Neuropharmacological efficacy of metformin for stroke in rodents: A meta-analysis of preclinical trials.
Neuropharmacological efficacy of metformin for stroke in rodents: A meta-analysis of preclinical trials.
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二甲双胍治疗啮齿动物中风的神经药理学功效:临床前试验的荟萃分析
DOI:
10.3389/fphar.2022.1009169
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发表时间:
2022
影响因子:
5.6
通讯作者:
中科院分区:
文献类型:
--
作者:
Background: Stroke, including ischemic stroke, intracerebral hemorrhage, and subarachnoid hemorrhage (SAH), remains a leading cause of mortality globally. Different stroke subtypes have similar detrimental effects in multiple fields of health. Previous research has shown that metformin plays a neuroprotective role in experimental animal models of stroke; however, a preclinical quantitative analysis on the ability of metformin to treat stroke is still lacking. This meta-analysis evaluates the efficacy of metformin in improving stroke prognosis in rodent models of stroke. Methods: Relevant preclinical trials were retrieved from PubMed, EMBASE, and the Web of Science. The neurological score (NS), brain water content (BWC), infarct size, rotarod test, TUNEL, neuron quantity, microglia quantity, and p-AMPK levels were compared between a control group and a metformin group using the standardized mean difference (SMD) and corresponding confidence interval (CI). Quality was assessed with SYRCLE’s risk of bias tool. Results: Fifteen articles published from 2010 to 2022 were included in the meta-analysis. The metformin group had statistically significant differences compared to the control group in the following aspects: NS (SMD −1.45; 95% CI −2.32, −0.58; p = 0.001), BWC (SMD −3.22; 95% CI −4.69, −1.76; p < 0.0001), infarct size (SMD −2.90; 95% CI −3.95, −1.85; p < 0.00001), rotarod test (SMD 2.55; 95% CI 1.87, 3.23; p < 0.00001), TUNEL (SMD -3.63; 95% CI −5.77, −1.48; p = 0.0009), neuron quantity (SMD 3.42; 95% CI 2.51, 4.34; p < 0.00001), microglia quantity (SMD −3.06; 95% CI -4.69, −1.44; p = 0.0002), and p-AMPK levels (SMD 2.92; 95% CI 2.02, 3.82; p < 0.00001). Furthermore, sensitivity analysis and stratified analysis were conducted for heterogeneous outcome indicators. Conclusion: Overall, metformin treatment improves severe outcomes triggered by stroke. Despite the limitations intrinsic to animal studies, this systematic review may provide a vital reference for future high-quality preclinical trials and clinical use.
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影响因子:
5.6
作者:
Liu, Ke;Li, Lulu;Liu, Zhijun;Li, Gang;Wu, Yanqing;Jiang, Xingjun;Wang, Mengdie;Chang, Yanmin;Jiang, Tingting;Luo, Jianheng;Zhu, Jiahui;Li, Hongge;Wang, Yong
通讯作者:
Wang, Yong
影响因子:
13.8
作者:
Gu HQ;Yang X;Wang CJ;Zhao XQ;Wang YL;Liu LP;Meng X;Jiang Y;Li H;Liu C;Wangqin R;Fonarow GC;Schwamm LH;Xian Y;Li ZX;Wang YJ
通讯作者:
Wang YJ
影响因子:
5.5
作者:
Liu, Jiu-Hong;Feng, Dan;Pei, Lei
通讯作者:
Pei, Lei
DOI:
10.1016/j.jstrokecerebrovasdis.2013.09.001
发表时间:
2014-02-01
影响因子:
2.5
作者:
Cheng, Yuan-Yang;Leu, Hsin-Bang;Kao, Chung-Lan
通讯作者:
Kao, Chung-Lan
影响因子:
9.3
作者:
Liu Y;Tang G;Li Y;Wang Y;Chen X;Gu X;Zhang Z;Wang Y;Yang GY
通讯作者:
Yang GY