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Article

Identification of Adolescents with Adiposities and Elevated Blood Pressure and Implementation of Preventive Measures Warrants the Use of Multiple Clinical Assessment Tools

1
Department of Health Sciences, Qatar University, Doha P.O. Box 2713, Qatar
2
Faculty of Nursing, Jordan University of Science & Technology (JUST), P.O. Box 3030, Irbid 22110, Jordan
3
Department of Nutrition and Food Technology, Jordan University of Science and Technology, P.O. Box 3030, Irbid 22110, Jordan
*
Author to whom correspondence should be addressed.
J. Pers. Med. 2021, 11(9), 873; https://doi.org/10.3390/jpm11090873
Submission received: 17 June 2021 / Revised: 9 August 2021 / Accepted: 23 August 2021 / Published: 31 August 2021
(This article belongs to the Special Issue Personalized Medicine in Epidemics)

Abstract: Background

The burden of abdominal adiposity has increased globally, which is recognized as a key condition for the development of obesity-related disorders among youth, including type 2 diabetes, cardiovascular disease, and hypertension. High blood pressure (BP) and cardiovascular diseases increase the rates of premature mortality and morbidity substantially. Aims: to investigate the relation between abdominal adiposity and elevated BP among adolescent males in Jordan. Methods: Nationally representative sample of male adolescents was selected using multi-cluster sampling technique. Study sample included 1035 adolescent males aged 12 to 17 years. Multiple indicators were used to assess adiposity including waist circumference (WC) and total body fat (TF), truncal fat (TrF), and visceral fat (VF). Systolic blood pressure was measured to assess hypertension. Results: After adjusting for age, smoking status, and physical activity, the odds of having stage two hypertension increased 6, 7, and 8 times for adolescents who were on 90th percentile or above for Trf, VF, and WC, respectively. Conclusion: Elevated BP was significantly associated with total and abdominal adiposity among adolescent males in Jordan. Use of multiple clinical assessment tools is essential to assess abdominal obesity among adolescents.

1. Introduction

Obesity is considered the most serious future-health threatening problem among children and adolescents. In Jordan, about 17.3% of children and adolescents were overweight, and 15.7% were obese, as documented by Zayed and colleagues (2016) [1]. Recent research indicates that abdominal or central obesity is a more robust predictor for several debilitating and deadly chronic diseases than overall adiposity [2,3]. Besides being considered an important predictor of adult obesity, abdominal obesity among children and adolescents is also linked to several life threatening diseases, including cardiovascular diseases, diabetes, orthopaedic problems, cancers, metabolic syndrome, and high blood pressure [4,5,6,7]. Obesity does this through a variety of pathways, some as straightforward as the mechanical stress of carrying extra pounds and some involving multipart alterations in both hormones and cellular metabolism [8].
In the last decade, elevated BP increased among children and adolescents [9]. Adolescents with elevated BP can develop several chronic diseases and body organ damage [10,11]. Children with high BMI are more prone to have elevated BP [12]. Premature mortality is attributed to elevated BP by increasing the incidence of cardiovascular disease [13]. Prevention of childhood obesity initiates reduction in BP which leads to substantial prevention of cardiovascular disease [14]. Several studies supported the association between elevated BP and obesity among children and adolescents [15,16]. In Jordan, there are not enough data available about rates of abdominal obesity among children and adolescents, nor the association between abdominal adiposity and elevated blood pressure among this vulnerable group. The limited data available in Jordan used a single assessment tool for obesity with no consideration for identification and specification of risk and precision of preventive treatment. Therefore, this study aimed to investigate the relation between abdominal adiposity and elevated BP among adolescent males in Jordan by implementing a panel of assessment tools.

2. Materials and Methods

2.1. Study Design

A population-based, nationally representative cross-sectional study was conducted, and included 1035 male adolescents from 18 elementary and high schools in Jordan across the whole kingdom of Jordan. The study protocol was examined and approved by Jordan University of Science, Technology, and Ministry of Education-Jordan.
A list of all males’ schools (341 schools) in Jordan was obtained from Ministry of Education (MOE). Three geographical zones were identified based on MOE classification; north, mid, and south Jordan. Distribution of Schools over the geographical zones was also obtained from MOE; 130 schools in north area, 159 schools in middle area, and 52 schools in south area. Based on this distribution, a sample of 5% of schools (n = 18 schools) were selected as follows: 7 schools in northern Jordan, 8 schools in mid-Jordan, and 3 schools in southern Jordan. Classes in each school and adolescents in each class were selected using simple random selection.

