Evaluation of Bone and Body Mineral Profile in Association with Protein Content, Fat, Fat-Free, Skeletal Muscle Tissues According to Obesity Classification among Adult Men
Authors: Orkide Donma, Mustafa M. Donma
Abstract:
Obesity is associated with increased fat mass as well as fat percentage. Minerals are the elements, which are of vital importance. In this study, the relationships between body as well as bone mineral profile and the percentage as well as mass values of fat, fat-free portion, protein, skeletal muscle were evaluated in adult men with normal body mass index (N-BMI), and those classified according to different stages of obesity. A total of 103 adult men classified into five groups participated in this study. Ages were within 19-79 years range. Groups were N-BMI (Group 1), overweight (OW) (Group 2), first level of obesity (FLO) (Group 3), second level of obesity (SLO) (Group 4) and third level of obesity (TLO) (Group 5). Anthropometric measurements were performed. BMI values were calculated. Obesity degree, total body fat mass, fat percentage, basal metabolic rate (BMR), visceral adiposity, body mineral mass, body mineral percentage, bone mineral mass, bone mineral percentage, fat-free mass, fat-free percentage, protein mass, protein percentage, skeletal muscle mass and skeletal muscle percentage were determined by TANITA body composition monitor using bioelectrical impedance analysis technology. Statistical package (SPSS) for Windows Version 16.0 was used for statistical evaluations. The values below 0.05 were accepted as statistically significant. All the groups were matched based upon age (p > 0.05). BMI values were calculated as 22.6 ± 1.7 kg/m2, 27.1 ± 1.4 kg/m2, 32.0 ± 1.2 kg/m2, 37.2 ± 1.8 kg/m2, and 47.1 ± 6.1 kg/m2 for groups 1, 2, 3, 4, and 5, respectively. Visceral adiposity and BMR values were also within an increasing trend. Percentage values of mineral, protein, fat-free portion and skeletal muscle masses were decreasing going from normal to TLO. Upon evaluation of the percentages of protein, fat-free portion and skeletal muscle, statistically significant differences were noted between NW and OW as well as OW and FLO (p < 0.05). However, such differences were not observed for body and bone mineral percentages. Correlation existed between visceral adiposity and BMI was stronger than that detected between visceral adiposity and obesity degree. Correlation between visceral adiposity and BMR was significant at the 0.05 level. Visceral adiposity was not correlated with body mineral mass but correlated with bone mineral mass whereas significant negative correlations were observed with percentages of these parameters (p < 0.001). BMR was not correlated with body mineral percentage whereas a negative correlation was found between BMR and bone mineral percentage (p < 0.01). It is interesting to note that mineral percentages of both body as well as bone are highly affected by the visceral adiposity. Bone mineral percentage was also associated with BMR. From these findings, it is plausible to state that minerals are highly associated with the critical stages of obesity as prominent parameters.
Keywords: Bone, men, minerals, obesity.
Digital Object Identifier (DOI): doi.org/10.5281/zenodo.3455567
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[1] J. van Leeuwen, B. W. Koes, W. D. Paulis, and M. van Middelkoop, “Differences in bone mineral density between normal-weight children and children with overweight and obesity: a systematic review and meta-analysis,” Obes. Rev., vol. 18, pp. 526–546, May 2017.
[2] E. Chaplais, G. Naughton, D. Greene, F. Dutheil, B. Pereira, D. Thivel, and D. Courteix, “Effects of interventions with a physical activity component on bone health in obese children and adolescents: a systematic review and meta-analysis,” J. Bone Miner. Metab., vol.36, pp.12-30, Jan. 2018.
[3] S. L. Edelstein, and E. Barrett-Connor, “Relation between body size and bone mineral density in elderly men and women,” Am. J. Epidemiol., vol. 138, pp. 160-169, Aug. 1993.
[4] D. T. Felson, Y. Zhang, M. T. Hannan, and J. J. Anderson, “Effects of weight and body mass index on bone mineral density in men and women: the Framingham study,” J. Bone Miner. Res., vol. 8, pp. 567-573, May 1993.
[5] J. J. Cao, “Effects of obesity on bone metabolism,” J. Orthop. Surg. Res., vol.6, pp.30, Jun. 2011.
