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Gene expression biomarkers of response to citalopram treatment in major depressive disorder

There is significant variability in antidepressant treatment outcome, with ∼30–40% of patients with major depressive disorder (MDD) not presenting with adequate response even following several trials. To identify potential biomarkers of response, we investigated peripheral gene expression patterns o...

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Autores principales: Mamdani, F, Berlim, M T, Beaulieu, M-M, Labbe, A, Merette, C, Turecki, G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3309465/
https://www.ncbi.nlm.nih.gov/pubmed/22832429
http://dx.doi.org/10.1038/tp.2011.12
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author Mamdani, F
Berlim, M T
Beaulieu, M-M
Labbe, A
Merette, C
Turecki, G
author_facet Mamdani, F
Berlim, M T
Beaulieu, M-M
Labbe, A
Merette, C
Turecki, G
author_sort Mamdani, F
collection PubMed
description There is significant variability in antidepressant treatment outcome, with ∼30–40% of patients with major depressive disorder (MDD) not presenting with adequate response even following several trials. To identify potential biomarkers of response, we investigated peripheral gene expression patterns of response to antidepressant treatment in MDD. We did this using Affymetrix HG-U133 Plus2 microarrays in blood samples, from untreated individuals with MDD (N=63) ascertained at a community outpatient clinic, pre and post 8-week treatment with citalopram, and used a regression model to assess the impact of gene expression differences on antidepressant response. We carried out technical validation of significant probesets by quantitative reverse transcriptase PCR and conducted central nervous system follow-up of the most significant result in post-mortem brain samples from 15 subjects who died during a current MDD episode and 11 sudden-death controls. A total of 32 probesets were differentially expressed according to response to citalopram treatment following false discovery rate correction. Interferon regulatory factor 7 (IRF7) was the most significant differentially expressed gene and its expression was upregulated by citalopram treatment in individuals who responded to treatment. We found these results to be concordant with our observation of decreased expression of IRF7 in the prefrontal cortex of MDDs with negative toxicological evidence for antidepressant treatment at the time of death. These findings point to IRF7 as a gene of interest in studies investigating genomic factors associated with antidepressant response.
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spelling pubmed-33094652012-04-03 Gene expression biomarkers of response to citalopram treatment in major depressive disorder Mamdani, F Berlim, M T Beaulieu, M-M Labbe, A Merette, C Turecki, G Transl Psychiatry Original Article There is significant variability in antidepressant treatment outcome, with ∼30–40% of patients with major depressive disorder (MDD) not presenting with adequate response even following several trials. To identify potential biomarkers of response, we investigated peripheral gene expression patterns of response to antidepressant treatment in MDD. We did this using Affymetrix HG-U133 Plus2 microarrays in blood samples, from untreated individuals with MDD (N=63) ascertained at a community outpatient clinic, pre and post 8-week treatment with citalopram, and used a regression model to assess the impact of gene expression differences on antidepressant response. We carried out technical validation of significant probesets by quantitative reverse transcriptase PCR and conducted central nervous system follow-up of the most significant result in post-mortem brain samples from 15 subjects who died during a current MDD episode and 11 sudden-death controls. A total of 32 probesets were differentially expressed according to response to citalopram treatment following false discovery rate correction. Interferon regulatory factor 7 (IRF7) was the most significant differentially expressed gene and its expression was upregulated by citalopram treatment in individuals who responded to treatment. We found these results to be concordant with our observation of decreased expression of IRF7 in the prefrontal cortex of MDDs with negative toxicological evidence for antidepressant treatment at the time of death. These findings point to IRF7 as a gene of interest in studies investigating genomic factors associated with antidepressant response. Nature Publishing Group 2011-06 2011-06-21 /pmc/articles/PMC3309465/ /pubmed/22832429 http://dx.doi.org/10.1038/tp.2011.12 Text en Copyright © 2011 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Original Article
Mamdani, F
Berlim, M T
Beaulieu, M-M
Labbe, A
Merette, C
Turecki, G
Gene expression biomarkers of response to citalopram treatment in major depressive disorder
title Gene expression biomarkers of response to citalopram treatment in major depressive disorder
title_full Gene expression biomarkers of response to citalopram treatment in major depressive disorder
title_fullStr Gene expression biomarkers of response to citalopram treatment in major depressive disorder
title_full_unstemmed Gene expression biomarkers of response to citalopram treatment in major depressive disorder
title_short Gene expression biomarkers of response to citalopram treatment in major depressive disorder
title_sort gene expression biomarkers of response to citalopram treatment in major depressive disorder
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3309465/
https://www.ncbi.nlm.nih.gov/pubmed/22832429
http://dx.doi.org/10.1038/tp.2011.12
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