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Association of thromboxane A2 receptor gene polymorphism with the phenotype of acetyl salicylic acid-intolerant asthma

Association of thromboxane A2 receptor gene polymorphism with the phenotype of acetyl salicylic acid-intolerant asthma
Association of thromboxane A2 receptor gene polymorphism with the phenotype of acetyl salicylic acid-intolerant asthma
Background and objective The thromboxane A2 receptor (TBXA2R) is a receptor for a potent bronchoconstrictor, TBXA2 which is known to be related to bronchial asthma and myocardial infarction. TBXA2R antagonist and TBX synthase inhibitors have been found to be effective in the management of asthmatic patients. This study was aimed to evaluate whether genetic variants of TBXA2R may be related with development of acetyl salicylic acid (ASA)-intolerant asthma (AIA).
Methods TBXA2R gene polymorphisms (TBXA2R+795T>C, TBXA2R+924T>C) were determined using a single-base extension method in 93 AIA patients compared with 172 patients with ASA-tolerant asthma (ATA) and 118 normal controls (NCs) recruited from the Korean population. HLA DPB1*0301 genotype was performed using a direct sequencing method.
Results The rare C allele frequency of TBXA2R+795T>C was significantly higher in AIA than in ATA (P=0.03) and the TBXA2R+795T>C polymorphism was also associated with extent of percent fall in forced expiratory volume in 1 s (FEV1) after the inhalation of lysine–acetyl salicylic acid in AIA patients (P=0.009); AIA patients homozygous for the +795 C allele had a greater percent fall of FEV1 compared with individuals with TBXA2R+795 CT or TT genotypes. The frequency of patients carrying both the TBXA2R+795T>C rare allele and HLA DPB1*0301 was significantly higher in AIA patients (29.4%) than in ATA patients (7.3%) (P=0.008, odds ratio=5.3).
Conclusion These results suggest that the polymorphism of TBXA2R+795T>C may increase bronchoconstrictive response to ASA, which could contribute to the development of the AIA phenotype.
0954-7894
585-590
Kim, S.H.
1e5e8a15-6524-419a-b2f9-73e9653de401
Choi, J.H.
af9e8c00-3940-455d-aec3-a6f1e29a6abb
Park, H.S.
37395c90-bc75-4c48-9d46-daac0107844b
Holloway, J.W.
4bbd77e6-c095-445d-a36b-a50a72f6fe1a
Lee, S.K.
2bda7741-8d13-42f7-937a-a865fe2df798
Park, C.S.
50cefa27-eae1-4536-8d92-4d3362225d84
Shin, H.D.
06c51fc6-48d5-4795-82c4-573de62641b7
Kim, S.H.
1e5e8a15-6524-419a-b2f9-73e9653de401
Choi, J.H.
af9e8c00-3940-455d-aec3-a6f1e29a6abb
Park, H.S.
37395c90-bc75-4c48-9d46-daac0107844b
Holloway, J.W.
4bbd77e6-c095-445d-a36b-a50a72f6fe1a
Lee, S.K.
2bda7741-8d13-42f7-937a-a865fe2df798
Park, C.S.
50cefa27-eae1-4536-8d92-4d3362225d84
Shin, H.D.
06c51fc6-48d5-4795-82c4-573de62641b7

Kim, S.H., Choi, J.H., Park, H.S., Holloway, J.W., Lee, S.K., Park, C.S. and Shin, H.D. (2005) Association of thromboxane A2 receptor gene polymorphism with the phenotype of acetyl salicylic acid-intolerant asthma. Clinical & Experimental Allergy, 35 (5), 585-590. (doi:10.1111/j.1365-2222.2005.02220.x).

Record type: Article

Abstract

Background and objective The thromboxane A2 receptor (TBXA2R) is a receptor for a potent bronchoconstrictor, TBXA2 which is known to be related to bronchial asthma and myocardial infarction. TBXA2R antagonist and TBX synthase inhibitors have been found to be effective in the management of asthmatic patients. This study was aimed to evaluate whether genetic variants of TBXA2R may be related with development of acetyl salicylic acid (ASA)-intolerant asthma (AIA).
Methods TBXA2R gene polymorphisms (TBXA2R+795T>C, TBXA2R+924T>C) were determined using a single-base extension method in 93 AIA patients compared with 172 patients with ASA-tolerant asthma (ATA) and 118 normal controls (NCs) recruited from the Korean population. HLA DPB1*0301 genotype was performed using a direct sequencing method.
Results The rare C allele frequency of TBXA2R+795T>C was significantly higher in AIA than in ATA (P=0.03) and the TBXA2R+795T>C polymorphism was also associated with extent of percent fall in forced expiratory volume in 1 s (FEV1) after the inhalation of lysine–acetyl salicylic acid in AIA patients (P=0.009); AIA patients homozygous for the +795 C allele had a greater percent fall of FEV1 compared with individuals with TBXA2R+795 CT or TT genotypes. The frequency of patients carrying both the TBXA2R+795T>C rare allele and HLA DPB1*0301 was significantly higher in AIA patients (29.4%) than in ATA patients (7.3%) (P=0.008, odds ratio=5.3).
Conclusion These results suggest that the polymorphism of TBXA2R+795T>C may increase bronchoconstrictive response to ASA, which could contribute to the development of the AIA phenotype.

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Published date: 2005

Identifiers

Local EPrints ID: 27205
URI: http://eprints.soton.ac.uk/id/eprint/27205
ISSN: 0954-7894
PURE UUID: 9d1889e9-d051-4b2e-8cd3-02886eb3329b
ORCID for J.W. Holloway: ORCID iD orcid.org/0000-0001-9998-0464

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Date deposited: 25 Apr 2006
Last modified: 16 Mar 2024 02:57

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Contributors

Author: S.H. Kim
Author: J.H. Choi
Author: H.S. Park
Author: J.W. Holloway ORCID iD
Author: S.K. Lee
Author: C.S. Park
Author: H.D. Shin

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