抗核抗体在感染后嗅觉丧失中的应用-一项初步研究

U. Walliczek-Dworschak, A. Zimmermann, S. Poletti, T. Hummel
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引用次数: 2

摘要

背景:许多疾病是由自身免疫机制介导的,其中一些已被证明与嗅觉功能下降有关,如系统性红斑狼疮、Sjögren综合征、寻常性牛皮癣。感染后嗅觉丧失是嗅觉功能障碍的常见原因。然而,其性质尚不完全清楚,但可能与免疫介导的过程有关。因此,本研究的主要目的是研究感染后嗅觉丧失与自身免疫过程的可能关系。方法:52例患者,其中女性35例,男性17例;平均年龄(57岁±12岁),感染后嗅觉丧失,对照组56例(女性21例,男性35例;平均年龄58岁±13岁),伴有其他原因(鼻窦、创伤后或特发性)嗅觉功能障碍的患者被纳入本研究。使用“嗅探棒”扩展测试电池测量患者的嗅觉功能。同时采集静脉血进行抗核自身抗体分析。结果:与对照组相比,患者出现抗核抗体(ANA)的频率明显更高,尽管ANAs通常仅在1:100的临界值下存在。此外,ANAs的存在与气味阈值之间存在显著关联。结论:本研究的结果表明,感染后嗅觉功能障碍可能与自身免疫过程有关,因为与其他来源的嗅觉缺陷患者相比,它们表现出更多的ANAs,尽管在临床上没有显著水平。
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Antinuclear antibodies in postinfectious smell loss - a pilot study
Background: Numerous diseases are mediated by autoimmune mechanisms some of which have been shown to be associated with reduced olfactory function, e.g. systemic lupus erythematosus, Sjögren syndrome, psoriasis vulgaris. Postinfectious smell loss is a frequent cause of olfactory dysfunction. However, its nature is not fully understood, but connections to immune mediated processes might be possible. The primary aim of the present study was therefore to investigate the possible relation of postinfectious smell loss with autoimmune processes. Methods: Fifty-two patients (35 female, 17 male; mean age 57 years ± 12 years) with postinfectious smell loss and 56 controls (21 female, 35 male; mean age 58 years ± 13 years), with olfactory dysfunction of other causes (sinunasal, posttraumatic or idiopathic) were included in the present study. The patients’ olfactory function was measured using the extended test battery of the "Sniffin’ Sticks“. Furthermore venous blood samples were taken and analyzed for antinuclear autoantibodies. Results: Patients showed anti-nuclear antibodies (ANA) significantly more frequently compared to controls, although ANAs were typically only present at cut off levels of 1:100. In addition, there was a significant association between the presence of ANAs and odor thresholds. Conclusions: Results from this study indicate that postinfectious olfactory dysfunction may be associated with autoimmune processes, as they show significantly more ANAs – although not at a clincially significant level compared to patients with olfactory deficits of other origin.
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