中国东南部汉族人群中TLR7和TLR8多态性与哮喘风险和哮喘相关表型相关

Qian Zhang , Fenhong Qian , Linfu Zhou , Guozhen Wei , Ying Wang , Zhibin Hu , Guangfu Jin , Jianling Bai , Kaisheng Yin
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引用次数: 6

摘要

目的探讨TLR7和TLR8基因多态性对哮喘发病风险和哮喘相关表型的影响。方法从中国东南部同一地区连续招募318例无关联成人哮喘患者和352例健康志愿者。使用多重PCR结合标记阵列单碱基扩展技术对每个选定的SNP进行基因分型。我们在TLR7和TLR8中选定的snp与哮喘或哮喘相关表型之间进行了病例对照和仅病例关联研究。结果TLR7中rs5935436 SNP的T等位基因对男性哮喘发病具有保护作用(调整后or = 0.126, 95% ci = 0.016-0.995)。CT/TT基因型rs5935436在女性哮喘合并变应性鼻炎患者中较少出现(调整后or = 0.18, 95% ci = 0.04-0.90)。rs3761623的纯合子AA和rs3764880的GG与女性哮喘患者低FEV1%和哮喘严重程度呈正相关。单倍型分析证实了上述结果。结论tlr7和TLR8基因多态性可能在哮喘性别依赖的发病机制中起重要作用。这在临床上可能是有用的,既可以识别有哮喘风险的患者,也可以预防哮喘的发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Polymorphisms of TLR7 and TLR8 associated with risk of asthma and asthma-related phenotypes in a southeastern Chinese Han population

Objective

To evaluate the effects of polymorphisms in TLR7 and TLR8(as potential candidate genes) on asthma risk and asthma-related phenotypes.

Methods

We consecutively recruited 318 unrelated adult asthmatic patients and 352 healthy volunteers from the same area of southeast China. Genotyping of each selected SNP was performed using multiplex PCR in conjunction with tagged array single base extension technology. We conducted case-control and case-only association studies between the selected SNPs in TLR7 and TLR8 and asthma or asthma-related phenotypes.

Results

The T allele of rs5935436 SNP in TLR7 was protective from developing asthma in males (adjusted ORs = 0.126, 95% CIs = 0.016-0.995). The CT/TT genotype of rs5935436 was less frequent in female asthmatics with allergic rhinitis (adjusted ORs = 0.18, 95% CIs = 0.04-0.90). The homozygote AA of rs3761623 and GG of rs3764880 were positively associated with lower FEV1% and asthma severity in female asthmatics. These results were confirmed by haplotype analysis.

Conclusion

TLR7 and TLR8 polymorphisms may play an important role in the pathogenesis of asthma that is gender-dependent. This could be clinically useful, both for identifying patients at risk of asthma and for preventing its occurrence.

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