Please use this identifier to cite or link to this item: https://doi.org/10.3389/fendo.2020.609135
Title: Sodium-Glucose Co-Transporter 2 Inhibitors for Non-Alcoholic Fatty Liver Disease in Asian Patients With Type 2 Diabetes: A Meta-Analysis
Authors: 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
Keywords: Science & Technology
Life Sciences & Biomedicine
Endocrinology & Metabolism
hepatic fat
non-alcoholic fatty liver disease
sodium-glucose co-transporter-2 inhibitors
type 2 diabetes
meta-analysis
WEIGHT-LOSS
Issue Date: 11-Feb-2021
Publisher: FRONTIERS MEDIA SA
Citation: 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 (2021-02-11). Sodium-Glucose Co-Transporter 2 Inhibitors for Non-Alcoholic Fatty Liver Disease in Asian Patients With Type 2 Diabetes: A Meta-Analysis. FRONTIERS IN ENDOCRINOLOGY 11. ScholarBank@NUS Repository. https://doi.org/10.3389/fendo.2020.609135
Abstract: Objective: 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. Methods: 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). Results: 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. Conclusions: 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.
Source Title: FRONTIERS IN ENDOCRINOLOGY
URI: https://scholarbank.nus.edu.sg/handle/10635/206119
ISSN: 16642392
DOI: 10.3389/fendo.2020.609135
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