Attention deficit hyperactivity disorder symptoms as antecedents of later psychotic outcomes in 22q11.2 deletion syndrome.


Journal

Schizophrenia research
ISSN: 1573-2509
Titre abrégé: Schizophr Res
Pays: Netherlands
ID NLM: 8804207

Informations de publication

Date de publication:
02 2019
Historique:
received: 18 05 2018
revised: 16 07 2018
accepted: 31 07 2018
pubmed: 11 8 2018
medline: 5 3 2020
entrez: 11 8 2018
Statut: ppublish

Résumé

Individuals with 22q11.2 Deletion Syndrome (22q11.2DS) are at substantially heightened risk for psychosis. Thus, prevention and early intervention strategies that target the antecedents of psychosis in this high-risk group are a clinical priority. Attention Deficit Hyperactivity Disorder (ADHD) is one the most prevalent psychiatric disorders in children with 22q11.2DS, particularly the inattentive subtype. The aim of this study was to test the hypothesis that ADHD inattention symptoms predict later psychotic symptoms and/or psychotic disorder in those with 22q11.2DS. 250 children and adolescents with 22q11.2DS without psychotic symptoms at baseline took part in a longitudinal study. Assessments were performed using well-validated structured diagnostic instruments at two time points (T1 (mean age = 11.2, SD = 3.1) and T2 (mean age = 14.3, SD = 3.6)). Inattention symptoms at T1 were associated with development of psychotic symptoms at T2 (OR:1.2, p = 0.01) but weak associations were found with development of psychotic disorder (OR:1.2, p = 0.15). ADHD diagnosis at T1 was strongly associated with development of psychotic symptoms at T2 (OR:4.5, p < 0.001) and psychotic disorder (OR:5.9, p = 0.02). Our findings that inattention symptoms and the diagnosis of ADHD are associated with subsequent psychotic outcomes in 22q11.2DS have important clinical implications. Future studies examining the effects of stimulant and other ADHD treatments on individuals with 22q11.2DS are warranted.

Identifiants

pubmed: 30093352
pii: S0920-9964(18)30490-0
doi: 10.1016/j.schres.2018.07.044
pmc: PMC6406019
pii:
doi:

Types de publication

Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

320-325

Subventions

Organisme : NIMH NIH HHS
ID : U01 MH101720
Pays : United States
Organisme : MRF
ID : MRF_MRF-154-0001-RG-SKUSE
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/L011166/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/L010305/1
Pays : United Kingdom
Organisme : NIMH NIH HHS
ID : R01 MH085953
Pays : United States
Organisme : NIBIB NIH HHS
ID : U54 EB020403
Pays : United States
Organisme : Medical Research Council
ID : MR/P005748/1
Pays : United Kingdom
Organisme : NIMH NIH HHS
ID : U01 MH101719
Pays : United States
Organisme : Wellcome Trust
ID : 110222/Z/15/Z
Pays : United Kingdom

Informations de copyright

Copyright © 2018 The Authors. Published by Elsevier B.V. All rights reserved.

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Auteurs

Maria Niarchou (M)

Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, United Kingdom; Institute for Molecular Bioscience, University of Queensland, Brisbane, Australia. Electronic address: niarchoum@cardiff.ac.uk.

Samuel J R A Chawner (SJRA)

Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, United Kingdom.

Ania Fiksinski (A)

Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, the Netherlands; Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada; The Dalglish Family 22q Clinic for 22q11.2 Deletion Syndrome, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada.

Jacob A S Vorstman (JAS)

Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada; The Dalglish Family 22q Clinic for 22q11.2 Deletion Syndrome, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada; The Hospital for Sick Children, Toronto, Canada.

Johanna Maeder (J)

Department of Psychiatry, University of Geneva, Geneva, Switzerland.

Maude Schneider (M)

Department of Psychiatry, University of Geneva, Geneva, Switzerland.

Stephan Eliez (S)

Department of Psychiatry, University of Geneva, Geneva, Switzerland.

Marco Armando (M)

Department of Psychiatry, University of Geneva, Geneva, Switzerland.

Maria Pontillo (M)

Paediatric Hospital Bambino Gesu, Rome, Italy.

Stefano Vicari (S)

Paediatric Hospital Bambino Gesu, Rome, Italy.

Donna M McDonald-McGinn (DM)

Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.

Beverly S Emanuel (BS)

Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.

Elaine H Zackai (EH)

Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.

Carrie E Bearden (CE)

Semel Institute for Neuroscience and Human Behavior and Department of Psychology, UCLA, CA, USA.

Vandana Shashi (V)

Department of Pediatrics, Duke University School of Medicine, Durham, USA.

Stephen R Hooper (SR)

Department of Allied Health Sciences, University of North Carolina School of Medicine, Chapel Hill, NC, USA.

Michael J Owen (MJ)

Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, United Kingdom.

Raquel E Gur (RE)

Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA; Department of Psychiatry, Neuropsychiatry Section, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA; Department of Child and Adolescent Psychiatry, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.

Naomi R Wray (NR)

Institute for Molecular Bioscience, University of Queensland, Brisbane, Australia.

Marianne B M van den Bree (MBM)

Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, United Kingdom.

Anita Thapar (A)

Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, United Kingdom.

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