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Clinical course of patients with aspirin-exacerbated respiratory disease: can we predict the prognosis?
DC Field | Value | Language |
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dc.contributor.author | Kim, JH | - |
dc.contributor.author | Choi, GS | - |
dc.contributor.author | Kim, JE | - |
dc.contributor.author | Jin, HJ | - |
dc.contributor.author | Ye, YM | - |
dc.contributor.author | Kim, SH | - |
dc.contributor.author | Park, HS | - |
dc.date.accessioned | 2016-09-26T09:49:23Z | - |
dc.date.available | 2016-09-26T09:49:23Z | - |
dc.date.issued | 2014 | - |
dc.identifier.issn | 1462-2416 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/12577 | - |
dc.description.abstract | AIM: This study aimed to identify prognostic factors of aspirin-exacerbated
respiratory disease by comparing clinical and genetic data with the clinical course. PATIENTS & METHODS: Patients were classified into two groups according to their response to inhalation rechallenge with lysine-aspirin after at least 1 year of regular treatment with antiasthmatic medications. RESULTS: Forty eight patients (39.3%, group I) had negative responses, whereas 74 patients (60.7%, group II) had positive responses (n = 23) or were not rechallenged owing to persistent symptoms (n = 51). FEV(1) at diagnosis and follow-up were significantly lower in group II than in group I. The CCR3 polymorphism at -520T/G differed significantly between the two groups, whereas no difference was found in other SNPs. CONCLUSION: Baseline FEV(1) and lower lung function after treatment were clinical factors indicating a poor prognosis of aspirin-exacerbated respiratory disease. The G allele of CCR3 -520T>G was associated with persistent bronchial hypersensitivity to aspirin. | - |
dc.language.iso | en | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Alleles | - |
dc.subject.MESH | Aspirin | - |
dc.subject.MESH | Asthma, Aspirin-Induced | - |
dc.subject.MESH | Drug Hypersensitivity | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Forced Expiratory Volume | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Polymorphism, Single Nucleotide | - |
dc.subject.MESH | Prognosis | - |
dc.title | Clinical course of patients with aspirin-exacerbated respiratory disease: can we predict the prognosis? | - |
dc.type | Article | - |
dc.identifier.pmid | 24624912 | - |
dc.identifier.url | http://www.futuremedicine.com/doi/abs/10.2217/pgs.14.2?url_ver=Z39.88-2003&rfr_id=ori%3Arid%3Acrossref.org&rfr_dat=cr_pub%3Dpubmed& | - |
dc.contributor.affiliatedAuthor | 예, 영민 | - |
dc.contributor.affiliatedAuthor | 김, 승현 | - |
dc.contributor.affiliatedAuthor | 박, 해심 | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.2217/pgs.14.2 | - |
dc.citation.title | Pharmacogenomics | - |
dc.citation.volume | 15 | - |
dc.citation.number | 4 | - |
dc.citation.date | 2014 | - |
dc.citation.startPage | 449 | - |
dc.citation.endPage | 457 | - |
dc.identifier.bibliographicCitation | Pharmacogenomics, 15(4). : 449-457, 2014 | - |
dc.identifier.eissn | 1744-8042 | - |
dc.relation.journalid | J014622416 | - |
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