Gut Microbiota Dysbiosis in Chinese Children with Type 1 Diabetes Mellitus: An Observational Study
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Background: Gut microbiota dysbiosis is reportedly actively involved in autoimmune diseases such as type 1 diabetes mellitus (T1DM). However, the alterations in the gut microbiota and their correlation with fasting blood glucose (FBG) in Chinese children with T1DM remain unclear.
Aim: To investigate alterations in the gut microbiota in Chinese children with T1DM and their associations with clinical indicators.
Methods: Samples from 51 children with T1DM and 47 age-matched and gender-matched healthy controls were obtained, to explore the structural and functional alterations in the fecal microbiota. The V3-V4 regions of the 16S rRNA gene were sequenced on a MiSeq instrument, and the association with FBG were analyzed.
Results: We found that the bacterial diversity was significantly increased in the T1DM-associated fecal microbiota, and changes in the microbial composition were observed at different taxonomic levels. The T1DM-reduced differential taxa, such as ATCC8482, , , and , were negatively correlated with FBG, while the T1DM-enriched taxa, such as , group, , and , were positively correlated with FBG. ATCC8482, , the group, and , either alone or in combination, could be used as noninvasive diagnostic biomarkers to discriminate children with T1DM from healthy controls. In addition, the functional changes in the T1DM-associated fecal microbiota also suggest that these fecal microbes were associated with altered functions and metabolic activities, such as glycan biosynthesis and metabolism and lipid metabolism, which might play vital roles in the pathogenesis and development of T1DM.
Conclusion: Our present comprehensive investigation of the T1DM-associated fecal microbiota provides novel insights into the pathogenesis of the disease and sheds light on the diagnosis and treatment of T1DM.
Donohue M, Lamb A, Absangba A, Noromalala E, Weisenbeck D, Stumpf R Am J Primatol. 2025; 87(2):e23732.
PMID: 39905243 PMC: 11794673. DOI: 10.1002/ajp.23732.
Prapa I, Kompoura V, Pavlatou C, Nelios G, Mitropoulou G, Kostomitsopoulos N Microorganisms. 2024; 12(10).
PMID: 39458313 PMC: 11509866. DOI: 10.3390/microorganisms12102004.
Gut microbiome-immune interactions and their role in rheumatoid arthritis development.
Nurgaziyev M, Issilbayeva A, Bersimbaev R, Ilderbayev O, Vinogradova E, Jarmukhanov Z PeerJ. 2024; 12:e17477.
PMID: 39006008 PMC: 11246623. DOI: 10.7717/peerj.17477.
Villani A, Fontana A, Panebianco C, Ferro C, Copetti M, Pavlovic R Gut Microbes. 2024; 16(1):2375483.
PMID: 38972056 PMC: 11229760. DOI: 10.1080/19490976.2024.2375483.
Wang L, Gong C, Wang R, Wang J, Yang Z, Wang X Front Pediatr. 2024; 12:1382466.
PMID: 38938502 PMC: 11208633. DOI: 10.3389/fped.2024.1382466.