ALCOHOL-ASSOCIATED LIVER DISEASE: NATURAL HISTORY, MANAGEMENT AND NOVEL TARGETED THERAPIES.


Journal

Clinical and molecular hepatology
ISSN: 2287-285X
Titre abrégé: Clin Mol Hepatol
Pays: Korea (South)
ID NLM: 101586730

Informations de publication

Date de publication:
31 Oct 2024
Historique:
received: 24 08 2024
accepted: 29 10 2024
medline: 1 11 2024
pubmed: 1 11 2024
entrez: 31 10 2024
Statut: aheadofprint

Résumé

Alcohol consumption is a leading cause of preventable morbidity and mortality worldwide and the primary cause of advanced liver disease. Alcohol use disorder (AUD) is a chronic, frequently relapsing condition characterized by persistent alcohol consumption despite its negative consequences. Alcohol-associated liver disease (ALD) encompasses a series of stages, from fatty liver (steatosis) to inflammation (steatohepatitis), fibrosis, and, ultimately, liver cirrhosis and its complications. The development of ALD is complex, involving both genetic and environmental factors, yet the exact mechanisms at play remain unclear. Alcohol-associated hepatitis (AH), a severe form of ALD, presents with sudden jaundice and liver failure. Currently, there are no approved targeted therapies able to interfere in the pathogenesis of ALD to stop the progression of the disease, making alcohol abstinence the most effective way to improve prognosis across all stages of ALD. For patients with advanced ALD who do not respond to medical therapy, liver transplantation is the only option that can improve prognosis. Recently, AH has become an early indication for liver transplantation in non-responders to medical treatment, showing promising results in carefully selected patients. This review provides an update on the epidemiology, natural history, pathogenesis, and current treatments for ALD. A deeper insight into novel targeted therapies investigated for AH focusing on new pathophysiologically-based agents is also discussed, including anti-inflammatory and antioxidative stress drugs, gut-liver axis modulators, and hepatocyte regenerative molecules.

Identifiants

pubmed: 39481875
pii: cmh.2024.0709
doi: 10.3350/cmh.2024.0709
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Edilmar Alvarado-Tapias (E)

Gastroenterology and Hepatology department. Hospital of Santa Creu and Sant Pau, Autonomus University of Barcelona. Barcelona, Spain.
Centre for Biomedical Research in Liver and Digestive Diseases Network (CIBERehd). Madrid. Spain.

Elisa Pose (E)

Centre for Biomedical Research in Liver and Digestive Diseases Network (CIBERehd). Madrid. Spain.
Liver Unit, Hospital Clinic,Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.

Jordi Gratacós (J)

Centre for Biomedical Research in Liver and Digestive Diseases Network (CIBERehd). Madrid. Spain.
Liver Unit, Hospital Clinic,Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.

Ana Clemente-Sánchez (A)

Centre for Biomedical Research in Liver and Digestive Diseases Network (CIBERehd). Madrid. Spain.
Department of Gastroenterology and Hepatology, Hospital General Universitario Gregorio Marañón (IiSGM), Madrid, Spain.

Hugo Hugo López-Pelayo (HH)

Addictions Unit, Psychiatry and Psychology Service, ICN, Hospital Clinic Barcelona, Barcelona, Spain. Health and Addictions Research Group, IDIBAPS, Barcelona, Spain.

Ramón Bataller (R)

Centre for Biomedical Research in Liver and Digestive Diseases Network (CIBERehd). Madrid. Spain.
Liver Unit, Hospital Clinic,Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.

Classifications MeSH