https://orcid.org/0000-0002-0799-8411
Figures
Abstract
Background
The association between obesity and fracture risk may be skeletal site- and sex-specific but results among studies are inconsistent. Whilst several studies reported higher bone mineral density (BMD) in patients with obesity, altered bone quality could be a major determinant of bone fragility in this population.
Objectives
This systematic review and meta-analysis aimed to compare, in men, premenopausal women and postmenopausal women with obesity vs. individuals without obesity: 1) the incidence of fractures overall and by site; 2) BMD; and 3) bone quality parameters (circulating bone turnover markers and bone microarchitecture and strength by advanced imaging techniques).
Data sources
PubMed (MEDLINE), EMBASE, Cochrane Library and Web of Science were searched from inception of databases until the 13th of January 2021.
Data synthesis
Each outcome was stratified by sex and menopausal status in women. The meta-analysis was performed using a random-effect model with inverse-variance method. The risks of hip and wrist fracture were reduced by 25% (n = 8: RR = 0.75, 95% CI: 0.62, 0.91, P = 0.003, I2 = 95%) and 15% (n = 2 studies: RR = 0.85, 95% CI: 0.81, 0.88), respectively, while ankle fracture risk was increased by 60% (n = 2 studies: RR = 1.60, 95% CI: 1.52, 1.68) in postmenopausal women with obesity compared with those without obesity. In men with obesity, hip fracture risk was decreased by 41% (n = 5 studies: RR = 0.59, 95% CI: 0.44, 0.79). Obesity was associated with increased BMD, better bone microarchitecture and strength, and generally lower or unchanged circulating bone resorption, formation and osteocyte markers. However, heterogeneity among studies was high for most outcomes, and overall quality of evidence was very low to low for all outcomes.
Citation: Turcotte A-F, O’Connor S, Morin SN, Gibbs JC, Willie BM, Jean S, et al. (2021) Association between obesity and risk of fracture, bone mineral density and bone quality in adults: A systematic review and meta-analysis. PLoS ONE 16(6): e0252487. https://doi.org/10.1371/journal.pone.0252487
Editor: Tuan Van Nguyen, Garvan Institute of Medical Research, AUSTRALIA
Received: January 19, 2021; Accepted: May 15, 2021; Published: June 8, 2021
Copyright: © 2021 Turcotte et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files. The protocol of this systematic review and meta-analysis has been registered in the Prospective Register of Systematic Reviews (PROSPERO) (registration number: CRD42020159189).
Funding: No authors received specific funding for this work. AFT received a doctoral scholarship from the Fonds de recherche du Québec-Santé (FRQ-S) (2019-2020) and the Canadian Institutes for Health Research (CIHR) (2020-2023). SO received a doctoral scholarship from the FRQ-S (2019-2020) and CIHR (2020-2024). CG is a scholar from the FRQ-S and a recipient of a New investigator award from Diabetes Canada. JG is a recipient of a Natural Sciences and Engineering Research Council (NSERC) Discovery Grant and Early Career Researcher Launch Supplement. BW is supported by the Shriners Hospitals for Children and is a scholar from the FRQ-S. SNM is a scholar from the FRQ-S.
Competing interests: No authors have competing interests.
Introduction
The incidence of fractures has been predicted to increase as the population is aging worldwide [1, 2]. Osteoporotic fractures are associated with excess mortality [3–5] in addition to being amongst the most frequent causes of disability and morbidity worldwide [6]. Consequently, fractures impose a financial burden on society in direct medical costs and indirect costs, which are projected to increase to $25.3 billion by 2025 in the United States [7]. Although the overall prevalence of fragility fractures is higher in women (especially in postmenopausal women) [8, 9], men generally have higher rates of fracture-related mortality [3].
Several clinical risk factors besides age, sex and menopausal status are known to affect fracture risk including a low body mass index (BMI) [10, 11]. Conversely, it still remains uncertain whether obesity is protective or not against fractures [12, 13]. Since obesity is projected to affect more than 50% of the population by 2030 [14, 15], it is imperative to determine how obesity should be considered in fracture risk assessment. The relationship between obesity and the risk of fracture is complex and appears to vary depending on skeletal site [16, 17], and may differ in men and women [11]. For example, a previous meta-analysis of the association of fracture risk and BMI in 398,610 women revealed that low BMI was a risk factor for hip and all osteoporotic fractures, but was a protective factor for lower leg fracture, whereas high BMI was a risk factor for humerus and elbow fractures [18].
Moreover, whilst numerous studies have consistently shown that areal bone mineral density (aBMD) is higher in patients with obesity [19], it appears that altered bone quality may be a major determinant of fracture risk in this population. Bone quality comprises bone microarchitecture, bone remodeling and bone tissue material properties, which includes bone strength, fracture toughness and fatigue strength. Bone strength can also be estimated through finite element analysis, which predicts bone resistance to stresses and strains. In recent years, few studies have evaluated the impact of obesity on bone microarchitecture and strength using advanced imaging techniques, such as peripheral quantitative computed tomography (pQCT) and high resolution-pQCT (HR-pQCT) [20–22]. Some studies also reported lower bone turnover in obesity, with a predominance of reduced bone formation over bone resorption [23, 24]. Besides, some studies also used obesity criteria other than BMI to assess the association between obesity and bone fragility [25–27]. Furthermore, coexistence of obesity with type 2 diabetes, which has also been associated with an increased risk of fracture [19], deteriorated bone microarchitecture (e.g., increased cortical porosity) and altered bone turnover [19, 28], may further impair bone health in individuals with obesity.
Previously published meta-analyses on the relationship between obesity and the risk of fractures targeted only women [18], hip fractures [29, 30], vertebral fractures [31], or overall fractures [32]. Moreover, no meta-analysis assessed whether bone quality parameters differ between adults with or without obesity. It is thus timely to summarize the available evidence and provide a more complete picture of bone health and fracture risk in men and women with obesity. The aims of this systematic review and meta-analysis were to compare, in men, premenopausal women and postmenopausal women with obesity vs. without obesity: 1) the incidence of fractures overall and by site; 2) BMD; and 3) bone quality parameters (i.e. bone microarchitecture and strength by advanced imaging techniques and circulating bone turnover markers). Secondary aims were to investigate whether the presence of type 2 diabetes in people with obesity further affects fracture risk, BMD and bone quality parameters.
Materials and methods
Protocol and registration
We conducted this systematic review using the Cochrane review methodology [33], and reported our results according to the Preferred reporting items for systematic review and meta-analysis (PRISMA) [34]. The protocol was registered with the Prospective Register of Systematic Reviews (PROSPERO) on 28th April 2020 (registration number: CRD42020159189). Eligibility criteria and analysis were detailed and documented in the protocol. They are also described in the following sections of the manuscript.
Eligibility criteria
Eligibility criteria were defined using an adaptation of the PICOS approach (Population, Exposure, Comparator, Outcomes and Study design) [34].
Population.
The study population were men and women of any ethnicity or setting. Only studies that included a majority of adults (i.e. at least 80% of the sample was aged 18 years or older, which is an arbitrary criterion commonly used in systematic reviews) [33] were selected, as findings among the paediatric population may be distinct due to ongoing bone development [35]. Studies including only individuals who experienced a fracture at baseline or had a joint replacement were excluded.
Exposure.
Studies were included when the exposure group was composed of individuals with obesity, characterized by an excessive fat accumulation that presents a risk to health. Any definition of obesity provided by the authors was considered. When multiple BMI categories were used, we used 25 kg/m2 for threshold between obese/non-obese groups. Therefore, when results were reported for obese, overweight and normal-weight individuals, obese and overweight individuals were combined in the “obesity” exposure group. Studies comparing equal categories (tertiles, quartiles or quintiles) were excluded since the ranges used were not comparable.
Comparator.
Studies were included when the comparison group was composed of individuals without obesity. Any definition provided by the authors was considered.
Outcomes.
The primary outcomes were incident fractures at any or specific skeletal sites, that were either self-reported or confirmed by imaging. Secondary outcomes were: 1) aBMD at the total hip, femoral neck, lumbar spine and radius as well as volumetric BMD (vBMD) at the tibia and radius; 2) bone microarchitecture parameters [cortical thickness, cortical porosity, trabecular number, trabecular separation and trabecular connectivity, finite element modeling (FEM) estimated bone strength (failure load and stiffness) by pQCT or HR-pQCT]; and 3) circulating bone turnover markers [C-terminal telopeptide (CTX), N-terminal telopeptide (NTX), procollagen type 1 intact N-terminal propeptide (P1NP), osteocalcin and sclerostin]. Bone specific alkaline phosphatase, 25-hydroxyvitamin D and parathyroid hormone were not considered.
Study design.
For fracture outcomes, only studies using a prospective follow-up were considered; experimental studies with an intervention (e.g. nutrition, physical activity, bariatric surgery, pharmacotherapy, etc.) were excluded. For BMD, bone microarchitecture parameters and circulating bone turnover markers, all quantitative study designs, namely cross-sectional studies, cohort studies, clinical trials, case-control studies, retrospective studies, experimental studies and interrupted time series were considered. In longitudinal studies, only the baseline data were considered for secondary outcomes. Qualitative and descriptive studies, reviews, conference abstracts, letters to the editor or other non-peer reviewed publications were also excluded.
Search strategy
Studies were identified by searching electronic databases, scanning the reference list of included studies and consulting experts in the field. The search was applied to PubMed (MEDLINE), EMBASE, Cochrane Library and Web of Science from inception of databases until the 1st of November 2019. The search was then updated on the 13th of January 2021 to ensure the most up-to-date review of the literature.
The search strategy (S1 Table) was revised by an information specialist (F. Bergeron) at Laval University, Québec City. Highly-sensitive and precision maximizing filters from the Evidence-Based Medicine (EBM) Toolkit form BMJ Best Practice were used for study design in PubMed and EMBASE [36]. No restriction was imposed on publication date, publication status or language. Results from the different databases were merged and duplicates were manually removed using EndNote X8.2 (Clarivate Analytics) reference software when the title, authors, journal and year of publication were identical.
Study selection
Pilot testing was performed prior to the study selection process. Two reviewers (AFT and SO) independently screened titles and abstracts in duplicate to identify irrelevant manuscripts. Afterwards, eligibility assessment was performed independently by AFT and SO, in duplicate, using full-text reports. The eligibility process was conducted in an adapted electronic data collection form determined a priori and containing the inclusion and exclusion criteria described above. Multiple publications from the same studies were clustered. In case of uncertainty, AFT and SO deliberated to find consensus. In case of disagreement, a third reviewer (CG) was invited to the discussion. We assessed inter-reviewer agreement for full text selection using the kappa statistic. A kappa value of 0–0.20 was considered as no agreement, 0.21–0.39 was considered minimal agreement, 0.40–0.59 was considered weak agreement, 0.60–0.79 was considered moderate agreement, 0.80–0.90 was considered strong agreement, and 0.90 and above was considered perfect agreement [37]. The same selection process was used for the initial search and the update. A flow diagram (Fig 1) from the PRISMA statement [34] was generated to map out the study selection process.
Data extraction
A data collection form, adapted from the Data collection form for RCTs from Cochrane Airways and the Cochrane Handbook of Systematic Reviews of Intervention [38], was used. Pilot testing was performed on ten randomly-selected included studies, prior to the data extraction and amendments were made consequently. Data from the included studies were extracted independently in duplicate by AFT and SO. Disagreements were resolved by discussion between the two reviewers. CG was invited to the discussion if no agreement could be reached. In case of duplicate reporting, the reports with the largest number of participants were used. We tried to retrieve the missing data from the corresponding authors by sending emails twice. We contacted 8 authors for further information, among whom 3 authors responded.
A codification guide was generated to ensure the accuracy of the extraction process by the two reviewers. The following information was extracted from each included study: 1) study publication information (name of first author, year of publication, country of population); 2) population characteristics (total sample size, follow-up length (for fracture outcome only), size of exposure group, size of comparator group, mean age, sex, ethnicity, menopausal status, number of participants with type 2 diabetes, number of participants with a history of fracture, comorbidities or diseases affecting the participants and number of participants using medications known to affect bone metabolism); 3) exposure and comparator characteristics (group name, definition used); 4) outcomes characteristics (name of the outcome, reporting method for fractures (self-reported or confirmed), measurement tool and units of measurement); 5) measure of effect (type of effect, crude effect amplitude, crude 95% confidence interval and p-value, adjusted effect amplitude, covariates used in the adjusted model, adjusted 95% confidence interval and p-value). Two variables related to bone quality that provide information on bone strength, the estimated failure load and stiffness, were added after the beginning of the data extraction process. As those variables are estimated using finite element analysis, based on images captured by pQCT and HR-pQCT, we assumed they were already considered in the search strategy.
