Ya-Ting Li, Qi-Qing Ye, Ya-Xin Lu, Ke-Xin Yang, Ping-Ping Zhang, Chang Chen, Min Zhou, Pei-Ying Feng, Zhuang-Gui Chen
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Multivariate logistic regression analyzed the associations between AR multimorbidity and allergen sensitivity, allergen-specific IgE levels, and the count of positive allergens.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>A cohort of 2275 patients with AR was included, of which 1100 (48.4%) presented with AR alone, while 1175 (51.6%) exhibited AR multimorbidity. Patients with AR multimorbidity had a more diverse allergen profile than those with AR alone. An increased number of positive ingested allergens had a higher odds ratio (OR) for AR multimorbidity compared with inhaled allergens (1.46 vs. 1.96) across all phenotypes. Sensitization to allergens and their allergen-specific IgE levels, including dust mites, cat dander, and milk (<i>p</i> < 0.05), were associated with AR multimorbidity. In children, cat and dog dander were significant allergens associated with AR multimorbidity (<i>p</i> < 0.05).</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>Allergen sensitization patterns in AR multimorbidity differ from those in AR alone. Polysensitization, particularly to ingested allergens, increases the risk of allergic multimorbidity. 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引用次数: 0
摘要
背景:变应性鼻炎(AR)多病可能需要被认为是一种特殊的疾病,因为变应性鼻炎的临床和免疫学差异明显。过敏性多病通常涉及多致敏,其中过敏原特异性免疫球蛋白E (IgE)起重要作用。目的:本研究旨在探讨过敏性鼻炎单发和多发性鼻炎患者过敏原IgE致敏模式的差异。方法:对诊断为AR的患者进行现实世界病例对照研究,多因素logistic回归分析AR多发病与过敏原敏感性、过敏原特异性IgE水平和阳性过敏原计数之间的关系。结果:纳入2275例AR患者,其中1100例(48.4%)单独表现为AR, 1175例(51.6%)表现为AR多病。AR多病患者的过敏原谱比单纯AR患者的过敏原谱更多样化。在所有表型中,摄入阳性过敏原数量的增加与吸入过敏原相比,具有更高的AR多发病优势比(OR) (1.46 vs 1.96)。对过敏原及其过敏原特异性IgE水平的致敏,包括尘螨、猫皮屑和牛奶(p结论:过敏性过敏原在过敏性过敏原多发病中的致敏模式不同于单独的过敏性过敏原。多致敏,特别是对摄入的过敏原,增加了过敏性多病的风险。过敏性多病的风险也随着特定过敏原阳性和更高的过敏原特异性IgE水平而增加。
Allergen sensitization patterns: Allergic rhinitis with multimorbidity versus alone—A real-world study
Background
Allergic rhinitis (AR) multimorbidity may need to be considered a specific disease because of distinct clinical and immunological differences from AR alone. Allergic multimorbidity often involves polysensitization, where allergen-specific immunoglobulin E (IgE) plays a significant role.
Objective
This study aims to explore differences in allergen IgE sensitization patterns between AR alone and AR multimorbidity.
Methods
A real-world case-control study was conducted with patients diagnosed with AR. Multivariate logistic regression analyzed the associations between AR multimorbidity and allergen sensitivity, allergen-specific IgE levels, and the count of positive allergens.
Results
A cohort of 2275 patients with AR was included, of which 1100 (48.4%) presented with AR alone, while 1175 (51.6%) exhibited AR multimorbidity. Patients with AR multimorbidity had a more diverse allergen profile than those with AR alone. An increased number of positive ingested allergens had a higher odds ratio (OR) for AR multimorbidity compared with inhaled allergens (1.46 vs. 1.96) across all phenotypes. Sensitization to allergens and their allergen-specific IgE levels, including dust mites, cat dander, and milk (p < 0.05), were associated with AR multimorbidity. In children, cat and dog dander were significant allergens associated with AR multimorbidity (p < 0.05).
Conclusions
Allergen sensitization patterns in AR multimorbidity differ from those in AR alone. Polysensitization, particularly to ingested allergens, increases the risk of allergic multimorbidity. The risk of allergic multimorbidity also increases with specific allergen positivity and higher allergen-specific IgE levels.
期刊介绍:
Clinical and Translational Allergy, one of several journals in the portfolio of the European Academy of Allergy and Clinical Immunology, provides a platform for the dissemination of allergy research and reviews, as well as EAACI position papers, task force reports and guidelines, amongst an international scientific audience.
Clinical and Translational Allergy accepts clinical and translational research in the following areas and other related topics: asthma, rhinitis, rhinosinusitis, drug hypersensitivity, allergic conjunctivitis, allergic skin diseases, atopic eczema, urticaria, angioedema, venom hypersensitivity, anaphylaxis, food allergy, immunotherapy, immune modulators and biologics, animal models of allergic disease, immune mechanisms, or any other topic related to allergic disease.