Carle Illinois College of Medicine, University of Illinois Urbana-Champaign, Champaign, IL 61820, USA.
Mayo Clinic Alix School of Medicine, Mayo Clinic Arizona, Scottsdale, AZ 85259, USA.
Int J Mol Sci. 2023 Jun 30;24(13):10902. doi: 10.3390/ijms241310902.
Despite the high incidence and burden of stroke, biological biomarkers are not used routinely in clinical practice to diagnose, determine progression, or prognosticate outcomes of acute ischemic stroke (AIS). Because of its direct interface with neural tissue, cerebrospinal fluid (CSF) is a potentially valuable source for biomarker development. This systematic review was conducted using three databases. All trials investigating clinical and preclinical models for CSF biomarkers for AIS diagnosis, prognostication, and severity grading were included, yielding 22 human trials and five animal studies for analysis. In total, 21 biomarkers and other multiomic proteomic markers were identified. S100B, inflammatory markers (including tumor necrosis factor-alpha and interleukin 6), and free fatty acids were the most frequently studied biomarkers. The review showed that CSF is an effective medium for biomarker acquisition for AIS. Although CSF is not routinely clinically obtained, a potential benefit of CSF studies is identifying valuable biomarkers from the pathophysiologic microenvironment that ultimately inform optimization of targeted low-abundance assays from peripheral biofluid samples (e.g., plasma). Several important catabolic and anabolic markers can serve as effective measures of diagnosis, etiology identification, prognostication, and severity grading. Trials with large cohorts studying the efficacy of biomarkers in altering clinical management are still needed.
尽管中风的发病率和负担很高,但生物标志物并未常规用于临床实践,以诊断、确定进展或预测急性缺血性中风 (AIS) 的结局。由于其与神经组织的直接界面,脑脊液 (CSF) 是开发生物标志物的潜在有价值来源。本系统评价使用了三个数据库进行。所有研究 CSF 标志物用于 AIS 诊断、预后和严重程度分级的临床和临床前模型的试验均包括在内,分析了 22 项人类试验和 5 项动物研究。总共确定了 21 种生物标志物和其他多组学蛋白质标志物。S100B、炎症标志物(包括肿瘤坏死因子-α和白细胞介素 6)和游离脂肪酸是研究最多的生物标志物。该综述表明,CSF 是获取 AIS 生物标志物的有效介质。尽管 CSF 临床上通常不常规获取,但 CSF 研究的潜在益处是从病理生理微环境中识别有价值的生物标志物,最终为优化来自外周生物流体样本(例如血浆)的靶向低丰度检测提供信息。一些重要的分解代谢和合成代谢标志物可以作为诊断、病因识别、预后和严重程度分级的有效措施。仍需要进行大型队列试验,研究生物标志物在改变临床管理方面的功效。