COVID-19 and Vitamin D: A lesson from the skin.
Radomir M SlominskiJoanna StefanMohammad AtharMichael F HolickAnton M JettenChander RamanAndrzej T SłominskiPublished in: Experimental dermatology (2020)
The negative outcomes of COVID-19 diseases respiratory distress (ARDS) and the damage to other organs are secondary to a "cytokine storm" and to the attendant oxidative stress. Active hydroxyl forms of vitamin D are anti-inflammatory, induce antioxidative responses, and stimulate innate immunity against infectious agents. These properties are shared by calcitriol and the CYP11A1-generated non-calcemic hydroxyderivatives. They inhibit the production of pro-inflammatory cytokines, downregulate NF-κΒ, show inverse agonism on RORγ and counteract oxidative stress through the activation of NRF-2. Therefore, a direct delivery of hydroxyderivatives of vitamin D deserves consideration in the treatment of COVID-19 or ARDS of different aetiology. We also recommend treatment of COVID-19 patients with high-dose vitamin D since populations most vulnerable to this disease are likely vitamin D deficient and patients are already under supervision in the clinics. We hypothesize that different routes of delivery (oral and parenteral) will have different impact on the final outcome.
Keyphrases
- oxidative stress
- coronavirus disease
- sars cov
- anti inflammatory
- high dose
- end stage renal disease
- acute respiratory distress syndrome
- newly diagnosed
- ischemia reperfusion injury
- ejection fraction
- mechanical ventilation
- diabetic rats
- signaling pathway
- peritoneal dialysis
- chronic kidney disease
- lps induced
- prognostic factors
- low dose
- intensive care unit
- combination therapy
- immune response
- skeletal muscle
- smoking cessation
- genetic diversity
- respiratory tract