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Treatment of 95 post-Covid patients with SSRIs
After Covid-19 infection, 12.5% develops post-Covid-syndrome (PCS). Symptoms indicate numerous affected organ systems. After a year, chronic fatigue, dysautonomia and neurological and neuropsychiatric complaints predominate. In this study, 95 PCS patients were treated with selective serotonin reupta...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10622561/ https://www.ncbi.nlm.nih.gov/pubmed/37919310 http://dx.doi.org/10.1038/s41598-023-45072-9 |
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author | Rus, Carla P. de Vries, Bert E. K. de Vries, Ingmar E. J. Nutma, Idelette Kooij, J. J. Sandra |
author_facet | Rus, Carla P. de Vries, Bert E. K. de Vries, Ingmar E. J. Nutma, Idelette Kooij, J. J. Sandra |
author_sort | Rus, Carla P. |
collection | PubMed |
description | After Covid-19 infection, 12.5% develops post-Covid-syndrome (PCS). Symptoms indicate numerous affected organ systems. After a year, chronic fatigue, dysautonomia and neurological and neuropsychiatric complaints predominate. In this study, 95 PCS patients were treated with selective serotonin reuptake inhibitors (SSRIs). This study used an exploratory questionnaire and found that two-thirds of patients had a reasonably good to strong response on SSRIs, over a quarter of patients had moderate response, while 10% reported no response. Overall, patients experienced substantial improved well-being. Brainfog and sensory overload decreased most, followed by chronic fatigue and dysautonomia. Outcomes were measured with three different measures that correlated strongly with each other. The response to SSRIs in PCS conditions was explained by seven possible neurobiological mechanisms based on recent literature on PCS integrated with already existing knowledge. Important for understanding these mechanisms is the underlying biochemical interaction between various neurotransmitter systems and parts of the immune system, and their dysregulation in PCS. The main link appears to be with the metabolic kynurenine pathway (KP) which interacts extensively with the immune system. The KP uses the same precursor as serotonin: tryptophan. The KP is overactive in PCS which maintains inflammation and which causes a lack of tryptophan. Finally, potential avenues for future research to advance this line of clinical research are discussed. |
format | Online Article Text |
id | pubmed-10622561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106225612023-11-04 Treatment of 95 post-Covid patients with SSRIs Rus, Carla P. de Vries, Bert E. K. de Vries, Ingmar E. J. Nutma, Idelette Kooij, J. J. Sandra Sci Rep Article After Covid-19 infection, 12.5% develops post-Covid-syndrome (PCS). Symptoms indicate numerous affected organ systems. After a year, chronic fatigue, dysautonomia and neurological and neuropsychiatric complaints predominate. In this study, 95 PCS patients were treated with selective serotonin reuptake inhibitors (SSRIs). This study used an exploratory questionnaire and found that two-thirds of patients had a reasonably good to strong response on SSRIs, over a quarter of patients had moderate response, while 10% reported no response. Overall, patients experienced substantial improved well-being. Brainfog and sensory overload decreased most, followed by chronic fatigue and dysautonomia. Outcomes were measured with three different measures that correlated strongly with each other. The response to SSRIs in PCS conditions was explained by seven possible neurobiological mechanisms based on recent literature on PCS integrated with already existing knowledge. Important for understanding these mechanisms is the underlying biochemical interaction between various neurotransmitter systems and parts of the immune system, and their dysregulation in PCS. The main link appears to be with the metabolic kynurenine pathway (KP) which interacts extensively with the immune system. The KP uses the same precursor as serotonin: tryptophan. The KP is overactive in PCS which maintains inflammation and which causes a lack of tryptophan. Finally, potential avenues for future research to advance this line of clinical research are discussed. Nature Publishing Group UK 2023-11-02 /pmc/articles/PMC10622561/ /pubmed/37919310 http://dx.doi.org/10.1038/s41598-023-45072-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Rus, Carla P. de Vries, Bert E. K. de Vries, Ingmar E. J. Nutma, Idelette Kooij, J. J. Sandra Treatment of 95 post-Covid patients with SSRIs |
title | Treatment of 95 post-Covid patients with SSRIs |
title_full | Treatment of 95 post-Covid patients with SSRIs |
title_fullStr | Treatment of 95 post-Covid patients with SSRIs |
title_full_unstemmed | Treatment of 95 post-Covid patients with SSRIs |
title_short | Treatment of 95 post-Covid patients with SSRIs |
title_sort | treatment of 95 post-covid patients with ssris |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10622561/ https://www.ncbi.nlm.nih.gov/pubmed/37919310 http://dx.doi.org/10.1038/s41598-023-45072-9 |
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