Department of Pharmaceutical Sciences & Technology, BIT Mesra, Ranchi, 835215, India.
Naunyn Schmiedebergs Arch Pharmacol. 2024 Nov;397(11):8421-8443. doi: 10.1007/s00210-024-03204-6. Epub 2024 Jun 11.
Nonalcoholic fatty liver disease (NAFLD), more appropriately known as metabolic (dysfunction) associated fatty liver disease (MAFLD), a prevalent condition in type 2 diabetes mellitus (T2DM) patients, is a complex condition involving hepatic lipid accumulation, inflammation, and liver fibrosis. The gut-liver axis is closely linked to metabolic dysfunction, insulin resistance, inflammation, and oxidative stress that are leading to the cooccurrence of MAFLD and T2DM cardiovascular diseases (CVDs). The purpose of this review is to raise awareness about the role of the gut-liver axis in the progression of MAFLD, T2DM and CVDs with a critical analysis of available treatment options for T2DM and MAFLD and their impact on cardiovascular health. This study analysed over 100 articles on this topic, using online searches and predefined keywords, to understand and summarise published research. Numerous studies have shown a strong correlation between gut dysfunction, particularly the gut microbiota and its metabolites, and the occurrence and progression of MAFLD and type 2 diabetes mellitus (T2DM). Herein, this article also examines the impact of the gut-liver axis on MAFLD, T2DM, and related complications, focusing on the role of gut microbiota dysbiosis in insulin resistance, T2DM and obesity-related cardiovascular complications. The study suggests potential treatment targets for MAFLD linked to T2DM, focusing on cardiovascular outcomes and the molecular mechanism of the gut-liver axis, as gut microbiota dysbiosis contributes to obesity-related metabolic abnormalities.
非酒精性脂肪性肝病(NAFLD),更恰当地称为代谢(功能)相关脂肪性肝病(MAFLD),是 2 型糖尿病(T2DM)患者中普遍存在的一种疾病,是一种涉及肝脂质积聚、炎症和肝纤维化的复杂疾病。肠-肝轴与代谢功能障碍、胰岛素抵抗、炎症和氧化应激密切相关,这些因素导致 MAFLD 和 T2DM 心血管疾病(CVDs)同时发生。本综述的目的是提高对肠-肝轴在 MAFLD、T2DM 和 CVDs 进展中的作用的认识,对 T2DM 和 MAFLD 的现有治疗选择及其对心血管健康的影响进行批判性分析。本研究通过在线搜索和预定义的关键词,对这一主题的 100 多篇文章进行了分析,以了解和总结已发表的研究。大量研究表明,肠道功能障碍,特别是肠道微生物群及其代谢物,与 MAFLD 和 2 型糖尿病(T2DM)的发生和进展密切相关。本文还研究了肠-肝轴对 MAFLD、T2DM 及相关并发症的影响,重点关注肠道微生物群失调在胰岛素抵抗、T2DM 和肥胖相关心血管并发症中的作用。该研究提出了与 T2DM 相关的 MAFLD 的潜在治疗靶点,重点关注心血管结局和肠-肝轴的分子机制,因为肠道微生物群失调导致与肥胖相关的代谢异常。