University of Washington, Seattle, Washington.
Washington University School of Medicine, St. Louis, Missouri.
Ann Am Thorac Soc. 2020 Sep;17(9):1085-1093. doi: 10.1513/AnnalsATS.201905-375OC.
In cystic fibrosis (CF), the lung clearance index (LCI), derived from multiple breath washout (MBW), is more sensitive in detecting early lung disease than FEV; MBW has been less thoroughly evaluated in young patients with primary ciliary dyskinesia (PCD). Our objectives were ) to evaluate the sensitivity of MBW and spirometry for the detection of mild lung disease in young children with PCD and CF compared with healthy control (HC) subjects and ) to compare patterns of airway obstruction between disease populations. We used a multicenter, single-visit, observational study in children with PCD and CF with a forced expiratory volume in 1 second (FEV) greater than 60% predicted and HC subjects, ages 3-12 years. Nitrogen MBW and spirometry were performed and overread for acceptability. χ and Kruskall-Wallis tests compared demographics and lung function measures between groups, linear regression evaluated the effect of disease state, and Spearman's rank correlation coefficient compared the LCI and spirometric measurements. Twenty-five children with PCD, 49 children with CF, and 80 HC children were enrolled, among whom 17 children with PCD (68%), 36 children with CF (73%), and 53 (66%) HC children performed both acceptable spirometry and MBW; these children made up the analytic cohort. The median age was 9.0 years (interquartile range [IQR], 6.8-11.1). The LCI was abnormal (more than 7.8) in 10 of 17 (59%) patients with PCD and 21 of 36 (58%) patients with CF, whereas FEV was abnormal in three of 17 (18%) patients with PCD and six of 36 (17%) patients with CF. The LCI was significantly elevated in patients with PCD and CF compared with HC subjects (ratio of geometric mean vs. HC: PCD 1.27; 95% confidence interval [CI], 1.15-1.39; and CF 1.24; 95% CI, 1.15-1.33]). Children with PCD had lower midexpiratory-phase forced expiratory flow % predicted compared with children with CF (62% [IQR, 50-78%] vs. 85% [IQR, 68-99%]; = 0.05). LCI did not correlate with FEV. The LCI is more sensitive than FEV in detecting lung disease in young patients with PCD, similar to CF. LCI holds promise as a sensitive endpoint for the assessment of early PCD lung disease.
在囊性纤维化 (CF) 中,源自多次呼吸冲洗 (MBW) 的肺清除指数 (LCI) 比 FEV 更能敏感地检测早期肺疾病;MBW 在原发性纤毛运动障碍 (PCD) 的年轻患者中评估得不够充分。我们的目标是)评估 MBW 和肺活量计在检测与健康对照 (HC) 受试者相比,年轻 PCD 和 CF 患者轻度肺疾病的敏感性)比较疾病人群之间气道阻塞的模式。我们使用多中心、单次就诊、观察性研究,纳入了年龄在 3-12 岁之间 FEV 大于 60%预计值的 PCD 和 CF 患儿和 HC 受试者。进行了氮 MBW 和肺活量计检查,并进行了可接受性复查。组间比较采用 χ 和 Kruskal-Wallis 检验,比较人口统计学和肺功能指标,线性回归评估疾病状态的影响,Spearman 秩相关系数比较 LCI 和肺活量计测量值。共纳入 25 名 PCD 患儿、49 名 CF 患儿和 80 名 HC 患儿,其中 17 名 PCD 患儿(68%)、36 名 CF 患儿(73%)和 53 名(66%)HC 患儿同时进行了可接受的肺活量计和 MBW 检查;这些患儿构成了分析队列。中位年龄为 9.0 岁(四分位距 [IQR],6.8-11.1)。17 名 PCD 患儿中有 10 名(59%)和 36 名 CF 患儿中有 21 名(58%)的 LCI 异常(大于 7.8),而 17 名 PCD 患儿中有 3 名(18%)和 36 名 CF 患儿中有 6 名(17%)的 FEV 异常。与 HC 受试者相比,PCD 和 CF 患者的 LCI 显著升高(几何均数比与 HC:PCD 1.27;95%置信区间 [CI],1.15-1.39;和 CF 1.24;95% CI,1.15-1.33])。与 CF 患儿相比,PCD 患儿的中期呼气流量 %预计值较低(62%[IQR,50-78%]与 85%[IQR,68-99%];=0.05)。LCI 与 FEV 无相关性。LCI 比 FEV 更能敏感地检测年轻 PCD 患者的肺疾病,与 CF 相似。LCI 有望成为评估早期 PCD 肺疾病的敏感终点。