{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Bostrand SMK"],"funding":["Medical Research Council Canada","Scottish Funding Council","British Heart Foundation","Cancer Research UK","NIA NIH HHS","Medical Research Council","National Institute for Health Research (NIHR)","Chief Scientist Office","Brain and Behavior Research Foundation","National Institutes of Health","Wellcome Trust","UK Research and Innovation"],"pagination":["e13100"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC7614236"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["27(1)"],"pubmed_abstract":["Harmful alcohol use is a leading cause of premature death and is associated with age-related disease. Biological ageing is highly variable between individuals and may deviate from chronological ageing, suggesting that biomarkers of biological ageing (derived from DNA methylation or brain structural measures) may be clinically relevant. Here, we investigated the relationships between alcohol phenotypes and both brain and DNA methylation age estimates. First, using data from UK Biobank and Generation Scotland, we tested the association between alcohol consumption (units/week) or hazardous use (Alcohol Use Disorders Identification Test [AUDIT] scores) and accelerated brain and epigenetic ageing in 20,258 and 8051 individuals, respectively. Second, we used Mendelian randomisation (MR) to test for a causal effect of alcohol consumption levels and alcohol use disorder (AUD) on biological ageing. Alcohol use showed a consistent positive association with higher predicted brain age (AUDIT-C: β = 0.053, p = 3.16 × 10<sup>-13</sup> ; AUDIT-P: β = 0.052, p = 1.6 × 10<sup>-13</sup> ; total AUDIT score: β = 0.062, p = 5.52 × 10<sup>-16</sup> ; units/week: β = 0.078, p = 2.20 × 10<sup>-16</sup> ), and two DNA methylation-based estimates of ageing, GrimAge (units/week: β = 0.053, p = 1.48 × 10<sup>-7</sup> ) and PhenoAge (units/week: β = 0.077, p = 2.18x10<sup>-10</sup> ). MR analyses revealed limited evidence for a causal effect of AUD on accelerated brain ageing (β = 0.118, p = 0.044). However, this result should be interpreted cautiously as the significant effect was driven by a single genetic variant. We found no evidence for a causal effect of alcohol consumption levels on accelerated biological ageing. Future studies investigating the mechanisms associating alcohol use with accelerated biological ageing are warranted."],"journal":["Addiction biology"],"pubmed_title":["Associations between alcohol use and accelerated biological ageing."],"pmcid":["PMC7614236"],"funding_grant_id":["MC_PC_17228","MC_UU_00011/3","HR03006","MR/R024790/2","MC_UU_00011/1","104036","MR/R024065/1","27404","108890","108890/Z/15/Z","104036/Z/14/Z","R01AG054628","R01 AG054628","CZD/16/6","MC_QA137853"],"pubmed_authors":["McCartney DL","Wootton RE","Walker RM","Harris MA","de Nooij L","Whalley HC","Vaher K","Cole JH","Cox SR","Marioni RE","Evans KL","McIntosh AM","Bostrand SMK","Clarke TK"],"additional_accession":[]},"is_claimable":false,"name":"Associations between alcohol use and accelerated biological ageing.","description":"Harmful alcohol use is a leading cause of premature death and is associated with age-related disease. Biological ageing is highly variable between individuals and may deviate from chronological ageing, suggesting that biomarkers of biological ageing (derived from DNA methylation or brain structural measures) may be clinically relevant. Here, we investigated the relationships between alcohol phenotypes and both brain and DNA methylation age estimates. First, using data from UK Biobank and Generation Scotland, we tested the association between alcohol consumption (units/week) or hazardous use (Alcohol Use Disorders Identification Test [AUDIT] scores) and accelerated brain and epigenetic ageing in 20,258 and 8051 individuals, respectively. Second, we used Mendelian randomisation (MR) to test for a causal effect of alcohol consumption levels and alcohol use disorder (AUD) on biological ageing. Alcohol use showed a consistent positive association with higher predicted brain age (AUDIT-C: β = 0.053, p = 3.16 × 10<sup>-13</sup> ; AUDIT-P: β = 0.052, p = 1.6 × 10<sup>-13</sup> ; total AUDIT score: β = 0.062, p = 5.52 × 10<sup>-16</sup> ; units/week: β = 0.078, p = 2.20 × 10<sup>-16</sup> ), and two DNA methylation-based estimates of ageing, GrimAge (units/week: β = 0.053, p = 1.48 × 10<sup>-7</sup> ) and PhenoAge (units/week: β = 0.077, p = 2.18x10<sup>-10</sup> ). MR analyses revealed limited evidence for a causal effect of AUD on accelerated brain ageing (β = 0.118, p = 0.044). However, this result should be interpreted cautiously as the significant effect was driven by a single genetic variant. We found no evidence for a causal effect of alcohol consumption levels on accelerated biological ageing. Future studies investigating the mechanisms associating alcohol use with accelerated biological ageing are warranted.","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Jan","modification":"2026-05-29T05:29:14.405Z","creation":"2025-02-18T23:44:38.486Z"},"accession":"S-EPMC7614236","cross_references":{"pubmed":["34636470"],"doi":["10.1111/adb.13100"]}}