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  3. Developing Psychosis and Its Risk States Through the Lens of Schizotypy
 

Developing Psychosis and Its Risk States Through the Lens of Schizotypy

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BORIS DOI
10.7892/boris.62102
Date of Publication
2015
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Contributor
Debbané, Martin
Eliez, Stephan
Badoud, Deborah
Conus, Philippe
Flückiger, Rahel
Universitätsklinik für Kinder- und Jugendpsychiatrie und Psychotherapie
Schultze-Lutter, Frauke
Universitätsklinik für Kinder- und Jugendpsychiatrie und Psychotherapie (KJP)
Subject(s)

600 - Technology::610...

Series
Schizophrenia bulletin
ISSN or ISBN (if monograph)
0586-7614
Publisher
Oxford University Press
Language
English
Publisher DOI
10.1093/schbul/sbu176
PubMed ID
25548386
Uncontrolled Keywords

adolescence

basic symptoms

development

prodrome

schizophrenia

Description
Starting from the early descriptions of Kraepelin and Bleuler, the construct of schizotypy was developed from observations of aberrations in nonpsychotic family members of schizophrenia patients. In contemporary diagnostic manuals, the positive symptoms of schizotypal personality disorder were included in the ultra high-risk (UHR) criteria 20 years ago, and nowadays are broadly employed in clinical early detection of psychosis. The schizotypy construct, now dissociated from strict familial risk, also informed research on the liability to develop any psychotic disorder, and in particular schizophrenia-spectrum disorders, even outside clinical settings. Against the historical background of schizotypy it is surprising that evidence from longitudinal studies linking schizotypy, UHR, and conversion to psychosis has only recently emerged; and it still remains unclear how schizotypy may be positioned in high-risk research. Following a comprehensive literature search, we review 18 prospective studies on 15 samples examining the evidence for a link between trait schizotypy and conversion to psychosis in 4 different types of samples: general population, clinical risk samples according to UHR and/or basic symptom criteria, genetic (familial) risk, and clinical samples at-risk for a nonpsychotic schizophrenia-spectrum diagnosis. These prospective studies underline the value of schizotypy in high-risk research, but also point to the lack of evidence needed to better define the position of the construct of schizotypy within a developmental psychopathology perspective of emerging psychosis and schizophrenia-spectrum disorders
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/128596
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sbu176.pdftextAdobe PDF1.49 MBpublisherotherOpen
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