非创伤性 SAH 中的 GFAP 和 UCHL1:迄今为止的故事。文献的系统回顾。

Filippos Psochias, Georgios Mavrovounis, George Stranjalis, Theodosis Kalamatianos
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引用次数: 0

摘要

目的:非创伤性蛛网膜下腔出血(SAH非创伤性蛛网膜下腔出血(SAH)的误诊率高、预后差。生物标志物对 SAH 患者的鉴别、治疗/管理指导和预后改善很有帮助。本系统综述旨在研究生物标志物 GFAP(胶质纤维酸性蛋白)和 UCH-L1(泛素 C 端水解酶 L1)在非创伤性 SAH 诊断和预后中的潜在作用:方法:对 PubMed、Scopus 和 Web of Science 数据库进行了系统性检索,检索期从开始到 2023 年 2 月:结果:17 项研究符合纳入标准并被纳入本综述。纳入的绝大多数研究(82%)是关于 GFAP 的。大多数研究使用了血液和/或 CSF 样本,并在最初住院的几天内进行了多次测量。大多数已确定的研究都明显报告了结果不佳的 SAH 患者 GFAP 和 UCHL1 水平较高。标本类型和采样时间存在明显差异:结论:在住院初期对 GFAP 和 UCHL1 进行定量分析有望预测 SAH 患者的预后。尽管如此,仍有必要开展进一步的研究来证实这些发现,并进一步明确这两种生物标志物在 SAH 诊断以及严重程度和继发事件预测中的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GFAP and UCHL1 in Non-traumatic SAH: The Story thus Far. A Systematic Review of the Literature.

Objective: Non-traumatic subarachnoid hemorrhage (SAH) is associated with a high percentage of misdiagnosis and poor prognosis. Biomarkers could be useful in the identification, treatment/management guidance, and outcome improvement of SAH patients. The current systematic review aims to investigate the potential role of biomarkers GFAP (Glial Fibrillary Acidic Protein) and UCH-L1 (Ubiquitin C-Terminal Hydrolase L1) in the diagnosis and prognosis of non-traumatic SAH.

Methods: A systematic search of PubMed, Scopus, and Web of Science databases was conducted from their inception through February 2023.

Results: 17 studies met the inclusion criteria and were included in this review. The vast majority of the included studies (82%) were on GFAP. Most studies used blood and/or CSF samples and incorporated multiple measurements through the initial hospitalization days. The majority of identified studies reported significantly higher levels of GFAP and UCHL1 in SAH patients with poor outcomes. There was notable variation in the specimen type and the timing of sampling.

Conclusion: Quantification of GFAP and UCHL1 through the initial days of hospitalization shows promise in the prediction of SAH patient outcomes. Further research is nevertheless warranted to confirm these findings and further clarify the use of the two biomarkers in SAH diagnosis and the prediction of severity and secondary events.

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