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Monoamine Oxidase A and B Gene Polymorphisms and Negative and Positive Symptoms in Schizophrenia
Given that schizophrenia is a heterogeneous disorder, the analysis of clinical characteristics could help to identify homogeneous phenotypes that may be of relevance in genetic studies. Linkage and association studies have suggested that a locus predisposing to schizophrenia may reside within Xp11....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scholarly Research Network
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3658801/ https://www.ncbi.nlm.nih.gov/pubmed/23738213 http://dx.doi.org/10.5402/2012/852949 |
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author | Camarena, Beatriz Fresán, Ana Aguilar, Alejandro Escamilla, Raúl Saracco, Ricardo Palacios, Jorge Tovilla, Alfonso Nicolini, Humberto |
author_facet | Camarena, Beatriz Fresán, Ana Aguilar, Alejandro Escamilla, Raúl Saracco, Ricardo Palacios, Jorge Tovilla, Alfonso Nicolini, Humberto |
author_sort | Camarena, Beatriz |
collection | PubMed |
description | Given that schizophrenia is a heterogeneous disorder, the analysis of clinical characteristics could help to identify homogeneous phenotypes that may be of relevance in genetic studies. Linkage and association studies have suggested that a locus predisposing to schizophrenia may reside within Xp11. We analyzed uVNTR and rs1137070, polymorphisms from MAOA and rs1799836 of MAOB genes to perform single SNP case-control association study in a sample of 344 schizophrenia patients and 124 control subjects. Single polymorphism analysis of uVNTR, rs1137070 and rs1799836 SNPs did not show statistical differences between cases and controls. Multivariate ANOVA analysis of clinical characteristics showed statistical differences between MAOB/rs1799836 and affective flattening scores (F = 4.852, P = 0.009), and significant association between MAOA/uVNTR and affective flattening in female schizophrenia patients (F = 4.236, P = 0.016) after Bonferroni's correction. Our preliminary findings could suggest that severity of affective flattening may be associated by modifier variants of MAOA and MAOB genes in female Mexican patients with schizophrenia. However, further large-scale studies using quantitative symptom-based phenotypes and several candidate variants should be analyzed to obtain a final conclusion. |
format | Online Article Text |
id | pubmed-3658801 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Scholarly Research Network |
record_format | MEDLINE/PubMed |
spelling | pubmed-36588012013-06-04 Monoamine Oxidase A and B Gene Polymorphisms and Negative and Positive Symptoms in Schizophrenia Camarena, Beatriz Fresán, Ana Aguilar, Alejandro Escamilla, Raúl Saracco, Ricardo Palacios, Jorge Tovilla, Alfonso Nicolini, Humberto ISRN Psychiatry Clinical Study Given that schizophrenia is a heterogeneous disorder, the analysis of clinical characteristics could help to identify homogeneous phenotypes that may be of relevance in genetic studies. Linkage and association studies have suggested that a locus predisposing to schizophrenia may reside within Xp11. We analyzed uVNTR and rs1137070, polymorphisms from MAOA and rs1799836 of MAOB genes to perform single SNP case-control association study in a sample of 344 schizophrenia patients and 124 control subjects. Single polymorphism analysis of uVNTR, rs1137070 and rs1799836 SNPs did not show statistical differences between cases and controls. Multivariate ANOVA analysis of clinical characteristics showed statistical differences between MAOB/rs1799836 and affective flattening scores (F = 4.852, P = 0.009), and significant association between MAOA/uVNTR and affective flattening in female schizophrenia patients (F = 4.236, P = 0.016) after Bonferroni's correction. Our preliminary findings could suggest that severity of affective flattening may be associated by modifier variants of MAOA and MAOB genes in female Mexican patients with schizophrenia. However, further large-scale studies using quantitative symptom-based phenotypes and several candidate variants should be analyzed to obtain a final conclusion. International Scholarly Research Network 2012-04-19 /pmc/articles/PMC3658801/ /pubmed/23738213 http://dx.doi.org/10.5402/2012/852949 Text en Copyright © 2012 Beatriz Camarena et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Study Camarena, Beatriz Fresán, Ana Aguilar, Alejandro Escamilla, Raúl Saracco, Ricardo Palacios, Jorge Tovilla, Alfonso Nicolini, Humberto Monoamine Oxidase A and B Gene Polymorphisms and Negative and Positive Symptoms in Schizophrenia |
title | Monoamine Oxidase A and B Gene Polymorphisms and Negative and Positive Symptoms in Schizophrenia |
title_full | Monoamine Oxidase A and B Gene Polymorphisms and Negative and Positive Symptoms in Schizophrenia |
title_fullStr | Monoamine Oxidase A and B Gene Polymorphisms and Negative and Positive Symptoms in Schizophrenia |
title_full_unstemmed | Monoamine Oxidase A and B Gene Polymorphisms and Negative and Positive Symptoms in Schizophrenia |
title_short | Monoamine Oxidase A and B Gene Polymorphisms and Negative and Positive Symptoms in Schizophrenia |
title_sort | monoamine oxidase a and b gene polymorphisms and negative and positive symptoms in schizophrenia |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3658801/ https://www.ncbi.nlm.nih.gov/pubmed/23738213 http://dx.doi.org/10.5402/2012/852949 |
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