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Osteoporosis is a worldwide problem and mostly result from the age-dependent bone loss. Literatures
show factors involved in bone loss, but impacts of that are not totally clarify. This study primary aimed to
investigate whether basal metabolic rate and body composition affect bone mass in elderly and adult.
Cross-sectional study was performed to collect the data set of bone mass, muscle mass, fat mass, and basal
metabolic rate. The result showed that bone mass was highly correlate with basal metabolic rate (r = 0.979,
0.971; p = 0.000) and muscle mass (r = 0.947, 0.924; p = 0.000) in elderly and adult. Aged bone mass also related to fat mass. Bone mass in both age-groups were mostly influenced by basal metabolic rate (adjusted beta coefficients = 0.979, 0.971; p = 0.000). In conclusion, basal metabolic rate was correlate with bone mass and may be the factor affecting bone mass in both elderly and adult.
มูลนิธิโรคกระดูกพรุนแห่งประเทศไทย. แนวปฏิบัติบริการสาธารณสุข โรคกระดูกพรุน พ.ศ. 2553. จาก http://www.bangkokhealth.com/index.php/health/health-system/bone/2219-2012-10-18-03-27-04.html
Wang, W.J., Kuo, K.L., Liaw, C.K., et al. (2017). Bone health among older adults in Taiwan. Arch Gerontol Geriatr. 70, 155-161.
Cosman, F., Krege, J.H., Looker, A.C., et al. Spine fracture prevalence in a nationally representative sample of US women and men aged ≥40 years: results from the National Health and Nutrition Examination Survey (NHANES) 2013-2014. Osteoporos Int. doi: 10.1007/s00198-017-3948-9. [Epub ahead of print]
Campos-Obando, N., Koek, W.N., Hooker, E.R., et al., Serum phosphate is associated with fracture risk: the Rotterdam Study and MrOS. J Bone Miner Res. doi: 10.1002/jbmr.3094. [Epub ahead of print]
Lassen, N.E., Andersen, T.L., Pløen, G.G., et al., Coupling of bone resorption and formation in real time: new knowledge gained from Human Haversian BMUs. J Bone Miner Res. doi: 10.1002/jbmr.3091. [Epub ahead of print]
Nahar, V.K., Nelson, K.M., Ford, M.A., et al. (2016). Predictors of bone mineral density among Asian Indians in Northern Mississippi: a pilot study. J Res Health Sci. 16(4), 228-232.
Kenny, A.M., Prestwood, K.M., Marcello, K.M., et al. (2000). Determinants of bone density in healthy older men with low testosterone levels. J Gerontol A Biol Sci Med Sci. 55(9), M492-M497.
Kang, D.H., Guo, L.F., Guo, T., et al. (2015). Association of body composition with bone mineral density in northern Chinese men by different criteria for obesity. J Endocrinol Invest. 38(3), 323-331.
Jiang, Y., Zhang, Y., Jin, M., et al. (2015). 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. 10. doi: 10.1371/journal.pone.0130400.
Lee, H.J., Yang, S.J. (2017). Aging-related correlation between serum Sirtuin 1 activities and basal metabolic rate in women, but not in Men. Clin Nutr Res. 6(1), 18-26.
White, E., Mehnert, J.M., Chan, C.S. (2015).
Autophagy, Metabolism, and Cancer. Clin Cancer Res. 21(22), 5037-5046.
Fukagawa, N.K., Bandini, L.G., Young, J.B. (1990). Effect of age on body composition and resting metabolic rate. Am J Physiol. 259(2 Pt 1), E233-E238.
Poehlman, E.T., Goran, M.I., Gardner, A.W., et al. (1993). Determinants of decline in resting metabolic rate in aging females. Am J Physiol. 264(3 Pt 1), E450-E455.
Hsu, W.H., Fan, C.H., Lin, Z.R., et al. (2013). Effect of basal metabolic rate on the bone mineral density in middle to old age women in Taiwan. Maturitas. 76(1), 70-74.
Yilmaz, B., Yasar, E., Goktepe, A.S., et al. (2007). The relationship between basal metabolic rate and femur bone mineral density in men with traumatic spinal cord injury. Arch Phys Med Rehabil. 88(6), 758-761.
Burr, D.B. (1997). Muscle strength, bone mass, and age-related bone loss. J Bone Miner Res. 12(10), 1547-1551.
Baumgartner, R.N. (2000). Body composition in healthy aging. Ann N Y Acad Sci. 904, 437-448.
Soares, M.J., Cummings, N.K., Ping-Delfos, W.L. (2011). Energy metabolism and the metabolic syndrome: Does a lower basal metabolic rate signal recovery following weight loss? Diabetes Metab Syndr. 5(2), 98-101.
Andreoli, A., Garaci, F., Cafarelli, F.P., et al. (2016). Body composition in clinical practice. Eur J Radiol. 85(8), 1461-1468.
Johnstone, A.M., Murison, S.D., Duncan, J.S., et al, (2005). Factors influencing variation in basal metabolic rate include fat-free mass, fat mass, age, and circulating thyroxine but not sex, circulating leptin, or triiodothyronine. Am J Clin Nutr. 82(5), 941-948.