Impact of CFTR Modulator Therapies on Liver Function in Cystic Fibrosis Patients: A Systematic Review of Hepatic Biomarkers

Authors

  • Elena Simona Moiceanu Pediatric Poison Centre, Grigore Alexandrescu Clinical Emergency Hospital for Children, Bucharest; Iuliu Hațieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania
  • Daniel Corneliu Leucuța Medical Informatics and Biostatistics Dept, Iuliu Hațieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania
  • Viorela Gabriela Nițescu Pediatric Poison Centre, Grigore Alexandrescu Clinical Emergency Hospital for Children, Bucharest; Carol Davila University of Medicine and Pharmacy, Bucharest, Romania
  • Andreea Lescaie Pediatric Poison Centre, Grigore Alexandrescu Clinical Emergency Hospital for Children, Bucharest; Carol Davila University of Medicine and Pharmacy, Bucharest, Romania
  • Maria Iacobescu Institute of Medical Research and Life Sciences – MEDFUTURE, Iuliu Hațieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania
  • Iustina Violeta Stan Alessandrescu-Rusescu National Institute for Mother and Child Health, Bucharest; Carol Davila University of Medicine and Pharmacy, Bucharest, Romania
  • Simona Elena Moșescu Alessandrescu-Rusescu National Institute for Mother and Child Health, Bucharest, Romania
  • Iolanda Cristina Vivisenco Dept. of Pediatrics, Grigore Alexandrescu Clinical Emergency Hospital for Children, Bucharest; Carol Davila University of Medicine and Pharmacy, Bucharest, Romania
  • Dan Lucian Dumitrașcu 2nd Dept. of Internal Medicine, Emergency Clinical County Hospital, Cluj-Napoca; Iuliu Hațieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania

DOI:

https://doi.org/10.15403/jgld-5879

Keywords:

cystic fibrosis, CFTR modulators, liver function, ALT, AST, GGT, AP, bilirubin, albumin, systematic review

Abstract

Background and Aims: Cystic fibrosis transmembrane conductance regulator (CFTR) modulators, including elexacaftor/ivacaftor/tezacaftor (ETI) and lumacaftor/ivacaftor (LI), have revolutionized the treatment of cystic fibrosis. However, their impact on liver function remains unclear, with varying effects reported across studies. The aim of this study was to systematically review the effects of CFTR modulators on liver function in cystic fibrosis patients by evaluating changes in key hepatic biomarkers.

Methods: A comprehensive literature search was conducted in Europe PubMed Central and PubMed databases for studies published between January 1, 2010, and December 31, 2023. Eligible studies included those assessing the impact of CFTR modulators on liver biomarkers in cystic fibrosis patients. Meta-analyses were performed where possible.

Results: Six studies encompassing 195 patients were included, with significant heterogeneity in study design, population, and outcomes. The review found mixed results for alanine aminotransferase (ALT), aspartate aminotransferase (AST), and gamma glutamyltransferase (GGT) levels, with some studies reporting increases and others decreases. LI therapy was associated with significant reductions in GGT and alkaline phosphatase (AP) levels, while ETI therapy showed significant increases in bilirubin levels. Albumin levels increased significantly with both therapies.

Conclusions: CFTR modulators have varying effects on liver function biomarkers in cystic fibrosis patients, with LI therapy generally showing more favorable outcomes on liver health. The significant heterogeneity among studies underscores the need for more standardized research to better understand these effects and guide clinical management.

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Published

2025-03-28

How to Cite

1.
Moiceanu ES, Leucuța DC, Nițescu VG, Lescaie A, Iacobescu M, Stan IV, Moșescu SE, Vivisenco IC, Dumitrașcu DL. Impact of CFTR Modulator Therapies on Liver Function in Cystic Fibrosis Patients: A Systematic Review of Hepatic Biomarkers. JGLD [Internet]. 2025 Mar. 28 [cited 2026 Jul. 22];34(1):115-21. Available from: https://www.jgld.ro/jgld/index.php/jgld/article/view/5879

Issue

Section

Systematic Review