Tang Rui, Lyu Xiaohong, Li Hong, Sun Jinlyu
Allergy Department, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Allergy Department, Beijing Key Laboratory of Precision Medicine for Diagnosis and Treatment of Allergic Diseases, National Clinical Research Center for Dermatologic and Immunologic Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Front Genet. 2023 Feb 24;14:1139813. doi: 10.3389/fgene.2023.1139813. eCollection 2023.
It has been suggested that genetic factors may be substantially linked to allergy disorders. This study aims to investigate the relationship between the genetic susceptibility of Chinese patients with allergy disorders and the polymorphisms of plasminogen activator inhibitor 1 gene () rs1799762, cysteinyl leukotriene receptor 1 gene () rs320995, gasdermin B gene () rs7216389, glycoprotein IIIa gene () rs5918, glycoprotein Ib alpha gene () rs6065, platelet endothelial aggregation receptor 1 gene () rs12041331, and tumor necrosis factor alpha gene () rs1800629. From the Peking Union Medical College Hospital, this study enrolled 60 healthy participants and 286 participants with allergic diseases. TaqMan-minor groove binder (MGB) quantitative polymerase chain reaction (qPCR) was used to examine the gene polymorphisms in each group. The TaqMan-MGB qPCR results were completely consistent with the DNA sequencing results, according to other studies in this medical center (Kappa = 1, < .001). Only the distribution of PAI-1 rs1799762 was different between patients with allergic cough and healthy people (χ2 = 7.48, = .0238). With regard to cough patients, the 4G4G and 5G5G genotypes were more frequent (allergic cough vs. healthy individuals: 4G4G 57.9% vs. 26.7%; 5G5G 20.0% vs. 13.3%), but the 4G5G genotype was more frequent in healthy people (allergic cough vs. healthy individuals: 45.7% vs. 60.0%). The rs320995, rs7216389, a rs5918, rs6065, rs12041331, and rs1800629 polymorphisms, however, did not show any of such relationships. The rs1799762 polymorphisms may be associated with the genetic susceptibility of Chinese allergic disease patients with cough performance.
有人提出,遗传因素可能与过敏症密切相关。本研究旨在调查中国过敏症患者的遗传易感性与纤溶酶原激活物抑制剂1基因()rs1799762、半胱氨酰白三烯受体1基因()rs320995、gasdermin B基因()rs7216389、糖蛋白IIIa基因()rs5918、糖蛋白Ibα基因()rs6065、血小板内皮聚集受体1基因()rs12041331和肿瘤坏死因子α基因()rs1800629多态性之间的关系。本研究从北京协和医院招募了60名健康参与者和286名患有过敏性疾病的参与者。采用TaqMan-小沟结合剂(MGB)定量聚合酶链反应(qPCR)检测每组的基因多态性。根据该医学中心的其他研究(Kappa = 1,P <.001),TaqMan-MGB qPCR结果与DNA测序结果完全一致。只有过敏咳嗽患者和健康人之间PAI-1 rs1799762的分布不同(χ2 = 7.48,P =.0238)。对于咳嗽患者,4G4G和5G5G基因型更为常见(过敏性咳嗽与健康个体:4G4G 57.9%对26.7%;5G5G 20.0%对13.3%),但4G5G基因型在健康人中更为常见(过敏性咳嗽与健康个体:45.7%对60.0%)。然而,rs320995、rs7216389、rs5918、rs6065、rs12041331和rs1800629多态性并未显示出任何此类关系。rs1799762多态性可能与中国过敏性疾病咳嗽患者的遗传易感性有关。