TY - JOUR
T1 - Obesity, Diabetes, Coffee, Tea, and Cannabis Use Alter Risk for Alcohol-Related Cirrhosis in 2 Large Cohorts of High-Risk Drinkers
AU - Whitfield, John B.
AU - Masson, Steven
AU - Liangpunsakul, Suthat
AU - Mueller, Sebastian
AU - Aithal, Guruprasad P.
AU - Eyer, Florian
AU - Gleeson, Dermot
AU - Thompson, Andrew
AU - Stickel, Felix
AU - Soyka, Michael
AU - Muellhaupt, Beat
AU - Daly, Ann K.
AU - Cordell, Heather J.
AU - Foroud, Tatiana
AU - Lumeng, Lawrence
AU - Pirmohamed, Munir
AU - Nalpas, Bertrand
AU - Jacquet, Jean Marc
AU - Moirand, Romain
AU - Nahon, Pierre
AU - Naveau, Sylvie
AU - Perney, Pascal
AU - Haber, Paul S.
AU - Seitz, Helmut K.
AU - Day, Christopher P.
AU - Mathurin, Philippe
AU - Morgan, Timothy R.
AU - Seth, Devanshi
N1 - Publisher Copyright:
© 2021 Wolters Kluwer Health. All rights reserved.
PY - 2021/1/1
Y1 - 2021/1/1
N2 - INTRODUCTION: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.
AB - INTRODUCTION: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.
UR - http://www.scopus.com/inward/record.url?scp=85099321411&partnerID=8YFLogxK
U2 - 10.14309/ajg.0000000000000833
DO - 10.14309/ajg.0000000000000833
M3 - Article
C2 - 32868629
AN - SCOPUS:85099321411
SN - 0002-9270
VL - 116
SP - 106
EP - 115
JO - American Journal of Gastroenterology
JF - American Journal of Gastroenterology
IS - 1
ER -