Association of β2-adrenergic receptor polymorphism with the phenotype of aspirin-intolerant acute urticaria

Citations

SCOPUS

10

초록

The genetic mechanism of aspirin intolerant acute urticaria. (AIAU) is unknown. To demonstrate an association between the β2 adrenergic receptor (ADRB2) polymorphism and the phenotype of AIAU, one hundred fourteen patients with AIAU, 110 patients with aspirin intolerant chronic urticaria. (AICU), and 498 normal healthy controls (NC) based on a Korean population were enrolled. The genotype of ADRB2 at 46 A > G was analyzed using a direct sequencing method. The ADRB2 polymorphism at 46 A > G showed a significant difference between AIAU and NC; the frequency of the major genotype was significantly higher in the AIAU group (p = 0.017 in recessive model), while no differences were noted in allele and genotype frequencies between AICU and NC. In conclusion, the ADRB2 (46 A > G) gene polymorphism may contribute to the development of the phenotype of AIAU.

키워드

ADRB2 polymorphism; Aspirin sensitivity; Urticaria; acetylsalicylic acid; beta 2 adrenergic receptor; immunoglobulin E; adult; allergic rhinitis; allergic urticaria; article; aspirin intolerant acute urticaria; aspirin intolerant chronic urticaria; asthma; atopy; controlled study; disease association; disease duration; DNA extraction; female; genetic polymorphism; genotype; human; Korea; major clinical study; male; nonhuman; phenotype; provocation test; statistical significance
제목
Association of β2-adrenergic receptor polymorphism with the phenotype of aspirin-intolerant acute urticaria
저자
Kim H.-A.; Ye Y.-M.; Kim S.-H.; Hur G.-Y.; Park H.S.
DOI
10.3349/ymj.2007.48.6.1079
발행일
2007
유형
Article
저널명
Yonsei Medical Journal
권
48
호
6
페이지
1079 ~ 1081