Homozygosity for rs738409:G in PNPLA3 is associated with increased mortality following an episode of severe alcoholic hepatitis

被引:55
作者
Atkinson, Stephen R. [1 ]
Way, Michael J. [2 ,3 ]
McQuillin, Andrew [3 ]
Morgan, Marsha Y. [2 ]
Thursz, Mark R. [1 ]
机构
[1] Imperial Coll London, Div Surg & Canc, Dept Hepatol, London, England
[2] UCL, UCL Inst Liver & Digest Hlth, Div Med, Royal Free Campus, London, England
[3] UCL, Div Psychiat, Mol Psychiat Lab, London, England
基金
英国医学研究理事会;
关键词
Alcohol dependence; Hepatitis; alcoholic; Liver cirrhosis; Genetic polymorphism; PNPLA3; Genotype; Prednisolone; Prognostic scores; Risk allele; Survival; GREATER-THAN-G; HEPATOCELLULAR-CARCINOMA; LIVER-DISEASE; TERM SURVIVAL; RISK; CIRRHOSIS; VARIANT; POLYMORPHISM; METAANALYSIS; MODEL;
D O I
10.1016/j.jhep.2017.01.018
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Background & Aims: Carriage of rs738409: G in PNPLA3 is associated with an increased risk of developing alcohol-related cirrhosis and has a significant negative effect on survival. Short-term mortality in patients with severe alcoholic hepatitis is high; drinking behaviour is a major determinant of outcome in survivors. The aim of this study was to determine whether carriage of rs738409: G has an additional detrimental effect on survival in this patient group. Methods: Genotyping was undertaken in 898 cases with severe alcoholic hepatitis, recruited through the UK Steroids or Pentoxifylline for Alcoholic Hepatitis (STOPAH) trial, and 1188 White British/Irish alcohol dependent controls with no liver injury, recruited via University College London. Subsequent drinking behaviour was classified, in cases surviving >= 90 days, as abstinent or drinking. The relationship between rs738409 genotype, drinking behaviour and survival was explored. Results: The frequency of rs738409: G was significantly higher in cases than controls (29.5% vs. 18.9%; p = 2.15 x 10(-15); odds ratio 1.80 [95% confidence interval (CI) 1.55-2.08]). Case-mortality at days 28, 90 and 450 was 16%, 25% and 41% respectively. There was no association between rs738409: G and 28-day mortality. Mortality in the 90 to 450-day period was higher in survivors who subsequently resumed drinking (hazard ratio [HR] 2.77, 95% CI 1.79-4.29; p < 0.0001) and in individuals homozygous for rs738409: G (HR 1.69, 95% CI 1.02-2.81, p = 0.04). Conclusion: Homozygosity for rs738409: G in PNPLA3 confers significant additional risk of medium-term mortality in patients with severe alcoholic hepatitis. Rs738409 genotype may be taken into account when considering treatment options for these patients. Lay summary: Individuals misusing alcohol who carry a particular variant of the gene PNPLA3 are more at risk of developing severe alcoholic hepatitis, a condition with a poor chance of survival. The longer-term outcome in people with this condition who survive the initial illness is strongly influenced by their ability to remain abstinent from alcohol. However, carriers of this gene variant are less likely to survive even if they are able to stop drinking completely. Knowing if someone carries this gene variant could influence the way in which they are managed. Clinical trial numbers: EudraCT reference number: 2009-013897-42; ISRCTN reference number: ISRCTN88782125. Clinical trial numbers: EudraCT reference number: 2009-013897-42; ISRCTN reference number: ISRCTN88782125. (C) 2017 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:120 / 127
页数:8
相关论文
共 41 条
[1]
ALEXANDER JF, 1971, AM J GASTROENTEROL, V56, P515
[2]
A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis [J].
Buch, Stephan ;
Stickel, Felix ;
Trepo, Eric ;
Way, Michael ;
Herrmann, Alexander ;
Nischalke, Hans Dieter ;
Brosch, Mario ;
Rosendahl, Jonas ;
Berg, Thomas ;
Ridinger, Monika ;
Rietschel, Marcella ;
McQuillin, Andrew ;
Frank, Josef ;
Kiefer, Falk ;
Schreiber, Stefan ;
Lieb, Wolfgang ;
Soyka, Michael ;
Semmo, Nasser ;
Aigner, Elmar ;
Datz, Christian ;
Schmelz, Renate ;
Brueckner, Stefan ;
Zeissig, Sebastian ;
Stephan, Anna-Magdalena ;
Wodarz, Norbert ;
Deviere, Jacques ;
Clumeck, Nicolas ;
Sarrazin, Christoph ;
Lammert, Frank ;
Gustot, Thierry ;
Deltenre, Pierre ;
Voelzke, Henry ;
Lerch, Markus M. ;
Mayerle, Julia ;
Eyer, Florian ;
Schafmayer, Clemens ;
Cichon, Sven ;
Noethen, Markus M. ;
Nothnagel, Michael ;
Ellinghaus, David ;
Huse, Klaus ;
Franke, Andre ;
Zopf, Steffen ;
Hellerbrand, Claus ;
Moreno, Christophe ;
Franchimont, Denis ;
Morgan, Marsha Y. ;
Hampe, Jochen .
