Department of Neurosurgery, University Hospital of Essen, D-45147, Essen, Germany.
Institute for Medical Biometry and Statistics, Faculty of Medicine and Medical Center, University of Freiburg, Freiburg, Germany.
Neurosurg Rev. 2020 Jun;43(3):825-833. doi: 10.1007/s10143-018-1037-y. Epub 2018 Oct 10.
Delayed cerebral ischemia (DCI) is a severe complication of subarachnoid hemorrhage (SAH). Clinical and radiographic features of SAH may be helpful in identification of individuals prone to DCI. The aim of this systematic review was to analyze the present evidence on predictive value of blood and cerebrospinal fluid (CSF) biomarkers of DCI after SAH. We systematically searched in PubMed, Scopus, Web of Science, and Cochrane Library databases for publications before July 15, 2018, reporting correlations between blood/CSF biomarkers and occurrence of DCI and/or vasospasm in SAH patients. Included studies underwent quality assessment according to QUIPS and STARD guidelines. Level of evidence (I-IV) for each of tested biomarkers was assessed according to GRADE guidelines. Of 2181 unique records identified in four databases, 270 original articles and 5 meta-analyses were included to this review. Of 257 blood and CSF parameters analyzed in 16.914 SAH patients, there was no biomarker with positive association with DCI/vasospasm showing level I evidence. Twenty-one biomarkers achieved level II evidence and could be confirmed as predictive biomarkers. In this review, six single nucleotide polymorphisms (for EET metabolic pathways, COMT, HMGB1, ACE, PAI-1 promoter, and Hp genes) and 15 non-genetic biomarkers (pNF-H, ADAMTS13, NPY, Copeptin, HMGB1, GFAP, periostin, Tau, BNP, NT pro-BNP, hs-TnT, PA-TEGMA, MPV:PLT, NLR, and PLR) were selected as predictive DCI biomarkers. We propose that a panel analysis of the selected genetic and protein biomarker candidates would be needed for further validation in a large SAH cohort.
迟发性脑缺血(DCI)是蛛网膜下腔出血(SAH)的严重并发症。SAH 的临床和影像学特征有助于识别易发生 DCI 的个体。本系统评价的目的是分析目前关于 SAH 后 DCI 的血液和脑脊液(CSF)生物标志物的预测价值的证据。我们系统地在 PubMed、Scopus、Web of Science 和 Cochrane Library 数据库中检索了截至 2018 年 7 月 15 日之前发表的关于血液/CSF 生物标志物与 SAH 患者 DCI 和/或血管痉挛发生之间相关性的报告。纳入的研究根据 QUIPS 和 STARD 指南进行了质量评估。根据 GRADE 指南评估了每个测试生物标志物的证据水平(I-IV)。在四个数据库中确定的 2181 个独特记录中,有 270 篇原始文章和 5 篇荟萃分析被纳入本综述。在 16914 名 SAH 患者中分析了 257 个血液和 CSF 参数,没有生物标志物与 DCI/血管痉挛呈阳性关联,具有 I 级证据。21 个生物标志物达到 II 级证据,可以确认为预测性生物标志物。在本综述中,六个单核苷酸多态性(用于 EET 代谢途径、COMT、HMGB1、ACE、PAI-1 启动子和 Hp 基因)和 15 个非遗传生物标志物(pNF-H、ADAMTS13、NPY、Copeptin、HMGB1、GFAP、periostin、Tau、BNP、NT pro-BNP、hs-TnT、PA-TEGMA、MPV:PLT、NLR 和 PLR)被选为预测 DCI 的生物标志物。我们建议对选定的遗传和蛋白质生物标志物候选物进行联合分析,以在大型 SAH 队列中进一步验证。