Zanjan Metabolic Disease Research Center, Vali-e-Asr Hospital, Zanjan University of Medical Science, Zanjan, Iran.
Clin Mol Hepatol. 2018 Sep;24(3):331-338. doi: 10.3350/cmh.2018.0006. Epub 2018 Jun 12.
BACKGROUND/AIMS: Non-alcoholic fatty liver disease (NAFLD) is one of the most prevalent chronic liver diseases in recent years. The aim of this study was to evaluate the effects of sitagliptin with and without a synbiotic supplement in the treatment of patients with NAFLD.
In total, 138 NAFLD patients aged 18-60 years were enrolled in the study. Patients were randomized to one of the following treatments for 16 weeks: Group I (n=68), sitagliptin 50 mg daily plus placebo (one capsule per day) or group II (n=70) sitagliptin 50 mg daily plus synbiotic (one capsule per day). Changes in fasting blood glucose (FBS), liver enzymes, lipid profile, and body mass index were compared between the groups.
The mean change in FBS with sitagliptin-placebo from baseline was -10.47±5.77 mg/dL, and that with sitagliptin-synbiotic was -13.52±4.16 mg/dL. There was a significant difference between the groups (P<0.001). The mean change in cholesterol (Chol) was -8.34±28.83 mg/dL with sitagliptin-placebo and -21.25±15.50 mg/dL with sitagliptinsynbiotic. There was a significant difference between the two groups (P=0.029). The administration of sitagliptin-placebo induced an increase of 6.13±27.04 mg/dL in low density lipoprotein (LDL), whereas sitagliptin-synbiotic induced a decrease of 14.92±15.85 mg/dL in LDL. A significant difference was observed between the two groups (P<0.001). On the other hand, in the sitagliptin-synbiotic group, there was significant improvement in aspartate aminotransferase (AST) level compared to the sitagliptin-placebo group (P=0.018).
Sitagliptin-synbiotic produced greater improvement in FBS, AST, Chol, and LDL compared to sitagliptin alone in patients with NAFLD.
背景/目的:非酒精性脂肪性肝病(NAFLD)是近年来最常见的慢性肝病之一。本研究旨在评估西他列汀联合或不联合益生菌补充剂治疗非酒精性脂肪性肝病患者的疗效。
共纳入 138 例年龄在 18-60 岁的非酒精性脂肪性肝病患者,随机分为以下治疗组:I 组(n=68),西他列汀 50mg/d 联合安慰剂(每日 1 粒);II 组(n=70),西他列汀 50mg/d 联合益生菌(每日 1 粒)。比较两组患者空腹血糖(FBS)、肝酶、血脂谱和体重指数的变化。
西他列汀-安慰剂组治疗前后 FBS 平均变化为-10.47±5.77mg/dL,西他列汀-益生菌组为-13.52±4.16mg/dL。两组间差异有统计学意义(P<0.001)。西他列汀-安慰剂组胆固醇(Chol)平均变化为-8.34±28.83mg/dL,西他列汀-益生菌组为-21.25±15.50mg/dL。两组间差异有统计学意义(P=0.029)。西他列汀-安慰剂组 LDL 水平升高 6.13±27.04mg/dL,而西他列汀-益生菌组 LDL 水平降低 14.92±15.85mg/dL。两组间差异有统计学意义(P<0.001)。另一方面,与西他列汀-安慰剂组相比,西他列汀-益生菌组天冬氨酸氨基转移酶(AST)水平显著改善(P=0.018)。
与西他列汀单药治疗相比,西他列汀联合益生菌在改善非酒精性脂肪性肝病患者的 FBS、AST、Chol 和 LDL 方面更具优势。