摘要
目的:通过对血管紧张素转换酶(ACE)基因插入/缺失的多态性及CD14/-159C/T基因的多态性分析,探讨其在变应性鼻炎发病中的作用。方法:采用聚合酶链反应(PCR)扩增及限制性内切酶片段多态性(PCR-RFLP)分析方法测定60例变应性鼻炎患者和40例健康对照者的ACE基因型和CD14/-159C/T基因型的分布情况,并采用相关统计学方法对结果进行分析。结果:(1)ACE等位基因I、D频率在变应性鼻炎组和对照组的分布差异有统计学意义(χ2=17.37,P<0.01)。等位基因D与变应性鼻炎高度相关(OR=3.46,95%CI=1.92 ̄6.23,P<0.01)。(2)CD14/-159C/T等位基因C、T频率在变应性鼻炎组和对照组的分布差别具有统计学意义(χ2=14.53,P<0.01),等位基因C与变应性鼻炎高度相关(OR=3.1,95%CI=1.75~5.47,P<0.01)。2组基因型(CC型、CT型、TT型)频率的分布比较差别也有统计学意义(χ2=11.77,P<0.01)。结论:ACE基因多态性与CD14基因的多态性是影响变应性鼻炎的重要候选基因,其中ACE的D等位基因与CD14-159C/T的C等位基因与变应性鼻炎相关。
Objective: To investigate the correlation of angiotensin-converting enzyme (ACE) gene polymorphism and - 159C/T polymorphism of CD14 gene promoter with allergic rhinitis and to approach its pathogenesis for guiding future prophylaxis and therapies. Methods: ACE genotype and CD14 genotype were detected in 60 allergic rhinitis patients and 40 health control by polymerase chain reaction (PCR) and restriction fragment length polymorphism (PCR-RFLP). A series of statistic were used to analysis the experimental results. Results: (1) There were significant differences in I and D allele frequencies at ACE gene (X^2 = 17.37,P 〈 0.01). Allele D was associated with allergic rhinitis (OR = 3.46, 95% CI = 1.92-6.23, P 〈 0.01). (2) There were significant differences in C and T allele frequencies at CD14/-159 locus (X2 = 14.53,P 〈 0.01). Allele C was associated with allergic rhinitis (OR=3.1, 95%CI = 1.75-5.47, P 〈 0.01). There was a statistical significance in frequency distribution between two gene types (X^2= 11.77, P 〈 0.01). Conclusion:ACE gene and CD 14 locus polymorphism may be an important candidate gene for allergic rhinitis. Allele D and allele C are associated with allergic rhinitis.
出处
《天津医药》
CAS
北大核心
2006年第12期860-862,共3页
Tianjin Medical Journal