Relationship between cognitive flexibility and subsequent course of mood symptoms and suicidal ideation in young adults with childhood-onset bipolar disorder

• Published in: European child & adolescent psychiatry 2022-02, Vol.31 (2), p.299-312
• Main Authors: MacPherson, Heather A., Kudinova, Anastacia Y., Schettini, Elana, Jenkins, Gracie A., Gilbert, Anna C., Thomas, Sarah A., Kim, Kerri L., Radoeva, Petya D., Fenerci, Rebecca L. Babcock, Yen, Shirley, Hower, Heather, Hunt, Jeffrey, Keller, Martin B., Dickstein, Daniel P.
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Age of onset; Bipolar disorder; Bipolar Disorder - complications; Bipolar Disorder - epidemiology; Chi-square test; Child; Child & adolescent psychiatry; Child and Adolescent Psychiatry; Childhood; Children; Cognition; Cognitive ability; Cognitive flexibility; Comorbidity; Cross-Sectional Studies; Executive Function; Flexibility; Functional impairment; Humans; Intelligence tests; Medical prognosis; Medicine; Medicine & Public Health; Memory; Mental depression; Mood; Neuropsychological Tests; Original Contribution; Psychiatry; Short term memory; Spatial memory; Suicidal Ideation; Suicide; Symptoms; Young Adult; Young adults
• ISSN: 1018-8827; 1435-165X
• DOI: 10.1007/s00787-020-01688-0

Neurocognitive deficits, such as cognitive flexibility impairments, are common in bipolar disorder (BD) and predict poor academic, occupational, and functional outcomes. However, the association between neurocognition and illness trajectory is not well understood, especially across developmental transitions. This study examined cognitive flexibility and subsequent mood symptom and suicidal ideation (SI) course in young adults with childhood-onset BD-I (with distinct mood episodes) vs. BD-not otherwise specified (BD-NOS) vs. typically-developing controls (TDCs). Sample included 93 young adults (ages 18–30) with prospectively verified childhood-onset DSM-IV BD-I ( n  = 34) or BD-NOS ( n  = 15) and TDCs ( n  = 44). Participants completed cross-sectional neuropsychological tasks and clinical measures. Then participants with BD completed longitudinal assessments of mood symptoms and SI at 6-month intervals ( M  = 39.18 ± 16.57 months of follow-up data). Analyses included ANOVAs, independent-samples t tests, chi-square analyses, and multiple linear regressions. Participants with BD-I had significant deficits in cognitive flexibility and executive functioning vs. BD-NOS and TDCs, and impaired spatial working memory vs. TDCs only. Two significant BD subtype-by-cognitive flexibility interactions revealed that cognitive flexibility deficits were associated with subsequent percentage of time depressed and with SI in BD-I but not BD-NOS, regardless of other neurocognitive factors (full-scale IQ, executive functioning, spatial working memory) and clinical factors (current and prior mood and SI symptoms, age of BD onset, global functioning, psychiatric medications, comorbidity). Thus, cognitive flexibility may be an important etiological brain/behavior mechanism, prognostic indicator, and intervention target for childhood-onset BD-I, as this deficit appears to endure into young adulthood and is associated with worse prognosis for subsequent depression and SI.