[Relationship between interleukin-17A gene polymorphisms and the susceptibility to childhood asthma]

Zhongguo Dang Dai Er Ke Za Zhi. 2016 Dec;18(12):1264-1268. doi: 10.7499/j.issn.1008-8830.2016.12.013.
[Article in Chinese]

Abstract

Objective: To explore the relationship between polymorphisms of interleukin-17A (IL-17A) gene promoter (-197G/A and -692C/T) and the susceptibility to childhood asthma, to further identify the candidate genes for asthma, and to provide a basis for early prevention of asthma in high-risk children.

Methods: Sixty-five outpatients or inpatients with childhood asthma between August 2013 and August 2015 were assigned to asthma group. Seventy healthy children within the same period were assigned to control group. Using peripheral venous blood from the two groups, PCR with sequence-specific primers was carried out to determine single nucleotide polymorphisms at positions -197G/A and -692C/T in IL-17A gene promoter. A statistical analysis was used to evaluate differences in genotype and allele frequencies between the two groups.

Results: Compared with the control group, the asthma group had significantly higher frequencies of TT genotype (29% vs 16%; P=0.012) and T allele (52% vs 42%; P=0.039) at position -692C/T of IL-17A gene. Children with T allele had 1.413-fold higher risk of childhood asthma than those with C allele (OR=1.413, 95%CI: 1.015-1.917). There were no significant differences in genotype and allele frequencies at position -197G/A in IL-17A gene between the two groups (p>0.05).

Conclusions: Polymorphisms at position -692C/T in IL-17A gene promoter is associated with the susceptibility to childhood asthma. Children with -692T allele are more susceptible to childhood asthma. There is no significant relationship between polymorphisms at position -197G/A in IL-17A gene promoter and the susceptibility to childhood asthma.

目的: 探讨儿童IL-17A启动子区域(-197G/A和-692C/T)基因多态性与儿童哮喘易感性的关系,为能进一步寻找到哮喘的候选基因从而为患病高风险儿童早期预防奠定基础。

方法: 选取2013年8月至2015年8月门诊随访或住院的哮喘患儿65例为哮喘组,另选取同期行健康体检儿童70例为健康对照组,采集两组儿童外周静脉血,应用序列特异性引物聚合酶链反应(SSP-PCR)法检测IL-17A基因-197G/A和-692C/T两个位点的单核苷酸多态性(SNP),统计分析两组间基因型及等位基因分布频率的差异。

结果: IL-17A基因-692C/T位点哮喘组患儿TT基因型的分布频率(29%)显著高于健康对照组(16%)(P=0.012);哮喘组-692T等位基因分布频率(52%)显著高于健康对照组(42%)(P=0.039);罹患儿童哮喘的风险T等位基因携带者是C等位基因携带者的1.413倍(OR=1.413,95%CI:1.015~1.917);而IL-17A基因-197G/A位点基因型及等位基因分布频率在哮喘组和健康对照组间比较差异无统计学意义(P > 0.05)。

结论: IL-17A基因启动子区域-692C/T位点基因多态性与儿童哮喘的易感性相关,-692T等位基因携带者更易罹患儿童哮喘,而IL-17A-197G/A位点多态性与儿童哮喘的易感性无显著相关。

MeSH terms

  • Asthma / genetics*
  • Female
  • Genetic Predisposition to Disease*
  • Genotype
  • Humans
  • Interleukin-17 / genetics*
  • Male
  • Polymorphism, Single Nucleotide*

Substances

  • IL17A protein, human
  • Interleukin-17

Grants and funding

西南医科大学附属医院科研基金(2015-QS-032)