2.2. Data Collection

All adolescents were asked to complete a self-administered questionnaire including data about socio demographic status, dietary habits, and physical activity level. The questionnaire was pilot tested to check for any vague, poorly stated items.

2.3. Measurements

2.3.1. Total Adiposity

Total adiposity was assessed using body mass index (BMI) and total body fat (TF) percentage. Anthropometric measurements were performed by a trained dietitian. Weight was measured to the nearest 0.1 kg (Tanita BF-350, Tanita Corporation, Tokyo, Japan). Height was measured to the nearest 0.1 cm with a portable Harpenden stadiometer. BMI was then calculated as the ratio of weight (kg) to height (m) squared (kg/m2) [17]. BMI for age charts were used to assess overweight and obesity [18]. BMI and age were plotted to obtain adolescents’ BMI-age percentiles. Data were interpreted as follows: <5th percentile were assessed as underweight, 5th–85th percentile were assessed as normal weight, 85th–95th percentile were assessed as overweight, and ≥95th percentile were assessed as obese [19].
TF% was estimated using bioelectrical impedance technique (Tanita BF-350, Tanita Corporation, Tokyo, Japan). Age and gender sensitive cut-off points for TF% were used to assess obesity [19].

2.3.2. Abdominal Adiposity

Several indicators were used to assess abdominal adiposity; waist circumference (WC), truncal fat (TrF) %, and visceral fat (VF). WC was measured at the narrowest area of the torso, as seen from the anterior aspect, to the nearest 0.1 cm with a non-elastic tape measure snugly fitted to measure WC at the level of the natural waist. The WC value corresponding to ≥90th percentile of WC for gender and age were used as cut-off values to identify adolescents with abdominal obesity [20].
Truncal fat (TrF)% and VF were estimated using bioelectrical impedance technique (Tanita AB-140 ViScan; Tanita Corporation, Tokyo, Japan). Adolescents were asked to lie back and expose their abdominal region. Electrodes were attached to the impedance meter and placed across the navel of the subject with the electrodes facing down. The positioning line was aligned on the impedance meter with the laser to adjust the position. Values associated with ≥90th percentile were considered high.

2.4. Blood Pressure Measurement

Blood pressure (BP) was measured by a registered nurse using validated automated oscillometric device (Omron HEM-7051, Omron Corporation, Kyoto, Japan) [21]. Blood pressure was measured according to a standardized protocol. Blood pressure was measured first on the right arm and then at left arm. Both readings were taken after the participants were allowed to sit and rest for 5 min to relieve anxiety with their back supported, feet on the floor, arm supported, and cubital fossa at heart level. The same technique was followed for right and left arm measurement. Two readings were obtained at a 1-min interval, and the average of the two readings was recorded. Systolic BP was determined by the onset of the “tapping” KSs (K1) and the fifth KS (K5), or the disappearance of KS, as the definition of Diastolic BP. After measuring the mean values of BP, the BP percentiles were determined accordingly.
The following criteria were used to categorize adolescents according to their BP: normal BP for adolescents with systolic BP <90th percentile; prehypertension for adolescents with 90th to <95th percentile; stage 1 hypertension for adolescents with 95th to <99th percentile and stage 2 hypertension for adolescents with >99th percentile [22]. Only Systolic BP was used in this study as indicator for hypertension, as the literature suggests that diastolic hypertension rarely occurs without Systolic hypertension in children and adolescents [23,24].

2.5. Statistical Analysis

Statistical analysis was performed using SPSS for Windows version 11.5 (Statistical Package for the Social Sciences). Data were expressed as frequencies and percentages. Multivariate logistic regression was performed to investigate the association between adolescent’s risk of elevated systolic blood pressure and anthropometric measurements. Odds ratios (OR) and 95% confidence intervals (95% CI) were calculated and p-value was set at p < 0.05.

