Determinants of the effectiveness of bezafibrate combined with ursodeoxycholic acid in patients with primary biliary cholangitis

Author:

Matsumoto Kosuke1,Hirohara Junko2,Takeuchi Akihito1,Miura Ryo1,Asaoka Yoshinari1ORCID,Nakano Toshiaki2,Tanaka Atsushi1ORCID

Affiliation:

1. Department of Medicine Teikyo University School of Medicine Tokyo Japan

2. The Third Department of Internal Medicine Kansai Medical University Osaka Japan

Abstract

AbstractBackground and AimsFor patients with primary biliary cholangitis (PBC) exhibiting suboptimal responses to ursodeoxycholic acid (UDCA), obeticholic acid (OCA), and bezafibrate (BZF) are currently used and shown to improve long‐term outcomes. Nevertheless, we encounter patients who die or undergo liver transplantation (LT) even with combination treatment. In this study, we explored prognostic indicators in patients receiving combination treatment of UDCA and BZF.MethodsWe took advantage of the Japanese PBC registry and enrolled patients who received both UDCA and BZF therapy in 2000 or later. The covariates investigated included baseline covariates as well as treatment covariates. Two main outcomes (all‐cause death or LT and liver‐related death or LT) were assessed using multivariable‐adjusted Cox proportional hazards models.ResultsIn total, 772 patients were included. The median follow‐up was 7.1 years. Using the Cox regression model, bilirubin (hazard ratio [HR] 6.85, 95% confidence interval [CI] 1.73–27.1, p = 0.006), alkaline phosphatase (HR 5.46, 95% CI 1.32–22.6, p = 0.019), and histological stage (HR 4.87, 95% CI 1.16–20.5, p = 0.031) were found associated with LT‐free survival. For survival free from liver disease‐related death or LT, albumin (HR 7.72, 95% CI 1.48–40.4, p = 0.016) and bilirubin (HR 14.5, 95% CI 2.37–88.5, p = 0.004) were found significantly associated.ConclusionIn patients with PBC receiving combination therapy, prognostic variables were similar to those in patients receiving UDCA monotherapy. These results indicate the importance of diagnosing patients with PBC at an earlier stage because of the reduced effectiveness of BZF at advanced stages.

Publisher

Wiley

Subject

Infectious Diseases,Hepatology

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