Dopamine transporter genotype modulates brain activity during a working memory task in children with ADHD
Dopamine active transporter gene (DAT1) is a candidate gene associated with attention-deficit/hyperactivity disorder (ADHD). The DAT1 variable number tandem repeat (VNTR)-3’ polymorphism is functional and 9R carriers have been shown to produce more DAT than 10R homozygotes. We used functional magnet...
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Veröffentlicht in: | Research in developmental disabilities 2019-09, Vol.92, p.103430-103430, Article 103430 |
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creator | Pineau, Guillaume Villemonteix, Thomas Slama, Hichem Kavec, Martin Balériaux, Danielle Metens, Thierry Baijot, Simon Mary, Alison Ramoz, Nicolas Gorwood, Philip Peigneux, Philippe Massat, Isabelle |
description | Dopamine active transporter gene (DAT1) is a candidate gene associated with attention-deficit/hyperactivity disorder (ADHD). The DAT1 variable number tandem repeat (VNTR)-3’ polymorphism is functional and 9R carriers have been shown to produce more DAT than 10R homozygotes. We used functional magnetic resonance imaging (fMRI) to investigate the effects of this polymorphism on the neural substrates of working memory (WM) in a small but selected population of children with ADHD, naïve of any psychotropic treatment and without comorbidity. MRI and genotype data were obtained for 36 children (mean age: 10,36 +/− 1,49 years) with combined-type ADHD (9R n = 15) and 25 typically developing children (TDC) (mean age: 9,55 +/− 1,25 years) (9R n = 12). WM performance was similar between conditions. We found a cross-over interaction effect between gene (9R vs. 10R) and diagnosis (TDC vs. ADHD) in the orbito-frontal gyrus, cerebellum and inferior temporal lobe. In these areas, WM-related activity was higher for 9R carriers in ADHD subjects and lower in TDC. In ADHD children only, 10R homozygotes exhibited higher WM-related activity than 9R carriers in a network encompassing the parietal and the temporal lobes, the ventral visual cortex, the orbito-frontal gyrus and the head of the caudate nucleus. There was no significant results in TDC group. Our preliminary findings suggest that DAT1 VNTR polymorphism can modulate WM-related brain activity ADHD children. |
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The DAT1 variable number tandem repeat (VNTR)-3’ polymorphism is functional and 9R carriers have been shown to produce more DAT than 10R homozygotes. We used functional magnetic resonance imaging (fMRI) to investigate the effects of this polymorphism on the neural substrates of working memory (WM) in a small but selected population of children with ADHD, naïve of any psychotropic treatment and without comorbidity. MRI and genotype data were obtained for 36 children (mean age: 10,36 +/− 1,49 years) with combined-type ADHD (9R n = 15) and 25 typically developing children (TDC) (mean age: 9,55 +/− 1,25 years) (9R n = 12). WM performance was similar between conditions. We found a cross-over interaction effect between gene (9R vs. 10R) and diagnosis (TDC vs. ADHD) in the orbito-frontal gyrus, cerebellum and inferior temporal lobe. In these areas, WM-related activity was higher for 9R carriers in ADHD subjects and lower in TDC. In ADHD children only, 10R homozygotes exhibited higher WM-related activity than 9R carriers in a network encompassing the parietal and the temporal lobes, the ventral visual cortex, the orbito-frontal gyrus and the head of the caudate nucleus. There was no significant results in TDC group. Our preliminary findings suggest that DAT1 VNTR polymorphism can modulate WM-related brain activity ADHD children.