Evidence map›Paper›PMID 42120611›Full record

ArticleJournal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine2026

Obstructive sleep apnea and primary snoring in children are associated with oropharyngeal dysbiosis and a mild compositional imbalance in the gastrointestinal tract.

Jennifer Hudson, Azleena Akhand, Moe Thant Nwe, Michael J Coffey, Josie van Dorst, Sandra Chuang, Chee Y Ooi

Abstract read
In one paragraph

Article in Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Jennifer HudsonSchool of Clinical Medicine, Discipline of Pediatrics and Child Health, The University of New South Wales, Sydney, Australia. jennifer.hudson@unsw.edu.au.ORCID 0000-0002-4688-9154
Azleena AkhandSchool of Clinical Medicine, Discipline of Pediatrics and Child Health, The University of New South Wales, Sydney, Australia.
Moe Thant NweSchool of Clinical Medicine, Discipline of Pediatrics and Child Health, The University of New South Wales, Sydney, Australia.
Michael J CoffeySchool of Clinical Medicine, Discipline of Pediatrics and Child Health, The University of New South Wales, Sydney, Australia.
Josie van DorstSchool of Clinical Medicine, Discipline of Pediatrics and Child Health, The University of New South Wales, Sydney, Australia.
Sandra ChuangSchool of Clinical Medicine, Discipline of Pediatrics and Child Health, The University of New South Wales, Sydney, Australia.
Chee Y OoiSchool of Clinical Medicine, Discipline of Pediatrics and Child Health, The University of New South Wales, Sydney, Australia.

Funding

National Health and Medical Research Council 2020/GNT1194358
6 · The paper itself

Abstract

backgroundObstructive sleep apnea (OSA) and primary snoring (PS) represent a spectrum of sleep-related breathing conditions. Emerging evidence links OSA to perturbations in the oropharyngeal and gut microbiomes and the pathogenesis of OSA-related comorbidities. However, the microbiome composition and factors driving dysbiosis in children remain unresolved.

methodsTwo pediatric cohorts were examined to assess the microbiome associated with sleep-disordered breathing in the airway (Cohort A) and gut (Cohort B) using 16S rRNA gene profiling. Oropharyngeal swabs were collected from participants with OSA, PS, and healthy controls (HC) (n = 60). Cohort B participants (OSA and HC, n = 46) provided stool samples for microbiome and fecal calprotectin measurements and completed a dietary survey.

resultsOropharyngeal microbial diversity differed between OSA and HC, characterized by an increase in gastrointestinal specific taxa and reduced oral commensals. Similar shifts were observed between PS and HC, with few taxa differing between OSA and PS. In the gut, children with OSA showed an imbalance marked by an increase in opportunistic pathogens and reduced beneficial organisms. However, diversity assessments did not show any indication of dysbiosis or inflammation, and there were no overall differences in dietary intake.

conclusionsDysbiosis in the oropharyngeal microbiomes of OSA and PS points to shared pathophysiological factors (e.g., snoring) as possible drivers of microbiome disruption across the spectrum of sleep-disordered breathing. The gastrointestinal microbiome of children with OSA indicates a mild microbial imbalance that may elicit harmful outcomes or manifest as dysbiosis if left untreated. Together, these findings support a role of the microbiome as a possible mediator of comorbidities across the spectrum of sleep-disordered breathing. Current knowledge/study rationale: Obstructive sleep apnea (OSA) and primary snoring (PS) represent a continuum of sleep-related breathing disorders. While adult and animal studies suggest OSA-induced microbiome disruptions contribute to the onset of comorbidities, the factors driving dysbiosis in children remain unresolved. This study investigated the airway and gut microbiomes in pediatric OSA, PS, and healthy controls to identify microbial alterations linked to these conditions. Study impact: This study revealed that children with obstructive sleep apnea and primary snoring exhibit similar altered oropharyngeal microbiomes, distinct from that of healthy controls, suggesting common underlying pathophysiological factors.

Indexed as

DysbiosisGastrointestinal MicrobiomeGastrointestinal TractOropharynxSleep Apnea, ObstructiveSnoringChildCohort StudiesFecesFemaleHumansMaleGastrointestinal microbiomeObstructive sleep apneaOropharyngeal microbiomePediatricPrimary snoring

Identifiers

PMID42120611
PMCPMC13168413

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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 OpenQuestion graph.