Please use this identifier to cite or link to this item: 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
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