Please use this identifier to cite or link to this item: https://doi.org/10.1038/ncomms16015
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dc.titleLarge-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness
dc.contributor.authorWillems, S.M
dc.contributor.authorWright, D.J
dc.contributor.authorDay, F.R
dc.date.accessioned2020-10-26T02:44:43Z
dc.date.available2020-10-26T02:44:43Z
dc.date.issued2017
dc.identifier.citationWillems, 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
dc.identifier.issn2041-1723
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/179708
dc.description.abstractHand 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.
dc.publisherNature Publishing Group
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectanalytical method
dc.subjectbiomechanics
dc.subjectfitness
dc.subjectgene
dc.subjectgenetic analysis
dc.subjectgenetic structure
dc.subjectgenome
dc.subjectmorbidity
dc.subjectmortality
dc.subjectmuscle
dc.subjectACTG1 gene
dc.subjectArticle
dc.subjectfemale
dc.subjectgene
dc.subjectgene locus
dc.subjectgenome-wide association study
dc.subjectgrip strength
dc.subjecthand grip
dc.subjecthuman
dc.subjectKANSL1 gene
dc.subjectLRPPRC gene
dc.subjectmajor clinical study
dc.subjectmale
dc.subjectMendelian randomization analysis
dc.subjectmuscle cell
dc.subjectmuscle strength
dc.subjectPEX14 gene
dc.subjectpsychomotor disorder
dc.subjectsignal transduction
dc.subjectskeletal muscle
dc.subjectSYT1 gene
dc.subjectTGFA gene
dc.subjectadult
dc.subjectaged
dc.subjectCaucasian
dc.subjectcohort analysis
dc.subjectgene locus
dc.subjectgenetics
dc.subjecthand
dc.subjecthand strength
dc.subjectmiddle aged
dc.subjectphysiology
dc.subjectpopulation genetics
dc.subjectsingle nucleotide polymorphism
dc.subjectUnited Kingdom
dc.subjectACTG1 protein, human
dc.subjectactin
dc.subjectKANSL1 protein, human
dc.subjectLRPPRC protein, human
dc.subjectmembrane protein
dc.subjectnuclear protein
dc.subjectPEX14 protein, human
dc.subjectrepressor protein
dc.subjectTGFA protein, human
dc.subjecttransforming growth factor alpha
dc.subjecttumor protein
dc.subjectActins
dc.subjectAdult
dc.subjectAged
dc.subjectCohort Studies
dc.subjectEuropean Continental Ancestry Group
dc.subjectFemale
dc.subjectGenetic Loci
dc.subjectGenetics, Population
dc.subjectGenome-Wide Association Study
dc.subjectHand
dc.subjectHand Strength
dc.subjectHumans
dc.subjectMale
dc.subjectMembrane Proteins
dc.subjectMiddle Aged
dc.subjectNeoplasm Proteins
dc.subjectNuclear Proteins
dc.subjectPolymorphism, Single Nucleotide
dc.subjectRepressor Proteins
dc.subjectTransforming Growth Factor alpha
dc.subjectUnited Kingdom
dc.typeArticle
dc.contributor.departmentOBSTETRICS & GYNAECOLOGY
dc.description.doi10.1038/ncomms16015
dc.description.sourcetitleNature Communications
dc.description.volume8
dc.description.page16015
dc.published.statepublished
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