Neuropsychological functioning in adolescents and young adults at genetic risk for schizophrenia and affective psychoses: results from the Harvard and Hillside Adolescent High Risk Studies
- PMID: 16707777
- PMCID: PMC2632246
- DOI: 10.1093/schbul/sbj078
Neuropsychological functioning in adolescents and young adults at genetic risk for schizophrenia and affective psychoses: results from the Harvard and Hillside Adolescent High Risk Studies
Abstract
Siblings and offspring of persons with schizophrenia carry elevated genetic risk for the illness and manifest attentional and memory impairments. Because less is known about other neuropsychological functions and their specificity in adolescents, we conducted a genetic high-risk (HR) study of schizophrenia (HR-SCZ) and affective psychosis (HR-AFF). Participants (ages 12-25) were from the Harvard Adolescent High-Risk and Hillside Family studies, including 73 HR-SCZ, 18 HR-AFF, and 84 community controls (CCs) recruited in metropolitan Boston and New York. Groups were compared on overall neurocognitive functioning, 6 domains, and 13 test scores, controlling for age, parental education, and correlated data within families. The HR-SCZ group was significantly impaired overall, while the HR-AFF group demonstrated a trend toward overall impairment. HR-SCZ subjects showed significantly lower Verbal Ability (d = .73) and Executive Functioning/Working Memory (d = .47) than CCs. HR-AFF subjects showed reduced Verbal Ability (d = .64) compared to CCs. Excluding 12 CCs with a parental history of depression (without psychosis) led to larger differences between HR and CC groups across domains. Moreover, HR-SCZ and CC group differences in Verbal Memory (d = .39) and Visual-Spatial (d = .34) became statistically significant. There were no significant differences between HR-SCZ and HR-AFF groups. Data support a modest neuropsychological deficit in persons at genetic HR for psychosis, with a broader range of deficits in HR-SCZ. Future work should assess the relationship of neurocognition to adaptive functioning and possible onset of psychosis in HR samples. Ascertainment criteria for controls may markedly influence results and interpretation of group differences.
Figures
Similar articles
-
Verbal and visual-spatial memory impairment in youth at familial risk for schizophrenia or affective psychosis: a pilot study.Schizophr Res. 2013 Mar;144(1-3):122-8. doi: 10.1016/j.schres.2012.11.027. Epub 2013 Jan 9. Schizophr Res. 2013. PMID: 23312552 Free PMC article.
-
Auditory Vigilance and Working Memory in Youth at Familial Risk for Schizophrenia or Affective Psychosis in the Harvard Adolescent Family High Risk Study.J Int Neuropsychol Soc. 2016 Nov;22(10):1026-1037. doi: 10.1017/S1355617716000242. J Int Neuropsychol Soc. 2016. PMID: 27903327
-
Cognitive functioning in young people with first episode psychosis: relationship to diagnosis and clinical characteristics.Aust N Z J Psychiatry. 2004 Jul;38(7):501-10. doi: 10.1080/j.1440-1614.2004.01403.x. Aust N Z J Psychiatry. 2004. PMID: 15255822
-
Shared and divergent neurocognitive impairments in adult patients with schizophrenia and bipolar disorder: Whither the evidence?Neurosci Biobehav Rev. 2016 Feb;61:66-89. doi: 10.1016/j.neubiorev.2015.12.002. Epub 2015 Dec 12. Neurosci Biobehav Rev. 2016. PMID: 26691725 Review.
-
Memory Impairments and Psychosis Prediction: A Scoping Review and Theoretical Overview.Neuropsychol Rev. 2020 Dec;30(4):521-545. doi: 10.1007/s11065-020-09464-2. Epub 2020 Nov 23. Neuropsychol Rev. 2020. PMID: 33226539
Cited by
-
Maternal Bacterial Infection During Pregnancy and Offspring Risk of Psychotic Disorders: Variation by Severity of Infection and Offspring Sex.Am J Psychiatry. 2020 Jan 1;177(1):66-75. doi: 10.1176/appi.ajp.2019.18101206. Epub 2019 Oct 4. Am J Psychiatry. 2020. PMID: 31581799 Free PMC article.
-
Premorbid cognitive deficits in young relatives of schizophrenia patients.Front Hum Neurosci. 2010 Mar 9;3:62. doi: 10.3389/neuro.09.062.2009. eCollection 2010. Front Hum Neurosci. 2010. PMID: 20300465 Free PMC article.
-
Neurocognitive allied phenotypes for schizophrenia and bipolar disorder.Schizophr Bull. 2008 Jul;34(4):743-59. doi: 10.1093/schbul/sbn027. Epub 2008 Apr 29. Schizophr Bull. 2008. PMID: 18448479 Free PMC article. Review.
-
Frequency of normative word associations in the speech of individuals at familial high-risk for schizophrenia.Schizophr Res. 2012 Sep;140(1-3):99-103. doi: 10.1016/j.schres.2012.06.034. Epub 2012 Jul 21. Schizophr Res. 2012. PMID: 22819779 Free PMC article.
-
The Consortium on the Genetics of Schizophrenia: neurocognitive endophenotypes.Schizophr Bull. 2007 Jan;33(1):49-68. doi: 10.1093/schbul/sbl055. Epub 2006 Nov 13. Schizophr Bull. 2007. PMID: 17101692 Free PMC article. Review.
References
-
- Tsuang M, Stone W, Faraone S. Schizophrenia: a review of genetic studies. Harv Rev Psychiatry. 1999;7:185–207. - PubMed
-
- Gottesman I, Gould T. The endophenotype concept in psychiatry: etymology and strategic intentions. Am J Psychiatry. 2003;160:636–645. - PubMed
-
- Tsuang M, Gilbertson M, Faraone S. Genetic transmission of negative and positive symptoms in the biological relatives of schizophrenics. In: Marneros A, Andersen N, Tsuang M, editors. Negative Versus Positive Schizophrenia. Berlin: Springer; 1991. pp. 265–291.
-
- Green M. What are the functional consequences of neurocognitive deficits in schizophrenia? Am J Psychiatry. 1996;153:321–330. - PubMed
-
- Nuechterlein K, Dawson M. Information processing and attentional functioning in the developmental course of schizophrenic disorders. Schizophr Bull. 1984;10:160–203. - PubMed
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Medical