Plasma Renin Activity Predicts Prognosis and Liver Disease-Related Events in Liver Cirrhosis Patients with Ascites Treated by Tolvaptan.


Journal

Digestive diseases (Basel, Switzerland)
ISSN: 1421-9875
Titre abrégé: Dig Dis
Pays: Switzerland
ID NLM: 8701186

Informations de publication

Date de publication:
2022
Historique:
received: 29 01 2021
accepted: 27 06 2021
pubmed: 5 8 2021
medline: 7 7 2022
entrez: 4 8 2021
Statut: ppublish

Résumé

A retrospective study was to analyze the association of plasma renin activity (PRA) with overall survival and liver disease-related events in decompensated liver cirrhosis with ascites treated by tolvaptan. We included 196 patients with decompensated cirrhosis treated with tolvaptan and for whom hepatic ascites had remained uncontrolled by conventional diuretics. Factors associated with prognosis and appearance of liver disease-related events were investigated, including vasopressin, sympathetic nervous system hormones (adrenaline, noradrenaline, and dopamine), and the renin-angiotensin system (PRA and aldosterone) at the beginning of tolvaptan treatment. Age, history of hepatocellular carcinoma (HCC), and PRA were identified as independent factors for prognosis after tolvaptan treatment. The median survival time in patients with PRA ≥9.5 ng/mL/h at the beginning of tolvaptan treatment was significantly shorter than in patients with PRA <9.5 ng/mL/h (193 vs. 893 days, p < 0.001). PRA and a history of HCC were independent factors for the occurrence of liver disease-related events. The median event-free period in patients with PRA ≥3.2 ng/mL/h was significantly shorter than that of patients with PRA <3.2 ng/mL/h (89 vs. 222 days, p < 0.001). PRA is an independent predictor of prognosis and appearance of liver disease-related events in patients with decompensated cirrhosis who have started tolvaptan treatment.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
A retrospective study was to analyze the association of plasma renin activity (PRA) with overall survival and liver disease-related events in decompensated liver cirrhosis with ascites treated by tolvaptan.
METHODS METHODS
We included 196 patients with decompensated cirrhosis treated with tolvaptan and for whom hepatic ascites had remained uncontrolled by conventional diuretics. Factors associated with prognosis and appearance of liver disease-related events were investigated, including vasopressin, sympathetic nervous system hormones (adrenaline, noradrenaline, and dopamine), and the renin-angiotensin system (PRA and aldosterone) at the beginning of tolvaptan treatment.
RESULTS RESULTS
Age, history of hepatocellular carcinoma (HCC), and PRA were identified as independent factors for prognosis after tolvaptan treatment. The median survival time in patients with PRA ≥9.5 ng/mL/h at the beginning of tolvaptan treatment was significantly shorter than in patients with PRA <9.5 ng/mL/h (193 vs. 893 days, p < 0.001). PRA and a history of HCC were independent factors for the occurrence of liver disease-related events. The median event-free period in patients with PRA ≥3.2 ng/mL/h was significantly shorter than that of patients with PRA <3.2 ng/mL/h (89 vs. 222 days, p < 0.001).
CONCLUSIONS CONCLUSIONS
PRA is an independent predictor of prognosis and appearance of liver disease-related events in patients with decompensated cirrhosis who have started tolvaptan treatment.

Identifiants

pubmed: 34348262
pii: 000518099
doi: 10.1159/000518099
doi:

Substances chimiques

Tolvaptan 21G72T1950
Renin EC 3.4.23.15

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

479-488

Informations de copyright

© 2021 S. Karger AG, Basel.

Auteurs

Leona Osawa (L)

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan.
First Department of Internal Medicine, Faculty of Medicine, University of Yamanashi, Kofu, Japan.

Hiroyuki Nakanishi (H)

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan.

Masayuki Kurosaki (M)

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan.

Sakura Kirino (S)

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan.

Kento Inada (K)

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan.

Koji Yamashita (K)

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan.

Yuka Hayakawa (Y)

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan.

Shuhei Sekiguchi (S)

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan.

Wan Wang (W)

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan.

Mao Okada (M)

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan.

Mayu Higuchi (M)

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan.

Yasuyuki Komiyama (Y)

First Department of Internal Medicine, Faculty of Medicine, University of Yamanashi, Kofu, Japan.

Kenta Takaura (K)

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan.

Hitomi Takada (H)

First Department of Internal Medicine, Faculty of Medicine, University of Yamanashi, Kofu, Japan.

Shun Kaneko (S)

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan.

Chiaki Maeyashiki (C)

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan.

Nobuharu Tamaki (N)

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan.

Yutaka Yasui (Y)

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan.

Kaoru Tsuchiya (K)

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan.

Jun Itakura (J)

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan.

Yuka Takahashi (Y)

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan.

Nobuyuki Enomoto (N)

First Department of Internal Medicine, Faculty of Medicine, University of Yamanashi, Kofu, Japan.

Namiki Izumi (N)

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan.

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Classifications MeSH