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Celecoxib for Mood Disorders: A Systematic Review and Meta-Analysis of Randomized Controlled Trials
The effects of celecoxib on a broad spectrum of mood disorders and on inflammatory parameters have not yet been comprehensively evaluated. The aim of this study was to systematically summarize the available knowledge on this topic. Data from both preclinical and clinical studies were analyzed, consi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10218898/ https://www.ncbi.nlm.nih.gov/pubmed/37240605 http://dx.doi.org/10.3390/jcm12103497 |
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author | Gędek, Adam Szular, Zofia Antosik, Anna Z. Mierzejewski, Paweł Dominiak, Monika |
author_facet | Gędek, Adam Szular, Zofia Antosik, Anna Z. Mierzejewski, Paweł Dominiak, Monika |
author_sort | Gędek, Adam |
collection | PubMed |
description | The effects of celecoxib on a broad spectrum of mood disorders and on inflammatory parameters have not yet been comprehensively evaluated. The aim of this study was to systematically summarize the available knowledge on this topic. Data from both preclinical and clinical studies were analyzed, considering the efficacy and safety of celecoxib in the treatment of mood disorders, as well as the correlation of inflammatory parameters with the effect of celecoxib treatment. Forty-four studies were included. We found evidence supporting the antidepressant efficacy of celecoxib in a dose of 400 mg/day used for 6 weeks as an add-on treatment in major depression (SMD = −1.12 [95%Cl: −1.71,−0.52], p = 0.0002) and mania (SMD = −0.82 [95% CI:−1.62,−0.01], p = 0.05). The antidepressant efficacy of celecoxib in the above dosage used as sole treatment was also confirmed in depressed patients with somatic comorbidity (SMD = −1.35 [95% CI:−1.95,−0.75], p < 0.0001). We found no conclusive evidence for the effectiveness of celecoxib in bipolar depression. Celecoxib at a dose of 400 mg/d used for up to 12 weeks appeared to be a safe treatment in patients with mood disorders. Although an association between celecoxib response and inflammatory parameters has been found in preclinical studies, this has not been confirmed in clinical trials. Further studies are needed to evaluate the efficacy of celecoxib in bipolar depression, as well as long-term studies evaluating the safety and efficacy of celecoxib in recurrent mood disorders, studies involving treatment-resistant populations, and assessing the association of celecoxib treatment with inflammatory markers. |
format | Online Article Text |
id | pubmed-10218898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102188982023-05-27 Celecoxib for Mood Disorders: A Systematic Review and Meta-Analysis of Randomized Controlled Trials Gędek, Adam Szular, Zofia Antosik, Anna Z. Mierzejewski, Paweł Dominiak, Monika J Clin Med Systematic Review The effects of celecoxib on a broad spectrum of mood disorders and on inflammatory parameters have not yet been comprehensively evaluated. The aim of this study was to systematically summarize the available knowledge on this topic. Data from both preclinical and clinical studies were analyzed, considering the efficacy and safety of celecoxib in the treatment of mood disorders, as well as the correlation of inflammatory parameters with the effect of celecoxib treatment. Forty-four studies were included. We found evidence supporting the antidepressant efficacy of celecoxib in a dose of 400 mg/day used for 6 weeks as an add-on treatment in major depression (SMD = −1.12 [95%Cl: −1.71,−0.52], p = 0.0002) and mania (SMD = −0.82 [95% CI:−1.62,−0.01], p = 0.05). The antidepressant efficacy of celecoxib in the above dosage used as sole treatment was also confirmed in depressed patients with somatic comorbidity (SMD = −1.35 [95% CI:−1.95,−0.75], p < 0.0001). We found no conclusive evidence for the effectiveness of celecoxib in bipolar depression. Celecoxib at a dose of 400 mg/d used for up to 12 weeks appeared to be a safe treatment in patients with mood disorders. Although an association between celecoxib response and inflammatory parameters has been found in preclinical studies, this has not been confirmed in clinical trials. Further studies are needed to evaluate the efficacy of celecoxib in bipolar depression, as well as long-term studies evaluating the safety and efficacy of celecoxib in recurrent mood disorders, studies involving treatment-resistant populations, and assessing the association of celecoxib treatment with inflammatory markers. MDPI 2023-05-16 /pmc/articles/PMC10218898/ /pubmed/37240605 http://dx.doi.org/10.3390/jcm12103497 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Systematic Review Gędek, Adam Szular, Zofia Antosik, Anna Z. Mierzejewski, Paweł Dominiak, Monika Celecoxib for Mood Disorders: A Systematic Review and Meta-Analysis of Randomized Controlled Trials |
title | Celecoxib for Mood Disorders: A Systematic Review and Meta-Analysis of Randomized Controlled Trials |
title_full | Celecoxib for Mood Disorders: A Systematic Review and Meta-Analysis of Randomized Controlled Trials |
title_fullStr | Celecoxib for Mood Disorders: A Systematic Review and Meta-Analysis of Randomized Controlled Trials |
title_full_unstemmed | Celecoxib for Mood Disorders: A Systematic Review and Meta-Analysis of Randomized Controlled Trials |
title_short | Celecoxib for Mood Disorders: A Systematic Review and Meta-Analysis of Randomized Controlled Trials |
title_sort | celecoxib for mood disorders: a systematic review and meta-analysis of randomized controlled trials |
topic | Systematic Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10218898/ https://www.ncbi.nlm.nih.gov/pubmed/37240605 http://dx.doi.org/10.3390/jcm12103497 |
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