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Oral Biofilm Sampling for Microbiome Analysis in Healthy Children
Published on: December 31, 2017
Preliminary analysis of gut microbiome characteristics in children with obstructive sleep apnea hypopnea syndrome
Zhihui Wang1,2, Luting Zhou1, Yanyu He1
1Department of Respiration, Children's Hospital of Soochow University, Suzhou, China.
Insights
Children with obstructive sleep apnea-hypopnea syndrome (OSAHS) show altered gut microbiomes. Specific gut bacteria correlate with polysomnography (PSG) indicators, though microbiome changes have limited diagnostic prediction for OSAHS.
Area of Science:
- Microbiome research
- Pediatric sleep medicine
- Gastroenterology
Background:
- Obstructive sleep apnea-hypopnea syndrome (OSAHS) is prevalent in children.
- The gut microbiome's role in OSAHS pathophysiology is increasingly recognized.
- Understanding gut microbiome alterations in pediatric OSAHS is crucial for potential therapeutic targets.
Purpose of the Study:
- To characterize gut microbiome changes in children with OSAHS.
- To explore the relationship between gut microbiota composition and polysomnography (PSG) results in pediatric OSAHS.
Main Methods:
- 16S rRNA high-throughput sequencing was used to analyze stool samples from children with OSAHS, primary snoring, and controls.
- Gut microbiome diversity (alpha and beta) and composition were assessed.
- Correlation analyses were performed between gut microbiota and PSG parameters.
Main Results:
- Significant differences in gut microbiome diversity and composition were observed between OSAHS and control groups.
- The Firmicutes/Bacteroidetes ratio increased with OSAHS severity.
- Specific genera (Akkermansia, Dialister, Escherichia-Shigella, Faecalibacterium) showed correlations with PSG metrics like sleep efficiency and oxygen saturation.
Conclusions:
- Pediatric OSAHS is associated with subtle alterations in gut microbiome composition.
- While the Firmicutes/Bacteroidetes ratio has limited predictive value for OSAHS diagnosis, specific gut genera correlate with key PSG indicators.
- Gut microbiota may play a role in OSAHS pathophysiology and warrant further investigation.
Objective:
To analyze the characteristic changes in the gut microbiome in children with obstructive sleep apnea-hypopnea syndrome (OSAHS) and to investigate the relationship between the gut microbiome and polysomnography (PSG) results.
Methods:
Children diagnosed with primary snoring and OSAHS by PSG were enrolled in the study group. Nonsnoring children undergoing elective surgery were selected as the control group. Stool, sleep monitoring data, and medical history data were collected. The clinical history data were analyzed by SPSS 25.0 software. 16S rRNA high-throughput sequencing technology was used to analyze the gut microbiome, and relevant biostatistical methods were used to analyze and describe the characteristics of the gut microbiome.
Results:
A total of 62 OSAHS patients (42 mild OSAHS and 20 moderate to severe OSAHS), 16 primary snoring patients and 46 controls were enrolled in this study. There were significant differences in the partial alpha diversity index (observed otus index, Chao1 index) and beta diversity under the Jaccard and unweighted UniFrac distance methods between the mild OSAHS group and the moderate to severe OSAHS group. There were differences in some gut microbiome at different levels of phylum, class, order, family, genus and species between the control group and OSAHS group. There was a significant difference in the abundance ratio between Firmicutes and Bacteroidetes (F/B), and the ratio gradually increased among the three groups. The predictive model for OSAHS diagnosis established by the receiver operating characteristic (ROC) curve showed that the area under the curve (AUC) of Firmicutes and the F/B were more than 50%. At the genus level, Akkermansia was positively correlated with sleep efficiency (SE), Dialister was positively correlated with mean oxygen saturation (SaO2mean) and lowest oxygen saturation (LSaO2), Escherichia-Shigella was negatively correlated with total sleep time (TST), and Faecalibacterium was negatively correlated with the obstructive apnea index (OAI).
Conclusion:
The gut microbiome of children with OSAHS is slightly different at the phylum, class, order, family, genus and species levels. The F/B and Firmicutes abundance detection have limited predictive capability for the diagnosis of OSAHS. At the genus level, some gut microbiota were correlated with PSG indicators.
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