CFTR 调节器疗法对囊性纤维化患者肝功能的影响:肝脏生物标志物的系统回顾

Elena Simona Moiceanu, Daniel Corneliu Leucuța, Viorela Gabriela Nițescu, Andreea Lescaie, Maria Iacobescu, Iustina Violeta Stan, Simona Elena Moșescu, Iolanda Cristina Vivisenco, Dan Lucian Dumitrașcu
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引用次数: 0

摘要

背景和目的:囊性纤维化跨膜传导调节器(CFTR)调节剂,包括 elexacaftor/ivacaftor/tezacaftor (ETI) 和 lumacaftor/ivacaftor (LI),已经彻底改变了囊性纤维化的治疗。然而,它们对肝功能的影响仍不明确,不同研究报告的影响也不尽相同。本研究旨在通过评估关键肝脏生物标志物的变化,系统回顾CFTR调节剂对囊性纤维化患者肝功能的影响:在欧洲 PubMed Central 和 PubMed 数据库中对 2010 年 1 月 1 日至 2023 年 12 月 31 日期间发表的研究进行了全面的文献检索。符合条件的研究包括那些评估CFTR调节剂对囊性纤维化患者肝脏生物标志物影响的研究。尽可能进行元分析:共纳入六项研究,涵盖 195 名患者,研究设计、研究人群和研究结果存在显著异质性。综述发现,丙氨酸氨基转移酶(ALT)、天门冬氨酸氨基转移酶(AST)和γ谷氨酰转移酶(GGT)水平的研究结果不一,一些研究报告了丙氨酸氨基转移酶(ALT)水平的升高,而另一些研究报告了丙氨酸氨基转移酶(AST)水平的降低。LI疗法能显著降低谷丙转氨酶和碱性磷酸酶(AP)水平,而ETI疗法则能显著提高胆红素水平。两种疗法均可使白蛋白水平明显升高:CFTR调节剂对囊性纤维化患者肝功能生物标志物的影响各不相同,LI疗法通常对肝脏健康更有利。不同研究之间存在明显的异质性,这突出表明需要进行更多的标准化研究,以更好地了解这些影响并指导临床治疗。
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Impact of CFTR Modulator Therapies on Liver Function in Cystic Fibrosis Patients: A Systematic Review of Hepatic Biomarkers.

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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