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J Am Coll Nutr ; 39(8): 694-699, 2020.
Article in English | MEDLINE | ID: covidwho-641763

ABSTRACT

Early reports indicate an association between the severity of the COVID-19 infection and the widespread 25-hydroxy vitamin D deficiency known to exist in populations around the world. Vitamin D deficiency is extremely common among African American (AA) communities, where the COVID-19 infection rate is three-fold higher, and the mortality rate nearly six-fold higher, compared with rates in predominantly white communities. COVID-19 infection primarily affects the lungs and airways. Previous reports have linked 25-hydroxy vitamin D deficiency with subclinical interstitial lung disease. AA are at risk for lower cellular glutathione (GSH) levels, and GSH deficiency epigenetically impairs VD biosynthesis pathway genes. Compared with vitamin D alone, co-supplementation of vitamin D and L-cysteine (a GSH precursor) showed a better efficacy in improving levels of GSH and VD-regulatory genes at the cellular/tissue level, increasing 25(OH) vitamin D levels, and reducing inflammation biomarkers in the blood in mice studies. We propose that randomized clinical trials are needed to examine the potential of co-supplementation with anti-inflammatory antioxidants, vitamin D and L-cysteine in correcting the 25(OH)VD deficiency and preventing the 'cytokine storm,' one of the most severe consequences of infection with COVID-19, thereby preventing the adverse clinical effects of COVID-19 infection in the vulnerable AA population.


Subject(s)
Black or African American , COVID-19 Drug Treatment , Cysteine/therapeutic use , Dietary Supplements , Glutathione/metabolism , Vitamin D Deficiency/drug therapy , Vitamin D/therapeutic use , Animals , Anti-Inflammatory Agents/pharmacology , Anti-Inflammatory Agents/therapeutic use , Antioxidants/pharmacology , Antioxidants/therapeutic use , Biomarkers/blood , COVID-19/ethnology , COVID-19/metabolism , COVID-19/mortality , Cysteine/pharmacology , Cytokines/metabolism , Epigenesis, Genetic , Genetic Predisposition to Disease , Humans , Inflammation/etiology , Inflammation/metabolism , Inflammation/prevention & control , Mice , Vitamin D/analogs & derivatives , Vitamin D/blood , Vitamin D/pharmacology , Vitamin D Deficiency/ethnology , Vitamin D Deficiency/metabolism , Vitamins/blood , Vitamins/pharmacology , Vitamins/therapeutic use
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