Gibbons W J, Sharma A, Lougheed D, Macklem P T
Montreal Chest Hospital Centre, McGill University, Quebec, Canada.
Am J Respir Crit Care Med. 1996 Feb;153(2):582-9. doi: 10.1164/ajrccm.153.2.8564102.
Airway hyperresponsiveness is easily assessed by measuring the concentration or dose of an inhaled agonist that produces a defined response, e.g., PC20 or PD20. However, this measure does not assess excessive bronchoconstriction. We report the results of analyzing bronchial dose-response curves by measuring percent fall in vital capacity (delta FVC%) as the response rather than the PC20. In our analysis, delta FVC% was measured at the PC20, and therefore it was the dependent variable, whereas the concentration of agonist was the independent variable, in contrast to the usual bronchoprovocation tests in which the response is the independent variable and the dose is the dependent variable. We reasoned that a dose-dependent increase in gas trapping with histamine would detect excessive bronchoconstriction as a decrease in FVC; in contrast, PC20 measures only the ease of bronchoconstriction. In 10 patients with mild asthma the reproducibility of delta FVC% when FEV1 fell by 20%, i.e., at the PC20 concentration of histamine, taken from a greater than 6-s FVC on an otherwise standard histamine challenge test was comparable to that of PC20. In 10 healthy asymptomatic subjects there were only trivial falls (0.3%) in FVC to as much as 16 mg/ml histamine. In a retrospective study of 146 patients with mild asthma, the delta FVC% was normally distributed (13.2 +/- 5.5 SD%) and did not correlate with the number of beta 2-agonist prescriptions or the PC20, but it did correlate with the number of prescriptions written per month for oral prednisone (r = 0.55, p < 0.02). We conclude that delta FVC% when FEV1 falls by 20% is a safe method of detecting excessive bronchoconstriction, and it reveals that different asthmatics react in fundamentally different ways to the same agonist. This may be useful in detecting the asthmatic at risk for serious disease.
气道高反应性可通过测量产生特定反应的吸入激动剂的浓度或剂量来轻松评估,例如PC20或PD20。然而,这种测量方法并不能评估过度支气管收缩。我们报告了通过测量肺活量下降百分比(ΔFVC%)作为反应而非PC20来分析支气管剂量反应曲线的结果。在我们的分析中,ΔFVC%是在PC20时测量的,因此它是因变量,而激动剂浓度是自变量,这与通常的支气管激发试验相反,在通常的试验中反应是自变量而剂量是因变量。我们推断,组胺导致的气体潴留剂量依赖性增加会检测到FVC降低所反映的过度支气管收缩;相比之下,PC20仅测量支气管收缩的易感性。在10例轻度哮喘患者中,当FEV1下降20%时,即在组胺PC20浓度下,从标准组胺激发试验中大于6秒的FVC得出的ΔFVC%的可重复性与PC20相当。在10名健康无症状受试者中,高达16 mg/ml组胺时FVC仅有微小下降(0.3%)。在一项对146例轻度哮喘患者的回顾性研究中,ΔFVC%呈正态分布(13.2±5.5 SD%),与β2激动剂处方数量或PC20无关,但与每月口服泼尼松的处方数量相关(r = 0.55,p < 0.02)。我们得出结论,当FEV1下降20%时的ΔFVC%是检测过度支气管收缩的一种安全方法,并且它揭示了不同哮喘患者对同一激动剂的反应在根本上存在差异。这可能有助于检测有严重疾病风险的哮喘患者。