Liver-Related and Cardiovascular Outcome of Patients Transplanted for Nonalcoholic Fatty Liver Disease: A European Single-Center Study.


Journal

Transplantation proceedings
ISSN: 1873-2623
Titre abrégé: Transplant Proc
Pays: United States
ID NLM: 0243532

Informations de publication

Date de publication:
Jun 2021
Historique:
received: 27 07 2020
revised: 18 01 2021
accepted: 25 02 2021
pubmed: 22 5 2021
medline: 7 7 2021
entrez: 21 5 2021
Statut: ppublish

Résumé

The increasing rate of liver transplantation (LT) for nonalcoholic fatty liver disease (NAFLD) raises concerns on cardiovascular morbidity and mortality after LT in these patients. We collected variables regarding the presence of metabolic risk factors, NAFLD recurrence, cardiovascular morbidity, and overall survival at time of listing and after LT of 112 patients with NAFLD and a control group of 120 patients with hepatitis C (HCV). Metabolic syndrome and cardiovascular morbidity component rates (24.1% vs 12.5%) at the time of LT listing were higher in patients with NAFLD compared with patients with HCV (for all, P < .0390). Median follow-up after LT was 5.6 years in patients with NAFLD vs 13.5 years in patients with HCV (P = .0009). There was no difference in 6-weeks postoperative mortality (1.7% vs 2.5%) (P =1.0000). Metabolic syndrome components after LT were more frequent in patients with NAFLD than in patients with HCV (for all, P < .0008). The incidence of NAFLD 5 years after LT was higher in patients transplanted for NAFLD compared with HCV (43.5% vs 4.2%) (P < .0001). Patients with recurrent NAFLD more often had myocardial infarction compared with those without recurrence (8.3% vs 0%) (P = .0313). Five years after LT, cardiovascular morbidity was more frequent in the NAFLD group than in the HCV group (12.8% vs 9.3%) (P = .0256), whereas no difference in overall survival was observed. LT for NAFLD is associated with satisfactory 5-year outcomes; however, our data underscore the need for close monitoring and aggressive management of cardiovascular risk factors in these patients.

Sections du résumé

BACKGROUND BACKGROUND
The increasing rate of liver transplantation (LT) for nonalcoholic fatty liver disease (NAFLD) raises concerns on cardiovascular morbidity and mortality after LT in these patients.
METHODS METHODS
We collected variables regarding the presence of metabolic risk factors, NAFLD recurrence, cardiovascular morbidity, and overall survival at time of listing and after LT of 112 patients with NAFLD and a control group of 120 patients with hepatitis C (HCV).
RESULTS RESULTS
Metabolic syndrome and cardiovascular morbidity component rates (24.1% vs 12.5%) at the time of LT listing were higher in patients with NAFLD compared with patients with HCV (for all, P < .0390). Median follow-up after LT was 5.6 years in patients with NAFLD vs 13.5 years in patients with HCV (P = .0009). There was no difference in 6-weeks postoperative mortality (1.7% vs 2.5%) (P =1.0000). Metabolic syndrome components after LT were more frequent in patients with NAFLD than in patients with HCV (for all, P < .0008). The incidence of NAFLD 5 years after LT was higher in patients transplanted for NAFLD compared with HCV (43.5% vs 4.2%) (P < .0001). Patients with recurrent NAFLD more often had myocardial infarction compared with those without recurrence (8.3% vs 0%) (P = .0313). Five years after LT, cardiovascular morbidity was more frequent in the NAFLD group than in the HCV group (12.8% vs 9.3%) (P = .0256), whereas no difference in overall survival was observed.
CONCLUSION CONCLUSIONS
LT for NAFLD is associated with satisfactory 5-year outcomes; however, our data underscore the need for close monitoring and aggressive management of cardiovascular risk factors in these patients.

Identifiants

pubmed: 34016462
pii: S0041-1345(21)00227-X
doi: 10.1016/j.transproceed.2021.02.025
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1674-1681

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Jakob Van Herck (J)

Department of General Internal Medicine, University Hospital KU Leuven, Leuven, Belgium.

Jef Verbeek (J)

Department of Gastroenterology and Hepatology, University Hospital KU Leuven, Leuven, Belgium.

Hannah van Malenstein (H)

Department of Gastroenterology and Hepatology, University Hospital KU Leuven, Leuven, Belgium.

Wim Laleman (W)

Department of Gastroenterology and Hepatology, University Hospital KU Leuven, Leuven, Belgium.

David Cassiman (D)

Department of Gastroenterology and Hepatology, University Hospital KU Leuven, Leuven, Belgium.

Chris Verslype (C)

Department of Gastroenterology and Hepatology, University Hospital KU Leuven, Leuven, Belgium.

Schalk van der Merwe (S)

Department of Gastroenterology and Hepatology, University Hospital KU Leuven, Leuven, Belgium.

Ina Jochmans (I)

Abdominal Transplantation, Transplantation Research Group, Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium; Abdominal Transplantation Surgery, University Hospitals Leuven, Leuven, Belgium.

Mauricio Sainz-Barriga (M)

Abdominal Transplantation, Transplantation Research Group, Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium; Abdominal Transplantation Surgery, University Hospitals Leuven, Leuven, Belgium.

Diethard Monbaliu (D)

Abdominal Transplantation, Transplantation Research Group, Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium; Abdominal Transplantation Surgery, University Hospitals Leuven, Leuven, Belgium.

Jacques Pirenne (J)

Abdominal Transplantation, Transplantation Research Group, Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium; Abdominal Transplantation Surgery, University Hospitals Leuven, Leuven, Belgium.

Frederik Nevens (F)

Department of Gastroenterology and Hepatology, University Hospital KU Leuven, Leuven, Belgium. Electronic address: frederik.nevens@uzleuven.be.

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Classifications MeSH