Risk of subsequent gastrointestinal disease assessed by skeletal muscle strength and mass in a prospective cohort study

Skeletal muscle may mutually interact with gastrointestinal disease through metabolic homeostasis and nutritional status and therefore may be a marker for early risk detection. We conducted a prospective cohort analysis including 393,606 participants (mean age 56.0 years, 53.9% female) from the UK B...

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Veröffentlicht in:iScience 2024-04, Vol.27 (4), p.109341-109341, Article 109341
Hauptverfasser: Dan, Lintao, Qin, Pei, Xie, Siyuan, Sun, Yuhao, Fu, Tian, Ruan, Xixian, Shi, Wenming, Chen, Jie, Cai, Jianting, Li, Xue
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Sprache:eng
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Zusammenfassung:Skeletal muscle may mutually interact with gastrointestinal disease through metabolic homeostasis and nutritional status and therefore may be a marker for early risk detection. We conducted a prospective cohort analysis including 393,606 participants (mean age 56.0 years, 53.9% female) from the UK Biobank. The exposures were grip strength and skeletal muscle mass (SMM). The primary outcomes were 24 incident gastrointestinal diseases. During a mean follow-up of 12.1 years, we found that one sex-specific SD increase in grip strength and SMM were associated with reduced risk of 16 and 19 gastrointestinal diseases, respectively. For grip strength, the HRs ranged from 0.94 (for ulcerative colitis) to 0.80 (for liver cancers). For SMM, the HRs ranged from 0.92 (for colorectal cancer) to 0.51 (for non-alcoholic fatty liver disease). Our finding suggested that grip strength and SMM might be significant indicators for gastrointestinal diseases risk screen. [Display omitted] •Higher grip strength was associated with reduced risk of 16 gastrointestinal diseases•Higher muscle mass was associated with reduced risk of 19 gastrointestinal diseases•Reveal unreported associations of muscle indicators with 10 gastrointestinal diseases•Highlight the potential of muscle indicators as early risk screen manners Gastroenterology; Public health; Risk stratification
ISSN:2589-0042
2589-0042
DOI:10.1016/j.isci.2024.109341