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Specific IgE positivity against inhalant allergens and development of autoimmune disease

机译:针对吸入性过敏原和自身免疫性疾病发展的特异性IgE阳性

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Background: Allergic and autoimmune diseases have been suggested to be inversely associated. We investigated the association between atopy and development of any and specific types of autoimmune disease. Methods: We included a total of 14 849 individuals from five population-based studies with measurements of atopy defined as specific IgE positivity against inhalant allergens. We followed the participants by linkage to the Danish National Patient Register (median follow-up time 11.2 years). Hazard ratio (HR) and 95% confidence interval (CI) of autoimmune disease were estimated by Cox regression. Results: The risk for atopics versus non-atopics was: for any autoimmune disease (HR = 0.99, 95% CI: 0.83, 1.18), thyrotoxicosis (HR = 0.69, 95% CI: 0.34, 1.37), type 1 diabetes (HR = 1.16, 95% CI: 0.84, 1.60), multiple sclerosis (HR = 1.97, 95% CI: 0.95, 4.11), iridocyclitis (HR = 0.82, 95% CI: 0.38, 1.74), Crohn's disease (HR = 1.03, 95% CI: 0.47, 2.25), ulcerative colitis (HR = 0.93, 95% CI: 0.52, 1.69), psoriasis vulgaris (HR = 1.50, 95% CI: 0.86, 2.62), seropositive rheumatoid arthritis (HR = 0.74, 95% CI: 0.48, 1.14) and polymyalgia rheumatica (HR = 0.79, 95% CI: 0.44, 1.44). Conclusions: We found no statistically significant associations between atopy and autoimmune disease, but we cannot exclude relatively small to moderate effects - protective or promotive - of atopy on autoimmune disease.
机译:背景:过敏和自身免疫性疾病被认为是负相关的。我们调查了特应性疾病与任何和特定类型的自身免疫性疾病发展之间的关联。方法:我们纳入了来自五项基于人群的研究的14 849名个体,其中特应性的测量被定义为针对吸入性过敏原的特异性IgE阳性。我们通过与丹麦国家患者登记簿的链接跟踪参与者(中位随访时间为11.2年)。通过Cox回归评估自身免疫疾病的危险比(HR)和95%置信区间(CI)。结果:特应性与非特应性的风险是:对于任何自身免疫性疾病(HR = 0.99,95%CI:0.83,1.18),甲状腺毒症(HR = 0.69,95%CI:0.34,1.37),1型糖尿病(HR = 1.16,95%CI:0.84,1.60),多发性硬化症(HR = 1.97,95%CI:0.95,4.11),虹膜睫状体炎(HR = 0.82,95%CI:0.38,1.74),克罗恩病(HR = 1.03, 95%CI:0.47,2.25),溃疡性结肠炎(HR = 0.93,95%CI:0.52,1.69),寻常型牛皮癣(HR = 1.50,95%CI:0.86,2.62),血清反应阳性的类风湿关节炎(HR = 0.74,95) %CI:0.48、1.14)和风湿性多肌痛(HR = 0.79,95%CI:0.44、1.44)。结论:我们发现特应性疾病与自身免疫性疾病之间无统计学意义的关联,但我们不能排除特应性疾病对自身免疫性疾病的相对较小至中度的影响(保护性或促进性)。

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