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Secondary Mania induced by TNF‐α inhibitors: A systematic review
A growing number of studies support a bidirectional relationship between inflammation and bipolar disorders. Tumor necrosis factor‐α (TNF‐α) inhibitors have recently attracted interest as potential therapeutic compounds for treating depressive symptoms, but the risk for triggering mood switches in p...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9298409/ https://www.ncbi.nlm.nih.gov/pubmed/34590391 http://dx.doi.org/10.1111/pcn.13302 |
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author | Miola, Alessandro Dal Porto, Veronica Meda, Nicola Perini, Giulia Solmi, Marco Sambataro, Fabio |
author_facet | Miola, Alessandro Dal Porto, Veronica Meda, Nicola Perini, Giulia Solmi, Marco Sambataro, Fabio |
author_sort | Miola, Alessandro |
collection | PubMed |
description | A growing number of studies support a bidirectional relationship between inflammation and bipolar disorders. Tumor necrosis factor‐α (TNF‐α) inhibitors have recently attracted interest as potential therapeutic compounds for treating depressive symptoms, but the risk for triggering mood switches in patients with or without bipolar disorders remains controversial. Thus, we conducted a systematic review to study the anti‐TNF‐α medication‐induced manic or hypomanic episodes. PubMed, Scopus, Medline, and Embase databases were screened for a comprehensive literature search from inception until November 2020, using The Preferred Reporting Items for Systematic Reviews and Meta‐Analyses guidelines. Out of the initial 75 references, the screening resulted in the inclusion of four case reports (each describing one patient) and a cohort study (in which 40 patients out of 7600–0.53% – experienced elated mood episodes after infliximab administration). Of these 44 patients, 97.7% experienced a manic episode and 2.3% hypomania. 93.2% of patients had no history of psychiatric disorder or psychotropic treatment. Only 6.8% had a history of psychiatric disorders with the affective spectrum (4.6% dysthymia and 2.3% bipolar disorder). The time of onset of manic or hypomanic symptoms varied across TNF‐α inhibitors with an early onset for Infliximab and a later onset for Adalimumab and Etanercept. These findings suggest that medications targeting the TNF‐α pathway may trigger a manic episode in patients with or without affective disorders. However, prospective studies are needed to evaluate the relative risk of such side effects and identify the population susceptible to secondary mania. |
format | Online Article Text |
id | pubmed-9298409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-92984092022-07-21 Secondary Mania induced by TNF‐α inhibitors: A systematic review Miola, Alessandro Dal Porto, Veronica Meda, Nicola Perini, Giulia Solmi, Marco Sambataro, Fabio Psychiatry Clin Neurosci Review Article A growing number of studies support a bidirectional relationship between inflammation and bipolar disorders. Tumor necrosis factor‐α (TNF‐α) inhibitors have recently attracted interest as potential therapeutic compounds for treating depressive symptoms, but the risk for triggering mood switches in patients with or without bipolar disorders remains controversial. Thus, we conducted a systematic review to study the anti‐TNF‐α medication‐induced manic or hypomanic episodes. PubMed, Scopus, Medline, and Embase databases were screened for a comprehensive literature search from inception until November 2020, using The Preferred Reporting Items for Systematic Reviews and Meta‐Analyses guidelines. Out of the initial 75 references, the screening resulted in the inclusion of four case reports (each describing one patient) and a cohort study (in which 40 patients out of 7600–0.53% – experienced elated mood episodes after infliximab administration). Of these 44 patients, 97.7% experienced a manic episode and 2.3% hypomania. 93.2% of patients had no history of psychiatric disorder or psychotropic treatment. Only 6.8% had a history of psychiatric disorders with the affective spectrum (4.6% dysthymia and 2.3% bipolar disorder). The time of onset of manic or hypomanic symptoms varied across TNF‐α inhibitors with an early onset for Infliximab and a later onset for Adalimumab and Etanercept. These findings suggest that medications targeting the TNF‐α pathway may trigger a manic episode in patients with or without affective disorders. However, prospective studies are needed to evaluate the relative risk of such side effects and identify the population susceptible to secondary mania. John Wiley & Sons Australia, Ltd 2021-11-02 2022-01 /pmc/articles/PMC9298409/ /pubmed/34590391 http://dx.doi.org/10.1111/pcn.13302 Text en © 2021 The Authors Psychiatry and Clinical Neurosciences published by John Wiley & Sons Australia, Ltd on behalf of Japanese Society of Psychiatry and Neurology https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Miola, Alessandro Dal Porto, Veronica Meda, Nicola Perini, Giulia Solmi, Marco Sambataro, Fabio Secondary Mania induced by TNF‐α inhibitors: A systematic review |
title | Secondary Mania induced by TNF‐α inhibitors: A systematic review |
title_full | Secondary Mania induced by TNF‐α inhibitors: A systematic review |
title_fullStr | Secondary Mania induced by TNF‐α inhibitors: A systematic review |
title_full_unstemmed | Secondary Mania induced by TNF‐α inhibitors: A systematic review |
title_short | Secondary Mania induced by TNF‐α inhibitors: A systematic review |
title_sort | secondary mania induced by tnf‐α inhibitors: a systematic review |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9298409/ https://www.ncbi.nlm.nih.gov/pubmed/34590391 http://dx.doi.org/10.1111/pcn.13302 |
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