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The reproducibility and effect on non-specific airway responsiveness of inhaled prostaglandin D2 and leukotriene D4 in asthmatic subjects.

机译:哮喘患者吸入前列腺素D2和白三烯D4的可重复性及其对非特异性气道反应性的影响。

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摘要

1. Mast cell mediators PGD2 and LTD4 may play important roles in asthma pathogenesis. There is little information on the repeatability of inhalation challenge with these agonists in the laboratory. 2. We assessed the repeatability of inhalation challenges using PGD2 and LTD4 in two groups of 10 asthmatic volunteers. Non-specific bronchial responsiveness was assessed by histamine inhalation challenges. 3. Using the Bland-Altman method, we found the coefficient of repeatability to be 1.2 doubling doses for LTD4 and 2.1 for PGD2 at a 1 week interval. Repeatability for histamine inhalation challenge over the same time period was similar at 1.4 and 2.1 doubling doses respectively. 4. Non-specific bronchial responsiveness following LTD4 challenge decreased significantly, mean PD20FEV1 increasing from 169 nmol on day 1 to 278 nmol on day 3 (P = 0.001), before returning to baseline levels. 5. A progressive decrease in non-specific bronchial responsiveness occurred following PGD2 challenge. Baseline PD20FEV1 was 195 nmol, increasing to 238 nmol by day 3 (NS) and 313 nmol by day 8 (P = 0.016). 6. PGD2 inhalation challenges performed a week apart are less reproducible than LTD4 challenges, possibly as a result of significant changes in histamine bronchial responsiveness. Our findings allow accurate power calculations to be made for studies to assess new pharmacological antagonists to these mediators.
机译:1.肥大细胞介质PGD2和LTD4可能在哮喘发病中起重要作用。这些激动剂在实验室中的吸入攻击可重复性的信息很少。 2.我们评估了使用PGD2和LTD4在两组10名哮喘志愿者中进行吸入挑战的可重复性。非特异性支气管反应性通过组胺吸入攻击进行评估。 3.使用Bland-Altman方法,我们发现在1周的间隔内,LTD4的重复系数为1.2倍,PGD2的重复系数为2.1。组胺吸入攻击在相同时间段内的重复性分别为1.4和2.1倍剂量时相似。 4. LTD4攻击后的非特异性支气管反应性显着降低,平均PD20FEV1从第1天的169 nmol增加到第3天的278 nmol(P = 0.001),然后恢复至基线水平。 5. PGD2攻击后,非特异性支气管反应性逐渐降低。基线PD20FEV1为195 nmol,到第3天(NS)增加到238 nmol,到第8天增加到313 nmol(P = 0.016)。 6.间隔一周进行的PGD2吸入刺激比LTD4刺激的重现性差,这可能是由于组胺支气管反应性发生显着变化所致。我们的发现允许进行准确的功率计算,以进行研究以评估这些介体的新药理拮抗剂。

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