Quality assessment
To verify the internal validity of included studies, AFT and SO independently assessed the risk of bias for each individual study. The Newcastle-Ottawa Scale (NOS) was used to evaluate the risk of bias for case-control and cohort studies [39]. The NOS tool assesses the quality of selection (4 items, 1 point each), comparability (1 item, 2 points) and outcome (3 items, 1 point each) of studies. The NOS tool generates a total score ranging from 0 (worst score) to 9 (best score). A score of 7 and above was considered low risk of bias, a score of 4–6 was considered moderate risk of bias and a score under 4 was considered high risk of bias [40]. The Joanna Briggs Institute (JBI) tool was used to assess the risk of bias for cross-sectional studies and for longitudinal studies from which we used cross-sectional data [41]. For each item, answers were either “Yes”, “No”, “Unclear” or “Not applicable”. Scores ranged from 0 (worst score) to 8 (best score) and studies were judged as low risk of bias when the scores were above 6, moderate risk of bias when scores were between 4 and 6 and high risk of bias when scores were 3 or under [42]. Pilot testing was made on ten randomly-selected included studies to confirm adequate reliability prior to the risk of bias assessment, and amendments were made subsequently. Selection bias for each study was evaluated by verifying the eligibility criteria and selection of participants into the study. Confounding bias was assessed by evaluating if a confounding domain has not been measured at all or was not controlled for in the analysis. Information bias was evaluated by verifying if the exposure status was misclassified, if bias is introduced due to missing data, or if outcomes were misclassified or measured with error. Disagreements between AFT and SO were resolved by consensus.
Statistical analyses
Descriptive analyses were completed to report characteristics of included studies, based on the PICOS approach. Moreover, descriptive synthesis was made for outcomes for which a meta-analysis could not be performed. Each outcome was evaluated comparing individuals with versus without obesity. When studies used different measures of effect size for an outcome, a transformation was performed whenever possible to enable comparison and combination of the studies for the meta-analysis. Relative risk (RR) with 95% confidence interval (CI) were used for fracture outcome. Mean differences (MD) with 95% CI were used to compare BMD at each bone site and bone quality parameters between the exposure and comparator groups. The meta-analysis was performed using a random-effect model with inverse-variance method, following the Cochrane review methodology for data analysis recommendations [43, 44]. For each outcome, estimates of the effect measure with their 95% CI are illustrated in forest plots.
All statistical analyses were performed with Review Manager software [45]. Each outcome was stratified based on sex and menopausal status (men, premenopausal women, postmenopausal women) since there are major differences in bone metabolism and risk of fracture between those populations [11, 31]. We included in the men or women’s groups a mixed population when composed of at least 70% of either men or women. This arbitrary cut-off was chosen to minimise heterogeneity while maximizing statistical power within each group. When a mixed population included less than 70% of either men or women, men and women were combined and reported in a category called “studies combining men and women”. In studies with multiple categories of obesity, we pooled groups together to allow comparison. We tested for heterogeneity with the I2 statistic to measure inconsistency of the effects between studies [46]. I2 over 50% was considered substantial heterogeneity and I2 over 75% was considered considerable heterogeneity [47]. To explore potential causes of heterogeneity, subgroup analyses were planned a priori, and based on obesity cut-off criteria (as above, obesity criteria or overweight criteria according to the World health organization classification44), type 2 diabetes status (according to the author’s definition), studies including or not individuals with comorbidities or use of medication known to affect bone metabolism, and overall risk of bias (low, moderate, high). After extraction of the data, only subgroup analyses based on obesity cut-off criterion and risk of bias were conducted since insufficient information on type 2 diabetes, presence of disease or use of medication was reported in these studies to allow analysis. A p-value <0.05 was considered statistically significant.
Risk of bias across studies
Publication bias was assessed by visual evaluation of funnel plots [48, 49] produced by Review Manager software [45]. We evaluated the study mean differences for asymmetry, which can result from the non-publication of small studies with negative results. Quality of evidence for each outcome was assessed according to the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach [50]. The GRADE approach defines the quality of evidence based on within-study risk of bias (methodological quality), directness of evidence, heterogeneity, precision of effect estimates and risk of publication bias.
Additional analyses
Sensitivity analyses were conducted to explore the robustness and accuracy of the results. To do so, studies were removed one at a time to explore how each study individually influenced the global estimate [51]. Sensitivity analysis based on the definition of exposure (BMI vs other obesity measures) could not be performed as the number of studies using measures other than BMI to define the exposure and comparator groups was too small.
Results
Study selection
The study selection process is described in Fig 1. We identified 14,741 citations through databases and screened 9,455 after the removal of duplicates. From those, 8,914 were discarded based on the title and abstract as they did not meet the eligibility criteria. Fifty-four studies were also discarded because the full-text was not available. The full-text of the remaining 487 reports was assessed for eligibility: 353 studies were excluded, leaving 134 for inclusion in the systematic review [20–22, 25, 52–181]. All included studies were in English or French. The kappa statistic was 0.82, displaying a strong inter-reviewer agreement for the full-text selection. Finally, 121 studies were included in the meta-analysis [20–22, 25, 52–153, 163–167, 169, 171–173, 175, 177–181]: 13 [154–162, 168, 170, 174, 176] were excluded because data was missing, could not be transformed, or could not be obtained from corresponding authors.
Study characteristics
Study characteristics of the included studies are presented in Table 1 (fracture), Table 2 (aBMD and vBMD), Table 3 (bone microarchitecture parameters) and S2 Table (circulating bone turnover markers). Moreover, S3 Table describes the methods used for measurement of bone turnover markers. All of the included studies were published between 1987 and 2021. Eighty-six studies selected for the review were cross-sectional studies, 34 were prospective cohort studies, 11 were case-control studies and 3 were epidemiological studies. Fifty-one studies were from Europe, 42 from Asia, 20 from North America, 8 from South America, 5 from Africa and 8 from Oceania. Fifty-six studies were conducted in postmenopausal women, 46 in a mixed population of men and women, 20 in premenopausal women and 12 in men. The studies included in this systematic review involved a total of 5,450,315 participants, including 2,798,344 individuals with obesity and 2,651,971 individuals without obesity. The mean age of the participants ranged between 18.2 and 78.3 years. Some information could not be retrieved from most of the studies such as the number of participants using medication or having comorbidities or diseases known to affect bone metabolism (e.g. diabetes), and the number of individuals with a history of fracture.
Risk of bias within studies
The risk of bias assessment results for included studies are presented in Tables 1–3 and S2. The overall risk of bias was considered “low” for 57 studies, “moderate” for 69 studies and “high” for 8 studies. The main criteria that were not reached for cross-sectional studies were: “the study subjects and setting described in detail” and “strategies to deal with confounding factors stated”. In cohort studies, the quality criteria that received the lowest score were: “demonstration that outcome of interest was not present at start of study” and “was follow-up long enough for outcomes to occur”.
Results of individual studies
Summary data of individual outcomes for each study are presented using forest plots (Figs 2–4 and S1–S8). Results from subgroup analyses for BMD and circulating bone turnover markers outcomes are presented in S4 Table.
Forest plot of pooled effect size for the risk of fracture at any site in A) postmenopausal women, B) premenopausal women, and C) men with vs. without obesity, using a random-effect model.
Forest plot of pooled effect size for the risk of hip fracture in A) postmenopausal women and B) men with vs. without obesity, using a random-effect model.
Forest plot of pooled effect size for the total hip aBMD by DXA mean difference between A) postmenopausal women, B) premenopausal women and C) men with vs. without obesity, using a random-effect model.
Syntheses of results
Association between obesity and risk of fractures.
Any fracture. Fracture data was available in 20 studies [25, 55, 66, 82, 83, 90, 98, 99, 112, 116, 117, 125, 127, 132, 133, 137, 140, 144, 164, 169], totalizing 3,582,437 participants in whom 60,754 fracture events occurred during a mean follow-up of 6.6 years. In the pooled analysis, obesity was associated with a lower risk of fracture in postmenopausal women (n = 12: RR = 0.86, 95% CI: 0.77, 0.97, P = 0.02, I2 = 97%) and men (n = 9: RR = 0.77, 95% CI: 0.64, 0.93, P = 0.006, I2 = 91%). No association between obesity and risk of fracture at any site in premenopausal women was found (n = 2: RR = 1.16, 95% CI: 0.80, 1.67, P = 0.43, I2 = 81%) (Fig 2). Moreover, there was no association between obesity and risk of fracture in studies combining men and women (n = 4: RR = 0.97, 95% CI: 0.72, 1.31, P = 0.84, I2 = 96%). Subgroup analyses did not explain the heterogeneity within groups.
Hip fracture. Hip fracture data was available in 11 studies [55, 66, 82, 99, 116, 117, 127, 137, 140, 144, 164], including 1,911,715 participants in whom 16,055 fracture events occurred during a mean follow-up length of 7.9 years. Obesity was associated with a lower risk of hip fracture in postmenopausal women (n = 8: RR = 0.75, 95% CI: 0.62, 0.91, P = 0.003, I2 = 95%) and men (n = 5: RR = 0.59, 95% CI: 0.44, 0.79, P = 0.0004, I2 = 91%) (Fig 3), but not in studies combining men and women (n = 2: RR = 0.98, 95% CI: 0.55, 1.76, P = 0.96, I2 = 94%). Hip fracture data was not available for studies involving premenopausal women. Subgroup analyses did not explain the heterogeneity within groups.
Clinical vertebral fracture. Three studies reported clinical vertebral fractures in postmenopausal women [25, 66, 144], totalizing 315,136 participants in whom 1,694 fracture events occurred during a mean follow-up length of 6.6 years. These studies revealed that obesity was not associated with clinical vertebral fracture risk (S1 Fig). Subgroup analyses could not be performed.
Upper limb fracture. Two studies reported wrist and forearm fractures [55, 66, 144], including a total of 1,200,573 participants in whom 10,681 fracture events happened during a mean follow-up length of 5.7 years. Studies were conducted in postmenopausal women and showed an association between obesity and a reduced risk of wrist fracture (n = 2: RR = 0.85, 95% CI: 0.81, 0.88, P<0.00001, I2 = 0%) (S1 Fig). No difference between groups was observed for forearm fracture (n = 2). Subgroup analyses could not be performed. Meta-analysis could not be performed on humerus fracture since only one included study specifically assessed this site. This study reported that high BMI was a risk factor for humerus fracture in postmenopausal women [144].
Lower limb fracture. Ankle fracture risk was reported in two studies [55, 66], including 1,198,360 participants in whom 7,221 fracture events arose during a mean follow-up length of 5.4 years. Studies included postmenopausal women and showed that obesity was associated with an increased risk of ankle fracture (RR = 1.60, 95% CI: 1.52, 1.68, P<0.00001, I2 = 0%) (S1 Fig). Subgroup analysis could not be performed. Moreover, meta-analysis could not be performed on either tibia/fibula or femur (non-hip) fracture. Yet, one study reported an increased risk of upper leg fracture in postmenopausal women with obesity [17].
Association between obesity and BMD.
Total hip aBMD by DXA. Total hip aBMD by DXA was reported in 33 studies [21, 52, 54, 56, 58, 68, 70, 71, 87, 89, 93, 96, 97, 107, 110–114, 117, 118, 130, 132, 133, 143, 148, 151–153, 163, 173, 178, 179], including 29,279 participants. Obesity was associated with a higher total hip aBMD in postmenopausal women (n = 12: MD = 0.11 g/cm2, 95% CI: 0.08, 0.13, P<0.00001, I2 = 96%), premenopausal women (n = 9: MD = 0.08 g/cm2, 95% CI: 0.06, 0.10, P<0.00001, I2 = 91%), men (n = 9: MD = 0.07 g/cm2, 95% CI: 0.05, 0.09, P<0.00001, I2 = 82%), and in studies combining men and women (n = 7: MD = 0.09 g/cm2, 95% CI: 0.07, 0.11, P<0.00001, I2 = 77%) (Fig 4). Subgroup analyses did not explain the heterogeneity within groups.
Femoral neck aBMD by DXA. Femoral neck aBMD by DXA was reported in 48 studies [52, 54, 56, 58–60, 67–72, 84, 85, 88, 89, 92, 93, 96, 97, 101, 103, 106–108, 110–114, 118, 120, 121, 124, 128, 130, 142, 144, 148–153, 167, 173, 177, 180, 181], including 30,577 participants. Obesity was associated with increased femoral neck aBMD in postmenopausal women (n = 21: MD = 0.06 g/cm2, 95% CI: 0.05, 0.08, P<0.00001, I2 = 90%), premenopausal women (n = 13: MD = 0.05 g/cm2, 95% CI: 0.03, 0.07, P<0.00001, I2 = 92%), men (n = 8: MD = 0.05 g/cm2, 95% CI: 0.03, 0.07, P<0.00001, I2 = 79%), and in studies combining men and women (n = 7: MD = 0.07 g/cm2, 95% CI: 0.04, 0.10, P<0.00001, I2 = 77%) (S2 Fig). Subgroup analyses did not explain the heterogeneity within groups.
