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Obesity, diabetes, coffee, tea and cannabis use alter risk for alcohol-related cirrhosis in two large cohorts of high-risk drinkers

Whitfield, John B.; Masson, Steven; Liangpunsakul, Suthat; Mueller, Sebastian; Aithal, Guruprasad P.; Eyer, Florian; Gleeson, Dermot; Thompson, Andrew; Stickel, Felix; Soyka, Michael; Daly, Ann K.; Cordell, Heather J.; Foroud, Tatiana; Lumeng, Lawrence; Pirmohamed, Munir; Nalpas, Bertrand; Jacquet, Jean-Marc; Moirand, Romain; Nahon, Pierre; Naveau, Sylvie; Perney, Pascal; Haber, Paul S.; Seitz, Helmut K.; Day, Christopher P.; Mathurin, Philippe; Morgan, Timothy R.; Seth, Devanshi

Obesity, diabetes, coffee, tea and cannabis use alter risk for alcohol-related cirrhosis in two large cohorts of high-risk drinkers Thumbnail


Authors

John B. Whitfield

Steven Masson

Suthat Liangpunsakul

Sebastian Mueller

Florian Eyer

Dermot Gleeson

Andrew Thompson

Felix Stickel

Michael Soyka

Ann K. Daly

Heather J. Cordell

Tatiana Foroud

Lawrence Lumeng

Munir Pirmohamed

Bertrand Nalpas

Jean-Marc Jacquet

Romain Moirand

Pierre Nahon

Sylvie Naveau

Pascal Perney

Paul S. Haber

Helmut K. Seitz

Christopher P. Day

Philippe Mathurin

Timothy R. Morgan

Devanshi Seth



Abstract

Background:
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 multi-centre case-control study (GenomALC) comparing 1293 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 6573 controls from UK Biobank.

Results:
The GenomALC case and control groups reported similar lifetime alcohol intake (1374 versus 1412 kg). Cases had a higher prevalence of diabetes (20.5% (262/1288) versus 6.5% (48/734), p = 2.27 x 10 -18 ) and higher pre-morbid BMI (26.37 ± 0.16 kg/m 2 ) than controls (24.44 ± 0.18 kg/m 2 , p = 5.77 x 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 from liver disease than controls (OR 2.25 95% CI 1.55 to 3.26). Data from UK Biobank confirmed these findings for diabetes, BMI, proportion of alcohol as wine and coffee consumption.

Conclusions:
If these relationships are causal, measures such as weight loss, intensive treatment of diabetes or pre-diabetic states, and coffee consumption should reduce risk of alcoholrelated cirrhosis.

Citation

Whitfield, J. B., Masson, S., Liangpunsakul, S., Mueller, S., Aithal, G. P., Eyer, F., …Seth, D. (2021). Obesity, diabetes, coffee, tea and cannabis use alter risk for alcohol-related cirrhosis in two large cohorts of high-risk drinkers. American Journal of Gastroenterology, 116(1), 106-115. https://doi.org/10.14309/ajg.0000000000000833

Journal Article Type Article
Acceptance Date Jun 18, 2020
Online Publication Date Aug 31, 2020
Publication Date Jan 1, 2021
Deposit Date Jun 25, 2020
Publicly Available Date Mar 1, 2021
Journal American Journal of Gastroenterology
Print ISSN 0002-9270
Publisher Lippincott, Williams & Wilkins
Peer Reviewed Peer Reviewed
Volume 116
Issue 1
Pages 106-115
DOI https://doi.org/10.14309/ajg.0000000000000833
Keywords Alcohol, cirrhosis, coffee, familial risk, cannabis, diabetes
Public URL https://nottingham-repository.worktribe.com/output/4709670
Publisher URL https://journals.lww.com/ajg/Abstract/9000/Obesity,_Diabetes,_Coffee,_Tea,_and_Cannabis_Use.99148.aspx