Efficacy of ginkgo diterpene lactone meglumine on cognitive function in patients with acute ischemic stroke: a predefined exploratory analysis of a multicenter, double-blind, randomized controlled trial

被引:0
|
作者
Tian, Xue [1 ,2 ,3 ,4 ]
Xu, Qin [1 ,2 ]
Xia, Xue [1 ,2 ]
Zhang, Yijun [1 ,2 ,3 ,4 ]
Meng, Xia [1 ,2 ]
Wang, Anxin [1 ,2 ,4 ,5 ]
机构
[1] Capital Med Univ, Beijing Tiantan Hosp, Dept Neurol, 119 South 4th Ring West Rd, Beijing 100070, Peoples R China
[2] Capital Med Univ, Beijing Tiantan Hosp, China Natl Clin Res Ctr Neurol Dis, Beijing, Peoples R China
[3] Capital Med Univ, Sch Publ Hlth, Dept Epidemiol & Hlth Stat, Beijing, Peoples R China
[4] Beijing Municipal Key Lab Clin Epidemiol, Beijing, Peoples R China
[5] Capital Med Univ, Dept Clin Epidemiol & Clin Trial, Beijing, Peoples R China
关键词
Acute ischemic stroke; Ginkgo diterpene lactone meglumine; Neuroprotective drugs; Cognitive function; RISK-FACTORS; SAFETY; IMPAIRMENT; CHINA;
D O I
10.1007/s00415-024-12272-w
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background Ginkgo diterpene lactone meglumine (GDLM) could improve the functional outcome in patients with acute ischemic stroke (AIS). This study aimed to investigate the efficacy of GDLM on cognitive function in patients with AIS. Methods This is a predefined exploratory analysis of the Efficacy and Safety of Ginkgo Diterpene Lactone Meglumine in Acute Ischemic Stroke trial, which was primarily designed to investigate the efficacy and safety of GDLM versus placebo on functional outcome at 100 centers in China. Cognitive function was measured using the Montreal Cognitive Assessment (MoCA) test. The primary outcomes were changes of MoCA from baseline to Day 14 and Day 90 after randomization. Results A total of 3163 patients with completed data on MoCA were enrolled. There was statistically significant difference of changes in MoCA scores between the GDLM group and the placebo group from baseline to Day 14 (mean difference, 0.31; 95% confidence interval [CI], 0.08-0.53; P = 0.007) and to Day 90 after randomization (mean difference, 0.47; 95% CI, 0.22-0.72; P < 0.001). Additionally, GDLM was associated with a higher proportion of patients who reached a clinically significant level of improvement in MoCA from baseline to Day 14 (odds ratio [OR], 1.25; 95% CI, 1.08-1.44; P = 0.002) and Day 90 after randomization (OR, 1.21; 95% CI, 1.03-1.41; P = 0.02). Specially, GDLM could significantly improve the scores of visuo-spatial and executive function and language. Conclusions In this predefined analysis of patients with AIS, GDLM could improve the 14-day and 90-day cognitive function compared with the placebo.
引用
收藏
页码:3321 / 3327
页数:7
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