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Meta-analysis of GWAS on both Chinese and European populations identifies GPR173 as a novel X chromosome susceptibility gene for SLE

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dc.contributor.author Zhang, Huoru
dc.contributor.author Zhang, Yan
dc.contributor.author Wang, Yong-Fei
dc.contributor.author Morris, David
dc.contributor.author Nattiya Hirankarn
dc.contributor.author Sheng, Yujun
dc.contributor.author Shen, Jiangshan
dc.contributor.author Pan, Hai-Feng
dc.contributor.author Yang, Jing
dc.contributor.author Yang, Sen
dc.contributor.author Cui, Yong
dc.contributor.author Ye, Dong-Qing
dc.contributor.author Vyse, Timothy J.
dc.contributor.author Zhang, Xuejun
dc.contributor.author Lau, Yu Lung
dc.contributor.author Yang, Wanling
dc.contributor.other Chulalongkorn University. Faculty of Medicine
dc.date.accessioned 2019-05-12T09:52:15Z
dc.date.available 2019-05-12T09:52:15Z
dc.date.issued 2018-05-03
dc.identifier.citation Arthritis Research & Therapy. Vol.20, Article no. 92 (2018), 8 pages en_US
dc.identifier.issn 1478-6362
dc.identifier.uri http://cuir.car.chula.ac.th/handle/123456789/61728
dc.description.abstract Background : Systemic lupus erythematous (SLE) is a complex autoimmune disease with female predominance, particularly affecting those of childbearing age. We performed analysis of three genome-wide genotyping datasets of populations of both Chinese and European origin. Methods : This study involved 5695 cases and 10,357 controls in the discovery stage. The lead signal on chromosome X was followed by replication in three additional Asian cohorts, with 2300 cases and 4244 controls in total. Conditional analysis of the known associated loci on chromosome X was also performed to further explore independent signals. Results : Single-nucleotide polymorphism rs13440883 in GPR173 was found to be significantly associated with SLE (Pmeta = 7.53 × 10− 9, ORmeta= 1.16), whereas conditional analysis provided evidence of a potential independent signal in the L1CAM-IRAK1-MECP2 region in Asian populations (rs5987175 [LCA10]). Conclusions : We identified a novel SLE susceptibility locus on the X chromosome. This finding emphasizes the importance of the X chromosome in disease pathogenesis and highlights the role of sex chromosomes in the female bias of SLE. en_US
dc.language.iso en en_US
dc.publisher BioMed Central Ltd. en_US
dc.relation.uri https://doi.org/10.1186/s13075-018-1590-3
dc.relation.uri https://arthritis-research.biomedcentral.com/articles/10.1186/s13075-018-1590-3
dc.rights © The Author(s) 2018 en_US
dc.title Meta-analysis of GWAS on both Chinese and European populations identifies GPR173 as a novel X chromosome susceptibility gene for SLE en_US
dc.type Article en_US
dc.email.author No information provided
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dc.email.author No information provided
dc.email.author Nattiya.H@Chula.ac.th
dc.email.author No information provided
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dc.subject.keyword Systemic lupus erythematosus en_US
dc.subject.keyword X chromosome en_US
dc.subject.keyword Association en_US
dc.subject.keyword Genetics en_US
dc.subject.keyword Single-nucleotide polymorphisms en_US
dc.identifier.DOI 10.1186/s13075-018-1590-3


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