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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.
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Handan Melike Dönertaş
Leibniz Association
Daniel K. Fabian
SUNY Upstate Medical University
Matías Fuentealba
Buck Institute for Research on Aging
Nature Aging
University College London
Wellcome Trust
European Bioinformatics Institute
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Dönertaş et al. (Thu,) studied this question.
synapsesocial.com/papers/69da52350d540cafc5838e1a — DOI: https://doi.org/10.1038/s43587-021-00051-5