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An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves' disease.

ABSTRACT: BACKGROUND: Graves' disease is a female preponderant autoimmune illness and the contribution of the X chromosome to its risk has long been appreciated. However, no X-linked susceptibility loci have been indentified from recent genome-wide association studies (GWAS). METHODS: We re-examined the X chromosome data from our recent GWAS for Graves' disease by including males that were previously excluded from the X chromosome analyses. The data were analysed using logistic regression analysis including sex as a covariate, and an additive method assuming X chromosome inactivation, implemented in snpMatrix. RESULTS: A cluster of single nucleotide polymorphism (SNPs) at Xq21.1 was found showing association with genome-wide significance, among which rs3827440 was a non-synonymous SNP of GPR174 (P(logistic regression)= 9.52×10(-8); P(snpMatrix)=4.60×10(-9); OR=1.76, 95% CI 1.45 to 2.13). The association was reproduced in an independent sample collection set including 4564 Graves' disease cases and 3968 sex matched controls (combined P(logistic regression)=5.53×10(-21); combined P(snpMatrix)=4.26×10(-22); OR=1.69, 95% CI 1.53 to 1.86). Notably, GPR174 was widely expressed in immune related tissues and rs3827440 genotypes were associated with distinct mRNA levels (p=0.002). GPR174 did not show sex biased gene expression in our expression analysis. Resequencing study suggested the contribution of some rare variants in the GPR174 gene region to disease risk with a collapsing p value of 1.16×10(-3). CONCLUSIONS: The finding of an X-linked risk locus for Graves' disease expands our understanding of the role of the X chromosome in disease susceptibility.

SUBMITTER: Chu X

PROVIDER: S-EPMC3686253 | biostudies-literature | 2013 Jul

REPOSITORIES: biostudies-literature

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An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves' disease.

Chu Xun X Shen Min M Xie Fang F Miao Xiao-Jing XJ Shou Wei-Hua WH Liu Lin L Yang Peng-Peng PP Bai Ya-Nan YN Zhang Kai-Yue KY Yang Lin L Hua Qi Q Liu Wen-Dong WD Dong Yan Y Wang Hai-Feng HF Shi Jin-Xiu JX Wang Yi Y Song Huai-Dong HD Chen Sai-Juan SJ Chen Zhu Z Huang Wei W

Journal of medical genetics 20130510 7

<h4>Background</h4>Graves' disease is a female preponderant autoimmune illness and the contribution of the X chromosome to its risk has long been appreciated. However, no X-linked susceptibility loci have been indentified from recent genome-wide association studies (GWAS).<h4>Methods</h4>We re-examined the X chromosome data from our recent GWAS for Graves' disease by including males that were previously excluded from the X chromosome analyses. The data were analysed using logistic regression ana ...[more]

PMID: 23667180

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An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves' disease.

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An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves' disease.

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