A genetic risk score and diabetes predict development of alcohol-related cirrhosis in drinkers

dc.contributor.authorWhitfield, John B.
dc.contributor.authorSchwantes-An, Tae-Hwi
dc.contributor.authorDarlay, Rebecca
dc.contributor.authorAithal, Guruprasad P.
dc.contributor.authorAtkinson, Stephen R.
dc.contributor.authorBataller, Ramon
dc.contributor.authorBotwin, Greg
dc.contributor.authorChalasani, Naga P.
dc.contributor.authorCordell, Heather J.
dc.contributor.authorDaly, Ann K.
dc.contributor.authorDay, Christopher P.
dc.contributor.authorEyer, Florian
dc.contributor.authorForoud, Tatiana
dc.contributor.authorGleeson, Dermot
dc.contributor.authorGoldman, David
dc.contributor.authorHaber, Paul S.
dc.contributor.authorJacquet, Jean-Marc
dc.contributor.authorLiang, Tiebing
dc.contributor.authorLiangpunsakul, Suthat
dc.contributor.authorMasson, Steven
dc.contributor.authorMathurin, Philippe
dc.contributor.authorMoirand, Romain
dc.contributor.authorMcQuillin, Andrew
dc.contributor.authorMoreno, Christophe
dc.contributor.authorMorgan, Marsha Y.
dc.contributor.authorMueller, Sebastian
dc.contributor.authorMüllhaupt, Beat
dc.contributor.authorNagy, Laura E.
dc.contributor.authorNahon, Pierre
dc.contributor.authorNalpas, Bertrand
dc.contributor.authorNaveau, Sylvie
dc.contributor.authorPerney, Pascal
dc.contributor.authorPirmohamed, Munir
dc.contributor.authorSeitz, Helmut K.
dc.contributor.authorSoyka, Michael
dc.contributor.authorStickel, Felix
dc.contributor.authorThompson, Andrew
dc.contributor.authorThursz, Mark R.
dc.contributor.authorTrépo, Eric
dc.contributor.authorMorgan, Timothy R.
dc.contributor.authorSeth, Devanshi
dc.contributor.authorGenomALC Consortium
dc.contributor.departmentMedical and Molecular Genetics, School of Medicine
dc.date.accessioned2023-10-25T16:31:43Z
dc.date.available2023-10-25T16:31:43Z
dc.date.issued2022
dc.description.abstractBackground & aims: Only a minority of excess alcohol drinkers develop cirrhosis. We developed and evaluated risk stratification scores to identify those at highest risk. Methods: Three cohorts (GenomALC-1: n = 1,690, GenomALC-2: n = 3,037, UK Biobank: relevant n = 6,898) with a history of heavy alcohol consumption (≥80 g/day (men), ≥50 g/day (women), for ≥10 years) were included. Cases were participants with alcohol-related cirrhosis. Controls had a history of similar alcohol consumption but no evidence of liver disease. Risk scores were computed from up to 8 genetic loci identified previously as associated with alcohol-related cirrhosis and 3 clinical risk factors. Score performance for the stratification of alcohol-related cirrhosis risk was assessed and compared across the alcohol-related liver disease spectrum, including hepatocellular carcinoma (HCC). Results: A combination of 3 single nucleotide polymorphisms (SNPs) (PNPLA3:rs738409, SUGP1-TM6SF2:rs10401969, HSD17B13:rs6834314) and diabetes status best discriminated cirrhosis risk. The odds ratios (ORs) and (95% CIs) between the lowest (Q1) and highest (Q5) score quintiles of the 3-SNP score, based on independent allelic effect size estimates, were 5.99 (4.18-8.60) (GenomALC-1), 2.81 (2.03-3.89) (GenomALC-2), and 3.10 (2.32-4.14) (UK Biobank). Patients with diabetes and high risk scores had ORs of 14.7 (7.69-28.1) (GenomALC-1) and 17.1 (11.3-25.7) (UK Biobank) compared to those without diabetes and with low risk scores. Patients with cirrhosis and HCC had significantly higher mean risk scores than patients with cirrhosis alone (0.76 ± 0.06 vs. 0.61 ± 0.02, p = 0.007). Score performance was not significantly enhanced by information on additional genetic risk variants, body mass index or coffee consumption. Conclusions: A risk score based on 3 genetic risk variants and diabetes status enables the stratification of heavy drinkers based on their risk of cirrhosis, allowing for the provision of earlier preventative interventions. Lay summary: Excessive chronic drinking leads to cirrhosis in some people, but so far there is no way to identify those at high risk of developing this debilitating disease. We developed a genetic risk score that can identify patients at high risk. The risk of cirrhosis is increased >10-fold with just two risk factors - diabetes and a high genetic risk score. Risk assessment using this test could enable the early and personalised management of this disease in high-risk patients.
dc.eprint.versionAuthor's manuscript
dc.identifier.citationWhitfield JB, Schwantes-An TH, Darlay R, et al. A genetic risk score and diabetes predict development of alcohol-related cirrhosis in drinkers [published correction appears in J Hepatol. 2022 May;76(5):1244-1245]. J Hepatol. 2022;76(2):275-282. doi:10.1016/j.jhep.2021.10.005
dc.identifier.urihttps://hdl.handle.net/1805/36662
dc.language.isoen_US
dc.publisherElsevier
dc.relation.isversionof10.1016/j.jhep.2021.10.005
dc.relation.journalJournal of Hepatology
dc.rightsPublisher Policy
dc.sourcePMC
dc.subjectHepatocellular carcinoma
dc.subjectRisk stratification
dc.subjectChronic alcohol use
dc.subjectGenome wide association
dc.subjectSingle nucleotide polymorphism
dc.subjectCoffee
dc.titleA genetic risk score and diabetes predict development of alcohol-related cirrhosis in drinkers
dc.typeArticle
Files
Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
nihms-1748321.pdf
Size:
890.31 KB
Format:
Adobe Portable Document Format
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.99 KB
Format:
Item-specific license agreed upon to submission
Description: