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Profiling gut microbiome dynamics in subacute thyroiditis: Implications for pathogenesis, diagnosis, and treatment
Jiayun Li1,2, Jiasheng Ju3, Qian Xu1
1Department of Endocrinology, 920th Hospital of the Joint Logistics Support Force of the Chinese People's Liberation Army, Kunming, Yunnan, 650032, China.
Subacute thyroiditis (SAT) is linked to gut microbiome changes, with specific bacteria increasing or decreasing. Prednisolone treatment partially restores gut bacteria, suggesting a role in SAT development and response.
Area of Science:
- Microbiology
- Endocrinology
- Gastroenterology
Background:
- Subacute thyroiditis (SAT) is an inflammatory thyroid condition with an unknown etiology.
- The gut microbiome plays a crucial role in immune system regulation and has been implicated in various autoimmune diseases.
Purpose of the Study:
- To characterize gut microbiome alterations in newly diagnosed SAT patients.
- To identify microbial signatures associated with SAT and its treatment response.
Main Methods:
- 16S ribosomal RNA gene sequencing of fecal samples from 20 SAT patients and 20 healthy controls.
- Bioinformatics analysis of microbial alpha/beta diversity, taxonomic composition, and differential abundance.
- Investigation of correlations between gut microbiome and clinical parameters.
Main Results:
- SAT patients showed altered gut microbiota with increased Escherichia-Shigella, Bifidobacterium, Akkermansia, Veillonella, and Streptococcus.
- Decreased abundance of Bacteroidetes, Faecalibacterium, Prevotella, Roseburia, and Ruminococcus was observed in SAT patients.
- Prednisolone treatment partially normalized the gut microbiota, with Lactobacillus, Lactobacillaceae, Lactobacillus reuteri, and Prevotella identified as post-treatment biomarkers.
Conclusions:
- SAT is associated with distinct gut microbiome alterations.
- These alterations are partially reversible with prednisolone treatment.
- The gut microbiome may play a role in SAT pathogenesis and treatment response.
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