基质金属蛋白酶在急性缺血性脑卒中患者预后中的重要性

E. Costru-Tasnic, Mihail Gavriliuc, E. Manole
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引用次数: 1

摘要

背景:缺血性中风是世界范围内导致死亡和残疾的主要原因之一。进行了大量的研究来评估急性缺血性卒中患者临床恶化的风险,包括出血转化的风险。脑缺血病理的复杂性增加了许多候选分子作为脑卒中生物标志物进行研究的可能性。血脑屏障完整性生物标志物在基础研究和临床研究中均显示出良好的效果。基质金属蛋白酶已被广泛分析,并给出了令人鼓舞的结果,预测不利的神经预后,包括出血转化的风险。基质金属蛋白酶-9在局灶性缺血性脑卒中后血脑屏障的破坏中起关键作用。基质金属蛋白酶-2水平升高与紧密连接蛋白降解、缺血后基底膜和神经元损伤有关,并可能导致梗死和出血量增加。本文综述了基质金属蛋白酶在急性缺血性卒中患者预后中的作用,包括卒中结局和出血转化的风险。结论:基质金属蛋白酶,尤其是明胶酶,因其在缺血性脑卒中发展中的预测价值而被广泛研究。基质金属蛋白酶-2和基质金属蛋白酶-9与急性缺血性卒中的中风严重程度和出血转化相关,但需要大量的验证研究来实际翻译。未来的研究应侧重于开发一种生物标志物面板来预测中风患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The importance of matrix metalloproteinases in the prognosis of acute ischemic stroke patients
Background: Ischemic stroke is one of the leading causes of mortality and disability worldwide. Numerous studies were performed to assess the risk of clinical deterioration of acute ischemic stroke patients, including the risk of haemorrhagic transformation. The complexity of cerebral ischemia pathology raised the possibility of a multitude of candidate-molecules to be studied as stroke biomarkers. The blood brain barrier integrity biomarkers have shown promising results both in fundamental and clinical studies. Matrix metalloproteinases have been extensively analysed and gave encouraging results for predicting unfavourable neurological outcome, including the risk for haemorrhagic transformation. Matrix metalloproteinase-9 plays a crucial role in the disruption of the blood-brain barrier following focal cerebral ischemic stroke. Elevated matrix metalloproteinase-2 levels are responsible for the degradation of tight junction proteins, basal lamina and neuronal injury after ischemia, and may contribute to infarction and hemorrhagic volume. The review provides an overview of matrix metalloproteinases’ role in the prognosis of acute ischemic stroke patients, regarding the stroke outcome and the risk of haemorrhagic transformation. Conclusions: Matrix metalloproteinases, especially gelatinases, are extensively studied for their predictive value in ischemic stroke evolution. Matrix metalloproteinase-2 and matrix metalloproteinase-9 correlate with stroke severity and haemorrhagic transformation in acute ischemic stroke, but large validation studies are needed for practical translation. Future studies should focus on developing a biomarker panel for predicting outcomes in stroke patients.
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