Lumbar spine aBMD by DXA. Lumbar spine aBMD measured by DXA was reported in 56 studies [20–22, 52, 54, 56, 59–61, 67–72, 78, 81, 84, 85, 87–89, 92–94, 97, 100, 103, 106–108, 110, 112–115, 118, 120, 121, 124, 126, 128, 130–132, 134, 135, 142–144, 148, 150–153, 163, 167, 173, 177–181], including 29,420 participants. Obesity was associated with increased lumbar spine aBMD in postmenopausal women (n = 27: MD = 0.07 g/cm2, 95% CI: 0.05, 0.09, P<0.00001, I2 = 92%), premenopausal women (n = 17: MD = 0.07 g/cm2, 95% CI: 0.04, 0.09, P<0.0001, I2 = 90%), men (n = 8: MD = 0.06 g/cm2, 95% CI: 0.04, 0.08, P<0.00001, I2 = 48%), and in studies combining men and women (n = 12: MD = 0.06 g/cm2, 95% CI: 0.03, 0.08, P<0.00001, I2 = 93%) (S3 Fig). Subgroup analyses did not explain the heterogeneity within groups.
Radius aBMD by DXA. Radius aBMD measured by DXA was available in 16 studies [21, 58, 69, 70, 73, 75, 102, 106, 110, 121, 124, 138, 145, 165, 178, 179], including 10,008 participants. Obesity was associated with higher aBMD at the radius in postmenopausal women (n = 6: MD = 0.07 g/cm2, 95% CI: 0.05, 0.08, P<0.00001, I2 = 65%), premenopausal women (n = 10: MD = 0.03 g/cm2, 95% CI: 0.02, 0.04, P<0.00001, I2 = 84%) and men (n = 2: MD = 0.02 g/cm2, 95% CI: 0.01, 0.03, P<0.00001, I2 = 0%) (S4 Fig). Subgroup analyses did not explain the heterogeneity within groups.
Radius volumetric BMD (vBMD) by pQCT and HR-pQCT. The two studies that reported radius vBMD by pQCT in premenopausal women revealed no difference between those with or without obesity (S5 Fig) [122, 123].
Tibia vBMD by pQCT and HR-pQCT. Two studies reported tibia vBMD measured by pQCT, which included 331 premenopausal women [122, 123]. Similar to the radius vBMD findings by pQCT, obesity was not associated with any difference in tibia vBMD (S5 Fig) [122, 123].
Associations between obesity, bone microarchitecture and strength.
Radius cortical thickness by pQCT and HR-pQCT. Radius cortical thickness by pQCT was reported in two studies [122, 123], which included 163 premenopausal women. Those studies did not reveal any association between radius cortical thickness and obesity (S6 Fig).
Tibia cortical thickness by pQCT and HR-pQCT. Three studies reported tibia cortical thickness by pQCT [95, 122, 123] in premenopausal women and found no difference between premenopausal women with and without obesity (S6 Fig).
Radius and tibia cortical porosity by HR-pQCT. Three studies excluded from the meta-analysis reported radius and tibia cortical porosity by HR-pQCT [20–22]. At both sites, cortical porosity was lower in postmenopausal women with obesity compared to women without obesity [21]. Another study revealed significantly lower cortical porosity at the tibia in men aged 55–75 years and postmenopausal women with obesity, whereas no significant difference was observed at the radius [22]. In the third study, cortical porosity at the radius and tibia was not different between individuals with or without obesity in a mixed population of men and women (mean age 41 years, 66.7% women) [20].
Radius and tibia trabecular number and trabecular separation by HR-pQCT. The same studies reported radius and tibia trabecular number and trabecular separation by HR-pQCT [20–22]. Radius trabecular number was significantly greater in individuals with obesity in all studies, whereas radius trabecular separation was significantly lower in postmenopausal women [21, 22], men and premenopausal women with obesity [22], compared controls without obesity. Moreover, tibia trabecular number was significantly greater, and trabecular separation was significantly lower in men [22], pre- and postmenopausal women [21, 22], and in a mixed population of men and women with obesity (mean age 41 years, 66.7% women) [20].
Radius and tibia estimated stiffness and failure load by HR-pQCT. The same studies also reported radius and tibia estimated stiffness and failure load by HR-pQCT [20–22]. At the radius, the estimated stiffness was higher in postmenopausal women [21, 22] and men aged 55–75 years with obesity [22], whereas no difference was observed in premenopausal women and in younger men aged 25–40 years [22]. Nevertheless, the estimated failure load at the radius was greater for men [22], pre- and postmenopausal women with obesity [21, 22]. At the tibia, both the estimated stiffness and failure load were higher in postmenopausal women [21, 22], premenopausal women and men with obesity [22]. However, the study conducted in a mixed population of men and women found no difference between individuals with and without obesity for both the radius and tibia estimated stiffness and failure load (mean age 41 years, 66.7% women) [20].
Association between obesity and circulating bone turnover markers.
P1NP levels. P1NP levels were reported in 13 studies [21, 22, 64, 70, 88, 104, 112, 118, 129, 139, 146, 147, 153], including 5,808 participants. Obesity was associated with lower P1NP levels in studies combining men and women (n = 5: MD = -7.66 ng/ml, 95% CI: -13.36, -1.96, P = 0.008, I2 = 68%), but not in postmenopausal women (n = 8) (S7 Fig). Subgroup analyses did not explain the heterogeneity within groups.
Total osteocalcin levels. Total osteocalcin levels were reported in 29 studies [21, 53, 60, 62–65, 68, 74, 76, 77, 80, 81, 84, 92, 97, 105, 107, 119, 126, 129, 135, 144, 146, 147, 151, 153, 166, 175], including 6,332 participants. Obesity was not associated with any difference in osteocalcin levels between individuals with and without obesity (S7 Fig), except in studies combining men and women (n = 9: MD = -3.86 ng/ml, 95% CI: -6.78, -0.95, P = 0.009, I2 = 97%). Subgroup analyses did not explain the heterogeneity within groups.
CTX levels. CTX levels were reported in 21 studies [21, 22, 60, 63, 64, 68, 70, 81, 86, 88, 91, 97, 104, 107, 112, 118, 129, 139, 146, 147, 171], including 10,375 participants. Obesity was associated with reduced CTX levels in postmenopausal women (n = 12: MD = -0.08 ng/ml, 95% CI: -0.12, -0.04, P<0.0001, I2 = 75%) (S8 Fig) and in studies combining men and women (n = 9: MD = -0.08 ng/ml, 95% CI: -0.12, -0.04, P<0.0001, I2 = 74%). Subgroup analyses did not explain the heterogeneity within groups.
Urinary NTX levels. Urinary NTX levels were reported in 5 studies [79, 135, 144, 153, 182], including 3,329 participants. No difference between individuals with and without obesity was observed in postmenopausal women (n = 3) (S8 Fig) and in studies with a mixed population (n = 2). No subgroup analyses were performed.
Sclerostin levels. Sclerostin levels were reported in 3 studies [53, 57, 79], including 380 participants. In those studies, no difference between individuals with and without obesity was observed. No subgroup analyses were performed.
Risk of bias across studies and quality of evidence
Strong evidence of heterogeneity was observed between studies for the majority of the outcomes. Publication bias for all outcomes were assessed using funnel plots (S9–S19 Figs). We saw no evidence of asymmetry; therefore, no publication bias was detected. Publication bias could only be assessed for the outcomes that had a sufficient sample size [49]: fracture at any site in postmenopausal women and men, hip fracture in postmenopausal women, total hip aBMD in postmenopausal women, femoral neck aBMD in postmenopausal and premenopausal women, lumbar spine aBMD in postmenopausal women, premenopausal women and in studies with a mixed population of men and women, osteocalcin levels and CTX levels in postmenopausal women. The quality of evidence assessed following the GRADE approach was considered very low for all fracture outcomes except for wrist fracture in postmenopausal women, where the quality of evidence was considered low. The quality of evidence was also considered low for lumbar spine aBMD in men, radius and tibia vBMD by pQCT, radius and tibia cortical thickness by pQCT, and P1NP levels in premenopausal women. The quality of evidence was considered very low for all other outcomes. Of note, the quality of evidence was downgraded mainly because of the study design of included studies (which were not randomized controlled trials) and the inconsistency in results.
Heterogeneity exploration
When studies were removed from the analysis one at a time, we found one study [111] that had a strong effect on the heterogeneity for total hip aBMD in a mixed population of men and women. Indeed, we found that the study by Lloyd et al. [111] was responsible for the majority of the heterogeneity. When this study was removed from the pooled estimate, the Higgin’s I2 decreased from 80% to 1% and the pooled mean difference decreased from 0.09 to 0.08 g/cm2 (95% CI: 0.07, 0.09, P<0.00001). Even if the study by Lloyd et al. [111] was the main source of heterogeneity for this outcome, we decided to maintain this study in the analyses since it was not significantly affecting the pooled estimate, had a group with and without obesity with a similar proportion of men and women with comparable age, and a low risk of bias. However, potential explanation for the observed heterogeneity may be the higher prevalence of diabetes and proportion of black individuals in the group with obesity compared with the group without obesity, which are both known to be associated with higher BMD [183, 184]. Heterogeneity exploration was performed for all outcomes. However, no other study was found to have a strong effect on heterogeneity.
Discussion
Summary of evidence
One hundred and thirty-four studies totalizing more than 5 million individuals were included in this systematic review, of which 121 studies were incorporated in the meta-analysis. Our results showed a significantly reduced risk of fracture in postmenopausal women and men with obesity compared with individuals without obesity. Assessment of fracture risk by anatomical site revealed that postmenopausal women with obesity had a lower risk of hip and wrist fracture by 25% and 15%, respectively, whilst ankle fracture risk was increased by 1.6-fold compared with postmenopausal women without obesity. Hip fracture risk was reduced by 41% in men with vs. without obesity. Finally, obesity was not associated with clinical vertebral fracture risk, but only a handful of studies assessed this outcome specifically, and it is not clear if ascertainment was complete in these studies. These results confirm that fracture risk varies by skeletal site in individuals with obesity, and also suggests that the impact of obesity on fracture differs in men and postmenopausal women. No conclusion could be drawn regarding the association between obesity and fracture incidence in premenopausal women given the small number of studies. Moreover, the impact of combined obesity and type 2 diabetes on fracture risk could not be assessed, as no study specifically addressed this question. High heterogeneity was observed between studies for most outcomes, which was not fully explained in subgroup or sensitivity analyses. Lastly, the overall quality of evidence based on the GRADE approach was very low to low for all outcomes, due to the study designs and risk of bias of the included studies, and the high heterogeneity between studies.
Regarding BMD and bone microarchitecture, the available evidence suggests favorable findings in people with obesity vs. controls without obesity. Indeed, aBMD by DXA was higher at the total hip, femoral neck, lumbar spine and radius in men, premenopausal women and postmenopausal women with obesity compared with their counterpart without obesity. Only two studies conducted in postmenopausal women as well as in premenopausal women and men found superior HR-pQCT-derived bone microarchitecture and strength in individuals with obesity compared with controls without obesity: tibia vBMD was greater, radius cortical thickness was higher, radius and tibia trabecular number were increased, trabecular separation was reduced, and estimated stiffness and failure load were increased. Finally, the bone resorption marker CTX was generally lower in people with obesity. However, conflicting results were reported for the bone formation markers P1NP and osteocalcin, with either no difference or lower levels in those with vs without obesity. In a limited number of studies, no difference between groups was observed in the osteocyte marker sclerostin. To the best of our knowledge, our meta-analysis is the first to evaluate, altogether, the relationship between obesity, fracture risk, BMD and bone quality parameters by sex and menopausal status.
Our finding of a decreased risk of hip fracture in men and postmenopausal women with obesity is consistent with a previous meta-analysis, which reported that high BMI is a protective factor for hip fracture in postmenopausal women [18], as well as in men and women of all age [29]. This fracture risk reduction is clinically significant since hip fractures are associated with the highest morbidity and mortality rates [1, 185], and impose a financial burden on society [7]. However, opposite to our results, another meta-analysis found that abdominal obesity is associated with a higher risk of hip fracture in men and women aged 40 years and older [30]. These conflicting results may be explained by the fact that the majority of the studies included in our meta-analysis and previous meta-analyses focused on general obesity, mostly defined by BMI, rather than abdominal obesity. While abdominal obesity has been recognized as a stronger risk factor of metabolic disorders than BMI, this may also be the case for bone fragility [186, 187]. Abdominal obesity is associated with greater insulin resistance as well as systemic inflammation and oxidative stress [188, 189], increased circulating inflammatory cytokines, and altered levels of bone-regulating hormones [190], which are all known to adversely affect bone metabolism. Moreover, using BMI as a measure of adiposity has been shown to be less accurate in older adults due to change in body composition associated with aging [191]. Altogether, those with abdominal obesity may have a distinct fracture risk pattern, highlighting the necessity to consider abdominal obesity when assessing fracture risk in adults [25].
In addition, type 2 diabetes, which frequently coexists with obesity, may further impact fracture risk. Indeed, many studies reported increased risk of hip and non-vertebral fracture in individuals with type 2 diabetes [19, 192]. However, studies considering presence of type 2 diabetes in the association between obesity and fracture risk are limited: most studies used type 2 diabetes as an adjustment factor and did not assess whether the presence of type 2 diabetes modifies the association between obesity and fracture incidence.
