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Endothelial progenitor cells, potential biomarkers for diagnosis and prognosis of ischemic stroke: protocol for an observational case-control study

机译:内皮祖细胞,缺血性脑卒中诊断和预后的潜在生物标志物:观察病例对照研究的方案

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Ischemic stroke is a devastating, life altering event which can severely reduce patient quality of life. Despite years of research there have been minimal therapeutic advances. Endothelial progenitor cells (EPCs), stem cells involved in both vasculogenesis and angiogenesis, may be a potential therapeutic target. After a stroke, EPCs migrate to the site of ischemic injury to repair cerebrovascular damage, and their numbers and functional capacity may determine patients’ outcome. This study aims to determine whether the number of circulating EPCs and their functional aspects may be used as biomarkers to identify the type (cortical or lacunar) and/or severity of ischemic stroke. The study will also investigate if there are any differences in these characteristics between healthy volunteers over and under 65 years of age. 100 stroke patients (50 lacunar and 50 cortical strokes) will be recruited in this prospective, observational case-controlled study. Blood samples will be taken from stroke patients at baseline (within 48 hours of stroke) and days 7, 30 and 90. EPCs will be counted with flow cytometry. The plasma levels of pro- and anti-angiogenic factors and inflammatory cytokines will also be determined. Outgrowth endothelial cells will be cultured to be used in tube formation, migration and proliferation functional assays. Primary outcome is disability or dependence on day 90 after stroke, assessed by the modified Rankin Scale. Secondary outcomes are changes in circulating EPC numbers and/or functional capacity between patient and healthy volunteers, between patient subgroups and between elderly and young healthy volunteers. Recruitment started in February 2017, 167 participants have been recruited. Recruitment will end in November 2019. West Midlands - Coventry & Warwickshire Research Ethics Committee approved this study (REC number: 16/WM/0304) on September 8, 2016. Protocol version: 2.0. The Bayraktutan Dunhill Medical Trust EPC Study was registered in ClinicalTrials.gov (NCT02980354) on November 15, 2016. This study will determine whether the number of EPCs can be used as a prognostic or diagnostic marker for ischemic strokes and is a step towards discovering if transplantation of EPCs may aid patient recovery.
机译:缺血性卒中是一种毁灭性的,生活改变的事件,可以严重降低患者的生活质量。尽管有多年的研究,但有最少的治疗性进展。内皮祖细胞(EPC),血管生成和血管生成的干细胞可以是潜在的治疗靶标。中风后,EPC迁移到缺血性损伤部位以修复脑血管损伤,它们的数量和功能能力可能会确定患者的结果。该研究旨在确定循环EPC的数量及其功能方面是否可以用作生物标志物,以鉴定缺血性卒中的类型(皮质或皮疹)和/或严重程度。该研究还将调查在65岁以下的健康志愿者之间的这些特征是否存在任何差异。在这项前瞻性,观测的病例对照研究中,将招募100脑卒中患者(50只花格拉达和50例皮质中风)。血液样品将从基线(卒中48小时内)的中风患者免受血液样本,并将EPCS与流式细胞术计数。还将确定诸如抗血管生成因子和炎症细胞因子的血浆水平。将培养出来的外皮细胞以用于管形成,迁移和增殖功能测定。主要结果是在中风后第90天的残疾或依赖,由改进的rankin规模评估。二次结果是患者和健康志愿者之间的循环循环和/或功能能力,患者亚组和老年人和年轻的健康志愿者之间的循环和/或功能能力。招聘始于2017年2月,167名参与者已被招募。招聘将于2019年11月结束。西米德兰兹 - 考文垂&沃里克郡研究伦理委员会于2016年9月8日批准了这项研究(REC编号:16 / WM / 0304)。议定书版:2.0。 2016年11月15日在Clinicaltrials.gov(NCT02980354)中登记了Bayraktutan Dunhill医疗信托EPC研究。该研究将确定EPC的数量是否可用作缺血卒中的预后或诊断标志物,并且是朝向发现if的一步EPC的移植可能有助于患者恢复。

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