Nature CommunicationsGenetic & Genomic MedicinePeer-reviewed journal article
Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women
Garan JonesiD, Katerina TrajanoskaiD, Adam J. SantanastoiD, Najada StringaiD, Chia‐Ling KuoiD, Janice L. AtkinsiD, Joshua Richard LewisiD, ThuyVy DuongiD, Shengjun HongiD, Mary Lou Biggs, Jian’an LuaniD, Chloé SarnowskiiD, Kathryn L. LunettaiD, Toshiko TanakaiD, Mary K. WojczynskiiD, Ryan CvejkusiD, Maria NethanderiD, Sahar Ghasemi, Jingyun YangiD, M. Carola ZillikensiD, Stefan WalteriD, Kamil SicinskiiD, Érika KagueiD, Cheryl L. Ackert‐BicknelliD, Dan E. ArkingiD, , Luke C. PillingiD
- Citations
- 222
- FWCI
- 5.38
- Field percentile
- top 2%
Abstract
Low muscle strength is an important heritable indicator of poor health linked to morbidity and mortality in older people. In a genome-wide association study meta-analysis of 256,523 Europeans aged 60 years and over from 22 cohorts we identified 15 loci associated with muscle weakness (European Working Group on Sarcopenia in Older People definition: n=48,596 cases, 18.9% of total), including 12 loci not implicated in previous analyses of continuous measures of grip strength. Loci include genes reportedly involved in autoimmune disease (HLA-DQA1 p=4*10-17), arthritis (GDF5 p=4*10-13), cell cycle control and cancer protection, regulation of transcription, and others involved in the development and maintenance of the musculoskeletal system. Using Mendelian randomization we report possible overlapping causal pathways, including diabetes susceptibility, hematological parameters, and the immune system. We conclude that muscle weakness in older adults has distinct mechanisms from continuous strength, including several pathways considered to be hallmarks of ageing.
- organism: human
- assay: GWAS summary statistics
- research focus: GWAS / association mapping
- approach: statistical model
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