Please use this identifier to cite or link to this item: https://doi.org/10.3389/fendo.2020.609135
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dc.titleSodium-Glucose Co-Transporter 2 Inhibitors for Non-Alcoholic Fatty Liver Disease in Asian Patients With Type 2 Diabetes: A Meta-Analysis
dc.contributor.authorWong, Chloe
dc.contributor.authorYaow, Clyve Yu Leon
dc.contributor.authorNg, Cheng Han
dc.contributor.authorChin, Yip Han
dc.contributor.authorLow, Yi Fen
dc.contributor.authorLim, Amanda Yuan Ling
dc.contributor.authorMuthiah, Mark Dhinesh
dc.contributor.authorKhoo, Chin Meng
dc.date.accessioned2021-11-15T01:58:21Z
dc.date.available2021-11-15T01:58:21Z
dc.date.issued2021-02-11
dc.identifier.citationWong, 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
dc.identifier.issn16642392
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/206119
dc.description.abstractObjective: 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.
dc.language.isoen
dc.publisherFRONTIERS MEDIA SA
dc.sourceElements
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectEndocrinology & Metabolism
dc.subjecthepatic fat
dc.subjectnon-alcoholic fatty liver disease
dc.subjectsodium-glucose co-transporter-2 inhibitors
dc.subjecttype 2 diabetes
dc.subjectmeta-analysis
dc.subjectWEIGHT-LOSS
dc.typeReview
dc.date.updated2021-11-15T01:23:41Z
dc.contributor.departmentCOMMUNICATIONS AND NEW MEDIA
dc.description.doi10.3389/fendo.2020.609135
dc.description.sourcetitleFRONTIERS IN ENDOCRINOLOGY
dc.description.volume11
dc.published.statePublished
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