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Clinical course of patients with aspirin-exacerbated respiratory disease: can we predict the prognosis?

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dc.contributor.authorKim, JH-
dc.contributor.authorChoi, GS-
dc.contributor.authorKim, JE-
dc.contributor.authorJin, HJ-
dc.contributor.authorYe, YM-
dc.contributor.authorKim, SH-
dc.contributor.authorPark, HS-
dc.date.accessioned2016-09-26T09:49:23Z-
dc.date.available2016-09-26T09:49:23Z-
dc.date.issued2014-
dc.identifier.issn1462-2416-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/12577-
dc.description.abstractAIM: 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.
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dc.language.isoen-
dc.subject.MESHAdult-
dc.subject.MESHAlleles-
dc.subject.MESHAspirin-
dc.subject.MESHAsthma, Aspirin-Induced-
dc.subject.MESHDrug Hypersensitivity-
dc.subject.MESHFemale-
dc.subject.MESHForced Expiratory Volume-
dc.subject.MESHHumans-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPolymorphism, Single Nucleotide-
dc.subject.MESHPrognosis-
dc.titleClinical course of patients with aspirin-exacerbated respiratory disease: can we predict the prognosis?-
dc.typeArticle-
dc.identifier.pmid24624912-
dc.identifier.urlhttp://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.affiliatedAuthor예, 영민-
dc.contributor.affiliatedAuthor김, 승현-
dc.contributor.affiliatedAuthor박, 해심-
dc.type.localJournal Papers-
dc.identifier.doi10.2217/pgs.14.2-
dc.citation.titlePharmacogenomics-
dc.citation.volume15-
dc.citation.number4-
dc.citation.date2014-
dc.citation.startPage449-
dc.citation.endPage457-
dc.identifier.bibliographicCitationPharmacogenomics, 15(4). : 449-457, 2014-
dc.identifier.eissn1744-8042-
dc.relation.journalidJ014622416-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Allergy
Journal Papers > Hospital > Clinical Trial Center
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