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大规模 GWAS 鉴定出多个与握力相关的位点,为肌肉健康提供了生物学见解。

Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness.

机构信息

MRC Epidemiology Unit, University of Cambridge School of Clinical Medicine, Cambridge CB2 0QQ, UK.

Department of Internal Medicine, Erasmus Medical Center, 3015 CE Rotterdam, The Netherlands.

出版信息

Nat Commun. 2017 Jul 12;8:16015. doi: 10.1038/ncomms16015.

Abstract

Hand grip strength is a widely used proxy of muscular fitness, a marker of frailty, and predictor of a range of morbidities and all-cause mortality. To investigate the genetic determinants of variation in grip strength, we perform a large-scale genetic discovery analysis in a combined sample of 195,180 individuals and identify 16 loci associated with grip strength (P<5 × 10) in combined analyses. A number of these loci contain genes implicated in structure and function of skeletal muscle fibres (ACTG1), neuronal maintenance and signal transduction (PEX14, TGFA, SYT1), or monogenic syndromes with involvement of psychomotor impairment (PEX14, LRPPRC and KANSL1). Mendelian randomization analyses are consistent with a causal effect of higher genetically predicted grip strength on lower fracture risk. In conclusion, our findings provide new biological insight into the mechanistic underpinnings of grip strength and the causal role of muscular strength in age-related morbidities and mortality.

摘要

握力是肌肉健康的常用指标,也是身体虚弱的标志,能够预测多种疾病和全因死亡率。为了探究握力变化的遗传决定因素,我们在一个包含 195180 人的综合样本中进行了大规模的遗传发现分析,在综合分析中鉴定出 16 个与握力相关的位点(P<5 × 10)。其中一些位点包含与骨骼肌纤维结构和功能相关的基因(ACTG1)、神经元维持和信号转导(PEX14、TGFA、SYT1),或涉及精神运动障碍的单基因综合征(PEX14、LRPPRC 和 KANSL1)。孟德尔随机化分析结果与更高的遗传预测握力与更低的骨折风险之间存在因果关系一致。总之,我们的研究结果为握力的潜在机制以及肌肉力量在与年龄相关的疾病和死亡率中的因果作用提供了新的生物学见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d53/5510175/669d13d07074/ncomms16015-f1.jpg

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