3. Results

This study included 1035 adolescents aged between 12 and 17 years. Socio-demographic characteristics of Jordanian adolescents were presented in Table 1. Half of participants were from Mid Jordan (49%), followed by North (35%), and South (16%). Participant’s school grades ranged from 7th grade up to 11th grade. Students’ parenteral educational levels were high school diplomas and college education in most cases. Few students reported either an illiterate mother or father.
Table 2 presents data related to systolic hypertension according to their dietary habits. Students’ self-reported regular consumption of vegetables (p = 0.008), fruits (p = 0.033) and chocolate (p = 0.013) were related to their systolic blood pressure. On the other hand, milk and dairy products, meat, fish, legumes, canned fruit juice, soda, and nuts were not significantly associated with blood pressure. Table 3 shows adjusted odds ratios for adolescents’ SHTN based on their general and abdominal obesity. After adjusting for confounding variables—age, smoking status, and physical activity—it was found that BMI, WC, TF, TrF, and VF are positively related to increased odds of SHTN.
Odds of pre-hypertension increased in a dose–response pattern among overweight (OR, 2.3; 95% CI, 1.4–3.8) and obese (OR, 2.7; 95% CI, 1.6–4.5) adolescents as compared to adolescents with normal body weight. Similarly, odds of stage 1 hypertension increased in a dose–response pattern across overweight (OR,1.8; 95% CI, 1.01–3.1) and obesity (OR, 2.7; 95% CI, 1.6–4.6) classes. A similar trend was observed for stage 2 SHTN.
With regard to WC, and after adjusting for age, smoking status, and physical activity, adolescents with the highest 10th percentile of WC had 5 times higher odds of having stage 1 hypertension (OR, 95% CI, 2.3–10.6) and 8.6 higher odds of having stage 2 hypertension (OR, 95% CI, 4,5–16.4). A similar relation was found with total body fat. Obese adolescents had twice as high odds of having stage 1 hypertension (OR, 95% CI, 1.3–3.8) and 3.5 times higher odds of having stage 2 hypertension (OR, 95% CI, 2.3–5.5).
With regard to TrF, and after adjusting for age, smoking status, and physical activity, adolescents with the highest 10th percentile of TF had 4 times higher odds of having stage 1 hypertension (OR, 95% CI, 2.2–7.1) and 5.5 higher odds of having stage 2 hypertension (OR, 95% CI, 3.4–9.1). Similar relation was found with VF. Adolescents with the highest 10th percentile of VF had 4.2 times higher odds of having stage 1 hypertension (OR, 95% CI, 1.8–9.4) and 7.2 times higher odds of having stage 2 hypertension (OR, 95% CI, 3.7–14.1).

4. Discussion

Health consequences of overweight and obesity in adolescence are strongly associated with risk factors for chronic health conditions such as cardiovascular disease, diabetes, and elevated blood pressure [4,6].
Fruit and vegetable consumption was significantly related to blood pressure (p = 0.008 and p = 0.033, respectively). This finding was consistent with the findings of several studies [25,26,27,28]. Apple et al. (2006) studied the contents of fruit and vegetables for vitamins, minerals, and fibers. Fruits and vegetables also contained potassium; and this increase consumption of potassium intake was associated with reduction in blood pressure. The increase in potassium intake had same lowering effect on blood pressure as a decrease in sodium intake. Potassium plays a major role in balancing out the negative effects of sodium. Whelton et al. (1997) recommended potassium for prevention and treatment of hypertension. Increasing serum levels of vitamins A, C, E [25], and D [28] were associated with lowering blood pressure. Meta-analysis suggested that increasing the dietary fiber intake had a lowering effect on blood pressure [27]. According to this study, chocolate was significantly related to blood pressure (p = 0.013). Studies explained chocolate’s role to lower blood pressure [29,30,31]. Chocolate contained coca that include polyphenols, especially flavones. Strong effects of flavones on blood pressure as a vasodilator were applied by increasing the formation of endothelial nitric oxide.
