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https://doi.org/10.1038/ncomms16015
Title: | Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness | Authors: | Willems, S.M Wright, D.J Day, F.R |
Keywords: | analytical method biomechanics fitness gene genetic analysis genetic structure genome morbidity mortality muscle ACTG1 gene Article female gene gene locus genome-wide association study grip strength hand grip human KANSL1 gene LRPPRC gene major clinical study male Mendelian randomization analysis muscle cell muscle strength PEX14 gene psychomotor disorder signal transduction skeletal muscle SYT1 gene TGFA gene adult aged Caucasian cohort analysis gene locus genetics hand hand strength middle aged physiology population genetics single nucleotide polymorphism United Kingdom ACTG1 protein, human actin KANSL1 protein, human LRPPRC protein, human membrane protein nuclear protein PEX14 protein, human repressor protein TGFA protein, human transforming growth factor alpha tumor protein Actins Adult Aged Cohort Studies European Continental Ancestry Group Female Genetic Loci Genetics, Population Genome-Wide Association Study Hand Hand Strength Humans Male Membrane Proteins Middle Aged Neoplasm Proteins Nuclear Proteins Polymorphism, Single Nucleotide Repressor Proteins Transforming Growth Factor alpha United Kingdom |
Issue Date: | 2017 | Publisher: | Nature Publishing Group | Citation: | Willems, S.M, Wright, D.J, Day, F.R (2017). Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness. Nature Communications 8 : 16015. ScholarBank@NUS Repository. https://doi.org/10.1038/ncomms16015 | Rights: | Attribution 4.0 International | 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 × 10-8) 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. © The Author(s) 2017. | Source Title: | Nature Communications | URI: | https://scholarbank.nus.edu.sg/handle/10635/179708 | ISSN: | 2041-1723 | DOI: | 10.1038/ncomms16015 | Rights: | Attribution 4.0 International |
Appears in Collections: | Elements Staff Publications |
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