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使用经验证的 Ara h 2 截断值可准确预测三分之一成年人的花生过敏。

Accurate Prediction of Peanut Allergy in One-Third of Adults Using a Validated Ara h 2 Cutoff.

机构信息

Department of Dermatology and Allergology, University Medical Center, Utrecht University, Utrecht, the Netherlands; Department of Pediatric Pulmonology and Allergology, Wilhelmina Children's Hospital, University Medical Center, Utrecht University, Utrecht, the Netherlands.

Department of Dermatology and Allergology, University Medical Center, Utrecht University, Utrecht, the Netherlands.

出版信息

J Allergy Clin Immunol Pract. 2021 Apr;9(4):1667-1674.e3. doi: 10.1016/j.jaip.2020.11.024. Epub 2020 Nov 26.

Abstract

BACKGROUND

The diagnostic value of peanut components is extensively studied in children, but to a lesser extent in adults with suspected peanut allergy. The use of peanut components in daily practice may reduce the need for double-blind placebo-controlled food challenges (DBPCFCs); however, validation studies are currently lacking.

OBJECTIVE

To evaluate the diagnostic value of (combined) peanut components and validate a previously found Ara h 2 cutoff level with 100% positive predictive value (PPV) in adults with suspected peanut allergy.

METHODS

Adults who underwent a peanut DBPCFC were included: 84 patients from a previous study (2002-2012) and 70 new patients (2012-2019). Specific IgE (sIgE) to peanut extract, Ara h 1, 2, 3, 6, and 8 was measured using ImmunoCAP. Diagnostic value was assessed with an area under the curve (AUC) analysis.

RESULTS

In total, 95 (62%) patients were peanut allergic. sIgE to Ara h 2 and Ara h 6 were the best predictors with an AUC (95% confidence interval) of 0.85 (0.79-0.91) and 0.85 (0.79-0.92), respectively. The Ara h 2 cutoff level with 100% PPV (≥1.75 kU/L) was validated in the 70 new patients. Thirty percent of all included patients could be classified correctly as peanut allergic using this validated cutoff level.

CONCLUSION

sIgE to Ara h 2 and Ara h 6 have equally high discriminative ability. Peanut allergy can be predicted accurately in one-third of adults using a validated cutoff level of sIgE to Ara h 2.

摘要

背景

在儿童中广泛研究了花生成分的诊断价值,但在疑似花生过敏的成年人中研究较少。在日常实践中使用花生成分可能会减少对双盲安慰剂对照食物挑战(DBPCFC)的需求;然而,目前缺乏验证研究。

目的

评估(组合)花生成分的诊断价值,并验证之前在疑似花生过敏的成年人中发现的 Ara h 2 截断值,其具有 100%的阳性预测值(PPV)。

方法

纳入接受花生 DBPCFC 的成年人:来自先前研究(2002-2012 年)的 84 名患者和 70 名新患者(2012-2019 年)。使用 ImmunoCAP 测量花生提取物、Ara h 1、2、3、6 和 8 的特异性 IgE(sIgE)。使用曲线下面积(AUC)分析评估诊断价值。

结果

共有 95 名(62%)患者对花生过敏。sIgE 对 Ara h 2 和 Ara h 6 是最佳预测因子,AUC(95%置信区间)分别为 0.85(0.79-0.91)和 0.85(0.79-0.92)。在 70 名新患者中验证了 Ara h 2 截断值为 100%PPV(≥1.75 kU/L)。使用此经过验证的截断值,可正确分类三分之一的所有纳入患者为花生过敏。

结论

sIgE 对 Ara h 2 和 Ara h 6 具有相同的区分能力。使用经过验证的 Ara h 2 sIgE 截断值,可准确预测三分之一的成年人是否患有花生过敏。

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