Chen Xingyu, Zhuang Xiaorong, Peng Zhongwei, Yang Huili, Chen Liangyi, Yang Qingwei
Department of Neurology, Zhongshan Hospital Affiliated to Xiamen University, Xiamen, China.
Department of Neurology, Zhongshan Hospital Affiliated to Xiamen University, Xiamen, China,
Eur Neurol. 2018;80(3-4):163-170. doi: 10.1159/000494989. Epub 2018 Nov 28.
To assess whether intensive statin therapy reduces the occurrence of microemboli in patients with acute ischemic stroke.
Patients with acute ischemic stroke within 72 h of onset were randomized to the intensive statin (atorvastatin 60 mg/day, adjusted to 20 mg/day after 7 days) and control (atorvastatin 20 mg/day) groups. Combined aspirin and clopidogrel were used for antiplatelet therapy. Microemboli were monitored by transcranial Doppler on days 1 (pre-treatment), 3, and 7. Metalloproteinase-9 (MMP-9), high-sensitivity C-reactive protein (hs-CRP), and National Institutes of Health Stroke Scale (NIHSS) score were assessed on days 1 and 7. The modified Rankin scale (mRS) was used on day 90. The primary outcome was the proportion of patients with microemboli on day 3.
There were 35 (58.3%) and 30 (52.6%) patients with microemboli in the intensive statin (n = 60) and control (n = 57) groups, respectively, on day 1 (p = 0.342). On day 3, there were significantly less microemboli in the intensive statin group (n = 9; 15.0%) compared with controls (n = 16; 28.1%; p = 0.002). No difference was observed in MMP-9 and hs-CRP levels on day 1, but on day 7, MMP-9 (median 79.3 vs. 95.9 μg/L; p = 0.004) and hs-CRP (median 2.01 vs. 3.60 mg/L; p = 0.020) levels were lower in the intensive statin group compared with controls. There were no differences in NIHSS scores on days 1 and 7. There was no difference in mRS on day 90.
Intensive atorvastatin therapy in patients with acute ischemic stroke reduces the occurrence of microemboli and inflammation, with no overt adverse events.
评估强化他汀类药物治疗是否能降低急性缺血性脑卒中患者微栓子的发生率。
将发病72小时内的急性缺血性脑卒中患者随机分为强化他汀组(阿托伐他汀60毫克/天,7天后调整为20毫克/天)和对照组(阿托伐他汀20毫克/天)。联合使用阿司匹林和氯吡格雷进行抗血小板治疗。在第1天(治疗前)、第3天和第7天通过经颅多普勒监测微栓子。在第1天和第7天评估金属蛋白酶-9(MMP-9)、高敏C反应蛋白(hs-CRP)和美国国立卫生研究院卒中量表(NIHSS)评分。在第90天使用改良Rankin量表(mRS)。主要结局是第3天出现微栓子的患者比例。
强化他汀组(n = 60)和对照组(n = 57)在第1天分别有35例(58.3%)和30例(52.6%)患者出现微栓子(p = 0.342)。在第3天,强化他汀组的微栓子明显少于对照组(n = 9;15.0%),对照组为(n = 16;28.1%;p = 0.002)。第1天MMP-9和hs-CRP水平无差异,但在第7天,强化他汀组的MMP-9(中位数79.3对95.9μg/L;p = 0.004)和hs-CRP(中位数2.01对3.60mg/L;p = 0.020)水平低于对照组。第1天和第7天NIHSS评分无差异。第90天mRS无差异。
急性缺血性脑卒中患者接受强化阿托伐他汀治疗可降低微栓子的发生率和炎症反应,且无明显不良事件。