All polymorphisms studied in this paper [PMID: 19950296] , total : 65 polymorphisms

Title : Contribution of a haplotype in the HLA region to anti-cyclic citrullinated peptide antibody positivity in rheumatoid arthritis, independently of HLA-DRB1.
Abstract : OBJECTIVE: To examine the risk of anti-cyclic citrullinated peptide (anti-CCP) antibody positivity in rheumatoid arthritis (RA) patients carrying certain haplotypes in the HLA region. METHODS: A total of 1,389 Japanese patients with RA were genotyped for 30 single-nucleotide polymorphisms (SNPs) in the HLA region using commercial oligonucleotide arrays (from Perlegen or Affymetrix) as well as for HLA-DRB1 alleles using a sequence-specific polymerase chain reaction method. Stepwise logistic regression was used to select from among the 30 SNPs the ones that represented a risk of anti-CCP antibody positivity. Haplotypes of the selected SNPs were inferred using an expectation-maximization algorithm. Associations of individual SNPs were evaluated with the Cochran-Armitage test for trend. DRB1 alleles and haplotypes were evaluated with the chi-square test. Heterogeneities of risks among the shared epitope (SE) and non-SE HLA-DRB1 alleles were examined using the exact test. Haplotype associations that were independent of individual HLA-DRB1 alleles were evaluated using the likelihood ratio test. RESULTS: Significant associations were found for 9 SNPs (smallest P value being 2.4x10(-8)) and in 4 HLA-DRB1 alleles (smallest P value being 2.0x10(-10) in DRB1*0405). Stepwise logistic regression selected 4 SNPs (rs9262638, rs7775228, rs4713580, and rs9277359). Among the 16 inferred haplotypes of these 4 SNPs, 6 indicated significant associations (smallest P value being 1.9x10(-11)). Risks among SE and non-SE alleles were significantly heterogeneous (P=0.0095 and P=9.8x10(-9), respectively), indicating the importance of stratification with individual DRB1 alleles rather than SE alleles. Conditional analysis of the risk associated with individual DRB1 alleles identified a risk haplotype that was independent of DRB1 (odds ratio 2.00 [95% confidence interval 1.44-2.79], P=2.6x10(-5)). CONCLUSION: Heterogeneous risks of anti-CCP antibody positivity were confirmed among SE and non-SE alleles in our patient population. A risk haplotype in the HLA region that is independent of HLA-DRB1 was confirmed.
Author : Okada Y,Yamada R,Suzuki A,Kochi Y,Shimane K,Myouzen K,Kubo M,Nakamura Y,Yamamoto K,
Source : Arthritis Rheum. 2009 Dec;60(12):3582-90. doi: 10.1002/art.24939.
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No.Polymorphism nameGene SymbolEntrez Gene ID
31 NA HLA-DRB1 3123
32 NA HLA-DRB1 3123
33 NA HLA-DRB1 3123
34 NA HLA-DRB1 3123
35 NA HLA-DRB1 3123
36 NA HLA-DRB1 3123
37 NA HLA-DRB1 3123
38 NA HLA-DRB1 3123
39 NA HLA-DRB1 3123
40 NA HLA-DRB1 3123
41 NA HLA-DRB1 3123
42 NA HLA-DRB1 3123
43 NA HLA-DRB1 3123
44 NA HLA-DRB1 3123
45 NA HLA-DRB1 3123
46 NA HLA-DRB1 3123
47 NA HLA-DRB1 3123
48 NA HLA-DRB1 3123
49 NA HLA-DRB1 3123
50 NA HLA-DRB1 3123
51 NA HLA-DRB1 3123
52 NA HLA-DRB1 3123
53 NA HLA-DRB1 3123
54 NA HLA-DRB1 3123
55 NA HLA-DRB1 3123
56 NA HLA-DRB1 3123
57 NA HLA-DRB1 3123
58 NA HLA-DRB1 3123
59 NA HLA-DRB1 3123
60 NA HLA-DRB1 3123
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