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ABSTRACT: Background
Phenotypic age acceleration (PhenoAgeAccel) is a promising biological aging metric, but its associations with chronic digestive disease risk are unclear. This study evaluated these associations and assessed modification by genetic risk and lifestyle.Methods
We analyzed 292,639 UK Biobank participants. PhenoAge and PhenoAgeAccel were calculated using a validated algorithm based on clinical biomarkers. Cox proportional hazards models estimated associations of PhenoAgeAccel, genetic risk, and lifestyle with incident chronic digestive diseases, including interaction and stratified analyses. Variance decomposition quantified contributions of aging, genetics, and lifestyle.Results
Over a median 13.67-year follow-up, PhenoAgeAccel > 0 (accelerated aging) was ind
SUBMITTER: Xiang S
PROVIDER: S-EPMC12835587 | biostudies-literature | 2026 Feb
REPOSITORIES: biostudies-literature