Our meta-analysis supports that the association between obesity and risk of fracture is skeletal site-specific. This is also supported by another meta-analysis which found that obesity was a risk factor of lower limb fracture and upper arm fracture (humerus and elbow) in women of all age [18]. Reasons for this site-specific association are still not completely understood, but it appears that specific bone sites may require enhancement of different material properties to resist fracture depending on the predominant failure mechanism at that site [193]. Thus, the hip and wrist in individuals with obesity may be more protected from fracture due to the increased BMD which improves bone strength, while sites such as the vertebrae or lower limbs fracture via other failure mechanisms, which require enhancement in other material properties (i.e. fatigue strength and fracture toughness). Although individuals with obesity are more likely to fall due to reduced mobility, postural control and protective responses [194, 195], and even weakened psychomotor abilities [196], soft tissue padding around the hip area may allow energy dissipation after trauma or a fall, subsequently contributing to the protective effect of obesity against hip fracture [197]. Moreover, a different falls pattern may exist between individuals with and without obesity, as individuals with obesity are more likely to fall backward or sideways, rather than forward [196]. Therefore, wrists are less exposed to trauma, which may explain the reduced risk of fracture at this site. Another possible explanation is that ankles are not protected by adipose tissue padding, and have to support greater body weight when falling, perhaps explaining the increased risk of fracture at these sites. Besides, higher body weight increases the impact forces during the fall.
Another goal of this meta-analysis was to evaluate differences in BMD, bone microarchitecture and bone remodeling markers between adults with and without obesity to help understand the bone parameters involved in the obesity-associated bone fragility. To our knowledge, this is the first meta-analysis to address and quantify the differences in BMD and bone quality parameters in this population. Our results showed that overall, individuals with obesity have higher aBMD, vBMD (when assessed by HR-pQCT) and better bone microarchitecture and strength at all sites. However, conflicting results remain for cortical porosity, since either lower or similar cortical porosity was observed between individuals with and without obesity at both sites. In all studies, cortical porosity was measured using a first-generation HR-pQCT scanner, which limited the measurement to peripheral rather than diaphyseal sites of the radius and tibia, and it is known that cortical porosity has poor precision [198]. Moreover, one of the studies excluded participants with type 2 diabetes [22] whereas the other two studies did not mention the diabetes status of the population [20, 21]. Since cortical porosity has been shown to be increased in individuals with type 2 diabetes but decreased in obesity, it may explain, at least partly, the conflicting results for this outcome. Nevertheless, it is unknown whether the increase in BMD and bone strength as well as favorable bone microarchitecture seen in individuals with obesity is sufficient to resist the larger strains applied on bones during trauma or fall in the context of excess weight. Besides, it is difficult to make any definitive conclusions since only a limited number of studies compared these bone quality parameters using advanced imaging techniques in individuals with or without obesity. Finally, with regards to circulating bone turnover markers, our meta-analysis revealed significantly lower levels of the bone resorption marker CTX in individuals with obesity but results on the bone formation markers P1NP and osteocalcin were mixed. Potential causes for these inconsistent results are the heterogeneity of the populations included (i.e. diabetes status) and the preanalytical and analytical variability of the bone turnover markers measurements (i.e. fasting status and time of day of the measurement, measurement in serum or plasma, analysis in a single batch or not, type of assay).
Limitations and strengths
Our systematic review and meta-analysis has strengths, such as the exhaustive search strategy and number of outcomes investigated. Indeed, it included 134 studies, which allowed us to highlight the magnitude of the association between obesity and risk of any and site-specific fracture, and the difference in BMD, bone microarchitecture parameters and circulating bone remodeling markers between individuals with and without obesity, stratified by sex and menopausal status. The quality of all included studies was also assessed with validated quality assessment tools for cross-sectional, cohort and case-control studies. We carried out an extensive quality assessment for individual studies and for each outcome using the GRADE approach. We also investigated heterogeneity with subgroup analyses and performed sensitivity analyses.
Our meta-analysis has also limitations. First, conclusions could not be drawn with regards to fracture incidence in premenopausal women, in men (except for hip fracture), and for humerus, tibia/fibula and femur (non-hip) fracture incidence in postmenopausal women. Second, high heterogeneity was observed between the included studies, which was not totally explained in subgroup analyses. The inclusion of studies using a cut-off of 70% of men and pre- and postmenopausal women to categorize groups by sex and menopausal status may have increased heterogeneity within groups. Heterogeneity may also be the result of the combination of obese with overweight individuals in some studies as well as of a wide range of BMI across studies. Unfortunately, we could not perform subgroup analyses based on BMI categories, as very few studies classified the obese group based on BMI obesity categories. Moreover, very few studies considered a different criterion for obesity than BMI, which does not necessarily follow the dose-response relationship between obesity and fracture risk. Therefore, using BMI as a criterion does not discriminate individuals who are at higher risk vs lower risk of fracture. Remaining heterogeneity may be related, at least partly, to the demographic diversity of the populations across studies (i.e., ethnicity, age and socioeconomic level), the presence of conditions or use of certain medications that may affect bone outcomes for some individuals (e.g. diabetes status), and the method used to report fractures (adjudicated or self-reported). Also, for fracture outcomes, adjustment for covariates and lengths of follow-up were not consistent across studies, and mechanism of fracture was not always reported (fragility vs. non-fragility fracture). Third, risk of vertebral fractures may have been underestimated since only clinical vertebral fractures were reported. Fourth, while type 2 diabetes often coexists with obesity and may further impair bone quality and reduce bone strength in this population, we have not been able to examine the association between obesity, with and without type 2 diabetes, on bone outcomes. Indeed, most studies only reported prevalence of participants with type 2 diabetes and used it as an adjustment factor in the statistical analyses. Fifth, only a few studies compared bone microarchitecture parameters in people with or without obesity. Finally, the inclusiveness of our analysis may be limited by the fact that studies reporting correlation analyses or relative or absolute measures of effect without the number of fracture events were not included.
Conclusions
In conclusion, we found that obesity is associated with higher bone mass and favorable bone microarchitecture while bone turnover, as assessed by circulating bone turnover markers, was either lower or similar to controls without obesity. Obesity was associated with a lower risk of fracture at the hip (in men and postmenopausal women) and at the wrist (in postmenopausal women) but with a higher risk of ankle fracture (in postmenopausal women). Results should however be interpreted with caution given the high heterogeneity among studies for most outcomes, and the low quality of evidence for all outcomes. Moreover, no conclusion could be drawn for premenopausal women and for certain fracture sites in all groups given the paucity of data. This meta-analysis highlights areas for future research including the need for site-specific fracture studies in premenopausal women with obesity, studies evaluating fracture sites other than the hip in men with obesity or comparing bone microarchitecture between pre- and postmenopausal women as well as men with and without obesity. It also emphasizes the need to standardize the assessment of bone turnover markers in research. Moreover, studies looking at the impact of fat distribution on bone outcomes may find obesity patterns that may be more susceptible to bone fragility, as defining obesity with BMI may not be specific enough to portray bone metabolism impairment in individuals with obesity. Finally, as type 2 diabetes often coexists with obesity and is a well-known risk factor for fracture, studies addressing specifically the impact of type 2 diabetes in this population are necessary.
Supporting information
S2 Table. Study characteristics of included studies for bone turnover markers outcome.
https://doi.org/10.1371/journal.pone.0252487.s003
(DOCX)
S3 Table. Assessment methods used for bone turnover markers.
https://doi.org/10.1371/journal.pone.0252487.s004
(DOCX)
S4 Table. Results of subgroup analysis by obesity and risk of bias criterion for bone mineral density and bone turnover markers outcomes in postmenopausal women, premenopausal women and men.
https://doi.org/10.1371/journal.pone.0252487.s005
(DOCX)
S1 Fig.
Forest plot of pooled effect size for the risk of A) clinical vertebral fracture, B) wrist fracture, C) forearm fracture and D) ankle fracture in postmenopausal women with vs. without obesity, using a random-effect model.
https://doi.org/10.1371/journal.pone.0252487.s006
(DOCX)
S2 Fig.
Forest plot of pooled effect size for the femoral neck aBMD by DXA mean difference between A) postmenopausal women, B) premenopausal women and C) men with vs. without obesity, using a random-effect model.
https://doi.org/10.1371/journal.pone.0252487.s007
(DOCX)
S3 Fig.
Forest plot of pooled effect size for the lumbar spine aBMD by DXA mean difference between A) postmenopausal women, B) premenopausal women and C) men with vs. without obesity, using a random-effect model.
https://doi.org/10.1371/journal.pone.0252487.s008
(DOCX)
S4 Fig.
Forest plot of pooled effect size for the radius aBMD by DXA mean difference between A) postmenopausal women, B) premenopausal women and C) men with vs. without obesity, using a random-effect model.
https://doi.org/10.1371/journal.pone.0252487.s009
(DOCX)
S5 Fig.
Forest plot of pooled effect size for the A) radius vBMD and B) tibia vBMD by pQCT mean difference between premenopausal women with vs. without obesity, using a random-effect model.
https://doi.org/10.1371/journal.pone.0252487.s010
(DOCX)
S6 Fig.
Forest plot of pooled effect size for the A) radius cortical thickness and B) tibia cortical thickness by pQCT mean difference between premenopausal women with vs. without obesity, using a random-effect model.
https://doi.org/10.1371/journal.pone.0252487.s011
(DOCX)
S7 Fig.
Forest plot of pooled effect size for A) P1NP levels mean difference between postmenopausal women with vs. without obesity, and total osteocalcin levels mean difference between B) postmenopausal women, C) premenopausal women and D) men with vs. without obesity, using a random-effect model.
https://doi.org/10.1371/journal.pone.0252487.s012
(DOCX)
S8 Fig.
Forest plot of pooled effect size for A) CTX levels and B) NTX levels mean difference between postmenopausal women with vs. without obesity, using a random-effect model.
https://doi.org/10.1371/journal.pone.0252487.s013
(DOCX)
S9 Fig. Funnel plot for fracture at any site in postmenopausal women.
https://doi.org/10.1371/journal.pone.0252487.s014
(DOCX)
S10 Fig. Funnel plot for fracture at any site in men.
https://doi.org/10.1371/journal.pone.0252487.s015
(DOCX)
S11 Fig. Funnel plot for hip fracture in postmenopausal women.
https://doi.org/10.1371/journal.pone.0252487.s016
(DOCX)
S12 Fig. Funnel plot for total hip aBMD in postmenopausal women.
https://doi.org/10.1371/journal.pone.0252487.s017
(DOCX)
S13 Fig. Funnel plot for femoral neck aBMD in postmenopausal women.
https://doi.org/10.1371/journal.pone.0252487.s018
(DOCX)
S14 Fig. Funnel plot for femoral neck aBMD in premenopausal women.
https://doi.org/10.1371/journal.pone.0252487.s019
(DOCX)
S15 Fig. Funnel plot for lumbar spine aBMD in postmenopausal women.
https://doi.org/10.1371/journal.pone.0252487.s020
(DOCX)
S16 Fig. Funnel plot for lumbar spine aBMD in premenopausal women.
https://doi.org/10.1371/journal.pone.0252487.s021
(DOCX)
S17 Fig. Funnel plot for lumbar spine aBMD in studies combining men and women.
https://doi.org/10.1371/journal.pone.0252487.s022
(DOCX)
S18 Fig. Funnel plot for osteocalcin levels in postmenopausal women.
https://doi.org/10.1371/journal.pone.0252487.s023
(DOCX)
S19 Fig. Funnel plot for CTX levels in postmenopausal women.
https://doi.org/10.1371/journal.pone.0252487.s024
(DOCX)
References
- 1. Strom O, Borgstrom F, Kanis JA, Compston J, Cooper C, McCloskey EV, et al. Osteoporosis: burden, health care provision and opportunities in the EU: a report prepared in collaboration with the International Osteoporosis Foundation (IOF) and the European Federation of Pharmaceutical Industry Associations (EFPIA). Archives of osteoporosis. 2011;6:59–155. pmid:22886101
- 2. Gullberg B, Johnell O, Kanis JA. World-wide projections for hip fracture. Osteoporosis international: a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA. 1997;7(5):407–13. pmid:9425497
- 3. Center JR, Nguyen TV, Schneider D, Sambrook PN, Eisman JA. Mortality after all major types of osteoporotic fracture in men and women: an observational study. Lancet (London, England). 1999;353(9156):878–82. pmid:10093980
- 4. Bliuc D, Nguyen ND, Milch VE, Nguyen TV, Eisman JA, Center JR. Mortality risk associated with low-trauma osteoporotic fracture and subsequent fracture in men and women. Jama. 2009;301(5):513–21. pmid:19190316
- 5. Morin S, Lix LM, Azimaee M, Metge C, Caetano P, Leslie WD. Mortality rates after incident non-traumatic fractures in older men and women. Osteoporosis international: a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA. 2011;22(9):2439–48. pmid:21161507
- 6. Melton LJ 3rd. Adverse outcomes of osteoporotic fractures in the general population. Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research. 2003;18(6):1139–41. pmid:12817771
- 7. Burge R, Dawson-Hughes B, Solomon DH, Wong JB, King A, Tosteson A. Incidence and economic burden of osteoporosis-related fractures in the United States, 2005–2025. Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research. 2007;22(3):465–75. pmid:17144789
- 8. Melton LJ 3rd, Chrischilles EA, Cooper C, Lane AW, Riggs BL. Perspective. How many women have osteoporosis? Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research. 1992;7(9):1005–10. pmid:1414493
- 9. Cawthon PM. Gender differences in osteoporosis and fractures. Clinical orthopaedics and related research. 2011;469(7):1900–5. pmid:21264553
- 10. Nielson CM, Srikanth P, Orwoll ES. Obesity and fracture in men and women: an epidemiologic perspective. Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research. 2012;27(1):1–10.
