Liver transplantation in the patient with physical frailty.


Journal

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

Informations de publication

Date de publication:
06 2023
Historique:
received: 13 02 2023
revised: 23 03 2023
accepted: 26 03 2023
medline: 22 5 2023
pubmed: 20 5 2023
entrez: 19 5 2023
Statut: ppublish

Résumé

Frailty is a decline in functional reserve across multiple physiological systems. A key component of frailty is sarcopenia, which denotes a loss of skeletal muscle mass and impaired contractile function that ultimately result in physical frailty. Physical frailty/sarcopenia are frequent and contribute to adverse clinical outcomes before and after liver transplantation. Frailty indices, including the liver frailty index, focus on contractile dysfunction (physical frailty), while cross-sectional image analysis of muscle area is the most accepted and reproducible measure to define sarcopenia. Thus, physical frailty and sarcopenia are interrelated. The prevalence of physical frailty/sarcopenia is high in liver transplant candidates and these conditions have been shown to adversely impact clinical outcomes including mortality, hospitalisations, infections, and cost of care both before and after transplantation. Data on the prevalence of frailty/sarcopenia and their sex- and age-dependent impact on outcomes are not consistent in patients on the liver transplant waitlist. Physical frailty and sarcopenic obesity are frequent in the obese patient with cirrhosis, and adversely affect outcomes after liver transplantation. Nutritional interventions and physical activity remain the mainstay of management before and after transplantation, despite limited data from large scale trials. In addition to physical frailty, there is recognition that a global evaluation including a multidisciplinary approach to other components of frailty (e.g., cognition, emotional, psychosocial) also need to be addressed in patients on the transplant waitlist. Recent advances in our understanding of the underlying mechanisms of sarcopenia and contractile dysfunction have helped identify novel therapeutic targets.

Identifiants

pubmed: 37208097
pii: S0168-8278(23)00202-7
doi: 10.1016/j.jhep.2023.03.025
pii:
doi:

Types de publication

Journal Article Review Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1105-1117

Subventions

Organisme : NIGMS NIH HHS
ID : R01 GM119174
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK113196
Pays : United States
Organisme : NIAAA NIH HHS
ID : P50 AA024333
Pays : United States
Organisme : NIAAA NIH HHS
ID : R01 AA012180
Pays : United States
Organisme : NIAAA NIH HHS
ID : U01 AA026976
Pays : United States
Organisme : NHLBI NIH HHS
ID : R56 HL141744
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK061732
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK062470
Pays : United States
Organisme : NIAMS NIH HHS
ID : R21 AR071046
Pays : United States

Informations de copyright

Copyright © 2023. Published by Elsevier B.V.

Auteurs

Puneeta Tandon (P)

Division of Gastroenterology (Liver Unit), Department of Medicine, University of Alberta, Edmonton, Alberta, Canada.

Alberto Zanetto (A)

Gastroenterology and Multivisceral Transplant Unit, Department of Surgery, Oncology, and Gastroenterology, Padova University Hospital, Italy.

Salvatore Piano (S)

Unit of Internal Medicine and Hepatology, Department of Medicine - DIMED, University and Hospital of Padova, Padova, Italy.

Julie K Heimbach (JK)

William J von Liebig Transplant Center Mayo Clinic College of Medicine, Rochester, MN 55905, USA. Electronic address: Heimbach.julie@mayo.edu.

Srinivasan Dasarathy (S)

Division of Gastroenterology and Hepatology, Cleveland Clinic, Cleveland, OH 44195, USA.

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