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Huperzine A for treatment of cognitive impairment in major depressive disorder: a systematic review of randomized controlled trials
BACKGROUND: Acetylcholinesterase (AChE) inhibitors have been shown to be effective in treating cognitive impairment in animal models and in human subjects with major depressive disorder (MDD). Huperzine A (HupA), a Traditional Chinese Medicine derived from a genus of clubmosses known as Huperzineser...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shanghai Municipal Bureau of Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5004090/ https://www.ncbi.nlm.nih.gov/pubmed/27605862 http://dx.doi.org/10.11919/j.issn.1002-0829.216003 |
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author | ZHENG, Wei XIANG, Ying-Qiang UNGVARI, Gabor S. CHIU, F.K. Helen H. NG, Chee WANG, Ying XIANG, Yu-Tao |
author_facet | ZHENG, Wei XIANG, Ying-Qiang UNGVARI, Gabor S. CHIU, F.K. Helen H. NG, Chee WANG, Ying XIANG, Yu-Tao |
author_sort | ZHENG, Wei |
collection | PubMed |
description | BACKGROUND: Acetylcholinesterase (AChE) inhibitors have been shown to be effective in treating cognitive impairment in animal models and in human subjects with major depressive disorder (MDD). Huperzine A (HupA), a Traditional Chinese Medicine derived from a genus of clubmosses known as Huperzineserrata, is a powerful AChE inhibitor that has been used as an adjunctive treatment for MDD, but no meta-analysis on HupA augmentation for MDD has yet been reported. AIM: Conduct a systematic review and meta-analysis of randomized controlled trials (RCTS) about HupA augmentation in the treatment of MDD to evaluate its efficacy and safety. METHODS: Two evaluators independently searched nine English-language and Chinese-language databases, selected relevant studies that met pre-determined inclusion criteria, extracted data about outcome and safety, and conducted quality assessments and data synthesis. RESULTS: Three low-quality RCTs (pooled n=238) from China were identified that compared monotherapy antidepressant treatment for depression versus combined treatment with antidepressants and HupA. Participants in the studies ranged from 16 to 60 years of age. The average duration of adjunctive antidepressant and HupA treatment in the studies was only 6.7 weeks. All three studies were open label and non-blinded, so their overall quality was judged as poor. Meta-analysis of the pooled sample found no significant difference in the improvement in depressive symptoms between the two groups (weighted mean difference: -1.90 (95%CI: -4.23, 0.44), p=0.11). However, the adjunctive HupA group did have significantly greater improvement than the antidepressant only group in cognitive functioning (as assessed by the Wisconsin Card Sorting Test and the Wechsler Memory Scale-Revised) and in quality of life. There was no significant difference in the incidence of adverse drug reactions between groups. CONCLUSIONS: The data available on the effectiveness and safety of adjunctive treatment using HupA in patients with MDD who are receiving antidepressants is insufficient to arrive at a definitive conclusion about its efficacy and safety. Pooling of the data from three low-quality RCTs from China found no advantage of adjunctive HupA in the treatment of depressive symptoms, but adjunctive treatment with HupA was associated with a faster resolution of the cognitive symptoms that frequently accompany MDD. |
format | Online Article Text |
id | pubmed-5004090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Shanghai Municipal Bureau of Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-50040902016-09-07 Huperzine A for treatment of cognitive impairment in major depressive disorder: a systematic review of randomized controlled trials ZHENG, Wei XIANG, Ying-Qiang UNGVARI, Gabor S. CHIU, F.K. Helen H. NG, Chee WANG, Ying XIANG, Yu-Tao Shanghai Arch Psychiatry Systematic Review and Meta-Analysis BACKGROUND: Acetylcholinesterase (AChE) inhibitors have been shown to be effective in treating cognitive impairment in animal models and in human subjects with major depressive disorder (MDD). Huperzine A (HupA), a Traditional Chinese Medicine derived from a genus of clubmosses known as Huperzineserrata, is a powerful AChE inhibitor that has been used as an adjunctive treatment for MDD, but no meta-analysis on HupA augmentation for MDD has yet been reported. AIM: Conduct a systematic review and meta-analysis of randomized controlled trials (RCTS) about HupA augmentation in the treatment of MDD to evaluate its efficacy and safety. METHODS: Two evaluators independently searched nine English-language and Chinese-language databases, selected relevant studies that met pre-determined inclusion criteria, extracted data about outcome and safety, and conducted quality assessments and data synthesis. RESULTS: Three low-quality RCTs (pooled n=238) from China were identified that compared monotherapy antidepressant treatment for depression versus combined treatment with antidepressants and HupA. Participants in the studies ranged from 16 to 60 years of age. The average duration of adjunctive antidepressant and HupA treatment in the studies was only 6.7 weeks. All three studies were open label and non-blinded, so their overall quality was judged as poor. Meta-analysis of the pooled sample found no significant difference in the improvement in depressive symptoms between the two groups (weighted mean difference: -1.90 (95%CI: -4.23, 0.44), p=0.11). However, the adjunctive HupA group did have significantly greater improvement than the antidepressant only group in cognitive functioning (as assessed by the Wisconsin Card Sorting Test and the Wechsler Memory Scale-Revised) and in quality of life. There was no significant difference in the incidence of adverse drug reactions between groups. CONCLUSIONS: The data available on the effectiveness and safety of adjunctive treatment using HupA in patients with MDD who are receiving antidepressants is insufficient to arrive at a definitive conclusion about its efficacy and safety. Pooling of the data from three low-quality RCTs from China found no advantage of adjunctive HupA in the treatment of depressive symptoms, but adjunctive treatment with HupA was associated with a faster resolution of the cognitive symptoms that frequently accompany MDD. Shanghai Municipal Bureau of Publishing 2016-04-25 /pmc/articles/PMC5004090/ /pubmed/27605862 http://dx.doi.org/10.11919/j.issn.1002-0829.216003 Text en Copyright © 2016 by Shanghai Municipal Bureau of Publishing http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Systematic Review and Meta-Analysis ZHENG, Wei XIANG, Ying-Qiang UNGVARI, Gabor S. CHIU, F.K. Helen H. NG, Chee WANG, Ying XIANG, Yu-Tao Huperzine A for treatment of cognitive impairment in major depressive disorder: a systematic review of randomized controlled trials |
title | Huperzine A for treatment of cognitive impairment in major depressive disorder: a systematic review of randomized controlled trials |
title_full | Huperzine A for treatment of cognitive impairment in major depressive disorder: a systematic review of randomized controlled trials |
title_fullStr | Huperzine A for treatment of cognitive impairment in major depressive disorder: a systematic review of randomized controlled trials |
title_full_unstemmed | Huperzine A for treatment of cognitive impairment in major depressive disorder: a systematic review of randomized controlled trials |
title_short | Huperzine A for treatment of cognitive impairment in major depressive disorder: a systematic review of randomized controlled trials |
title_sort | huperzine a for treatment of cognitive impairment in major depressive disorder: a systematic review of randomized controlled trials |
topic | Systematic Review and Meta-Analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5004090/ https://www.ncbi.nlm.nih.gov/pubmed/27605862 http://dx.doi.org/10.11919/j.issn.1002-0829.216003 |
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