Lack of Association between Eotaxin-1 Gene Polymorphisms and Nasal Polyposis

被引:4
作者
Ekinci, Suna [1 ]
Erbek, Selim S. [1 ]
Yurtcu, Erkan [2 ]
Sahin, Feride I. [3 ]
机构
[1] Baskent Univ, Dept Otolaryngol, Fac Med, TR-06490 Ankara, Turkey
[2] Baskent Univ, Dept Med Biol, Fac Med, TR-06490 Ankara, Turkey
[3] Baskent Univ, Dept Med Genet, Fac Med, TR-06490 Ankara, Turkey
关键词
eotaxin; nasal polyposis; genotype; polymorphism; SINGLE-NUCLEOTIDE POLYMORPHISMS; SERUM TOTAL IGE; ATOPIC-DERMATITIS; ASTHMA; PROMOTER; CHILDREN; FAMILY;
D O I
10.1177/0194599811417359
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Objective. To examine whether there is an association of eotaxin-1 gene polymorphisms with nasal polyposis (NP). Study Design. Cross-sectional study. Setting. Tertiary referral center. Subjects and Methods. The study group included 85 patients with NP and 93 controls without sinonasal disease. Genotypes of eotaxin-1 (2384 A>G and 167 G>A) were identified by restriction fragment length polymorphism analyses after polymerase chain reaction. Results. The -384 A>G and 167 G>A single nucleotide polymorphisms were higher in patients with NP than in controls (P = .044 and P = .019, respectively). However, their relation was statistically poor (association coefficient = 0.18). Consistent with this result, comparisons of allele frequencies for both single nucleotide polymorphisms were not significantly different (-384 A>G, P = .164; 167 G>A, P = .144). Conclusion. In this study, eotaxin-1 -384 A>G or 67 G>A genotypes were not associated with susceptibility to NP.
引用
收藏
页码:1036 / 1039
页数:4
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