Medical Department of Lishui University, Lishui, Zhejiang 323000, P.R. China.
Mol Med Rep. 2012 Dec;6(6):1385-8. doi: 10.3892/mmr.2012.1098. Epub 2012 Sep 26.
To study the association of polymorphisms of the IL-18 promoter (-607C/A and -137G/C) with bronchial asthma, 120 subjects with bronchial asthma were selected as the experimental group (49 cases with bronchial asthma and allergic rhinitis as experimental group 1 and 71 cases with bronchial asthma without allergic rhinitis as experimental group 2) and 120 healthy individuals were selected as the control group. A polymerase chain reaction sequence-specific primer (PCR-SSP) was used to identify the genotypic polymorphisms between the experimental and control groups. The results revealed that the frequencies of the CC, CA and AA genotypes at -607C/A in experimental group 1 were 18.37, 40.82 and 40.82%, respectively; these frequencies were 32.39, 54.92 and 12.68%, respectively, in experimental group 2. There was a statistically significant difference in the genotype distribution between experimental groups 1 and 2 (χ²=12.81; P<0.05). The allele frequencies of genotypes C and A were 38.78 and 61.22%, respectively, in experimental group 1 and 59.86 and 40.14%, respectively, in experimental group 2. The allele frequencies at -607C/A were significantly different between experimental groups 1 and 2 (χ²=10.32; P<0.05). Frequencies of genotypes GG, GC and CC at -137C/A in experimental group 1 were 48.98, 46.94 and 4.08%, respectively, and 80.28, 14.08 and 4.08% in experimental group 2 with significant difference (χ²=15.73, P<0.05). Allele frequencies of G and C in experimental group 1 were 72.45 and 27.55%, and 87.32 and 12.68% in experimental group 2 with statistically significant difference (χ²=8.42, P<0.05). In conclusion, polymorphisms of the IL-18 gene promoter at -607C/A and -137G/C were associated with allergic rhinitis in bronchial asthma, indicating that polymorphisms of the IL-18 gene promoter at -607C/A and -137G/C differentially affect the pathogenesis of asthma and allergic rhinitis.
为了研究白细胞介素-18(IL-18)启动子(-607C/A 和-137G/C)多态性与支气管哮喘的关系,选择 120 例支气管哮喘患者作为实验组(49 例支气管哮喘合并变应性鼻炎为实验组 1,71 例支气管哮喘无变应性鼻炎为实验组 2),选择 120 例健康个体作为对照组。采用聚合酶链反应序列特异性引物(PCR-SSP)鉴定实验组和对照组之间的基因型多态性。结果显示,实验组 1-607C/A 处 CC、CA 和 AA 基因型的频率分别为 18.37%、40.82%和 40.82%;实验组 2 分别为 32.39%、54.92%和 12.68%。实验组 1 和 2 的基因型分布差异有统计学意义(χ²=12.81,P<0.05)。基因型 C 和 A 的等位基因频率分别为实验组 1 中的 38.78%和 61.22%,实验组 2 中的 59.86%和 40.14%。实验组 1 和 2 之间-607C/A 的等位基因频率差异有统计学意义(χ²=10.32,P<0.05)。实验组 1-137C/A 处 GG、GC 和 CC 基因型的频率分别为 48.98%、46.94%和 4.08%,实验组 2 分别为 80.28%、14.08%和 4.08%,差异有统计学意义(χ²=15.73,P<0.05)。实验组 1 中 G 和 C 的等位基因频率分别为 72.45%和 27.55%,实验组 2 中分别为 87.32%和 12.68%,差异有统计学意义(χ²=8.42,P<0.05)。综上所述,白细胞介素-18 基因启动子-607C/A 和-137G/C 多态性与支气管哮喘合并变应性鼻炎有关,表明白细胞介素-18 基因启动子-607C/A 和-137G/C 多态性对哮喘和变应性鼻炎的发病机制有不同的影响。