Pifferi M, Ragazzo V, Caramella D, Baldini G
Department of Pediatrics, University of Pisa, Italy.
Pediatr Pulmonol. 2001 Jun;31(6):419-24. doi: 10.1002/ppul.1069.
Infants with acute bronchiolitis during the first months of life are at increased risk of developing persistent wheezing and bronchial asthma later in life. The study of eosinophil cationic protein (ECP) suggests that eosinophil-related inflammatory mechanisms may play a role in respiratory syncytial virus (RSV) bronchiolitis. The aim of our study was to verify whether serum ECP (s-ECP) measurements are useful in predicting the development of persistent wheezing in children affected by RSV bronchiolitis during a 5 years follow-up period. Forty-eight infants were enrolled prospectively (mean age: 153.5 days). All had a clinical and radiological diagnosis of acute bronchiolitis and confirmed RSV infection. Peripheral eosinophil counts, levels of s-ECP, and serum IgE concentrations were measured during bronchiolitis. Five years later the children were re-evaluated in regard to their respiratory symptoms (standardized questionnaires) and atopic status (specific IgE levels). We observed significantly higher s-ECP levels (P < 0.001) at enrollment in subjects who developed persistent wheezing compared to subjects who did not show late wheezing. Initial s-ECP values allowed significant and correct prediction of persistent wheezing (P < 0.001). The risk to develop respiratory symptoms was 9.73 higher for infants with s-ECP levels > or = 8 microg/L than for those with s-ECP levels <8 microg/L (P < 0.0001). In conclusion, our study suggests that s-ECP levels in infants with bronchiolitis are useful in predicting the risk to develop wheezing in the subsequent 5 years.
出生后最初几个月患急性细支气管炎的婴儿,日后发生持续性喘息和支气管哮喘的风险会增加。对嗜酸性粒细胞阳离子蛋白(ECP)的研究表明,嗜酸性粒细胞相关的炎症机制可能在呼吸道合胞病毒(RSV)细支气管炎中起作用。我们研究的目的是验证在5年随访期内,检测血清ECP(s-ECP)是否有助于预测受RSV细支气管炎影响的儿童发生持续性喘息的情况。前瞻性纳入了48例婴儿(平均年龄:153.5天)。所有患儿均有急性细支气管炎的临床和影像学诊断,且确诊为RSV感染。在细支气管炎期间检测外周嗜酸性粒细胞计数、s-ECP水平和血清IgE浓度。5年后,对这些儿童的呼吸道症状(标准化问卷)和特应性状态(特异性IgE水平)进行重新评估。我们观察到,与未出现后期喘息的患儿相比,发生持续性喘息的患儿在入组时s-ECP水平显著更高(P < 0.001)。初始s-ECP值能够显著且正确地预测持续性喘息(P < 0.001)。s-ECP水平≥8 μg/L的婴儿出现呼吸道症状的风险比s-ECP水平<8 μg/L的婴儿高9.73倍(P < 0.0001)。总之,我们的研究表明,细支气管炎婴儿的s-ECP水平有助于预测其在随后5年发生喘息的风险。