Zhao Hongru, Yun Wenwei, Zhang Qunying, Cai Xiuying, Li Xuemin, Hui Guozhen, Zhou Xianju, Ni Jianqiang
Department of Neurology, First Affiliated Hospital of Soochow University, Suzhou, Jiangsu Province, China.
Department of Neurosurgery, First Affiliated Hospital of Soochow University, Suzhou, Jiangsu Province, China.
J Stroke Cerebrovasc Dis. 2016 Apr;25(4):752-60. doi: 10.1016/j.jstrokecerebrovasdis.2015.11.018. Epub 2016 Jan 13.
The research aim was to investigate the effects of dl-3-n-butylphthalide (NBP) on the level of circulating endothelial progenitor cells (EPCs) and clinical outcome in patients with acute ischemic stroke (AIS).
A total of 170 patients were included and randomly assigned to NBP group and control group. All patients were administrated a basic antiplatelet and lipid-lowering therapy. Among the patients, 86 received additional NBP administration for 30 days, whereas 84 received only basic therapy (the control). The level of circulating EPCs (marked with CD34(+)/CD133(+)/KDR(+)) was determined by flow cytometry at baseline and days 7, 14, and 30 after therapy. Impairment of neurological function was evaluated by the National Institutes of Health Stroke Scale (NIHSS) on days 7, 14, 30, and 90 after therapy. The association between the increased level of circulating EPCs and improvement of NIHSS score was evaluated by Pearson analysis. The clinical outcome was evaluated by modified Rankin Scale (mRS) on day 90. During the observation period, any adverse events related to drugs were reported.
The levels of circulating EPCs on days 14 and 30 were significantly higher in the NBP group than in the control group. In contrast, NIHSS score was notably lower in NBP group on day 14, 30 and day 90. Pearson correlation analysis revealed a significant association between the increased level of EPCs and improvement of NIHSS score. Also, the mRS score in the NBP group was lower on day 90. Importantly, the reported adverse events in the 2 groups were comparable.
NBP significantly increases the circulating level and improves clinical outcome in patients with AIS.
本研究旨在探讨丁苯酞(NBP)对急性缺血性脑卒中(AIS)患者循环内皮祖细胞(EPCs)水平及临床结局的影响。
共纳入170例患者,随机分为NBP组和对照组。所有患者均接受基础抗血小板和降脂治疗。其中,86例患者额外接受NBP治疗30天,而84例患者仅接受基础治疗(对照组)。在基线及治疗后第7、14和30天,通过流式细胞术测定循环EPCs(标记为CD34(+)/CD133(+)/KDR(+))水平。在治疗后第7、14、30和90天,采用美国国立卫生研究院卒中量表(NIHSS)评估神经功能缺损情况。通过Pearson分析评估循环EPCs水平升高与NIHSS评分改善之间的相关性。在第90天,采用改良Rankin量表(mRS)评估临床结局。在观察期内,报告任何与药物相关的不良事件。
NBP组在第14天和30天的循环EPCs水平显著高于对照组。相比之下,NBP组在第14天、30天和90天的NIHSS评分显著更低。Pearson相关性分析显示,EPCs水平升高与NIHSS评分改善之间存在显著相关性。此外,NBP组在第90天的mRS评分更低。重要的是,两组报告的不良事件具有可比性。
NBP可显著提高AIS患者的循环水平并改善临床结局。