</description><identifier>ISSN: 0891-4222</identifier><identifier>EISSN: 1873-3379</identifier><identifier>DOI: 10.1016/j.ridd.2019.103430</identifier><identifier>PMID: 31306870</identifier><language>eng</language><publisher>United States: Elsevier Ltd</publisher><subject>Attention Deficit Disorder with Hyperactivity - genetics ; Attention Deficit Disorder with Hyperactivity - psychology ; Attention deficit/hyperactivity disorder (ADHD) ; Brain - diagnostic imaging ; Brain - physiopathology ; Caudate nucleus ; Cerebellum ; Child ; Cognitive science ; Correlation of Data ; DAT1 VNTR polymorphism ; Dopamine Plasma Membrane Transport Proteins - genetics ; Female ; fMRI ; Humans ; Magnetic Resonance Imaging - methods ; Male ; Memory, Short-Term - physiology ; Minisatellite Repeats - genetics ; Polymorphism, Genetic ; Working memory</subject><ispartof>Research in developmental disabilities, 2019-09, Vol.92, p.103430-103430, Article 103430</ispartof><rights>2019 Elsevier Ltd</rights><rights>Copyright © 2019 Elsevier Ltd. All rights reserved.</rights><rights>Attribution - NonCommercial</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c434t-3bf682151f36e09180e2392d8a815fd50d5c23a6de6f44376b8d2e5f746915d63</citedby><cites>FETCH-LOGICAL-c434t-3bf682151f36e09180e2392d8a815fd50d5c23a6de6f44376b8d2e5f746915d63</cites><orcidid>0000-0002-8070-9938</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ridd.2019.103430$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31306870$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-03487339$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Pineau, Guillaume</creatorcontrib><creatorcontrib>Villemonteix, Thomas</creatorcontrib><creatorcontrib>Slama, Hichem</creatorcontrib><creatorcontrib>Kavec, Martin</creatorcontrib><creatorcontrib>Balériaux, Danielle</creatorcontrib><creatorcontrib>Metens, Thierry</creatorcontrib><creatorcontrib>Baijot, Simon</creatorcontrib><creatorcontrib>Mary, Alison</creatorcontrib><creatorcontrib>Ramoz, Nicolas</creatorcontrib><creatorcontrib>Gorwood, Philip</creatorcontrib><creatorcontrib>Peigneux, Philippe</creatorcontrib><creatorcontrib>Massat, Isabelle</creatorcontrib><title>Dopamine transporter genotype modulates brain activity during a working memory task in children with ADHD</title><title>Research in developmental disabilities</title><addtitle>Res Dev Disabil</addtitle><description>Dopamine active transporter gene (DAT1) is a candidate gene associated with attention-deficit/hyperactivity disorder (ADHD). The DAT1 variable number tandem repeat (VNTR)-3’ polymorphism is functional and 9R carriers have been shown to produce more DAT than 10R homozygotes. We used functional magnetic resonance imaging (fMRI) to investigate the effects of this polymorphism on the neural substrates of working memory (WM) in a small but selected population of children with ADHD, naïve of any psychotropic treatment and without comorbidity. MRI and genotype data were obtained for 36 children (mean age: 10,36 +/− 1,49 years) with combined-type ADHD (9R n = 15) and 25 typically developing children (TDC) (mean age: 9,55 +/− 1,25 years) (9R n = 12). WM performance was similar between conditions. We found a cross-over interaction effect between gene (9R vs. 10R) and diagnosis (TDC vs. ADHD) in the orbito-frontal gyrus, cerebellum and inferior temporal lobe. In these areas, WM-related activity was higher for 9R carriers in ADHD subjects and lower in TDC. In ADHD children only, 10R homozygotes exhibited higher WM-related activity than 9R carriers in a network encompassing the parietal and the temporal lobes, the ventral visual cortex, the orbito-frontal gyrus and the head of the caudate nucleus. There was no significant results in TDC group. Our preliminary findings suggest that DAT1 VNTR polymorphism can modulate WM-related brain activity ADHD children.