Association of VDR and CYP2R1 Polymorphisms with Mite-Sensitized Persistent Allergic Rhinitis in a Chinese Population

Adult Male China Adolescent Science 03 medical and health sciences 0302 clinical medicine Asian People Gene Frequency Animals Humans Genetic Predisposition to Disease Child Cytochrome P450 Family 2 Genetic Association Studies Aged Q R Epistasis, Genetic Middle Aged 3. Good health Genetic Loci Case-Control Studies Child, Preschool Medicine Cholestanetriol 26-Monooxygenase Female Research Article
DOI: 10.1371/journal.pone.0133162 Publication Date: 2015-07-15T14:41:30Z
ABSTRACT
As recent studies have described an association between vitamin D and allergic rhinitis, we hypothesized that pathway-related genes may be candidate for susceptibility to rhinitis. Thus, sought evaluate whether polymorphisms in the receptor (VDR) CYP2R1 are associated with mite-sensitized persistent rhinitis (PER) a Han Chinese population. A hospital-based case-control study consisting of 519 patients PER 447 healthy controls was conducted. Five single nucleotide (SNPs) VDR were selected genotyping. The genotype allele frequencies rs9729, rs2228570, rs1544410, rs731236 as well rs2060793 not significantly PER. After stratification analyses, however, both CT CT/TT genotypes rs2228570 exhibited decreased risk (CT: adjusted odds ratio (OR)=0.58, 95% confidence intervals (CI)=0.37-0.91; CT/TT: OR=0.61, CI=0.40-0.93) PER, while AA increased (adjusted OR=1.85, CI=1.03-3.34) age subgroup <16 years old. Both AG AG/GG (AG: OR=0.43, CI=0.21-0.89; AG/GG: OR=0.46, CI=0.23-0.94) female subgroup. Analysis locus-locus interactions revealed two models involved combined SNPs statistically significant (P<0.05). Our data suggest gender impact on three (rs2228570, rs731236, rs2060793) pathway this variants genetic pathogenesis
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