Home Research Feeds Comparative assessment of gut microbial composition and function in patients with Graves' disease and Graves' orbitopathy

Comparative assessment of gut microbial composition and function in patients with Graves' disease and Graves' orbitopathyOriginal paper

Researched by:

  • Karen Pendergrass

Last Updated: 2026-07-05

Karen Pendergrass
Karen Pendergrass

Karen Pendergrass is a microbiome researcher specializing in microbiome-targeted interventions (MBTIs). She systematically analyzes scientific literature to identify microbial patterns, develop hypotheses, and validate interventions. As the founder of the Microbiome Signatures Database, she bridges microbiome research with clinical practice. In 2012, based on her own investigative research, she became the first documented case of FMT for Celiac Disease, four years before the first published case study.

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Location
China
Sample Site
Feces
Species
Homo sapiens

What was studied?

This study asked whether gut bacteria differ between Graves' disease with and without eye involvement. Researchers compared fecal microbial communities across three groups using 16S ribosomal RNA gene sequencing. The goal was to identify intestinal bacteria specific to Graves' disease and to Graves' orbitopathy. Random forest analysis was used to rank taxa that best separated the groups. Predicted metabolic functions of the bacteria were also compared.

Who was studied?

The study analyzed fecal samples from 95 adults in China. This included 30 patients with Graves' disease but no orbitopathy and 33 patients with Graves' orbitopathy. A further 32 healthy subjects served as controls. All analyses used 16S ribosomal RNA gene sequencing of stool. This was a case-control comparative design in humans.

What were the most important findings?

At the phylum level, Deinococcus-Thermus and Chloroflexi were significantly lower in orbitopathy patients than in Graves' disease alone. At the genus level, Subdoligranulum and Bilophila rose in the orbitopathy group. Several genera fell in orbitopathy versus Graves' disease. These included Blautia, Anaerostipes, Dorea, Butyricicoccus, Romboutsia, Fusicatenibacter, Collinsella, Intestinibacter, and Phascolarctobacterium. Deinococcus-Thermus, Cyanobacteria, and Chloroflexi ranked in the top ten for classifying samples. Enriched pathways in patients included nucleotide, enzyme family, and energy metabolism.

What are the greatest implications of this study?

The findings suggest gut bacteria differ measurably once Graves' disease progresses to eye involvement. Lower abundance of butyrate-related genera like Blautia, Butyricicoccus, and Fusicatenibacter may mark this shift. These patterns point to the microbiome as a possible contributor to orbitopathy development. The study is cross-sectional, so it cannot prove the bacteria cause eye disease. The associations warrant confirmation in larger, longitudinal cohorts.

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