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Topiramate and other kainate receptor antagonists for depression: A systematic review of randomized controlled trials

BACKGROUND: Depression is a common disorder that affects patients' quality of life and incurs health system costs. Due to the resistance to treat depression, better understanding of neurophysiology was considered; one of the implications is the glutamatergic system. This study aims to systemati...

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Autor principal: Shamabadi, Ahmad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9773746/
https://www.ncbi.nlm.nih.gov/pubmed/35912516
http://dx.doi.org/10.1002/npr2.12284
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author Shamabadi, Ahmad
author_facet Shamabadi, Ahmad
author_sort Shamabadi, Ahmad
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description BACKGROUND: Depression is a common disorder that affects patients' quality of life and incurs health system costs. Due to the resistance to treat depression, better understanding of neurophysiology was considered; one of the implications is the glutamatergic system. This study aims to systematically review clinical trials investigating the antidepressant effects of kainate receptor antagonists. METHODS: The study protocol was registered in PROSPERO (CRD42021213912). Scopus, ISI, Embase, PubMed, Cochrane Library, Google Scholar, and two trial registries were searched for randomized controlled trials on the effectiveness of topiramate, phenobarbital, and other ten barbiturates in depression. The difference with control groups in terms of changing depressive symptoms was the primary outcome. RESULTS: Nine trials were identified, in which 784 patients were studied. The efficacy of thiopental was comparable to that of imipramine, with fewer side effects. When administered with electroconvulsive therapy, it had fewer to similar effects and fewer side effects than ketamine. Both monotherapy and adjunctive therapy with topiramate were effective and tolerable in treating depressed patients. Phenobarbital had therapeutic effects compared to imipramine and amitriptyline with fewer side effects. CONCLUSION: Regarding the glutamatergic hypothesis of depression and obtained promising results, further studies of kainate receptor antagonists in high‐quality trials are recommended. Given the high prevalence of depression in epileptic patients, more problems with its treatment, and the fact that the studied agents were anticonvulsants, it is recommended that future studies prioritize depressed‐epileptic patients.
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spelling pubmed-97737462022-12-23 Topiramate and other kainate receptor antagonists for depression: A systematic review of randomized controlled trials Shamabadi, Ahmad Neuropsychopharmacol Rep Review Articles BACKGROUND: Depression is a common disorder that affects patients' quality of life and incurs health system costs. Due to the resistance to treat depression, better understanding of neurophysiology was considered; one of the implications is the glutamatergic system. This study aims to systematically review clinical trials investigating the antidepressant effects of kainate receptor antagonists. METHODS: The study protocol was registered in PROSPERO (CRD42021213912). Scopus, ISI, Embase, PubMed, Cochrane Library, Google Scholar, and two trial registries were searched for randomized controlled trials on the effectiveness of topiramate, phenobarbital, and other ten barbiturates in depression. The difference with control groups in terms of changing depressive symptoms was the primary outcome. RESULTS: Nine trials were identified, in which 784 patients were studied. The efficacy of thiopental was comparable to that of imipramine, with fewer side effects. When administered with electroconvulsive therapy, it had fewer to similar effects and fewer side effects than ketamine. Both monotherapy and adjunctive therapy with topiramate were effective and tolerable in treating depressed patients. Phenobarbital had therapeutic effects compared to imipramine and amitriptyline with fewer side effects. CONCLUSION: Regarding the glutamatergic hypothesis of depression and obtained promising results, further studies of kainate receptor antagonists in high‐quality trials are recommended. Given the high prevalence of depression in epileptic patients, more problems with its treatment, and the fact that the studied agents were anticonvulsants, it is recommended that future studies prioritize depressed‐epileptic patients. John Wiley and Sons Inc. 2022-08-01 /pmc/articles/PMC9773746/ /pubmed/35912516 http://dx.doi.org/10.1002/npr2.12284 Text en © 2022 The Author. Neuropsychopharmacology Reports published by John Wiley & Sons Australia, Ltd on behalf of The Japanese Society of Neuropsychopharmacology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Review Articles
Shamabadi, Ahmad
Topiramate and other kainate receptor antagonists for depression: A systematic review of randomized controlled trials
title Topiramate and other kainate receptor antagonists for depression: A systematic review of randomized controlled trials
title_full Topiramate and other kainate receptor antagonists for depression: A systematic review of randomized controlled trials
title_fullStr Topiramate and other kainate receptor antagonists for depression: A systematic review of randomized controlled trials
title_full_unstemmed Topiramate and other kainate receptor antagonists for depression: A systematic review of randomized controlled trials
title_short Topiramate and other kainate receptor antagonists for depression: A systematic review of randomized controlled trials
title_sort topiramate and other kainate receptor antagonists for depression: a systematic review of randomized controlled trials
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9773746/
https://www.ncbi.nlm.nih.gov/pubmed/35912516
http://dx.doi.org/10.1002/npr2.12284
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