The Effect of Intensive Statin Therapy on Symptomatic Intracranial Arterial Stenosis

被引:1
|
作者
Zhou, Peiyang [1 ]
Cao, Zhihua [1 ]
Wang, Pu [1 ]
Liu, Guangzhi [1 ]
Yao, Xuan [1 ]
Wang, Puqing [1 ]
Li, Guang [2 ]
Zhang, Guibin [1 ]
Gao, Ping [2 ]
机构
[1] Hubei Univ Med, Xiangyang Peoples Hosp 1, Dept Neurol, Xiangyang, Peoples R China
[2] Hubei Univ Med, Xiangyang Peoples Hosp 1, Dept Radiol, Xiangyang, Peoples R China
关键词
Statin; Enhanced lipid-lowering; Intracranial atherosclerotic stenosis; CT perfusion imaging; STROKE; ATHEROSCLEROSIS; PREDICTION;
D O I
暂无
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: The aim of this study was to observe the effect of intensive statin therapy on symptomatic intracranial arterial stenosis. Methods: overall, 120 patients with symptomatic intracranial arterial stenosis were admitted to the Xiangyang No. 1 People's Hospital, Hubei University of Medicine, Xiangyang, China from January 2010 to May 2013. They were randomly divided into three groups and were given different doses of atorvastatin orally for 1 year or more, and followed up for 12 months. The three groups were assessed for clinical end-point event rates and changes in cerebral blood flow value before and after treatment to assess the effectiveness of intensive statin therapy. Results: The incidence rates of end-point cerebrovascular events in the low-dose group (10 mg/d), the generaldose group (20 mg/d) and the intensive treatment group (40 mg/d) were 26.3%, 13.5% and 5.4% respectively during the 12-month follow-up after treatment. There was a significant difference between the low dose group and the intensive treatment group (P<0.05). The relative cerebral blood flow and relative cerebral blood volume of the three groups were significantly higher than those before treatment (P<0.05), and the relative time to peak for the intensive treatment group was shorter than that before treatment (P<0.001). Conclusion: Atorvastatin at 40 mg/d has a significant advantage compared with atorvastatin at 20 mg/d and 10 mg/d in reducing cerebrovascular events and improving cerebral blood flow.
引用
收藏
页码:231 / 236
页数:6
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