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Distinct Gut Microbiota Structure and Function of Children with Idiopathic Central and Peripheral Precocious Puberty
Congfu Huang1, Haiying Liu2, Wei Yang3
1Department of Pediatrics, Longgang District Maternity & Child Healthcare Hospital, Shenzhen, China.
Insights
Children with precocious puberty (PP) have distinct gut microbiota (GM) compared to healthy children. This study reveals differences in GM composition and function, suggesting GM as a potential therapeutic target for PP.
Area of Science:
- Microbiology
- Endocrinology
- Pediatrics
Background:
- Precocious puberty (PP) is a common pediatric endocrine disorder with unknown pathogenesis.
- Emerging research highlights the gut-brain axis and the gut microbiota's role in childhood endocrine diseases.
- Understanding gut microbiota (GM) variations in different PP types is crucial.
Purpose of the Study:
- To investigate and compare the gut microbiota composition and predicted functional pathways in children with idiopathic central precocious puberty (ICPP), peripheral precocious puberty (PPP), and healthy controls (HC).
- To explore the relationship between gut microbiota and the different types of precocious puberty.
- To provide a theoretical basis for gut microbiota-based clinical interventions for PP.
Main Methods:
- Recruited 27 children with ICPP, 18 with PPP, and 23 healthy children (HC).
- Performed 16S rDNA sequencing on stool samples to analyze gut microbiota composition.
- Utilized bioinformatics to predict metabolic pathways and analyze microbial community structure and function.
Main Results:
- Children with ICPP and PPP exhibited significantly higher gut microbiota diversity (OTUs, annotated genera, α-diversity) compared to HC.
- Increased abundance of butyrate-producing bacteria (e.g., Prevotella, Roseburia) was observed in ICPP and PPP groups, while Bacteroides and Faecalibacterium were higher in HC.
- Metabolic pathway analysis revealed enrichment in cell motility, signal transduction, and environmental adaptation in ICPP/PPP groups, and reduced carbohydrate metabolism compared to HC.
Conclusions:
- Gut microbiota composition and predicted functional patterns differ significantly between children with ICPP/PPP and healthy children.
- Peripheral precocious puberty (PPP) may represent an intermediate stage between idiopathic central precocious puberty (ICPP) and healthy controls.
- These findings support the gut microbiota as a potential target for therapeutic interventions in precocious puberty.
Abstract:
Precocious puberty (PP) is one of the most common endocrine diseases in children, and the pathogenesis is currently unknown. Recent studies on the gut-brain axis have shown that there is a correlation between childhood endocrine diseases and the gut microbiota (GM). To explore the GM characteristics of children with different types of PP, we recruited 27 idiopathic central precocious puberty children (ICPP group), 18 peripheral precocious puberty children (PPP group), and 23 healthy children of the same age (HC group). Their stool samples were subjected to 16S rDNA sequencing. In this study, we found that the OTUs numbers, the annotated genera, and α-diversity of GM of the ICPP and PPP group were all significantly higher than that in the HC group (P < 0.05). The abundance of butyrate-producing bacteria Prevotella, Lachnospiracea incertae sedis, Roseburia, Ruminococcus, and Alistipes was significantly higher in the ICPP group and the PPP group, and Bacteroides and Faecalibacterium showed significantly higher abundance in the HC group. The GM symbiosis network showed that both Bacteroides and Faecalibacterium were negatively correlated with these butyrate-producing bacteria. The abundances of most significantly changed genera were gradually increased from HC to PPP, and to the ICPP group, while only Bacteroides was gradually decreased. After the prediction of the metabolic pathways of the GM, the cell motility, signal transduction, and environmental adaptation were significantly enriched in the ICPP and the PPP groups (P < 0.05), while the carbohydrate metabolism pathway was significantly lower (P < 0.001). Overall, this study showed that the GM composition and predicted functional pattern of children with ICPP and PPP are different from healthy children, and PPP may be a transitional stage between ICPP and HC children, which provide a theoretical basis for clinical intervention based on GM in the treatment of PP.
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