# The role of gut microbiota in autoimmune thyroid diseases: nutritional determinants and diet-based modulation

**Authors:** Hubert Lewandowski, Maciej Maslyk, Halla Kaminska, Lukasz Szarpak

PMC · DOI: 10.3389/fendo.2026.1785878 · Frontiers in Endocrinology · 2026-02-19

## TL;DR

This review explores how gut microbiota may influence autoimmune thyroid diseases and discusses dietary strategies to modulate the gut microbiota.

## Contribution

The paper provides a comprehensive overview of the role of gut microbiota in autoimmune thyroid diseases and evaluates diet-based modulation strategies.

## Key findings

- Gut microbiota alterations may contribute to immune dysregulation in autoimmune thyroid diseases.
- Dietary components like fiber, selenium, and probiotics may influence gut microbiota composition.
- Current evidence supports dietary interventions as a complementary approach rather than a standalone treatment.

## Abstract

Autoimmune thyroid diseases (AITD), primarily Hashimoto’s thyroiditis and Graves’ disease, represent the most common organ-specific autoimmune disorders and remain a significant clinical challenge due to their chronic course, frequent comorbidities, and limited options for causal treatment. In recent years, increasing attention has been directed toward the gut microbiota as a potential modulator of immune tolerance and endocrine autoimmunity. Accumulating evidence suggests that alterations in gut microbial composition and function may contribute to immune dysregulation, intestinal barrier dysfunction, and low-grade inflammation observed in patients with AITD. This narrative review summarizes current knowledge on the role of gut microbiota in the pathophysiology of autoimmune thyroid diseases, with a particular focus on nutritional determinants and diet-based strategies for microbiota modulation. We discuss mechanisms linking diet, microbial metabolites, intestinal permeability, and immune responses relevant to thyroid autoimmunity. Special attention is given to dietary patterns, specific nutrients, and bioactive food components that may influence gut microbiota composition and function, including fiber, selenium, iodine, vitamin D, polyphenols, and probiotic-containing foods. From a clinical standpoint, the available evidence remains limited and largely heterogeneous, with most data derived from observational studies rather than interventional trials. Although growing interest surrounds diet-driven modulation of the gut microbiota, current findings do not support its use as an independent therapeutic approach in autoimmune thyroid diseases. Instead, dietary interventions may be best viewed as a complementary element of overall patient care. Well-designed prospective studies are still needed to determine whether such strategies can meaningfully influence disease course, to define which patients may benefit, and to translate these observations into practical, evidence-based dietary guidance. Future progress will depend on function-focused, phenotype-informed studies integrating microbiota readouts with clinically meaningful endocrine endpoints.

## Linked entities

- **Chemicals:** selenium (PubChem CID 6326970), iodine (PubChem CID 807)
- **Diseases:** Hashimoto’s thyroiditis (MONDO:0007699), Graves’ disease (MONDO:0005364)

