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Efficacy and Safety of DL-3-n-Butylphthalide in the Treatment of Poststroke Cognitive Impairment: A Systematic Review and Meta-Analysis

Background: Poststroke cognitive impairment (PSCI) is a common complication observed after stroke. Current pharmacologic therapies have no definitive evidence for cognitive recovery or disease progression. Recent studies have verified the positive effect of DL-3-n-butylphthalide (NBP). However, the...

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Autores principales: Fan, Xueming, Shen, Wei, Wang, Liuding, Zhang, Yunling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8823901/
https://www.ncbi.nlm.nih.gov/pubmed/35145408
http://dx.doi.org/10.3389/fphar.2021.810297
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author Fan, Xueming
Shen, Wei
Wang, Liuding
Zhang, Yunling
author_facet Fan, Xueming
Shen, Wei
Wang, Liuding
Zhang, Yunling
author_sort Fan, Xueming
collection PubMed
description Background: Poststroke cognitive impairment (PSCI) is a common complication observed after stroke. Current pharmacologic therapies have no definitive evidence for cognitive recovery or disease progression. Recent studies have verified the positive effect of DL-3-n-butylphthalide (NBP). However, the clinical efficacy and safety are still unclear. The aim of this study was to assess the efficacy of NBP and its harmful effect in the treatment of PSCI. Method: Eligible randomized controlled trials (RCTs) were retrieved from inception to June 2021 from seven medical databases and two clinical registries. The revised Cochrane risk of bias tool (RoB 2.0) was used for methodological quality. RevMan v5.4.1 from Cochrane Collaboration was used for statistical analysis, and Hartung-Knapp-Sidik-Jonkman (HKSJ) method was used for post hoc testing depend on the number of studies. This study has been submitted to PROSPERO with registration number is CRD42021274123. Result: We identified 26 studies with a total sample size of 2,571 patients. The results of this study showed that NBP as monotherapy or combination therapy had better performance in increasing the MoCA (monotherapy: SMD(N) = 1.05, 95% CI [0.69, 1.42], p < 0.00001; SMD(P) = 1.06, 95% CI [0.59, 1.52], p < 0.00001. combination: SMD(O) = 0.81, 95% CI [0.62, 1.01], p < 0.00001; SMD(N) = 0.90, 95% CI [0.46, 1.33], p < 0.0001; SMD(D) = 1.04, 95% CI [0.71, 1.38], p < 0.00001), MMSE (monotherapy: MD(N) = 4.89, 95% CI [4.14, 5.63]), p < 0.00001). combination: SMD(O) = 1.26, 95% CI [0.97, 1.56], p < 0.00001; SMD(C) = 1.63, 95% CI [1.28, 1.98], p < 0.00001; SMD(N) = 2.13, 95% CI [1.52, 2.75], p < 0.00001) and BI (monotherapy: MD(N) = 13.53, HKSJ 95% CI [9.84, 17.22], p = 0.014. combination: SMD(O) = 2.24, HKSJ 95%CI [0.37, 4.11], p = 0.032; SMD(C) = 3.36, 95%CI [2.80, 3.93], p < 0.00001; SMD(D) = 1.48, 95%CI [1.13, 1.83], p < 0.00001); and decreasing the NIHSS (monotherapy: MD(N) = −3.86, 95% CI [−5.22, −2.50], p < 0.00001. combination: SMD(O) = −1.15, 95% CI [−1.31, −0.98], p < 0.00001; SMD(C) = −1.82, 95% CI [−2.25, −1.40], p < 0.00001) and CSS (combination: MD(O) = −7.11, 95% CI [−8.42, −5.80], p < 0.00001), with no serious adverse reactions observed. The funnel plot verified the possibility of publication bias. Conclusion: NBP maintains a stable pattern in promoting the recovery of cognitive function and abilities of daily living, as well as reducing the symptoms of neurological deficits. However, there is still a need for more high-quality RCTs to verify its efficacy and safety.
