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Efficacy and safety of intensive statin therapy in Chinese patients with atherosclerotic intracranial arterial stenosis: A single-center, randomized, single-blind, parallel-group study with one-year follow-up

机译:他汀类药物强化治疗在中国动脉粥样硬化性颅内动脉狭窄患者中的疗效和安全性:一项为期一年的随访,单中心,随机,单盲,平行分组研究

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Objectives: The purpose of this study is to validate the efficacy of intensive statin therapy for patients with atherosclerotic intracranial arterial stenosis (AICAS).Methods: In this study, we performed a single-center, randomized, single-blind, parallel-group clinical trial. A total of 120 Chinese patients with AICAS were enrolled and randomly divided into three groups [low-dose atorvastatin therapy (LAT, 10mg/day), standard-dose atorvastatin therapy (SAT, 20mg/day), and intensive-dose atorvastatin therapy (IAT, 40mg/day) groups] in a 1:1:1 ratio. Evaluation variables, including changes in serum lipid profiles, degree of stenosis, and perfusion-related parameters derived from computed tomography perfusion (CTP) imaging from baseline to weeks 26 and 52, as well as the occurrence of cerebrovascular events during the study period, were used to compare the benefits of these three statin therapies.Results: After 52 weeks of treatment, improvement of serum lipid profiles, degree of stenosis, and perfusion-related parameters were all significantly better in the IAT group. In addition, the cumulative probability of cerebrovascular events at 52 weeks was significantly lower in the IAT group than in the LAT group, although there was no statistical difference between the IAT group and the SAT group. The proportion of patients experiencing any adverse event was similar among the three treatment groups. Adverse events caused by IAT were generally mild; no serious adverse events occurred throughout the entire period of study.Conclusion: In conclusion, long-term use of IAT appears to be a safe and effective treatment at least for Chinese patients with AICAS.
机译:目的:本研究旨在验证强化他汀类药物治疗对动脉粥样硬化性颅内动脉狭窄(AICAS)患者的疗效。方法:在本研究中,我们进行了单中心,随机,单盲,平行组临床研究试用。共有120例中国AICAS患者入选,并随机分为三组:低剂量阿托伐他汀治疗(LAT,10mg /天),标准剂量阿托伐他汀治疗(SAT,20mg /天)和大剂量阿托伐他汀治疗( IAT,40mg /天)],比例为1:1:1。评价变量包括从基线到第26周和第52周的计算机断层扫描灌注(CTP)成像得出的血清脂质谱,狭窄程度和灌注相关参数的变化,以及研究期间脑血管事件的发生。结果:在治疗52周后,IAT组的血脂水平,狭窄程度和灌注相关参数的改善均明显好于后者。另外,尽管IAT组和SAT组之间没有统计学差异,但IAT组52周时脑血管事件的累积概率显着低于LAT组。在三个治疗组中,发生任何不良事件的患者比例相似。 IAT引起的不良事件一般较轻;结论:总之,长期使用IAT至少对于中国AICAS患者似乎是一种安全有效的治疗方法。

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