Evidence map›Paper›PMID 40152070›Full record

ArticlePediatric pulmonology2025

Oscillometry Phenotypes in Children With Down Syndrome.

Katharine L Hamlington, Emily H Cooper, Kristine Wolter-Warmerdam, Monica L Vielkind, John T Brinton, Allison Keck, Rawan J Bresselsmith, Jennifer Maybee, Arwen Jackson, Francis Hickey and 1 more

Abstract read
In one paragraph

Article in Pediatric pulmonology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Katharine L HamlingtonDepartment of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA.ORCID http://orcid.org/0000-0002-5221-2123
Emily H CooperUniversity of Colorado School of Medicine, Aurora, Colorado, USA.
Kristine Wolter-WarmerdamAnna and John J. Sie Center for Down Syndrome, Children's Hospital Colorado, Aurora, Colorado, USA.
Monica L VielkindPediatric Pulmonology, University of Rochester Medical Center, Rochester, New York, USA.
John T BrintonUniversity of Colorado School of Medicine, Aurora, Colorado, USA.
Allison KeckChildren's Hospital Colorado, Aurora, Colorado, USA.
Rawan J BresselsmithChildren's Hospital Colorado, Aurora, Colorado, USA.
Jennifer MaybeeChildren's Hospital Colorado, Aurora, Colorado, USA.ORCID http://orcid.org/0000-0003-4665-6630
Arwen JacksonChildren's Hospital Colorado, Aurora, Colorado, USA.
Francis HickeyDepartment of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA.
Emily M DeBoerDepartment of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA.ORCID http://orcid.org/0000-0002-0924-9342

Funding

Identifying Measures of Pulmonary Morbidity for Clinical Trials in Children with Down Syndrome and AspirationR21HL151261 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI DEBOER, EMILY M · 2019 to 2020
$344k
NHLBI NIH HHS R21 HL151261This research was supported by NIH/NHLBI R21 HL151261-01 (DeBoer), the Linda Crnic Institute, and the Sie Center for Down syndrome.
6 · The paper itself

Abstract

objectiveTo 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.

resultsIn 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.

conclusionsIn 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.

Indexed as

Down SyndromeOscillometryAdolescentAirway ResistanceAlbuterolChildChild, PreschoolCross-Sectional StudiesDeglutition DisordersFemaleHeart Defects, CongenitalHumansLungMalePhenotypeRespiratory Function TestsAlbuterolaspirationlung functionpulmonarytracheomalaciatrisomy 21

Identifiers

PMID40152070
PMCPMC12536560

What Socratic holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.