Findings of the current study are in line with previously published studies suggesting that obesity is an independent risk factor for early hypertension [4,6,23,24]. Abdominal adiposity showed stronger association that between fatness and the risks of stage 1 and stage 2 systolic hypertension among study participants. Risks increased up to 8 times with abdominal adiposity indicators. Our findings were similar to those reported by Pausova et al. (2012) and Pazin et al. (2020), where an association was found between adolescents abdominal adiposity and high BP, especially among in boys [32,33].
The relationship between abdominal adiposity and elevated blood pressure is not fully explained yet. However, researchers linked abdominal adiposity to elevated blood pressure via insulin resistance and related inflammation [8,24,34,35,36,37]. Abdominal adiposity stimulates the state of insulin resistance and the inflammatory process [38]. Inflammation leads several changes vascular endothelial function, which in turn leads to the development of hypertension [39]. Visceral fat that accumulates around individual internal organs decreases body sensitivity to insulin, which contributes to oxidative stress, inflammation, vascular endothelial dysfunction, and hypertension [35,37].
Landsberg et al. (2013) explained that the pathophysiology of fat accumulation in the abdominal region led to an increase in BP through the stimulation of insulin resistance, increasing central nervous system activity, renin-angiotensin-aldosterone system activity, angiotensinogen from intra-abdominal adipocytes, aldosterone production, and the renal sodium reabsorption [40]. High adiposity can lead to adiposopathy in adolescence, with associated increases in inflammation and oxidative stress, changes in adipokines and endocrinopathy [39]. This manifests as cardio-metabolic risk factors in similar patterns to those in noted in obese adults [5]. Both obesity and cardio-metabolic risk factors have been shown to be associated with vascular changes indicative of early hypertension, atherosclerosis, as well as ventricular hypertrophy, dilation, and dysfunction [8,24].
Ke and colleagues (2018) clarified that high BP is being induced by VF due to high levels of free fatty acids excretion in liver via portal circulation after lipogenesis and lipolysis activity, gluconeogenesis, lipid synthesis, and insulin resistance [41]. This elevated amount of free fatty acids will induce hypertension and eventually atherosclerosis [42,43].
Many studies revealed that applying different anthropometric assessment methods is essential to evaluate body weight status accurately [44,45,46,47]. Body composition can be assessed at the molecular, cellular, and tissue levels using several different methods [44,46]. Specific limitations of anthropometry in the obese are obvious. These limitations include the inability to distinguish subcutaneous fat from visceral adipose tissue, which is helpful to assess disease risk [47] and accuracy may be lowered in the severely obese, due to difficulties finding the actual waistline or drooping abdominal fat can interfere with hip measurement [46]. Therefore, no single measurement is recommended to assess the body composition of obese people. Yet, each modality has benefits and drawbacks [46].
This study has several strengths, including the representation of the sample to the Jordanian adolescent males and multiple tools used to operationalize adiposity. However, the study is limited as it did not include intensive dietary data which were not to feasible in the school setting, especially with all the measurements being performed.
In conclusion, excess fat, especially abdominal fat, is associated with increased risk of systolic hypertension among adolescent males. The physiological relation between obesity and hypertension could not attribute to a single factor. It is critical to use multiple clinical assessment tools for obesity to optimizes identification of adolescents at risk; hence preventive measures can be timely considered. Findings of this study must be taken with high level of importance to prevent early hypertension and associated cardiovascular diseases risk later in adulthood.

