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http://purl.uniprot.org/citations/23257407http://www.w3.org/2000/01/rdf-schema#comment"

Background

Human leukocyte antigen (HLA) antigens and genes have long been reported associated with systemic lupus erythematosus (SLE) susceptibility in many populations. With the advance in technologies such as genome-wide association studies, many newly discovered SLE-associated single-nucleotide polymorphisms (SNPs) have been reported in recent years. These include HLA-DRB1/HLA-DQA1 rs9271366 and HLA-DQB1/HLA-DQA2 rs9275328. Our aim was to investigate these SNPs in a Malaysian SLE cohort.

Materials and methods

SNPs rs9271366 and rs9275328 were screened across 790 Malaysian citizens from three ethnic groups (360 patients and 430 healthy volunteers) by Taqman SNP genotyping assays. Allele and genotyping frequencies, Hardy-Weinberg equilibrium, Fisher's exact test and odds ratio were calculated for each SNP and ethnic group. Linkage disequilibrium and interaction between the two SNPs were also evaluated.

Results

The minor allele G and its homozygous genotype GG of HLA-DRB1/HLA-DQA1 rs9271366 significantly increased the SLE susceptibility in Malaysian patients, including those of Malay and Chinese ethnicity (odds ratio (OR) > 1, p < 0.05). As for HLA-DQB1/HLA-DQA2 rs9275328, the minor allele T and the heterozygous genotype CT conferred protective effect to SLE in Malaysians, as well as in Malays and Chinese, by having OR < 1 and p value <0.05. Both SNPs did not show associations to SLE in Indians. D' and r (2) values for the two SNPs in LD analysis were 0.941 and 0.065, respectively, with haplotype GC and AT being significantly associated with SLE (p < 5.0 × 10(-4)) after 10,000 permutations were performed. The MDR test clustered the genotype combinations of GG and CC, and AG and CC of rs9271366 and rs9275328, accordingly, as high-risk group, and the two SNPs interacted redundantly by removing 1.96% of the entropy.

Conclusions

Our findings suggest that in addition to some classical HLA variants, rs9271366 and rs9275328 are additional polymorphisms worth considering in the Malaysian and possibly in a larger Asian SLE scenario."xsd:string
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http://purl.uniprot.org/citations/23257407http://purl.uniprot.org/core/author"Othman I."xsd:string
http://purl.uniprot.org/citations/23257407http://purl.uniprot.org/core/author"Chua K.H."xsd:string
http://purl.uniprot.org/citations/23257407http://purl.uniprot.org/core/author"Phipps M.E."xsd:string
http://purl.uniprot.org/citations/23257407http://purl.uniprot.org/core/author"Tan L.P."xsd:string
http://purl.uniprot.org/citations/23257407http://purl.uniprot.org/core/author"Chai H.C."xsd:string
http://purl.uniprot.org/citations/23257407http://purl.uniprot.org/core/date"2013"xsd:gYear
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http://purl.uniprot.org/citations/23257407http://purl.uniprot.org/core/pages"198-204"xsd:string
http://purl.uniprot.org/citations/23257407http://purl.uniprot.org/core/title"HLA variants rs9271366 and rs9275328 are associated with systemic lupus erythematosus susceptibility in Malays and Chinese."xsd:string
http://purl.uniprot.org/citations/23257407http://purl.uniprot.org/core/volume"22"xsd:string
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