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Influence of COMT val158met Genotype on the Depressed Brain during Emotional Processing and Working Memory

Major depressive disorder (MDD) has been associated with abnormal prefrontal-limbic interactions and altered catecholaminergic neurotransmission. The val158met polymorphism on the catechol-O-methyltransferase (COMT) gene has been shown to influence prefrontal cortex (PFC) activation during both emot...

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Autores principales: Opmeer, Esther M., Kortekaas, Rudie, van Tol, Marie-José, van der Wee, Nic J. A., Woudstra, Saskia, van Buchem, Mark A., Penninx, Brenda W., Veltman, Dick J., Aleman, André
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3772077/
https://www.ncbi.nlm.nih.gov/pubmed/24069183
http://dx.doi.org/10.1371/journal.pone.0073290
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author Opmeer, Esther M.
Kortekaas, Rudie
van Tol, Marie-José
van der Wee, Nic J. A.
Woudstra, Saskia
van Buchem, Mark A.
Penninx, Brenda W.
Veltman, Dick J.
Aleman, André
author_facet Opmeer, Esther M.
Kortekaas, Rudie
van Tol, Marie-José
van der Wee, Nic J. A.
Woudstra, Saskia
van Buchem, Mark A.
Penninx, Brenda W.
Veltman, Dick J.
Aleman, André
author_sort Opmeer, Esther M.
collection PubMed
description Major depressive disorder (MDD) has been associated with abnormal prefrontal-limbic interactions and altered catecholaminergic neurotransmission. The val158met polymorphism on the catechol-O-methyltransferase (COMT) gene has been shown to influence prefrontal cortex (PFC) activation during both emotional processing and working memory (WM). Although COMT-genotype is not directly associated with MDD, it may affect MDD pathology by altering PFC activation, an endophenotype associated with both COMT and MDD. 125 participants, including healthy controls (HC, n=28) and MDD patients were genotyped for the COMT val158met polymorphism and underwent functional magnetic resonance imaging (fMRI-neuroimaging) during emotion processing (viewing of emotional facial expressions) and a WM task (visuospatial planning). Within HC, we observed a positive correlation between the number of met-alleles and right inferior frontal gyrus activation during emotional processing, whereas within patients the number of met-alleles was not correlated with PFC activation. During WM a negative correlation between the number of met-alleles and middle frontal gyrus activation was present in the total sample. In addition, during emotional processing there was an effect of genotype in a cluster including the amygdala and hippocampus. These results demonstrate that COMT genotype is associated with relevant endophenotypes for MDD. In addition, presence of MDD only interacts with genotype during emotional processing and not working memory.
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spelling pubmed-37720772013-09-25 Influence of COMT val158met Genotype on the Depressed Brain during Emotional Processing and Working Memory Opmeer, Esther M. Kortekaas, Rudie van Tol, Marie-José van der Wee, Nic J. A. Woudstra, Saskia van Buchem, Mark A. Penninx, Brenda W. Veltman, Dick J. Aleman, André PLoS One Research Article Major depressive disorder (MDD) has been associated with abnormal prefrontal-limbic interactions and altered catecholaminergic neurotransmission. The val158met polymorphism on the catechol-O-methyltransferase (COMT) gene has been shown to influence prefrontal cortex (PFC) activation during both emotional processing and working memory (WM). Although COMT-genotype is not directly associated with MDD, it may affect MDD pathology by altering PFC activation, an endophenotype associated with both COMT and MDD. 125 participants, including healthy controls (HC, n=28) and MDD patients were genotyped for the COMT val158met polymorphism and underwent functional magnetic resonance imaging (fMRI-neuroimaging) during emotion processing (viewing of emotional facial expressions) and a WM task (visuospatial planning). Within HC, we observed a positive correlation between the number of met-alleles and right inferior frontal gyrus activation during emotional processing, whereas within patients the number of met-alleles was not correlated with PFC activation. During WM a negative correlation between the number of met-alleles and middle frontal gyrus activation was present in the total sample. In addition, during emotional processing there was an effect of genotype in a cluster including the amygdala and hippocampus. These results demonstrate that COMT genotype is associated with relevant endophenotypes for MDD. In addition, presence of MDD only interacts with genotype during emotional processing and not working memory. Public Library of Science 2013-09-12 /pmc/articles/PMC3772077/ /pubmed/24069183 http://dx.doi.org/10.1371/journal.pone.0073290 Text en © 2013 Opmeer et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Opmeer, Esther M.
Kortekaas, Rudie
van Tol, Marie-José
van der Wee, Nic J. A.
Woudstra, Saskia
van Buchem, Mark A.
Penninx, Brenda W.
Veltman, Dick J.
Aleman, André
Influence of COMT val158met Genotype on the Depressed Brain during Emotional Processing and Working Memory
title Influence of COMT val158met Genotype on the Depressed Brain during Emotional Processing and Working Memory
title_full Influence of COMT val158met Genotype on the Depressed Brain during Emotional Processing and Working Memory
title_fullStr Influence of COMT val158met Genotype on the Depressed Brain during Emotional Processing and Working Memory
title_full_unstemmed Influence of COMT val158met Genotype on the Depressed Brain during Emotional Processing and Working Memory
title_short Influence of COMT val158met Genotype on the Depressed Brain during Emotional Processing and Working Memory
title_sort influence of comt val158met genotype on the depressed brain during emotional processing and working memory
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3772077/
https://www.ncbi.nlm.nih.gov/pubmed/24069183
http://dx.doi.org/10.1371/journal.pone.0073290
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