# Adipose Tissue Dysfunction and Metabolic Diseases: The Role of Vitamin D/Vitamin D Receptor Axis

**Authors:** Flavia Agata Cimini, Federica Sentinelli, Alessandro Oldani, Ilaria Barchetta, Maria Gisella Cavallo

PMC · DOI: 10.3390/ijms262110256 · 2025-10-22

## TL;DR

This review explores how vitamin D and its receptor help regulate fat tissue health and prevent metabolic diseases like diabetes and fatty liver.

## Contribution

The paper provides a comprehensive review of the vitamin D/VDR axis's role in adipose tissue biology and metabolic disease.

## Key findings

- Vitamin D influences adipogenesis, inflammation, and insulin sensitivity in adipose tissue.
- Genetic variability and tissue-specific VDR signaling affect metabolic outcomes.
- Adequate vitamin D levels are important for preventing adipose tissue dysfunction.

## Abstract

Obesity-associated adipose tissue dysfunction represents a key driver of metabolic disorders, including type 2 diabetes, cardiovascular diseases, and fatty liver disease. Emerging evidence highlights the vitamin D/vitamin D receptor (VD/VDR) axis as an important regulator of adipose tissue homeostasis. Beyond its classical role in mineral metabolism, vitamin D influences adipogenesis, inflammation, and insulin sensitivity, thereby modulating systemic metabolic health. In this review, we summarize the current understanding of the VD/VDR axis in adipose tissue biology, from molecular pathways controlling lipid turnover and immune responses to experimental and clinical evidence linking vitamin D status with obesity-related complications. We also discuss the role of genetic variability and tissue-specific VDR signaling in shaping metabolic outcomes. While results from supplementation trials remain inconsistent, maintaining adequate vitamin D levels appears crucial for the prevention of adipose tissue dysfunction and its cardiometabolic consequences. Future studies are warranted to define optimal strategies for harnessing the VD/VDR axis in therapeutic approaches to obesity and metabolic disease.

## Linked entities

- **Diseases:** type 2 diabetes (MONDO:0005148), fatty liver disease (MONDO:0004790), obesity (MONDO:0011122)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, VDR (vitamin D receptor) [NCBI Gene 7421] {aka NR1I1, PPP1R163}
- **Diseases:** cardiovascular diseases (MESH:D002318), fatty liver disease (MESH:D005234), Obesity (MESH:D009765), inflammation (MESH:D007249), Adipose Tissue Dysfunction (MESH:D018205), Metabolic Diseases (MESH:D008659), type 2 diabetes (MESH:D003924)
- **Chemicals:** lipid (MESH:D008055), Vitamin D (MESH:D014807)

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12610601/full.md

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Source: https://tomesphere.com/paper/PMC12610601