Gamma‐glutamyl transferase predicts pemafibrate treatment response in non‐alcoholic fatty liver disease

Author:

Takahashi Yusuke1,Seko Yuya1ORCID,Yamaguchi Kanji1,Takeuchi Kento1,Yano Kota1,Kataoka Seita1,Moriguchi Michihisa1,Itoh Yoshito1

Affiliation:

1. Department of Molecular Gastroenterology and Hepatology, Graduate School of Medical Science Kyoto Prefectural University of Medicine Kyoto Japan

Abstract

AbstractBackground and AimPemafibrate, a selective peroxisome proliferator activated receptor α modulator, has been shown to improve liver function among nonalcoholic fatty liver disease (NAFLD) patients with dyslipidemia. The aim of this retrospective study is to identify predictors of pemafibrate efficacy in NAFLD patients.MethodsA total of 75 NAFLD patients with dyslipidemia who received pemafibrate twice per day for 48 weeks were enrolled in this study. We used the FibroScan‐aspartate aminotransferase (FAST) score as a benchmark for treatment efficacy.ResultsMedian FAST score significantly decreased from 0.96 at baseline to 0.93 at week 48 (P < 0.001). Significant improvements in levels of aspartate aminotransferase (AST), alanine aminotransferase (ALT), gamma‐glutamyl transferase (GGT), and triglycerides were also noted. The serum level of GGT at baseline was correlated with change in FAST score (r = −0.22, P = 0.049). Changes in AST, ALT, and GGT were positively correlated with change in FAST score (r = 0.71, r = 0.61, and r = 0.38). Multivariate analyses identified age and GGT level at baseline as significantly associated with improvement of FAST score by pemafibrate therapy (odds ratio 1.11, 1.02, respectively). Patients over 50 years of age and with a GGT of 90 IU/L or higher showed significantly greater improvement in the FAST score than other groups.ConclusionsPemafibrate improves the FAST score of NAFLD patients with complicating dyslipidemia, especially in older patients with high GGT level. GGT is useful as an indicator of optimal treatment choice for NAFLD patients with dyslipidemia.

Funder

Ministry of Education, Culture, Sports, Science and Technology

Publisher

Wiley

Subject

Gastroenterology,Hepatology

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