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The association between immune activation and manic symptoms in patients with a depressive disorder

Although recent studies have shown that immunological processes play an important role in the pathophysiology of mood disorders, immune activation may only be present in specific subgroups of patients. Our study aimed to examine whether immune activation was associated with (a) the presence of manic...

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Autores principales: Becking, K, Boschloo, L, Vogelzangs, N, Haarman, B C M, Riemersma-van der Lek, R, Penninx, B W J H, Schoevers, R A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3818012/
https://www.ncbi.nlm.nih.gov/pubmed/24150223
http://dx.doi.org/10.1038/tp.2013.87
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author Becking, K
Boschloo, L
Vogelzangs, N
Haarman, B C M
Riemersma-van der Lek, R
Penninx, B W J H
Schoevers, R A
author_facet Becking, K
Boschloo, L
Vogelzangs, N
Haarman, B C M
Riemersma-van der Lek, R
Penninx, B W J H
Schoevers, R A
author_sort Becking, K
collection PubMed
description Although recent studies have shown that immunological processes play an important role in the pathophysiology of mood disorders, immune activation may only be present in specific subgroups of patients. Our study aimed to examine whether immune activation was associated with (a) the presence of manic symptoms and (b) the onset of manic symptoms during 2 years of follow-up in depressed patients. Patients with a depressive disorder at baseline (N=957) and healthy controls (N=430) were selected from the Netherlands Study of Depression and Anxiety. Assessments included lifetime manic symptoms at baseline and two-year follow up, as well as C-reactive protein (CRP), interleukin-6 (IL-6) and tumor necrosis factor alpha (TNF-α) at baseline. Within depressed patients, immune activation was not related to the presence or absence of lifetime manic symptoms at baseline. However, CRP levels were strongly elevated in depressed men who developed manic symptoms compared with those who did not develop manic symptoms over 2 years (P<0.001, Cohen's d=0.89). IL-6 and TNF-α were also higher in depressed men with an onset of manic symptoms, but this association was not significant. However, we found that the onset of manic symptoms was particularly high in men with multiple elevated levels of inflammatory markers. Depressed men who developed manic symptoms during follow-up had increased immunological activity (especially CRP) compared with depressed men who did not develop manic symptoms. Further research should explore whether a treatment approach focusing on inflammatory processes may be more effective in this specific subgroup of depressed patients.
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spelling pubmed-38180122013-11-06 The association between immune activation and manic symptoms in patients with a depressive disorder Becking, K Boschloo, L Vogelzangs, N Haarman, B C M Riemersma-van der Lek, R Penninx, B W J H Schoevers, R A Transl Psychiatry Original Article Although recent studies have shown that immunological processes play an important role in the pathophysiology of mood disorders, immune activation may only be present in specific subgroups of patients. Our study aimed to examine whether immune activation was associated with (a) the presence of manic symptoms and (b) the onset of manic symptoms during 2 years of follow-up in depressed patients. Patients with a depressive disorder at baseline (N=957) and healthy controls (N=430) were selected from the Netherlands Study of Depression and Anxiety. Assessments included lifetime manic symptoms at baseline and two-year follow up, as well as C-reactive protein (CRP), interleukin-6 (IL-6) and tumor necrosis factor alpha (TNF-α) at baseline. Within depressed patients, immune activation was not related to the presence or absence of lifetime manic symptoms at baseline. However, CRP levels were strongly elevated in depressed men who developed manic symptoms compared with those who did not develop manic symptoms over 2 years (P<0.001, Cohen's d=0.89). IL-6 and TNF-α were also higher in depressed men with an onset of manic symptoms, but this association was not significant. However, we found that the onset of manic symptoms was particularly high in men with multiple elevated levels of inflammatory markers. Depressed men who developed manic symptoms during follow-up had increased immunological activity (especially CRP) compared with depressed men who did not develop manic symptoms. Further research should explore whether a treatment approach focusing on inflammatory processes may be more effective in this specific subgroup of depressed patients. Nature Publishing Group 2013-10 2013-10-22 /pmc/articles/PMC3818012/ /pubmed/24150223 http://dx.doi.org/10.1038/tp.2013.87 Text en Copyright © 2013 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Original Article
Becking, K
Boschloo, L
Vogelzangs, N
Haarman, B C M
Riemersma-van der Lek, R
Penninx, B W J H
Schoevers, R A
The association between immune activation and manic symptoms in patients with a depressive disorder
title The association between immune activation and manic symptoms in patients with a depressive disorder
title_full The association between immune activation and manic symptoms in patients with a depressive disorder
title_fullStr The association between immune activation and manic symptoms in patients with a depressive disorder
title_full_unstemmed The association between immune activation and manic symptoms in patients with a depressive disorder
title_short The association between immune activation and manic symptoms in patients with a depressive disorder
title_sort association between immune activation and manic symptoms in patients with a depressive disorder
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3818012/
https://www.ncbi.nlm.nih.gov/pubmed/24150223
http://dx.doi.org/10.1038/tp.2013.87
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