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The DAOA/G30 locus and affective disorders: haplotype based association study in a polydiagnostic approach
BACKGROUND: The DAOA/G30 (D-amino acid oxidase activator) gene complex at chromosomal region 13q32-33 is one of the most intriguing susceptibility loci for the major psychiatric disorders, although there is no consensus about the specific risk alleles or haplotypes across studies. METHODS: In a case...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2921107/ https://www.ncbi.nlm.nih.gov/pubmed/20667145 http://dx.doi.org/10.1186/1471-244X-10-59 |
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author | Gawlik, Micha Wehner, Ingeborg Mende, Meinhard Jung, Sven Pfuhlmann, Bruno Knapp, Michael Stöber, Gerald |
author_facet | Gawlik, Micha Wehner, Ingeborg Mende, Meinhard Jung, Sven Pfuhlmann, Bruno Knapp, Michael Stöber, Gerald |
author_sort | Gawlik, Micha |
collection | PubMed |
description | BACKGROUND: The DAOA/G30 (D-amino acid oxidase activator) gene complex at chromosomal region 13q32-33 is one of the most intriguing susceptibility loci for the major psychiatric disorders, although there is no consensus about the specific risk alleles or haplotypes across studies. METHODS: In a case-control sample of German descent (affective psychosis: n = 248; controls: n = 188) we examined seven single nucleotide polymorphisms (SNPs) around DAOA/G30 (rs3916966, rs1935058, rs2391191, rs1935062, rs947267, rs3918342, and rs9558575) for genetic association in a polydiagnostic approach (ICD 10; Leonhard's classification). RESULTS: No single marker showed evidence of overall association with affective disorder neither in ICD10 nor Leonhard's classification. Haplotype analysis revealed no association with recurrent unipolar depression or bipolar disorder according to ICD10, within Leonhard's classification manic-depression was associated with a 3-locus haplotype (rs2391191, rs1935062, and rs3916966; P = 0.022) and monopolar depression with a 5-locus combination at the DAOA/G30 core region (P = 0.036). CONCLUSION: Our data revealed potential evidence for partially overlapping risk haplotypes at the DAOA/G30 locus in Leonhard's affective psychoses, but do not support a common genetic contribution of the DAOA/G30 gene complex to the pathogenesis of affective disorders. |
format | Text |
id | pubmed-2921107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29211072010-08-13 The DAOA/G30 locus and affective disorders: haplotype based association study in a polydiagnostic approach Gawlik, Micha Wehner, Ingeborg Mende, Meinhard Jung, Sven Pfuhlmann, Bruno Knapp, Michael Stöber, Gerald BMC Psychiatry Research Article BACKGROUND: The DAOA/G30 (D-amino acid oxidase activator) gene complex at chromosomal region 13q32-33 is one of the most intriguing susceptibility loci for the major psychiatric disorders, although there is no consensus about the specific risk alleles or haplotypes across studies. METHODS: In a case-control sample of German descent (affective psychosis: n = 248; controls: n = 188) we examined seven single nucleotide polymorphisms (SNPs) around DAOA/G30 (rs3916966, rs1935058, rs2391191, rs1935062, rs947267, rs3918342, and rs9558575) for genetic association in a polydiagnostic approach (ICD 10; Leonhard's classification). RESULTS: No single marker showed evidence of overall association with affective disorder neither in ICD10 nor Leonhard's classification. Haplotype analysis revealed no association with recurrent unipolar depression or bipolar disorder according to ICD10, within Leonhard's classification manic-depression was associated with a 3-locus haplotype (rs2391191, rs1935062, and rs3916966; P = 0.022) and monopolar depression with a 5-locus combination at the DAOA/G30 core region (P = 0.036). CONCLUSION: Our data revealed potential evidence for partially overlapping risk haplotypes at the DAOA/G30 locus in Leonhard's affective psychoses, but do not support a common genetic contribution of the DAOA/G30 gene complex to the pathogenesis of affective disorders. BioMed Central 2010-07-29 /pmc/articles/PMC2921107/ /pubmed/20667145 http://dx.doi.org/10.1186/1471-244X-10-59 Text en Copyright ©2010 Gawlik et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Gawlik, Micha Wehner, Ingeborg Mende, Meinhard Jung, Sven Pfuhlmann, Bruno Knapp, Michael Stöber, Gerald The DAOA/G30 locus and affective disorders: haplotype based association study in a polydiagnostic approach |
title | The DAOA/G30 locus and affective disorders: haplotype based association study in a polydiagnostic approach |
title_full | The DAOA/G30 locus and affective disorders: haplotype based association study in a polydiagnostic approach |
title_fullStr | The DAOA/G30 locus and affective disorders: haplotype based association study in a polydiagnostic approach |
title_full_unstemmed | The DAOA/G30 locus and affective disorders: haplotype based association study in a polydiagnostic approach |
title_short | The DAOA/G30 locus and affective disorders: haplotype based association study in a polydiagnostic approach |
title_sort | daoa/g30 locus and affective disorders: haplotype based association study in a polydiagnostic approach |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2921107/ https://www.ncbi.nlm.nih.gov/pubmed/20667145 http://dx.doi.org/10.1186/1471-244X-10-59 |
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