Washington University School of Medicine, St Louis, Missouri; St Louis VA Medical Center, St Louis, Missouri.
Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland; Johns Hopkins University School of Medicine, Baltimore, Maryland.
Ann Allergy Asthma Immunol. 2014 Apr;112(4):354-60.e1. doi: 10.1016/j.anai.2014.01.013. Epub 2014 Feb 5.
The methacholine challenge test quantifies airway hyper-responsiveness, which is measured by the provocative concentration of methacholine causing a 20% decrease in forced expiration volume in 1 second (PC20). The dose-response effect of inhaled corticosteroids (ICS) on PC20 has been inconsistent and within-patient variability of PC20 is not well established.
To determine the effect of high- vs low-dose ICS on PC20 and within-patient variability in those with repeated measurements of PC20.
A randomized, double-masked, crossover trial was conducted in patients with asthma on controller medications with PC20 of 8 mg/mL or lower (n = 64) to evaluate the effect of high-dose (1,000 μg/d) vs low-dose (250 μg/d) fluticasone for 4 weeks on PC20. In addition, the variability of PC20 was assessed in participants who underwent 2 or 3 PC20 measurements on the same dose of ICS (n = 27) over a 4-week interval.
Because there was a significant period effect, dose comparison of the change in PC20 was assessed in the first treatment period. There was no significant difference in the change in PC20 for high- vs low-dose ICS (39% vs 30% increase, respectively; P = .87). The within- and between-participant variances for log PC20 were 0.84 and 0.96, respectively, with an intra-class correlation of 0.53, and 37% of participants had more than 2 doubling dose changes in PC20 in those with repeated measurements.
The effect of ICS on PC20 is not dose dependent at fluticasone levels of 250 and 1,000 μg/d. Interpersonal variability for PC20 is large. A lack of precise measurements should be taken into account when interpreting any change in PC20.
乙酰甲胆碱挑战试验量化了气道高反应性,其通过引起用力呼气量在 1 秒内下降 20%的乙酰甲胆碱激发浓度(PC20)来测量。吸入性皮质类固醇(ICS)对 PC20 的剂量反应效应一直不一致,并且 PC20 的个体内变异性尚未得到充分确立。
确定高剂量与低剂量 ICS 对 PC20 的影响,以及对 PC20 进行重复测量的患者个体内变异性。
对接受控制性药物治疗且 PC20 为 8mg/ml 或更低的哮喘患者(n=64)进行了一项随机、双盲、交叉试验,以评估高剂量(1000μg/d)与低剂量(250μg/d)氟替卡松治疗 4 周对 PC20 的影响。此外,在接受相同剂量 ICS(n=27)进行 2 或 3 次 PC20 测量的参与者中,评估了 PC20 的变异性。
由于存在显著的周期效应,因此在第一个治疗期评估了 PC20 变化的剂量比较。高剂量与低剂量 ICS 对 PC20 变化的影响无显著差异(分别增加 39%和 30%;P=.87)。log PC20 的个体内和个体间方差分别为 0.84 和 0.96,组内相关系数为 0.53,有 37%的参与者在重复测量中 PC20 的加倍剂量变化超过 2 次。
在氟替卡松 250μg/d 和 1000μg/d 水平下,ICS 对 PC20 的影响与剂量无关。PC20 的个体间变异性很大。在解释 PC20 的任何变化时,都应考虑到精确测量的缺乏。