Author Contributions

H.B.: proposal writing, data analysis, data interpretation, and writing manuscript. M.K.: data interpretation and writing manuscript. A.H.Z.: data collection and writing manuscript. R.T.: data interpretation and writing manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Deanship of Research in Jordan University of Science and Technology (project No. 2014/97).

Institutional Review Board Statement

This study was conducted according to the guidelines laid down in the Declaration of Helsinki and all procedures involving research study participants were approved by the IRB at Ministry of Education. IRB Approval number was 3/10/21299.

Informed Consent Statement

Written informed consent was obtained from all subjects/parents.

Acknowledgments

Authors would like to thank Fawzieh Hammad for her help in the data entry and analysis.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Zayed, A.A.; Beano, A.M.; Haddadin, F.I.; Radwan, S.S.; Allauzy, S.A.; Alkhayyat, M.M.; Al-Dahabrah, Z.A.; Al-Hasan, Y.G.; Yousef, A.-M.F. Prevalence of short stature, underweight, overweight, and obesity among school children in Jordan. BMC Public Health 2016, 16, 1040. [Google Scholar] [CrossRef] [Green Version]
  2. Tchernof, A.; Després, J.-P. Pathophysiology of human visceral obesity: An update. Physiol. Rev. 2013. [Google Scholar] [CrossRef]
  3. Wang, S.; Ren, J. Obesity paradox in aging: From prevalence to pathophysiology. Progress Cardiovasc. Dis. 2018, 61, 182–189. [Google Scholar] [CrossRef]
  4. Albuquerque, D.; Nóbrega, C.; Samouda, H.; Manco, L. Assessment of obesity and abdominal obesity among Portuguese children. Acta Med. Portuguesa 2012, 25, 169–173. [Google Scholar]
  5. Bendor, C.D.; Bardugo, A.; Pinhas-Hamiel, O.; Afek, A.; Twig, G. Cardiovascular morbidity, diabetes and cancer risk among children and adolescents with severe obesity. Cardiovasc. Diabetol. 2020, 19, 79. [Google Scholar] [CrossRef]
  6. Branca, F.; Nikogosian, H.; Lobstein, T. The Challenge Obesity in the WHO European Region and the Strategies for Response: Summary; World Health Organization: Geneva, Switzerland, 2007. [Google Scholar]
  7. Güngör, N.K. Overweight and obesity in children and adolescents. J. Clin. Res. Pediatr. Endocrinol. 2014, 6, 129. [Google Scholar] [CrossRef] [PubMed]
  8. Chait, A.; den Hartigh, L.J. Adipose tissue distribution, inflammation and its metabolic consequences, including diabetes and cardiovascular disease. Front. Cardiovasc. Med. 2020, 7, 22. [Google Scholar] [CrossRef] [Green Version]
  9. Prastowo, N.A.; Haryono, I.R. Elevated blood pressure and its relationship with bodyweight and anthropometric measurements among 8–11-year-old Indonesian school children. J. Public Health Res. 2020, 9, 1723. [Google Scholar] [CrossRef]
  10. Lande, M.B.; Carson, N.L.; Roy, J.; Meagher, C.C. Effects of childhood primary hypertension on carotid intima media thickness: A matched controlled study. Hypertension 2006, 48, 40–44. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  11. Must, A.; Jacques, P.F.; Dallal, G.E.; Bajema, C.J.; Dietz, W.H. Long-term morbidity and mortality of overweight adolescents: A follow-up of the Harvard Growth Study of 1922 to 1935. N. Engl. J. Med. 1992, 327, 1350–1355. [Google Scholar] [CrossRef] [PubMed]
  12. Freedman, D.S.; Mei, Z.; Srinivasan, S.R.; Berenson, G.S.; Dietz, W.H. Cardiovascular risk factors and excess adiposity among overweight children and adolescents: The Bogalusa Heart Study. J. Pediatr. 2007, 150, 12–17. [Google Scholar] [CrossRef] [PubMed]
  13. Stamler, J.; Stamler, R.; Neaton, J.D. Blood pressure, systolic and diastolic, and cardiovascular risks: US population data. Arch. Int. Med. 1993, 153, 598–615. [Google Scholar] [CrossRef]
  14. Freedman, D.S.; Dietz, W.H.; Srinivasan, S.R.; Berenson, G.S. The relation of overweight to cardiovascular risk factors among children and adolescents: The Bogalusa Heart Study. Pediatrics 1999, 103, 1175–1182. [Google Scholar] [CrossRef] [PubMed]
  15. Genovesi, S.; Giussani, M.; Pieruzzi, F.; Vigorita, F.; Arcovio, C.; Cavuto, S.; Stella, A. Results of blood pressure screening in a population of school-aged children in the province of Milan: Role of overweight. J. Hypertens. 2005, 23, 493–497. [Google Scholar] [CrossRef]
