Literature DB >> 10945082

Factor structure and familiality of first-rank symptoms in sibling pairs with schizophrenia and schizoaffective disorder.

J Loftus1, L E Delisi, T J Crow.   

Abstract

BACKGROUND: Since their introduction as diagnostic criteria by Schneider in 1937, nuclear symptoms have played a key role in concepts of schizophrenia, but their relationship to each other and to genetic predisposition has been unclear. AIMS: To ascertain the factor structure and familiality of nuclear symptoms.
METHODS: Nuclear (Schneiderian) symptoms were extracted from case notes and interviews in a study of 103 sibling pairs with DSM-III-R schizophrenia or schizoaffective disorder.
RESULTS: Principal components analysis demonstrated two major factors: one, accounting for about 50% of the variance, groups thought withdrawal, insertion and broadcasting, with delusions of control; and the second, accounting for < 20% of the variance, groups together third-person voices, thought echo and running commentary. Factor I was significantly correlated within sibling pairs.
CONCLUSIONS: The correlation within sibling pairs suggests that, contrary to the conclusion of some previous studies, some nuclear symptoms do show a degree of familiality and therefore perhaps heritability.

Entities:  

Mesh:

Year:  2000        PMID: 10945082     DOI: 10.1192/bjp.177.1.15

Source DB:  PubMed          Journal:  Br J Psychiatry        ISSN: 0007-1250            Impact factor:   9.319


  10 in total

Review 1.  First rank symptoms for schizophrenia.

Authors:  Karla Soares-Weiser; Nicola Maayan; Hanna Bergman; Clare Davenport; Amanda J Kirkham; Sarah Grabowski; Clive E Adams
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2.  Concordance between chart review and structured interview assessments of schizophrenic symptoms.

Authors:  Ayman H Fanous; Richard L Amdur; Francis A O'Neill; Dermot Walsh; Kenneth S Kendler
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Review 3.  Molecular genetics of the psychosis phenotype.

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4.  [The psychopathology of ego disturbances: history and phenomenology].

Authors:  M Bürgy
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5.  Personality in relation to genetic liability for schizophrenia and bipolar disorder: differential associations with the COMT Val 108/158 Met polymorphism.

Authors:  Amy L Silberschmidt; Scott R Sponheim
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6.  The genetics of symptom-based phenotypes: toward a molecular classification of schizophrenia.

Authors:  Pamela DeRosse; Todd Lencz; Katherine E Burdick; Samuel G Siris; John M Kane; Anil K Malhotra
Journal:  Schizophr Bull       Date:  2008-07-15       Impact factor: 9.306

Review 7.  The diagnostic status of first-rank symptoms.

Authors:  Julie Nordgaard; Sidse M Arnfred; Peter Handest; Josef Parnas
Journal:  Schizophr Bull       Date:  2007-06-11       Impact factor: 9.306

8.  Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia.

Authors:  Pei-Lung Chen; Dimitrios Avramopoulos; Virginia K Lasseter; John A McGrath; M Daniele Fallin; Kung-Yee Liang; Gerald Nestadt; Ningping Feng; Gary Steel; Andrew S Cutting; Paula Wolyniec; Ann E Pulver; David Valle
Journal:  Am J Hum Genet       Date:  2009-01       Impact factor: 11.025

9.  Investigating the relationship between thought interference, somatic passivity and outcomes in patients with psychosis: a natural language processing approach using a clinical records search platform in south London.

Authors:  Thibault Thierry Magrangeas; Anna Kolliakou; Jyoti Sanyal; Rashmi Patel; Robert Stewart
Journal:  BMJ Open       Date:  2022-08-02       Impact factor: 3.006

10.  Structural MRI Differences between Patients with and without First Rank Symptoms: A Delusion?

Authors:  Henriette D Heering; Godefridus J C Koevoets; Laura Koenders; Marise W J Machielsen; Carin J Meijer; Manabu Kubota; Jessica de Nijs; Wiepke Cahn; Hilleke E Hulshoff Pol; Lieuwe de Haan; Rene S Kahn; Neeltje E M van Haren
Journal:  Front Psychiatry       Date:  2015-07-29       Impact factor: 4.157

  10 in total

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