Xepapadaki Paraskevi, Papadopoulos Nikolaos G, Bossios Apostolos, Manoussakis Emmanuel, Manousakas Theodoros, Saxoni-Papageorgiou Photini
Allergy Unit, 2nd Pediatric Clinic, University of Athens.
J Allergy Clin Immunol. 2005 Aug;116(2):299-304. doi: 10.1016/j.jaci.2005.04.007.
Respiratory viruses induce asthma exacerbations and airway hyperresponsiveness (AHR). Atopy is an important risk factor for asthma persistence.
We sought to evaluate whether atopy is a risk factor for prolonged AHR after upper respiratory tract infections (URIs).
Twenty-five children (13 atopic and 12 nonatopic children) with intermittent virus-induced asthma were studied. Clinical evaluation, skin prick tests, methacholine bronchoprovocation, questionnaires, and a nasal wash specimen were obtained at baseline. For 9 months, subjects completed diary cards with respiratory symptoms. During their first reported cold, a nasal wash specimen was obtained. Methacholine provocation was performed 10 days and 5, 7, 9, and 11 weeks later. In case a new cold developed, the provocation schedule was followed from the beginning.
Viruses were detected in 17 (68%) of 25 patients during their first cold, with rhinovirus being most commonly identified (82%). AHR increased significantly 10 days after the URI, equally in both groups (P = .67), and remained so up to the fifth week. Duration of AHR in subjects experiencing a single URI ranged from 5 to 11 weeks, without a significant difference between groups. In the duration of the study, atopic children experienced more colds and asthma exacerbations than nonatopic children. Thus for duration of AHR, significant prolongation was noted in the atopic group when assessed cumulatively.
In asthmatic children the duration of AHR after a single natural cold is 5 to 11 weeks. However, an increased rate of symptomatic cold and asthma episodes in atopic children is associated with considerable cumulative prolongation of AHR, which might help explain the role of atopy as a risk factor for asthma persistence.
呼吸道病毒可诱发哮喘急性发作和气道高反应性(AHR)。特应性是哮喘持续存在的重要危险因素。
我们旨在评估特应性是否为上呼吸道感染(URIs)后AHR持续时间延长的危险因素。
对25名患有间歇性病毒诱发哮喘的儿童(13名特应性儿童和12名非特应性儿童)进行研究。在基线时进行临床评估、皮肤点刺试验、乙酰甲胆碱支气管激发试验、问卷调查,并采集鼻洗液样本。在9个月的时间里,受试者填写记录呼吸道症状的日记卡。在他们首次报告感冒时,采集鼻洗液样本。在感冒后10天以及5、7、9和11周后进行乙酰甲胆碱激发试验。如果出现新的感冒,则重新开始激发试验流程。
25名患者中有17名(68%)在首次感冒时检测到病毒,其中鼻病毒最为常见(82%)。感冒后10天,两组患者的AHR均显著增加(P = 0.67),并一直持续到第五周。经历单次URIs的受试者AHR持续时间为5至11周,两组之间无显著差异。在研究期间,特应性儿童比非特应性儿童患感冒和哮喘急性发作的次数更多。因此,累计评估时,特应性组的AHR持续时间显著延长。
在哮喘儿童中,单次自然感冒后AHR的持续时间为5至11周。然而,特应性儿童有症状的感冒和哮喘发作率增加,与AHR的显著累计延长相关,这可能有助于解释特应性作为哮喘持续存在危险因素的作用。