Li Ya-Ting, Ye Qi-Qing, Lu Ya-Xin, Yang Ke-Xin, Zhang Ping-Ping, Chen Chang, Zhou Min, Feng Pei-Ying, Chen Zhuang-Gui
Department of Allergy, Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Children's Medicine Centre, Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Clin Transl Allergy. 2025 Jan;15(1):e70030. doi: 10.1002/clt2.70030.
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.
This study aims to explore differences in allergen IgE sensitization patterns between AR alone and AR multimorbidity.
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.
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).
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.
变应性鼻炎(AR)合并症可能需要被视为一种特定疾病,因为其在临床和免疫学方面与单纯的AR存在明显差异。变应性合并症常涉及多致敏,其中变应原特异性免疫球蛋白E(IgE)起着重要作用。
本研究旨在探讨单纯AR与AR合并症之间变应原IgE致敏模式的差异。
对诊断为AR的患者进行一项真实世界病例对照研究。多因素逻辑回归分析AR合并症与变应原敏感性、变应原特异性IgE水平及阳性变应原数量之间的关联。
纳入了2275例AR患者队列,其中1100例(48.4%)为单纯AR,而1175例(51.6%)表现为AR合并症。与单纯AR患者相比,AR合并症患者的变应原谱更为多样。在所有表型中,摄入性变应原阳性数量增加与AR合并症的比值比(OR)高于吸入性变应原(1.46对1.96)。对包括尘螨、猫皮屑和牛奶在内的变应原致敏及其变应原特异性IgE水平与AR合并症相关(p<0.05)。在儿童中,猫和狗皮屑是与AR合并症相关的重要变应原(p<0.05)。
AR合并症的变应原致敏模式与单纯AR不同。多致敏,尤其是对摄入性变应原的多致敏,增加了变应性合并症的风险。变应性合并症的风险也随着特定变应原阳性和更高的变应原特异性IgE水平而增加。