Kumar Ashish
Professor, Department of Gastroenterology, Institute of Liver, Gastroenterology, and Pancreatico-Biliary Sciences, Sir Ganga Ram Hospital, Delhi, India, Corresponding Author, Orcid: https://orcid.org/0000-0001-6680-7227.
J Assoc Physicians India. 2025 Jul;73(7):e45-e60. doi: 10.59556/japi.73.1058.
Metabolic dysfunction-associated steatotic liver disease (MASLD), formerly known as nonalcoholic fatty liver disease (NAFLD), has become a significant public health issue worldwide, with a pronounced impact in India due to the escalating rates of obesity and type 2 diabetes mellitus (T2DM) driving its prevalence. This condition spans a range of hepatic disorders, from uncomplicated steatosis to metabolic dysfunction-associated steatohepatitis (MASH), accompanied by differing levels of hepatic fibrosis, heightening the likelihood of progression to cirrhosis, liver cancer, and cardiovascular complications. While lifestyle modification remains the cornerstone of MASLD management, pharmacologic therapies are increasingly recognized as essential for patients with progressive disease or those at higher risk of complications. Recent insights into the pathogenesis of MASLD have led to the development of innovative therapies targeting key mechanisms such as hepatic steatosis, insulin resistance, inflammation, and hepatic fibrosis. Several pharmacological agents have shown encouraging results in clinical trials, including thyroid hormone receptor-β agonist resmetirom, glucagon-like peptide-1 receptor agonists (GLP-1RAs) like semaglutide, peroxisome proliferator-activated receptor (PPAR) agonists such as pioglitazone and saroglitazar, sodium-glucose cotransporter-2 inhibitors (SGLT2i), and vitamin E. Furthermore, emerging therapies, including the dual incretin agonist tirzepatide and fibroblast growth factor (FGF) analogs, hold the potential to transform future treatment strategies. This review provides a comprehensive overview of current and evolving pharmacologic options for MASLD, with a focus on practical recommendations tailored for Indian physicians. A structured treatment algorithm for noncirrhotic MASLD (F0-F3 fibrosis) is presented, incorporating only drugs currently available in India and stratified based on diabetes status and hepatic fibrosis severity. Given India's vast and diverse patient population, ensuring access to cost-effective therapies remains a challenge, necessitating a pragmatic approach that balances efficacy, affordability, and real-world feasibility. This review serves as a practical clinical guide, equipping physicians with evidence-based recommendations to optimize MASLD management in routine practice.
代谢功能障碍相关脂肪性肝病(MASLD),以前称为非酒精性脂肪性肝病(NAFLD),已成为全球重大的公共卫生问题,由于肥胖率和2型糖尿病(T2DM)患病率不断上升,在印度的影响尤为显著。这种疾病涵盖了一系列肝脏疾病,从不复杂的脂肪变性到代谢功能障碍相关脂肪性肝炎(MASH),伴有不同程度的肝纤维化,增加了进展为肝硬化、肝癌和心血管并发症的可能性。虽然生活方式改变仍然是MASLD管理的基石,但药物治疗对于病情进展的患者或并发症风险较高的患者越来越被认为是必不可少的。最近对MASLD发病机制的深入了解导致了针对肝脂肪变性、胰岛素抵抗、炎症和肝纤维化等关键机制的创新疗法的开发。几种药物在临床试验中显示出令人鼓舞的结果,包括甲状腺激素受体-β激动剂瑞美替昂、司美格鲁肽等胰高血糖素样肽-1受体激动剂(GLP-1RAs)、吡格列酮和沙罗格列扎等过氧化物酶体增殖物激活受体(PPAR)激动剂、钠-葡萄糖协同转运蛋白-2抑制剂(SGLT2i)和维生素E。此外,包括双效肠促胰岛素激动剂替尔泊肽和成纤维细胞生长因子(FGF)类似物在内的新兴疗法有可能改变未来的治疗策略。本综述全面概述了目前和不断发展的MASLD药物选择,重点是为印度医生量身定制的实用建议。提出了非肝硬化MASLD(F0-F3纤维化)的结构化治疗算法,仅纳入印度目前可用的药物,并根据糖尿病状态和肝纤维化严重程度进行分层。鉴于印度庞大且多样化的患者群体,确保获得具有成本效益的疗法仍然是一项挑战,需要一种务实的方法来平衡疗效