Low alcohol consumption influences outcomes in individuals with alcohol-related compensated cirrhosis in a French multicenter cohort.


Journal

Journal of hepatology
ISSN: 1600-0641
Titre abrégé: J Hepatol
Pays: Netherlands
ID NLM: 8503886

Informations de publication

Date de publication:
03 2023
Historique:
received: 07 04 2022
revised: 24 10 2022
accepted: 04 11 2022
pubmed: 25 11 2022
medline: 3 3 2023
entrez: 24 11 2022
Statut: ppublish

Résumé

The harmful impact of heavy alcohol consumption and recurrence in patients with alcohol-related cirrhosis is long-established, although this is based on old studies. However, the drivers of long-term outcome still need to be clearly investigated. All patients with biopsy-proven compensated alcohol-related cirrhosis included in the CIRRAL cohort (22 centers) were prospectively studied. Prognostic variables of survival and liver event-free survival were assessed using multivariable Cox models with stepwise selection. The prognostic impact of alcohol recurrence during follow-up (computed in glass-years in the same way as pack-years for tobacco) was assessed using a time-dependent covariable. From 2010 to 2016, 650 patients were included. The median age at baseline was 58.4 years, 67.4% were men and the median BMI was 27.8 kg/m This prospective study in patients with compensated alcohol-related cirrhosis identifies factors predictive of alcohol recurrence during follow-up and shows that moderate alcohol consumption during follow-up negatively impacts outcomes. Patients with alcohol-related cirrhosis should be advised to completely stop drinking alcohol. CIRRAL (NCT01213927) cohort was registered at ClinicalTrials.gov and the full protocol is available at the following link: https://clinicaltrials.gov/ct2/show/NCT01213927. In patients with alcohol-related cirrhosis, data are lacking about the impact of the amount of alcohol consumed on both survival and liver-related events. The present study based on the CIRRAL cohort demonstrates that alcohol recurrence occurs in more than 30% of patients with compensated cirrhosis and that even a moderate recurrence strongly influences outcomes. Patients with compensated alcohol-related cirrhosis should be advised to completely discontinue alcohol consumption, even in small amounts, as the present study shows that no alcohol consumption can be regarded as safe when cirrhosis has developed.

Sections du résumé

BACKGROUND & AIMS
The harmful impact of heavy alcohol consumption and recurrence in patients with alcohol-related cirrhosis is long-established, although this is based on old studies. However, the drivers of long-term outcome still need to be clearly investigated.
METHOD
All patients with biopsy-proven compensated alcohol-related cirrhosis included in the CIRRAL cohort (22 centers) were prospectively studied. Prognostic variables of survival and liver event-free survival were assessed using multivariable Cox models with stepwise selection. The prognostic impact of alcohol recurrence during follow-up (computed in glass-years in the same way as pack-years for tobacco) was assessed using a time-dependent covariable.
RESULTS
From 2010 to 2016, 650 patients were included. The median age at baseline was 58.4 years, 67.4% were men and the median BMI was 27.8 kg/m
CONCLUSION
This prospective study in patients with compensated alcohol-related cirrhosis identifies factors predictive of alcohol recurrence during follow-up and shows that moderate alcohol consumption during follow-up negatively impacts outcomes. Patients with alcohol-related cirrhosis should be advised to completely stop drinking alcohol.
REGISTRATION
CIRRAL (NCT01213927) cohort was registered at ClinicalTrials.gov and the full protocol is available at the following link: https://clinicaltrials.gov/ct2/show/NCT01213927.
IMPACT AND IMPLICATIONS
In patients with alcohol-related cirrhosis, data are lacking about the impact of the amount of alcohol consumed on both survival and liver-related events. The present study based on the CIRRAL cohort demonstrates that alcohol recurrence occurs in more than 30% of patients with compensated cirrhosis and that even a moderate recurrence strongly influences outcomes. Patients with compensated alcohol-related cirrhosis should be advised to completely discontinue alcohol consumption, even in small amounts, as the present study shows that no alcohol consumption can be regarded as safe when cirrhosis has developed.

