A genetic risk score and diabetes predict ...
Type de document :
Article dans une revue scientifique: Article original
PMID :
URL permanente :
Titre :
A genetic risk score and diabetes predict development of alcohol-related cirrhosis in drinkers.
Auteur(s) :
Whitfield, J. B. [Auteur]
Schwantes-An, T. H. [Auteur]
Darlay, R. [Auteur]
Aithal, G. P. [Auteur]
Atkinson, S. R. [Auteur]
Bataller, R. [Auteur]
Botwin, G. [Auteur]
Chalasani, N. P. [Auteur]
Cordell, H. J. [Auteur]
Daly, A. K. [Auteur]
Day, C. P. [Auteur]
Eyer, F. [Auteur]
Foroud, T. [Auteur]
Gleeson, D. [Auteur]
Goldman, D. [Auteur]
Haber, P. S. [Auteur]
Jacquet, Jean-Marc [Auteur]
Hôpital Universitaire Carémeau [Nîmes] [CHU Nîmes]
Service Addictologie [CHU Nîmes] [Pôle ICAGNE]
Liang, T. [Auteur]
Liangpunsakul, S. [Auteur]
Masson, S. [Auteur]
Mathurin, Philippe [Auteur]
Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286
Moirand, Romain [Auteur]
Nutrition, Métabolismes et Cancer [NuMeCan]
Centre Hospitalier Universitaire [Rennes]
Université de Rennes [UR]
Mcquillin, A. [Auteur]
Moreno, C. [Auteur]
Morgan, M. Y. [Auteur]
Mueller, S. [Auteur]
Müllhaupt, B. [Auteur]
Nagy, L. E. [Auteur]
Nahon, Pierre [Auteur]
Université Paris 13 [UP13]
Hôpital Avicenne [AP-HP]
Génomique Fonctionnelle des Tumeurs Solides [U1162]
Nalpas, Bertrand [Auteur]
Hôpital Universitaire Carémeau [Nîmes] [CHU Nîmes]
Information Scientifique et Technique [DISC/IST]
Naveau, Sylvie [Auteur]
AP-HP - Hôpital Antoine Béclère [Clamart]
Perney, P. [Auteur]
Service Addictologie [CHU Nîmes] [Pôle ICAGNE]
Pirmohamed, M. [Auteur]
Seitz, H. K. [Auteur]
Soyka, M. [Auteur]
Stickel, F. [Auteur]
Thompson, A. [Auteur]
Thursz, M. R. [Auteur]
Trépo, E. [Auteur]
Morgan, T. R. [Auteur]
Seth, D. [Auteur]
Schwantes-An, T. H. [Auteur]
Darlay, R. [Auteur]
Aithal, G. P. [Auteur]
Atkinson, S. R. [Auteur]
Bataller, R. [Auteur]
Botwin, G. [Auteur]
Chalasani, N. P. [Auteur]
Cordell, H. J. [Auteur]
Daly, A. K. [Auteur]
Day, C. P. [Auteur]
Eyer, F. [Auteur]
Foroud, T. [Auteur]
Gleeson, D. [Auteur]
Goldman, D. [Auteur]
Haber, P. S. [Auteur]
Jacquet, Jean-Marc [Auteur]
Hôpital Universitaire Carémeau [Nîmes] [CHU Nîmes]
Service Addictologie [CHU Nîmes] [Pôle ICAGNE]
Liang, T. [Auteur]
Liangpunsakul, S. [Auteur]
Masson, S. [Auteur]
Mathurin, Philippe [Auteur]
Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286
Moirand, Romain [Auteur]
Nutrition, Métabolismes et Cancer [NuMeCan]
Centre Hospitalier Universitaire [Rennes]
Université de Rennes [UR]
Mcquillin, A. [Auteur]
Moreno, C. [Auteur]
Morgan, M. Y. [Auteur]
Mueller, S. [Auteur]
Müllhaupt, B. [Auteur]
Nagy, L. E. [Auteur]
Nahon, Pierre [Auteur]
Université Paris 13 [UP13]
Hôpital Avicenne [AP-HP]
Génomique Fonctionnelle des Tumeurs Solides [U1162]
Nalpas, Bertrand [Auteur]
Hôpital Universitaire Carémeau [Nîmes] [CHU Nîmes]
Information Scientifique et Technique [DISC/IST]
Naveau, Sylvie [Auteur]
AP-HP - Hôpital Antoine Béclère [Clamart]
Perney, P. [Auteur]
Service Addictologie [CHU Nîmes] [Pôle ICAGNE]
Pirmohamed, M. [Auteur]
Seitz, H. K. [Auteur]
Soyka, M. [Auteur]
Stickel, F. [Auteur]
Thompson, A. [Auteur]
Thursz, M. R. [Auteur]
Trépo, E. [Auteur]
Morgan, T. R. [Auteur]
Seth, D. [Auteur]
Titre de la revue :
Journal of Hepatology
Nom court de la revue :
J Hepatol
Date de publication :
2021-10-23
ISSN :
1600-0641
Mot(s)-clé(s) en anglais :
Hepatocellular carcinoma
risk stratification
chronic alcohol use
genome-wide association
single nucleotide polymorphism
coffee
risk stratification
chronic alcohol use
genome-wide association
single nucleotide polymorphism
coffee
Discipline(s) HAL :
Sciences du Vivant [q-bio]
Résumé en anglais : [en]
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, ...
Lire la suite >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.Lire moins >
Lire la suite >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.Lire moins >
Langue :
Anglais
Comité de lecture :
Oui
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
Université de Lille
Inserm
CHU Lille
Inserm
CHU Lille
Date de dépôt :
2024-01-12T05:50:51Z
2024-03-01T13:06:09Z
2024-03-01T13:06:09Z
Fichiers
- document
- Accès libre
- Accéder au document