NATURE GENETICS, 2015, 47 (12) :1443-+
[3]
PNPLA3 I148M (rs738409) genetic variant and age at onset of at-risk alcohol consumption are independent risk factors for alcoholic cirrhosis [J].
Burza, Maria Antonella ;
Molinaro, Antonio ;
Attilia, Maria Luisa ;
Rotondo, Claudia ;
Attilia, Fabio ;
Ceccanti, Mauro ;
Ferri, Flaminia ;
Maldarelli, Federica ;
Maffongelli, Angela ;
De Santis, Adriano ;
Attili, Adolfo Francesco ;
Romeo, Stefano ;
Corradini, Stefano Ginanni .
LIVER INTERNATIONAL, 2014, 34 (04) :514-520
[4]
Systematic review with meta-analysis: the I148M variant of patatin-like phospholipase domain-containing 3 gene (PNPLA3) is significantly associated with alcoholic liver cirrhosis [J].
Chamorro, A-J. ;
Torres, J-L. ;
Miron-Canelo, J-A. ;
Gonzalez-Sarmiento, R. ;
Laso, F-J. ;
Marcos, M. .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2014, 40 (06) :571-581
[5]
Second-generation PLINK: rising to the challenge of larger and richer datasets [J].
Chang, Christopher C. ;
Chow, Carson C. ;
Tellier, Laurent C. A. M. ;
Vattikuti, Shashaank ;
Purcell, Shaun M. ;
Lee, James J. .
GIGASCIENCE, 2015, 4
[6]
PNPLA3 rs738409C/G polymorphism in cirrhosis: relationship with the aetiology of liver disease and hepatocellular carcinoma occurrence [J].
Falleti, Edmondo ;
Fabris, Carlo ;
Cmet, Sara ;
Cussigh, Annarosa ;
Bitetto, Davide ;
Fontanini, Elisabetta ;
Fornasiere, Ezio ;
Bignulin, Sara ;
Fumolo, Elisa ;
Bignulin, Eleonora ;
Pirisi, Mario ;
Toniutto, Pierluigi .
LIVER INTERNATIONAL, 2011, 31 (08) :1137-1143
[7]
The Glasgow alcoholic hepatitis score identifies patients who may benefit from corticosteroids [J].
Forrest, E. H. ;
Morris, A. J. ;
Stewart, S. ;
Phillips, M. ;
Oo, Y. H. ;
Fisher, N. C. ;
Haydon, G. ;
O'Grady, J. ;
Day, C. P. .
GUT, 2007, 56 (12) :1743-1746
[8]
Steroids or pentoxifylline for alcoholic hepatitis (STOPAH): study protocol for a randomised controlled trial [J].
Forrest, Ewan ;
Mellor, Jane ;
Stanton, Louise ;
Bowers, Megan ;
Ryder, Priscilla ;
Austin, Andrew ;
Day, Christopher ;
Gleeson, Dermot ;
O'Grady, John ;
Masson, Steven ;
McCune, Anne ;
Patch, David ;
Richardson, Paul ;
Roderick, Paul ;
Ryder, Stephen ;
Wright, Mark ;
Thursz, Mark .
TRIALS, 2013, 14
[9]
PNPLA3 in end-stage liver disease: Alcohol consumption, hepatocellular carcinoma development, and transplantation-free survival [J].
Friedrich, Kilian ;
Wannhoff, Andreas ;
Kattner, Stefan ;
Brune, Maik ;
Hov, Johannes Roksund ;
Weiss, Karl Heinz ;
Antoni, Christoph ;
Dollinger, Matthias ;
Neumann-Haefelin, Christoph ;
Seufferlein, Thomas ;
Schemmer, Peter ;
Schirmacher, Peter ;
Stremmel, Wolfgang ;
Gotthardt, Daniel Nils .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2014, 29 (07) :1477-1484
[10]
GOLDBERG S, 1986, AM J GASTROENTEROL, V81, P1029