4.5 Article

Effect of vitamin D supplementation on microvascular reactivity in obese adolescents: A randomized controlled trial

Journal

NUTRITION METABOLISM AND CARDIOVASCULAR DISEASES
Volume 31, Issue 8, Pages 2474-2483

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.numecd.2021.04.025

Keywords

Obese adolescents; Vitamin D; Vascular function

Funding

  1. University Hospital of Nimes, France [LOCAL/2015]

Ask authors/readers for more resources

This study is the first to assess the effect of vitamin D supplementation on microvascular reactivity in obese adolescents, finding that vitamin D supplementation can improve vascular function, attenuate microvascular dysfunction, without altering macrovascular function.
Background and aim: Childhood obesity is associated with vitamin D (VD) deficiency and vascular dysfunction. Considering evidence indicates that VD may improve vascular func-tion, this study, for the first time, assessed the effect of VD supplementation on microvascular reactivity in obese adolescents (OA). Methods and results: This randomized controlled trial included 26 OA, receiving fruit juice with (n = 13) or without VD (4000 IU/d; n = 13) over a 3-month lifestyle program, as well as 23 normal-weight adolescents (controls). The primary outcome was the pre-to-post-program change in microvascular reactivity determined by laser speckle contrast imaging with acetylcho-line and sodium nitroprusside iontophoresis. Changes in 25 hydroxyvitamin D (25(OH)D), flow-mediated dilation (FMD), nitrate-mediated dilation (NMD), insulin resistance (HOMA-IR) and in-flammatory markers (C-reactive protein [CRP]) were monitored. At inclusion, in comparison to controls, OA exhibited lower total and free 25(OH)D, impaired microvascular responses, and impaired FMD, but similar NMD. After the lifestyle program, total and free 25(OH)D increased in all OA, with a greater increase in those receiving VD supplements. HOMA-IR and CRP decreased in all OA. Neither FMD nor NMD were altered in either group. Endothelium-dependent microvascular reactivity only increased in the VD-supplemented group, reaching values comparable to that of controls. Similar results were found when analyzing only OA with a VD deficiency at baseline. Conclusion: VD supplementation during a lifestyle program attenuated microvascular dysfunc-tion in OA without altering macrovascular function. Registration number for clinical trial: NCT02400151. (c) 2021 The Italian Diabetes Society, the Italian Society for the Study of Atherosclerosis, the Italian Society of Human Nutrition and the Department of Clinical Medicine and Surgery, Federico II University. Published by Elsevier B.V. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available