# Associations between genetic variants of vitamin D metabolic pathway and gestational diabetes mellitus: the potential mediation role of serum 25(OH)D3

**Authors:** Linlin Hua, Lina Wang, Lingling Cui, Zhiqian Li, Jiajia Chen, Bing Wang, Xia Zhang, Le Ma

PMC · DOI: 10.1186/s12902-026-02199-w · BMC Endocrine Disorders · 2026-02-24

## TL;DR

This study found that genetic variations in the VDR gene are linked to gestational diabetes risk, with vitamin D levels partially explaining this connection.

## Contribution

The study identifies specific VDR gene variants and their mediation through serum 25(OH)D3 in gestational diabetes risk among a Chinese population.

## Key findings

- The VDR rs731236-G allele was associated with a reduced risk of gestational diabetes mellitus.
- The VDR rs7975232-A allele was linked to an increased risk of gestational diabetes mellitus.
- Higher 25(OH)D3 levels were inversely associated with gestational diabetes risk.

## Abstract

Circulating vitamin D concentrations have been recognized as a risk factor for GDM. The pathway genes of vitamin D synthesis and metabolism have been shown to be strongly associated with serum vitamin D. This study aimed to evaluate the association between genetic variations and GDM risk, and to further explore the potential mediating role of serum 25(OH)D3 in these relationships.

A nested case-control study including 131 cases of GDM and 131 controls from the Zhengzhou Birth Cohort established since 2021. We genotyped nine SNPs using the TaqMan probe method and measured serum 25(OH)D3 by ELISA.

The VDR rs731236-G allele was associated with reduced GDM risk: the OR (95% CI) was 0.56 (0.34, 0.93) in the multivariable adjusted model. Conversely, the VDR rs7975232-A allele was associated with a higher risk of GDM (OR: 1.56; 95% CI: 1.04, 2.33). Higher 25(OH)D3 levels were inversely associated with GDM risk (OR: 0.36; 95% CI: 0.20, 0.67; Ptrend <0.01). Each 1-unit increment of log-transformed 25(OH)D3 level was associated with a 79% lower risk of GDM (OR 0.21, 95% CI: 0.09, 0.46). Mediation analyses indicated that 25(OH)D3 explained 24.7% of the protective effect of the VDR rs731236 variant [Indirect effect= -0.06 (-0.12, -0.01)], and 29.6% of the detrimental effect of VDR rs7975232 and GDM risk [indirect effect = 0.07 (0.03, 0.13)].

The study suggested a significant association of VDR rs7975232 and rs731236 polymorphisms with GDM risk among the Chinese population. Higher 25(OH)D3 levels were associated with a decreased risk of GDM. Additionally, circulating 25(OH)D3 partially mediated the association between variant genotype of SNPs at VDR-rs731236 and VDR-rs7975232 and GDM risk, but the relatively wide CI prompted cautious interpretation. These findings emphasize the important role of genetic variants in VDR in the pathogenesis of GDM. Further studies with larger cohort sample sizes should be conducted to confirm the present findings.

Not applicable.

The online version contains supplementary material available at 10.1186/s12902-026-02199-w.

## Linked entities

- **Genes:** VDR (vitamin D receptor) [NCBI Gene 7421]
- **Chemicals:** 25(OH)D3 (PubChem CID 5283731)
- **Diseases:** gestational diabetes mellitus (MONDO:0005406)

## Full-text entities

- **Diseases:** gestational diabetes mellitus (MESH:D016640)
- **Chemicals:** vitamin D (MESH:D014807), 25(OH)D3 (-)

## Full text

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## Figures

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## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC13041490/full.md

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Source: https://tomesphere.com/paper/PMC13041490