  16. Wang, M.; Kelishadi, R.; Khadilkar, A.; Hong, Y.M.; Nawarycz, T.; Krzywińska-Wiewiorowska, M.; Aounallah-Skhiri, H.; Motlagh, M.E.; Kim, H.S.; Khadilkar, V. Body mass index percentiles and elevated blood pressure among children and adolescents. J. Human Hypertens. 2020, 34, 319–325. [Google Scholar] [CrossRef] [PubMed]
  17. Lohman, T.G.; Roche, A.F.; Martorell, R. Anthropometric Standardization Reference Manual; Human Kinetics Books: Champaign, IL, USA, 1988. [Google Scholar]
  18. Jebb, S.; McCarthy, D.; Fry, T.; Prentice, A. New body fat reference curves for children. Int. J. Obes. 2006, 30, A156–A157. [Google Scholar]
  19. Siegel, M.J.; Hildebolt, C.F.; Bae, K.T.; Hong, C.; White, N.H. Total and intraabdominal fat distribution in preadolescents and adolescents: Measurement with MR imaging. Radiology 2007, 242, 846–856. [Google Scholar] [CrossRef]
  20. Pandit, D.S.; Khadilkar, A.V.; Chiplonkar, S.A.; Khadilkar, V.V.; Kinare, A.S. Arterial stiffness in obese children: Role of adiposity and physical activity. Indian J. Endocrinol. Metabol. 2014, 18, 70. [Google Scholar]
  21. Umer, A.; Kelley, G.A.; Cottrell, L.E.; Giacobbi, P.; Innes, K.E.; Lilly, C.L. Childhood obesity and adult cardiovascular disease risk factors: A systematic review with meta-analysis. BMC Public Health 2017, 17, 683. [Google Scholar] [CrossRef] [Green Version]
  22. Kelishadi, R.; Heshmat, R.; Ardalan, G.; Qorbani, M.; Taslimi, M.; Poursafa, P.; Keramatian, K.; Taheri, M.; Motlagh, M.-E. First report on simplified diagnostic criteria for pre-hypertension and hypertension in a national sample of adolescents from the Middle East and North Africa: The CASPIAN-III study. J. Pediatr. 2014, 90, 85–91. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Alp, H.; Karaarslan, S.; Eklioğlu, B.S.; Atabek, M.E.; Altın, H.; Baysal, T. Association between nonalcoholic fatty liver disease and cardiovascular risk in obese children and adolescents. Canadian J. Cardiol. 2013, 29, 1118–1125. [Google Scholar] [CrossRef]
  24. Gupta, P.P.; Fonarow, G.C.; Horwich, T.B. Obesity and the obesity paradox in heart failure. Canadian J. Cardiol. 2015, 31, 195–202. [Google Scholar] [CrossRef]
  25. Appel, L.J.; Brands, M.W.; Daniels, S.R.; Karanja, N.; Elmer, P.J.; Sacks, F.M. Dietary approaches to prevent and treat hypertension: A scientific statement from the American Heart Association. Hypertension 2006, 47, 296–308. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Whelton, P.K.; He, J.; Cutler, J.A.; Brancati, F.L.; Appel, L.J.; Follmann, D.; Klag, M.J. Effects of oral potassium on blood pressure: Meta-analysis of randomized controlled clinical trials. JAMA 1997, 277, 1624–1632. [Google Scholar] [CrossRef] [PubMed]
  27. Whelton, S.P.; Hyre, A.D.; Pedersen, B.; Yi, Y.; Whelton, P.K.; He, J. Effect of dietary fiber intake on blood pressure: A meta-analysis of randomized, controlled clinical trials. LWW 2005, 2005, 475–481. [Google Scholar] [CrossRef] [PubMed]
  28. Witham, M.D.; Nadir, M.A.; Struthers, A.D. Effect of vitamin D on blood pressure: A systematic review and meta-analysis. J. Hypertens. 2009, 27, 1948–1954. [Google Scholar] [CrossRef]
  29. Fisher, N.D.; Hollenberg, N.K. Aging and vascular responses to flavanol-rich cocoa. J. Hypertens. 2006, 24, 1575–1580. [Google Scholar] [CrossRef] [Green Version]
  30. Karim, M.; McCormick, K.; Kappagoda, C.T. Effects of cocoa extracts on endothelium-dependent relaxation. J. Nutr. 2000, 130, 2105S–2108S. [Google Scholar] [CrossRef]
  31. Taubert, D.; Roesen, R.; Schömig, E. Effect of cocoa and tea intake on blood pressure: A meta-analysis. Arch. Int. Med. 2007, 167, 626–634. [Google Scholar] [CrossRef] [Green Version]
  32. Pausova, Z.; Mahboubi, A.; Abrahamowicz, M.; Leonard, G.T.; Perron, M.; Richer, L.; Veillette, S.; Gaudet, D.; Paus, T. Sex differences in the contributions of visceral and total body fat to blood pressure in adolescence. Hypertension 2012, 59, 572–579. [Google Scholar] [CrossRef] [Green Version]
