Prieto Luis, Bruno Laura, Gutiérrez Valentina, Uixera Sonia, Pérez-Francés Carmen, Lanuza Amparo, Ferrer Ana
Sección de Alergología, Hospital Universitario Dr. Peset, and Universidad de Valencia, Valencia, Spain.
Chest. 2003 Oct;124(4):1325-33. doi: 10.1378/chest.124.4.1325.
To investigate the utility of the determination of airway responsiveness to inhaled adenosine 5'-monophosphate (AMP) and exhaled nitric oxide (ENO) levels as markers for safely reducing the dose of inhaled corticosteroids (ICS) in patients with asthma well controlled with a moderately high ICS dose.
A total of 37 patients with asthma well controlled for at least 3 months by treatment with a moderately high ICS dose (beclomethasone dipropionate, 500 to 1,000 microg or equivalent daily) were included in the study. Patients were treated for a 2-week run-in (baseline) period with their usual dose of ICS. For the next 12 weeks, patients were treated with ICS at half the previous dose, maintaining the same inhalation device. At the end of the baseline period and after 2 weeks, 8 weeks, and 12 weeks of treatment with a reduced dose of ICS, measurements were made in the following order: ENO, spirometry, and AMP challenge. Furthermore, patients completed a diary twice daily recording peak expiratory flow, daytime and nighttime symptoms, and use of rescue albuterol.
Ten patients had an asthma exacerbation. Using a Kaplan-Meier survival analysis, the significant predictors of a failure of ICS reduction were having both bronchoconstriction in response to AMP and ENO levels > or = 15 parts per billion (ppb) at baseline (p = 0.006), as well as having both bronchoconstriction in response to AMP and ENO levels > or = 20 ppb at baseline (p = 0.033). Having a decrease in the provocative concentration of AMP causing a 20% fall in FEV(1) of at least one doubling concentration 2 weeks after the dose of ICS was halved was a borderline significant predictor for failure of ICS reduction (p = 0.062).
These observations suggest that in asthmatic patients well controlled with ICS, the determination of AMP responsiveness and ENO levels may be useful to identifying those subjects whose condition will or will not deteriorate when the dose of ICS is reduced.
探讨测定气道对吸入5'-单磷酸腺苷(AMP)的反应性和呼出一氧化氮(ENO)水平,作为安全降低中度高剂量吸入性糖皮质激素(ICS)治疗的哮喘控制良好患者ICS剂量的标志物的效用。
本研究共纳入37例经中度高剂量ICS(二丙酸倍氯米松,500至1000微克/天或等效剂量)治疗至少3个月病情控制良好的哮喘患者。患者先用其常用剂量的ICS进行为期2周的导入期(基线期)治疗。在接下来的12周内,患者接受剂量减半的ICS治疗,使用相同的吸入装置。在基线期结束时以及在剂量减半的ICS治疗2周、8周和12周后,按以下顺序进行测量:ENO、肺量计检查和AMP激发试验。此外,患者每天记录两次日记,记录呼气峰值流速、白天和夜间症状以及急救沙丁胺醇的使用情况。
10例患者哮喘发作。采用Kaplan-Meier生存分析,ICS减量失败的显著预测因素为基线时对AMP有支气管收缩反应且ENO水平≥15 ppb(十亿分之一)(p = 0.006),以及基线时对AMP有支气管收缩反应且ENO水平≥20 ppb(p = 0.033)。在ICS剂量减半2周后,引起FEV(1)下降20%的AMP激发浓度至少降低一个加倍浓度是ICS减量失败的临界显著预测因素(p = 0.062)。
这些观察结果表明,在ICS控制良好的哮喘患者中,测定AMP反应性和ENO水平可能有助于识别那些在ICS剂量降低时病情是否会恶化的患者。