Evidence map›Paper›PMID 42082982›Full record

ArticleThyroid research2026

Thyroid functional state-dependent dysbiosis of gut microbiota in Hashimoto's thyroiditis: a cross-sectional metagenomic profiling study.

Jie Li, Suhang Guo, Hua Yu, Xiaobo Hong, Jing Nie, Hua Sun

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Article in Thyroid research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 citing paper in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Jie Li *The Second Clinical Medical College of Zhejiang, Chinese Medical University, Hangzhou, Zhejiang Province, 310053, China.
Suhang Guo *Department of Pharmacy, Hangzhou Red Cross Hospital, No.208 East Huancheng Road, Hangzhou, Zhejiang Province, 310003, China.
Hua YuMicrobiology Laboratory, Hangzhou Center for Disease Control and Prevention, Hangzhou, Zhejiang Province, 310021, China.
Xiaobo HongDepartment of Pharmacy, The First Affiliated Hospital of Ningbo University, Ningbo, Zhejiang Province, 315211, China.
Jing NieDepartment of Geriatrics, Hangzhou Red Cross Hospital, No.208 East Huancheng Road, Hangzhou, Zhejiang Province, 310003, China.
Hua SunDepartment of Geriatrics, Hangzhou Red Cross Hospital, No.208 East Huancheng Road, Hangzhou, Zhejiang Province, 310003, China. sunshine918@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHashimoto's thyroiditis (HT) is a prevalent autoimmune thyroid disease (AITD) closely linked to genetic predisposition and environmental factors. Gut microbiota dysbiosis has recently been implicated as a critical contributor to AITDs' pathogenesis. Our study aims to systematically investigate the dynamic alterations in gut microbial communities under varying thyroid functional statuses and elucidate their underlying mechanisms.

methods67 HT patients with varying thyroid functional statuses and 23 healthy controls were enrolled. Fecal 16 S rDNA sequencing and analyses (alpha diversity, LEfSe, correlation, functional pathways) assessed microbiota-thyroid function links.

resultsHT patients with hypo/hyperthyroidism had lower gut microbiota richness than euthyroid patients (more reduced in hyperthyroidism). The hyperthyroid group exhibited enrichment of Fusobacterium, the hypothyroid group was dominated by Clostridium sensu stricto_1, and the euthyroid group showed a predominance of short-chain fatty acid (SCFA)-producing bacteria (e.g., Lactobacillus). Clostridium sensu stricto_1 positively correlated with TPO-Ab levels but negatively correlated with FT3.Pro-inflammatory genera(e.g., Escherichia-Shigella, Streptococcus) demonstrated negative correlations with FT3.Functional prediction analysis revealed potential associations with L-tyrosine degradation in the hyperthyroid group, reduced proportions of bile acid metabolism pathways in the hypothyroid group, and enriched proportions of fatty acid metabolism pathways in the euthyroid group.

conclusionsThis study revealed that gut microbiota dysbiosis is closely associated with thyroid functional statuses in HT. Specific bacterial genera, such as Clostridium sensu stricto_1 and Fusobacterium, may contribute to immune regulation and disease progression. The dynamic alterations in gut microbial profiles provide potential biomarkers for precision diagnosis and treatment of HT.

Identifiers

PMID42082982
PMCPMC13137569

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