  33. Pazin, D.C.; da Luz Kaestner, T.L.; Olandoski, M.; Baena, C.P.; de Azevedo Abreu, G.; Kuschnir, M.C.C.; Bloch, K.V.; Faria-Neto, J.R. Association Between Abdominal Waist Circumference and Blood Pressure In Brazilian Adolescents With Normal Body Mass Index: Waist circumference and blood pressure in Adolescents. Glob. Heart 2020, 15. [Google Scholar] [CrossRef] [Green Version]
  34. Poirier, P.; Giles, T.D.; Bray, G.A.; Hong, Y.; Stern, J.S.; Pi-Sunyer, F.X.; Eckel, R.H. Obesity and cardiovascular disease: Pathophysiology, evaluation, and effect of weight loss: An update of the 1997 American Heart Association Scientific Statement on Obesity and Heart Disease from the Obesity Committee of the Council on Nutrition, Physical Activity, and Metabolism. Circulation 2006, 113, 898–918. [Google Scholar]
  35. Reddy, P.; Lent-Schochet, D.; Ramakrishnan, N.; McLaughlin, M.; Jialal, I. Metabolic syndrome is an inflammatory disorder: A conspiracy between adipose tissue and phagocytes. Clin. Chim. Acta 2019, 496, 35–44. [Google Scholar] [CrossRef] [PubMed]
  36. Tsioufis, C.; Kordalis, A.; Flessas, D.; Anastasopoulos, I.; Tsiachris, D.; Papademetriou, V.; Stefanadis, C. Pathophysiology of resistant hypertension: The role of sympathetic nervous system. Int. J. Hypertens. 2011, 2011. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. Zhou, Y.; Li, H.; Xia, N. The Interplay Between Adipose Tissue and Vasculature: Role of Oxidative Stress in Obesity. Front. Cardiovasc. Med. 2021, 8, 131. [Google Scholar] [CrossRef]
  38. Xu, H.; Barnes, G.T.; Yang, Q.; Tan, G.; Yang, D.; Chou, C.J.; Sole, J.; Nichols, A.; Ross, J.S.; Tartaglia, L.A. Chronic inflammation in fat plays a crucial role in the development of obesity-related insulin resistance. J. Clin. Investig. 2003, 112, 1821–1830. [Google Scholar] [CrossRef] [PubMed]
  39. Dinh, Q.N.; Drummond, G.R.; Sobey, C.G.; Chrissobolis, S. Roles of inflammation, oxidative stress, and vascular dysfunction in hypertension. BioMed Res. Int. 2014, 2014. [Google Scholar] [CrossRef] [Green Version]
  40. Landsberg, L.; Aronne, L.J.; Beilin, L.J.; Burke, V.; Igel, L.I.; Lloyd-Jones, D.; Sowers, J. Obesity-related hypertension: Pathogenesis, cardiovascular risk, and treatment—A position paper of the The Obesity Society and the American Society of Hypertension. Obesity 2013, 21, 8–24. [Google Scholar] [CrossRef] [PubMed]
  41. Ke, C.; Zhu, X.; Zhang, Y.; Shen, Y. Metabolomic characterization of hypertension and dyslipidemia. Metabolomics 2018, 14, 117. [Google Scholar] [CrossRef]
  42. Artwohl, M.; Roden, M.; Waldhäusl, W.; Freudenthaler, A.; Baumgartner-Parzer, S.M. Free fatty acids trigger apoptosis and inhibit cell cycle progression in human vascular endothelial cells. FASEB J. 2004, 18, 146–148. [Google Scholar] [CrossRef] [Green Version]
  43. Boden, G.; She, P.; Mozzoli, M.; Cheung, P.; Gumireddy, K.; Reddy, P.; Xiang, X.; Luo, Z.; Ruderman, N. Free fatty acids produce insulin resistance and activate the proinflammatory nuclear factor-κB pathway in rat liver. Diabetes 2005, 54, 3458–3465. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  44. Baumgartner, R.N.; Ross, R.; Heymsfield, S.B. Does adipose tissue influence bioelectric impedance in obese men and women? J. Appl. Physiol. 1998, 84, 257–262. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  45. Beechy, L.; Galpern, J.; Petrone, A.; Das, S.K. Assessment tools in obesity—Psychological measures, diet, activity, and body composition. Physiol. Behav. 2012, 107, 154–171. [Google Scholar] [CrossRef]
  46. Das, S.K. Body composition measurement in severe obesity. Curr. Opin. Clin. Nutr. Metab. Care 2005, 8, 602–606. [Google Scholar] [CrossRef] [Green Version]
  47. Duren, D.L.; Sherwood, R.J.; Czerwinski, S.A.; Lee, M.; Choh, A.C.; Siervogel, R.M.; Chumlea, W.C. Body composition methods: Comparisons and interpretation. J. Diabetes Sci. Technol. 2008, 2, 1139–1146. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Table 1. Socio-demographic characteristic of Jordanian adolescents.
Table 1. Socio-demographic characteristic of Jordanian adolescents.
Variablen (%)
Region
Northern Jordan363 (35.1)
Mid-Jordan508 (49.1)
