V体育安卓版 - Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci
- PMID: 18204446
- PMCID: PMC3712260
- DOI: 10.1038/ng.81
Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci
Abstract
Systemic lupus erythematosus (SLE) is a common systemic autoimmune disease with complex etiology but strong clustering in families (lambda(S) = approximately 30). We performed a genome-wide association scan using 317,501 SNPs in 720 women of European ancestry with SLE and in 2,337 controls, and we genotyped consistently associated SNPs in two additional independent sample sets totaling 1,846 affected women and 1,825 controls. Aside from the expected strong association between SLE and the HLA region on chromosome 6p21 and the previously confirmed non-HLA locus IRF5 on chromosome 7q32, we found evidence of association with replication (1. 1 x 10(-7) < P(overall) < 1. 6 x 10(-23); odds ratio = 0. 82-1 VSports手机版. 62) in four regions: 16p11. 2 (ITGAM), 11p15. 5 (KIAA1542), 3p14. 3 (PXK) and 1q25. 1 (rs10798269). We also found evidence for association (P < 1 x 10(-5)) at FCGR2A, PTPN22 and STAT4, regions previously associated with SLE and other autoimmune diseases, as well as at > or =9 other loci (P < 2 x 10(-7)). Our results show that numerous genes, some with known immune-related functions, predispose to SLE. .
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Comment in
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The developing mosaic of autoimmune disease risk.Nat Genet. 2008 Feb;40(2):131-2. doi: 10.1038/ng0208-131. Nat Genet. 2008. PMID: 18227869 No abstract available.
"VSports注册入口" References
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- Danchenko N, Satia JA, Anthony MS. Epidemiology of systemic lupus erythematosus: a comparison of worldwide disease burden. Lupus. 2006;15:308–318. - PubMed
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- Deapen D, et al. A revised estimate of twin concordance in systemic lupus erythematosus. Arthritis Rheum. 1992;35:311–318. - PubMed (VSports在线直播)
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