# The Role of Vitamin D in Severity and Control of Asthma in Children and Adolescents: A Systematic Review and Meta‐Analysis

**Authors:** Joelia M. Ladeira, Olívia Zacas, Amanda Miranda Ferreira, Patrícia Chaib Gomes Stegun, Milena Baptistella Grotta, Adyleia A. D. Contrera Toro

PMC · DOI: 10.1002/ppul.71541 · Pediatric Pulmonology · 2026-02-27

## TL;DR

This study finds that children with asthma have lower vitamin D levels than healthy children, and lower vitamin D is linked to more severe asthma but not better asthma control or lung function.

## Contribution

A systematic review and meta-analysis revealing a link between vitamin D deficiency and asthma severity in children.

## Key findings

- Children with asthma had significantly lower vitamin D levels than healthy controls.
- Severe asthma was associated with lower vitamin D levels compared to mild asthma.
- Vitamin D showed a moderate inverse association with total IgE but not with eosinophil counts or IL-10.

## Abstract

Vitamin D may modulate the inflammatory processes involved in asthma.

To synthesize evidence on the association between serum 25‐hydroxyvitamin D levels and asthma control, severity, pulmonary function, and inflammatory markers in children and adolescents.

MEDLINE PubMed, BIREME, EBSCOhost, Scopus, Web of Science, EMBASE, Cochrane Library, and ProQuest until May 2025.

Eligible studies enrolled participants aged 2–18 years with clinically diagnosed asthma and evaluated serum vitamin D levels in relation to asthma severity and/or control and pulmonary function parameters or type 2 inflammatory biomarkers. We included observational and randomized studies.

The risk of bias for studies was assessed. Random‐effects models estimated pooled outcomes. The heterogeneity was assessed using Cochran's Q and the I² statistic.

Forty‐one studies (7780 participants) were included; 25 contributed to meta‐analyses. Children with asthma had significantly lower serum 25(OH)D levels than healthy controls (mean difference −4.89 ng/mL; 95% CI −7.38 to −2.40; p < 0.001). Severe asthma was associated with lower vitamin D compared with mild disease (−4.21 ng/mL; 95% CI −6.43 to −1.98; p = 0.0002). No significant difference was observed between controlled and uncontrolled asthma. Correlations with pulmonary function were weak and non‐significant (FEV₁ r = 0.18; p = 0.08). Vitamin D showed a moderate inverse association with total IgE (r = −0.37; p = 0.02), but not with eosinophil counts or IL‐10. Heterogeneity was high across analyses.

Children with asthma exhibit lower serum vitamin D levels compared with healthy peers, and these levels are inversely associated with asthma severity and total IgE. No consistent associations were observed with pulmonary function or asthma control. Further research is needed to determine whether correcting vitamin D deficiency can improve clinical and immunologic outcomes in pediatric asthma.

## Linked entities

- **Proteins:** IGHE (immunoglobulin heavy constant epsilon), IL10 (interleukin 10)
- **Chemicals:** 25-hydroxyvitamin D (PubChem CID 5353325)
- **Diseases:** asthma (MONDO:0004979)

## Full-text entities

- **Genes:** TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}, NOS2 (nitric oxide synthase 2) [NCBI Gene 4843] {aka HEP-NOS, INOS, NOS, NOS2A}, IL2RA (interleukin 2 receptor subunit alpha) [NCBI Gene 3559] {aka CD25, IDDM10, IL2R, IMD41, TCGFR, p55}, FOXP3 (forkhead box P3) [NCBI Gene 50943] {aka AIID, DIETER, IPEX, JM2, PIDX, XPID}
- **Diseases:** PICOS (MESH:D011248), Bronchial (MESH:D001982), immune dysregulation (OMIM:614878), allergic (MESH:D004342), Asthma (MESH:D001249), Insufficiency (MESH:D000309), dyspnea (MESH:D004417), reduced pulmonary function (MESH:D001523), asthmatic (MESH:D013224), atopic (MESH:C566404), Inflammation (MESH:D007249), Vitamin D deficiency (MESH:D014808), impaired pulmonary function (OMIM:608852)
- **Chemicals:** Cholecalciferol (MESH:D002762), 25(OH)D3 (MESH:C104450), D (MESH:D003903), 25(OH)D (-), calcium (MESH:D002118), Vitamin D (MESH:D014807), nitric oxide (MESH:D009569), Vitamin A (MESH:D014801)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12947299/full.md

## References

68 references — full list in the complete paper: https://tomesphere.com/paper/PMC12947299/full.md

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Source: https://tomesphere.com/paper/PMC12947299