Fondazione Policlinico Universitario Campus Bio-Medico, Via Alvaro del Portillo, 00128 Roma, Italy.
Brain Innovations Lab, Università Campus Bio-Medico di Roma, Via Álvaro del Portillo 21, 00128 Rome, Italy.
Int J Mol Sci. 2023 Jul 17;24(14):11545. doi: 10.3390/ijms241411545.
Stroke, a complex and heterogeneous disease, is a leading cause of morbidity and mortality worldwide. The timely therapeutic intervention significantly impacts patient outcomes, but early stroke diagnosis is challenging due to the lack of specific diagnostic biomarkers. This review critically examines the literature for potential biomarkers that may aid in early diagnosis, differentiation between ischemic and hemorrhagic stroke, and prediction of hemorrhagic transformation in ischemic stroke. After a thorough analysis, four promising biomarkers were identified: Antithrombin III (ATIII), fibrinogen, and ischemia-modified albumin (IMA) for diagnostic purposes; glial fibrillary acidic protein (GFAP), micro RNA 124-3p, and a panel of 11 metabolites for distinguishing between ischemic and hemorrhagic stroke; and matrix metalloproteinase-9 (MMP-9), s100b, and interleukin 33 for predicting hemorrhagic transformation. We propose a biomarker panel integrating these markers, each reflecting different pathophysiological stages of stroke, that could significantly improve stroke patients' early detection and treatment. Despite promising results, further research and validation are needed to demonstrate the clinical utility of this proposed panel for routine stroke treatment.
中风是一种复杂且异质性的疾病,是全球发病率和死亡率的主要原因。及时的治疗干预对患者的预后有重大影响,但由于缺乏特定的诊断生物标志物,早期中风的诊断具有挑战性。本综述批判性地评估了文献中可能有助于早期诊断、区分缺血性和出血性中风以及预测缺血性中风的出血性转化的潜在生物标志物。经过彻底分析,确定了四个有前途的生物标志物:抗凝血酶 III(ATIII)、纤维蛋白原和缺血修饰白蛋白(IMA)用于诊断目的;神经胶质纤维酸性蛋白(GFAP)、微小 RNA 124-3p 和一组 11 种代谢物用于区分缺血性和出血性中风;基质金属蛋白酶 9(MMP-9)、S100B 和白细胞介素 33 用于预测出血性转化。我们提出了一个生物标志物小组,整合了这些标志物,每个标志物反映中风不同的病理生理阶段,这可以显著提高中风患者的早期检测和治疗效果。尽管有很有前景的结果,但仍需要进一步的研究和验证,以证明这个提出的小组对常规中风治疗的临床应用价值。