- 11. De Laet C, Kanis JA, Oden A, Johanson H, Johnell O, Delmas P, et al. Body mass index as a predictor of fracture risk: a meta-analysis. Osteoporosis international: a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA. 2005;16(11):1330–8. pmid:15928804
- 12. Dimitri P, Bishop N, Walsh JS, Eastell R. Obesity is a risk factor for fracture in children but is protective against fracture in adults: a paradox. Bone. 2012;50(2):457–66. pmid:21619952
- 13. Fassio A, Idolazzi L, Rossini M, Gatti D, Adami G, Giollo A, et al. The obesity paradox and osteoporosis. Eating and weight disorders: EWD. 2018;23(3):293–302. pmid:29637521
- 14. Finkelstein EA, Khavjou OA, Thompson H, Trogdon JG, Pan L, Sherry B, et al. Obesity and severe obesity forecasts through 2030. American journal of preventive medicine. 2012;42(6):563–70. pmid:22608371
- 15. Wang YC, McPherson K, Marsh T, Gortmaker SL, Brown M. Health and economic burden of the projected obesity trends in the USA and the UK. Lancet (London, England). 2011;378(9793):815–25. pmid:21872750
- 16. Prieto-Alhambra D, Premaor MO, Fina Aviles F, Hermosilla E, Martinez-Laguna D, Carbonell-Abella C, et al. The association between fracture and obesity is site-dependent: a population-based study in postmenopausal women. Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research. 2012;27(2):294–300. pmid:22095911
- 17. Compston JE, Watts NB, Chapurlat R, Cooper C, Boonen S, Greenspan S, et al. Obesity is not protective against fracture in postmenopausal women: GLOW. The American journal of medicine. 2011;124(11):1043–50. pmid:22017783
- 18. Johansson H, Kanis JA, Oden A, McCloskey E, Chapurlat RD, Christiansen C, et al. A meta-analysis of the association of fracture risk and body mass index in women. Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research. 2014;29(1):223–33. pmid:23775829
- 19. Walsh JS, Vilaca T. Obesity, Type 2 Diabetes and Bone in Adults. Calcified tissue international. 2017;100(5):528–35. pmid:28280846
- 20. Andersen SF K. D.; Hansen S.; Brixen K.; Gram J.; Stoving R. K. Bone Structure and Estimated Bone Strength in Obese Patients Evaluated by High-Resolution Peripheral Quantitative Computed Tomography. Calcified Tissue International. 2014;95(1):19–28. pmid:24736885
- 21. Sornay-Rendu EB S.; Vilayphiou N.; Claustrat B.; Chapurlat R. D. In obese postmenopausal women, bone microarchitecture and strength are not commensurate to greater body weight: the Os des Femmes de Lyon (OFELY) study. Exp Clin Endocrinol Diabetes. 2013;121(7):377–83. Epub 2013 Jul 9. pmid:23839538
- 22. Evans AL, Paggiosi MA, Eastell R, Walsh JS. Bone density, microstructure and strength in obese and normal weight men and women in younger and older adulthood. Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research. 2015;30(5):920–8. pmid:25400253
- 23. Cao JJ. Effects of obesity on bone metabolism. Journal of orthopaedic surgery and research. 2011;6:30. pmid:21676245
- 24. Shapses SA, Sukumar D. Bone metabolism in obesity and weight loss. Annual review of nutrition. 2012;32:287–309. pmid:22809104
- 25. Luo J, Lee RY. How Does Obesity Influence the Risk of Vertebral Fracture? Findings From the UK Biobank Participants. JBMR Plus. 2020;4(5):e10358. pmid:32382691
- 26. Hind K, Pearce M, Birrell F. Total and Visceral Adiposity Are Associated With Prevalent Vertebral Fracture in Women but Not Men at Age 62 Years: The Newcastle Thousand Families Study. Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research. 2017;32(5):1109–15.
- 27. Kim KC, Shin DH, Lee SY, Im JA, Lee DC. Relation between obesity and bone mineral density and vertebral fractures in Korean postmenopausal women. Yonsei medical journal. 2010;51(6):857–63. pmid:20879051
- 28. Compston J. Type 2 diabetes mellitus and bone. Journal of internal medicine. 2018;283(2):140–53. pmid:29265670
- 29. Tang X, Liu G, Kang J, Hou Y, Jiang F, Yuan W, et al. Obesity and risk of hip fracture in adults: a meta-analysis of prospective cohort studies. PloS one. 2013;8(4):e55077. pmid:23593112
- 30. Sadeghi O, Saneei P, Nasiri M, Larijani B, Esmaillzadeh A. Abdominal Obesity and Risk of Hip Fracture: A Systematic Review and Meta-Analysis of Prospective Studies. Advances in nutrition (Bethesda, Md). 2017;8(5):728–38. pmid:28916573
- 31. Kaze AD, Rosen HN, Paik JM. A meta-analysis of the association between body mass index and risk of vertebral fracture. Osteoporosis international: a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA. 2018;29(1):31–9. pmid:29098347
- 32. Xiang BYH W.; Zhou G. Q.; Hu N.; Chen H.; Chen C. Body mass index and the risk of low bone mass-related fractures in women compared with men A PRISMA-compliant meta-analysis of prospective cohort studies. Medicine. 2017;96(12).
- 33.
Higgins JPT TJ CJ, Cumpston M, Li T, Page MJ, Welch VA. Cochrane Handbook for Systematic Reviews of Interventions version 6.0 (Updated July 2019). Cochrane Available from wwwtrainingcochraneorg/handbook. 2019.
- 34. Liberati A, Altman DG, Tetzlaff J, Mulrow C, Gotzsche PC, Ioannidis JP, et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate healthcare interventions: explanation and elaboration. BMJ (Clinical research ed). 2009;339:b2700. pmid:19622552
- 35. Boskey AL, Coleman R. Aging and bone. Journal of dental research. 2010;89(12):1333–48. pmid:20924069
- 36.
Study Design Search Filters. BMJ Best Pratice 2019;Evidence-Based Medicine Toolkit.
- 37. McHugh ML. Interrater reliability: the kappa statistic. Biochemia medica. 2012;22(3):276–82. pmid:23092060
- 38.
Higgins J, Green S. Cochrane Handbook for Systematic Reviews of Interventions [Internet]. The Cochrane Collaboration. 2011;Version 5.1.0 [updated March 2011](Available from www.handbook.cochrane.org).
- 39.
Wells G SB, O’connell D, Peterson J, Welch V, Losos M, et al. The Newcastle-Ottawa Scale (NOS) for assessing the quality of nonrandomised studies in meta-analyses. Ottawa: Ottawa Hospital Research Institute. 2011;Available: www.ohri.ca/programs/clinical_epidemiology/oxford.asp.
- 40.
Viswanathan M AM, Berkman ND, Chang S, Hartling L, McPheeters LM, Santaguida PL, et al. Assessing the Risk of Bias of Individual Studies in Systematic Reviews of Health Care Interventions. Agency for Healthcare Research and Quality Methods Guide for Comparative Effectiveness Reviews. 2012;AHRQ Publication No. 12-EHC047-EF.
- 41. Munn Z, Moola S, Riitano D, Lisy K. The development of a critical appraisal tool for use in systematic reviews addressing questions of prevalence. International journal of health policy and management. 2014;3(3):123–8. pmid:25197676
- 42.
The Institute Joanna Briggs. Joanna Briggs Institute Reviewers’ Manual, 2014th edn. 2014;Adelaide, SA: The Joanna Briggs Institute.
- 43. Mueller M, D’Addario M, Egger M, Cevallos M, Dekkers O, Mugglin C, et al. Methods to systematically review and meta-analyse observational studies: a systematic scoping review of recommendations. BMC medical research methodology. 2018;18(1):44. pmid:29783954
- 44. DerSimonian R, Laird N. Meta-analysis in clinical trials. Control Clin Trials. 1986;7(3):177–88. pmid:3802833
- 45.
Review Manager (RevMan) [Computer program]. Version 5.3. Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration. 2014.
- 46. Higgins JP, Thompson SG. Quantifying heterogeneity in a meta-analysis. Statistics in medicine. 2002;21(11):1539–58. pmid:12111919
- 47. Higgins JP, Thompson SG, Deeks JJ, Altman DG. Measuring inconsistency in meta-analyses. BMJ (Clinical research ed). 2003;327(7414):557–60. pmid:12958120
- 48. Sterne JA, Egger M. Funnel plots for detecting bias in meta-analysis: guidelines on choice of axis. Journal of clinical epidemiology. 2001;54(10):1046–55. pmid:11576817
- 49. Sterne JA, Sutton AJ, Ioannidis JP, Terrin N, Jones DR, Lau J, et al. Recommendations for examining and interpreting funnel plot asymmetry in meta-analyses of randomised controlled trials. BMJ (Clinical research ed). 2011;343:d4002. pmid:21784880
- 50.
Berkman ND, Lohr KN, Ansari M, McDonagh M, Balk E, Whitlock E, et al. Grading the Strength of a Body of Evidence When Assessing Health Care Interventions for the Effective Health Care Program of the Agency for Healthcare Research and Quality: An Update. Methods Guide for Effectiveness and Comparative Effectiveness Reviews. Rockville (MD): Agency for Healthcare Research and Quality (US); 2008.
- 51. Tobias A. Assessing the influence of a single study in the meta-anyalysis estimate. Stata Technical Bulletin. 1999;8(47).
- 52. Al-Shoumer KAN V. Prevalence of low bone mass in postmenopausal Kuwaiti women residents in the largest province of Kuwait. Ann Nutr Metab. 2012;60(1):6–16. Epub 2011 Dec 16. pmid:22179189
- 53. Albassam RSS S.; Alnaami A. M.; Khattak M. N. K.; Lei K. Y.; Al-Daghri N. M.; Reginster J. Y. et al. Consequences of bariatric surgery on outcomes in rheumatic diseases. Osteoporos Int. 2019;30(4):845–52. Epub 2019 Jan 6. pmid:30613867
- 54. Amarendra Reddy GK B.; Shatrugna V.; Thilak Ravindra Reddy P.; Nagalla B.; Ajeya Kumar P.; Usha Rani K. Bone mass of overweight affluent Indian youth and its sex-specific association with body composition. Archives of Osteoporosis. 2009;4(1–2):31–9. pmid:20234857
- 55. Armstrong MEC B. J.; Banks E.; Green J.; Reeves G. K.; Beral V. Different effects of age, adiposity and physical activity on the risk of ankle, wrist and hip fractures in postmenopausal women. Aging Male. 2012;15(2):96–102. Epub 2012 Mar 23. pmid:22439807
- 56. Ayoub MLEK G.; Zakhem E.; El Khoury C.; Cortet B.; El Hage R. Trabecular Bone Score in obese, overweight and normal-weight young men. Science and Sports. 2017;32(1):33–8.
- 57. Azzam EZA M. N.; Younan D. N.; Salem T. M.; Abdul-Aziz A. A. DObesity: Relationship between vitamin D deficiency, obesity and sclerostin as a novel biomarker of bone metabolism. Journal of Clinical and Translational Endocrinology. 2019;17.
- 58. Bachmann KNF P. K.; Lawson E. A.; Russell B. M.; Riccio A. D.; Meenaghan E.; Gerweck A. V. et al. Comparison of hip geometry, strength, and estimated fracture risk in women with anorexia nervosa and overweight/obese women. J Clin Endocrinol Metab. 2014;99(12):4641–8. pmid:25243571
- 59. Baheiraei AP N. A.; Eisman J. A.; Nguyen N. D.; Nguyen T. V. Bone mineral density, body mass index and cigarette smoking among Iranian women: Implications for prevention. BMC Musculoskeletal Disorders. 2005;6. pmid:15703067
- 60. Bilic-Curcic IM S.; Mihaljevic I.; Franceschi M.; Jukic T. Bone Mineral Density in Relation to Metabolic Syndrome Components in Postmenopausal Women With Diabetes Mellitus Type 2. Nutr Metab (Lond). 2017;14:25. eCollection 2017. pmid:28286536
- 61. Buta CV C.; Ungureanu D.; Mogos V.; Branisteanu D. D. Lean body mass and leptin, but not fat mass are independent predictors of bone mass in postmenopausal women. Revista Romana De Medicina De Laborator. 2012;20(3):29–37.
- 62. Caglar GSO E. D.; Kiseli M.; Demirtas S.; Cengiz S. D. The association of osteocalcin and adiponectin with glucose metabolism in nondiabetic postmenopausal women. Foot Ankle Int. 2014;35(1):8–13. Epub 2013 Oct 14. pmid:24127268
- 63. Cakmak AP C.; Dogan E.; Caliskan S.; Guclu S.; Altunyurt S. Raloxifene increases serum leptin levels in postmenopausal women: a prospective study. Obes Res. 2005;13(9):1505–9. pmid:16222049
- 64. Carsote MP S. A.; Mitroi M.; Camen A.; Radu L. Serum Osteocalcin, P1NP, Alkaline Phosphase, and CrossLaps in Humans The relationship with body mass index. Revista De Chimie. 2019;70(5):1615–8.
