Bone mineral density is cross sectionally associated with cartilage volume in healthy, asymptomatic adult females: Geelong Osteoporosis Study
Highlights
► We examine BMD measured by DXA and cartilage measured by MRI in 160 adult females. ► Site-specific BMD is associated with cartilage volume at the hip. ► Cartilage volume and axial/lower limb BMD may have common local factors.
Introduction
The association between osteoporosis and osteoarthritis (OA) is controversial. The relationship between these diseases is most often assessed by linking bone mineral density (BMD), as a surrogate marker for osteoporosis, and the radiological features of OA. Cross-sectional studies consistently suggest that BMD is associated with the presence of knee OA as measured by osteophytes [1], [2], joint space narrowing [3]. Similarly, longitudinal studies have shown higher BMD to be associated with incidence of knee OA in older women [4], and to predict greater joint space narrowing [5]. However, there are conflicting data regarding the association between BMD and OA, for instance a recent longitudinal study identified that BMD was positively associated with increased odds of developing joint space narrowing and Kellgren–Lawrence grade ≥ 2 in subjects without OA, but was not associated with progression in those with prevalent disease [6]. Furthermore, in those with OA, despite increased BMD, it is not clear that fracture risk is reduced, with studies providing conflicting results [7], [8]. These discrepancies may be related to subchondral bone attrition, which as a key feature of OA, has been associated with systemic BMD [9].
One of the defining characteristics of OA is articular cartilage loss. By the time the first signs of radiographic OA are present, even with grade 1 joint space narrowing, 10% of articular cartilage volume loss has already occurred [10]. The use of magnetic resonance imaging (MRI) enables the direct visualisation of cartilage, and allows the direct examination of knee structure, before radiographic changes are present, allowing the characterisation of the pre-radiographic structural changes of OA. Reduced cartilage volume, increased prevalence and severity of defects and increased tibial plateau area have been related to the severity of radiographic OA [11], [12]. Bone marrow lesions (BMLs) have been related to pain and increased disease progression, measured by cartilage loss [13]. Initial work has shown that cartilage volume of older subjects without OA is positively associated with total body BMD in both genders, and also with hip BMD for men [1]. It is possible that factors associated with reduced cartilage volume in asymptomatic individuals will increase the risk of OA onset.
Whilst previous studies have examined the relationship between BMD and cartilage volume [1], the relationships between BMD (at sites distant to the knee) and other knee structures have not been examined. Furthermore, the mechanisms behind the relationship between BMD and knee cartilage volume are not known; thus, examination of the association between site specific measures of BMD and components of knee structure in asymptomatic young to middle-aged adult females without clinical OA may help us to understand these mechanisms. Additionally, the use of peripheral measures of BMD to determine properties of the knee may be useful in community-based settings, due to quick, cheap and easy access.
The aim of this study was to determine the associations between BMD at eight skeletal sites, and knee structure, including cartilage volume, defects, and BMLs in healthy, asymptomatic young to middle-aged female subjects without any clinical signs of OA.
Section snippets
Subjects
Data were derived from an age-stratified random sample of population-based adult females enrolled in the Geelong Osteoporosis Study (GOS) who had attended the 10-year follow up (2004–07, 82.1% retention rate). GOS subjects had been randomly selected within 10 yr age stratum, and recruited from the Commonwealth electoral rolls for the Barwon Statistical Division, Australia [14]. Subjects for this analysis (n = 160) were aged between 29 and 50 yr (mean ± SD, 41.4 ± 5.3 yr). Exclusion criteria included
Results
The characteristics of study subjects are shown in Table 1. Of the small number of prevalent osteophytes (n = 15) there were no statistical differences in those with and without (data not shown).
The relationships between SD of BMD and knee cartilage volume are presented in Table 2. In univariable analyses, cartilage volume was positively associated with BMD as measured by DXA at the total body, femoral neck, Ward's triangle and trochanter (all p ≤ 0.03), with a trend in the same direction at the
Discussion
To date, no study has examined the association between site-specific BMD and properties of knee structure in asymptomatic young to middle-aged adult females. In this study, cartilage volume in the medial compartment showed a positive association with BMD at the hip and spine. Cartilage defects in the medial compartment showed a trend for association with BMD at the spine mid and forearm. No further associations were observed between measures of BMD at the forearms, and none was observed at the
Competing interests
The authors declare they have no competing interests.
Author contributions
SLB, JAP, FMC and AEW conceived and designed the study. SLB, JAP, FMC, MJH, MAK, GCN, and AEW had the major role in analysis and interpretation of the data and in drafting the report. MJH, JAP, FMC, and AEW supervised the statistical analysis. SLB undertook measurement of knee structures. All authors contributed to drafting the report, and interpretation of the data. All authors had full access to all of the data (including statistical reports and tables) in the study and can take
Acknowledgments
This study was funded by the National Health and Medical Research Council (NHMRC) of Australia (251638, 436665), the Victorian Health Promotion Foundation, LEW Carty Foundation and Arthritis Australia. SL Brennan was supported by NHMRC PhD Scholarship (519404, 2010) and NHMRC Early Career Fellowship (1012472, 2011). AE Wluka is the recipient of NHMRC Clinical Career Development Award (545876). We thank the participants who made this study possible and the MRI technicians at Barwon Medical
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