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根据对变应原的皮肤敏感性和对组胺的气道反应性预测气道对变应原的反应性。

Prediction of airway responsiveness to allergen from skin sensitivity to allergen and airway responsiveness to histamine.

作者信息

Cockcroft D W, Murdock K Y, Kirby J, Hargreave F

出版信息

Am Rev Respir Dis. 1987 Jan;135(1):264-7. doi: 10.1164/arrd.1987.135.1.264.

Abstract

Previous data have indicated that airway responsiveness to allergen, expressed as the provocation concentration causing a 20% FEV1 fall (PC20), was dependent on nonallergic airway responsiveness (histamine PC20) and sensitivity to allergen (skin sensitivity or end-point titration). From retrospective data in 24 subjects, we developed a formula to predict allergen PC20 and examined its accuracy prospectively in 26 new subjects undergoing allergen inhalation test with doubling allergen concentrations. Allergen PC20 (APC20) was predicted from histamine PC20 (HPC20) and skin sensitivity (SS) by the formula: Log10 (APC20) = 0.69 Log10 (HPC20 X SS) + 0.11 (r = 0.85). Allergen PC20 was accurately predicted in 6, and overestimated or underestimated by 1 doubling concentration in 11, by 2 concentrations in 6, by 3 concentrations in 3, and by greater than 3 concentrations in none. From the total of 50 subjects, a new relationship was developed: Log10 (APC10) = 0.68 log10 (HPC20 X SS) (r = 0.82) from which 46 of 50 (92%) of allergen PC20 values fall within 2 doubling concentrations of the regression line (and all within 3). Early airway responsiveness to a given allergen can be predicted within a +/- 8-fold range, which is better than some investigator's test reproducibility of +/- 1 log (10-fold). Allergen inhalation tests to determine early asthmatic responsiveness to different IgE-mediated allergens can probably be replaced by the simpler and safer determinations of allergen sensitivity (SS, RAST) and histamine or methacholine airway responsiveness.

摘要

先前的数据表明,气道对过敏原的反应性,以引起第一秒用力呼气量(FEV1)下降20%的激发浓度(PC20)来表示,取决于非过敏性气道反应性(组胺PC20)和对过敏原的敏感性(皮肤敏感性或终点滴定法)。根据24名受试者的回顾性数据,我们制定了一个预测过敏原PC20的公式,并在26名接受过敏原浓度加倍的过敏原吸入试验的新受试者中对其准确性进行了前瞻性研究。通过以下公式根据组胺PC20(HPC20)和皮肤敏感性(SS)预测过敏原PC20(APC20):Log10(APC20)=0.69 Log10(HPC20×SS)+0.11(r = 0.85)。6名受试者的过敏原PC20得到准确预测,11名受试者的预测值高估或低估了1个加倍浓度,6名受试者高估或低估了2个浓度,3名受试者高估或低估了3个浓度,没有受试者高估或低估超过3个浓度。在总共50名受试者中,得出了一个新的关系:Log10(APC10)=0.68 log10(HPC20×SS)(r = 0.82),50名受试者中有46名(92%)的过敏原PC20值落在回归线的2个加倍浓度范围内(且全部在3个加倍浓度范围内)。对给定过敏原的早期气道反应性可在±8倍范围内预测,这比一些研究者测试的±1 log(10倍)的可重复性要好。确定对不同IgE介导的过敏原的早期哮喘反应性的过敏原吸入试验可能可以被更简单、更安全的过敏原敏感性(SS、放射性变应原吸附试验)以及组胺或乙酰甲胆碱气道反应性测定所取代。

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