Southern Jordan164 (15.8)
School grade
7th 181 (17.5)
8th 230 (22.2)
9th224 (21.6)
10th220 (21.3)
11th180 (17.4)
Father educational level
Illiterate23 (2.2)
≤12 years 538 (52.0)
>12 years474 (45.8)
Mother educational level
Illiterate17 (1.6)
≤12 years 576 (55.7)
>12 years442 (42.7)
Family Income (JD) *
≤300 176 (17.0)
301–499 297 (28.7)
500–799 234 (22.6)
≥800 296 (28.6)
Cigarette smoking
Yes243 (23.5)
No792 (76.5)
* Jordanian Dinar (JD) = USD 1.408. education level: ≤12 years: include elementary and high schools, ≥12 years: include after high school education.
Table 2. Prevalence of hypertension according to adolescents food group intake.
Table 2. Prevalence of hypertension according to adolescents food group intake.
Frequency of Eating Different Food/WeekMean ± SDp-ValueFrequency of Eating Different Food/WeekMean ± SDp-Value
VegetableNuts
Daily121.25 a ± 13.220.008Daily120.63 ± 13.110.162
4–6123.78 b ± 13.384–6122.90 ± 13.93
1–3123.08 b ± 13.291–3123.38 ± 13.29
No128.40 c ± 16.77No123.91 ± 13.65
FruitChocolate0.013
Daily121.07 a ± 13.220.033Daily121.81 a ± 13.23
4–6122.79 b ± 13.184–6121.07 a ± 12.66
1–3124.22 b ± 13.761–3124.56 b ± 13.89
No125.21 c ± 15.28No124.59 c ± 14.31
Milk and dairy productsSoda
Daily121.76 ± 12.890.113Daily122.90 ± 12.650.198
4–6122.27 ± 13.464–6122.03 ± 13.41
1–3124.31 ± 13.751–3123.24 ± 13.71
No122.82 ± 14.48No122.59 ± 15.42
MeatCanned fruit juice
Daily121.69 ± 12.710.061Daily122.28 ± 12.820.187
4–6122.55 ± 12.814–6121.22 ± 13.44
1–3122.59 ± 13.681–3123.05 ± 13.64
No126.36 ± 15.70No125.03 ± 15.29
FishLegumes
Daily122.04 ± 18.140.898Daily122.05 ± 12.980.337
4–6121.62 ± 12.814–6121.72 ± 13.59
1–3122.53 ± 13.431–3123.34 ± 13.60
No123.96 ± 13.52No124.31 ± 13.24
Different letters means that there is a statistically significant difference between the groups.
Table 3. Multivariate logistic regression between adolescent’s systolic hypertension and anthropometric measurements.
Table 3. Multivariate logistic regression between adolescent’s systolic hypertension and anthropometric measurements.
Multivariate Analysis
VariablesPre-SHTN
OR (95% CI)
p-ValueStage 1 SHTN
OR (95% CI)
p-ValueStage 2 SHTN
OR (95% CI)
p-Value
Body Mass Index *
Overweight2.3 (1.4, 3.8)0.0011.8 (1.01, 3.1)0.0473.2 (2.1, 5.1)<0.001
Obesity2.7 (1.6, 4.5)<0.0012.7 (1.6, 4.6)<0.0017.1 (4.7, 10.9)<0.001
Waist circumferences
≥90th percentile 2.3 (1, 5.5)0.0495 (2.3, 10.6)<0.0018.6 (4.5, 16.4)<0.001
Total Fat †
Over fat1.5 (0.8, 3.1)0.2091.1 (0.5, 2.4) 0.757 1.9 (1, 3.3)0.032
Obese2 (1.2, 3.4)0.0092.2 (1.3, 3.8)0.0043.5 (2.3, 5.5)<0.001
Trunk Fat
≥90th percentile1.6 (0.8, 3.2)0.1954 (2.2, 7.1)<0.0015.5(3.4, 9.1)<0.001
Visceral Fat
≥90th percentile1.8 (0.7, 4.6)0.2374.2 (1.9, 9.4)<0.0017.2 (3.7, 14.1)<0.001
* BMI for age was obtained and categorized according WHO cutoff point underweight (for age BMI < 5% percentile), normal weight (5% percentile < BMI < 85% percentile), overweight (85% percentile < BMI < 95% percentile), obese (BMI ≥ 95% percentile) (Riley and Bluhm, 2012). TOTAL FAT cut off point were determined. SHTN refer to systolic hypertension.
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Bawadi, H.; Kassab, M.; Zanabili, A.H.; Tayyem, R. Identification of Adolescents with Adiposities and Elevated Blood Pressure and Implementation of Preventive Measures Warrants the Use of Multiple Clinical Assessment Tools. J. Pers. Med. 2021, 11, 873. https://doi.org/10.3390/jpm11090873

AMA Style

Bawadi H, Kassab M, Zanabili AH, Tayyem R. Identification of Adolescents with Adiposities and Elevated Blood Pressure and Implementation of Preventive Measures Warrants the Use of Multiple Clinical Assessment Tools. Journal of Personalized Medicine. 2021; 11(9):873. https://doi.org/10.3390/jpm11090873

Chicago/Turabian Style

Bawadi, Hiba, Manal Kassab, Abdel Hadi Zanabili, and Reema Tayyem. 2021. "Identification of Adolescents with Adiposities and Elevated Blood Pressure and Implementation of Preventive Measures Warrants the Use of Multiple Clinical Assessment Tools" Journal of Personalized Medicine 11, no. 9: 873. https://doi.org/10.3390/jpm11090873

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