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The silent side of the spectrum: schizotypy and the schizotaxic self.

Andrea Raballo, Josef Parnas

Schizophrenia Bulletin February 22, 2010 DOI: 10.1093/schbul/sbq008 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Observational family high-risk study Peer reviewed
Sample size 218
Population Unaffected members of six extended multiplex families with schizophrenia, assessed in the Copenhagen Schizophrenia Linkage Study
Keywords Humans Regression analysis Ego Schizotypal personality disorder Schizophrenia Schizophrenic psychology Adult Middle aged Denmark Female Genetic linkage
Key findings Self-disorders rose in a stepwise pattern from unaffected members with no mental illness through schizotypal traits, other personality disorders, and schizotypal personality disorder, and were associated with a markedly increased risk of belonging to a more affected group. The authors argue this supports self-disorders as an expression of schizotaxic vulnerability and a multidimensional model of schizotypy.

Abstract

The identification of individuals carrying unexpressed genetic liability to schizophrenia is crucial for both etiological research and clinical risk stratification. Subclinical psychopathological features detectable in the nonpsychotic part of the schizophrenia spectrum could improve the delineation of informative vulnerability phenotypes. Inspired by Meehl's schizotaxia-schizotypy heuristic model, we tested anomalous subjective experiences (self-disorders, SDs) as a candidate vulnerability phenotype in a sample of nonpsychotic, genetically high-risk subjects. A total of 218 unaffected members of 6 extended multiplex families (assessed between 1989 and 1999 during the Copenhagen Schizophrenia Linkage Study) were stratified into 4 groups of increasing psychopathological expressivity: no mental illness (NMI), no mental illness with schizotypal traits (NMI-ST), personality disorders not fulfilling other personality disorders (OPDs), and schizotypal personality disorder (SPD). We tested the distribution of SDs among the subgroups, the effect of SDs on the risk of belonging to the different subgroups, and the effect of experimental grouping and concomitant psychopathology (ie, negative symptoms (NSs) and subpsychotic formal thought disorder [FTD]) on the chances of experiencing SDs. SDs distribution followed an incremental pattern from NMI to SPD. SDs were associated with a markedly increased risk of NMI-ST, OPDs, or SPD. The odds of SDs increased as a function of the diagnostic category assignment, independently of sociodemographics and concomitant subclinical psychopathology (NSs and FTD). The results support SDs as an expression of schizotaxic vulnerability and indicate a multidimensional model of schizotypy--characterized by SDs, NSs, FTD--as a promising heuristic construct to address liability phenotypes in genetically high-risk studies.

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