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ORIGINAL RESEARCH article

Front. Microbiol.

Sec. Microorganisms in Vertebrate Digestive Systems

Volume 16 - 2025 | doi: 10.3389/fmicb.2025.1621167

This article is part of the Research TopicBifidobacteria: Exploring the Roles of These Microbiome Guardians and Their Effects on Human HealthView all 11 articles

Bifidobacterium Depletion Promotes Goiter via Gut-Thyroid Axis: Evidence from Mendelian Randomization and Experimental Validation

Provisionally accepted
Wenyong  LiaoWenyong LiaoYang  JiangYang JiangJiwen  ZhangJiwen ZhangYinghao  WuYinghao WuXue  YuXue YuShaohong  ChenShaohong ChenHaiyan  LiuHaiyan LiuLinlin  XiuLinlin Xiu*Gansheng  ZhongGansheng Zhong*
  • School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China

The final, formatted version of the article will be published soon.

Background: While gut microbiota dysbiosis has been associated with thyroid disorders, its causal role in goiter pathogenesis remains unclear. We aimed to investigate whether specific gut microbial taxa causally influence goiter risk through the short-chain fatty acid (SCFA)-iodine-thyroid axis.We performed Mendelian randomization (MR) analysis using gut microbiota genome-wide association study (GWAS) data (MiBioGen consortium, n=18,340) and goiter GWAS data (FinnGen R10, 10,312 cases/401,869 controls). Experimental validation included: (1) establishing a propylthiouracil (PTU)-induced goiter rat model with 16S rRNA sequencing of fecal samples, (2) targeted SCFAs quantification, (3) thyroid/serum iodine measurement, (4) thyroid hormone assays, and (5) sodium-iodide symporter (NIS) protein expression analysis.Results: MR analysis identified 10 gut microbial taxa causally associated with goiter risk (all P < 0.05), with Bifidobacterium bifidum showing protective effects (OR=0.861, 95% CI: 0.764-0.971, P=0.014). In goiter rats, 16S rRNA sequencing revealed eight differentially abundant microbial taxa including significantly reduced B. bifidum, accompanied by: (1) impairment of two butyrate synthesis pathways, (2) decreased levels of six SCFAs (including butyrate), (3) impaired thyroid iodine uptake, (4) downregulated NIS expression, and ( 5) thyroid dysfunction (reduced triiodothyronine [T3], thyroxine [T4], free T3 [FT3], free T4 [FT4] with elevated thyroid-stimulating hormone [TSH]) -all measurements showing statistical significance (P < 0.05).This study provides causal evidence that Bifidobacterium depletion may contribute to goiter development through SCFA-mediated impairment of NIS-dependent iodine uptake and thyroid hormone synthesis, highlighting the association of the "gut-thyroid axis" and laying the foundation for early prevention and therapeutic intervention of goiter.

Keywords: Gut Microbiota, Goiter, Mendelian randomization, 16S rRNA sequencing, Bifidobacterium, gut-thyroid axis

Received: 30 Apr 2025; Accepted: 12 Jun 2025.

Copyright: © 2025 Liao, Jiang, Zhang, Wu, Yu, Chen, Liu, Xiu and Zhong. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence:
Linlin Xiu, School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China
Gansheng Zhong, School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China

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