A genetic risk score and diabetes predict development of alcohol-related cirrhosis in drinkers
dc.contributor.author | Whitfield, John B. | |
dc.contributor.author | Schwantes-An, Tae-Hwi | |
dc.contributor.author | Darlay, Rebecca | |
dc.contributor.author | Aithal, Guruprasad P. | |
dc.contributor.author | Atkinson, Stephen R. | |
dc.contributor.author | Bataller, Ramon | |
dc.contributor.author | Botwin, Greg | |
dc.contributor.author | Chalasani, Naga P. | |
dc.contributor.author | Cordell, Heather J. | |
dc.contributor.author | Daly, Ann K. | |
dc.contributor.author | Day, Christopher P. | |
dc.contributor.author | Eyer, Florian | |
dc.contributor.author | Foroud, Tatiana | |
dc.contributor.author | Gleeson, Dermot | |
dc.contributor.author | Goldman, David | |
dc.contributor.author | Haber, Paul S. | |
dc.contributor.author | Jacquet, Jean-Marc | |
dc.contributor.author | Liang, Tiebing | |
dc.contributor.author | Liangpunsakul, Suthat | |
dc.contributor.author | Masson, Steven | |
dc.contributor.author | Mathurin, Philippe | |
dc.contributor.author | Moirand, Romain | |
dc.contributor.author | McQuillin, Andrew | |
dc.contributor.author | Moreno, Christophe | |
dc.contributor.author | Morgan, Marsha Y. | |
dc.contributor.author | Mueller, Sebastian | |
dc.contributor.author | Müllhaupt, Beat | |
dc.contributor.author | Nagy, Laura E. | |
dc.contributor.author | Nahon, Pierre | |
dc.contributor.author | Nalpas, Bertrand | |
dc.contributor.author | Naveau, Sylvie | |
dc.contributor.author | Perney, Pascal | |
dc.contributor.author | Pirmohamed, Munir | |
dc.contributor.author | Seitz, Helmut K. | |
dc.contributor.author | Soyka, Michael | |
dc.contributor.author | Stickel, Felix | |
dc.contributor.author | Thompson, Andrew | |
dc.contributor.author | Thursz, Mark R. | |
dc.contributor.author | Trépo, Eric | |
dc.contributor.author | Morgan, Timothy R. | |
dc.contributor.author | Seth, Devanshi | |
dc.contributor.author | GenomALC Consortium | |
dc.contributor.department | Medical and Molecular Genetics, School of Medicine | |
dc.date.accessioned | 2023-10-25T16:31:43Z | |
dc.date.available | 2023-10-25T16:31:43Z | |
dc.date.issued | 2022 | |
dc.description.abstract | Background & 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.version | Author's manuscript | |
dc.identifier.citation | Whitfield 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.uri | https://hdl.handle.net/1805/36662 | |
dc.language.iso | en_US | |
dc.publisher | Elsevier | |
dc.relation.isversionof | 10.1016/j.jhep.2021.10.005 | |
dc.relation.journal | Journal of Hepatology | |
dc.rights | Publisher Policy | |
dc.source | PMC | |
dc.subject | Hepatocellular carcinoma | |
dc.subject | Risk stratification | |
dc.subject | Chronic alcohol use | |
dc.subject | Genome wide association | |
dc.subject | Single nucleotide polymorphism | |
dc.subject | Coffee | |
dc.title | A genetic risk score and diabetes predict development of alcohol-related cirrhosis in drinkers | |
dc.type | Article |