- 65. Cifuentes MJ M. A.; Lewis R. D.; Heymsfield S. B.; Chowdhury H. A.; Modlesky C. M.; Shapses S. A. Bone turnover and body weight relationships differ in normal-weight compared with heavier postmenopausal women. Osteoporosis International. 2003;14(2):116–22. pmid:12730781
- 66. Compston JEW N. B.; Chapurlat R.; Cooper C.; Boonen S.; Greenspan S.; Pfeilschifter J. et al. Obesity is not protective against fracture in postmenopausal women: GLOW. Orthop Traumatol Surg Res. 2011;97(8 Suppl):S160–6. Epub Oct 28. pmid:22036243
- 67. Silva HGM L. M.; Conceicao F. L.; Zahar S. E.; Farias M. L. Influence of obesity on bone density in postmenopausal women. Am J Orthod Dentofacial Orthop. 2007;132(2):185–90. pmid:17693368
- 68. de Araujo IMS C. E.; Nahas A. K.; Nogueira-Barbosa M. H.; Elias J. Jr.; de Paula F. J. Marrow adipose tissue spectrum in obesity and type 2 diabetes mellitus. Endocr Metab Immune Disord Drug Targets. 2017;17(3):207–12. pmid:28847266
- 69. DeSimone DPS J.; Edwards J.; Shary J.; Gordon L.; Bell N. H. Influence of body habitus and race on bone mineral density of the midradius, hip, and spine in aging women. Am J Surg. 1990;159(1):118–23; discussion 23–4. pmid:2294788
- 70. Tay YD, Cusano NE, Rubin MR, Williams J, Omeragic B, Bilezikian JP. Trabecular Bone Score in Obese and Nonobese Subjects With Primary Hyperparathyroidism Before and After Parathyroidectomy. The Journal of clinical endocrinology and metabolism. 2018;103(4):1512–21. pmid:29373705
- 71. Dubois EFW M. F.; Verdouw B. C.; Zwinderman A. H.; van Boxtel C. J.; Dekhuijzen P. N. R.; Schweitzer D. H. Lack of relationships between cumulative methylprednisolone dose and bone mineral density in healthy men and postmenopausal women with chronic low back pain. Clinical Rheumatology. 2003;22(1):12–7. pmid:12605311
- 72. Dytfeld JI-S M.; Gowin E.; Michalak M.; Horst-Sikorska W. Influence of lean and fat mass on bone mineral density (BMD) in postmenopausal women with osteoporosis. BMC Public Health. 2011;11:735. pmid:21943301
- 73. El Hage RB F.; Khairallah W.; Bedran F.; Maalouf N.; Zakhem E.; Issa M. et al. The influence of obesity and overweight on hip bone mineral density in Lebanese women. J Bone Miner Res. 2014;29(1):223–33. pmid:23775829
- 74. El-Eshmawy MAA I. Relationships between preptin and osteocalcin in obese, overweight, and normal weight adults. Am Surg. 2015;81(3):239–44. pmid:25760198
- 75. Gafane LFS R.; Kruger I. M.; Schutte A. E. Large artery stiffness and carotid intima-media thickness in relation to markers of calcium and bone mineral metabolism in African women older than 46 years. J Endocrinol Invest. 2015;38(3):323–31. Epub 2014 Sep 25. pmid:25252817
- 76. Garcia-Martin AC-B M.; Luque-Fernandez I.; Rozas-Moreno P.; Quesada-Charneco M.; Munoz-Torres M. Osteocalcin as a marker of metabolic risk in healthy postmenopausal women. J Pediatr. 2011;158(5):727–34. Epub 1 Jan 13. pmid:21232765
- 77. Genazzani ADS M.; Strucchi C.; Puccetti S.; Luisi S.; Genazzani A. R. Oral dehydroepiandrosterone supplementation modulates spontaneous and growth hormone-releasing hormone-induced growth hormone and insulin-like growth factor-1 secretion in early and late postmenopausal women. Obes Res. 2001;9(9):544–51. pmid:11557835
- 78. Glogowska-Szelag JK-K B.; Marek B.; Nowak M.; Sieminska L. Assessment of selected adipocytokines in obese women with postmenopausal osteoporosis. Endokrynol Pol. 2019;30(65217).
- 79. Grethen EH K. M.; Jones R.; Cacucci B. M.; Gupta C. E.; Acton A.; Considine R. V. et al. Serum leptin, parathyroid hormone, 1,25-dihydroxyvitamin D, fibroblast growth factor 23, bone alkaline phosphatase, and sclerostin relationships in obesity. J Clin Endocrinol Metab. 2012;97(5):1508–16. Epub 2 Mar 14. pmid:22419720
- 80. Gu PL Y.; Ding Q.; Yang Q.; Su J.; Chen Y.; Zheng H. et al. Correlation between osteocalcin and visceral fat area in overweight and obese male population. International Journal of Clinical and Experimental Medicine. 2017;10(4):6980–6.
- 81. Holecki MZ-M B.; Janowska J.; Nieszporek T.; Wojaczynska-Stanek K.; Zak-Golab A.; Wiecek A. The influence of weight loss on serum osteoprotegerin concentration in obese perimenopausal women. Int J Obes (Lond). 2007;31(8):1232–9. Epub 2007 Mar 6.
- 82. Huang HL, Pan CC, Hsiao YF, Chen MC, Kung CY, Kung PT, et al. Associations of body mass index and diabetes with hip fracture risk: a nationwide cohort study. BMC public health. 2018;18(1):1325. pmid:30497430
- 83. Huopio JH R.; Jurvelin J.; Saarikoski S.; Alhava E.; Kroger H. Role of chronic health disorders in perimenopausal fractures. J Foot Ankle Surg. 2005;44(6):450–4. pmid:16257674
- 84. Ibrahim SEE H. F.; Helmy A.; Galal Z. A.; Abdel Salam M. H. Serum leptin concentration, bone mineral density and bone biochemical markers in a sample of Egyptian women: A possible relationship. Egyptian Rheumatologist. 2011;33(4):171–7.
- 85. Indhavivadhana SR P. The relationship between bone mineral density and metabolic syndrome in peri- and post-menopausal Thai women. Bonekey Rep. 2015;4:758. eCollection. pmid:26587227
- 86. Jacobs CAV A. M.; Thompson K. L.; Lattermann C. Rapid Progression of Knee Pain and Osteoarthritis Biomarkers Greatest for Patients with Combined Obesity and Depression: Data from the Osteoarthritis Initiative. Cartilage. 2018.
- 87. Jang DGK J. Y.; Choi S. K.; Ko H. S.; Shin J. C.; Park I. Y. Prevalence of Low Bone Mineral Density and Associated Risk Factors in Korean Puerperal Women. J Investig Clin Dent. 2016;7(4):376–82. Epub 2015 Jun 19. pmid:26097179
- 88. Jiajue RJ Y.; Wang O.; Li M.; Xing X.; Cui L.; Yin J. et al. Suppressed bone turnover was associated with increased osteoporotic fracture risks in non-obese postmenopausal Chinese women with type 2 diabetes mellitus. Osteoporosis International. 2014;25(8):1999–2005. pmid:24760246
- 89. Jiang YZ Y.; Jin M. M.; Gu Z. Y.; Pei Y.; Meng P. Aged-Related Changes in Body Composition and Association between Body Composition with Bone Mass Density by Body Mass Index in Chinese Han Men over 50-year-old. Plos One. 2015;10(6).
- 90. Jordan SL L.; Berecki-Gisolf J.; Bain C.; Seubsman S. A.; Sleigh A.; Banks E. Body mass index, physical activity, and fracture among young adults: longitudinal results from the Thai cohort study. J Clin Endocrinol Metab. 2013;98(1):345–51. Epub Nov 16. pmid:23162093
- 91. Kadric L, Zylla S, Nauck M, Völzke H, Friedrich N, Hannemann A. Associations Between Plasma Chemerin Concentrations and Bone Quality in Adults From the General Population. Endocrinology. 2018;159(6):2378–85. pmid:29701774
- 92. Kanazawa IY T.; Yamamoto M.; Yamauchi M.; Yano S.; Sugimoto T. Combination of obesity with hyperglycemia is a risk factor for the presence of vertebral fractures in type 2 diabetic men. Acta Orthop Traumatol Turc. 2008;42(5):322–7. pmid:19158452
- 93. Kang DL Z.; Wang Y.; Zhang H.; Feng X.; Cao W.; Wang P. Relationship of body composition with bone mineral density in northern Chinese men by body mass index levels. J Bone Miner Res. 2014;29(4):1015–24. pmid:24014423
- 94. Kao CHC C. C.; Wang S. J. Normal data for lumbar spine bone mineral content in healthy elderly Chinese: influences of sex, age, obesity and ethnicity. Ann Intern Med. 1994;121(10):745–9. pmid:7944051
- 95. Kassanos DT E.; Baltas C. S.; Papakonstantinou O.; Simeonidis G.; Salamalekis G.; Grammatikakis I. et al. Augmentation of cortical bone mineral density in women with polycystic ovary syndrome: a peripheral quantitative computed tomography (pQCT) study. Endocrine. 2010;38(1):113–7. Epub 2010 Jul 3. pmid:20960111
- 96. Khukhlina OSL O. D.; Kaniovska L. V.; Shuper V. O.; Horbatiuk I. B.; Hryniuk O. Ye. Characteristics of bone mineral density and densitometry data in patients with osteoarthritis, non-alcoholic steatohepatitis and obesity. Archives of the Balkan Medical Union. 2019;54(3):467–72.
- 97. Kim SWC E. H. High Levels of Serum DPP-4 Activity Are Associated with Low Bone Mineral Density in Obese Postmenopausal Women. Contemp Clin Trials. 2016;47:315–24. Epub Feb 23. pmid:26924671
- 98. Kim JHH A. R.; Choi H. J.; Ku E. J.; Cho N. H.; Shin C. S. Sex-based Differences in the Association between Body Composition and Incident Fracture Risk in Koreans. Scientific Reports. 2017;7. pmid:28127057
- 99. Kim SH, Yi SW, Yi JJ, Kim YM, Won YJ. Association Between Body Mass Index and the Risk of Hip Fracture by Sex and Age: A Prospective Cohort Study. Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research. 2018;33(9):1603–11. pmid:29750839
- 100. Kin KK K.; Yamazaki K.; Okamoto S.; Inoue T. Bone mineral density of the spine in normal Japanese subjects using dual-energy X-ray absorptiometry: effect of obesity and menopausal status. J Nutr Sci Vitaminol (Tokyo). 1991;37(Suppl):S65–70. pmid:1820447
- 101. Kirchengast SK W.; Hauser G. Protective effect of moderate overweight on bone density of the hip joint in elderly and old Austrians. Urology. 2002;60(1):120–4. pmid:12100936
- 102. Korpelainen RK J.; Heikkinen J.; Vaananen K.; Keinanen-Kiukaanniemi S. Lifestyle factors are associated with osteoporosis in lean women but not in normal and overweight women: a population-based cohort study of 1222 women. J Pediatr Orthop. 2003;23(1):27–9. pmid:12499938
- 103. Kumar AS A. K.; Mittal S.; Kumar G. The Relationship Between Body Mass Index and Bone Mineral Density in Premenopausal and Postmenopausal North Indian Women. Journal of Obstetrics and Gynecology of India. 2016;66(1):52–6. pmid:26924908
- 104. Kyvernitakis IK D.; Struck M.; Hars O.; Bauer T.; Hadji P. Impact of BMI on serum estradiol and bone turnover markers in postmenopausal women with hormone-sensitive early breast cancer treated with anastrozole. Journal of Cancer Research and Clinical Oncology. 2014;140(1):159–66. pmid:24292402
- 105. Lee SWJ H. H.; Kim M. R.; You Y. O.; Kim J. H. Association between obesity, metabolic risks and serum osteocalcin level in postmenopausal women. Front Biosci (Elite Ed). 2012;4:2586–606.
- 106. Liel YE J.; Shary J.; Spicer K. M.; Gordon L.; Bell N. H. The effects of race and body habitus on bone mineral density of the radius, hip, and spine in premenopausal women. Acta Paediatr Scand. 1988;77(5):741–6. pmid:2849283
- 107. Lim JSJ G. C.; Moon K. R.; Kim E. Y. Combined aerobic and resistance exercise is effective for achieving weight loss and reducing cardiovascular risk factors without deteriorating bone health in obese young adults. Acta Neurochir (Wien). 2013;155(3):479–84; discussion 84. Epub 2013 Jan 13. pmid:23314986
- 108. Lim HSB D. W.; Suh K. I.; Park H. K.; Kim H. J.; Kim T. H.; Lee H. H. Is there a difference in serum vitamin D levels and bone mineral density according to body mass index in young adult women? Journal of Bone Metabolism. 2019;26(3):145–50. pmid:31555611
- 109. Lingaiah SM-P L.; Risteli J.; Tapanainen J. S. Metformin decreases bone turnover markers in polycystic ovary syndrome: a post hoc study. Fertility and sterility. 2019.