## Full-text entities

- **Genes:** OCLN (occludin) [NCBI Gene 100506658] {aka BLCPMG, PPP1R115, PTORCH1}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, NR1H4 (nuclear receptor subfamily 1 group H member 4) [NCBI Gene 9971] {aka BAR, FXR, HRR-1, HRR1, PFIC5, RIP14}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, FFAR3 (free fatty acid receptor 3) [NCBI Gene 2865] {aka FFA3R, GPR41}, ARSH (arylsulfatase family member H) [NCBI Gene 347527] {aka sulfatase}, AHR (aryl hydrocarbon receptor) [NCBI Gene 196] {aka FVH3, RP85, bHLHe76}, GUSB (glucuronidase beta) [NCBI Gene 2990] {aka BG, MPS7}, CD79A (CD79a molecule) [NCBI Gene 973] {aka IGA, IGAlpha, MB-1, MB1}, GPBAR1 (G protein-coupled bile acid receptor 1) [NCBI Gene 151306] {aka BG37, GPCR19, GPR131, M-BAR, TGR5}, FFAR2 (free fatty acid receptor 2) [NCBI Gene 2867] {aka FFA2R, GPR43}, TPO (thyroid peroxidase) [NCBI Gene 7173] {aka MSA, TDH2A, TPX}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, HLA-A (major histocompatibility complex, class I, A) [NCBI Gene 3105] {aka HLAA}, TJP1 (tight junction protein 1) [NCBI Gene 7082] {aka ZO-1}, TSHR (thyroid stimulating hormone receptor) [NCBI Gene 7253] {aka CHNG1, LGR3, hTSHR-I}, IL21 (interleukin 21) [NCBI Gene 59067] {aka CVID11, IL-21, Za11}, FABP2 (fatty acid binding protein 2) [NCBI Gene 2169] {aka FABPI, I-FABP}, LBP (lipopolysaccharide binding protein) [NCBI Gene 3929] {aka BPIFD2}, HP (haptoglobin) [NCBI Gene 3240] {aka HP2ALPHA2, HPA1S}, HCAR2 (hydroxycarboxylic acid receptor 2) [NCBI Gene 338442] {aka GPR109A, HCA2, HM74a, HM74b, NIACR1, PUMAG}
- **Diseases:** Helicobacter pylori infection (MESH:D016481), malabsorption (MESH:D008286), nutritional deficiencies (MESH:D044342), acid suppression (MESH:D000550), micronutrient deficiencies (MESH:D007153), Hypothyroidism (MESH:D007037), fibrosis (MESH:D005355), GI symptom (MESH:D012816), critical illness (MESH:D016638), endotoxemia (MESH:D019446), HL (MESH:C538324), coeliac disease (MESH:D004194), gastrointestinal symptoms (MESH:D012817), inflammation (MESH:D007249), atrophic gastritis (MESH:D005757), weight loss (MESH:D015431), Dysbiosis (MESH:D064806), IBS (MESH:D053560), autoimmune gastrointestinal disorders (MESH:D005767), ATD (MESH:D001260), infections (MESH:D007239), iodine deficiency (MESH:D003409), GO (MESH:D049970), thyrotoxicosis (MESH:C566386), diarrhea (MESH:D003967), Hyperthyroidism (MESH:D006980), B12 deficiency (MESH:D014806), fatigue (MESH:D005221), orbital (MESH:D009916), autoimmune (MESH:D001327), GI (MESH:D006470), thyroid disease (MESH:D013959), Autoimmune thyroid diseases (MESH:D013967), Iron deficiency (MESH:D000090463), Celiac disease (MESH:D002446), HT (MESH:D050031), GD (MESH:D006111), Yersinia enterocolitica (MESH:D015009), immune dysregulation (OMIM:614878), bloating (MESH:C535647), dyspepsia (MESH:D004415), genetic (MESH:D030342)
- **Chemicals:** Zinc (MESH:D015032), bile acid (MESH:D001647), Vitamin D (MESH:D014807), LT4 (MESH:D013974), antithyroid (-), olive oil (MESH:D000069463), carbohydrate (MESH:D002241), Selenium (MESH:D012643), propionate (MESH:D011422), fructo-oligosaccharides (MESH:C116580), butyrate (MESH:D002087), lactulose (MESH:D007792), Iodine (MESH:D007455), vitamin B12 (MESH:D014805), lithium (MESH:D008094), LPS (MESH:D008070), Iron (MESH:D007501), metformin (MESH:D008687), prebiotics (MESH:D056692), mannitol (MESH:D008353), amiodarone (MESH:D000638), polyphenols (MESH:D059808), SCFA (MESH:D005232), calcium (MESH:D002118), indole (MESH:C030374), tryptophan (MESH:D014364), kynurenine (MESH:D007737), indole-3-acetic acid (MESH:C030737), acetate (MESH:D000085)
- **Species:** Borreliella burgdorferi (Lyme disease spirochete, species) [taxon 139], Lacticaseibacillus casei (species) [taxon 1582], Bacteroides fragilis YCH46 (strain) [taxon 295405], Bifidobacterium longum (species) [taxon 216816], Homo sapiens (human, species) [taxon 9606], Faecalibacterium prausnitzii (species) [taxon 853], Lacticaseibacillus rhamnosus (species) [taxon 47715], Helicobacter pylori (species) [taxon 210], Yersinia enterocolitica (species) [taxon 630], Lactobacillus delbrueckii subsp. bulgaricus (subspecies) [taxon 1585], Lactobacillus acidophilus (species) [taxon 1579], Bifidobacterium breve (species) [taxon 1685], Streptococcus thermophilus (species) [taxon 1308]

## Full text

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## Figures

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## References

73 references — full list in the complete paper: https://tomesphere.com/paper/PMC12960086/full.md

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Source: https://tomesphere.com/paper/PMC12960086