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dc.date.accessioned2024-03-10T20:41:53Z
dc.date.available2024-03-10T20:41:53Z
dc.date.created2023-09-22T12:37:30Z
dc.date.issued2023
dc.identifier.citationWechsler, Daniel L. Rijsdijk, Fruhling V. Adamo, Nicoletta Eilertsen, Espen Moen Ahmadzadeh, Yasmin I. Badini, Isabella Hannigan, Laurie John Ystrøm, Eivind McAdams, Thomas Andrew . Assessing aetiological overlap between child and adult attention-deficit hyperactivity disorder symptoms in an extended family design. BJPsych Open. 2023, 9(5)
dc.identifier.urihttp://hdl.handle.net/10852/109448
dc.description.abstractBackground Several longitudinal studies have cast doubt on the aetiological overlap between child and adult attention-deficit hyperactivity disorder (ADHD). However, a lack of genetically sensitive data following children across adulthood precludes direct evaluation of aetiological overlap between child and adult ADHD. Aims We circumvent the existing gap in longitudinal data by exploring genetic overlap between maternal (adult) and offspring (child) ADHD and comorbid symptoms in an extended family cohort. Method Data were drawn from the Norwegian Mother, Father and Child Cohort Study, a Norwegian birth registry cohort of 114 500 children and their parents. Medical Birth Registry of Norway data were used to link extended families. Mothers self-reported their own ADHD symptoms when children were aged 3 years; reported children's ADHD symptoms at age 5 years; and children's ADHD, oppositional defiant disorder (ODD), conduct disorder, anxiety and depression symptoms at age 8 years. Genetic correlations were derived from Multiple-Children-of-Twins-and-Siblings and extended bivariate twin models. Results Phenotypic correlations between adult ADHD symptoms and child ADHD, ODD, conduct disorder, anxiety and depression symptoms at age 8 years were underpinned by medium-to-large genetic correlations (child ADHD: rG = 0.55, 95% CI 0.43−0.93; ODD: rG = 0.80, 95% CI 0.46−1; conduct disorder: rG = 0.44, 95% CI 0.28−1; anxiety: rG = 0.72, 95% CI 0.48−1; depression: rG = 1, 95% CI 0.66−1). These cross-generational adult–child genetic correlations were of a comparable magnitude to equivalent child–child genetic correlations with ADHD symptoms at age 5 years. Conclusions Our findings provide genetically sensitive evidence that ADHD symptoms in adulthood share a common genetic architecture with symptoms of ADHD and four comorbid disorders at age 8 years. These findings suggest that in the majority of cases, ADHD symptoms in adulthood are not aetiologically distinct from in childhood.
dc.languageEN
dc.publisherRoyal College of Psychiatrists
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleAssessing aetiological overlap between child and adult attention-deficit hyperactivity disorder symptoms in an extended family design
dc.title.alternativeENEngelskEnglishAssessing aetiological overlap between child and adult attention-deficit hyperactivity disorder symptoms in an extended family design
dc.typeJournal article
dc.creator.authorWechsler, Daniel L.
dc.creator.authorRijsdijk, Fruhling V.
dc.creator.authorAdamo, Nicoletta
dc.creator.authorEilertsen, Espen Moen
dc.creator.authorAhmadzadeh, Yasmin I.
dc.creator.authorBadini, Isabella
dc.creator.authorHannigan, Laurie John
dc.creator.authorYstrøm, Eivind
dc.creator.authorMcAdams, Thomas Andrew
cristin.unitcode185,17,5,7
cristin.unitnameHelse-, utviklings- og personlighetspsyk
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin2177907
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=BJPsych Open&rft.volume=9&rft.spage=&rft.date=2023
dc.identifier.jtitleBJPsych Open
dc.identifier.volume9
dc.identifier.issue5
dc.identifier.pagecount7
dc.identifier.doihttps://doi.org/10.1192/bjo.2023.554
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn2056-4724
dc.type.versionPublishedVersion
cristin.articleide169
dc.relation.projectNFR/262177
dc.relation.projectNFR/288083
dc.relation.projectHSØ/2018059


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