Literature DB >> 19229852

Evidence that self-reported psychotic experiences represent the transitory developmental expression of genetic liability to psychosis in the general population.

Tineke Lataster1, Inez Myin-Germeys, Catherine Derom, Evert Thiery, Jim van Os.   

Abstract

It has been suggested that self-reported, common, non-clinical psychotic experiences may represent the transitory developmental expression of distributed genetic risk for psychosis. In a sample of female MZ (176 pairs) and DZ twins (113 pairs), cross-twin, cross-trait analyses were conducted to investigate the association between repeated continuous measures of self-reported psychotic experiences (PE-three measures over 18 months), assessed with the CAPE, in one twin and clinical interview categorical measures of psychotic symptoms (PS), assessed with SCID-I, in the other twin. The results showed that in MZ but not DZ pairs (interaction: chi(2) = 7.9, df = 1, P = 0.005), the cross-twin association between PE and PS was large and significant (standardized effect size: 0.26, 95% CI: 0.10-0.42) and of similar magnitude as the within-twin PE-PS association (standardized effect size: 0.28, 95% CI: 0.10-0.45), demonstrating both PE validity and genetic effects. In addition, the cross-twin association between PE and PS was significantly larger (interaction: chi(2) = 20.3, df = 1, P < 0.0001) for younger MZ twins (standardized effect size: 0.67, 95% CI: 0.44-0.90) than older MZ twins (standardized effect size: -0.05, 95% CI: -0.26 to 0.16), demonstrating developmental effects. This study indicates that self-reported psychotic experiences in the general population may represent the developmental expression of population genetic risk for psychosis. 2009 Wiley-Liss, Inc.

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Year:  2009        PMID: 19229852     DOI: 10.1002/ajmg.b.30933

Source DB:  PubMed          Journal:  Am J Med Genet B Neuropsychiatr Genet        ISSN: 1552-4841            Impact factor:   3.568


  14 in total

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4.  Schizophrenia candidate gene ERBB4: covert routes of vulnerability to psychosis detected at the population level.

Authors:  Nicholas C Stefanis; Alex Hatzimanolis; Nikolaos Smyrnis; Dimitrios Avramopoulos; Ioannis Evdokimidis; Jim van Os; Costas N Stefanis; Richard E Straub; Daniel R Weinberger
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5.  Correlation Between Levels of Delusional Beliefs and Perfusion of the Hippocampus and an Associated Network in a Non-Help-Seeking Population.

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6.  The CCC2000 Birth Cohort Study of Register-Based Family History of Mental Disorders and Psychotic Experiences in Offspring.

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7.  Striatal abnormalities and spontaneous dyskinesias in non-clinical psychosis.

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Journal:  Schizophr Res       Date:  2013-10-22       Impact factor: 4.939

8.  Dietary intake of fish, omega-3, omega-6 polyunsaturated fatty acids and vitamin D and the prevalence of psychotic-like symptoms in a cohort of 33,000 women from the general population.

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9.  Psychotic symptoms and gray matter deficits in clinical pediatric populations.

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10.  Psychosis as a transdiagnostic and extended phenotype in the general population.

Authors:  Jim van Os; Uli Reininghaus
Journal:  World Psychiatry       Date:  2016-06       Impact factor: 49.548

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