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Pioglitazone on nonalcoholic steatohepatitis: A systematic review and meta-analysis of 15 RCTs

Nonalcoholic steatohepatitis is regarded as a risk factor of many liver diseases. METHODS: Relevant studies were searched from The National Library of Medicine, Cochrane Library, Elsevier, China National Knowledge Infrastructure, Web of Science and WANFANG databases. A total of 15 eligible studies w...

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Detalles Bibliográficos
Autores principales: Zhao, Yan, Zhao, Wenli, Wang, Hongwu, Zhao, Ye, Bu, Huaien, Takahashi, Hirokazu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9678615/
https://www.ncbi.nlm.nih.gov/pubmed/36401449
http://dx.doi.org/10.1097/MD.0000000000031508
Descripción
Sumario:Nonalcoholic steatohepatitis is regarded as a risk factor of many liver diseases. METHODS: Relevant studies were searched from The National Library of Medicine, Cochrane Library, Elsevier, China National Knowledge Infrastructure, Web of Science and WANFANG databases. A total of 15 eligible studies were analyzed in the Reviewer Manager 5.3 software, including 7 English articles and 8 Chinese articles. RESULTS: Fifteen studies are selected for this meta-analysis, which includes totally 623 patients in the treatment group and 594 patients in the control group. As a result, 8 studies show that the total effective rate of the treatment group is higher than that of the control group [Z = 3.64, 95% confidence intervals (CI): 1.78 (1.31–2.43), P = .0003]; eleven studies show that fasting plasma glucose levels of the experimental group are lower than that of the control group [Z = 4.38, 95% CI: −0.95 (−1.38 to −0.53), P < .0001]; ten studies show that glutamic-pyruvic transaminase levels of the experimental group are lower than that of the control group [Z = 3.69, 95% CI: −11.76 (−18.01 to −5.51), P = .0002]; 6 studies show that glutamic oxalacetic transaminase levels of the experimental group are lower than that of the control group [Z = 7.40, 95% CI: −3.01 (−3.81 to −2.22), P < .00001]; 6 studies show that gamma-glutamyl transpeptidase levels of the experimental group are lower than that of the control group [Z = 2.43, 95% CI: −23.77 (−42.98 to −4.57), P = .02]; 9 studies show that triglyceride levels of the experimental group are lower than that of the control group [Z = 3.06, 95% CI: −0.62 (−1.01 to −0.22), P = .002]; 6 studies show that the homeostasis model assessment of insulin resistance of the experimental group is lower than that of the control group [Z = 3.22, 95% CI: −2.33 (−3.75 to −0.91), P = .001]; 6 studies show that the glycated hemoglobin A1c of the experimental group is lower than that of the control group [Z = 4.50, 95% CI: −1.90 (−2.72 to −1.07), P < .00001]; five studies show that the fasting insulin of the experimental group is lower than that of the control group [Z = 3.42, 95% CI: −2.25 (−3.53 to −0.96), P = .0006]. CONCLUSION: Pioglitazone intake is effective in nonalcoholic steatohepatitis management.