# Effect of vitamin D status on a disintegrin-like and metalloprotease with thrombospondin type 1 motif 13 (ADAMTS13) and interleukin 6 in patients with acute myeloid leukaemia

**Authors:** Dina Ashraf Abdelhady, Mervat Mostafa Mohamed Azab, Ahmed A. Alnagar, Nora Said

PMC · DOI: 10.1186/s40001-025-02879-8 · European Journal of Medical Research · 2025-07-16

## TL;DR

This study found that vitamin D supplementation may reduce inflammation in patients with acute myeloid leukemia, but does not affect a key enzyme linked to disease outcomes.

## Contribution

The study demonstrates that vitamin D supplementation can lower IL-6 levels in vitamin D-deficient AML patients, suggesting a potential anti-inflammatory role.

## Key findings

- Vitamin D-deficient AML patients who received supplementation showed significantly reduced IL-6 levels after 28 days.
- AML patients had significantly higher IL-6 and lower ADAMTS13 levels compared to healthy controls.
- A negative correlation was found between vitamin D and IL-6 levels on Day 28 of treatment.

## Abstract

Low levels of the enzyme ADAMTS13 and elevated inflammatory markers such as interleukin-6 (IL-6) are associated with worse outcomes in patients with acute myeloid leukaemia (AML). IL-6 produced by leukaemia cells suppresses ADAMTS13 activity and impairs hematopoietic differentiation. Vitamin D, which has known for its immunomodulatory effects, may reduce IL-6 levels. This study investigated the impact of vitamin D supplementation on IL-6 and ADAMTS13 levels in patients newly diagnosed with AML.

A total of 38 newly diagnosed AML patients and 14 healthy individuals were included. IL-6 and ADAMTS13 levels were measured in both groups at baseline. Among AML patients, 34 were found to have vitamin D deficiency. Seventeen of these patients received oral vitamin D supplementation for 28 days in addition to their standard chemotherapy. Serum levels of IL-6, ADAMTS13 and vitamin D were measured on the 1st and 28th days of chemotherapy. Statistical analyses included Mann–Whitney U test, Wilcoxon signed-rank test, and Spearman correlation.

AML patients had significantly higher IL-6 (7.19 vs. 1.15 pg/mL; p = 0.00001) and lower ADAMTS13 (684 vs. 1205 ng/mL; p = 0.001) compared to controls. ADAMTS13 significantly increased by Day 28 (p = 0.0001), while IL-6 showed no overall change. However, among vitamin D-deficient patients receiving supplementation, IL-6 levels decreased significantly by Day 28 (p = 0.049). A negative correlation was found between vitamin D and IL-6 on Day 28 (r = –0.485; p = 0.035). No significant effect of vitamin D status was observed on ADAMTS13 levels.

Vitamin D supplementation was associated with a reduction in IL-6 levels, but did not influence ADAMTS13 levels in patients with AML. These findings support the potential role of vitamin D as an adjunct anti-inflammatory agent during induction chemotherapy. Further studies with larger samples and longer follow-up are recommended to clarify its therapeutic relevance.

Trial registration number NCT05149339 in www.clinicaltrial.gov registered on 25/11/2021 'retrospectively registered’ with URL; https://register.clinicaltrials.gov/prs/app/action/SelectProtocol?sid=S000BKX8&selectaction=Edit&uid=U0005ZGQ&ts=98&cx=avh64j.

## Linked entities

- **Proteins:** ADAMTS13 (ADAM metallopeptidase with thrombospondin type 1 motif 13), IL6 (interleukin 6), IL6 (interleukin 6)
- **Diseases:** acute myeloid leukaemia (MONDO:0015667), AML (MONDO:0018874)

## Full-text entities

- **Genes:** ADAMTS13 (ADAM metallopeptidase with thrombospondin type 1 motif 13) [NCBI Gene 11093] {aka ADAM-TS13, ADAMTS-13, C9orf8, VWFCP, vWF-CP}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** inflammatory (MESH:D007249), leukaemia (MESH:D015458), vitamin D deficiency (MESH:D014808), AML (MESH:D054218)
- **Chemicals:** Vitamin D (MESH:D014807)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12269281