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Ginkgo biloba extract EGb 761(®) improves cognition and overall condition after ischemic stroke: Results from a pilot randomized trial

Background: Patients who experienced an ischemic stroke are at risk for cognitive impairment. Quantified Ginkgo biloba extract EGb 761(®) has been used to treat cognitive dysfunction, functional impairment and neuropsychiatric symptoms in mild cognitive impairment and dementia. Objectives: To assess...

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Autores principales: Cui, Mei, You, Tongyao, Zhao, Yuwu, Liu, Ruozhuo, Guan, Yangtai, Liu, Jianren, Liu, Xueyuan, Wang, Xin, Dong, Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10090660/
https://www.ncbi.nlm.nih.gov/pubmed/37063270
http://dx.doi.org/10.3389/fphar.2023.1147860
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author Cui, Mei
You, Tongyao
Zhao, Yuwu
Liu, Ruozhuo
Guan, Yangtai
Liu, Jianren
Liu, Xueyuan
Wang, Xin
Dong, Qiang
author_facet Cui, Mei
You, Tongyao
Zhao, Yuwu
Liu, Ruozhuo
Guan, Yangtai
Liu, Jianren
Liu, Xueyuan
Wang, Xin
Dong, Qiang
author_sort Cui, Mei
collection PubMed
description Background: Patients who experienced an ischemic stroke are at risk for cognitive impairment. Quantified Ginkgo biloba extract EGb 761(®) has been used to treat cognitive dysfunction, functional impairment and neuropsychiatric symptoms in mild cognitive impairment and dementia. Objectives: To assess the cognitive-related effects of EGb 761(®) treatment in patients after acute ischemic stroke, as well as the feasibility of patient selection and outcome measures. Methods: We conducted a randomized, multicentric, open-label trial at 7 centers in China. Patients scoring 20 or lower on the National Institutes of Health Stroke Scale were enrolled between 7 and 14 days after stroke onset and randomly assigned to receive 240 mg per day of EGb 761(®) or no additional therapy for 24 weeks in a 1:1 ratio. Both groups received standard treatments for the prevention of recurrent stroke during the trial. General cognitive function and a battery of cognitive tests for sub-domains were evaluated at 24 weeks. All patients were monitored for adverse events. Results: 201 patients ≥50 years old were included, with 100 assigned to the EGb 761(®) group and 101 to the reference group. The mean change from baseline on the global cognitive function as assessed by the Montreal Cognitive Assessment score was 2.92 in the EGb 761(®) group and 1.33 in the reference group (between-group difference: 1.59 points; 95% confidence interval [CI], 0.51 to 2.67; p < 0.005). For cognitive domains, EGb 761(®) showed greater effects on the Hopkins Verbal Learning Test Total Recall (EGb 761(®) change 1.40 vs. reference −0.49) and Form 1 of the Shape Trail Test (EGb 761(®) change −38.2 vs. reference −15.6). Potentially EGb 761(®)-related adverse events occurred in no more than 3% of patients. Conclusion: Over the 24-week period, EGb 761(®) treatment improved overall cognitive performance among patients with mild to moderate ischemic stroke. Our findings provide valuable recommendations for the design of future trials, including the criteria for patient selection. Clinical Trial Registration: www.isrctn.com, identifier ISRCTN11815543.
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spelling pubmed-100906602023-04-13 Ginkgo biloba extract EGb 761(®) improves cognition and overall condition after ischemic stroke: Results from a pilot randomized trial Cui, Mei You, Tongyao Zhao, Yuwu Liu, Ruozhuo Guan, Yangtai Liu, Jianren Liu, Xueyuan Wang, Xin Dong, Qiang Front Pharmacol Pharmacology Background: Patients who experienced an ischemic stroke are at risk for cognitive impairment. Quantified Ginkgo biloba extract EGb 761(®) has been used to treat cognitive dysfunction, functional impairment and neuropsychiatric symptoms in mild cognitive impairment and dementia. Objectives: To assess the cognitive-related effects of EGb 761(®) treatment in patients after acute ischemic stroke, as well as the feasibility of patient selection and outcome measures. Methods: We conducted a randomized, multicentric, open-label trial at 7 centers in China. Patients scoring 20 or lower on the National Institutes of Health Stroke Scale were enrolled between 7 and 14 days after stroke onset and randomly assigned to receive 240 mg per day of EGb 761(®) or no additional therapy for 24 weeks in a 1:1 ratio. Both groups received standard treatments for the prevention of recurrent stroke during the trial. General cognitive function and a battery of cognitive tests for sub-domains were evaluated at 24 weeks. All patients were monitored for adverse events. Results: 201 patients ≥50 years old were included, with 100 assigned to the EGb 761(®) group and 101 to the reference group. The mean change from baseline on the global cognitive function as assessed by the Montreal Cognitive Assessment score was 2.92 in the EGb 761(®) group and 1.33 in the reference group (between-group difference: 1.59 points; 95% confidence interval [CI], 0.51 to 2.67; p < 0.005). For cognitive domains, EGb 761(®) showed greater effects on the Hopkins Verbal Learning Test Total Recall (EGb 761(®) change 1.40 vs. reference −0.49) and Form 1 of the Shape Trail Test (EGb 761(®) change −38.2 vs. reference −15.6). Potentially EGb 761(®)-related adverse events occurred in no more than 3% of patients. Conclusion: Over the 24-week period, EGb 761(®) treatment improved overall cognitive performance among patients with mild to moderate ischemic stroke. Our findings provide valuable recommendations for the design of future trials, including the criteria for patient selection. Clinical Trial Registration: www.isrctn.com, identifier ISRCTN11815543. Frontiers Media S.A. 2023-03-29 /pmc/articles/PMC10090660/ /pubmed/37063270 http://dx.doi.org/10.3389/fphar.2023.1147860 Text en Copyright © 2023 Cui, You, Zhao, Liu, Guan, Liu, Liu, Wang and Dong. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Cui, Mei
You, Tongyao
Zhao, Yuwu
Liu, Ruozhuo
Guan, Yangtai
Liu, Jianren
Liu, Xueyuan
Wang, Xin
Dong, Qiang
Ginkgo biloba extract EGb 761(®) improves cognition and overall condition after ischemic stroke: Results from a pilot randomized trial
title Ginkgo biloba extract EGb 761(®) improves cognition and overall condition after ischemic stroke: Results from a pilot randomized trial
title_full Ginkgo biloba extract EGb 761(®) improves cognition and overall condition after ischemic stroke: Results from a pilot randomized trial
title_fullStr Ginkgo biloba extract EGb 761(®) improves cognition and overall condition after ischemic stroke: Results from a pilot randomized trial
title_full_unstemmed Ginkgo biloba extract EGb 761(®) improves cognition and overall condition after ischemic stroke: Results from a pilot randomized trial
title_short Ginkgo biloba extract EGb 761(®) improves cognition and overall condition after ischemic stroke: Results from a pilot randomized trial
title_sort ginkgo biloba extract egb 761(®) improves cognition and overall condition after ischemic stroke: results from a pilot randomized trial
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10090660/
https://www.ncbi.nlm.nih.gov/pubmed/37063270
http://dx.doi.org/10.3389/fphar.2023.1147860
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