Saglani Sejal, Payne Donald N, Zhu Jie, Wang Zhuo, Nicholson Andrew G, Bush Andrew, Jeffery Peter K
Department of Respiratory Paediatrics , Imperial College London, United Kingdom.
Am J Respir Crit Care Med. 2007 Nov 1;176(9):858-64. doi: 10.1164/rccm.200702-212OC. Epub 2007 Aug 16.
It is unclear when the pathologic features of asthma first appear. We hypothesized that eosinophilic airway inflammation and epithelial reticular basement membrane (RBM) thickening, absent in wheezy infants, would be present in preschool children with severe, recurrent wheeze.
To compare RBM thickness and inflammation in endobronchial biopsies (EBs) from wheezy preschool children and age-matched control subjects.
EBs were obtained from wheezy preschool children (aged 3 mo to 5 yr), undergoing a clinically indicated fiberoptic bronchoscopy. Subjects undergoing fiberoptic bronchoscopy to investigate stridor acted as nonasthmatic controls. RBM thickness was measured and the density of subepithelial, immunologically distinct inflammatory cells was determined and expressed as a volume fraction (%). EBs from 16 children (median age, 29 [7-57] mo) with wheeze confirmed by video questionnaire (confirmed wheezers [CWs]), 14 with reported wheeze (reported wheezers [RWs]) (median age, 17 [8-58] mo), and 10 control subjects (median age, 19 [5-42] mo) were assessed.
RBM thickness in the three groups was as follows: CWs: median, 4.6 (range, 2.9-8.0) microm; RWs: median, 3.5 (2.1-5.4) microm; control subjects: median, 3.8 (2.5-4.7) microm. RBM was significantly thicker in CWs than in control subjects (P < 0.05). Eosinophil density was as follows: CWs: median, 1.07% (range, 0.0-3.52%); RWs: median, 0.72% (0.0-2.04%); control subjects: median, 0.0% (0.0-1.05%). Eosinophilic inflammation was significantly greater in CWs compared with control subjects (P < 0.05). There were no between-group differences for any other inflammatory cell phenotype.
The characteristic pathologic features of asthma in adults and school-aged children develop in preschool children with confirmed wheeze between the ages of 1 and 3 years, a time when intervention may modify the natural history of asthma.
哮喘的病理特征最初何时出现尚不清楚。我们推测,喘息婴儿不存在的嗜酸性气道炎症和上皮网状基底膜(RBM)增厚,在重度复发性喘息的学龄前儿童中会出现。
比较喘息学龄前儿童和年龄匹配的对照受试者的支气管活检标本(EBs)中的RBM厚度和炎症情况。
从接受临床指征性纤维支气管镜检查的喘息学龄前儿童(3个月至5岁)获取EBs。接受纤维支气管镜检查以调查喘鸣的受试者作为非哮喘对照。测量RBM厚度,并确定上皮下免疫特异性炎症细胞的密度,并表示为体积分数(%)。对16名经视频问卷确认有喘息的儿童(中位年龄,29[7 - 57]个月)(确诊喘息者[CWs])、14名报告有喘息的儿童(报告喘息者[RWs])(中位年龄,17[8 - 58]个月)和10名对照受试者(中位年龄,19[5 - 42]个月)的EBs进行评估。
三组的RBM厚度如下:CWs:中位值4.6(范围,2.9 - 8.0)微米;RWs:中位值3.5(2.1 - 5.4)微米;对照受试者:中位值3.8(2.5 - 4.7)微米。CWs的RBM明显比对照受试者厚(P < 0.05)。嗜酸性粒细胞密度如下:CWs:中位值1.07%(范围,0.0 - 3.52%);RWs:中位值0.72%(0.0 - 2.04%);对照受试者:中位值0.0%(0.0 - 1.05%)。与对照受试者相比,CWs中的嗜酸性炎症明显更严重(P < 0.05)。其他炎症细胞表型在组间无差异。
成人和学龄儿童哮喘的特征性病理特征在1至3岁确诊喘息的学龄前儿童中出现,这是一个干预可能改变哮喘自然病程的时期。