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Plasma IL-17A levels in patients with late-life depression

OBJECTIVE: A consistent body of research has confirmed that patients with major depressive disorder (MDD) have increased concentrations of pro-inflammatory cytokines, including IL-6, TNF-α, IL-1β, the soluble IL-2 receptor, and C-reactive protein, compared to controls; however, there is limited info...

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Autores principales: Saraykar, Smita, Cao, Bo, Barroso, Lucelia S., Pereira, Kelly S., Bertola, Laiss, Nicolau, Mariana, Ferreira, Jessica D., Dias, Natalia S., Vieira, Erica L., Teixeira, Antonio L., Silva, Ana Paula M., Diniz, Breno S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação Brasileira de Psiquiatria 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6900762/
https://www.ncbi.nlm.nih.gov/pubmed/29069253
http://dx.doi.org/10.1590/1516-4446-2017-2299
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author Saraykar, Smita
Cao, Bo
Barroso, Lucelia S.
Pereira, Kelly S.
Bertola, Laiss
Nicolau, Mariana
Ferreira, Jessica D.
Dias, Natalia S.
Vieira, Erica L.
Teixeira, Antonio L.
Silva, Ana Paula M.
Diniz, Breno S.
author_facet Saraykar, Smita
Cao, Bo
Barroso, Lucelia S.
Pereira, Kelly S.
Bertola, Laiss
Nicolau, Mariana
Ferreira, Jessica D.
Dias, Natalia S.
Vieira, Erica L.
Teixeira, Antonio L.
Silva, Ana Paula M.
Diniz, Breno S.
author_sort Saraykar, Smita
collection PubMed
description OBJECTIVE: A consistent body of research has confirmed that patients with major depressive disorder (MDD) have increased concentrations of pro-inflammatory cytokines, including IL-6, TNF-α, IL-1β, the soluble IL-2 receptor, and C-reactive protein, compared to controls; however, there is limited information on IL-17A in MDD. Moreover, information about IL-17A in older populations, i.e., patients with late-life depression (LLD), is conspicuously missing from the literature. The purpose of this study was to investigate the role of IL-17A in LLD. METHODS: A convenience sample of 129 individuals, 74 with LLD and 55 non-depressed controls, were enrolled in this study. The Mann-Whitney U test was used to compare plasma IL-17A levels between LLD and controls subjects, and Spearman’s rank order correlation was used to investigate correlation of these levels with clinical, neuropsychological, and cognitive assessments. RESULTS: Plasma IL-17A levels were not statistically different between LLD patients and controls (p = 0.94). Among all subjects (LLD + control), plasma IL-17A did not correlate significantly with depressive symptoms (rho = -0.009, p = 0.92) but a significant correlation was observed with cognitive assessments (rho = 0.22, p = 0.01). CONCLUSION: Our findings do not support an association between plasma IL-17A levels and LLD. Nevertheless, IL-17A may be associated with cognitive impairment in LLD patients. If this finding is confirmed in future longitudinal studies, modulation of the T-helper 17 cell (T(h)17) immune response may be a treatment target for cognitive impairment in this population.
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spelling pubmed-69007622019-12-30 Plasma IL-17A levels in patients with late-life depression Saraykar, Smita Cao, Bo Barroso, Lucelia S. Pereira, Kelly S. Bertola, Laiss Nicolau, Mariana Ferreira, Jessica D. Dias, Natalia S. Vieira, Erica L. Teixeira, Antonio L. Silva, Ana Paula M. Diniz, Breno S. Braz J Psychiatry Brief Communication OBJECTIVE: A consistent body of research has confirmed that patients with major depressive disorder (MDD) have increased concentrations of pro-inflammatory cytokines, including IL-6, TNF-α, IL-1β, the soluble IL-2 receptor, and C-reactive protein, compared to controls; however, there is limited information on IL-17A in MDD. Moreover, information about IL-17A in older populations, i.e., patients with late-life depression (LLD), is conspicuously missing from the literature. The purpose of this study was to investigate the role of IL-17A in LLD. METHODS: A convenience sample of 129 individuals, 74 with LLD and 55 non-depressed controls, were enrolled in this study. The Mann-Whitney U test was used to compare plasma IL-17A levels between LLD and controls subjects, and Spearman’s rank order correlation was used to investigate correlation of these levels with clinical, neuropsychological, and cognitive assessments. RESULTS: Plasma IL-17A levels were not statistically different between LLD patients and controls (p = 0.94). Among all subjects (LLD + control), plasma IL-17A did not correlate significantly with depressive symptoms (rho = -0.009, p = 0.92) but a significant correlation was observed with cognitive assessments (rho = 0.22, p = 0.01). CONCLUSION: Our findings do not support an association between plasma IL-17A levels and LLD. Nevertheless, IL-17A may be associated with cognitive impairment in LLD patients. If this finding is confirmed in future longitudinal studies, modulation of the T-helper 17 cell (T(h)17) immune response may be a treatment target for cognitive impairment in this population. Associação Brasileira de Psiquiatria 2017-10-19 /pmc/articles/PMC6900762/ /pubmed/29069253 http://dx.doi.org/10.1590/1516-4446-2017-2299 Text en http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Communication
Saraykar, Smita
Cao, Bo
Barroso, Lucelia S.
Pereira, Kelly S.
Bertola, Laiss
Nicolau, Mariana
Ferreira, Jessica D.
Dias, Natalia S.
Vieira, Erica L.
Teixeira, Antonio L.
Silva, Ana Paula M.
Diniz, Breno S.
Plasma IL-17A levels in patients with late-life depression
title Plasma IL-17A levels in patients with late-life depression
title_full Plasma IL-17A levels in patients with late-life depression
title_fullStr Plasma IL-17A levels in patients with late-life depression
title_full_unstemmed Plasma IL-17A levels in patients with late-life depression
title_short Plasma IL-17A levels in patients with late-life depression
title_sort plasma il-17a levels in patients with late-life depression
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6900762/
https://www.ncbi.nlm.nih.gov/pubmed/29069253
http://dx.doi.org/10.1590/1516-4446-2017-2299
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