Dua Ankita, Kumari Rashmi, Singh Mona, Kumar Roushan, Pradeep Sunila, Ojesina Akinyemi I, Kumar Roshan
Department of Zoology, Shivaji College, University of Delhi, New Delhi, India.
Department of Zoology, College of Commerce, Arts & Science, Patliputra University, Patna, Bihar, India.
Front Med (Lausanne). 2025 Aug 14;12:1618275. doi: 10.3389/fmed.2025.1618275. eCollection 2025.
The global prevalence of Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) has reached alarming levels, affecting nearly one-third of the world's population. This review analyzes current evidence on the intricate relationships between MASLD, insulin resistance, and type 2 diabetes mellitus (T2DM), with particular emphasis on gut microbiome interactions. As MASLD progresses from simple steatosis to Metabolic Dysfunction-Associated Steatohepatitis (MASH), it can lead to severe complications including fibrosis, cirrhosis, and hepatocellular carcinoma. The pathogenesis of MASLD is multifactorial, involving hepatic lipid accumulation, oxidative stress, inflammation, and dysregulation of the gut-liver axis. Insulin resistance is a central driver of disease progression, closely linked to obesity and metabolic syndrome. Recent research highlights how gut microbiome dysbiosis exacerbates MASLD through mechanisms such as increased intestinal permeability, systemic inflammation, and altered metabolic signaling. Identification of microbial signatures offers promise for novel diagnostic and therapeutic strategies. By integrating metabolic, inflammatory, and microbial perspectives, this review provides a comprehensive overview of MASLD pathogenesis and its association with obesity, insulin resistance, and T2DM.
代谢功能障碍相关脂肪性肝病(MASLD)的全球患病率已达到惊人水平,影响了近三分之一的世界人口。本综述分析了关于MASLD、胰岛素抵抗和2型糖尿病(T2DM)之间复杂关系的现有证据,特别强调了肠道微生物群的相互作用。随着MASLD从单纯性脂肪变性发展为代谢功能障碍相关脂肪性肝炎(MASH),它可导致包括纤维化、肝硬化和肝细胞癌在内的严重并发症。MASLD的发病机制是多因素的,涉及肝脏脂质积累、氧化应激、炎症以及肠-肝轴失调。胰岛素抵抗是疾病进展的核心驱动因素,与肥胖和代谢综合征密切相关。最近的研究强调了肠道微生物群失调如何通过肠道通透性增加、全身炎症和代谢信号改变等机制加剧MASLD。微生物特征的识别为新型诊断和治疗策略带来了希望。通过整合代谢、炎症和微生物学观点,本综述全面概述了MASLD的发病机制及其与肥胖、胰岛素抵抗和T2DM的关联。