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HLA-DRA polymorphisms associated with risk of nasal polyposis in asthmatic patients

Authors
Kim, Jeong-HyunPark, Byung-LaeCheong, Hyun SubPasaje, Charisse Flerida A.Bae, Joon SeolPark, Jong SookUh, Soo-TaekKim, Yong-HoonKim, Mi-KyeongChoi, Inseon S.Choi, Byoung WhuiPark, Choon-SikShin, Hyoung Doo
Issue Date
Jan-2012
Publisher
OCEAN SIDE PUBLICATIONS INC
Citation
AMERICAN JOURNAL OF RHINOLOGY & ALLERGY, v.26, no.1, pp 12 - 17
Pages
6
Journal Title
AMERICAN JOURNAL OF RHINOLOGY & ALLERGY
Volume
26
Number
1
Start Page
12
End Page
17
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/20629
DOI
10.2500/ajra.2012.26.3692
ISSN
1945-8924
1945-8932
Abstract
Background: Nasal polyps, part of the aspirin triad symptoms, are edematous protrusions arising from the mucosa of the nasal sinuses. Although the causative factors and pathogenesis of the polyps are unknown, the significant effect of human leukocyte antigen-DR (HLA-DR) expression in nasal polyps and genetic associations of the major histocompatibility complex class II, DR alpha (HLA-DRA) with immune-mediated diseases have been revealed. Methods: To investigate the associations of HLA-DRA polymorphisms with nasal polyposis in asthmatic patients and in aspirin-hypersensitive subgroups, 22 single nucleotide polymorphisms (SNPs) were genotyped in a total of 467 asthmatic patients including 158 nasal polyp-positive and 309 polyp-negative subjects. Results: Statistical analysis showed that four SNPs (p = 0.0005-0.02; Pcorr = 0.009-0.033) and one haplotype (p = 0.002; Pcorr = 0.029) were significantly associated with the presence of nasal polyposis in asthmatic patients. In further analysis, although significant signals disappeared after corrections for multiple testing, two HLA-DRA polymorphisms (rs9268644C>A, rs3129878A>C) were found to be potential markers for nasal polyp development in aspirin-tolerant asthma (p = 0.005 and 0.007, respectively) compared with the aspirin-exacerbated respiratory disease (p > 0.05) subgroup. In silico analysis predicted major "C" allele of rs14004C>A in 5'-untranslated region as a potential binding site for regulatory glucocorticoid receptor. In addition, sequence nearby rs1051336G>A is suspected to be a pyrimidine-rich element that affects mRNA stability. Conclusion: Despite the need for replication in larger cohorts and/or functional evaluations, our findings suggest that HLA-DRA polymorphisms might contribute to nasal polyposis susceptibility in patients with asthma. (Am J Rhinol Allergy 26, 12-17, 2012; doi: 10.2500/ajra.2012.26.3692)
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