| Literature DB >> 33959723 |
Handan Melike Dönertaş1, Daniel K Fabian1,2, Matías Fuentealba Valenzuela1,2, Linda Partridge2,3, Janet M Thornton1.
Abstract
Age is a common risk factor in many diseases, but the molecular basis for this relationship is elusive. In this study we identified 4 disease clusters from 116 diseases in the UK Biobank data, defined by their age-of-onset profiles, and found that diseases with the same onset profile are genetically more similar, suggesting a common etiology. This similarity was not explained by disease categories, co-occurrences or disease cause-effect relationships. Two of the four disease clusters had an increased risk of occurrence from age 20 and 40 years respectively. They both showed an association with known aging-related genes, yet differed in functional enrichment and evolutionary profiles. Moreover, they both had age-related expression and methylation changes. We also tested mutation accumulation and antagonistic pleiotropy theories of aging and found support for both.Entities:
Keywords: Aging; GWAS; UK Biobank; age-related disease; antagonistic pleiotropy; mutation accumulation
Year: 2021 PMID: 33959723 PMCID: PMC7610725 DOI: 10.1038/s43587-021-00051-5
Source DB: PubMed Journal: Nat Aging ISSN: 2662-8465