Interaction between COMT Val158Met polymorphism and childhood adversity affects reward processing in adulthood

Accumulating evidence suggests that altered dopamine transmission may increase the risk of mental disorders such as ADHD, schizophrenia or depression, possibly mediated by reward system dysfunction. This study aimed to clarify the impact of the COMT Val158Met polymorphism in interaction with environ...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:NeuroImage (Orlando, Fla.) Fla.), 2016-05, Vol.132, p.556-570
Hauptverfasser: Boecker-Schlier, Regina, Holz, Nathalie E., Buchmann, Arlette F., Blomeyer, Dorothea, Plichta, Michael M., Jennen-Steinmetz, Christine, Wolf, Isabella, Baumeister, Sarah, Treutlein, Jens, Rietschel, Marcella, Meyer-Lindenberg, Andreas, Banaschewski, Tobias, Brandeis, Daniel, Laucht, Manfred
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 570
container_issue
container_start_page 556
container_title NeuroImage (Orlando, Fla.)
container_volume 132
creator Boecker-Schlier, Regina
Holz, Nathalie E.
Buchmann, Arlette F.
Blomeyer, Dorothea
Plichta, Michael M.
Jennen-Steinmetz, Christine
Wolf, Isabella
Baumeister, Sarah
Treutlein, Jens
Rietschel, Marcella
Meyer-Lindenberg, Andreas
Banaschewski, Tobias
Brandeis, Daniel
Laucht, Manfred
description Accumulating evidence suggests that altered dopamine transmission may increase the risk of mental disorders such as ADHD, schizophrenia or depression, possibly mediated by reward system dysfunction. This study aimed to clarify the impact of the COMT Val158Met polymorphism in interaction with environmental variation (G×E) on neuronal activity during reward processing. 168 healthy young adults from a prospective study conducted over 25years participated in a monetary incentive delay task measured with simultaneous EEG-fMRI. DNA was genotyped for COMT, and childhood family adversity (CFA) up to age 11 was assessed by a standardized parent interview. At reward delivery, a G×E revealed that fMRI activation for win vs. no-win trials in reward-related regions increased with the level of CFA in Met homozygotes as compared to Val/Met heterozygotes and Val homozygotes, who showed no significant effect. During the anticipation of monetary vs. verbal rewards, activation decreased with the level of CFA, which was also observed for EEG, in which the CNV declined with the level of CFA. These results identify convergent genetic and environmental effects on reward processing in a prospective study. Moreover, G×E effects during reward delivery suggest that stress during childhood is associated with higher reward sensitivity and reduced efficiency in processing rewarding stimuli in genetically at-risk individuals. Together with previous evidence, these results begin to define a specific system mediating interacting effects of early environmental and genetic risk factors, which may be targeted by early intervention and prevention. •Interaction between COMT and childhood adversity on reward processing was examined.•fMRI activity of Met homozygotes increased with adversity at reward delivery.•fMRI activity decreased with childhood adversity during reward anticipation.•Anticipatory EEG activity decreases with adversity provided converging evidence.
doi_str_mv 10.1016/j.neuroimage.2016.02.006
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1787958468</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S105381191600104X</els_id><sourcerecordid>4044399241</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2248-768f7f0c12bee34742b19c56a585697a6c51e9c40e45cfcd8a3f768d24d003a23</originalsourceid><addsrcrecordid>eNqFkU9LAzEQxRdRsFa_Q8CLl12T7GY3e9Tin0JLL9VrSJPZNmWb1GS3pd_eLBUEL55mGH5vmHkvSRDBGcGkfNxmFnrvzE6uIaNxkmGaYVxeJCOCa5bWrKKXQ8_ylBNSXyc3IWwxxjUp-CixU9uBl6ozzqIVdEcAiyaL-RJ9ypYwPocO7V172jm_35iwQ9JqpDam1RvnNJL6AD6Y7oRk04DqAvJwlF6jvXcKQjB2jYyNWN92g-A2uWpkG-Dup46Tj9eX5eQ9nS3eppOnWaooLXhalbypGqwIXQHkRVXQFakVKyXjrKwrWSpGoFYFhoKpRmku8yZqNC00xrmk-Th5OO-Nd3z1EDqxM0FB20oLrg-CVLyqGS9KHtH7P-jW9d7G6waqrHLGcB4pfqaUdyF4aMTeR8_9SRAshiDEVvwGIYYgBKYiBhGlz2cpxIcPBrwIyoBVoI2PlgntzP9LvgGv6Jdy</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1786735503</pqid></control><display><type>article</type><title>Interaction between COMT Val158Met polymorphism and childhood adversity affects reward processing in adulthood</title><source>Elsevier ScienceDirect Journals</source><creator>Boecker-Schlier, Regina ; Holz, Nathalie E. ; Buchmann, Arlette F. ; Blomeyer, Dorothea ; Plichta, Michael M. ; Jennen-Steinmetz, Christine ; Wolf, Isabella ; Baumeister, Sarah ; Treutlein, Jens ; Rietschel, Marcella ; Meyer-Lindenberg, Andreas ; Banaschewski, Tobias ; Brandeis, Daniel ; Laucht, Manfred</creator><creatorcontrib>Boecker-Schlier, Regina ; Holz, Nathalie E. ; Buchmann, Arlette F. ; Blomeyer, Dorothea ; Plichta, Michael M. ; Jennen-Steinmetz, Christine ; Wolf, Isabella ; Baumeister, Sarah ; Treutlein, Jens ; Rietschel, Marcella ; Meyer-Lindenberg, Andreas ; Banaschewski, Tobias ; Brandeis, Daniel ; Laucht, Manfred</creatorcontrib><description>Accumulating evidence suggests that altered dopamine transmission may increase the risk of mental disorders such as ADHD, schizophrenia or depression, possibly mediated by reward system dysfunction. This study aimed to clarify the impact of the COMT Val158Met polymorphism in interaction with environmental variation (G×E) on neuronal activity during reward processing. 168 healthy young adults from a prospective study conducted over 25years participated in a monetary incentive delay task measured with simultaneous EEG-fMRI. DNA was genotyped for COMT, and childhood family adversity (CFA) up to age 11 was assessed by a standardized parent interview. At reward delivery, a G×E revealed that fMRI activation for win vs. no-win trials in reward-related regions increased with the level of CFA in Met homozygotes as compared to Val/Met heterozygotes and Val homozygotes, who showed no significant effect. During the anticipation of monetary vs. verbal rewards, activation decreased with the level of CFA, which was also observed for EEG, in which the CNV declined with the level of CFA. These results identify convergent genetic and environmental effects on reward processing in a prospective study. Moreover, G×E effects during reward delivery suggest that stress during childhood is associated with higher reward sensitivity and reduced efficiency in processing rewarding stimuli in genetically at-risk individuals. Together with previous evidence, these results begin to define a specific system mediating interacting effects of early environmental and genetic risk factors, which may be targeted by early intervention and prevention. •Interaction between COMT and childhood adversity on reward processing was examined.•fMRI activity of Met homozygotes increased with adversity at reward delivery.•fMRI activity decreased with childhood adversity during reward anticipation.•Anticipatory EEG activity decreases with adversity provided converging evidence.</description><identifier>ISSN: 1053-8119</identifier><identifier>EISSN: 1095-9572</identifier><identifier>DOI: 10.1016/j.neuroimage.2016.02.006</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>Brain ; Childhood adversity ; COMT Val158Met polymorphism ; Dopamine ; Electroencephalography ; Functional magnetic resonance imaging ; Gene–environment interaction ; Genotype &amp; phenotype ; Reward processing</subject><ispartof>NeuroImage (Orlando, Fla.), 2016-05, Vol.132, p.556-570</ispartof><rights>2016 Elsevier Inc.</rights><rights>Copyright Elsevier Limited May 15, 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2248-768f7f0c12bee34742b19c56a585697a6c51e9c40e45cfcd8a3f768d24d003a23</citedby><cites>FETCH-LOGICAL-c2248-768f7f0c12bee34742b19c56a585697a6c51e9c40e45cfcd8a3f768d24d003a23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S105381191600104X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids></links><search><creatorcontrib>Boecker-Schlier, Regina</creatorcontrib><creatorcontrib>Holz, Nathalie E.</creatorcontrib><creatorcontrib>Buchmann, Arlette F.</creatorcontrib><creatorcontrib>Blomeyer, Dorothea</creatorcontrib><creatorcontrib>Plichta, Michael M.</creatorcontrib><creatorcontrib>Jennen-Steinmetz, Christine</creatorcontrib><creatorcontrib>Wolf, Isabella</creatorcontrib><creatorcontrib>Baumeister, Sarah</creatorcontrib><creatorcontrib>Treutlein, Jens</creatorcontrib><creatorcontrib>Rietschel, Marcella</creatorcontrib><creatorcontrib>Meyer-Lindenberg, Andreas</creatorcontrib><creatorcontrib>Banaschewski, Tobias</creatorcontrib><creatorcontrib>Brandeis, Daniel</creatorcontrib><creatorcontrib>Laucht, Manfred</creatorcontrib><title>Interaction between COMT Val158Met polymorphism and childhood adversity affects reward processing in adulthood</title><title>NeuroImage (Orlando, Fla.)</title><description>Accumulating evidence suggests that altered dopamine transmission may increase the risk of mental disorders such as ADHD, schizophrenia or depression, possibly mediated by reward system dysfunction. This study aimed to clarify the impact of the COMT Val158Met polymorphism in interaction with environmental variation (G×E) on neuronal activity during reward processing. 