Metabolically favorable adiposity and bone mineral density: a Mendelian randomization analysis

孟德尔随机化 骨矿物 医学 股骨颈 骨密度 内科学 体脂百分比 骨质疏松症 内分泌学 生理学 人体测量学 生物 基因型 遗传学 基因 遗传变异
作者
Victoria L. Bland,Jennifer W. Bea,Scott B. Going,Hanieh Yaghootkar,Amit Arora,Ferris A. Ramadan,Janet L. Funk,Zhao Chen,Yann C. Klimentidis
出处
期刊:Obesity [Wiley]
卷期号:31 (1): 267-278 被引量:5
标识
DOI:10.1002/oby.23604
摘要

Abstract Objective This analysis assessed the putative causal association between genetically predicted percent body fat and areal bone mineral density (aBMD) and, more specifically, the association between genetically predicted metabolically “favorable adiposity” (MFA) and aBMD at clinically relevant bone sites. Methods Mendelian randomization was used to assess the relationship of MFA and percent body fat with whole‐body, lumbar spine, femoral neck, and forearm aBMD. Sex‐stratified and age‐stratified exploratory analyses were conducted. Results In all MR analyses, genetically predicted MFA was inversely associated with aBMD for the whole body (β = −0.053, p = 0.0002), lumbar spine (β = −0.075; p = 0.0001), femoral neck (β = −0.045; p = 0.008), and forearm (β = −0.115; p = 0.001). This negative relationship was strongest in older individuals and did not differ by sex. The relationship between genetically predicted percent body fat and aBMD was nonsignificant across all Mendelian randomization analyses. Several loci that were associated at a genome‐wide significance level ( p < 5 × 10 −8 ) in opposite directions with body fat and aBMD measures were also identified. Conclusions This study did not support the hypothesis that MFA protects against low aBMD. Instead, it showed that MFA may result in lower aBMD. Further research is needed to understand how MFA affects aBMD and other components of bone health such as bone turnover, bone architecture, and osteoporotic fractures.
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