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Effect of Ginkgolide in Ischemic Stroke patients with large Artery Atherosclerosis: Results from a randomized trial

Authors :
Huisheng Chen
Zhilin Jiang
Biyun Zong
Ming Yu
Ping Sun
Wenjun Yu
Jianjun Guo
Baoshen Wang
Xin Wang
Shuangxing Hou
Chun Wang
Junyan Liu
Xiangyu Pu
Jiadong Zhang
Yong Zhao
Guiru Zhang
Lishu Wan
Wei Li
Jingyu Zhang
Guofang Chen
Hongtian Zhang
Jianhua Xu
Yan Wei
Dongjuan Xu
Jun Liu
Jifa Long
Shejun Feng
Xiao Bo
Chunhua Wei
Qingke Bai
Yun Xu
Lei Huang
Qiang Dong
Jun Tan
Xiaoya Feng
Yongge Hou
Caixiao Chen
Ming Zhang
Mingyao You
Houqin Chen
Liping Sun
Qing He
Weizhong Gu
Tao Sun
Zhenguo Liu
Xiaohong Li
Lihong Zhao
Wenjie Cao
Anding Xu
Run-Hui Li
Yang Yang
Xijing Mao
Yanxia Wang
Qingyou Zeng
Bihua Wu
Zhen Jiao
Yingmin Song
Mingzong Yan
Zhengqi Lu
Yi Dong
Guozhong Li
Ding Qin
Rongxia Ji
Source :
CNS Neuroscience & Therapeutics
Publication Year :
2021
Publisher :
Wiley, 2021.

Abstract

Background Dual antiplatelet therapy is considered beneficial in acute ischemic stroke (AIS) patients with intracranial artery stenosis (ICAS), with more bleeding events. Ginkgolide is shown to reduce platelet activation after infarction, which might be of benefit in AIS. We aimed to explore the effect of Ginkgolide in AIS patients with ICAS. Methods This was a randomized, double‐blinded, placebo‐controlled trial conducted at 61 centers in China. Within 72 h after onset, consecutive patients diagnosed as AIS with ICAS were randomized to either Ginkgolide or placebo treatment. The primary outcome was the composite of mortality and recurrent stroke (ischemic or hemorrhagic) during first 4 weeks in an intention‐to‐treat analysis. Secondary functional outcome was assessed by modified Rankin Scale and improvement of stroke severity was assessed by National Institution of Health Stroke Scale at day 28. Safety outcome was measured by the rate of severe adverse event (SAE). Results There were 936 patients randomized to either Ginkgolide or placebo treatment. Their average age was 64.2 ± 10.4 years old and 36.0% of the patients were female. The composite index event occurred in six patients in placebo group, and none occurred in Ginkgolide group (risk ratio 1.01; 95% CI 1.00–1.02). There were more patients who achieved favorable outcome in Ginkgolide group, compared with that of the placebo group (OR 2.16, 95%CI 1.37–3.41). SAE occurred in five (1.1%) patients in the Ginkgolide group and three (0.6%) in the placebo group (OR0.60, 95CI% 0.14–2.53). Intracranial hemorrhage occurred in 1/473 (0.2%) in the placebo group. Conclusions Ginkgolide, working as PAF antagonist, may reduce recurrent stroke in AIS with ICAS patients within 72 hours after onset. It might be an optional treatment in moderate‐to‐severe AIS patients with ICAS. (http://www.chictr.org.cn Number as ChiCTR‐IPR‐17012310).<br />Although dual antiplatelet therapy is considered benefit in acute ischemic stroke (AIS) patients with intracranial artery stenosis (ICAS), there are more bleeding events. Ginkgolide, works as PAF antagonist, may reduce recurrent and mortality in AIS with large artery stenosis within 72 hours atfer onset during 90 days follow‐up. It might play a role of neuroprotection in AIS patients with ICAS

Details

ISSN :
17555949 and 17555930
Volume :
27
Database :
OpenAIRE
Journal :
CNS Neuroscience & Therapeutics
Accession number :
edsair.doi.dedup.....ca4051c7e4ba5ad9bdd16a0f6a27f77c