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Published on: December 2, 2015
Executive Control and Associated Brain Activity in Children With Familial High-Risk of Schizophrenia or Bipolar
Line Korsgaard Johnsen1,2, Kit Melissa Larsen1,2, Søren Asp Fuglsang1
1Danish Research Centre for Magnetic Resonance, Centre for Functional and Diagnostic Imaging and Research, Copenhagen University Hospital, Amager and Hvidovre, Copenhagen, Denmark.
Insights
Children at high risk for schizophrenia or bipolar disorder show increased reaction time variability, suggesting a potential early marker for these conditions. This variability may indicate difficulties with sustained attention, independent of current illness.
Area of Science:
- Neuroscience
- Psychiatry
- Developmental Psychology
Background:
- Executive control is a potential prognostic and endophenotypic marker for schizophrenia (SZ) and bipolar disorder (BP).
- Assessing children with familial high-risk (FHR) for SZ or BP can identify early risk markers.
- Hypothesis: FHR children exhibit impaired executive control and aberrant brain activation compared to population-based controls (PBC).
Purpose of the Study:
- To examine executive control and brain activation in children at familial high-risk for SZ or BP.
- To identify potential early endophenotypic markers of SZ and BP risk in children.
- To compare executive control and neural responses between FHR-SZ, FHR-BP, and PBC children.
Main Methods:
- Utilized a flanker task and functional magnetic resonance imaging (fMRI).
- Included 11- to 12-year-old children: FHR-SZ (n=85), FHR-BP (n=63), and PBC (n=98).
- Analyzed reaction time (RT) variability (coefficient of variation, CVRT) and task-related brain activation.
Main Results:
- No group differences were found in executive control for resolving spatial visuomotor conflict.
- Significantly higher RT variability (CVRT) was observed in both FHR-BP and FHR-SZ groups compared to PBC children (Bayesian ANOVA, BF10 = 6.82).
- fMRI analyses showed no evidence of between-group differences in task-related brain activation; results remained consistent after excluding children with psychiatric illness.
Conclusions:
- Children aged 11-12 with FHR-SZ and FHR-BP demonstrate intact conflict resolution and neural efficiency.
- Increased RT variability, independent of psychiatric illness, may indicate difficulties in sustained attention and serve as a potential endophenotypic marker of risk.
- These findings highlight subtle executive function differences in at-risk youth, potentially preceding overt psychopathology.
Background And Hypotheses:
Impaired executive control is a potential prognostic and endophenotypic marker of schizophrenia (SZ) and bipolar disorder (BP). Assessing children with familial high-risk (FHR) of SZ or BP enables characterization of early risk markers and we hypothesize that they express impaired executive control as well as aberrant brain activation compared to population-based control (PBC) children.
Study Design:
Using a flanker task, we examined executive control together with functional magnetic resonance imaging (fMRI) in 11- to 12-year-old children with FHR of SZ (FHR-SZ) or FHR of BP (FHR-BP) and PBC children as part of a register-based, prospective cohort-study; The Danish High Risk and Resilience study-VIA 11.
Study Results:
We included 85 (44% female) FHR-SZ, 63 (52% female) FHR-BP and 98 (50% female) PBC in the analyses. Executive control effects, caused by the spatial visuomotor conflict, showed no differences between groups. Bayesian ANOVA of reaction time (RT) variability, quantified by the coefficient of variation (CVRT), revealed a group effect with similarly higher CVRT in FHR-BP and FHR-SZ compared to PBC (BF10 = 6.82). The fMRI analyses revealed no evidence for between-group differences in task-related brain activation. Post hoc analyses excluding children with psychiatric illness yielded same results.
Conclusion:
FHR-SZ and FHR-BP at age 11-12 show intact ability to resolve a spatial visuomotor conflict and neural efficacy. The increased variability in RT may reflect difficulties in maintaining sustained attention. Since variability in RT was independent of existing psychiatric illness, it may reflect a potential endophenotypic marker of risk.
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