Institute for Human Nutrition and Food Science, Christian-Albrechts-University, Düsternbrooker Weg 17, 24105, Kiel, Germany.
Institute of Nutritional Science, University of Potsdam, Potsdam, Germany.
Sci Rep. 2023 Mar 28;13(1):5030. doi: 10.1038/s41598-023-31642-4.
Lower bone mass in older adults may be mediated by the endocrine crosstalk between muscle, adipose tissue and bone. In 150 community-dwelling adults (59-86 years, BMI 17-37 kg/m; 58.7% female), skeletal muscle mass index, adipose tissue and fat mass index (FMI) were determined. Levels of myokines, adipokines, osteokines, inflammation markers and insulin were measured as potential determinants of bone mineral content (BMC) and density (BMD). FMI was negatively associated with BMC and BMD after adjustment for mechanical loading effects of body weight (r-values between -0.37 and -0.71, all p < 0.05). Higher FMI was associated with higher leptin levels in both sexes, with higher hsCRP in women and with lower adiponectin levels in men. In addition to weight and FMI, sclerostin, osteocalcin, leptin × sex and adiponectin were independent predictors of BMC in a stepwise multiple regression analysis. Muscle mass, but not myokines, showed positive correlations with bone parameters that were weakened after adjusting for body weight (r-values between 0.27 and 0.58, all p < 0.01). Whereas the anabolic effect of muscle mass on bone in older adults may be partly explained by mechanical loading, the adverse effect of obesity on bone is possibly mediated by low-grade inflammation, higher leptin and lower adiponectin levels.
老年人的骨量减少可能是由肌肉、脂肪组织和骨骼之间的内分泌串扰介导的。在 150 名社区居住的成年人(59-86 岁,BMI 17-37kg/m;58.7%为女性)中,测定了骨骼肌质量指数、脂肪组织和脂肪质量指数(FMI)。测量了肌因子、脂肪因子、骨因子、炎症标志物和胰岛素水平,作为骨矿物质含量(BMC)和密度(BMD)的潜在决定因素。在调整体重对身体力学负荷的影响后,FMI 与 BMC 和 BMD 呈负相关(r 值在-0.37 到-0.71 之间,所有 p 值均<0.05)。在两性中,较高的 FMI 与较高的瘦素水平相关,与女性中较高的 hsCRP 相关,与男性中较低的脂联素水平相关。除了体重和 FMI 之外,骨硬化蛋白、骨钙素、瘦素×性别和脂联素在逐步多元回归分析中是 BMC 的独立预测因子。肌肉质量,而不是肌因子,与骨参数呈正相关,在调整体重后,这些相关性减弱(r 值在 0.27 到 0.58 之间,所有 p 值均<0.01)。虽然肌肉质量对老年人骨骼的合成作用可能部分归因于力学负荷,但肥胖对骨骼的不良影响可能是由低度炎症、较高的瘦素和较低的脂联素水平介导的。