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Cerebrospinal fluid proteomic study of two bipolar disorder cohorts

The pathophysiology of bipolar disorder remains to be elucidated and there are no diagnostic or prognostic biomarkers for the condition. In this explorative proteomic study, we analyzed 201 proteins in cerebrospinal fluid (CSF) from mood stable bipolar disorder patients and control subjects sampled...

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Autores principales: Isgren, Anniella, Göteson, Andreas, Holmén-Larsson, Jessica, Pelanis, Aurimantas, Sellgren, Carl, Joas, Erik, Sparding, Timea, Zetterberg, Henrik, Smedler, Erik, Jakobsson, Joel, Landén, Mikael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9734044/
https://www.ncbi.nlm.nih.gov/pubmed/35986174
http://dx.doi.org/10.1038/s41380-022-01724-2
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author Isgren, Anniella
Göteson, Andreas
Holmén-Larsson, Jessica
Pelanis, Aurimantas
Sellgren, Carl
Joas, Erik
Sparding, Timea
Zetterberg, Henrik
Smedler, Erik
Jakobsson, Joel
Landén, Mikael
author_facet Isgren, Anniella
Göteson, Andreas
Holmén-Larsson, Jessica
Pelanis, Aurimantas
Sellgren, Carl
Joas, Erik
Sparding, Timea
Zetterberg, Henrik
Smedler, Erik
Jakobsson, Joel
Landén, Mikael
author_sort Isgren, Anniella
collection PubMed
description The pathophysiology of bipolar disorder remains to be elucidated and there are no diagnostic or prognostic biomarkers for the condition. In this explorative proteomic study, we analyzed 201 proteins in cerebrospinal fluid (CSF) from mood stable bipolar disorder patients and control subjects sampled from two independent cohorts, amounting to a total of 204 patients and 144 controls. We used three Olink Multiplex panels, whereof one specifically targets immune biomarkers, to assess a broad set of CSF protein concentrations. After quality control and removal of proteins with a low detection rate, 105 proteins remained for analyses in relation to case–control status and clinical variables. Only case–control differences that replicated across cohorts were considered. Results adjusted for potential confounders showed that CSF concentrations of growth hormone were lower in bipolar disorder compared with controls in both cohorts. The effect size was larger when the analysis was restricted to bipolar disorder type 1 and controls. We found no indications of immune activation or other aberrations. Growth hormone exerts many effects in the central nervous system and our findings suggest that growth hormone might be implicated in the pathophysiology of bipolar disorder.
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spelling pubmed-97340442022-12-11 Cerebrospinal fluid proteomic study of two bipolar disorder cohorts Isgren, Anniella Göteson, Andreas Holmén-Larsson, Jessica Pelanis, Aurimantas Sellgren, Carl Joas, Erik Sparding, Timea Zetterberg, Henrik Smedler, Erik Jakobsson, Joel Landén, Mikael Mol Psychiatry Article The pathophysiology of bipolar disorder remains to be elucidated and there are no diagnostic or prognostic biomarkers for the condition. In this explorative proteomic study, we analyzed 201 proteins in cerebrospinal fluid (CSF) from mood stable bipolar disorder patients and control subjects sampled from two independent cohorts, amounting to a total of 204 patients and 144 controls. We used three Olink Multiplex panels, whereof one specifically targets immune biomarkers, to assess a broad set of CSF protein concentrations. After quality control and removal of proteins with a low detection rate, 105 proteins remained for analyses in relation to case–control status and clinical variables. Only case–control differences that replicated across cohorts were considered. Results adjusted for potential confounders showed that CSF concentrations of growth hormone were lower in bipolar disorder compared with controls in both cohorts. The effect size was larger when the analysis was restricted to bipolar disorder type 1 and controls. We found no indications of immune activation or other aberrations. Growth hormone exerts many effects in the central nervous system and our findings suggest that growth hormone might be implicated in the pathophysiology of bipolar disorder. Nature Publishing Group UK 2022-08-19 2022 /pmc/articles/PMC9734044/ /pubmed/35986174 http://dx.doi.org/10.1038/s41380-022-01724-2 Text en © The Author(s) 2022 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Isgren, Anniella
Göteson, Andreas
Holmén-Larsson, Jessica
Pelanis, Aurimantas
Sellgren, Carl
Joas, Erik
Sparding, Timea
Zetterberg, Henrik
Smedler, Erik
Jakobsson, Joel
Landén, Mikael
Cerebrospinal fluid proteomic study of two bipolar disorder cohorts
title Cerebrospinal fluid proteomic study of two bipolar disorder cohorts
title_full Cerebrospinal fluid proteomic study of two bipolar disorder cohorts
title_fullStr Cerebrospinal fluid proteomic study of two bipolar disorder cohorts
title_full_unstemmed Cerebrospinal fluid proteomic study of two bipolar disorder cohorts
title_short Cerebrospinal fluid proteomic study of two bipolar disorder cohorts
title_sort cerebrospinal fluid proteomic study of two bipolar disorder cohorts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9734044/
https://www.ncbi.nlm.nih.gov/pubmed/35986174
http://dx.doi.org/10.1038/s41380-022-01724-2
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