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A Disrupted-in-Schizophrenia 1 Gene Variant is Associated with Clinical Symptomatology in Patients with First-Episode Psychosis
OBJECTIVE: DISC1 gene is one of the main candidate genes for schizophrenia since it has been associated to the illness in several populations. Moreover, variations in several DISC1 polymorphisms, and in particular Ser704Cys SNP, have been associated in schizophrenic patients to structural and functi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Neuropsychiatric Association
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4023094/ https://www.ncbi.nlm.nih.gov/pubmed/24843375 http://dx.doi.org/10.4306/pi.2014.11.2.186 |
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author | Vázquez-Bourgon, Javier Mata, Ignacio Roiz-Santiáñez, Roberto Ayesa-Arriola, Rosa Suárez Pinilla, Paula Tordesillas-Gutiérrez, Diana Vázquez-Barquero, José Luis Crespo-Facorro, Benedicto |
author_facet | Vázquez-Bourgon, Javier Mata, Ignacio Roiz-Santiáñez, Roberto Ayesa-Arriola, Rosa Suárez Pinilla, Paula Tordesillas-Gutiérrez, Diana Vázquez-Barquero, José Luis Crespo-Facorro, Benedicto |
author_sort | Vázquez-Bourgon, Javier |
collection | PubMed |
description | OBJECTIVE: DISC1 gene is one of the main candidate genes for schizophrenia since it has been associated to the illness in several populations. Moreover, variations in several DISC1 polymorphisms, and in particular Ser704Cys SNP, have been associated in schizophrenic patients to structural and functional modifications in two brain areas (pre-frontal cortex and hippocampus) that play a central role in the genesis of psychotic symptoms. This study tested the association between Ser704Cys DISC1 polymorphism and the clinical onset of psychosis. METHODS: Two hundred and thirteen Caucasian drug-naive patients experiencing a first episode of non-affective psychosis were genotyped for rs821616 (Ser704Cys) SNP of the DISC1 gene. The clinical severity of the illness was assessed using SAPS and SANS scales. Other clinical and socio-demographic variables were recorded to rule out possible confounding effects. RESULTS: Patients homozygous for the Ser allele of the Ser704Cys DISC1 SNP had significantly (p<0.05) higher rates at the positive symptoms dimension (SAPS-SANS scales) and hallucinations item, compared to Cys carriers. CONCLUSION: DISC1 gene variations may modulate the clinical severity of the psychosis at the onset of the disorder. |
format | Online Article Text |
id | pubmed-4023094 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Korean Neuropsychiatric Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-40230942014-05-19 A Disrupted-in-Schizophrenia 1 Gene Variant is Associated with Clinical Symptomatology in Patients with First-Episode Psychosis Vázquez-Bourgon, Javier Mata, Ignacio Roiz-Santiáñez, Roberto Ayesa-Arriola, Rosa Suárez Pinilla, Paula Tordesillas-Gutiérrez, Diana Vázquez-Barquero, José Luis Crespo-Facorro, Benedicto Psychiatry Investig Original Article OBJECTIVE: DISC1 gene is one of the main candidate genes for schizophrenia since it has been associated to the illness in several populations. Moreover, variations in several DISC1 polymorphisms, and in particular Ser704Cys SNP, have been associated in schizophrenic patients to structural and functional modifications in two brain areas (pre-frontal cortex and hippocampus) that play a central role in the genesis of psychotic symptoms. This study tested the association between Ser704Cys DISC1 polymorphism and the clinical onset of psychosis. METHODS: Two hundred and thirteen Caucasian drug-naive patients experiencing a first episode of non-affective psychosis were genotyped for rs821616 (Ser704Cys) SNP of the DISC1 gene. The clinical severity of the illness was assessed using SAPS and SANS scales. Other clinical and socio-demographic variables were recorded to rule out possible confounding effects. RESULTS: Patients homozygous for the Ser allele of the Ser704Cys DISC1 SNP had significantly (p<0.05) higher rates at the positive symptoms dimension (SAPS-SANS scales) and hallucinations item, compared to Cys carriers. CONCLUSION: DISC1 gene variations may modulate the clinical severity of the psychosis at the onset of the disorder. Korean Neuropsychiatric Association 2014-04 2014-04-11 /pmc/articles/PMC4023094/ /pubmed/24843375 http://dx.doi.org/10.4306/pi.2014.11.2.186 Text en Copyright © 2014 Korean Neuropsychiatric Association http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Vázquez-Bourgon, Javier Mata, Ignacio Roiz-Santiáñez, Roberto Ayesa-Arriola, Rosa Suárez Pinilla, Paula Tordesillas-Gutiérrez, Diana Vázquez-Barquero, José Luis Crespo-Facorro, Benedicto A Disrupted-in-Schizophrenia 1 Gene Variant is Associated with Clinical Symptomatology in Patients with First-Episode Psychosis |
title | A Disrupted-in-Schizophrenia 1 Gene Variant is Associated with Clinical Symptomatology in Patients with First-Episode Psychosis |
title_full | A Disrupted-in-Schizophrenia 1 Gene Variant is Associated with Clinical Symptomatology in Patients with First-Episode Psychosis |
title_fullStr | A Disrupted-in-Schizophrenia 1 Gene Variant is Associated with Clinical Symptomatology in Patients with First-Episode Psychosis |
title_full_unstemmed | A Disrupted-in-Schizophrenia 1 Gene Variant is Associated with Clinical Symptomatology in Patients with First-Episode Psychosis |
title_short | A Disrupted-in-Schizophrenia 1 Gene Variant is Associated with Clinical Symptomatology in Patients with First-Episode Psychosis |
title_sort | disrupted-in-schizophrenia 1 gene variant is associated with clinical symptomatology in patients with first-episode psychosis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4023094/ https://www.ncbi.nlm.nih.gov/pubmed/24843375 http://dx.doi.org/10.4306/pi.2014.11.2.186 |
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