168 healthy young adults from a prospective study conducted over 25years participated in a monetary incentive delay task measured with simultaneous EEG-fMRI. DNA was genotyped for COMT, and childhood family adversity (CFA) up to age 11 was assessed by a standardized parent interview. At reward delivery, a G×E revealed that fMRI activation for win vs. no-win trials in reward-related regions increased with the level of CFA in Met homozygotes as compared to Val/Met heterozygotes and Val homozygotes, who showed no significant effect. During the anticipation of monetary vs. verbal rewards, activation decreased with the level of CFA, which was also observed for EEG, in which the CNV declined with the level of CFA. These results identify convergent genetic and environmental effects on reward processing in a prospective study. Moreover, G×E effects during reward delivery suggest that stress during childhood is associated with higher reward sensitivity and reduced efficiency in processing rewarding stimuli in genetically at-risk individuals. Together with previous evidence, these results begin to define a specific system mediating interacting effects of early environmental and genetic risk factors, which may be targeted by early intervention and prevention. •Interaction between COMT and childhood adversity on reward processing was examined.•fMRI activity of Met homozygotes increased with adversity at reward delivery.•fMRI activity decreased with childhood adversity during reward anticipation.•Anticipatory EEG activity decreases with adversity provided converging evidence.</description><subject>Brain</subject><subject>Childhood adversity</subject><subject>COMT Val158Met polymorphism</subject><subject>Dopamine</subject><subject>Electroencephalography</subject><subject>Functional magnetic resonance imaging</subject><subject>Gene–environment interaction</subject><subject>Genotype &amp; phenotype</subject><subject>Reward processing</subject><issn>1053-8119</issn><issn>1095-9572</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNqFkU9LAzEQxRdRsFa_Q8CLl12T7GY3e9Tin0JLL9VrSJPZNmWb1GS3pd_eLBUEL55mGH5vmHkvSRDBGcGkfNxmFnrvzE6uIaNxkmGaYVxeJCOCa5bWrKKXQ8_ylBNSXyc3IWwxxjUp-CixU9uBl6ozzqIVdEcAiyaL-RJ9ypYwPocO7V172jm_35iwQ9JqpDam1RvnNJL6AD6Y7oRk04DqAvJwlF6jvXcKQjB2jYyNWN92g-A2uWpkG-Dup46Tj9eX5eQ9nS3eppOnWaooLXhalbypGqwIXQHkRVXQFakVKyXjrKwrWSpGoFYFhoKpRmku8yZqNC00xrmk-Th5OO-Nd3z1EDqxM0FB20oLrg-CVLyqGS9KHtH7P-jW9d7G6waqrHLGcB4pfqaUdyF4aMTeR8_9SRAshiDEVvwGIYYgBKYiBhGlz2cpxIcPBrwIyoBVoI2PlgntzP9LvgGv6Jdy</recordid><startdate>20160515</startdate><enddate>20160515</enddate><creator>Boecker-Schlier, Regina</creator><creator>Holz, Nathalie E.</creator><creator>Buchmann, Arlette F.</creator><creator>Blomeyer, Dorothea</creator><creator>Plichta, Michael M.</creator><creator>Jennen-Steinmetz, Christine</creator><creator>Wolf, Isabella</creator><creator>Baumeister, Sarah</creator><creator>Treutlein, Jens</creator><creator>Rietschel, Marcella</creator><creator>Meyer-Lindenberg, Andreas</creator><creator>Banaschewski, Tobias</creator><creator>Brandeis, Daniel</creator><creator>Laucht, Manfred</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>RC3</scope><scope>7QO</scope></search><sort><creationdate>20160515</creationdate><title>Interaction between COMT Val158Met polymorphism and childhood adversity affects reward processing in adulthood</title><author>Boecker-Schlier, Regina ; Holz, Nathalie E. ; Buchmann, Arlette F. ; Blomeyer, Dorothea ; Plichta, Michael M. ; Jennen-Steinmetz, Christine ; Wolf, Isabella ; Baumeister, Sarah ; Treutlein, Jens ; Rietschel, Marcella ; Meyer-Lindenberg, Andreas ; Banaschewski, Tobias ; Brandeis, Daniel ; Laucht, Manfred</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2248-768f7f0c12bee34742b19c56a585697a6c51e9c40e45cfcd8a3f768d24d003a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Brain</topic><topic>Childhood adversity</topic><topic>COMT Val158Met polymorphism</topic><topic>Dopamine</topic><topic>Electroencephalography</topic><topic>Functional magnetic resonance imaging</topic><topic>Gene–environment interaction</topic><topic>Genotype &amp; phenotype</topic><topic>Reward processing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Boecker-Schlier, Regina</creatorcontrib><creatorcontrib>Holz, Nathalie E.</creatorcontrib><creatorcontrib>Buchmann, Arlette F.</creatorcontrib><creatorcontrib>Blomeyer, Dorothea</creatorcontrib><creatorcontrib>Plichta, Michael M.