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http://purl.uniprot.org/citations/24332579http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/24332579http://www.w3.org/2000/01/rdf-schema#comment"

Background

Epidemiological research on the relationship between single nucleotide polymorphisms (SNPs) in the IL5RA gene and allergic disorders is limited. We examined the relationship between IL5RA SNPs and risk of rhinoconjunctivitis in young adult Japanese women.

Methods

Included were 393 women who met the criteria of the International Study of Asthma and Allergies in Childhood (ISAAC) for rhinoconjunctivitis. Controls were 767 women without rhinoconjunctivitis according to the ISAAC criteria who had not been diagnosed with allergic rhinitis by a doctor. Adjustment was made for age, region of residence, presence of older siblings, smoking, and education.

Results

Compared with the CC genotype of SNP rs6771148, the CG genotype, but not the GG genotype, was significantly associated with a reduced risk of rhinoconjunctivitis: the adjusted OR for the CG genotype was 0.76 (95% CI: 0.58-0.99). No evident associations were found between SNPs rs17882210, rs3804797, rs334809, rs9831572, or rs17881144 and rhinoconjunctivitis. The ACTAGA haplotype of rs17882210, rs3804797, rs334809, rs9831572, rs6771148, and rs17881144 was significantly inversely associated with rhinoconjunctivitis (crude OR=0.58, 95% CI: 0.37-0.88) while the GTAGCA haplotype was significantly positively related to rhinoconjunctivitis (crude OR=1.74, 95% CI: 1.14-2.65). No significant interactions affecting rhinoconjunctivitis were observed between any of the six SNPs and smoking.

Conclusion

This is the first study to show significant associations between IL5RA SNP rs6771148, the ACTAGA haplotype, and the GTAGCA haplotype and the risk of rhinoconjunctivitis. We did not find evidence for interactions affecting rhinoconjunctivitis between any of the IL5RA SNPs and smoking."xsd:string
http://purl.uniprot.org/citations/24332579http://purl.org/dc/terms/identifier"doi:10.1016/j.cyto.2013.11.006"xsd:string
http://purl.uniprot.org/citations/24332579http://purl.uniprot.org/core/author"Tanaka K."xsd:string
http://purl.uniprot.org/citations/24332579http://purl.uniprot.org/core/author"Miyake Y."xsd:string
http://purl.uniprot.org/citations/24332579http://purl.uniprot.org/core/author"Arakawa M."xsd:string
http://purl.uniprot.org/citations/24332579http://purl.uniprot.org/core/date"2014"xsd:gYear
http://purl.uniprot.org/citations/24332579http://purl.uniprot.org/core/name"Cytokine"xsd:string
http://purl.uniprot.org/citations/24332579http://purl.uniprot.org/core/pages"138-142"xsd:string
http://purl.uniprot.org/citations/24332579http://purl.uniprot.org/core/title"Case-control study of rhinoconjunctivitis associated with IL5RA polymorphisms in Japanese women: the Kyushu Okinawa Maternal and Child Health Study."xsd:string
http://purl.uniprot.org/citations/24332579http://purl.uniprot.org/core/volume"65"xsd:string
http://purl.uniprot.org/citations/24332579http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/24332579
http://purl.uniprot.org/citations/24332579http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/24332579
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http://purl.uniprot.org/uniprot/B3IU76http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/24332579
http://purl.uniprot.org/uniprot/Q14632http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/24332579
http://purl.uniprot.org/uniprot/Q01344http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/24332579
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