</description><subject>Attention Deficit Disorder with Hyperactivity - genetics</subject><subject>Attention Deficit Disorder with Hyperactivity - psychology</subject><subject>Attention deficit/hyperactivity disorder (ADHD)</subject><subject>Brain - diagnostic imaging</subject><subject>Brain - physiopathology</subject><subject>Caudate nucleus</subject><subject>Cerebellum</subject><subject>Child</subject><subject>Cognitive science</subject><subject>Correlation of Data</subject><subject>DAT1 VNTR polymorphism</subject><subject>Dopamine Plasma Membrane Transport Proteins - genetics</subject><subject>Female</subject><subject>fMRI</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Male</subject><subject>Memory, Short-Term - physiology</subject><subject>Minisatellite Repeats - genetics</subject><subject>Polymorphism, Genetic</subject><subject>Working memory</subject><issn>0891-4222</issn><issn>1873-3379</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kT9v2zAQxYmiReKk-QIdCo7tIJd_JIoCuhhxUxcw0KWdCZo8xXQkUSUpB_72paA0Y3HDHR5-94b3EPpAyZoSKr6c1sFZu2aENlngJSdv0IrKmhec181btCKyoUXJGLtGNzGeCKF1nit0zSknQtZkhdzWj7p3A-AU9BBHHxIE_AiDT5cRcO_t1OkEER-CdgPWJrmzSxdsp-CGR6zxsw9P89VD78MFJx2fcAbN0XU2wICfXTrizXa3fY_etbqLcPeyb9Hvh2-_7nfF_uf3H_ebfWFKXqaCH1ohGa1oywWQhkoCjDfMSi1p1dqK2MowroUF0ZYlr8VBWgZVW5eioZUV_BZ9XnyPulNjcL0OF-W1U7vNXs1aTipnxJszzeynhR2D_zNBTKp30UDX6QH8FBVjlazLhrI6o2xBTfAxBmhfvSlRcx3qpOY61FyHWurITx9f_KdDD_b15V_-Gfi6AJATOTsIKhoHgwHrApikrHf_8_8LgV2a2w</recordid><startdate>20190901</startdate><enddate>20190901</enddate><creator>Pineau, Guillaume</creator><creator>Villemonteix, Thomas</creator><creator>Slama, Hichem</creator><creator>Kavec, Martin</creator><creator>Balériaux, Danielle</creator><creator>Metens, Thierry</creator><creator>Baijot, Simon</creator><creator>Mary, Alison</creator><creator>Ramoz, Nicolas</creator><creator>Gorwood, Philip</creator><creator>Peigneux, Philippe</creator><creator>Massat, Isabelle</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0002-8070-9938</orcidid></search><sort><creationdate>20190901</creationdate><title>Dopamine transporter genotype modulates brain activity during a working memory task in children with ADHD</title><author>Pineau, Guillaume ; Villemonteix, Thomas ; Slama, Hichem ; Kavec, Martin ; Balériaux, Danielle ; Metens, Thierry ; Baijot, Simon ; Mary, Alison ; Ramoz, Nicolas ; Gorwood, Philip ; Peigneux, Philippe ; Massat, Isabelle</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c434t-3bf682151f36e09180e2392d8a815fd50d5c23a6de6f44376b8d2e5f746915d63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Attention Deficit Disorder with Hyperactivity - genetics</topic><topic>Attention Deficit Disorder with Hyperactivity - psychology</topic><topic>Attention deficit/hyperactivity disorder (ADHD)</topic><topic>Brain - diagnostic imaging</topic><topic>Brain - physiopathology</topic><topic>Caudate nucleus</topic><topic>Cerebellum</topic><topic>Child</topic><topic>Cognitive science</topic><topic>Correlation of Data</topic><topic>DAT1 VNTR polymorphism</topic><topic>Dopamine Plasma Membrane Transport Proteins - genetics</topic><topic>Female</topic><topic>fMRI</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Male</topic><topic>Memory, Short-Term - physiology</topic><topic>Minisatellite Repeats - genetics</topic><topic>Polymorphism, Genetic</topic><topic>Working