Department of Dermatology & Allergy Center, Odense University Hospital, Odense, Denmark.
Allergy. 2013 Feb;68(2):190-4. doi: 10.1111/all.12075. Epub 2012 Dec 14.
As replacement for the oral food challenge, decision-points for sensitization test have been established, but suboptimal sensitivity and/or specificity, as well as regional differences, have reduced the clinical usability. IgE toward specific peanut protein components has been reported to be of value, but data on correlation with clinical data are sparse. Our aim was to correlate IgE values with the outcome of peanut challenges.
Data from 175 positive and 30 negative peanut challenges in patients aged 1-26 years were retrospectively correlated with the levels of specific IgE to peanut and peanut components (Ara h 1-3, h 8, and h 9).
The best correlation between IgE and clinical thresholds was found for Ara h 2 (ρ(s) = -0.30, P < 0.01). A cutoff of Ara h 2 > 1.63 kU/l yielded a specificity = 1.00, with a corresponding sensitivity of 0.70. Symptom severity elicited during challenge correlated significantly with the levels of Ara h 2 (ρ(s) = 0.60, P < 0.0001), but large individual variation was found.
The level of IgE toward Ara h 2 can improve diagnostic accuracy by introducing a more clear-cut decision-point with an optimal specificity maintaining a high sensitivity. In our study, this would have reduced the necessary number of challenges to be performed from 205 to 92. Extrapolation between centers is difficult and decision-points need to be addressed in relation to settings and population. Further component-resolved diagnostic cannot replace oral challenge neither in determining thresholds nor in the assessment of severity of symptoms elicited during challenge.
为了替代口服食物挑战,已经确定了致敏试验的决策点,但由于敏感性和/或特异性不理想,以及地域差异,降低了其临床实用性。已经报道针对特定花生蛋白成分的 IgE 具有一定价值,但与临床数据的相关性数据较少。我们的目的是将 IgE 值与花生挑战的结果相关联。
回顾性分析了 175 例阳性和 30 例阴性花生挑战患者(年龄 1-26 岁)的数据,与花生和花生成分(Ara h 1-3、h 8 和 h 9)的特异性 IgE 水平相关联。
发现 IgE 与临床阈值之间的最佳相关性为 Ara h 2(ρ(s) = -0.30,P < 0.01)。Ara h 2 > 1.63 kU/l 的截点具有 1.00 的特异性,相应的敏感性为 0.70。挑战期间诱发的症状严重程度与 Ara h 2 的水平显著相关(ρ(s) = 0.60,P < 0.0001),但个体差异较大。
Ara h 2 的 IgE 水平可以通过引入更明确的决策点来提高诊断准确性,该决策点具有最佳特异性,同时保持高敏感性。在我们的研究中,这将使所需进行的挑战次数从 205 次减少到 92 次。中心之间的推断比较困难,需要根据环境和人群来确定决策点。进一步的成分解析诊断不能替代口服挑战,无论是在确定阈值还是在评估挑战期间诱发的症状严重程度方面。