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Specificity of the STAT4 Genetic Association for Severe Disease Manifestations of Systemic Lupus Erythematosus
Systemic lupus erythematosus (SLE) is a genetically complex disease with heterogeneous clinical manifestations. A polymorphism in the STAT4 gene has recently been established as a risk factor for SLE, but the relationship with specific SLE subphenotypes has not been studied. We studied 137 SNPs in t...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2377340/ https://www.ncbi.nlm.nih.gov/pubmed/18516230 http://dx.doi.org/10.1371/journal.pgen.1000084 |
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author | Taylor, Kimberly E. Remmers, Elaine F. Lee, Annette T. Ortmann, Ward A. Plenge, Robert M. Tian, Chao Chung, Sharon A. Nititham, Joanne Hom, Geoffrey Kao, Amy H. Demirci, F. Yesim Kamboh, M. Ilyas Petri, Michelle Manzi, Susan Kastner, Daniel L. Seldin, Michael F. Gregersen, Peter K. Behrens, Timothy W. Criswell, Lindsey A. |
author_facet | Taylor, Kimberly E. Remmers, Elaine F. Lee, Annette T. Ortmann, Ward A. Plenge, Robert M. Tian, Chao Chung, Sharon A. Nititham, Joanne Hom, Geoffrey Kao, Amy H. Demirci, F. Yesim Kamboh, M. Ilyas Petri, Michelle Manzi, Susan Kastner, Daniel L. Seldin, Michael F. Gregersen, Peter K. Behrens, Timothy W. Criswell, Lindsey A. |
author_sort | Taylor, Kimberly E. |
collection | PubMed |
description | Systemic lupus erythematosus (SLE) is a genetically complex disease with heterogeneous clinical manifestations. A polymorphism in the STAT4 gene has recently been established as a risk factor for SLE, but the relationship with specific SLE subphenotypes has not been studied. We studied 137 SNPs in the STAT4 region genotyped in 4 independent SLE case series (total n = 1398) and 2560 healthy controls, along with clinical data for the cases. Using conditional testing, we confirmed the most significant STAT4 haplotype for SLE risk. We then studied a SNP marking this haplotype for association with specific SLE subphenotypes, including autoantibody production, nephritis, arthritis, mucocutaneous manifestations, and age at diagnosis. To prevent possible type-I errors from population stratification, we reanalyzed the data using a subset of subjects determined to be most homogeneous based on principal components analysis of genome-wide data. We confirmed that four SNPs in very high LD (r(2) = 0.94 to 0.99) were most strongly associated with SLE, and there was no compelling evidence for additional SLE risk loci in the STAT4 region. SNP rs7574865 marking this haplotype had a minor allele frequency (MAF) = 31.1% in SLE cases compared with 22.5% in controls (OR = 1.56, p = 10(−16)). This SNP was more strongly associated with SLE characterized by double-stranded DNA autoantibodies (MAF = 35.1%, OR = 1.86, p<10(−19)), nephritis (MAF = 34.3%, OR = 1.80, p<10(−11)), and age at diagnosis<30 years (MAF = 33.8%, OR = 1.77, p<10(−13)). An association with severe nephritis was even more striking (MAF = 39.2%, OR = 2.35, p<10(−4) in the homogeneous subset of subjects). In contrast, STAT4 was less strongly associated with oral ulcers, a manifestation associated with milder disease. We conclude that this common polymorphism of STAT4 contributes to the phenotypic heterogeneity of SLE, predisposing specifically to more severe disease. |
format | Text |
