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Comparative Study
. 2013 Jan;43(1):119-31.
doi: 10.1017/S0033291712000773. Epub 2012 May 11.

Neuropsychological performance and family history in children at age 7 who develop adult schizophrenia or bipolar psychosis in the New England Family Studies

Affiliations
Comparative Study

Neuropsychological performance and family history in children at age 7 who develop adult schizophrenia or bipolar psychosis in the New England Family Studies

L J Seidman et al. Psychol Med. 2013 Jan.

Abstract

Background: Persons developing schizophrenia (SCZ) manifest various pre-morbid neuropsychological deficits, studied most often by measures of IQ. Far less is known about pre-morbid neuropsychological functioning in individuals who later develop bipolar psychoses (BP). We evaluated the specificity and impact of family history (FH) of psychosis on pre-morbid neuropsychological functioning.

Method: We conducted a nested case-control study investigating the associations of neuropsychological data collected systematically at age 7 years for 99 adults with psychotic diagnoses (including 45 SCZ and 35 BP) and 101 controls, drawn from the New England cohort of the Collaborative Perinatal Project (CPP). A mixed-model approach evaluated full-scale IQ, four neuropsychological factors derived from principal components analysis (PCA), and the profile of 10 intelligence and achievement tests, controlling for maternal education, race and intra-familial correlation. We used a deviant responder approach (<10th percentile) to calculate rates of impairment.

Results: There was a significant linear trend, with the SCZ group performing worst. The profile of childhood deficits for persons with SCZ did not differ significantly from BP. Neuropsychological impairment was identified in 42.2% of SCZ, 22.9% of BP and 7% of controls. The presence of psychosis in first-degree relatives (FH+) significantly increased the severity of childhood impairment for SCZ but not for BP.

Conclusions: Pre-morbid neuropsychological deficits are found in a substantial proportion of children who later develop SCZ, especially in the SCZ FH+ subgroup, but less so in BP, suggesting especially impaired neurodevelopment underlying cognition in pre-SCZ children. Future work should assess genetic and environmental factors that explain this FH effect.

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Conflict of interest statement

Conflict of Interest Statement: The following authors do not have any conflicts of interest to declare: Larry J. Seidman, Sara Cherkerzian, Jill M. Goldstein, Jessica Agnew-Blais, Ming T. Tsuang, Stephen L. Buka.

Figures

Figure 1
Figure 1
Full Scale IQ and Standardized Measures of Neuropsychological functioning at Age 7 in Adults who Developed Psychosis Including Persons with Schizophrenia Disorders (n=45), Bipolar Psychosis and Schizoaffective, Bipolar type combined (n=35), and Controls (n=101) *p < .05, **p<.01, ***p<.001 compared to controls (Least Square Means)
Figure 2
Figure 2
Profile analysis of mean performance and rates of abnormal performance on individual tests (<10%tile) of WRAT and WISC Performance at Age 7 for Adults who Subsequently Developed Psychosis, Including Schizophrenia and Schizoaffective Disorder, Depressed type (n=45), Bipolar Psychosis and Schizoaffective, Bipolar type combined (n=35), and Controls (n=101)
Figure 3
Figure 3
Full Scale IQ at 7 Years of Age for Adults That Subsequently Developed Psychosis With and Without a Family History of Psychosis in First-Degree Relatives, *p < .05, **p<.01, compared to controls. Controls (n=101), BP/SAB with no family history (N=13), BP/SAB with family history (N=16), Schizophrenia with no family history (N=28) and Schizophrenia with a positive family history of psychosis (N=8) (Least Square Means)

References

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