Literature DB >> 18562177

Investigating if psychosis-like symptoms (PLIKS) are associated with family history of schizophrenia or paternal age in the ALSPAC birth cohort.

Stanley Zammit1, Jeremy Horwood, Andrew Thompson, Kate Thomas, Paulo Menezes, David Gunnell, Chris Hollis, Dieter Wolke, Glyn Lewis, Glynn Harrison.   

Abstract

Psychosis-like symptoms (PLIKS) occur in about 15% of the population, but it is unclear to what extent PLIKS share aetiological mechanisms in common with those for schizophrenia. We examined whether the presence of PLIKS was associated with a family history of schizophrenia (FH-SCZ), or with advancing paternal age, using data from 6356 children in the ALSPAC birth cohort who participated in a semi-structured PLIKS interview at 12 years of age. We found no evidence of association between FH-SCZ and suspected or definite PLIKS (adjusted OR=0.94, 95%CI 0.44, 2.00; p=0.880). There was weak evidence that advancing paternal age was associated with increased PLIKS (adjusted OR per 10-year age increase=1.23, 95%CI 0.99, 1.55; p=0.058). Although not a priori hypotheses, family history of depression (adjusted OR=1.28, 95%CI 1.04, 1.57; p=0.018), and younger maternal age (adjusted OR per 10-year age increase=0.62, 95% CI 0.47, 0.82; p<0.001) both showed stronger evidence of association with suspected or definite PLIKS. Overall our findings provide little evidence that these established risk factors for schizophrenia show a similar relationship with PLIKS, suggesting that the presence of PLIKS is unlikely to be a strong marker of early expression of the pathology underlying schizophrenia. Whether future studies of PLIKS will increase our understanding of mechanisms underlying the development of schizophrenia, or prove useful in prediction of this disorder, remains to be seen.

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Year:  2008        PMID: 18562177     DOI: 10.1016/j.schres.2008.04.036

Source DB:  PubMed          Journal:  Schizophr Res        ISSN: 0920-9964            Impact factor:   4.939


  26 in total

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9.  Association of measures of fetal and childhood growth with non-clinical psychotic symptoms in 12-year-olds: the ALSPAC cohort.

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