Shared genetic background between children and adults with attention deficit/hyperactivity disorder
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRGS |
Texto Completo: | http://hdl.handle.net/10183/217931 |
Resumo: | Attention deficit/hyperactivity disorder (ADHD) is a common neurodevelopmental disorder characterized by age-inappropriate symptoms of inattention, impulsivity, and hyperactivity that persist into adulthood in the majority of the diagnosed children. Despite several risk factors during childhood predicting the persistence of ADHD symptoms into adulthood, the genetic architecture underlying the trajectory of ADHD over time is still unclear. We set out to study the contribution of common genetic variants to the risk for ADHD across the lifespan by conducting meta-analyses of genome-wide association studies on persistent ADHD in adults and ADHD in childhood separately and jointly, and by comparing the genetic background between them in a total sample of 17,149 cases and 32,411 controls. Our results show nine new independent loci and support a shared contribution of common genetic variants to ADHD in children and adults. No subgroup heterogeneity was observed among children, while this group consists of future remitting and persistent individuals. We report similar patterns of genetic correlation of ADHD with other ADHD-related datasets and different traits and disorders among adults, children, and when combining both groups. These findings confirm that persistent ADHD in adults is a neurodevelopmental disorder and extend the existing hypothesis of a shared genetic architecture underlying ADHD and different traits to a lifespan perspective |
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Rovira, PaulaGrevet, Eugenio HorácioHutz, Mara HelenaRovaris, Diego LuizOliveira, Angélica Salatino deSilva, Bruna Santos daBau, Claiton Henrique DottoRohde, Luis Augusto PaimRibasés, Marta2021-02-12T04:06:00Z20200893-133Xhttp://hdl.handle.net/10183/217931001121246Attention deficit/hyperactivity disorder (ADHD) is a common neurodevelopmental disorder characterized by age-inappropriate symptoms of inattention, impulsivity, and hyperactivity that persist into adulthood in the majority of the diagnosed children. Despite several risk factors during childhood predicting the persistence of ADHD symptoms into adulthood, the genetic architecture underlying the trajectory of ADHD over time is still unclear. We set out to study the contribution of common genetic variants to the risk for ADHD across the lifespan by conducting meta-analyses of genome-wide association studies on persistent ADHD in adults and ADHD in childhood separately and jointly, and by comparing the genetic background between them in a total sample of 17,149 cases and 32,411 controls. Our results show nine new independent loci and support a shared contribution of common genetic variants to ADHD in children and adults. No subgroup heterogeneity was observed among children, while this group consists of future remitting and persistent individuals. We report similar patterns of genetic correlation of ADHD with other ADHD-related datasets and different traits and disorders among adults, children, and when combining both groups. These findings confirm that persistent ADHD in adults is a neurodevelopmental disorder and extend the existing hypothesis of a shared genetic architecture underlying ADHD and different traits to a lifespan perspectiveapplication/pdfengNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology. London. Vol. 45 (2020), p. 1617–1626Marcadores genéticosTranstorno do déficit de atenção com hiperatividadeCriançaAdultoMetanálisePatrimônio genéticoShared genetic background between children and adults with attention deficit/hyperactivity disorderEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001121246.pdf.txt001121246.pdf.txtExtracted Texttext/plain70749http://www.lume.ufrgs.br/bitstream/10183/217931/2/001121246.pdf.txt32b199e62643f63f27a0fa7689aaa2ddMD52ORIGINAL001121246.pdfTexto completo (inglês)application/pdf2173454http://www.lume.ufrgs.br/bitstream/10183/217931/1/001121246.pdff8b7a6592ce0ca997a91a07e5abccd73MD5110183/2179312021-03-09 04:29:26.277583oai:www.lume.ufrgs.br:10183/217931Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2021-03-09T07:29:26Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.pt_BR.fl_str_mv |
Shared genetic background between children and adults with attention deficit/hyperactivity disorder |
title |
Shared genetic background between children and adults with attention deficit/hyperactivity disorder |
spellingShingle |
Shared genetic background between children and adults with attention deficit/hyperactivity disorder Rovira, Paula Marcadores genéticos Transtorno do déficit de atenção com hiperatividade Criança Adulto Metanálise Patrimônio genético |
title_short |
Shared genetic background between children and adults with attention deficit/hyperactivity disorder |
title_full |
Shared genetic background between children and adults with attention deficit/hyperactivity disorder |
title_fullStr |
Shared genetic background between children and adults with attention deficit/hyperactivity disorder |
title_full_unstemmed |
Shared genetic background between children and adults with attention deficit/hyperactivity disorder |
title_sort |
Shared genetic background between children and adults with attention deficit/hyperactivity disorder |
author |
Rovira, Paula |
author_facet |
Rovira, Paula Grevet, Eugenio Horácio Hutz, Mara Helena Rovaris, Diego Luiz Oliveira, Angélica Salatino de Silva, Bruna Santos da Bau, Claiton Henrique Dotto Rohde, Luis Augusto Paim Ribasés, Marta |
author_role |
author |
author2 |
Grevet, Eugenio Horácio Hutz, Mara Helena Rovaris, Diego Luiz Oliveira, Angélica Salatino de Silva, Bruna Santos da Bau, Claiton Henrique Dotto Rohde, Luis Augusto Paim Ribasés, Marta |
author2_role |
author author author author author author author author |
dc.contributor.author.fl_str_mv |
Rovira, Paula Grevet, Eugenio Horácio Hutz, Mara Helena Rovaris, Diego Luiz Oliveira, Angélica Salatino de Silva, Bruna Santos da Bau, Claiton Henrique Dotto Rohde, Luis Augusto Paim Ribasés, Marta |
dc.subject.por.fl_str_mv |
Marcadores genéticos Transtorno do déficit de atenção com hiperatividade Criança Adulto Metanálise Patrimônio genético |
topic |
Marcadores genéticos Transtorno do déficit de atenção com hiperatividade Criança Adulto Metanálise Patrimônio genético |
description |
Attention deficit/hyperactivity disorder (ADHD) is a common neurodevelopmental disorder characterized by age-inappropriate symptoms of inattention, impulsivity, and hyperactivity that persist into adulthood in the majority of the diagnosed children. Despite several risk factors during childhood predicting the persistence of ADHD symptoms into adulthood, the genetic architecture underlying the trajectory of ADHD over time is still unclear. We set out to study the contribution of common genetic variants to the risk for ADHD across the lifespan by conducting meta-analyses of genome-wide association studies on persistent ADHD in adults and ADHD in childhood separately and jointly, and by comparing the genetic background between them in a total sample of 17,149 cases and 32,411 controls. Our results show nine new independent loci and support a shared contribution of common genetic variants to ADHD in children and adults. No subgroup heterogeneity was observed among children, while this group consists of future remitting and persistent individuals. We report similar patterns of genetic correlation of ADHD with other ADHD-related datasets and different traits and disorders among adults, children, and when combining both groups. These findings confirm that persistent ADHD in adults is a neurodevelopmental disorder and extend the existing hypothesis of a shared genetic architecture underlying ADHD and different traits to a lifespan perspective |
publishDate |
2020 |
dc.date.issued.fl_str_mv |
2020 |
dc.date.accessioned.fl_str_mv |
2021-02-12T04:06:00Z |
dc.type.driver.fl_str_mv |
Estrangeiro info:eu-repo/semantics/article |
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0893-133X |
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001121246 |
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http://hdl.handle.net/10183/217931 |
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eng |
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eng |
dc.relation.ispartof.pt_BR.fl_str_mv |
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology. London. Vol. 45 (2020), p. 1617–1626 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf |
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