Division of Clinical Pharmacology, Centre for Interdisciplinary Research on Medicines (CIRM), University of Liège, and Division of Diabetes, Nutrition and Metabolic Disorders, Department of Medicine, CHU Liège, Liège, Belgium.
Diabetes Metab. 2019 Jun;45(3):213-223. doi: 10.1016/j.diabet.2019.01.008. Epub 2019 Jan 29.
Patients with type 2 diabetes mellitus (T2DM) are exposed to non-alcoholic fatty liver disease (NAFLD), a comorbidity associated with cardiovascular disease and chronic kidney disease, and which may progress to non-alcoholic steatohepatitis (NASH), fibrosis and cirrhosis. Sodium-glucose cotransporter type-2 (SGLT2) inhibitors are glucose-lowering agents that improve glucose control while promoting weight loss and lowering serum uric acid levels. These agents may exert cardiovascular and renal protection in T2DM patients with established cardiovascular disease. Recent findings from both randomized controlled trials and open-label studies have also shown that SGLT2 inhibitors are able to reduce fatty liver content, as assessed by different imaging techniques, and improve biological markers of NAFLD, especially serum liver enzymes, in patients with T2DM. In addition, there are emerging data to suggest a mechanism beyond the reduction of hyperglycaemia and body weight, and a potential role for the decrease in low-grade inflammation and oxidative stress associated with SGLT2 inhibitor therapy. This positive effect of SGLT2 inhibitors on NAFLD complements their already well-known effects on cardiovascular and chronic kidney diseases.
2 型糖尿病患者易患非酒精性脂肪性肝病(NAFLD),这是一种与心血管疾病和慢性肾脏病相关的合并症,可能进展为非酒精性脂肪性肝炎(NASH)、纤维化和肝硬化。钠-葡萄糖共转运蛋白 2(SGLT2)抑制剂是一种降血糖药物,可在降低血糖的同时促进体重减轻和降低血尿酸水平。这些药物可能对已患有心血管疾病的 2 型糖尿病患者发挥心血管和肾脏保护作用。最近的随机对照试验和开放标签研究结果还表明,SGLT2 抑制剂能够通过不同的影像学技术降低脂肪性肝病的肝内脂肪含量,并改善 2 型糖尿病患者的非酒精性脂肪性肝病的生物标志物,尤其是血清肝酶。此外,有新的数据表明,其作用机制不仅在于降低高血糖和体重,而且 SGLT2 抑制剂治疗还可能与降低低度炎症和氧化应激有关。SGLT2 抑制剂对非酒精性脂肪性肝病的这种积极影响补充了其对心血管疾病和慢性肾脏病的已有显著作用。