# Vitamin D supplementation and selected metabolic parameters in patients with type 2 diabetes and obesity: a prospective observational study

**Authors:** Karolina Hoffmann, Wiesław Bryl, Bhoomendra Bhongade, Ashot Avagimyan, Mohammed El-Tanani, Syed Arman Rabbani, Sirajunisa Talath, Imran Rashid Rangraze, Adil Farooq Wali, Walaa Ibraheem, Shakta Mani Satyam, Sorina Ispas, Ioannis Ilias, Viviana Maggio, Manfredi Rizzo, Anna Paczkowska

PMC · DOI: 10.3389/fendo.2025.1750040 · Frontiers in Endocrinology · 2026-01-14

## TL;DR

This study found that high-dose vitamin D3 improved vitamin D levels and slightly reduced blood sugar in obese type 2 diabetes patients, but had no effect on blood pressure or weight.

## Contribution

The study provides new evidence on the metabolic effects of high-dose vitamin D3 in obese type 2 diabetes patients on metformin.

## Key findings

- Vitamin D3 supplementation significantly increased serum 25(OH)D levels compared to controls.
- The intervention group showed modest reductions in fasting glucose and HbA1c.
- Baseline FSG, diabetes duration, and BMI predicted poor glycemic response to supplementation.

## Abstract

Vitamin D deficiency has been implicated in metabolic dysregulation, including insulin resistance and inflammation, commonly observed in patients with type 2 diabetes mellitus (T2DM) and obesity. Evidence on the metabolic impact of vitamin D supplementation in this population remains inconsistent.

To evaluate the effects of high-dose vitamin D3 supplementation on anthropometric and selected metabolic parameters in ambulatory obese patients with T2DM treated with metformin monotherapy.

This 12-week prospective cohort study included 200 patients with T2DM, allocated to a supplementation group (n = 100; vitamin D3 - 4,000 IU/day) or a control group (n = 100; no supplementation). Primary outcome was change in serum 25-hydroxyvitamin D [25(OH)D] concentration. Secondary outcomes included fasting serum glucose (FSG), glycated hemoglobin (HbA1c), blood pressure (BP), serum calcium, and body mass index (BMI). Predictors of failure to achieve target HbA1c ≤ 6.5% were identified using logistic regression.

After 12 weeks, serum 25(OH)D significantly increased in the supplementation group compared with controls (Δ +23.7 vs +1.3 ng/mL; p < 0.001). FSG and HbA1c decreased significantly in the intervention group (Δ –0.4 mmol/L, p = 0.02; Δ –0.6%, p = 0.01, respectively), while no significant changes were observed in systolic or diastolic BP, serum calcium, or BMI. Logistic regression identified higher baseline FSG (OR 1.34, 95% CI 1.12–1.61), longer diabetes duration (OR 1.28, 95% CI 1.07–1.54), and higher BMI (OR 1.21, 95% CI 1.01–1.47) as independent predictors of suboptimal glycemic response.

High-dose vitamin D3 supplementation significantly improved vitamin D status and was associated with modest improvements in glycemic control in obese patients with T2DM, without affecting blood pressure, calcium, or body weight. These findings support vitamin D repletion as a potential adjunctive strategy in diabetes management, while not allowing causal inference, and warrant further confirmation in randomized controlled trials with longer follow-up.

## Linked entities

- **Chemicals:** vitamin D3 (PubChem CID 5280795), metformin (PubChem CID 4091)
- **Diseases:** type 2 diabetes mellitus (MONDO:0005148), obesity (MONDO:0011122)

## Full-text entities

- **Diseases:** inflammation (MESH:D007249), diabetes (MESH:D003920), insulin resistance (MESH:D007333), metabolic dysregulation (MESH:D021081), T2DM (MESH:D003924), obese (MESH:D009765)
- **Chemicals:** Vitamin D (MESH:D014807), 25-hydroxyvitamin D (MESH:C104450), 25(OH)D (-), metformin (MESH:D008687), calcium (MESH:D002118), glucose (MESH:D005947), vitamin D3 (MESH:D002762)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12847046/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12847046/full.md

## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12847046/full.md

---
Source: https://tomesphere.com/paper/PMC12847046