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鞘氨醇-1-磷酸受体激动剂芬戈莫德在卒中动物模型中的疗效:一项更新的荟萃分析。

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

机构信息

Department of Neurology, Tianjin Neurological Institute, Tianjin Medical University General Hospital, Tianjin, China.

West China Medical Publishers, West China Hospital, Sichuan University, Chengdu, China.

出版信息

Int J Neurosci. 2021 Jan;131(1):85-94. doi: 10.1080/00207454.2020.1733556. Epub 2020 Mar 9.

Abstract

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. 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. 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%;  = 24; I = 90.0%;  < 0.0001) and consistently enhanced neurobehavioral outcome by 34.2% (95% CI 23.1%-45.2%;  = 14; I = 76.5%;  < 0.0001). No single factors accounted for heterogeneity. Our rigorous statistical evaluation confirmed the neuroprotective properties of fingolimod. New data can be used in designing future clinical trials.

摘要

神经炎症是脑缺血/再灌注损伤的核心部分。新型免疫抑制剂芬戈莫德是改善中风引起的损伤的有前途的候选药物。芬戈莫德在实验性缺血模型中有效,但缺乏严格的荟萃分析来考虑不同的实验变量如何影响结果。我们对中风模型中的芬戈莫德进行了系统的文献回顾,目的是严格评估芬戈莫德减少梗死体积和改善神经功能结局的效果。评估了 17 个变量作为异质性的来源协变量,并用标准化均数差荟萃分析来合并效应大小,以评估疗效。研究质量通过 CAMARADES 十项检查表进行评估,通过漏斗图和 Egger 检验评估发表偏倚。在文献研究中大约确定了 123 篇未重复的文章。在这些论文中,118 篇文章在阅读标题和摘要后被排除。在这项研究中又选择了另外 17 篇文章。研究质量为中等(中位数= 6;四分位距= 4),发表偏倚在统计学上无显著性。芬戈莫德使梗死体积减少 30.4%(95%置信区间 22.4%-38.3%;  = 24;I = 90.0%;  < 0.0001),并一致改善神经行为学结局 34.2%(95%置信区间 23.1%-45.2%;  = 14;I = 76.5%;  < 0.0001)。没有一个单一的因素可以解释异质性。我们严格的统计评估证实了芬戈莫德的神经保护特性。新的数据可用于设计未来的临床试验。

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