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Inevitability of disease recurrence after liver transplantation for NAFLD cirrhosis.
Villeret, François; Dharancy, Sébastien; Erard, Domitille; Abergel, Armand; Barbier, Louise; Besch, Camille; Boillot, Olivier; Boudjema, Karim; Coilly, Audrey; Conti, Filomena; Corpechot, Christophe; Duvoux, Christophe; Faitot, François; Faure, Stéphanie; Francoz, Claire; Giostra, Emiliano; Gugenheim, Jean; Hardwigsen, Jean; Hilleret, Marie-Noëlle; Hiriart, Jean-Baptiste; Houssel-Debry, Pauline; Kamar, Nassim; Lassailly, Guillaume; Latournerie, Marianne; Pageaux, Georges-Philippe; Samuel, Didier; Vanlemmens, Claire; Saliba, Faouzi; Dumortier, Jérôme.
Affiliation
  • Villeret F; Service d'Hépatologie et de Transplantation Hépatique, Institut d'Hépatologie de Lyon, Hôpital de la Croix Rousse, Hospices Civils de Lyon, Lyon, France.
  • Dharancy S; Université Claude Bernard Lyon 1, Lyon, France.
  • Erard D; Service des Maladies de l'Appareil Digestif, Hôpital Claude Huriez, CHRU Lille, Lille, France.
  • Abergel A; Service d'Hépatologie et de Transplantation Hépatique, Institut d'Hépatologie de Lyon, Hôpital de la Croix Rousse, Hospices Civils de Lyon, Lyon, France.
  • Barbier L; Département de Médecine digestive, CHU Estaing, Clermont-Ferrand, France.
  • Besch C; Service de Chirurgie digestive, Oncologique et Transplantation Hépatique, Hôpital Trousseau, CHU Tours, Tours, France.
  • Boillot O; Service de Chirurgie Hépato-bilio-pancréatique et Transplantation Hépatique, CHRU Hautepierre, Strasbourg, France.
  • Boudjema K; Fédération des Spécialités Digestives, Institut d'Hépatologie de Lyon, Hôpital Edouard Herriot, Hospices Civils de Lyon, Lyon, France.
  • Coilly A; Service de Chirurgie Hépatobiliaire et digestive, Hôpital Universitaire de Pontchaillou, Rennes, France.
  • Conti F; Centre Hépato-Biliaire, Hôpital Paul Brousse, Université Paris Saclay, Unité Inserm 1193, AP-HP, Villejuif, France.
  • Corpechot C; Sorbonne Université, CRSA, APHP, Unité Médicale de Transplantation Hépatique, Service d'Hépatogastroentérologie, Hôpital Pitié Salpêtrière, Paris, France.
  • Duvoux C; Service d'Hépatologie, Hôpital Saint-Antoine, CHU Saint-Antoine, APHP, Paris, France.
  • Faitot F; Service d'Hépatologie, Hôpital Henri Mondor, APHP, Créteil, France.
  • Faure S; Service de Chirurgie Hépato-bilio-pancréatique et Transplantation Hépatique, CHRU Hautepierre, Strasbourg, France.
  • Francoz C; Service d'Hépato-gastroentérologie et Transplantation Hépatique, CHU Saint-Eloi, Université de Montpellier, Montpellier, France.
  • Giostra E; Service d'Hépatologie et Transplantation Hépatique, Hôpital Beaujon, APHP, Clichy, France.
  • Gugenheim J; Service de Gastroentérologie et Hépatologie, Hôpitaux Universitaires de Genève, Genève, Switzerland.
  • Hardwigsen J; Service de Chirurgie Digestive et Centre de Transplantation Hépatique, Université Côte d'Azur, CHU l'Archet, Nice, France.
  • Hilleret MN; Service Chirurgie Générale et Transplantation Hépatique, Hôpital La Timone, APHM, Marseille, France.
  • Hiriart JB; Service d'hépato-gastro-entérologie, CHU Grenoble-Alpes, Grenoble, France.
  • Houssel-Debry P; Service d'Hépatologie et de Transplantation Hépatique, CHU Haut-Lévêque, Pessac, France.
  • Kamar N; Service des Maladies du Foie, Hôpital Universitaire de Pontchaillou, CHU de Rennes, Rennes, France.
  • Lassailly G; Département de Néphrologie et Transplantation d'Organes, CHU Rangueil, Toulouse, France.
  • Latournerie M; Service des Maladies de l'Appareil Digestif, Hôpital Claude Huriez, CHRU Lille, Lille, France.
  • Pageaux GP; Service d'hépatologie et de Gastro-entérologie, CHU Dijon-Bourgogne, Dijon, France.
  • Samuel D; Service d'Hépato-gastroentérologie et Transplantation Hépatique, CHU Saint-Eloi, Université de Montpellier, Montpellier, France.
  • Vanlemmens C; Centre Hépato-Biliaire, Hôpital Paul Brousse, Université Paris Saclay, Unité Inserm 1193, AP-HP, Villejuif, France.
  • Saliba F; Service d'Hépatologie et Soins Intensifs Digestifs, CHU Jean Minjoz, Besançon, France.
  • Dumortier J; Centre Hépato-Biliaire, Hôpital Paul Brousse, Université Paris Saclay, Unité Inserm 1193, AP-HP, Villejuif, France.
JHEP Rep ; 5(3): 100668, 2023 Mar.
Article in En | MEDLINE | ID: mdl-36852108
ABSTRACT
Background &

