Efficacy of the sphingosine-1-phosphate receptor agonist fingolimod in animal models of stroke: an updated meta-analysis

被引:18
|
作者
Dang, Chun [1 ,2 ]
Lu, Yaoheng [3 ]
Li, Qian [4 ]
Wang, Chunyang [1 ]
Ma, Xiaofeng [1 ,5 ]
机构
[1] Tianjin Med Univ, Tianjin Neurol Inst, Dept Neurol, Gen Hosp, Tianjin, Peoples R China
[2] Sichuan Univ, West China Hosp, West China Med Publishers, Chengdu, Peoples R China
[3] Chengdu Integrated TCM & Western Med Hosp, Dept Gen Surg, Chengdu, Peoples R China
[4] Harbin Med Univ, Dept Neurol, Affiliated Hosp 2, Harbin, Peoples R China
[5] Minist Educ & Tianjin City, Tianjin Neurol Inst, Key Lab Postneurotrauma Neurorepair & Regenerat C, Tianjin, Peoples R China
基金
中国国家自然科学基金;
关键词
Fingolimod; ischemic stroke; meta-analysis; neuroprotection; systematic review; animal studies; ACUTE ISCHEMIC-STROKE; IMMUNE MODULATOR FINGOLIMOD; FTY720; THERAPY; INFLAMMATION; BRAIN;
D O I
10.1080/00207454.2020.1733556
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Objective: Neuroinflammation is a central part of cerebral ischemia/reperfusion injury. The novel immune suppressant, fingolimod, is a promising candidate to ameliorate stroke-induced damage. Fingolimod is efficacious in experimental ischemic models, but a rigorous meta-analysis is lacking that considers how different experiment variables affect outcomes. Methods: We conducted a systematic literature review of fingolimod in stroke models, with the aim of rigorously evaluating fingolimod's effects on reducing infarct volume improving neurological outcomes. Seventeen variables were evaluated as covariates for the source of heterogeneity, and effect sizes were combined by using normalized mean difference meta-analysis to evaluate efficacy. Study quality was evaluated by the CAMARADES ten-item checklist, and publication bias was evaluated by funnel plots and Egger's tests. Results: About 123 unduplicated articles were identified in the literature research. Of these papers, 118 articles were excluded after reading titles and abstracts. Another 17 articles were selected in this study. Study quality was moderate (median = 6; interquartile range = 4), and publication bias was statistically insignificant. fingolimod reduced infarct volume by 30.4% (95% CI 22.4%-38.3%; n = 24; I-2 = 90.0%; p < 0.0001) and consistently enhanced neurobehavioral outcome by 34.2% (95% CI 23.1%-45.2%; n = 14; I-2 = 76.5%; p < 0.0001). No single factors accounted for heterogeneity. Conclusions: Our rigorous statistical evaluation confirmed the neuroprotective properties of fingolimod. New data can be used in designing future clinical trials.
引用
收藏
页码:85 / 94
页数:10
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