Koh Gerald Choon-Huat, Shek Lynette Pei-Chi, Kee Janine, Wee Andrew, Ng Vivian, Koh David
Department of Epidemiology and Public Health, Yong Loo Lin School of Medicine, National University of Singapore, National University Health System, Singapore 117597.
J Asthma. 2010 Feb;47(1):61-5. doi: 10.3109/02770900903350499.
Saliva eosinophil cationic protein (ECP) is higher in asthmatic adults than in healthy ones. However, its relationship with asthma severity, other atopic conditions and allergic sensitization have not been reported. Saliva collection is painless, readily acceptable to children and parents, and can be a potentially useful body fluid to measure asthma biomarkers. We recruited 102 physician-diagnosed young asthmatic subjects from outpatient clinics with change in FEV(1) > or = 12% with inhaled salbutamol and collected data on asthma severity, concurrent allergic rhinitis (AR) and atopic dermatitis (AD), and medication used (bronchodilator and corticosteroid). We measured whole saliva and serum ECP and performed skin prick tests (SPT) for three dust mites (Dermatophagoides pteronyssisinus, Dermatophagoides farinae and Blomia tropicalis) and two cockroaches (Periplaneta americana and Blatella germanica). Median salivary ECP was 84.6 microg/l (inter-quartile range [IQR]: 40.9-147.9) and median serum ECP was 14.7 microg/l (IQR: 6.4-32.1). Serum ECP was only higher in children whose sleep was disturbed by asthma in the past year than those who were not (geometric mean [GM]: 18.9 vs. 11.1 microg/l, relative mean difference [RMD]: 1.71 [95%CI: 1.09-2.69]). Serum ECP was increased among asthmatic children on inhaled corticosteroid than those not using them (GM: 15.6 vs. 8.1 microg/l, RMD: 1.93 [95%CI: 1.11-3.39]). Salivary ECP was not associated with asthma severity, concurrence of atopic conditions, medications used, or any SPT parameter. Saliva ECP did not correlate with serum ECP (r(s) = 0.032, p = 0.790). Salivary and serum ECP did not correlate with wheal size for any skin prick test.
哮喘成年患者唾液中的嗜酸性粒细胞阳离子蛋白(ECP)含量高于健康成年人。然而,其与哮喘严重程度、其他特应性疾病及过敏致敏之间的关系尚无报道。唾液采集无痛,儿童及家长易于接受,且可能是一种用于测量哮喘生物标志物的有用体液。我们从门诊招募了102名经医生诊断的年轻哮喘患者,这些患者吸入沙丁胺醇后FEV(1)变化≥12%,并收集了哮喘严重程度、并发过敏性鼻炎(AR)和特应性皮炎(AD)以及所用药物(支气管扩张剂和皮质类固醇)的数据。我们测量了全唾液和血清中的ECP,并对三种尘螨(屋尘螨、粉尘螨和热带无爪螨)和两种蟑螂(美洲大蠊和德国小蠊)进行了皮肤点刺试验(SPT)。唾液ECP中位数为84.6μg/l(四分位间距[IQR]:40.9 - 147.9),血清ECP中位数为14.7μg/l(IQR:6.4 - 32.1)。仅在过去一年睡眠受哮喘干扰的儿童中,血清ECP高于未受干扰的儿童(几何均值[GM]:18.9对11.1μg/l,相对均值差异[RMD]:1.71[95%CI:1.09 - 2.69])。使用吸入性皮质类固醇的哮喘儿童血清ECP高于未使用者(GM:15.6对8.1μg/l,RMD:1.93[95%CI:1.11 - 3.39])。唾液ECP与哮喘严重程度、特应性疾病并发情况、所用药物或任何皮肤点刺试验参数均无关联。唾液ECP与血清ECP不相关(r(s)=0.032,p = 0.790)。唾液和血清ECP与任何皮肤点刺试验的风团大小均不相关。