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spelling pubmed-88239012022-02-09 Efficacy and Safety of DL-3-n-Butylphthalide in the Treatment of Poststroke Cognitive Impairment: A Systematic Review and Meta-Analysis Fan, Xueming Shen, Wei Wang, Liuding Zhang, Yunling Front Pharmacol Pharmacology Background: Poststroke cognitive impairment (PSCI) is a common complication observed after stroke. Current pharmacologic therapies have no definitive evidence for cognitive recovery or disease progression. Recent studies have verified the positive effect of DL-3-n-butylphthalide (NBP). However, the clinical efficacy and safety are still unclear. The aim of this study was to assess the efficacy of NBP and its harmful effect in the treatment of PSCI. Method: Eligible randomized controlled trials (RCTs) were retrieved from inception to June 2021 from seven medical databases and two clinical registries. The revised Cochrane risk of bias tool (RoB 2.0) was used for methodological quality. RevMan v5.4.1 from Cochrane Collaboration was used for statistical analysis, and Hartung-Knapp-Sidik-Jonkman (HKSJ) method was used for post hoc testing depend on the number of studies. This study has been submitted to PROSPERO with registration number is CRD42021274123. Result: We identified 26 studies with a total sample size of 2,571 patients. The results of this study showed that NBP as monotherapy or combination therapy had better performance in increasing the MoCA (monotherapy: SMD(N) = 1.05, 95% CI [0.69, 1.42], p < 0.00001; SMD(P) = 1.06, 95% CI [0.59, 1.52], p < 0.00001. combination: SMD(O) = 0.81, 95% CI [0.62, 1.01], p < 0.00001; SMD(N) = 0.90, 95% CI [0.46, 1.33], p < 0.0001; SMD(D) = 1.04, 95% CI [0.71, 1.38], p < 0.00001), MMSE (monotherapy: MD(N) = 4.89, 95% CI [4.14, 5.63]), p < 0.00001). combination: SMD(O) = 1.26, 95% CI [0.97, 1.56], p < 0.00001; SMD(C) = 1.63, 95% CI [1.28, 1.98], p < 0.00001; SMD(N) = 2.13, 95% CI [1.52, 2.75], p < 0.00001) and BI (monotherapy: MD(N) = 13.53, HKSJ 95% CI [9.84, 17.22], p = 0.014. combination: SMD(O) = 2.24, HKSJ 95%CI [0.37, 4.11], p = 0.032; SMD(C) = 3.36, 95%CI [2.80, 3.93], p < 0.00001; SMD(D) = 1.48, 95%CI [1.13, 1.83], p < 0.00001); and decreasing the NIHSS (monotherapy: MD(N) = −3.86, 95% CI [−5.22, −2.50], p < 0.00001. combination: SMD(O) = −1.15, 95% CI [−1.31, −0.98], p < 0.00001; SMD(C) = −1.82, 95% CI [−2.25, −1.40], p < 0.00001) and CSS (combination: MD(O) = −7.11, 95% CI [−8.42, −5.80], p < 0.00001), with no serious adverse reactions observed. The funnel plot verified the possibility of publication bias. Conclusion: NBP maintains a stable pattern in promoting the recovery of cognitive function and abilities of daily living, as well as reducing the symptoms of neurological deficits. However, there is still a need for more high-quality RCTs to verify its efficacy and safety. Frontiers Media S.A. 2022-01-25 /pmc/articles/PMC8823901/ /pubmed/35145408 http://dx.doi.org/10.3389/fphar.2021.810297 Text en Copyright © 2022 Fan, Shen, Wang and Zhang. 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
Fan, Xueming
Shen, Wei
Wang, Liuding
Zhang, Yunling
Efficacy and Safety of DL-3-n-Butylphthalide in the Treatment of Poststroke Cognitive Impairment: A Systematic Review and Meta-Analysis
title Efficacy and Safety of DL-3-n-Butylphthalide in the Treatment of Poststroke Cognitive Impairment: A Systematic Review and Meta-Analysis
title_full Efficacy and Safety of DL-3-n-Butylphthalide in the Treatment of Poststroke Cognitive Impairment: A Systematic Review and Meta-Analysis
title_fullStr Efficacy and Safety of DL-3-n-Butylphthalide in the Treatment of Poststroke Cognitive Impairment: A Systematic Review and Meta-Analysis
title_full_unstemmed Efficacy and Safety of DL-3-n-Butylphthalide in the Treatment of Poststroke Cognitive Impairment: A Systematic Review and Meta-Analysis
title_short Efficacy and Safety of DL-3-n-Butylphthalide in the Treatment of Poststroke Cognitive Impairment: A Systematic Review and Meta-Analysis
title_sort efficacy and safety of dl-3-n-butylphthalide in the treatment of poststroke cognitive impairment: a systematic review and meta-analysis
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8823901/
https://www.ncbi.nlm.nih.gov/pubmed/35145408
http://dx.doi.org/10.3389/fphar.2021.810297
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