memory</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pineau, Guillaume</creatorcontrib><creatorcontrib>Villemonteix, Thomas</creatorcontrib><creatorcontrib>Slama, Hichem</creatorcontrib><creatorcontrib>Kavec, Martin</creatorcontrib><creatorcontrib>Balériaux, Danielle</creatorcontrib><creatorcontrib>Metens, Thierry</creatorcontrib><creatorcontrib>Baijot, Simon</creatorcontrib><creatorcontrib>Mary, Alison</creatorcontrib><creatorcontrib>Ramoz, Nicolas</creatorcontrib><creatorcontrib>Gorwood, Philip</creatorcontrib><creatorcontrib>Peigneux, Philippe</creatorcontrib><creatorcontrib>Massat, Isabelle</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Research in developmental disabilities</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pineau, Guillaume</au><au>Villemonteix, Thomas</au><au>Slama, Hichem</au><au>Kavec, Martin</au><au>Balériaux, Danielle</au><au>Metens, Thierry</au><au>Baijot, Simon</au><au>Mary, Alison</au><au>Ramoz, Nicolas</au><au>Gorwood, Philip</au><au>Peigneux, Philippe</au><au>Massat, Isabelle</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dopamine transporter genotype modulates brain activity during a working memory task in children with ADHD</atitle><jtitle>Research in developmental disabilities</jtitle><addtitle>Res Dev Disabil</addtitle><date>2019-09-01</date><risdate>2019</risdate><volume>92</volume><spage>103430</spage><epage>103430</epage><pages>103430-103430</pages><artnum>103430</artnum><issn>0891-4222</issn><eissn>1873-3379</eissn><abstract>Dopamine active transporter gene (DAT1) is a candidate gene associated with attention-deficit/hyperactivity disorder (ADHD). The DAT1 variable number tandem repeat (VNTR)-3’ polymorphism is functional and 9R carriers have been shown to produce more DAT than 10R homozygotes. We used functional magnetic resonance imaging (fMRI) to investigate the effects of this polymorphism on the neural substrates of working memory (WM) in a small but selected population of children with ADHD, naïve of any psychotropic treatment and without comorbidity. MRI and genotype data were obtained for 36 children (mean age: 10,36 +/− 1,49 years) with combined-type ADHD (9R n = 15) and 25 typically developing children (TDC) (mean age: 9,55 +/− 1,25 years) (9R n = 12). WM performance was similar between conditions. We found a cross-over interaction effect between gene (9R vs. 10R) and diagnosis (TDC vs. ADHD) in the orbito-frontal gyrus, cerebellum and inferior temporal lobe. In these areas, WM-related activity was higher for 9R carriers in ADHD subjects and lower in TDC. In ADHD children only, 10R homozygotes exhibited higher WM-related activity than 9R carriers in a network encompassing the parietal and the temporal lobes, the ventral visual cortex, the orbito-frontal gyrus and the head of the caudate nucleus. There was no significant results in TDC group. Our preliminary findings suggest that DAT1 VNTR polymorphism can modulate WM-related brain activity ADHD children.</abstract><cop>United States</cop><pub>Elsevier Ltd</pub><pmid>31306870</pmid><doi>10.1016/j.ridd.2019.103430</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-8070-9938</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Attention Deficit Disorder with Hyperactivity - genetics Attention Deficit Disorder with Hyperactivity - psychology Attention deficit/hyperactivity disorder (ADHD) Brain - diagnostic imaging Brain - physiopathology Caudate nucleus Cerebellum Child Cognitive science Correlation of Data DAT1 VNTR polymorphism Dopamine Plasma Membrane Transport Proteins - genetics Female fMRI Humans Magnetic Resonance Imaging - methods Male Memory, Short-Term - physiology Minisatellite Repeats - genetics Polymorphism, Genetic Working memory |
title | Dopamine transporter genotype modulates brain activity during a working memory task in children with ADHD |
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