[6] S. A. Shapses, L. C. Pop, and Y. Wang, “Obesity is a concern for bone health with aging,” Nutr. Res., vol.39, pp. 1-13, Mar. 2017.
[7] S. Gonnelli, C. Caffarelli, and R. Nuti, “Obesity and fracture risk,” Clin. Cases Miner. Bone Metab., vol.11, pp. 9-14, Jan. 2014.
[8] S. J. Lee, J. Y. Lee, and J. Sung, “Obesity and bone health revisited: A Mendelian randomization study for Koreans,” J. Bone Miner. Res.,vol. 28, pp.e3678, Feb. 2019.
[9] WHO. The world health report 1998 –Life in the 21st century: A vision for all. {https://www.who.int/1998/en}.
[10] E. Denova-Gutiérrez, P. Clark, R. F. Capozza, L. M. Nocciolino, J. L. Ferretti, R. Velázquez-Cruz, B. Rivera, G. R. Cointry, and J. Salmerón, “Differences in the relation between bone mineral content and lean body mass according to gender and reproductive status by age ranges,” J. Bone Miner. Metab., 2018 Dec 4. (Epub ahead of print)
[11] R. Cherif, F. Mahjoub, H. Sahli, E. Cheour, M. Sakly, and N. Attia, “Clinical and body composition predictors of bone turnover and mineral content in obese postmenopausal women,” Clin. Rheumatol., vol.38, pp.739-747, Mar 2019.
[12] A. Kęska, G. Lutosławska, J. Bertrandt, and M. Sobczak,”Relationships between bone mineral density and new indices of body composition in young, sedentary men and women,” Ann. Agric. Environ. Med., vol.25, pp.23-25, Mar. 2018.
[13] E. Sienkiewicz, F. Magkos, K. N. Aronis, M. Brinkoetter, J. P. Chamberland, and S. Chou, K. M. Arampatzi, C. Gao, A. Koniaris,and C. S. Mantzoros, “Long-term metreleptin treatment increases bone mineral density and content at the lumbar spine of lean hypoleptinemic women,” Metabolism, vol. 60, pp.1211-1221,Sept. 2011.
[14] T. Sutter, H. Toumi, A. Valery, R. El Hage, A. Pinti, and E. Lespessailles, “Relationships between muscle mass, strength and regional bone mineral density in young men,” PLoS One, vol. 14, pp. e0213681, Mar. 2019.
[15] A. Khawaja, P. Sabbagh, J. Prioux, G. Zunquin, G. Baquet, G. Maalouf, and R. El Hage, “Does muscular power predict bone mineral density in young adults?,” J. Clin. Densitom., vol.30283,pp.S1094-6950 Jan. 2019.
[16] I. Rodriguez-Gomez, A. Manas, J. Losa-Reyna, L. Rodriguez-Manas, S. F. M. Chastin, L. M. Alegre, F. J. Garcia-Garcia, and I. Ara, “ The impact of movement behaviors on bone health in elderly with adequate nutritional status: Compositional data analysis depending on the frailty status,” Nutrients, vol.11, pp. E582, Mar. 2019.
[17] F. J. Amaro-Gahete, O. A. de la, L. Jurado-Fasoli, J. R. Ruiz, M. J. Castillo, and A. Gutiérrez, “Effects of different exercise training programs on body composition: a randomized control trial,” Scand. J. Med. Sci. Sports, 2019 Mar 5. (Epub ahead of print).
[18] S. M. Bristow, G. D. Gamble, A. M. Horne, and I. R. Reid, “Longitudinal changes in bone mineral density, bone mineral content and bone area at the lumbar spine and hip in postmenopausal women, and the influence of abdominal aortic calcification,” Bone Rep., vol.10,pp.100190, Dec. 2018.
[19] J. M. Kindler, A. J. Lobene, K. A. Vogel, B. R. Martin, L. D. McCabe, M. Peacock, S. J. Warden, G. P. McCabe, and C. M. Weaver, ” Adiposity, insulin resistance, and bone mass in children and adolescents,” J. Clin. Endocrinol. Metab., vol.104, pp. 892-899, Mar. 2019.
[20] J. Jiang, P. Qiu, Y. Wang, C. Zhao, S. Fan, and X. Lin, “Association between serum high-density lipoprotein cholesterol and bone health in the general population: a large and multicenter study,” Arch. Osteoporos., vol.14, pp.36, Mar. 2019.