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Published on: December 31, 2017
Gut microbiota composition in children with obstructive sleep apnoea syndrome: a pilot study
Francesco Valentini1, Melania Evangelisti2, Marta Arpinelli1
1Pediatric Unit Sant'Andrea Hospital, Faculty of Medicine and Psychology, "Sapienza" University, Rome, Italy.
Insights
Children with obstructive sleep apnoea syndrome (OSAS) have reduced gut microbial diversity and increased inflammation-related gut bacteria. These changes correlate with sleep parameters, suggesting a link between OSAS, gut health, and intermittent hypoxia.
Area of Science:
- Microbiome research
- Pediatric sleep medicine
- Gastroenterology
Background:
- Obstructive Sleep Apnoea syndrome (OSAS) is a systemic inflammatory condition linked to intermittent hypoxia.
- Hypoxia can compromise intestinal barrier integrity and alter gut microbiota, as seen in adults and animal models.
- Limited research exists on pediatric OSAS-related gut dysbiosis, with only one study on snoring children and their microbiota.
Purpose of the Study:
- To assess gut microbiota composition in children with OSAS compared to healthy controls.
- To investigate the association between sleep parameters and gut microbiome alterations in pediatric OSAS.
Main Methods:
- A cohort of 16 children was divided into OSAS and healthy groups.
- Stool samples were analyzed for gut microbiota composition using 16S rRNA sequencing.
- OSAS children underwent nocturnal pulse oximetry and polysomnography.
Main Results:
- OSAS children exhibited significantly lower microbial diversity (species richness, Chao1 index) than healthy children (p=0.01).
- The Firmicutes/Bacteroidetes ratio positively correlated with the Sleep Clinical Record (p=0.03).
- Abundances of inflammation-related bacteria (Proteobacteria, Clostridiaceae, Oscillospiraceae, Klebsiella) and gut barrier bacteria (Desulfovibrionaceae, Bacteroides fragilis, Faecalibacterium prausnitzii) were significantly altered and correlated with sleep parameters.
Conclusions:
- Pediatric OSAS is associated with reduced gut microbiota diversity and an increase in bacteria linked to inflammation and gut barrier disruption.
- Intermittent hypoxia in OSAS may drive these gut microbiome changes.
- Further research is needed to elucidate the role of gut microbiota in pediatric OSAS pathophysiology and associated comorbidities.
Background:
Obstructive Sleep Apnoea syndrome (OSAS) is considered a systemic inflammatory disease and is characterized by intermittent hypoxia that can damage the integrity of intestinal barrier and alter gut microbiota composition in adults and animal models. To date there is only one study on snoring children and microbiota but no studies are present on paediatric OSAS related dysbiosis.
Study Objectives:
To evaluate gut microbiota composition in OSAS children in respect to healthy subjects and investigate the role of sleep parameters in changing gut microbiome.
Methods:
Sixteen children divided in OSAS and healthy groups. Stool samples were collected from both the two groups to assess gut microbiota composition using 16S rRNA sequencing and a nocturnal pulsossimetry and polysomnography were performed in OSAS children.
Results:
OSAS children showed a decreased microbial diversity in respect to healthy subjects in terms of number of observed species and Chao1 index (p = 0,01). Firmicutes/Bacteroidetes ratio was directly correlated to Sleep Clinical Record (p = 0,03). The abundance of several inflammation-related strains (Proteobacteria, Clostridiaceae, Oscillospiraceae, Klebsiella) were found significantly modified in relation to sleep parameters. Bacteria implied in the gut barrier integrity (Desulfovibrionaceae, Bacteroides fragilis and Faecalibacterium prausnitzii) were found significantly different in the two study groups and correlated with sleep parameters.
Conclusions:
OSAS children showed a lower microbiota diversity in respect to heathy subjects and an increase of inflammation and gut barrier disruptors-related strains probably induced by intermittent hypoxia. Further studies should be conducted to understand the role of gut microbiota in OSAS physiopathology and comorbidities in children.
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