</creatorcontrib><creatorcontrib>Jennen-Steinmetz, Christine</creatorcontrib><creatorcontrib>Wolf, Isabella</creatorcontrib><creatorcontrib>Baumeister, Sarah</creatorcontrib><creatorcontrib>Treutlein, Jens</creatorcontrib><creatorcontrib>Rietschel, Marcella</creatorcontrib><creatorcontrib>Meyer-Lindenberg, Andreas</creatorcontrib><creatorcontrib>Banaschewski, Tobias</creatorcontrib><creatorcontrib>Brandeis, Daniel</creatorcontrib><creatorcontrib>Laucht, Manfred</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>Biotechnology Research Abstracts</collection><jtitle>NeuroImage (Orlando, Fla.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Boecker-Schlier, Regina</au><au>Holz, Nathalie E.</au><au>Buchmann, Arlette F.</au><au>Blomeyer, Dorothea</au><au>Plichta, Michael M.</au><au>Jennen-Steinmetz, Christine</au><au>Wolf, Isabella</au><au>Baumeister, Sarah</au><au>Treutlein, Jens</au><au>Rietschel, Marcella</au><au>Meyer-Lindenberg, Andreas</au><au>Banaschewski, Tobias</au><au>Brandeis, Daniel</au><au>Laucht, Manfred</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interaction between COMT Val158Met polymorphism and childhood adversity affects reward processing in adulthood</atitle><jtitle>NeuroImage (Orlando, Fla.)</jtitle><date>2016-05-15</date><risdate>2016</risdate><volume>132</volume><spage>556</spage><epage>570</epage><pages>556-570</pages><issn>1053-8119</issn><eissn>1095-9572</eissn><abstract>Accumulating evidence suggests that altered dopamine transmission may increase the risk of mental disorders such as ADHD, schizophrenia or depression, possibly mediated by reward system dysfunction. This study aimed to clarify the impact of the COMT Val158Met polymorphism in interaction with environmental variation (G×E) on neuronal activity during reward processing. 168 healthy young adults from a prospective study conducted over 25years participated in a monetary incentive delay task measured with simultaneous EEG-fMRI. DNA was genotyped for COMT, and childhood family adversity (CFA) up to age 11 was assessed by a standardized parent interview. At reward delivery, a G×E revealed that fMRI activation for win vs. no-win trials in reward-related regions increased with the level of CFA in Met homozygotes as compared to Val/Met heterozygotes and Val homozygotes, who showed no significant effect. During the anticipation of monetary vs. verbal rewards, activation decreased with the level of CFA, which was also observed for EEG, in which the CNV declined with the level of CFA. These results identify convergent genetic and environmental effects on reward processing in a prospective study. Moreover, G×E effects during reward delivery suggest that stress during childhood is associated with higher reward sensitivity and reduced efficiency in processing rewarding stimuli in genetically at-risk individuals. Together with previous evidence, these results begin to define a specific system mediating interacting effects of early environmental and genetic risk factors, which may be targeted by early intervention and prevention. •Interaction between COMT and childhood adversity on reward processing was examined.•fMRI activity of Met homozygotes increased with adversity at reward delivery.•fMRI activity decreased with childhood adversity during reward anticipation.•Anticipatory EEG activity decreases with adversity provided converging evidence.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><doi>10.1016/j.neuroimage.2016.02.006</doi><tpages>15</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1053-8119
ispartof NeuroImage (Orlando, Fla.), 2016-05, Vol.132, p.556-570
issn 1053-8119
1095-9572
language eng
recordid cdi_proquest_miscellaneous_1787958468
source Elsevier ScienceDirect Journals
subjects Brain
Childhood adversity
COMT Val158Met polymorphism
Dopamine
Electroencephalography
Functional magnetic resonance imaging
Gene–environment interaction
Genotype & phenotype
Reward processing
title Interaction between COMT Val158Met polymorphism and childhood adversity affects reward processing in adulthood
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-04T21%3A51%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Interaction%20between%20COMT%20Val158Met%20polymorphism%20and%20childhood%20adversity%20affects%20reward%20processing%20in%20adulthood&rft.jtitle=NeuroImage%20(Orlando,%20Fla.)&rft.au=Boecker-Schlier,%20Regina&rft.date=2016-05-15&rft.volume=132&rft.spage=556&rft.epage=570&rft.pages=556-570&rft.issn=1053-8119&rft.eissn=1095-9572&rft_id=info:doi/10.1016/j.neuroimage.2016.02.006&rft_dat=%3Cproquest_cross%3E4044399241%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1786735503&rft_id=info:pmid/&rft_els_id=S105381191600104X&rfr_iscdi=true