# The role of vitamin D deficiency and modifiable risk factors in patients with Crohn’s disease

**Authors:** Xiaoyue Feng, Qin Yin, Ying Kang, Kang Jiang, Mengqing Xu, Fangyu Wang

PMC · DOI: 10.3389/fimmu.2025.1616924 · 2025-07-30

## TL;DR

This study explores how vitamin D deficiency is linked to Crohn’s disease and identifies factors that contribute to it.

## Contribution

The study identifies specific risk factors for vitamin D insufficiency in Crohn’s disease patients using regression analyses.

## Key findings

- Vitamin D levels were significantly lower in Crohn’s disease patients compared to healthy controls.
- Age, sex, iron levels, and 25-OH vitamin D were significant risk factors for vitamin D deficiency in CD patients.
- Vitamin D levels improved after Vedolizumab treatment in some patients.

## Abstract

Vitamin D insufficiency is usually seen in Crohn’s disease (CD). Our study aims to determine the risk factors for vitamin D insufficiency in CD patients.

Between May 2021 and December 2023, we enrolled 102 CD patients and 100 healthy people in our hospital who were eligible for the study. Changes in vitamin D levels were also analyzed. CD patients were divided into active and clinical remission, and further changes in micronutrient and vitamin D levels were analyzed. Lastly, risk factor analysis was conducted using univariate, multivariate, and LASSO regression analysis models.

The average age of CD patients was 38.91 ± 3.31 years, whereas the average age of the healthy people was 38.64 ± 2.26 years. Vitamin D levels were significantly lower in CD patients than in healthy controls (19.62 ± 2.68 vs. 22.68 ± 4.61), especially for patients with active CD. In 11 patients treated with vedolizumab, compared to the pre-treatment Vedolizumab group, vitamin D levels improved more dramatically post-Vedolizumab therapy. According to univariate analysis, Age (OR: 0.95, 95% CI 0.26-1.33, p=0.01), sex (OR: 0.26, 95% CI 0.25-0.99, p=0.03), recent biologics (OR: 0.54, 95% CI 0.44-1.25, p=0.02), iron (OR: 0.89, 95% CI 0.72-1.62, p=0.02), and total 25-OH vitamin D (OR: 1.25, 95% CI 1.02-1.99, p=0.02) did significantly differ between patients with and without vitamin D deficiency. After controlling for several variables, multivariate analysis revealed that a lower odds ratio was linked to increasing age at diagnosis (OR: 0.12, 95% CI 0.03-0.85, p=0.02), sex (OR: 0.58, 95% CI 0.44-0.95, p=0.01), iron (OR: 0.44, 95% CI 0.11-0.62, p=0.01), and 25-OH vitamin D total (OR: 0.48, 95% CI 0.25-0.95, p=0.03). In addition, Age, time since illness onset, and 25-OH vitamin D were found to be helpful indicators for CD patients using LASSO regression.

According to this study, vitamin D insufficiency was often linked to CD patients with active status and pre-treatment Vedolizumab. Furthermore, Age, time since illness onset, and 25-OH vitamin D were found to be significant risk factors for CD.

## Linked entities

- **Chemicals:** iron (PubChem CID 23925)
- **Diseases:** Crohn’s disease (MONDO:0005011)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, CD40 (CD40 molecule) [NCBI Gene 958] {aka Bp50, CDW40, TNFRSF5, p50}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL12B (interleukin 12B) [NCBI Gene 3593] {aka CLMF, CLMF2, IL-12B, IMD28, IMD29, NKSF}, CD83 (CD83 molecule) [NCBI Gene 9308] {aka BL11, HB15}, IL23A (interleukin 23 subunit alpha) [NCBI Gene 51561] {aka IL-23, IL-23A, IL23P19, P19, SGRF}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CD86 (CD86 molecule) [NCBI Gene 942] {aka B7-2, B7.2, B70, BU63, CD28LG2, CD86 v6}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** enterocolitis (MESH:D004760), Malabsorption syndromes (MESH:D008286), pancreatic insufficiency (MESH:D010188), celiac disease (MESH:D002446), Vertebral fractures (MESH:C535781), mental or emotional disorders (MESH:D001523), overweight (MESH:D050177), infections (MESH:D007239), VD deficit (MESH:D009461), obese (MESH:D009765), Vitamin D insufficiency (MESH:D014808), IBD (MESH:D015212), CD (MESH:D003424), colonic mucosal inflammation (MESH:D007249), Pregnancy or (MESH:D011254), infectious bowel disease (MESH:D003141), alcohol or drug abuse (MESH:D019966), diarrhea (MESH:D003967), gastrointestinal dysfunction (MESH:D005767), pan (MESH:C537931), renal/liver impairment (MESH:D017093)
- **Chemicals:** cholecalciferol (MESH:D002762), vitamin B12 (MESH:D014805), 5-aminosalicylic acid (MESH:D019804), Vedolizumab (MESH:C543529), magnesium (MESH:D008274), 25(OH)D (-), iron (MESH:D007501), Vitamin D (MESH:D014807), steroid (MESH:D013256), calcium (MESH:D002118), CDs (MESH:D002104)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12343588/full.md

---
Source: https://tomesphere.com/paper/PMC12343588