Publication:
Vitamin D receptor stimulation to reduce acute respiratory distress syndrome (ARDS) in patients with coronavirus SARS-CoV-2 infections: Revised Ms SBMB 2020_166.

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Date

2020-06-07

Authors

Quesada-Gomez, Jose Manuel
Entrenas-Castillo, Marta
Bouillon, Roger

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Elsevier
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Abstract

Coronavirus infection is a serious health problem awaiting an effective vaccine and/or antiviral treatment. The major complication of coronavirus disease 2019 (COVID-19), the Acute Respiratory Distress syndrome (ARDS), is due to a variety of mechanisms including cytokine storm, dysregulation of the renin-angiotensin system, neutrophil activation and increased (micro)coagulation. Based on many preclinical studies and observational data in humans, ARDS may be aggravated by vitamin D deficiency and tapered down by activation of the vitamin D receptor. Several randomized clinical trials using either oral vitamin D or oral Calcifediol (25OHD) are ongoing. Based on a pilot study, oral calcifediol may be the most promising approach. These studies are expected to provide guidelines within a few months.

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MeSH Terms

Administration, oral
Betacoronavirus
COVID-19
Calcifediol
Coronavirus infections
Humans
Pandemics
Pilot projects
Pneumonia, viral
Randomized controlled trials as topic
Renin-angiotensin system
Respiratory distress syndrome
SARS-CoV-2
Vitamin D
Vitamin D deficiency
Vitamins

DeCS Terms

Administración oral
Deficiencia de vitamina D
Infecciones por Coronavirus
Neumonía viral
Pandemias
Proyectos piloto
Sistema renina-angiotensina
Síndrome de dificultad respiratoria
Vitamina D

CIE Terms

Keywords

1α, 25(OH)2D or 1α, 25-dihydroxyvitamin D or calcitriol, Acute respiratory distress syndrome (ARDS), Calcifediol or 25-hydroxyvitamin D3, Corona virus, Cytokine storm, Hypercoagulability, Lung diseases, Renin-angiotensin system, SARS-CoV-2, Vitamin D, vitamin D3 or cholecalciferol

Citation

Quesada-Gomez JM, Entrenas-Castillo M, Bouillon R. Vitamin D receptor stimulation to reduce acute respiratory distress syndrome (ARDS) in patients with coronavirus SARS-CoV-2 infections: Revised Ms SBMB 2020_166. J Steroid Biochem Mol Biol. 2020 Sep;202:105719