Obesity, Diabetes, Coffee, Tea, and Cannabis Use Alter Risk for Alcohol-Related Cirrhosis in 2 Large Cohorts of High-Risk Drinkers

dc.contributor.authorWhitfield, John B.
dc.contributor.authorMasson, Steven
dc.contributor.authorLiangpunsakul, Suthat
dc.contributor.authorMueller, Sebastian
dc.contributor.authorAithal, Guruprasad P.
dc.contributor.authorEyer, Florian
dc.contributor.authorGleeson, Dermot
dc.contributor.authorThompson, Andrew
dc.contributor.authorStickel, Felix
dc.contributor.authorSoyka, Michael
dc.contributor.authorDaly, Ann K.
dc.contributor.authorCordell, Heather J.
dc.contributor.authorForoud, Tatiana
dc.contributor.authorLumeng, Lawrence
dc.contributor.authorPirmohamed, Munir
dc.contributor.authorNalpas, Bertrand
dc.contributor.authorJacquet, Jean-Marc
dc.contributor.authorMoirand, Romain
dc.contributor.authorNahon, Pierre
dc.contributor.authorNaveau, Sylvie
dc.contributor.authorPerney, Pascal
dc.contributor.authorHaber, Paul S.
dc.contributor.authorSeitz, Helmut K.
dc.contributor.authorDay, Christopher P.
dc.contributor.authorMathurin, Philippe
dc.contributor.authorMorgan, Timothy R.
dc.contributor.authorSeth, Devanshi
dc.contributor.authorGenomALC Consortium
dc.contributor.departmentMedicine, School of Medicine
dc.date.accessioned2024-08-15T15:41:55Z
dc.date.available2024-08-15T15:41:55Z
dc.date.issued2021
dc.description.abstractIntroduction: Sustained high alcohol intake is necessary but not sufficient to produce alcohol-related cirrhosis. Identification of risk factors, apart from lifetime alcohol exposure, would assist in discovery of mechanisms and prediction of risk. Methods: We conducted a multicenter case-control study (GenomALC) comparing 1,293 cases (with alcohol-related cirrhosis, 75.6% male) and 754 controls (with equivalent alcohol exposure but no evidence of liver disease, 73.6% male). Information confirming or excluding cirrhosis, and on alcohol intake and other potential risk factors, was obtained from clinical records and by interview. Case-control differences in risk factors discovered in the GenomALC participants were validated using similar data from 407 cases and 6,573 controls from UK Biobank. Results: The GenomALC case and control groups reported similar lifetime alcohol intake (1,374 vs 1,412 kg). Cases had a higher prevalence of diabetes (20.5% (262/1,288) vs 6.5% (48/734), P = 2.27 × 10-18) and higher premorbid body mass index (26.37 ± 0.16 kg/m2) than controls (24.44 ± 0.18 kg/m2, P = 5.77 × 10-15). Controls were significantly more likely to have been wine drinkers, coffee drinkers, smokers, and cannabis users than cases. Cases reported a higher proportion of parents who died of liver disease than controls (odds ratio 2.25 95% confidence interval 1.55-3.26). Data from UK Biobank confirmed these findings for diabetes, body mass index, proportion of alcohol as wine, and coffee consumption. Discussion: If these relationships are causal, measures such as weight loss, intensive treatment of diabetes or prediabetic states, and coffee consumption should reduce the risk of alcohol-related cirrhosis.
dc.eprint.versionAuthor's manuscript
dc.identifier.citationWhitfield JB, Masson S, Liangpunsakul S, et al. Obesity, Diabetes, Coffee, Tea, and Cannabis Use Alter Risk for Alcohol-Related Cirrhosis in 2 Large Cohorts of High-Risk Drinkers. Am J Gastroenterol. 2021;116(1):106-115. doi:10.14309/ajg.0000000000000833
dc.identifier.urihttps://hdl.handle.net/1805/42814
dc.language.isoen_US
dc.publisherWolters Kluwer
dc.relation.isversionof10.14309/ajg.0000000000000833
dc.relation.journalThe American Journal of Gastroenterology
dc.rightsPublisher Policy
dc.sourceAuthor
dc.subjectAlcohol
dc.subjectCirrhosis
dc.subjectCoffee
dc.subjectFamilial risk
dc.subjectCannabis
dc.subjectDiabetes
dc.titleObesity, Diabetes, Coffee, Tea, and Cannabis Use Alter Risk for Alcohol-Related Cirrhosis in 2 Large Cohorts of High-Risk Drinkers
dc.typeArticle
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