Han Hui, Lian Penggang, Chen Haiyuan, Shamsi Bilal Haider, Liu Yonglin, Niu Yongliang
Clinical Laboratory, Shenmu Hospital, the Affiliated Shenmu Hospital of Northwest University, Shenmu, 719300, People's Republic of China.
Otorhinolaryngologic Department, Shenmu Hospital, the Affiliated Shenmu Hospital of Northwest University, Shenmu, 719300, People's Republic of China.
J Asthma Allergy. 2023 Sep 18;16:979-986. doi: 10.2147/JAA.S421939. eCollection 2023.
Environmental factors and genetic predisposition can influence the occurrence and development of AR. Toll-like receptor 1 (TLR1) belongs to the TLR receptor family, which plays a fundamental role in the activation of innate immunity. This study aimed to explore the association between genetic loci and AR susceptibility in the Han Chinese from northern China.
Genotyping of three SNPs in the has proceeded using the Agena MassARRAY platform. Odds ratio (OR) and 95% confidence interval (CI) were used to assess the correlation between candidate SNPs and AR susceptibility. Using FPRP (false-positive report probability analysis) to detect whether the positive results are noteworthy findings. The SNP-SNP interactions were detected by multifactor dimensionality reduction (MDR).
-rs72493538 (Allele "G": OR=0.77, = 0.034) and -rs76600635 (Allele "G": OR=0.75, = 0.024) were associated with reducing the risk of AR among Han Chinese in northern China. In addition, we found evidence that -rs72493538 (males, participants with aging > 43 years, or coming from the wind-blown sand region) and -rs76600635 (males, participants with BMI ≤ 24 kg/m, or coming from the wind-blown sand region) were associated with AR risk in stratified analyses. FPRP showed that all positive results are noteworthy findings. MDR analysis showed that a two-loci genetic model composed of rs72493538 and rs76600635 can be chosen as the best genetic model to predict the risk of AR.
-rs72493538 and -rs76600635 have a close association with reducing the risk of AR.
环境因素和遗传易感性可影响变应性鼻炎(AR)的发生和发展。Toll样受体1(TLR1)属于TLR受体家族,在先天免疫激活中起重要作用。本研究旨在探讨中国北方汉族人群基因位点与AR易感性之间的关联。
使用Agena MassARRAY平台对[具体基因名称缺失]中的三个单核苷酸多态性(SNP)进行基因分型。采用优势比(OR)和95%置信区间(CI)评估候选SNP与AR易感性之间的相关性。使用假阳性报告概率分析(FPRP)检测阳性结果是否为值得关注的发现。通过多因素降维法(MDR)检测SNP-SNP相互作用。
-rs72493538(等位基因“G”:OR = 0.77,P = 0.034)和-rs76600635(等位基因“G”:OR = 0.75,P = 0.024)与降低中国北方汉族人群AR风险相关。此外,我们发现证据表明,在分层分析中,-rs72493538(男性、年龄>43岁的参与者或来自风沙地区的参与者)和-rs76600635(男性、体重指数≤24 kg/m²的参与者或来自风沙地区的参与者)与AR风险相关。FPRP显示所有阳性结果均为值得关注的发现。MDR分析表明,由rs72493538和rs76600635组成的双基因座遗传模型可作为预测AR风险的最佳遗传模型。
-rs72493538和-rs76600635与降低AR风险密切相关。