# The Role of Vitamin D in Autoimmune Thyroid Diseases: From Immunomodulation to Clinical Implications

**Authors:** Giulia Bendotti, Chiara Mele, Luisa Costantini, Alberto Ragni, Paola Leporati, Emilia Biamonte, Marco Gallo

PMC · DOI: 10.3390/nu18020217 · 2026-01-09

## TL;DR

Vitamin D may influence autoimmune thyroid diseases by modulating immune responses, but its role as a treatment is still unclear.

## Contribution

The paper reviews vitamin D's immunomodulatory effects and evaluates its potential as a risk marker versus a therapeutic target in autoimmune thyroid diseases.

## Key findings

- Low vitamin D levels are linked to increased risk of autoimmune thyroid diseases like Hashimoto’s and Graves’ disease.
- Vitamin D supplementation may reduce thyroid autoantibodies in some patients with Hashimoto’s and vitamin D deficiency.
- Clinical outcomes on disease progression or relapse prevention remain inconsistent and unproven.

## Abstract

Vitamin D is involved in immune regulation through effects on innate and adaptive immune responses mediated by vitamin D receptor activation within immune cells. Experimental and translational studies support its role in promoting regulatory T-cell activity, modulating Th1/Th17 responses, and influencing autoantibody production. At the population level, low serum 25-hydroxyvitamin D concentrations are consistently associated with an increased risk of autoimmune diseases, including autoimmune thyroid disorders such as Hashimoto’s thyroiditis (HT) and Graves’ disease (GD), suggesting a potential preventive association. In contrast, clinical evidence from interventional studies in patients with established disease is heterogeneous. Although vitamin D supplementation has been associated with reductions in thyroid autoantibody titers in some studies—particularly in patients with HT and baseline vitamin D deficiency—consistent effects on thyroid function, disease progression, or relapse prevention have not been demonstrated. Overall, current evidence supports vitamin D deficiency as a potentially modifiable risk marker rather than a confirmed disease-modifying therapeutic target in autoimmune thyroid diseases, highlighting the need for further studies focused on clinically meaningful outcomes.

## Linked entities

- **Diseases:** Hashimoto’s thyroiditis (MONDO:0007699), Graves’ disease (MONDO:0005364)

## Full-text entities

- **Genes:** VDR (vitamin D receptor) [NCBI Gene 7421] {aka NR1I1, PPP1R163}
- **Diseases:** autoimmune diseases (MESH:D001327), Autoimmune Thyroid Diseases (MESH:D013967), vitamin D deficiency (MESH:D014808), HT (MESH:D050031), GD (MESH:D006111)
- **Chemicals:** 25-hydroxyvitamin D (MESH:C104450), Vitamin D (MESH:D014807)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12845051/full.md

---
Source: https://tomesphere.com/paper/PMC12845051