在骨量峰值年龄的非糖尿病男性中,胰岛素抵抗与较小的皮质骨大小有关

C. Verroken, H. Zmierczak, S. Goemaere, J. Kaufman, B. Lapauw
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引用次数: 21

摘要

在2型糖尿病患者中,尽管骨密度保持不变,但骨折风险增加。虽然这种明显的矛盾可能部分解释为胰岛素抵抗影响骨结构和/或材料特性,但很少有研究调查胰岛素抵抗和骨几何之间的关系。目的:在骨量达到峰值年龄的非糖尿病男性队列中探讨这种相关性。设计、环境和参与者:在一所大学研究中心进行了一项横断面、基于人群的兄弟姐妹配对研究,招募了996名年龄在25至45岁之间的非糖尿病男性。胰岛素抵抗采用胰岛素抵抗稳态模型(HOMA-IR)评估,空腹血清样本中测量胰岛素和葡萄糖。采用桡骨远端、桡骨和胫骨轴的外围定量计算机断层扫描评估骨几何形状。结果在年龄、身高和体重调整分析中,HOMA-IR与桡骨远端小梁面积、皮质面积、骨膜和骨膜内周长以及桡骨和胫骨轴的极强度应变指数呈负相关(β≤-0.13,P < 0.001)。在对双能x线吸收测量得出的身体成分、骨转换标志物、肌肉大小或功能测量、脂联素、瘦素、胰岛素样生长因子1或性类固醇水平进行额外调整后,这些相关性基本保持不变。结论:在骨量峰值年龄的非糖尿病男性队列中,胰岛素抵抗与骨小梁和皮质骨大小呈负相关。在调整身体组成、肌肉大小或功能或性类固醇水平后,这些关联仍然存在,这表明胰岛素抵抗对骨骼几何形状有独立的影响。
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Insulin Resistance Is Associated With Smaller Cortical Bone Size in Nondiabetic Men at the Age of Peak Bone Mass
Context In type 2 diabetes mellitus, fracture risk is increased despite preserved areal bone mineral density. Although this apparent paradox may in part be explained by insulin resistance affecting bone structure and/or material properties, few studies have investigated the association between insulin resistance and bone geometry. Objective We aimed to explore this association in a cohort of nondiabetic men at the age of peak bone mass. Design, Setting, and Participants Nine hundred ninety-six nondiabetic men aged 25 to 45 years were recruited in a cross-sectional, population-based sibling pair study at a university research center. Main Outcome Measures Insulin resistance was evaluated using the homeostasis model assessment of insulin resistance (HOMA-IR), with insulin and glucose measured from fasting serum samples. Bone geometry was assessed using peripheral quantitative computed tomography at the distal radius and the radial and tibial shafts. Results In age-, height-, and weight-adjusted analyses, HOMA-IR was inversely associated with trabecular area at the distal radius and with cortical area, periosteal and endosteal circumference, and polar strength strain index at the radial and tibial shafts (β ≤ -0.13, P < 0.001). These associations remained essentially unchanged after additional adjustment for dual-energy X-ray absorptiometry-derived body composition, bone turnover markers, muscle size or function measurements, or adiponectin, leptin, insulin-like growth factor 1, or sex steroid levels. Conclusion In this cohort of nondiabetic men at the age of peak bone mass, insulin resistance is inversely associated with trabecular and cortical bone size. These associations persist after adjustment for body composition, muscle size or function, or sex steroid levels, suggesting an independent effect of insulin resistance on bone geometry.
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