Prevention of Cirrhosis Complications: Looking for Potential Disease Modifying Agents.

TIPS ascites decompensated cirrhosis human albumin non-selective beta-blockers portal hypertension rifaximin statins

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
05 Oct 2021
Historique:
received: 25 07 2021
revised: 29 09 2021
accepted: 04 10 2021
entrez: 13 10 2021
pubmed: 14 10 2021
medline: 14 10 2021
Statut: epublish

Résumé

The current therapeutic strategies for the management of patients with cirrhosis rely on the prevention or treatment of specific complications. The removal of the causative agents (i.e., viruses or alcohol) prevents decompensation in the vast majority of patients with compensated cirrhosis. In contrast, even when etiological treatment has been effective, a significant proportion of patients with decompensated cirrhosis remains at risk of further disease progression. Therefore, therapies targeting specific key points in the complex pathophysiological cascade of decompensated cirrhosis could represent a new approach for the management of these severely ill patients. Some of the interventions currently employed for treating or preventing specific complications of cirrhosis or used in other diseases (i.e., poorly absorbable oral antibiotics, statins, albumin) have been proposed as potential disease-modifying agents in cirrhosis (DMAC) since clinical studies have shown their capacity of improving survival. Additional multicenter, large randomized clinical trials are awaited to confirm these promising results. Finally, new drugs able to antagonize key pathophysiological mechanisms are under pre-clinical development or at the initial stages of clinical assessment.

Identifiants

pubmed: 34640608
pii: jcm10194590
doi: 10.3390/jcm10194590
pmc: PMC8509683
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

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Auteurs

Giacomo Zaccherini (G)

Department of Medical and Surgical Sciences, University of Bologna, 40138 Bologna, Italy.

Manuel Tufoni (M)

IRCCS AOU di Bologna-Policlinico di S. Orsola, 40138 Bologna, Italy.

Mauro Bernardi (M)

Department of Medical and Surgical Sciences, University of Bologna, 40138 Bologna, Italy.

Paolo Caraceni (P)

Department of Medical and Surgical Sciences, University of Bologna, 40138 Bologna, Italy.
IRCCS AOU di Bologna-Policlinico di S. Orsola, 40138 Bologna, Italy.
Center for Biomedical Applied Research, University of Bologna, 40138 Bologna, Italy.

Classifications MeSH