Shao Shih-Chieh, Kuo Liang-Tseng, Chien Rong-Nan, Hung Ming-Jui, Lai Edward Chia-Cheng
Department of Pharmacy, Keelung Chang Gung Memorial Hospital, Keelung, Taiwan.
School of Pharmacy, Institute of Clinical Pharmacy and Pharmaceutical Sciences, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
BMJ Open Diabetes Res Care. 2020 Dec;8(2). doi: 10.1136/bmjdrc-2020-001956.
Sodium glucose co-transporter 2 (SGLT2) inhibitors have been reported to benefit liver functions in patients with type 2 diabetes (T2D) with non-alcoholic fatty liver disease (NAFLD). The aim of this study is to critically appraise existing systematic reviews in order to consolidate evidence associating the use of SGLT2 inhibitors with beneficial hepatic results for patients with T2D with NAFLD.
This umbrella review searched relevant published systematic reviews of clinical trials from PubMed and Embase between inception and September 16, 2020. Two independent investigators appraised study quality using AMSTAR2 (Assessment of Multiple Systematic Reviews 2). The hepatic effects from SGLT2 inhibitors were summarized based on liver enzymes, liver fat, liver histology, liver cirrhosis and liver cancer.
Of 25 screened potential systematic reviews, we ultimately included 7 in this study. However, none of them could be rated as being of high methodological quality. Five systematic reviews indicated that SGLT2 inhibitors could effectively decrease liver fat and liver parameters of alanine aminotransferase and gamma-glutamyl transferase in patients with NAFLD. Two systematic reviews indicated that SGLT2 inhibitors could reduce hepatosteatosis, as supported by biopsy-proven evidence of improvement from a small clinical trial, but no evidence of liver fibrosis improvement was found.
There is some association between SGLT2 inhibitor use and observed benefits to liver functions in patients with T2D with NAFLD, although the quality of current systematic reviews remains relatively low. Further evaluation of long-term liver outcomes with SGLT2 inhibitors in cases of liver cirrhosis and liver cancer is warranted.
据报道,钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂对患有2型糖尿病(T2D)和非酒精性脂肪性肝病(NAFLD)的患者的肝功能有益。本研究的目的是严格评估现有的系统评价,以巩固关于SGLT2抑制剂的使用与T2D合并NAFLD患者肝脏有益结果之间关联的证据。
本伞形评价检索了从创刊至2020年9月16日PubMed和Embase上已发表的相关临床试验系统评价。两名独立研究人员使用AMSTAR2(多重系统评价评估2)评估研究质量。基于肝酶、肝脂肪、肝组织学、肝硬化和肝癌总结了SGLT2抑制剂的肝脏效应。
在筛选的25篇潜在系统评价中,本研究最终纳入了7篇。然而,它们均未被评为具有高方法学质量。五项系统评价表明,SGLT2抑制剂可有效降低NAFLD患者的肝脂肪以及丙氨酸转氨酶和γ-谷氨酰转移酶的肝脏参数。两项系统评价表明,SGLT2抑制剂可减少肝脂肪变性,一项小型临床试验的活检证实的改善证据支持了这一点,但未发现肝纤维化改善的证据。
在T2D合并NAFLD患者中,SGLT2抑制剂的使用与观察到的肝功能益处之间存在一定关联,尽管当前系统评价的质量仍然相对较低。有必要进一步评估SGLT2抑制剂在肝硬化和肝癌病例中的长期肝脏结局。