Modulatory effects of the piccolo genotype on emotional memory in health and depression.

Major depressive disorder (MDD) has been associated with biased memory formation for mood-congruent information, which may be related to altered monoamine levels. The piccolo (PCLO) gene, involved in monoaminergic neurotransmission, has previously been linked to depression in a genome-wide associati...

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Main Authors: Saskia Woudstra, Marie-José van Tol, Zoltán Bochdanovits, Nic J van der Wee, Frans G Zitman, Mark A van Buchem, Esther M Opmeer, André Aleman, Brenda W Penninx, Dick J Veltman, Witte J Hoogendijk
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3631241?pdf=render
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author Saskia Woudstra
Marie-José van Tol
Zoltán Bochdanovits
Nic J van der Wee
Frans G Zitman
Mark A van Buchem
Esther M Opmeer
André Aleman
Brenda W Penninx
Dick J Veltman
Witte J Hoogendijk
author_facet Saskia Woudstra
Marie-José van Tol
Zoltán Bochdanovits
Nic J van der Wee
Frans G Zitman
Mark A van Buchem
Esther M Opmeer
André Aleman
Brenda W Penninx
Dick J Veltman
Witte J Hoogendijk
author_sort Saskia Woudstra
collection DOAJ
description Major depressive disorder (MDD) has been associated with biased memory formation for mood-congruent information, which may be related to altered monoamine levels. The piccolo (PCLO) gene, involved in monoaminergic neurotransmission, has previously been linked to depression in a genome-wide association study. Here, we investigated the role of the PCLO risk allele on functional magnetic resonance imaging (MRI) correlates of emotional memory in a sample of 89 MDD patients (64 PCLO risk allele carriers) and 29 healthy controls (18 PCLO risk allele carriers). During negative word encoding, risk allele carriers showed significant lower activity relative to non-risk allele carriers in the insula, and trend-wise in the anterior cingulate cortex and inferior frontal gyrus. Moreover, depressed risk allele carriers showed significant lower activity relative to non-risk allele carriers in the striatum, an effect which was absent in healthy controls. Finally, amygdalar response during processing new positive words vs. known words was blunted in healthy PCLO+ carriers and in MDD patients irrespective of genotype, which may indicate that signalling of salient novel information does not occur to the same extent in PCLO+ carriers and MDD patients. The PCLO risk allele may increase vulnerability for MDD by modulating local brain function with regard to responsiveness to salient stimuli (i.e. insula) and processing novel negative information. Also, depression-specific effects of PCLO on dorsal striatal activation during negative word encoding and the absence of amygdalar salience signalling for novel positive information further suggest a role of PCLO in symptom maintenance in MDD.
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spelling doaj.art-111afbf5b34d48719109a9c6349935da2022-12-22T02:37:07ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0184e6149410.1371/journal.pone.0061494Modulatory effects of the piccolo genotype on emotional memory in health and depression.Saskia WoudstraMarie-José van TolZoltán BochdanovitsNic J van der WeeFrans G ZitmanMark A van BuchemEsther M OpmeerAndré AlemanBrenda W PenninxDick J VeltmanWitte J HoogendijkMajor depressive disorder (MDD) has been associated with biased memory formation for mood-congruent information, which may be related to altered monoamine levels. The piccolo (PCLO) gene, involved in monoaminergic neurotransmission, has previously been linked to depression in a genome-wide association study. Here, we investigated the role of the PCLO risk allele on functional magnetic resonance imaging (MRI) correlates of emotional memory in a sample of 89 MDD patients (64 PCLO risk allele carriers) and 29 healthy controls (18 PCLO risk allele carriers). During negative word encoding, risk allele carriers showed significant lower activity relative to non-risk allele carriers in the insula, and trend-wise in the anterior cingulate cortex and inferior frontal gyrus. Moreover, depressed risk allele carriers showed significant lower activity relative to non-risk allele carriers in the striatum, an effect which was absent in healthy controls. Finally, amygdalar response during processing new positive words vs. known words was blunted in healthy PCLO+ carriers and in MDD patients irrespective of genotype, which may indicate that signalling of salient novel information does not occur to the same extent in PCLO+ carriers and MDD patients. The PCLO risk allele may increase vulnerability for MDD by modulating local brain function with regard to responsiveness to salient stimuli (i.e. insula) and processing novel negative information. Also, depression-specific effects of PCLO on dorsal striatal activation during negative word encoding and the absence of amygdalar salience signalling for novel positive information further suggest a role of PCLO in symptom maintenance in MDD.http://europepmc.org/articles/PMC3631241?pdf=render
spellingShingle Saskia Woudstra
Marie-José van Tol
Zoltán Bochdanovits
Nic J van der Wee
Frans G Zitman
Mark A van Buchem
Esther M Opmeer
André Aleman
Brenda W Penninx
Dick J Veltman
Witte J Hoogendijk
Modulatory effects of the piccolo genotype on emotional memory in health and depression.
PLoS ONE
title Modulatory effects of the piccolo genotype on emotional memory in health and depression.
title_full Modulatory effects of the piccolo genotype on emotional memory in health and depression.
title_fullStr Modulatory effects of the piccolo genotype on emotional memory in health and depression.
title_full_unstemmed Modulatory effects of the piccolo genotype on emotional memory in health and depression.
title_short Modulatory effects of the piccolo genotype on emotional memory in health and depression.
title_sort modulatory effects of the piccolo genotype on emotional memory in health and depression
url http://europepmc.org/articles/PMC3631241?pdf=render
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