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Unveiling the gut connection: Exploring the link between microbiota and type 1 diabetes onset in pediatric patients
Amalia Ioana Arhire1,2, Teodora Papuc1,2, Sorin Ioacără1,2
1Department of General Medicine, The University of Medicine and Pharmacy 'Carol Davila', 020021 Bucharest, Romania.
Insights
Gut dysbiosis, an imbalance of gut bacteria and fungi, is linked to early-onset type 1 diabetes mellitus (T1DM) in children. This imbalance correlates with younger age and more severe disease onset, highlighting microbiota
Area of Science:
- Microbiology
- Immunology
- Pediatrics
Background:
- Type 1 diabetes mellitus (T1DM) is increasingly diagnosed in children, necessitating identification of contributing factors.
- Gut microbiota plays a crucial role in immune system development and metabolic regulation, potentially influencing T1DM pathogenesis.
- Previous research suggests a link between gut dysbiosis and autoimmune diseases, including T1DM.
Purpose of the Study:
- To investigate the association between gut microbiota composition and early-onset T1DM in children.
- To evaluate the correlation between gut dysbiosis, clinical parameters, and disease severity in pediatric T1DM patients.
- To explore the relationship between microbial imbalances, inflammation, and metabolic markers in T1DM.
Main Methods:
- A retrospective case-control pilot study involving 31 children diagnosed with T1DM within 6 months.
- Spearman correlation analysis was employed to assess associations between gut microbiota, clinical parameters, and disease markers.
- Comparison of gut microbiota composition between T1DM patients and a healthy control group.
Main Results:
- Gut dysbiosis characterized by an overabundance of bacteria and fungi was observed in T1DM children compared to controls.
- Specific bacterial genera showed significant correlations: *Butyricicoccus* with younger age and less severe disease markers, *Bacteroides* and *Clostridium leptum* with milder disease.
- Antibiotic use was linked to *Candida albicans* overgrowth, while inflammation markers correlated with specific bacterial groups.
Conclusions:
- Gut dysbiosis is prevalent in children with early-onset T1DM and is associated with younger age and more severe disease onset.
- Specific microbial alterations may play a role in pancreatic inflammation and T1DM progression.
- This study provides novel insights into the gastrointestinal dysbiosis in pediatric T1DM, suggesting potential therapeutic targets.
Abstract:
With the increasing occurrence of type 1 diabetes mellitus (T1DM) in younger individuals, it is important to identifying contributing factors. A retrospective case control pilot study involving 31 children within the first 6 months after diagnosis, was conducted in the Elias Hospital in Bucharest, Romania) between January 2019- December 2021. Spearman correlation analysis was performed, evaluating the association between microbiota and early onset T1DM, high-level onset glycaemia, ketoacidosis, thyroid autoimmunity and clinical parameters involving growth. Gut dysbiosis with an overabundance of bacteria and fungi was observed compared with the healthy control group. Butyricicoccus was positively associated with younger age at onset (r=0.6276, P=0.0018) but negatively correlated with markers of disease progression, such as T1DM recent diagnosis (r=-0.517, P=0.0164), homeostasis model assessment of β-cell function) (r=-0.5962, P=0.0034) and C-peptide values (r=-0.5005, P=0.0344). Bacteroides showed a negative association with early-stage diabetes (r=-0.4431, P=0.0442) and Clostridium leptum was negatively associated with recent diagnosis (r=-0.6278, P=0.0023). Antibiotic use prior to disease diagnosis was positively correlated with Candida albicans (r=0.4431, P=0.0442). Inflammation, determined by the systemic inflammatory index, was positively correlated with Enterobacteriaceae (r=0.4331, P=0.0441) and negatively correlated with Clostridium coccoides (r=-0.4241, P=0.0492). C-reactive protein levels were negatively associated with Bacteroides (r=-0.4331, P=0.0498). These findings highlighted the role of gut microbiota in pancreatic inflammation and T1DM progression. In conclusion, dysbiosis of children with T1DM was correlated with younger age and a more severe onset. Microbial metabolites levels differed in these patients compared with the healthy control group. To the best of our knowledge, the present study is the first to assess gastrointestinal dysbiosis in T1DM.
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