Aims:

Liver transplantation (LT) is the only available treatment for end-stage non-alcoholic fatty liver disease (NAFLD) (related decompensated cirrhosis and/or hepatocellular carcinoma). The aim of our study was to evaluate the risk of disease recurrence after LT and the factors influencing it.

Method:

This retrospective multicenter study included adults transplanted for NAFLD cirrhosis between 2000 and 2019 in 20 participating French-speaking centers. Disease recurrence (steatosis, steatohepatitis and fibrosis) was diagnosed from liver graft biopsies.

Results:

We analyzed 150 patients with at least one graft liver biopsy available ≥6 months after transplantation, among 361 patients transplanted for NAFLD. The median (IQR) age at LT was 61.3 (54.4-64.6) years. The median follow-up after LT was 4.7 (2.8-8.1) years. The cumulative recurrence rates of steatosis and steatohepatitis at 5 years were 80.0% and 60.3%, respectively. Significant risk factors for steatohepatitis recurrence in multivariate analysis were recipient age at LT <65 years (odds ratio [OR] 4.214; p = 0.044), high-density lipoprotein-cholesterol <1.15 mmol/L after LT (OR 3.463; p = 0.013) and grade ≥2 steatosis on the graft at 1 year after LT (OR 10.196; p = 0.001). The cumulative incidence of advanced fibrosis (F3-F4) was 20.0% at 5 years after LT and significant risk factors from multivariate analysis were metabolic syndrome before LT (OR 8.550; p = 0.038), long-term use of cyclosporine (OR 11.388; p = 0.031) and grade ≥2 steatosis at 1 year after LT (OR 10.720; p = 0.049). No re-LT was performed for NAFLD cirrhosis recurrence.

Conclusion:

Our results strongly suggest that recurrence of initial disease after LT for NAFLD is inevitable and progressive in a large proportion of patients; the means to prevent it remain to be further evaluated. Impact and implications Non-alcoholic fatty liver disease (NAFLD) is a growing indication for liver transplantation, but the analysis of disease recurrence, based on graft liver biopsies, has been poorly studied. Cumulative incidences of steatosis, steatohepatitis and NAFLD-related significant fibrosis recurrence at 5 years were 85.0%, 60.3% and 48.0%, respectively. Grade ≥2 steatosis on graft biopsy at 1 year (present in 25% of patients) is highly predictive of recurrence of steatohepatitis and advanced fibrosis bariatric surgery should be discussed in these patients specifically.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Prognostic_studies / Risk_factors_studies Language: En Journal: JHEP Rep Year: 2023 Document type: Article Affiliation country: France

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Prognostic_studies / Risk_factors_studies Language: En Journal: JHEP Rep Year: 2023 Document type: Article Affiliation country: France