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Association of the variants in AGT gene with modified drug response in Korean aspirin-intolerant asthma patients

Authors
Pasaje, Charisse Flerida A.Kim, Jeong-HyunPark, Byung-LaeCheong, Hyun SubPark, Tae-JoonLee, Jin-SolKim, YonghaBae, Joon SeolKim, Jin MooPark, Jong SookPark, Choon-SikShin, Hyoung Doo
Issue Date
Oct-2011
Publisher
Academic Press
Keywords
Aspirin-intolerant asthma; AGT; MLK; Polymorphism; Haplotype
Citation
Pulmonary Pharmacology and Therapeutics, v.24, no.5, pp 595 - 601
Pages
7
Journal Title
Pulmonary Pharmacology and Therapeutics
Volume
24
Number
5
Start Page
595
End Page
601
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/16171
DOI
10.1016/j.pupt.2011.05.007
ISSN
1094-5539
1522-9629
Abstract
The angiotensinogen (AGT) gene enhances the effect of several bronchoconstrictors and produces a peptide that is accumulated in the airways of asthma patients: events that may underpin the pathogenesis of aspirin-intolerant asthma (ALA). To carry out a case-control analysis between AGT and aspirin-induced bronchospasm following treatment with an anti-asthma drug, montelukast (MLK), 38 single nucleotide polymorphisms (SNPs) in AGT were genotyped in 56 AIA cohort. Genotyping was performed with TaqMan assay and haplotypes were inferred using PHASE algorithm ver. 2.0. Statistical analyses of each SNPs and haplotypes were performed using SAS version 9.1. Among 13 variants displaying significant signals, two SNPs (+2401C>G and +2476C>T) in the intronic region of AGT were significantly associated with modification of drug response even after correction for multiple testing (P=0.0009-0.002; P-corr=0.02-0.03). Furthermore, the two variants also exhibited associations with MLK response rate (P=0.0003-0.0006: P-corr=0.006-0.01). Although our results are preliminary and further replication in a larger-scale group of subjects should be warranted, these observations provide evidence that AGT variants might be one of genetic factors involved in the response of anti-asthma drugs in AIA patients. (C) 2011 Elsevier Ltd. All rights reserved.
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