Wong Chloe, Yaow Clyve Yu Leon, Ng Cheng Han, Chin Yip Han, Low Yi Fen, Lim Amanda Yuan Ling, Muthiah Mark Dhinesh, Khoo Chin Meng
Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Department of Medicine, National University Hospital, Singapore, Singapore.
Front Endocrinol (Lausanne). 2021 Feb 11;11:609135. doi: 10.3389/fendo.2020.609135. eCollection 2020.
Non-alcoholic fatty liver disease (NAFLD) is a very common disorder among patients with type 2 diabetes and may share causal relationship. Type 2 diabetes is a risk factor for progression and potential poor outcomes in NAFLD patients. This meta-analysis aimed to analyze the current evidence of sodium-glucose co-transporter-2 inhibitors (SGLT2i), a glucose-lowering drug to improve NAFLD in patients with Type 2 Diabetes.
Medline, Embase and Cochrane Central Register of Controlled Trials were searched for articles examining efficacy of SGLT2i on treatments of NAFLD in type 2 diabetes in July 2020, and articles were sieved. Continuous data were extracted in the form of mean and standard deviation and were pooled with standardized mean difference (SMD).
10 articles involving 555 patients from seven randomized controlled trials (RCTs) and three cohort studies, were included in this meta-analysis. Our analysis revealed significant improvements in hepatic fat content (after treatment: -0.789 (-1.404 to -0.175), p = 0.012; compared with control: -0.923 (-1.562 to -0.285), p = 0.005), AST (After Treatment: -0.539 (-0.720 to -0.357), p < 0.001; compared with control: -0.421 (-0.680 to -0.161), p = 0.001), ALT (after treatment: -0.633 (-0.892 to -0.373), p < 0.001; compared with Control: -0.468 (-0.685 to -0.251), p < 0.001), body composition (BMI: after treatment: -0.225 (-0.456 to 0.005), p = 0.055; compared with Control: -1.092 (-2.032 to -0.153), p = 0.023), glycemic control (HbA1c: After Treatment: -0.701 (-1.098 to -0.303), p = 0.001; compared with control: -0.210 (-0.603 to 0.183), p = 0.295), lipid parameters (Triglycerides: after treatment: -0.230 (-0.409 to -0.052), p = 0.011; compared with control: -0.336 (-0.597 to -0.076), p = 0.011), inflammatory markers (serum ferritin: after treatment: -0.409 (-0.694 to -0.124), p = 0.005; compared with control: -0.814 (-1.688 to 0.059), p = 0.068) after SGLT2i treatment, and when compared against controls. There was a trend in the improvement in fibrosis markers after SGLT2i treatment.
SGLT2i is an effective treatment to improve NAFLD among patients with type 2 diabetes. Further studies are needed to understand the direct and indirect effects of SGLT2i on NAFLD and if SGLT2i could prevent the progression of NAFLD or NASH. SGLT2i could potentially be considered for patients with type 2 diabetes and NAFLD, if there are no contraindications.
非酒精性脂肪性肝病(NAFLD)在2型糖尿病患者中非常常见,且可能存在因果关系。2型糖尿病是NAFLD患者病情进展及潜在不良结局的危险因素。本荟萃分析旨在分析钠-葡萄糖协同转运蛋白2抑制剂(SGLT2i)这一降糖药物改善2型糖尿病患者NAFLD的现有证据。
检索了Medline、Embase和Cochrane对照试验中央注册库,以查找2020年7月研究SGLT2i治疗2型糖尿病患者NAFLD疗效的文章,并对文章进行筛选。连续数据以均值和标准差的形式提取,并用标准化均值差(SMD)进行汇总。
本荟萃分析纳入了10篇文章,涉及来自7项随机对照试验(RCT)和3项队列研究的555例患者。我们的分析显示,SGLT2i治疗后及与对照组相比,肝脂肪含量(治疗后:-0.789(-1.404至-0.175),p = 0.012;与对照组相比:-0.923(-1.562至-0.285),p = 0.005)、谷草转氨酶(AST,治疗后:-0.539(-0.720至-0.357),p < 0.001;与对照组相比:-0.421(-0.680至-0.161),p = 0.001)、谷丙转氨酶(ALT,治疗后:-0.633(-0.892至-0.373),p < 0.001;与对照组相比:-0.468(-0.685至-0.251),p < 0.001)、身体成分(BMI,治疗后:-0.225(-0.456至0.005),p = 0.055;与对照组相比:-1.092(-2.032至-0.153),p = 0.023)、血糖控制(糖化血红蛋白HbA1c,治疗后:-0.701(-1.098至-0.303),p = 0.001;与对照组相比:-0.210(-0.603至0.183),p = 0.295)、血脂参数(甘油三酯,治疗后:-0.230(-0.409至-0.052),p = 0.011;与对照组相比:-0.336(-0.597至-0.076),p = 0.011)、炎症标志物(血清铁蛋白,治疗后:-0.409(-0.694至-0.124),p = 0.005;与对照组相比:-0.814(-1.688至0.059),p = 0.068)均有显著改善。SGLT2i治疗后纤维化标志物有改善趋势。
SGLT2i是改善2型糖尿病患者NAFLD的有效治疗方法。需要进一步研究以了解SGLT2i对NAFLD的直接和间接影响,以及SGLT2i是否能预防NAFLD或非酒精性脂肪性肝炎(NASH)的进展。如果没有禁忌证,对于2型糖尿病合并NAFLD患者,SGLT2i可能是一种可考虑的治疗药物。