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| Efficacy of Evolocumab Combined with Atorvastatin in the Treatment of Symptomatic Intracranial Atherosclerotic Stenosis |
| MAO Zhenya1, CHEN Jiansu2 |
1. Department of Pharmacy, Jiangsu Provincial People's Hospital, Nanjing Jiangsu 210000;
2. Department of Cardiovascular and Vascular Surgery,the Fourth Affiliated Hospital of Nanjing Medical University,Nanjing Jiangsu 210000 |
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Abstract 【Objective】 To investigate the efficacy of evolocumab combined with atorvastatin in the treatment of patients with symptomatic intracranial atherosclerotic stenosis (ICAS). 【Methods】 A total of 116 patients with symptomatic ICAS were randomly divided into the control group and the observation group, with 58 cases in each group. The control group was treated with atorvastatin calcium tablets, while the observation group was administered with evolocumab in addition to the control group's regimen. The blood lipid levels, carotid intima-media thickness (CIMT), plaque thickness, serum amyloid A1 (SAA1), cerebral blood volume (CBV) and cerebral blood flow (CBF) before and after treatment, as well as the incidence of adverse reactions during medication were compared between the two groups. The incidence of adverse endpoint events such as recurrent cerebral infarction, restenosis and death within 1 year after treatment was recorded. 【Results】 After treatment, the blood lipid metabolism level in the observation group was significantly improved compared with that in the control group. The levels of CIMT, plaque thickness and serum SAA1 in the observation group were lower than those in the control group, while CBV and CBF were higher than those in the control group (P<0.05). There was no statistically significant difference in the total incidence of adverse reactions between the two groups (P>0.05). The incidence of adverse endpoint events in the observation group was lower than that in the control group (P<0.05). 【Conclusion】 Evolocumab combined with atorvastatin can more effectively improve the blood lipid profile, carotid artery lesions and cerebral blood flow status of patients with symptomatic ICAS safely. It reduces the incidence of adverse endpoint events.
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Received: 23 October 2025
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