Effects of sitagliptin on intrahepatic lipid content in patients with non-alcoholic fatty liver disease

PurposeDipeptidyl peptidase-4 inhibitors (DPP-4I), key regulators of the actions of incretin hormones, exert anti-hyperglycemic effects in type 2 diabetes mellitus (T2DM) patients. A major unanswered question concerns the potential ability of DPP-4I to improve intrahepatic lipid (IHL) content in non...

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Veröffentlicht in:Frontiers in endocrinology (Lausanne) 2022-08, Vol.13, p.866189-866189
Hauptverfasser: Wang, Xingchun, Zhao, Bangfeng, Sun, Hang, You, Hui, Qu, Shen
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Sprache:eng
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Zusammenfassung:PurposeDipeptidyl peptidase-4 inhibitors (DPP-4I), key regulators of the actions of incretin hormones, exert anti-hyperglycemic effects in type 2 diabetes mellitus (T2DM) patients. A major unanswered question concerns the potential ability of DPP-4I to improve intrahepatic lipid (IHL) content in nonalcoholic fatty liver disease (NAFLD) patients. The aim of this study was to evaluate the effects of sitagliptin on IHL in NAFLD patients. MethodsA prospective, 24-week, single-center, open-label, comparative study enrolled 68 Chinese NAFLD patients with T2DM. Subjects were randomly divided into 4 groups: control group who did not take medicine (14 patients); sitagliptin group who received sitagliptin treatment (100mg per day) (17 patients); metformin group who received metformin (500mg three times per day) (17 patients); and sitagliptin plus metformin group who received sitagliptin (100mg per day) and metformin (500 mg three times per day) (20 patients). IHL, physical examination (waist circumstances, WC; body mass index, BMI), glucose-lipid metabolism (fasting plasma glucose, FPG; hemoglobin A1c, Hb1A1c; triglycerides; cholesterol; alanine aminotransferase, ALT; aspartate aminotransferase, AST) were measured at baseline and at 24 weeks. Results1) WC and BMI were decreased significantly in all groups except control group (all P0.05). Only the metformin group showed a statistically significant difference in IHL before and after treatment(P
ISSN:1664-2392
1664-2392
DOI:10.3389/fendo.2022.866189