id | pubmed-2377340 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-23773402008-05-30 Specificity of the STAT4 Genetic Association for Severe Disease Manifestations of Systemic Lupus Erythematosus Taylor, Kimberly E. Remmers, Elaine F. Lee, Annette T. Ortmann, Ward A. Plenge, Robert M. Tian, Chao Chung, Sharon A. Nititham, Joanne Hom, Geoffrey Kao, Amy H. Demirci, F. Yesim Kamboh, M. Ilyas Petri, Michelle Manzi, Susan Kastner, Daniel L. Seldin, Michael F. Gregersen, Peter K. Behrens, Timothy W. Criswell, Lindsey A. PLoS Genet Research Article Systemic lupus erythematosus (SLE) is a genetically complex disease with heterogeneous clinical manifestations. A polymorphism in the STAT4 gene has recently been established as a risk factor for SLE, but the relationship with specific SLE subphenotypes has not been studied. We studied 137 SNPs in the STAT4 region genotyped in 4 independent SLE case series (total n = 1398) and 2560 healthy controls, along with clinical data for the cases. Using conditional testing, we confirmed the most significant STAT4 haplotype for SLE risk. We then studied a SNP marking this haplotype for association with specific SLE subphenotypes, including autoantibody production, nephritis, arthritis, mucocutaneous manifestations, and age at diagnosis. To prevent possible type-I errors from population stratification, we reanalyzed the data using a subset of subjects determined to be most homogeneous based on principal components analysis of genome-wide data. We confirmed that four SNPs in very high LD (r(2) = 0.94 to 0.99) were most strongly associated with SLE, and there was no compelling evidence for additional SLE risk loci in the STAT4 region. SNP rs7574865 marking this haplotype had a minor allele frequency (MAF) = 31.1% in SLE cases compared with 22.5% in controls (OR = 1.56, p = 10(−16)). This SNP was more strongly associated with SLE characterized by double-stranded DNA autoantibodies (MAF = 35.1%, OR = 1.86, p<10(−19)), nephritis (MAF = 34.3%, OR = 1.80, p<10(−11)), and age at diagnosis<30 years (MAF = 33.8%, OR = 1.77, p<10(−13)). An association with severe nephritis was even more striking (MAF = 39.2%, OR = 2.35, p<10(−4) in the homogeneous subset of subjects). In contrast, STAT4 was less strongly associated with oral ulcers, a manifestation associated with milder disease. We conclude that this common polymorphism of STAT4 contributes to the phenotypic heterogeneity of SLE, predisposing specifically to more severe disease. Public Library of Science 2008-05-30 /pmc/articles/PMC2377340/ /pubmed/18516230 http://dx.doi.org/10.1371/journal.pgen.1000084 Text en This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Taylor, Kimberly E. Remmers, Elaine F. Lee, Annette T. Ortmann, Ward A. Plenge, Robert M. Tian, Chao Chung, Sharon A. Nititham, Joanne Hom, Geoffrey Kao, Amy H. Demirci, F. Yesim Kamboh, M. Ilyas Petri, Michelle Manzi, Susan Kastner, Daniel L. Seldin, Michael F. Gregersen, Peter K. Behrens, Timothy W. Criswell, Lindsey A. Specificity of the STAT4 Genetic Association for Severe Disease Manifestations of Systemic Lupus Erythematosus |
title | Specificity of the STAT4 Genetic Association for Severe Disease Manifestations of Systemic Lupus Erythematosus |
title_full | Specificity of the STAT4 Genetic Association for Severe Disease Manifestations of Systemic Lupus Erythematosus |
title_fullStr | Specificity of the STAT4 Genetic Association for Severe Disease Manifestations of Systemic Lupus Erythematosus |
title_full_unstemmed | Specificity of the STAT4 Genetic Association for Severe Disease Manifestations of Systemic Lupus Erythematosus |
title_short | Specificity of the STAT4 Genetic Association for Severe Disease Manifestations of Systemic Lupus Erythematosus |
title_sort | specificity of the stat4 genetic association for severe disease manifestations of systemic lupus erythematosus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2377340/ https://www.ncbi.nlm.nih.gov/pubmed/18516230 http://dx.doi.org/10.1371/journal.pgen.1000084 |
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