Pharmacological treatment for metabolic dysfunction-associated steatotic liver disease and related disorders: Current and emerging therapeutic options.

IF 19.3 1区 医学 Q1 PHARMACOLOGY & PHARMACY
Pharmacological Reviews Pub Date : 2025-03-01 Epub Date: 2024-11-22 DOI:10.1016/j.pharmr.2024.100018
Xiang Zhang, Harry Cheuk-Hay Lau, Jun Yu
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引用次数: 0

Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD; formerly known as nonalcoholic fatty liver disease) is a chronic liver disease affecting over a billion individuals worldwide. MASLD can gradually develop into more severe liver pathologies, including metabolic dysfunction-associated steatohepatitis (MASH), cirrhosis, and liver malignancy. Notably, although being a global health problem, there are very limited therapeutic options against MASLD and its related diseases. While a thyroid hormone receptor agonist (resmetirom) is recently approved for MASH treatment, other efforts to control these diseases remain unsatisfactory. Given the projected rise in MASLD and MASH incidence, it is urgent to develop novel and effective therapeutic strategies against these prevalent liver diseases. In this article, the pathogenic mechanisms of MASLD and MASH, including insulin resistance, dysregulated nuclear receptor signaling, and genetic risk factors (eg, patatin-like phospholipase domain-containing 3 and hydroxysteroid 17-β dehydrogenase-13), are introduced. Various therapeutic interventions against MASH are then explored, including approved medication (resmetirom), drugs that are currently in clinical trials (eg, glucagon-like peptide 1 receptor agonist, fibroblast growth factor 21 analog, and PPAR agonist), and those failed in previous trials (eg, obeticholic acid and stearoyl-CoA desaturase 1 antagonist). Moreover, given that the role of gut microbes in MASLD is increasingly acknowledged, alterations in the gut microbiota and microbial mechanisms in MASLD development are elucidated. Therapeutic approaches that target the gut microbiota (eg, dietary intervention and probiotics) against MASLD and related diseases are further explored. With better understanding of the multifaceted pathogenic mechanisms, the development of innovative therapeutics that target the root causes of MASLD and MASH is greatly facilitated. The possibility of alleviating MASH and achieving better patient outcomes is within reach. SIGNIFICANCE STATEMENT: Metabolic dysfunction-associated steatotic liver disease (MASLD) is the most common chronic liver disease worldwide, and it can progress to more severe pathologies, including steatohepatitis, cirrhosis, and liver cancer. Better understanding of the pathogenic mechanisms of these diseases has facilitated the development of innovative therapeutic strategies. Moreover, increasing evidence has illustrated the crucial role of gut microbiota in the pathogenesis of MASLD and related diseases. It may be clinically feasible to target gut microbes to alleviate MASLD in the future.

代谢功能障碍相关性脂肪性肝病(MASLD,以前称为非酒精性脂肪肝)是一种慢性肝病,影响着全球十多亿人。代谢性脂肪肝可逐渐发展为更严重的肝脏病变,包括代谢功能障碍相关性脂肪性肝炎(MASH)、肝硬化和肝脏恶性肿瘤。值得注意的是,尽管MASLD是一个全球性的健康问题,但针对MASLD及其相关疾病的治疗方案却非常有限。虽然最近批准了一种甲状腺激素受体激动剂(瑞美替罗)用于治疗 MASH,但控制这些疾病的其他努力仍不尽如人意。鉴于MASLD和MASH的发病率预计会上升,开发新的、有效的治疗策略来防治这些流行性肝病已迫在眉睫。本文介绍了MASLD和MASH的致病机制,包括胰岛素抵抗、核受体信号传导失调和遗传风险因素(如含类拍蛋白磷脂酶结构域的3和羟基类固醇17-β脱氢酶-13)。然后探讨了针对 MASH 的各种治疗干预措施,包括已获批准的药物(瑞美替罗)、目前正在进行临床试验的药物(如胰高血糖素样肽 1 受体激动剂、成纤维细胞生长因子 21 类似物和 PPAR 激动剂),以及在以前的试验中失败的药物(如奥贝胆酸和硬脂酰-CoA 去饱和酶 1 拮抗剂)。此外,鉴于肠道微生物在 MASLD 中的作用日益得到认可,肠道微生物群的改变和微生物在 MASLD 发病中的作用机制也得到了阐明。针对肠道微生物群(如饮食干预和益生菌)防治 MASLD 及相关疾病的治疗方法也在进一步探索之中。随着对多方面致病机制的深入了解,针对 MASLD 和 MASH 根本原因的创新疗法的开发将得到极大的促进。减轻 MASH 病情、改善患者预后指日可待。意义声明:代谢功能障碍相关性脂肪性肝病(MASLD)是全球最常见的慢性肝病,可发展为更严重的病变,包括脂肪性肝炎、肝硬化和肝癌。对这些疾病致病机制的深入了解促进了创新治疗策略的开发。此外,越来越多的证据表明,肠道微生物群在 MASLD 及相关疾病的发病机制中起着至关重要的作用。未来,以肠道微生物为靶点来缓解 MASLD 在临床上可能是可行的。
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来源期刊
Pharmacological Reviews
Pharmacological Reviews 医学-药学
CiteScore
34.70
自引率
0.50%
发文量
40
期刊介绍: Pharmacological Reviews is a highly popular and well-received journal that has a long and rich history of success. It was first published in 1949 and is currently published bimonthly online by the American Society for Pharmacology and Experimental Therapeutics. The journal is indexed or abstracted by various databases, including Biological Abstracts, BIOSIS Previews Database, Biosciences Information Service, Current Contents/Life Sciences, EMBASE/Excerpta Medica, Index Medicus, Index to Scientific Reviews, Medical Documentation Service, Reference Update, Research Alerts, Science Citation Index, and SciSearch. Pharmacological Reviews offers comprehensive reviews of new pharmacological fields and is able to stay up-to-date with published content. Overall, it is highly regarded by scholars.
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