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Casual associations between brain structure and sarcopenia: A large‐scale genetic correlation and mendelian randomization study

肌萎缩 孟德尔随机化 全基因组关联研究 人口 优势比 物理医学与康复 生物 内科学 医学 遗传学 单核苷酸多态性 基因型 遗传变异 环境卫生 基因
作者
Guang Yang,Wenqing Xie,Bin Li,Guihu Zhao,Jinchen Li,Wenfeng Xiao,Yusheng Li
出处
期刊:Aging Cell [Wiley]
卷期号:23 (10): e14252-e14252 被引量:6
标识
DOI:10.1111/acel.14252
摘要

Abstract Sarcopenia presenting a critical challenge in population‐aging healthcare. The elucidation of the interplay between brain structure and sarcopenia necessitates further research. The aim of this study is to explore the casual association between brain structure and sarcopenia. Linkage disequilibrium score regression (LDSC) was conducted to estimate the genetic correlations; MR was then performed to explore the causal relationship between Brain imaging‐derived phenotypes (BIDPs) and three sarcopenia‐related traits: handgrip strength, walking pace, and appendicular lean mass (ALM). The main analyses were conducted using the inverse‐variance weighted method. Moreover, weighted median and MR–Egger were conducted as sensitivity analyses. Genetic association between 6.41% of BIDPs and ALM was observed, and 4.68% of BIDPs exhibited causal MR association with handgrip strength, 2.11% of BIDPs were causally associated with walking pace, and 2.04% of BIDPs showed causal association with ALM. Volume of ventromedial hypothalamus was associated with increased odds of handgrip strength (OR: 1.18, 95% CI: 1.02 to 1.37) and ALM (OR: 1.05, 95% CI: 1.01 to 1.09). Mean thickness of G‐pariet‐inf‐Angular was associated with decreased odds of handgrip strength (OR: 0.83, 95% CI: 0.70 to 0.97) and walking pace (OR: 0.97, 95% CI: 0.93 to 0.99). As part of the brain structure forward causally influences sarcopenia, which may provide new perspectives for the prevention of sarcopenia and offer valuable insights for further research on the brain‐muscle axis.
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