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首页> 外文期刊>The Journal of Allergy and Clinical Immunology >Allergen reference doses for precautionary labeling (VITAL 2.0): Clinical implications
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Allergen reference doses for precautionary labeling (VITAL 2.0): Clinical implications

机译:预防标签的过敏原参考剂量(VITAL 2.0):临床意义

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Background There has been a dramatic proliferation of precautionary labeling by manufacturers to mitigate the perceived risk from low-level contamination from allergens in food. This has resulted in a significant reduction in choice of potentially safe foods for allergic consumers. Objectives We aimed to establish reference doses for 11 commonly allergenic foods to guide a rational approach by manufacturers based on all publically available valid oral food challenge data. Methods Reference doses were developed from statistical dose-distribution modeling of individual thresholds of patients in a dataset of more than 55 studies of clinical oral food challenges. Sufficient valid data were available for peanut, milk, egg, and hazelnut to allow assessment of the representativeness of the data used. Results The data were not significantly affected by the heterogeneity of the study methodology, including little effect of age on results for those foods for which sufficient numbers of adult challenge data were available (peanut and hazelnut). Thus by combining data from all studies, the eliciting dose for an allergic reaction in 1% of the population estimated for the following were 0.2 mg of protein for peanut, 0.1 mg for cow's milk, 0.03 mg for egg, and 0.1 mg for hazelnut. Conclusions These reference doses will form the basis of the revised Voluntary Incidental Trace Allergen Labeling (VITAL) 2.0 thresholds now recommended in Australia. These new levels will enable manufacturers to apply credible precautionary labeling and provide increased consumer confidence in their validity and reliability, as well as improving consumer safety.
机译:背景技术制造商已经广泛使用预防标签,以减轻食品中过敏原引起的低水平污染的风险。这大大减少了对过敏性消费者潜在安全食品的选择。目标我们旨在为11种常见的过敏性食品确定参考剂量,以指导制造商根据所有可公开获得的有效口服食品挑战数据来采取合理的方法。方法通过对55项临床口服食品挑战研究的数据集中的患者个体阈值进行统计剂量分布建模,开发了参考剂量。对于花生,牛奶,鸡蛋和榛子,有足够的有效数据可用来评估所用数据的代表性。结果研究方法的异质性对数据没有显着影响,包括年龄对那些具有足够数量的成人挑战数据(花生和榛子)的食品的结果影响很小。因此,通过结合所有研究的数据,在以下人群中估计有1%的人群引起过敏反应的剂量为:花生蛋白0.2 mg,牛奶0.1 mg,鸡蛋0.03 mg和榛子0.1 mg。结论这些参考剂量将构成澳大利亚现在建议的修订的自愿性偶然痕量过敏原标签(VITAL)2.0阈值的基础。这些新级别将使制造商能够应用可靠的预防性标签,并增强消费者对其有效性和可靠性的信心,并提高消费者的安全性。

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