Sustained Attention and Interference Control Among 7-Year-Old Children With a Familial High Risk of Schizophrenia or Bipolar Disorder-A Nationwide Observational Cohort Study

Biol Psychiatry Cogn Neurosci Neuroimaging. 2018 Aug;3(8):704-712. doi: 10.1016/j.bpsc.2018.04.012. Epub 2018 May 22.

Abstract

Background: Given the partially shared genetic liability between schizophrenia and bipolar disorder, we aimed to assess whether 7-year-old children with a familial high risk of schizophrenia or bipolar disorder display specific deficits of sustained attention and interference control compared with each other and with control children.

Methods: An observational cohort was identified through Danish registries and consisted of 522 children 7 years of age with no, one, or two parents with a diagnosis of schizophrenia or bipolar disorder. Control subjects were matched based on age, sex, and municipality. Sustained attention and interference control were assessed using Conners' Continuous Performance Test II and a modified Eriksen flanker task. Assessors were blinded to group membership of participants. The effect of higher genetic loading was not considered in the statistical models owing to low numbers.

Results: At 7 years of age, children with a familial high risk of schizophrenia displayed deficits of sustained attention and subtle deficits in interference control compared with control children and children with a familial high risk of bipolar disorder. Children with a familial high risk of bipolar disorder displayed similar abilities of sustained attention and interference control as control children except in terms of a lower accuracy.

Conclusions: Our findings suggest distinct neurodevelopmental characteristics in middle childhood of sustained attention and interference control for children of parents with schizophrenia or bipolar disorder.

Keywords: Attention; Bipolar disorder; Endophenotypes; First-degree relatives; Interference control; Schizophrenia.

Publication types

  • Observational Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Attention / physiology*
  • Bipolar Disorder / complications
  • Bipolar Disorder / physiopathology*
  • Child
  • Cognitive Dysfunction / etiology
  • Cognitive Dysfunction / physiopathology*
  • Cohort Studies
  • Denmark
  • Executive Function / physiology*
  • Female
  • Genetic Predisposition to Disease*
  • Humans
  • Male
  • Psychomotor Performance / physiology*
  • Registries
  • Risk
  • Schizophrenia / complications
  • Schizophrenia / physiopathology*