Wu Fan, Guan Wei-Jie, Gao Yi, An Jia-Ying, Xie Yan-Qing, Liu Wen-Ting, Yu Xin-Xin, Zheng Jin-Ping
State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, Guangzhou Institute of Respiratory Disease, First Affiliated Hospital of Guangzhou Medical University, Guangzhou Medical University, Guangzhou, Guangdong, China.
Affiliated Liwan Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China.
Clin Respir J. 2017 Jul;11(4):470-480. doi: 10.1111/crj.12360. Epub 2015 Sep 10.
Adenosine monophosphate (AMP) may reflect airway inflammation and hyperresponsiveness, but relationship between AMP and histamine (His, a conventional stimulus) bronchial provocation test (BPT) in asthma is not fully elucidated.
To compare both BPTs and determine their utility in reflecting changes of asthmatic symptoms.
BPTs were performed in a cross-over fashion, at 2-4 day intervals. Cumulative doses eliciting 20% FEV fall (PD FEV ), diagnostic performance and adverse events (AEs) were compared. Patients with PD FEV lower than geometric mean were defined as responders, otherwise poor responders. Patients with uncontrolled and partly controlled asthma, who maintained their original inhaled corticosteroids therapy, underwent reassessment of airway responsiveness and asthmatic symptoms 3 and 6 months after.
Nineteen uncontrolled, 22 partly controlled and 19 controlled asthmatic patients and 24 healthy subjects were recruited. Lower PD FEV geometric means were associated with poorer asthma control in His-BPT (0.424 μmol vs 1.684 μmol vs 3.757 μmol), but not AMP-BPT (11.810 μmol vs 7.781 μmol vs 10.220 μmol). Both BPTs yielded similar overall diagnostic performance in asthma (area under curve: 0.842 in AMP-BPT vs 0.850 in His-BPT). AEs, including wheezing and tachypnea, were similar and mild. Ten patients with uncontrolled and 10 partly controlled asthma were followed-up. At months 3 and 6, we documented an increase in PD FEV -AMP and PD FEV -His, which did not correlate with reduction asthmatic symptom scores. This overall applied in responders and poor responders of AMP-BPT and His-BPT.
Despite higher screening capacity of well-controlled asthma, AMP-BPT confers similar diagnostic performance and safety with His-BPT. AMP-BPT might not preferentially reflect changes asthmatic symptoms.
单磷酸腺苷(AMP)可能反映气道炎症和高反应性,但AMP与组胺(His,一种传统刺激物)支气管激发试验(BPT)在哮喘中的关系尚未完全阐明。
比较两种BPT并确定其在反映哮喘症状变化中的效用。
BPT以交叉方式进行,间隔2 - 4天。比较引起20%第一秒用力呼气容积(FEV)下降的累积剂量(PD20FEV)、诊断性能和不良事件(AE)。将PD20FEV低于几何平均值的患者定义为反应者,否则为反应不佳者。未控制和部分控制的哮喘患者,维持其原吸入糖皮质激素治疗,在3个月和6个月后重新评估气道反应性和哮喘症状。
招募了19例未控制、22例部分控制和19例控制的哮喘患者以及24名健康受试者。在组胺BPT中,较低的PD20FEV几何平均值与较差的哮喘控制相关(0.424μmol对1.684μmol对3.757μmol),但在AMP - BPT中并非如此(11.810μmol对7.781μmol对10.220μmol)。两种BPT在哮喘中的总体诊断性能相似(曲线下面积:AMP - BPT为0.842,组胺BPT为0.850)。不良事件,包括喘息和呼吸急促,相似且轻微。对10例未控制和10例部分控制的哮喘患者进行了随访。在第3个月和第6个月,我们记录到PD20FEV - AMP和PD20FEV - 组胺增加,这与哮喘症状评分的降低无关。这总体上适用于AMP - BPT和组胺BPT的反应者和反应不佳者。
尽管AMP - BPT对控制良好的哮喘筛查能力更高,但与组胺BPT具有相似的诊断性能和安全性。AMP - BPT可能无法优先反映哮喘症状的变化。