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Meta-analysis of genome-wide association data detects a risk locus for major mood disorders on chromosome 3p21.1

The major mood disorders, which include bipolar disorder (BD) and major depressive disorder (MDD), are substantially heritable, but few risk loci have been identified. We performed a meta-analysis of 5 major mood disorder case-control samples, including over 13,600 unique individuals genotyped with...

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Autores principales: McMahon, Francis J., Akula, Nirmala, Schulze, Thomas G., Muglia, Pierandrea, Tozzi, Federica, Detera-Wadleigh, Sevilla D., Steele, C.J.M., Breuer, René, Strohmaier, Jana, Wendland, Jens R., Mattheisen, Manuel, Mühleisen, Thomas W., Maier, Wolfgang, Nöthen, Markus M., Cichon, Sven, Farmer, Anne, Vincent, John B., Holsboer, Florian, Preisig, Martin, Rietschel, Marcella
Formato: Texto
Lenguaje:English
Publicado: 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2854040/
https://www.ncbi.nlm.nih.gov/pubmed/20081856
http://dx.doi.org/10.1038/ng.523
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author McMahon, Francis J.
Akula, Nirmala
Schulze, Thomas G.
Muglia, Pierandrea
Tozzi, Federica
Detera-Wadleigh, Sevilla D.
Steele, C.J.M.
Breuer, René
Strohmaier, Jana
Wendland, Jens R.
Mattheisen, Manuel
Mühleisen, Thomas W.
Maier, Wolfgang
Nöthen, Markus M.
Cichon, Sven
Farmer, Anne
Vincent, John B.
Holsboer, Florian
Preisig, Martin
Rietschel, Marcella
author_facet McMahon, Francis J.
Akula, Nirmala
Schulze, Thomas G.
Muglia, Pierandrea
Tozzi, Federica
Detera-Wadleigh, Sevilla D.
Steele, C.J.M.
Breuer, René
Strohmaier, Jana
Wendland, Jens R.
Mattheisen, Manuel
Mühleisen, Thomas W.
Maier, Wolfgang
Nöthen, Markus M.
Cichon, Sven
Farmer, Anne
Vincent, John B.
Holsboer, Florian
Preisig, Martin
Rietschel, Marcella
author_sort McMahon, Francis J.
collection PubMed
description The major mood disorders, which include bipolar disorder (BD) and major depressive disorder (MDD), are substantially heritable, but few risk loci have been identified. We performed a meta-analysis of 5 major mood disorder case-control samples, including over 13,600 unique individuals genotyped with approximately 500,000 to 1 million single nucleotide polymorphism (SNP) markers on high-density arrays. Allele-wise association results were meta-analyzed with a method that weights results by sample size. We found genome-wide significant evidence that SNPs in a region of chromosome 3p21.1were associated with major mood disorders. The SNP rs2251219 returned the smallest meta-analysis p-value, 3.63 × 10(−8), with a pooled odds ratio of 0.87. Supportive results were observed in 2 out of 3 independent samples tested in a replication study. These results implicate one or more genes in this region in the etiology of major mood disorders and suggest that BD and MDD share genetic risk factors.
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spelling pubmed-28540402010-08-01 Meta-analysis of genome-wide association data detects a risk locus for major mood disorders on chromosome 3p21.1 McMahon, Francis J. Akula, Nirmala Schulze, Thomas G. Muglia, Pierandrea Tozzi, Federica Detera-Wadleigh, Sevilla D. Steele, C.J.M. Breuer, René Strohmaier, Jana Wendland, Jens R. Mattheisen, Manuel Mühleisen, Thomas W. Maier, Wolfgang Nöthen, Markus M. Cichon, Sven Farmer, Anne Vincent, John B. Holsboer, Florian Preisig, Martin Rietschel, Marcella Nat Genet Article The major mood disorders, which include bipolar disorder (BD) and major depressive disorder (MDD), are substantially heritable, but few risk loci have been identified. We performed a meta-analysis of 5 major mood disorder case-control samples, including over 13,600 unique individuals genotyped with approximately 500,000 to 1 million single nucleotide polymorphism (SNP) markers on high-density arrays. Allele-wise association results were meta-analyzed with a method that weights results by sample size. We found genome-wide significant evidence that SNPs in a region of chromosome 3p21.1were associated with major mood disorders. The SNP rs2251219 returned the smallest meta-analysis p-value, 3.63 × 10(−8), with a pooled odds ratio of 0.87. Supportive results were observed in 2 out of 3 independent samples tested in a replication study. These results implicate one or more genes in this region in the etiology of major mood disorders and suggest that BD and MDD share genetic risk factors. 2010-01-17 2010-02 /pmc/articles/PMC2854040/ /pubmed/20081856 http://dx.doi.org/10.1038/ng.523 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
McMahon, Francis J.
Akula, Nirmala
Schulze, Thomas G.
Muglia, Pierandrea
Tozzi, Federica
Detera-Wadleigh, Sevilla D.
Steele, C.J.M.
Breuer, René
Strohmaier, Jana
Wendland, Jens R.
Mattheisen, Manuel
Mühleisen, Thomas W.
Maier, Wolfgang
Nöthen, Markus M.
Cichon, Sven
Farmer, Anne
Vincent, John B.
Holsboer, Florian
Preisig, Martin
Rietschel, Marcella
Meta-analysis of genome-wide association data detects a risk locus for major mood disorders on chromosome 3p21.1
title Meta-analysis of genome-wide association data detects a risk locus for major mood disorders on chromosome 3p21.1
title_full Meta-analysis of genome-wide association data detects a risk locus for major mood disorders on chromosome 3p21.1
title_fullStr Meta-analysis of genome-wide association data detects a risk locus for major mood disorders on chromosome 3p21.1
title_full_unstemmed Meta-analysis of genome-wide association data detects a risk locus for major mood disorders on chromosome 3p21.1
title_short Meta-analysis of genome-wide association data detects a risk locus for major mood disorders on chromosome 3p21.1
title_sort meta-analysis of genome-wide association data detects a risk locus for major mood disorders on chromosome 3p21.1
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2854040/
https://www.ncbi.nlm.nih.gov/pubmed/20081856
http://dx.doi.org/10.1038/ng.523
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