- 110. Liu PYI J. Z.; Brummel-Smith K.; Ghosh S. New insight into fat, muscle and bone relationship in women: Determining the threshold at which body fat assumes negative relationship with bone mineral density. International Journal of Preventive Medicine. 2014;5(11):1452–63. pmid:25538842
- 111. Lloyd JTA D. E.; Hochberg M. C.; Waldstein S. R.; Harris T. B.; Kritchevsky S. B.; Schwartz A. V. et al. Changes in bone mineral density over time by body mass index in the health ABC study. Obes Sci Pract. 2016;2(2):162–73. Epub 2016 May 31. pmid:27840689
- 112. Machado LGD D. S.; Figueiredo C. P.; Caparbo V. F.; Takayama L.; Oliveira R. M.; Lopes J. B. et al. Visceral fat measured by DXA is associated with increased risk of non-spine fractures in nonobese elderly women: a population-based prospective cohort analysis from the So Paulo Ageing & Health (SPAH) Study. Osteoporosis International. 2016;27(12):3525–33. pmid:27351667
- 113. Mazocco LC P. Association between body mass index and osteoporosis in women from northwestern Rio Grande do Sul. Oxid Med Cell Longev. 2017;2017:4807046. Epub 2017 Aug 23. pmid:28951766
- 114. Mendez JPR-M D.; Pedraza J.; Coral-Vazquez R. M.; Soriano R.; Garcia-Garcia E.; Aguirre-Garcia Mdel C. et al. Bone mineral density in postmenopausal Mexican-Mestizo women with normal body mass index, overweight, or obesity. J Orthop Trauma. 2013;27(5):e122–4. pmid:22648043
- 115. Messina CB C.; Menon G.; Magnani S.; Albano D.; Gitto S.; Ulivieri F. M. et al. Association Between 25-Hydroxyvitamin D and Bone Mineral Density in People With Obstructive Sleep Apnea Syndrome. J Clin Densitom. 2019;22(3):359–66. Epub Jan 5. pmid:30661747
- 116. Meyer HEW W. C.; Flint A. J.; Feskanich D. Abdominal obesity and hip fracture: results from the Nurses’ Health Study and the Health Professionals Follow-up Study. Osteoporos Int. 2016;27(6):2109–16. Epub 2016 Feb 8. pmid:26856584
- 117. Nielson CMM L. M.; Adams A. L.; LeBlanc E. S.; Cawthon P. M.; Ensrud K.; Stefanick M. L. et al. BMI and fracture risk in older men: the osteoporotic fractures in men study (MrOS). J Bone Miner Metab. 2011;29(2):201–6. Epub 2010 Aug 7. pmid:20694489
- 118. Olmos JMH J. L.; Pariente E.; Martinez J.; Gonzalez-Macias J. Use of prognostic factors of rheumatoid arthritis in clinical practice and perception of their predictive capacity before and after exposure to evidence. Obes Surg. 2018;28(12):3862–71. pmid:30069861
- 119. Ostrowska ZK-K B.; Marek B.; Kajdaniuk D.; Wolkowska-Pokrywa K. Circadian concentrations of free testosterone, selected markers of bone metabolism, osteoprotegerin and its ligand sRANKL in obese postmenopausal women. Transplant Proc. 2011;43(9):3470–5. pmid:22099822
- 120. Papakitsou EFM A. N.; Dretakis K. E.; Trovas G.; Zoras U.; Lyritis G.; Dretakis E. K. et al. Body mass index (BMI) and parameters of bone formation and resorption in postmenopausal women. J Endocrinol Invest. 2004;27(4):323–7. pmid:15233550
- 121. Pereira FAdC J. A.; dos Santos J. E.; Foss M. C.; Paula F. J. Impact of marked weight loss induced by bariatric surgery on bone mineral density and remodeling. Am J Clin Nutr. 2007;85(4):972–80. pmid:17413095
- 122. Pollock NKL E. M.; Hamrick M. W.; Baile C. A.; Hall D. B.; Lewis R. D. Bone and fat relationships in postadolescent black females: a pQCT study. Obes Surg. 2011;21(2):173–8. pmid:21104205
- 123. Pollock NKL E. M.; Baile C. A.; Hamrick M. W.; Hall D. B.; Lewis R. D. Is adiposity advantageous for bone strength? A peripheral quantitative computed tomography study in late adolescent females. Adv Ther. 2007;24(6):1314–20. pmid:18165214
- 124. Povoroznyuk VM L.; Dzerovych N.; Martynyuk L. Bone mineral density and trabecular bone score in Ukrainian postmenopausal women with metabolic syndrome. Maturitas. 2017;100:156.
- 125. Prieto-Alhambra DA F. F.; Judge A.; Van Staa T.; Nogues X.; Arden N. K.; Diez-Perez A. et al. Burden of pelvis fracture: a population-based study of incidence, hospitalisation and mortality. Osteoporosis International. 2012;23(12):2797–803. pmid:22310957
- 126. Ribot CT F.; Pouilles J. M.; Bonneu M.; Germain F.; Louvet J. P. Obesity and postmenopausal bone loss: the influence of obesity on vertebral density and bone turnover in postmenopausal women. Acta Chir Scand Suppl. 1987;536:1–60. pmid:3475886
- 127. Rousseau C, Jean S, Gamache P, Lebel S, Mac-Way F, Biertho L, et al. Change in fracture risk and fracture pattern after bariatric surgery: nested case-control study. BMJ (Clinical research ed). 2016;354:i3794. pmid:27814663
- 128. Rudman HAB F.; Pearce M. S.; Tuck S. P.; Francis R. M.; Treadgold L.; Hind K. Bone metabolism markers are associated with neck circumference in adult Arab women. Osteoporos Int. 2019;30(4):829–36. Epub 2019 Jan 8. pmid:30623213
- 129. Saarnio E, Pekkinen M, Itkonen ST, Kemi V, Karp H, Ivaska KK, et al. Low free 25-hydroxyvitamin D and high vitamin D binding protein and parathyroid hormone in obese Caucasians. A complex association with bone? PLoS One. 2018;13(2):e0192596. pmid:29489840
- 130. Salamat MRS A. H.; Abedi I.; Janghorbani M. Relationship between weight, body mass index, and bone mineral density in men referred for dual-energy X-ray absorptiometry scan in Isfahan, Iran. Journal of Osteoporosis. 2013;2013.
- 131. Schorr MF P. K.; Bachmann K. N.; Faje A. T.; Meenaghan E.; Kimball A.; Singhal V. et al. Differences in Trabecular Plate and Rod Structure in Premenopausal Women Across the Weight Spectrum. J Clin Endocrinol Metab. 2019;104(10):4501–10. pmid:31219580
- 132. Scott DC S. D.; Laslett L. L.; Cicuttini F.; Ebeling P. R.; Jones G. Associations of Sarcopenic Obesity and Dynapenic Obesity with Bone Mineral Density and Incident Fractures Over 5–10 Years in Community-Dwelling Older Adults. Arch Gerontol Geriatr. 2016;65:255–9. Epub Apr 20. pmid:27131229
- 133. Scott DS M.; Cumming R.; Naganathan V.; Blyth F.; Le Couteur D. G.; Handelsman D. J. et al. Sarcopenic Obesity and Its Temporal Associations With Changes in Bone Mineral Density, Incident Falls, and Fractures in Older Men: The Concord Health and Ageing in Men Project. Gastroenterology. 2017;152(4):706–15. pmid:28257716
- 134. Segall-Gutierrez PA R.; Ge M.; Lopez C.; Hernandez G.; Stanczyk F. Z. A pilot study examining short-term changes in bone mineral density among class 3 obese users of depot-medroxyprogesterone acetate. Breast. 2013;22(3):225–37. Epub Mar 25. pmid:23535509
- 135. Shaarawy MA A. F.; Hassan H.; Salem M. E. Relationship between serum leptin concentrations and bone mineral density as well as biochemical markers of bone turnover in women with postmenopausal osteoporosis. J Bone Miner Res. 2003;18(5):900–5. pmid:12733730
- 136. Shen JN C. M.; Marshall L. M.; Lee D. C.; Keaveny T. M.; Orwoll E. S.;Osteoporotic Fractures Men Mr, O. S. The Association Between BMI and QCT-Derived Proximal Hip Structure and Strength in Older Men: A Cross-Sectional Study. Journal of Bone and Mineral Research. 2015;30(7):1301–8. pmid:25565555
- 137. Shen JL W. D.; Nielson C. M.; Majumdar S. R.; Morin S. N.; Orwoll E. S. Associations of Body Mass Index With Incident Fractures and Hip Structural Parameters in a Large Canadian Cohort. J Cancer Surviv. 2016;10(1):21–30. Epub 2015 Mar 29. pmid:25820976
- 138. Shiraki MI H.; Fujimaki H.; Higuchi T. Relation between body size and bone mineral density with special reference to sex hormones and calcium regulating hormones in elderly females. Calcif Tissue Int. 1991;49(2):101–6. pmid:1913287
- 139. Sodi RH M. J.; Durham B. H.; Rees C.; Ranganath L. R.; Fraser W. D. The circulating concentration and ratio of total and high molecular weight adiponectin in post-menopausal women with and without osteoporosis and its association with body mass index and biochemical markers of bone metabolism. Am J Orthop (Belle Mead NJ). 2009;38(9):446–9.
- 140. Sogaard AJH K.; Omsland T. K.; Tell G. S.; Dahl C.; Schei B.; Meyer H. E. Age and Sex Differences in Body Mass Index as a Predictor of Hip Fracture: A NOREPOS Study. American Journal of Epidemiology. 2016;184(7):510–9. pmid:27630142
- 141. Sowers MRZ H.; Greendale G. A.; Neer R. M.; Cauley J. A.; Ellis J.; Johnson S. et al. Changes in bone resorption across the menopause transition: effects of reproductive hormones, body size, and ethnicity. J Clin Densitom. 2013;16(3):313–9. Epub Jun 12. pmid:22695056
- 142. Tajik EE F.; Rasouli B. Bone mineral density contributors, body mass index and calcium intake in postmenopausal women. Journal of Medical Sciences (Faisalabad). 2013;13(8):684–91.
- 143. Takata SI T.; Yonezu H. Characteristics of bone mineral density and soft tissue composition of obese Japanese women: Application of dual-energy X-ray absorptiometry. Journal of Bone and Mineral Metabolism. 1999;17(3):206–10. pmid:10757681
- 144. Tanaka SK T.; Saito M.; Shiraki M. Overweight/obesity and underweight are both risk factors for osteoporotic fractures at different sites in Japanese postmenopausal women. Nutr Res. 2013;33(1):67–75. Epub Dec 20. pmid:23351412
- 145. Tarquini BN N.; Perfetto F.; Piluso A.; Romano S.; Tarquini R. Evidence for bone mass and body fat distribution relationship in postmenopausal obese women. Archives of Gerontology and Geriatrics. 1997;24(1):15–21. pmid:15374132
- 146. Tonks KT, White CP, Center JR, Samocha-Bonet D, Greenfield JR. Bone Turnover Is Suppressed in Insulin Resistance, Independent of Adiposity. The Journal of clinical endocrinology and metabolism. 2017;102(4):1112–21. pmid:28324004
- 147. Viljakainen H, Ivaska KK, Paldanius P, Lipsanen-Nyman M, Saukkonen T, Pietilainen KH, et al. Suppressed bone turnover in obesity: a link to energy metabolism? A case-control study. The Journal of clinical endocrinology and metabolism. 2014;99(6):2155–63. pmid:24606073
- 148. Wampler NSC Z.; Jacobsen C.; Henderson J. A.; Howard B. V.; Rossouw J. E. Bone mineral density of American Indian and Alaska Native women compared with non-Hispanic white women: results from the Women’s Health Initiative Study. J Gastrointest Surg. 2005;9(7):955–60. pmid:16137591
- 149. Wiacek MS A.; Ignasiak Z.; Zubrzycki I. Z. The changes of bone mineral density in relation to body mass index and aging among Polish and different ethnic women in the United States: cross-sectional studies. J Am Coll Surg. 2010;211(1):49–54. Epub May 26. pmid:20610248
- 150. Wu SFD X. J. Body Mass Index May Positively Correlate with Bone Mineral Density of Lumbar Vertebra and Femoral Neck in Postmenopausal Females. Medical Science Monitor. 2016;22:145–51. pmid:26766815
- 151. Zhou YL Y.; Zhang D.; Wang J.; Yang H. Prevalence and predictors of osteopenia and osteoporosis in postmenopausal Chinese women with type 2 diabetes. Clin J Am Soc Nephrol. 2010;5(12):2297–304. Epub 2010 Aug 5. pmid:20688883
- 152. Choi WJH S. H. Blood Cadmium Is Associated with Osteoporosis in Obese Males but Not in Non-Obese Males: The Korea National Health and Nutrition Examination Survey 2008–2011. Surg Infect (Larchmt). 2015;16(5):577–82. Epub 5 Jul 31. pmid:26230521
- 153. Sukumar DA-S H.; Zurfluh R.; Schlussel Y.; Stahl T. J.; Gordon C. L.; Shapses S. A. Areal and Volumetric Bone Mineral Density and Geometry at Two Levels of Protein Intake During Caloric Restriction: A Randomized, Controlled Trial. Journal of Bone and Mineral Research. 2011;26(6):1339–48. pmid:21611972
- 154. Barghash AAS I.; Al Nozha O. M.; Baghdadi H. Adipose tissue cytokines: Relation to glycemic control, insulin resistance and biochemical bone markers in type 2 diabetic Saudi male patients. Journal of Taibah University Medical Sciences. 2014;9(2):151–7.
