Common strength 'genes' identified for first time

July 12, 2017, University of Cambridge
Skeletal muscle tissue. Credit: University of Michigan Medical School

Common genetic factors that influence muscle strength in humans have been identified for the first time in a study led by researchers from the University of Cambridge and published today in Nature Communications.

The researchers used data on hand grip from more than 140,000 participants in the UK Biobank study, combined with 50,000 additional individuals from the UK, Netherlands, Denmark and Australia, to identify sixteen common genetic variants that are associated with strength.

Dan Wright, joint first author on this paper and a PhD student at the Medical Research Council Epidemiology (MRC) Unit at the University of Cambridge, said: "The very large number of individuals participating in UK Biobank provides a powerful resource for identifying genes involved in complex traits such as muscle strength, and helps us understand their underlying biology and its relevance to health."

Many of these variants were located within or near to genes known to play a role in biological processes highly relevant to muscle function, including the structure and function of , and the communication of the nervous system with muscle cells.

Mutations in some of the genes highlighted are also known to be associated with severe monogenic syndromes - conditions caused by a single genetic mutations - characterised by compromised . This demonstrates that in genes which cause serious muscular conditions may also influence differences in strength in the general population.

Dr Robert Scott, who co-led the study with colleagues from the MRC Epidemiology Unit, said: "While we have long suspected a role for genetics in the variation in muscle strength, these findings give the first insights into some of the specific genetic variants that underpin variation in strength.

"These could be important steps towards identifying new treatments to prevent or treat muscle weakness."

Hand grip strength has been reported to be associated with many health outcomes, including risk of mortality, cardiovascular disease, and fracture - although it has been unclear whether variation in strength actually causes these outcomes, or simply reflects underlying disease processes.

Using the sixteen genetic variants identified for strength, the researchers were able to investigate the hypothesised causal link between strength and these adverse health outcomes. Their study found no evidence that lower strength causally increases risk of death or cardiovascular disease, but they did find evidence that higher muscular strength reduces risk of fracture, supporting the use of strength training interventions as a strategy to reduce risk of fractures.

Professor Nick Wareham, director of the MRC Epidemiology Unit and a senior author of the study, noted: "This work highlights the importance of in the prevention of fractures and the complications which can often follow a fall."

Explore further: Understanding the epidemiology of sarcopenia throughout the lifecourse

More information: Willems, SM et al. Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness. Nature Communications; 12 July 2017; DOI: 10.1038/ncomms16015

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