Identifiants

pubmed: 36423805
pii: S0168-8278(22)03304-9
doi: 10.1016/j.jhep.2022.11.013
pii:
doi:

Substances chimiques

Ethanol 3K9958V90M

Banques de données

ClinicalTrials.gov
['NCT01213927']

Types de publication

Multicenter Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

501-512

Investigateurs

Nathalie Ganne-Carrié (N)
Valérie Bourcier (V)
Cendrine Chaffaut (C)
Sylvie Chevret (S)
Isabelle Archambeaud (I)
Jérôme Gournay (J)
None Louis d'Alteroche
Laure Elkrief (L)
Frédéric Oberti (F)
Isabelle Fouchard-Hubert (I)
Dominique Roulot (D)
Christophe Moreno (C)
Alexandre Louvet (A)
Thông Dao (T)
Romain Moirand (R)
Jean-Charles Duclos-Vallée (JC)
Odile Goria (O)
Eric Nguyen-Khac (E)
Stanislas Pol (S)
Nicolas Carbonell (N)
Jean-Marie Péron (JM)
Victor de Lédinghen (V)
Violaine Ozenne (V)
Jean Henrion (J)
Albert Tran (A)
Gabriel Perlemuter (G)
Xavier Amiot (X)
Jean-Pierre Zarski (JP)

Informations de copyright

Copyright © 2022 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

Auteurs

Alexandre Louvet (A)

Liver Unit, University Hospital, Lille, France. Electronic address: alexandre.louvet@chru-lille.fr.

Valérie Bourcier (V)

AP-HP, Hôpital Avicenne, Service d'Hépatologie, Bobigny, Université Sorbonne Paris Nord, Bobigny et INSERM U1138, Université de Paris, France.

Isabelle Archambeaud (I)

Liver Unit, CHU, Nantes, France.

Louis d'Alteroche (L)

Liver Unit, University Hospital, Tours, France.

Cendrine Chaffaut (C)

SBIM, APHP, Hôpital Saint-Louis, Paris, Inserm, UMR-1153, ECSTRRA Team, Paris, France.

Frédéric Oberti (F)

Liver Unit, University Hospital, Angers, France.

Christophe Moreno (C)

Liver Unit, Hôpital Erasme, Université Libre de Bruxelles, Belgium.

Dominique Roulot (D)

AP-HP, Hôpital Avicenne, Service d'Hépatologie, Bobigny, Université Sorbonne Paris Nord, Bobigny et INSERM U1138, Université de Paris, France; Inserm U955 Université Paris Est, Créteil, France.

Thông Dao (T)

Liver Unit, University Hospital, Caen, France.

Romain Moirand (R)

Liver Unit, University Hospital, Rennes, France.

Jean-Charles Duclos-Vallée (JC)

Liver Unit, APHP, CHU Paul Brousse, Villejuif, France.

Odile Goria (O)

Liver Unit, University Hospital, Rouen, France.

Eric Nguyen-Khac (E)

Liver Unit, University Hospital, Amiens, France.

Stanislas Pol (S)

Liver Unit, Hôpital Cochin, INSERM U1223, Institut Pasteur, Paris, France.

Nicolas Carbonell (N)

Liver Unit, APHP, CHU Saint-Antoine, Paris, France.

Jérôme Gournay (J)

Liver Unit, CHU, Nantes, France.

Laure Elkrief (L)

Liver Unit, University Hospital, Tours, France.

Isabelle Fouchard-Hubert (I)

Liver Unit, University Hospital, Angers, France.

Sylvie Chevret (S)

SBIM, APHP, Hôpital Saint-Louis, Paris, Inserm, UMR-1153, ECSTRRA Team, Paris, France.

Nathalie Ganne-Carrié (N)

AP-HP, Hôpital Avicenne, Service d'Hépatologie, Bobigny, Université Sorbonne Paris Nord, Bobigny et INSERM U1138, Université de Paris, France. Electronic address: nathalie.ganne@aphp.fr.

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