학술논문

Within-family influences on dimensional neurobehavioral traits in a high-risk genetic model.
Document Type
Article
Source
Psychological Medicine. Oct2022, Vol. 52 Issue 14, p3184-3192. 9p.
Subject
*SCHIZOPHRENIA risk factors
*GENETICS of schizophrenia
*SOCIAL participation
*BIOLOGICAL models
*PSYCHOLOGY of parents
*22Q11 deletion syndrome
*EFFECT sizes (Statistics)
*QUANTITATIVE research
*COGNITION
*REGRESSION analysis
*GENETIC variation
*RISK assessment
*COMPARATIVE studies
*INTRACLASS correlation
*DESCRIPTIVE statistics
*DISEASE susceptibility
*COGNITIVE testing
*SOCIAL skills
*PHENOTYPES
*MOTOR ability
*INTELLIGENCE tests
*DISEASE complications
Language
ISSN
0033-2917
Abstract
Background: Genotype-first and within-family studies can elucidate factors that contribute to psychiatric illness. Combining these approaches, we investigated the patterns of influence of parental scores, a high-impact variant, and schizophrenia on dimensional neurobehavioral phenotypes implicated in major psychiatric disorders. Methods: We quantitatively assessed cognitive (FSIQ, VIQ, PIQ), social, and motor functioning in 82 adult individuals with a de novo 22q11.2 deletion (22 with schizophrenia), and 148 of their unaffected parents. We calculated within-family correlations and effect sizes of the 22q11.2 deletion and schizophrenia, and used linear regressions to assess contributions to neurobehavioral measures. Results: Proband-parent intra-class correlations (ICC) were significant for cognitive measures (e.g. FSIQ ICC = 0.549, p < 0.0001), but not for social or motor measures. Compared to biparental scores, the 22q11.2 deletion conferred significant impairments for all phenotypes assessed (effect sizes −1.39 to −2.07 s.d.), strongest for PIQ. There were further decrements in those with schizophrenia. Regression models explained up to 37.7% of the variance in IQ and indicated that for proband IQ, parental IQ had larger effects than schizophrenia. Conclusions: This study, for the first time, disentangles the impact of a high-impact variant from the modifying effects of parental scores and schizophrenia on relevant neurobehavioral phenotypes. The robust proband-parent correlations for cognitive measures, independent of the impact of the 22q11.2 deletion and of schizophrenia, suggest that, for certain phenotypes, shared genetic variation plays a significant role in expression. Molecular genetic and predictor studies are needed to elucidate shared factors and their contribution to psychiatric illness in this and other high-risk groups. [ABSTRACT FROM AUTHOR]