- 155. Vandevyver CW T.; Cassiman J. J.; Raus J.; Geusens P. Influence of the vitamin D receptor gene alleles on bone mineral density in postmenopausal and osteoporotic women. Journal of Bone and Mineral Research. 1997;12(2):241–7. pmid:9041056
- 156. Gomez-Cabello AA I.; Gonzalez-Aguero A.; Casajus J. A.; Vicente-Rodriguez G. Fat mass influence on bone mass is mediated by the independent association between lean mass and bone mass among elderly women: a cross-sectional study. J Pediatr Orthop B. 2013;22(1):70–5. pmid:22422007
- 157. Wolinsky FDB S. E.; Liu L.; Obrizan M.; Cook E. A.; Wright K. B.; Geweke J. F. et al. Recent hospitalization and the risk of hip fracture among older Americans. Eur Spine J. 2009;18(2):145–56. Epub 2008 Sep 13. pmid:18791749
- 158. Scott D, Shore-Lorenti C, McMillan L, Mesinovic J, Clark RA, Hayes A, et al. Associations of components of sarcopenic obesity with bone health and balance in older adults. Arch Gerontol Geriatr. 2018;75:125–31. pmid:29277040
- 159. Bener AH M.; Zirie M.; Heller R. F. Is obesity a protective factor for osteoporosis? APLAR Journal of Rheumatology. 2005;8(1):32–8.
- 160. Kouvonen AK M.; Oksanen T.; Pentti J.; De Vogli R.; Virtanen M.; Vahtera J. Obesity and occupational injury: a prospective cohort study of 69,515 public sector employees. PLoS One. 2013;8(10):e78653. eCollection 2013. pmid:24205288
- 161. Dickey WK N. Overweight in celiac disease: prevalence, clinical characteristics, and effect of a gluten-free diet. J Womens Health (Larchmt). 2006;15(9):1028–34.
- 162. Xu Y, Ma X, Pan X, He X, Xiao Y, Bao Y. Correlations between serum concentration of three bone-derived factors and obesity and visceral fat accumulation in a cohort of middle aged men and women. Cardiovasc Diabetol. 2018;17(1):143. pmid:30424752
- 163. Gandham A, Zengin A, Bonham MP, Winzenberg T, Balogun S, Wu F, et al. Incidence and predictors of fractures in older adults with and without obesity defined by body mass index versus body fat percentage. Bone. 2020;140:115546. pmid:32730938
- 164. Rikkonen T, Sund R, Sirola J, Honkanen R, Poole KES, Kröger H. Obesity is associated with early hip fracture risk in postmenopausal women: a 25-year follow-up. Osteoporosis international: a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA. 2020. pmid:33095419
- 165. Wang Y, Chen F, Wang H, Yu C, Shao S, Zhao M, et al. Association Between Forearm Bone Mineral Density and Metabolic Obesity in a Northern Chinese Population. Metab Syndr Relat Disord. 2020;18(5):251–9. pmid:32125926
- 166. Zhao H, Zheng C, Gan K, Qi C, Ren L, Song G. High Body Mass Index and Triglycerides Help Protect against Osteoporosis in Patients with Type 2 Diabetes Mellitus. J Diabetes Res. 2020;2020:1517879. pmid:33178837
- 167. Chain A, Faerstein E, Wahrlich V, Bezerra FF. Obesity, dynapenia, and their combination: Implications for bone mineral density in Brazilian adults-the Pró-Saúde study. Nutrition. 2021;81:110898. pmid:32739661
- 168. Gojkovic ZM R.; Harhaji V.; Ilincic B.; Barisic L.; Kupusinac A.; Radisic M. et al. Trends in bone mineral density among nutritional status categories of Vojvodina elderly population. Srpski Arhiv Za Celokupno Lekarstvo. 2020;148(9–10):577–83.
- 169. Hermenegildo-López Y, Sandoval-Insausti H, Donat-Vargas C, Banegas JR, Rodríguez-Artalejo F, Guallar-Castillón P. General and central obesity operate differently as predictors of falls requiring medical care in older women: a population-based cohort study in Spain. Age Ageing. 2021;50(1):213–9. pmid:32857126
- 170. Jawhar DSH N. A.; Shamssain M. H.; Malik A. T.; Quatman C. E.; Ly T. V.; Phieffer L. S. et al. Dual-energy x-ray absorptiometry scan (DXA) findings in diabetic and non-diabetic female: A retrospective cohort study;Refining Risk-Adjustment of 90-Day Costs Following Surgical Fixation of Ankle Fractures: An Analysis of Medicare Beneficiaries;Bone Mineral Density Assessment by DXA vs. QCT in Postmenopausal Females with Central Obesity;Effects of Roux-en-Y Gastric Bypass on Osteoclast Activity and Bone Density in Morbidly Obese Patients with Type 2 Diabetes. Med J Malaysia. 2020;75(1):47–51. pmid:32008020
- 171. Pham TTI K. K.; Hannukainen J. C.; Virtanen K. A.; Lidell M. E.; Enerback S.; Makela K. et al. Human Bone Marrow Adipose Tissue is a Metabolically Active and Insulin-Sensitive Distinct Fat Depot. Journal of Clinical Endocrinology & Metabolism. 2020;105(7):2300–10.
- 172. Scott DJ J.; Ebeling P. R.; Nordstrom P.; Nordstrom A. Adiposity Without Obesity: Associations with Osteoporosis, Sarcopenia, and Falls in the Healthy Ageing Initiative Cohort Study. Obesity. 2020;28(11):2232–41. pmid:33012137
- 173. Tencerova M, Frost M, Figeac F, Nielsen TK, Ali D, Lauterlein JL, et al. Obesity-Associated Hypermetabolism and Accelerated Senescence of Bone Marrow Stromal Stem Cells Suggest a Potential Mechanism for Bone Fragility. Cell Rep. 2019;27(7):2050-62.e6. pmid:31091445
- 174. Wyskida KF G.; Owczarek A. J.; Choręza P.; Kocełak P.; Madej P.; Chudek J. et al. Plasma sclerostin levels are associated with nutritional status and insulin resistance but not hormonal disturbances in women with polycystic ovary syndrome. Arch Gynecol Obstet. 2020;302(4):1025–31. pmid:32592042
- 175. Yaylali YT, Fidan-Yaylali G, Dedeoglu O, Senol H. Osteocalcin and epicardial adipose tissue in obesity: new hints for epicardial adipose tissue-bone crosstalk. Scand Cardiovasc J. 2019;53(6):296–8. pmid:31455100
- 176. Yoon JY, Choi IJ, Kim HJ, Cheon CK. Genotype and phenotype, growth outcome in 33 Korean patients with 21-hydroxylase deficiency. Hormone Research in Paediatrics. 2019;91:507.
- 177. Asli IN, Sheikhnezami M, Qutbi M, Farsad F, Asli SN, Ranji S, et al. Less influence of body mass index on bone mineral density of radius as compared to proximal femur: Possible role in the diagnosis of osteoporosis. World J Nucl Med. 2020;19(2):118–23. pmid:32939198
- 178. Maïmoun LM T.; Attalin V.; Dupuy A. M.; Cristol J. P.; Avignon A.; Mariano-Goulart D. et al. Modification of Muscle-Related Hormones in Women with Obesity: Potential Impact on Bone Metabolism. J Clin Med. 2020;9(4).
- 179. Maimoun LG P.; Mura T.; Nocca D.; Lefebvre P.; Philibert P.; Seneque M. et al. Specific Effects of Anorexia Nervosa and Obesity on Bone Mineral Density and Bone Turnover in Young Women. Journal of Clinical Endocrinology & Metabolism. 2020;105(4).
- 180. Shayganfar A, Ebrahimian S, Masjedi M.; Daryaei S. A study on bone mass density using dual energy X-ray absorptiometry: Does high body mass index have protective effect on bone density in obese patients? Journal of Research in Medical Sciences. 2020;25(1).
- 181. Zantut-Wittmann DEQ-M A.; dos Santos P. N. S.; Melhado-Kimura V.; Bahamondes L.; Fernandes A. Lack of Influence of Thyroid Hormone on Bone Mineral Density and Body Composition in Healthy Euthyroid Women. Frontiers in Endocrinology. 2020;10.
- 182. Zhou JZ L. J.; Watson P.; Zhang Q.; Lappe J. M. The effect of calcium and vitamin D supplementation on obesity in postmenopausal women: Secondary analysis for a large-scale, placebo controlled, double-blind, 4-year longitudinal clinical trial. Nutrition and Metabolism. 2010;7. pmid:20181022
- 183. Hochberg MC. Racial differences in bone strength. Transactions of the American Clinical and Climatological Association. 2007;118:305–15. pmid:18528512
- 184. Ma L, Oei L, Jiang L, Estrada K, Chen H, Wang Z, et al. Association between bone mineral density and type 2 diabetes mellitus: a meta-analysis of observational studies. European journal of epidemiology. 2012;27(5):319–32. pmid:22451239
- 185. Leibson CL, Tosteson AN, Gabriel SE, Ransom JE, Melton LJ. Mortality, disability, and nursing home use for persons with and without hip fracture: a population-based study. Journal of the American Geriatrics Society. 2002;50(10):1644–50. pmid:12366617
- 186. Després JP, Lemieux I. Abdominal obesity and metabolic syndrome. Nature. 2006;444(7121):881–7. pmid:17167477
- 187. Park J, Lee ES, Lee DY, Kim J, Park SE, Park CY, et al. Waist Circumference as a Marker of Obesity Is More Predictive of Coronary Artery Calcification than Body Mass Index in Apparently Healthy Korean Adults: The Kangbuk Samsung Health Study. Endocrinology and metabolism (Seoul, Korea). 2016;31(4):559–66. pmid:28029026
- 188. Pou KM, Massaro JM, Hoffmann U, Vasan RS, Maurovich-Horvat P, Larson MG, et al. Visceral and subcutaneous adipose tissue volumes are cross-sectionally related to markers of inflammation and oxidative stress: the Framingham Heart Study. Circulation. 2007;116(11):1234–41. pmid:17709633
- 189. Ding C, Parameswaran V, Udayan R, Burgess J, Jones G. Circulating levels of inflammatory markers predict change in bone mineral density and resorption in older adults: a longitudinal study. The Journal of clinical endocrinology and metabolism. 2008;93(5):1952–8. pmid:18285417
- 190. Shapses SA, Pop LC, Wang Y. Obesity is a concern for bone health with aging. Nutrition research (New York, NY). 2017;39:1–13. pmid:28385284
- 191. Villareal DT, Apovian CM, Kushner RF, Klein S. Obesity in older adults: technical review and position statement of the American Society for Nutrition and NAASO, The Obesity Society. The American journal of clinical nutrition. 2005;82(5):923–34. pmid:16280421
- 192. Vilaca T, Schini M, Harnan S, Sutton A, Poku E, Allen IE, et al. The risk of hip and non-vertebral fractures in type 1 and type 2 diabetes: A systematic review and meta-analysis update. Bone. 2020;137:115457. pmid:32480023
- 193. Hernandez CJ, van der Meulen MC. Understanding Bone Strength Is Not Enough. Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research. 2017;32(6):1157–62.
- 194. Corbeil P, Simoneau M, Rancourt D, Tremblay A, Teasdale N. Increased risk for falling associated with obesity: mathematical modeling of postural control. IEEE transactions on neural systems and rehabilitation engineering: a publication of the IEEE Engineering in Medicine and Biology Society. 2001;9(2):126–36.
- 195. Fjeldstad C, Fjeldstad AS, Acree LS, Nickel KJ, Gardner AW. The influence of obesity on falls and quality of life. Dynamic medicine: DM. 2008;7:4. pmid:18304350
- 196. Mignardot JB, Olivier I, Promayon E, Nougier V. Obesity impact on the attentional cost for controlling posture. PloS one. 2010;5(12):e14387. pmid:21187914
- 197. Bouxsein ML, Szulc P, Munoz F, Thrall E, Sornay-Rendu E, Delmas PD. Contribution of trochanteric soft tissues to fall force estimates, the factor of risk, and prediction of hip fracture risk. Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research. 2007;22(6):825–31.
- 198. Chiba K, Okazaki N, Kurogi A, Isobe Y, Yonekura A, Tomita M, et al. Precision of Second-Generation High-Resolution Peripheral Quantitative Computed Tomography: Intra- and Intertester Reproducibilities and Factors Involved in the Reproducibility of Cortical Porosity. Journal of clinical densitometry: the official journal of the International Society for Clinical Densitometry. 2018;21(2):295–302. pmid:28256308