# Vitamin D deficiency and risk of acute kidney injury after ischemic stroke: a propensity-matched cohort study

**Authors:** Kuo-Chuan Hung, Li-Chen Chang, Yi-Chen Lai, Ming Yew, Ping-Hsin Liu, I-Wen Chen

PMC · DOI: 10.3389/fnut.2025.1709491 · Frontiers in Nutrition · 2026-01-05

## TL;DR

Low vitamin D levels before a stroke are linked to a higher risk of kidney injury and other bad outcomes after the stroke.

## Contribution

This study is the first to show a link between pre-stroke vitamin D deficiency and post-stroke acute kidney injury using a large matched cohort.

## Key findings

- Vitamin D deficiency was associated with a 55% higher risk of acute kidney injury within 30 days after stroke.
- Vitamin D deficiency also increased risks of ICU admission, pneumonia, and dialysis requirement.
- The risk of progressing to end-stage renal disease was 69% higher in vitamin D-deficient patients over 1–12 months.

## Abstract

Vitamin D deficiency (VDD) has been linked to adverse outcomes in various clinical settings, but its relationship with post-stroke acute kidney injury (AKI) remains unexplored.

This retrospective cohort study utilized the TriNetX research network database to identify adult patients with first-documented ischemic stroke between January 2010 and December 2024. Patients were stratified based on serum 25-hydroxyvitamin D levels measured within 6 weeks pre-stroke: VDD group (<20 ng/mL) and control group (≥30 ng/mL). After 1:1 propensity score matching, we compared 30-day and 1–12 month outcomes between groups, with the primary outcome being AKI incidence within 30 days post-stroke.

After matching (n = 4,343 per group), patients with pre-stroke VDD demonstrated significantly higher 30-day AKI incidence compared with those with sufficient vitamin D levels (5.3% vs. 3.5%; odds ratio [OR] = 1.55, 95% confidence interval [CI] 1.26–1.92; p < 0.001). VDD was also associated with increased risks of all-cause mortality (OR = 1.63, 95% CI 1.26–2.12), intensive care unit (ICU) admission (OR = 1.55, 95% CI 1.30–1.84), pneumonia (OR = 1.48, 95% CI 1.09–2.02), and dialysis requirement (OR = 2.33, 95% CI 1.36–4.00). Vitamin D insufficiency (20–29 ng/mL) was associated with a milder but significant AKI risk increase (OR = 1.39, 95% CI 1.12–1.72; p = 0.003). The adverse effect of VDD persisted during 1–12 month follow-up, with higher risks of AKI (hazard ratio [HR] = 1.32, 95% CI 1.13–1.55) and progression to end-stage renal disease (HR = 1.69, 95% CI 1.16–2.46).

Pre-stroke VDD is associated with increased risk of post-stroke AKI and other adverse outcomes. The observed dose-dependent relationship suggests potential benefits from optimizing vitamin D status. These findings highlight the importance of assessing vitamin D levels in stroke risk stratification and suggest potential preventive strategies.

## Linked entities

- **Diseases:** acute kidney injury (MONDO:0002492), ischemic stroke (MONDO:1060198), pneumonia (MONDO:0005249), end-stage renal disease (MONDO:0004375)

## Full-text entities

- **Diseases:** end-stage renal disease (MESH:D007676), pneumonia (MESH:D011014), AKI (MESH:D058186), post-stroke (MESH:D020521), ischemic stroke (MESH:D002544), VDD (MESH:D014808)
- **Chemicals:** vitamin D (MESH:D014807), 25-hydroxyvitamin D (MESH:C104450)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC12812757/full.md

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Source: https://tomesphere.com/paper/PMC12812757