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分子诊断如何改变复杂花粉区域的变应原特异性免疫治疗方案。

How molecular diagnosis can change allergen-specific immunotherapy prescription in a complex pollen area.

机构信息

Allergy Department, Fundación Jiménez Díaz, Madrid, Spain.

出版信息

Allergy. 2012 May;67(5):709-11. doi: 10.1111/j.1398-9995.2012.02808.x. Epub 2012 Mar 2.

Abstract

BACKGROUND

The identification of disease-eliciting allergens is a prerequisite for accurate prescription of allergen-specific immunotherapy (SIT). The aim of this study was to determine whether molecular diagnosis (MD) may change indication and allergen prescription of SIT.

METHODS

A total of 141 patients with allergic rhinoconjunctivitis and/or asthma sensitized to pollen with or without concomitant food allergy were included. Skin prick testing with a panel of aeroallergens and a microarray-based panel of allergens (ISAC(®); Phadia, Sweden) was performed in all patients. Prior to learning the results of molecular diagnosis, three of the authors reached a consensus on the indication of SIT and use of allergens following EAACI recommendations, basing their judgment on clinical history and skin prick test results before and after obtaining the ISAC results. The agreement coefficient (kappa index) was used to analyze the results.

RESULTS

Fifty-nine percent of the patients were women with a mean age of 31 ± 13.63. Agreement in SIT indication before and after ISAC(®) results was found in only 62 (46%) patients (kappa = 0.1057 ± 0.0413). Concerning allergens used in the most common prescriptions before and after MD results, we obtained the following results: κ = 0.117 ± 0.0825 for grass; κ = 0.1624 ± 0.0639 for olive; κ = 0.0505 ± 0.0548 for olive and grass; κ = 0.1711 ± 0.0471 for grass and cypress; κ = 0.1897 ± 0.0493 for grass and London plane; κ = 1 ± 0.0842 for olive and cypress, and κ = 0.3586 ± 0.0798 for other combinations.

CONCLUSIONS

There was very low agreement concerning indication and use of allergens for SIT before and after performing MD. This discrepancy emphasizes the usefulness of MD, at least in areas of complex sensitization to pollen, in determining correct indication of SIT.

摘要

背景

鉴定疾病诱发过敏原是准确处方过敏原特异性免疫治疗(SIT)的前提。本研究旨在确定分子诊断(MD)是否可能改变 SIT 的适应证和过敏原处方。

方法

共纳入 141 例花粉过敏伴或不伴食物过敏的过敏性鼻结膜炎和/或哮喘患者。所有患者均行皮试,采用空气过敏原组合和基于微阵列的过敏原组合(ISAC(®);Phadia,瑞典)。在学习分子诊断结果之前,三位作者根据 EAACI 建议,根据临床病史和 ISAC 结果前后的皮肤点刺试验结果,就 SIT 适应证和过敏原使用达成共识。使用一致性系数(kappa 指数)分析结果。

结果

患者中 59%为女性,平均年龄 31 ± 13.63 岁。ISAC(®)结果前后 SIT 适应证的一致性仅在 62 例(46%)患者中发现(kappa = 0.1057 ± 0.0413)。关于 MD 结果前后最常见处方中使用的过敏原,我们得到以下结果:草的 κ = 0.117 ± 0.0825;橄榄的 κ = 0.1624 ± 0.0639;橄榄和草的 κ = 0.0505 ± 0.0548;草和柏树的 κ = 0.1711 ± 0.0471;草和伦敦梧桐的 κ = 0.1897 ± 0.0493;橄榄和柏树的 κ = 1 ± 0.0842;橄榄和草的 κ = 0.3586 ± 0.0798;其他组合的 κ 值<0.1。

结论

MD 前后 SIT 的适应证和过敏原使用的一致性非常低。这种差异强调了 MD 的有用性,至少在花粉过敏复杂的情况下,有助于确定 SIT 的正确适应证。

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