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      Persistence, Remission and Emergence of ADHD in Young Adulthood: Results from a Longitudinal, Prospective Population-Based Cohort

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          Abstract

          Importance

          ADHD is now recognized to occur in adulthood and is associated with a range of negative outcomes. However, less is known about the prospective course of ADHD into adulthood, the risk factors for its persistence past childhood, and the possibility of its emergence in young adulthood in non-clinical populations.

          Objective

          To investigate childhood risk factors and young adult functioning of individuals with persistent, remitted and late-onset ADHD.

          Design, Setting and Participants

          The study sample is the Environmental Risk (E-Risk) Longitudinal Twin Study, a UK nationally-representative birth cohort of 2,232 twins born in England and Wales in 1994–1995.

          Main Outcome Measures

          ADHD diagnoses were assessed in childhood at ages 5, 7, 10, and 12 and in young adulthood at age 18. Childhood predictors included pre/perinatal factors, child clinical characteristics and aspects of the family environment. Age-18 outcomes included ADHD symptoms and associated impairment, overall functioning and other mental health disorders.

          Results

          Among individuals with childhood ADHD (n=247), 21.1% met diagnostic criteria for the disorder at age 18. Persistence was associated with higher levels of symptoms and lower IQ in childhood. Persistent individuals had more functional impairment and higher rates of other mental health disorders at age 18 compared to those who remitted. Among individuals with adult ADHD (n=162), 67.9% did not meet criteria for ADHD at any assessment at or prior to age 12. In childhood, individuals with late-onset ADHD showed fewer behavior problems and higher IQ compared to the persistent group; at age 18, they showed comparable ADHD symptoms and impairment and similarly elevated rates of mental health disorders compared to the persistent group.

          Conclusion and Relevance

          In this general population cohort, the persistence of ADHD was largely driven by childhood ADHD severity and poorer neuropsychological functioning. Additionally, we identified heterogeneity in the adult ADHD population such that this group consisted of a large late-onset ADHD group with no childhood diagnosis and minimal neuropsychological impairment, and a smaller group with persistent ADHD and associated neuropsychological impairment. Our findings call into question the conceptualization of adult ADHD as a childhood-onset neurodevelopmental disorder.

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          Author and article information

          Journal
          101589550
          40869
          JAMA Psychiatry
          JAMA Psychiatry
          JAMA psychiatry
          2168-622X
          2168-6238
          12 April 2017
          01 July 2016
          01 July 2017
          : 73
          : 7
          : 713-720
          Affiliations
          [1 ]MRC Social Genetic and Developmental Psychiatry, Institute of Psychiatry, Psychology and Neuroscience, King’s College London, London, UK
          [2 ]Department of Psychiatry, University of São Paulo Medical School, São Paulo, Brazil; and the Department of Psychiatry, Federal University of Rio Grande do Sul, Porto Allegre, Brazil
          [3 ]Department of Child and Adolescent Psychiatry, Institute of Psychiatry, Psychology and Neuroscience, King’s College London, London, UK
          [4 ]National and Specialist Child Traumatic Stress and Anxiety Clinic, South London and Maudsley NHS Foundation Trust, London, UK
          [5 ]Department of Psychology and Neuroscience, Duke University, Durham, NC, USA
          [6 ]Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, NC, USA
          Author notes
          Correspondence concerning this article should be addressed to Louise Arseneault, Institute of Psychiatry, Psychology & Neuroscience, SGDP Centre, London, SE5 8AF, UK. louise.arseneault@ 123456kcl.ac.uk
          Article
          PMC5475268 PMC5475268 5475268 nihpa864742
          10.1001/jamapsychiatry.2016.0465
          5475268
          27192174
          4ecb1521-f01b-402d-9e6a-340071f2607e
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