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]
日期:2022-12-10
卷期号:31 (1): 267-278
被引量:5
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI