Bjerregaard A, Laing I A, Backer V, Sverrild A, Khoo S-K, Chidlow G, Sikazwe C, Smith D W, Le Souëf P, Porsbjerg C
Respiratory Research Unit, Bispebjerg University Hospital, Copenhagen, Denmark.
Telethon Kids Institute, Perth, WA, Australia.
Clin Exp Allergy. 2017 Aug;47(8):1007-1013. doi: 10.1111/cea.12935. Epub 2017 May 9.
The major trigger of asthma exacerbations is infection with a respiratory virus, most commonly rhinovirus. Type 2 inflammation is known to be associated with an increased risk of exacerbations in general. Whether type 2 inflammation at baseline increases the risk of future virus-induced exacerbations is unknown.
To assess whether type 2 inflammation is associated with an increased risk of virus-induced exacerbations of asthma.
Stable asthmatics had spirometry, skin prick test, measurement of FeNO and sputum induced for differential cell counts. Patients were followed up for 18 months, during which they were assessed at the research unit when they had symptoms of an exacerbation. Nasal swabs collected at these assessments underwent viral detection by PCR.
A total of 81 asthma patients were recruited, of which 22 (27%) experienced an exacerbation during the follow-up period. Of these, 15 (68%) had a respiratory virus detected at exacerbation. Sputum eosinophils >1% at baseline increased the risk of having a subsequent virus-induced exacerbation (HR 7.6 95% CI: 1.6-35.2, P=.010) as did having FeNO >25 ppb (HR 3.4 95% CI: 1.1-10.4, P=.033).
Established type 2 inflammation during stable disease is a risk factor for virus-induced exacerbations in a real-life setting. Measures of type 2 inflammation, such as sputum eosinophils and FeNO, could be included in the risk assessment of patients with asthma in future studies.
哮喘急性加重的主要诱因是呼吸道病毒感染,最常见的是鼻病毒。一般而言,已知2型炎症与急性加重风险增加有关。基线时的2型炎症是否会增加未来病毒诱发急性加重的风险尚不清楚。
评估2型炎症是否与病毒诱发的哮喘急性加重风险增加有关。
病情稳定的哮喘患者进行肺活量测定、皮肤点刺试验、呼出气一氧化氮(FeNO)测定以及诱导痰进行细胞分类计数。对患者进行18个月的随访,在此期间,当他们出现急性加重症状时在研究单位进行评估。在这些评估时采集的鼻拭子通过聚合酶链反应(PCR)进行病毒检测。
共招募了81例哮喘患者,其中22例(27%)在随访期间出现急性加重。其中,15例(68%)在急性加重时检测到呼吸道病毒。基线时痰嗜酸性粒细胞>1%会增加随后病毒诱发急性加重的风险(风险比[HR] 7.6,95%置信区间[CI]:1.6 - 35.2,P = 0.010),FeNO>25 ppb时也是如此(HR 3.4,95% CI:1.1 - 10.4,P = 0.033)。
在稳定期疾病中已确立的2型炎症是现实生活中病毒诱发急性加重的危险因素。在未来研究中,2型炎症指标,如痰嗜酸性粒细胞和FeNO,可纳入哮喘患者的风险评估。