Clinica Pediatrica, Dipartimento di Medicina e Chirurgia, Università di Parma, Azienda Ospedaliero-Universitaria di Parma, 43126 Parma, Italy.
UO Pediatria e Pronto Soccorso, Azienda Ospedaliero-Universitaria Consorziale Policlinico, Ospedale Pediatrico Giovanni XXIII, 70126 Bari, Italy.
Nutrients. 2021 Feb 16;13(2):640. doi: 10.3390/nu13020640.
Hazelnuts commonly elicit allergic reactions starting from childhood and adolescence, with a rare resolution over time. The definite diagnosis of a hazelnut allergy relies on an oral food challenge. The role of component resolved diagnostics in reducing the need for oral food challenges in the diagnosis of hazelnut allergies is still debated. Therefore, three electronic databases were systematically searched for studies on the diagnostic accuracy of specific-IgE (sIgE) on hazelnut proteins for identifying children with a hazelnut allergy. Studies regarding IgE testing on at least one hazelnut allergen component in children whose final diagnosis was determined by oral food challenges or a suggestive history of serious symptoms due to a hazelnut allergy were included. Study quality was assessed by the Quality Assessment of Diagnostic Accuracy Studies-2 tool. Eight studies enrolling 757 children, were identified. Overall, sensitivity, specificity, area under the curve and diagnostic odd ratio of Cor a 1 sIgE were lower than those of Cor a 9 and Cor a 14 sIge. When the test results were positive, the post-test probability of a hazelnut allergy was 34% for Cor a 1 sIgE, 60% for Cor a9 sIgE and 73% for Cor a 14 sIgE. When the test results were negative, the post-test probability of a hazelnut allergy was 55% for Cor a 1 sIgE, 16% for Cor a9 sIgE and 14% for Cor a 14 sIgE. Measurement of IgE levels to Cor a 9 and Cor a 14 might have the potential to improve specificity in detecting clinically tolerant children among hazelnut-sensitized ones, reducing the need to perform oral food challenges.
榛子通常会在儿童和青少年时期引发过敏反应,且随着时间的推移,过敏反应罕见地会自行消退。榛子过敏的明确诊断依赖于口服食物激发试验。在诊断榛子过敏时,成分解析诊断在减少口服食物激发试验需求方面的作用仍存在争议。因此,我们系统性地检索了三个电子数据库,以寻找关于榛子蛋白特异性 IgE(sIgE)用于识别榛子过敏儿童的诊断准确性的研究。纳入的研究对象为接受了至少一种榛子过敏原成分 IgE 检测且最终诊断由口服食物激发试验或因榛子过敏而出现严重症状的提示性病史确定的儿童。研究质量采用诊断准确性研究质量评估-2 工具进行评估。共确定了 8 项纳入了 757 名儿童的研究。总体而言,Cor a 1 sIgE 的敏感性、特异性、曲线下面积和诊断比值比均低于 Cor a 9 和 Cor a 14 sIgE。当检测结果为阳性时,Cor a 1 sIgE 检测结果阳性提示榛子过敏的后验概率为 34%,Cor a9 sIgE 为 60%,Cor a 14 sIgE 为 73%。当检测结果为阴性时,Cor a 1 sIgE 检测结果阴性提示榛子过敏的后验概率为 55%,Cor a9 sIgE 为 16%,Cor a 14 sIgE 为 14%。检测 Cor a 9 和 Cor a 14 的 IgE 水平可能有助于提高在榛子致敏儿童中检测临床耐受儿童的特异性,从而减少进行口服食物激发试验的需求。