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

被引:90
作者
Seidman, L. J. [1 ,2 ,3 ]
Cherkerzian, S. [4 ]
Goldstein, J. M. [2 ,3 ,4 ]
Agnew-Blais, J. [5 ]
Tsuang, M. T. [2 ,3 ,6 ,7 ,8 ]
Buka, S. L. [3 ,9 ]
机构
[1] Harvard Univ, Beth Israel Deaconess Med Ctr,Neuropsychol Lab, Massachusetts Mental Hlth Ctr,Div Publ Psychiat, Dept Psychiat,Med Sch,Commonwealth Res Ctr, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Psychiat, Boston, MA 02115 USA
[3] Harvard Inst Psychiat Epidemiol & Genet, Boston, MA USA
[4] Harvard Univ, Connors Ctr Womens Hlth & Gender Biol, Sch Med, Dept Psychiat,Div Womens Hlth, Boston, MA 02115 USA
[5] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[6] Univ Calif San Diego, Dept Psychiat, Ctr Behav Genom, La Jolla, CA 92093 USA
[7] Univ Calif San Diego, Inst Genom Med, La Jolla, CA 92093 USA
[8] Vet Med Res Fdn, San Diego, CA USA
[9] Brown Univ, Dept Community Hlth, Providence, RI 02912 USA
关键词
Bipolar psychosis; neurocognition; pre-morbid; schizophrenia; PREMORBID IQ; HIGH-RISK; GENETIC VULNERABILITY; DISORDER; CHILDHOOD; COHORT; COMPLICATIONS; INTELLIGENCE; IMPAIRMENT;
D O I
10.1017/S0033291712000773
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
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.
引用
收藏
页码:119 / 131
页数:13
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