晚期开发药物治疗代谢功能障碍相关脂肪性肝炎(MASH)的前景。

IF 16.9 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Brian Lee, Ussama Ghumman, Lisa D Pedicone, Andres Gomez Aldana, Eric Lawitz
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引用次数: 0

摘要

代谢功能障碍相关脂肪变性肝病(MASLD)是一种涉及脂肪性肝病的病理谱系,可发展为纤维化、肝硬化、肝细胞癌和肝功能衰竭。MASLD和代谢功能障碍相关脂肪性肝炎(MASH)的患病率持续上升,反映了全球相关合并症(如肥胖和2型糖尿病)患病率的上升。由于这些合并症的惊人增加,更大比例的人口面临发展MASLD和MASH的风险。因此,对于MASLD和MASH的有效治疗已经有了很大的努力。最近,美国食品和药物管理局(fda)批准了选择性甲状腺激素受体激动剂resmetirom作为MASH患者的第一种治疗方法。在印度,印度药品监督管理局批准了saroglitazar,一种双过氧化物酶体增殖激活受体(PPAR) α/γ激动剂,用于治疗MASLD。目前,我们有各种药物类别,包括肝脏特异性治疗,处于三期开发阶段,甚至更多的药物正在开发中。本文将讨论甲状腺激素受体-受体激动剂、PPAR激动剂、胰高血糖素样肽-1受体激动剂、成纤维细胞生长因子21激动剂和脂肪酸合成酶抑制剂等发展后期的前瞻性治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prospects of Late-Stage Development Agents in the Treatment of Metabolic Dysfunction-Associated Steatohepatitis (MASH).

Metabolic dysfunction-associated steatotic liver disease (MASLD) is a spectrum of pathology involving fatty liver disease that may progress to fibrosis, cirrhosis, hepatocellular carcinoma, and liver failure. The prevalence of MASLD and metabolic dysfunction-associated steatohepatitis (MASH) continues to increase, mirroring the rise in global prevalence of related comorbidities such as obesity and type 2 diabetes mellitus. Due to the alarming rise of these comorbidities, a greater proportion of the population is at risk for developing MASLD and MASH. As such, there has been a significant effort to develop effective therapies for MASLD and MASH. Recently, the U.S. Food and Drug Administration approved resmetirom, a selective thyroid hormone receptor-beta agonist, as the first treatment for patients with MASH. In India, the Drug Controller General of India approved saroglitazar, a dual peroxisome proliferator-activated receptor (PPAR) α/γ agonist, for the treatment of MASLD. Currently, we have various drug classes, including liver-specific therapies, in Phase 3 development with even more agents earlier in the pipeline. This review will discuss prospective therapies in later stages of development such as thyroid hormone receptor-beta agonists, PPAR agonists, glucagon-like peptide-1 receptor agonists, fibroblast growth factor 21 agonists, and fatty acid synthase inhibitors.

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来源期刊
Clinical and Molecular Hepatology
Clinical and Molecular Hepatology Medicine-Hepatology
CiteScore
15.60
自引率
9.00%
发文量
89
审稿时长
10 weeks
期刊介绍: Clinical and Molecular Hepatology is an internationally recognized, peer-reviewed, open-access journal published quarterly in English. Its mission is to disseminate cutting-edge knowledge, trends, and insights into hepatobiliary diseases, fostering an inclusive academic platform for robust debate and discussion among clinical practitioners, translational researchers, and basic scientists. With a multidisciplinary approach, the journal strives to enhance public health, particularly in the resource-limited Asia-Pacific region, which faces significant challenges such as high prevalence of B viral infection and hepatocellular carcinoma. Furthermore, Clinical and Molecular Hepatology prioritizes epidemiological studies of hepatobiliary diseases across diverse regions including East Asia, North Asia, Southeast Asia, Central Asia, South Asia, Southwest Asia, Pacific, Africa, Central Europe, Eastern Europe, Central America, and South America. The journal publishes a wide range of content, including original research papers, meta-analyses, letters to the editor, case reports, reviews, guidelines, editorials, and liver images and pathology, encompassing all facets of hepatology.
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