Otorhinolaryngologic Department, Shenmu Hospital, The Affiliated Shenmu Hospital of Northwest University, Shenmu, China.
Department of Science and Education, Shenmu Hospital, The Affiliated Shenmu Hospital of Northwest University, Shenmu, China.
Int Immunopharmacol. 2022 Jul;108:108874. doi: 10.1016/j.intimp.2022.108874. Epub 2022 May 26.
Allergic rhinitis (AR) is the most common inflammatory disorder induced by complex interactions between genetic and environmental factors. Genetic predisposition is the most important factor in the progression of AR. Previous studies have indicated that RORA is involved in the occurrence of AR. The present study aimed to determine the roles of RORA polymorphisms in AR susceptibility.
Peripheral blood samples were collected from 990 patients with AR and 1004 normal controls. Four single nucleotide polymorphisms (SNPs) in the RORA gene were detected by MassARRAY iPLEX platform. The associations of RORA polymorphisms with AR risk were determined according to logistic regression analysis. We further evaluated the impact of SNP-SNP interaction on AR risk using multifactor dimensionality reduction (MDR) method.
Our results showed that rs10519067 (OR 0.38, p = 0.021), rs10519068 (OR 0.45, p = 0.030), and rs11071559 (OR 0.83, p = 0.032) were significantly related to a decreased susceptibility to AR. Stratified analyses found that rs10519067 (OR 0.71, p = 0.046) and rs10519068 (OR 0.63, p = 0.010) could decrease the risk of AR in males. Rs10519068 (OR 0.73, p = 0.022), rs11071559 (OR 0.77, p = 0.041), and rs9302216 (OR 0.38, p = 0.017) significantly reduced the susceptibility to AR in people aged > 43 years. Furthermore, it was found that rs10519067 (OR 0.29, p = 0.032), rs10519068 (OR 0.72, p = 0.013), and rs11071559 (OR 0.36, p = 0.015) had a protective effect on AR patients with BMI ≤ 24 kg/m. MDR revealed that the combination of rs10519067, rs10519068, rs11071559, and rs9302216 was the best predictive model for AR.
Our study suggests that RORA polymorphisms may play a protective role in the development of AR.
过敏性鼻炎(AR)是由遗传和环境因素复杂相互作用引起的最常见的炎症性疾病。遗传易感性是 AR 进展的最重要因素。先前的研究表明 RORA 参与了 AR 的发生。本研究旨在确定 RORA 多态性在 AR 易感性中的作用。
采集 990 例 AR 患者和 1004 例正常对照者外周血样本。采用 MassARRAY iPLEX 平台检测 RORA 基因中的 4 个单核苷酸多态性(SNP)。根据逻辑回归分析确定 RORA 多态性与 AR 风险的关联。我们进一步使用多因素维度缩减(MDR)方法评估 SNP-SNP 相互作用对 AR 风险的影响。
我们的结果表明,rs10519067(OR 0.38,p=0.021)、rs10519068(OR 0.45,p=0.030)和 rs11071559(OR 0.83,p=0.032)与 AR 易感性降低显著相关。分层分析发现 rs10519067(OR 0.71,p=0.046)和 rs10519068(OR 0.63,p=0.010)可降低男性 AR 的发病风险。rs10519068(OR 0.73,p=0.022)、rs11071559(OR 0.77,p=0.041)和 rs9302216(OR 0.38,p=0.017)可显著降低>43 岁人群 AR 的易感性。此外,发现 rs10519067(OR 0.29,p=0.032)、rs10519068(OR 0.72,p=0.013)和 rs11071559(OR 0.36,p=0.015)对 BMI≤24kg/m2 的 AR 患者具有保护作用。MDR 显示 rs10519067、rs10519068、rs11071559 和 rs9302216 的组合是 AR 的最佳预测模型。
本研究表明 RORA 多态性可能在 AR 的发病机制中起保护作用。