00:01 🦠 Vitamin D supplementation reduces the incidence of COVID-19.
02:47 📊 Meta-analysis confirms significant association between vitamin D and COVID-19 protection.
03:02 📚 Vitamin D's crucial roles in health and immunity.
04:25 🧪 Understanding the role of vitamin D in immune response.
06:28 💡 Mechanisms of vitamin D action in the body.
08:01 🔬 Vitamin D's role in immune function and disease prevention.
09:34 💊 Immediate benefits of activated vitamin D (calcidiol) supplementation.
11:41 ✅ Advocating for vitamin D supplementation in healthcare.
You need Magnesium w/ Vitamin D....and vitamin K?
Vitamin D3 supplementation in the range of 4000 to 10,000 units (100 to 250 µg) needed to generate an optimal 40–60 ng/mL (100 to 150 nmol/L)
has been shown to be completely safe when combined with approximately 200 µg vitamin K2
Background: COVID-19 is a major pandemic that has killed more than 196,000 people. The COVID-19 disease course is strikingly divergent. Approximately 80-85% of patients experience mild or no symptoms, while the remainder develop severe disease. The mechanisms underlying these divergent outcomes are unclear. Emerging health disparities data regarding African American and homeless populations suggest that vitamin D insufficiency (VDI) may be an underlying driver of COVID-19 severity. To better define the VDI-COVID-19 link, we determined the prevalence of VDI among our COVID-19 intensive care unit (ICU) patients. Methods: In an Institutional Review Board approved study performed at a single, tertiary care academic medical center, the medical records of COVID-19 patients were retrospectively reviewed. Subjects were included for whom serum 25-hydroxycholecalcifoerol (25OHD) levels were determined. COVID-19-relevant data were compiled and analyzed. We determined the frequency of VDI among COVID-19 patients to evaluate the likelihood of a VDI-COVID-19 relationship. Results: Twenty COVID-19 patients with serum 25OHD levels were identified; 65.0% required ICU admission.The VDI prevalence in ICU patients was 84.6%, vs. 57.1% in floor patients. Strikingly, 100% of ICU patients less than 75 years old had VDI. Coagulopathy was present in 62.5% of ICU COVID-19 patients, and 92.3% were lymphocytopenic. Conclusions: VDI is highly prevalent in severe COVID-19 patients. VDI and severe COVID-19 share numerous associations including hypertension, obesity, male sex, advanced age, concentration in northern climates, coagulopathy, and immune dysfunction. Thus, we suggest that prospective, randomized controlled studies of VDI in COVID-19 patients are warranted.
The authors have declared no competing interest.
This work was supported by the following sources: 1) Louisiana State University Health Sciences Center; 2) 1R01HL118557-01A1, NIHLBI, NIH; 3) ASH Bridge Funding; 4) Texas A&M University System; 5) National Institutes of Health grant AI40165.
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All necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived.
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I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
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The authors confirm that the data supporting the findings of this study are available within the article.