Cognitive dysfunction is worse among pediatric patients with bipolar disorder Type I than Type II

Lindsay S Schenkel1, Amy E West, Rachel Jacobs

  • 1Department of Psychology, Rochester Institute of Technology, Rochester, NY 14623, USA. lssgsh@rit.edu

Insights

Pediatric patients with bipolar disorder (BD) show cognitive impairments. Bipolar I disorder (BD I) patients exhibit more severe deficits than Bipolar II disorder (BD II) patients, with verbal learning and memory potentially serving as a key endophenotype.

Area of Science:

  • Neuroscience
  • Psychiatry
  • Cognitive Psychology

Background:

  • Pediatric patients with bipolar disorder (BD) consistently exhibit impaired neurocognitive function.
  • These cognitive deficits may help identify endophenotypes across different BD subtypes.
  • Understanding these profiles is crucial for targeted interventions.

Purpose of the Study:

  • To determine the distinct phenotypic cognitive profiles of pediatric patients with Bipolar I disorder (BD I) and Bipolar II disorder (BD II).
  • To compare cognitive performance between BD subtypes and healthy controls (HC).

Main Methods:

  • A cohort of 79 participants, including 27 with BD I, 19 with BD II, and 33 demographically and intellectually matched HC, completed a comprehensive neurocognitive task battery.
  • Neurocognitive domains assessed included attention, executive function, working memory, visual memory, and verbal learning and memory.

Main Results:

  • BD I patients demonstrated significantly poorer performance than HC across all cognitive domains.
  • BD I patients also performed worse than BD II patients in most cognitive domains, except working memory.
  • BD II patients showed impairments relative to HC only in verbal learning and memory.

Conclusions:

  • Pediatric BD I patients exhibit more severe cognitive impairment than BD II patients, who show intermediate performance between BD I and HC.
  • Verbal learning and memory may serve as a cognitive endophenotype, effectively differentiating pediatric BD patients from controls across subtypes.
  • These findings support the development of subtype-specific cognitive interventions for pediatric BD.
Abstract

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