Variability of fractional exhaled nitric oxide is associated with the risk and aetiology of COPD exacerbations

被引:9
|
作者
Schumann, Desiree M. M. [1 ]
Papakonstantinou, Eleni [1 ,2 ,3 ]
Kostikas, Konstantinos [1 ,4 ]
Grize, Leticia [1 ]
Tamm, Michael [1 ]
Stolz, Daiana [1 ,2 ]
机构
[1] Univ Hosp, Clin Pneumol & Pulm Cell Res, Basel, Switzerland
[2] Univ Freiburg, Fac Med, Med Ctr, Dept Pneumol, Freiburg, Germany
[3] Aristotle Univ Thessaloniki, Dept Med, Lab Pharmacol, Thessaloniki, Greece
[4] Univ Ioannina, Dept Resp Med, Ioannina, Greece
关键词
aetiology; bacterial infection; COPD exacerbation; FeNO; fractional exhaled nitric oxide; prevention; viral infection; OBSTRUCTIVE PULMONARY-DISEASE; INHALED CORTICOSTEROIDS; AIRWAY INFLAMMATION; TREATMENT RESPONSE; FENO; INHALATION; INFECTION; ASTHMA;
D O I
10.1111/resp.14439
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background and ObjectiveAcute exacerbations of chronic obstructive pulmonary disease (AECOPD) are heterogeneous in aetiology and accelerate disease progression. Here, we aimed to investigate the association of fractional exhaled nitric oxide (FeNO) and its variability with AECOPD of different aetiology. MethodsFeNO was determined in 2157 visits (1697 stable, 133 AECOPD and 327 follow-up) of 421 COPD patients from the PREVENT study, an investigator-initiated, longitudinal and interventional study, who were on daily treatment with inhaled corticosteroids/long-acting beta 2-agonists. ResultsLongitudinal measurements of FeNO revealed an intra-subject variability of FeNO that was significantly higher in exacerbators compared to non-exacerbators (p < 0.001) and positively associated with the number of AECOPD. As FeNO variability increased, the probability of patients to remain AECOPD-free decreased. In patients included in the highest FeNO variability quartile (>= 15.0 ppb) the probability to remain free of AECOPD was only 35% as compared to 80% for patients included in the lowest FeNO variability quartile (0.50-4.39 ppb). The change of FeNO from the last stable visit to AECOPD was positively associated with the probability of viral infections and this association was stronger in current smokers than ex-smokers. In contrast, the change in FeNO from the last stable visit to an AECOPD visit was inversely associated with the probability of bacterial infections in ex-smokers but not in current smokers. ConclusionFeNO variability was associated with the risk and aetiology of AECOPD differentially in current and ex-smokers.
引用
收藏
页码:445 / 454
页数:10
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