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唐氏综合征患儿的示波测量表型

Oscillometry Phenotypes in Children With Down Syndrome.

作者信息

Hamlington Katharine L, Cooper Emily H, Wolter-Warmerdam Kristine, Vielkind Monica L, Brinton John T, Keck Allison, Bresselsmith Rawan J, Maybee Jennifer, Jackson Arwen, Hickey Francis, DeBoer Emily M

机构信息

Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA.

Children's Hospital Colorado, Aurora, Colorado, USA.

出版信息

Pediatr Pulmonol. 2025 Apr;60(4):e71069. doi: 10.1002/ppul.71069.

Abstract

OBJECTIVE

To evaluate lung function patterns measured by oscillometry in children with Down syndrome and determine associations with pulmonary diagnoses that may co-occur with Down syndrome, including evidence of dysphagia, obstructive sleep apnea, tracheomalacia, and congenital heart disease.

STUDY DESIGN AND PATIENTS

Cross-sectional study of children with Down syndrome who were enrolled during 2019-2022 at ages 4-18 years old.

MEASUREMENTS

Children performed oscillometry before and after albuterol administration to obtain respiratory impedance measures of resistance (R) and reactance (X). Aspiration from swallow study, obstructive sleep apnea from polysomnogram, tracheomalacia from flexible bronchoscopy, and congenital heart disease diagnoses were obtained from the electronic medical record.

RESULTS

In 50 children with Down syndrome, more negative X (median X5 z-score -0.93 [IQR - 2.15, 0.17]) was observed compared to a z-score of zero representing the mean in a pediatric reference population, but R was not increased at any frequency. Neither R nor X were related to tested pulmonary co-occurring diagnoses. Frequency dependence of resistance (R5-19) was elevated (median z-score 0.50 [IQR - 0.01, 1.14]), which, in combination with the more negative X, could indicate heterogeneity in peripheral and/or central airway sizes. After bronchodilator, R5 and AX decreased -26% [IQR -32%, -12%] and -43% [IQR -58%, -28%], respectively, and X5 increased 31% [IQR 12%, 45%], indicating physiological improvement.

CONCLUSIONS

In our population, a phenotype of lower lung compliance in 50% of children with Down syndrome was not associated with the presence of co-occurring pulmonary diagnoses. More work is needed to understand if this may be related to their diagnosis of DS.

摘要

目的

评估通过振荡法测量的唐氏综合征患儿的肺功能模式,并确定其与可能与唐氏综合征同时出现的肺部诊断之间的关联,包括吞咽困难、阻塞性睡眠呼吸暂停、气管软化和先天性心脏病的证据。

研究设计与患者

对2019年至2022年期间纳入的4至18岁唐氏综合征患儿进行横断面研究。

测量方法

患儿在使用沙丁胺醇前后进行振荡法检查,以获得呼吸阻抗的阻力(R)和电抗(X)测量值。吞咽研究中的误吸、多导睡眠图中的阻塞性睡眠呼吸暂停、柔性支气管镜检查中的气管软化以及先天性心脏病诊断均从电子病历中获取。

结果

在50名唐氏综合征患儿中,观察到X值更负(X5中位数z评分-0.93[四分位间距-2.15,0.17]),而儿科参考人群的平均值z评分为零,但在任何频率下R值均未增加。R值和X值均与所测试的肺部并发诊断无关。阻力的频率依赖性(R5-19)升高(中位数z评分0.50[四分位间距-0.01,1.14]),这与更负的X值相结合,可能表明外周和/或中央气道大小存在异质性。使用支气管扩张剂后,R5和AX分别下降了26%[四分位间距-32%,-12%]和-43%[四分位间距-58%,-28%],而X5增加了31%[四分位间距12%,45%],表明生理状况有所改善。

结论

在我们的研究人群中,50%的唐氏综合征患儿肺顺应性较低的表型与并发肺部诊断的存在无关。需要更多的研究来了解这是否可能与他们的唐氏综合征诊断有关。

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