Prus Katarzyna, Rejdak Konrad, Bilotta Federico
Department of Neurology, Stroke, and Early Post-Stroke Rehabilitation, University Clinical Hospital No. 4, 20-954 Lublin, Poland.
Department of Neurology, Medical University of Lublin, 20-954 Lublin, Poland.
Neurol Int. 2025 Apr 9;17(4):55. doi: 10.3390/neurolint17040055.
Ischemic stroke remains a leading cause of death and disability worldwide. Despite significant progress in reperfusion therapy, the optimal ischemic stroke management strategy has not been developed. Recent studies demonstrate that microRNA may play an essential role in the pathophysiology of ischemic stroke and its possible potential to be a treatment target point. The proposed systematic review aimed to report the relationship between IS's clinical severity and miRNA expression. Secondary outcomes included infarct volume, systemic inflammatory markers, and prognosis, as well as additional features such as stroke subtype, comorbidity, and risk of subsequent stroke in correlation to miRNA expression. : We have performed a systematic search of database resources according to PRISMA statement guidelines. Twenty-seven studies on a total number of 3906 patients were assessed as suitable for the present SR. Included studies analyzed the expression of 30 different miRNA fragments. : After investigating available data, we have identified a set of possible miRNA fragment candidates that may be used in stroke diagnostics and have the potential to be a base for the development of future treatment protocols. : Studies included in the presented SR indicate that miRNA expression may be significantly associated with clinical severity, infarct volume, and inflammation in ischemic stroke. More prospective, properly designed protocols with consistent methods of miRNA testing and optimized clinical assessment are needed to confirm the role of miRNA expression in the course of a stroke.
缺血性中风仍然是全球死亡和残疾的主要原因。尽管再灌注治疗取得了重大进展,但尚未制定出最佳的缺血性中风管理策略。最近的研究表明,微小RNA可能在缺血性中风的病理生理学中起重要作用,并且有可能成为治疗靶点。本系统评价旨在报告缺血性中风临床严重程度与微小RNA表达之间的关系。次要结局包括梗死体积、全身炎症标志物和预后,以及与微小RNA表达相关的其他特征,如中风亚型、合并症和后续中风风险。:我们根据PRISMA声明指南对数据库资源进行了系统检索。对总共3906例患者的27项研究被评估为适合本系统评价。纳入的研究分析了30种不同微小RNA片段的表达。:在研究现有数据后,我们确定了一组可能用于中风诊断的微小RNA片段候选物,它们有可能成为未来治疗方案开发的基础。:本系统评价中纳入的研究表明,微小RNA表达可能与缺血性中风的临床严重程度、梗死体积和炎症显著相关。需要更多前瞻性、设计合理的方案,采用一致的微小RNA检测方法和优化的临床评估,以确认微小RNA表达在中风病程中的作用。