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Psychotic-like Experiences and Polygenic Liability in the Adolescent Brain Cognitive Development Study
Nicole R Karcher1, Sarah E Paul2, Emma C Johnson1
1Department of Psychiatry, Washington University School of Medicine, St. Louis, Missouri.
Childhood psychotic-like experiences (PLEs) are linked to genetic risk for psychopathology. Brain structure and cognition may mediate this link, suggesting polygenic scores generalize to childhood risk.
Area of Science:
- Neuroscience
- Genetics
- Developmental Psychology
Background:
- Childhood psychotic-like experiences (PLEs) are early indicators of severe psychopathology.
- Understanding the genetic and mechanistic underpinnings of childhood PLEs is crucial for early intervention.
Purpose of the Study:
- To investigate the association between childhood PLEs and polygenic scores (PGSs) for various psychopathology-related traits.
- To explore potential neural and behavioral mechanisms, such as brain structure and cognitive performance, that may mediate the link between PGSs and PLEs.
Main Methods:
- Utilized baseline data from the Adolescent Brain Cognitive Development Study (N=4650, ages 9-10).
- Examined associations between PLEs and PGSs for schizophrenia, cross-disorder risk, PLEs, educational attainment, birth weight, and inflammation.
- Employed mediational models to assess indirect effects through brain structure indices and cognitive performance.
Main Results:
- Both total and distressing PLEs were significantly associated with PGSs for educational attainment and cross-disorder risk.
- Distressing PLEs showed significant associations with PGSs for schizophrenia and PLEs.
- Global brain volume and cognitive performance were found to indirectly link educational attainment PGS to PLEs.
Conclusions:
- Childhood PLEs are associated with genomic risk indices for broad psychopathology and psychosis.
- Brain structure and cognitive abilities may serve as intermediary phenotypes linking genetic risk to psychopathology.
- Polygenic scores developed in adult populations are applicable to assessing psychopathology risk in children.
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