The paper argues that the Institute of Medicine (IOM) made a statistical mistake when deriving the Recommended Dietary Allowance (RDA) for vitamin D, so 600 IU/day does not, in fact, ensure adequate vitamin D status for 97.5% of individuals.[1]
The IOM intended the vitamin D RDA to be the intake that gives at least 50 nmol/L of serum 25(OH)D in 97.5% of healthy people, and set this at 600 IU/day based on pooled supplementation studies at high latitudes in winter. The authors show that the IOM actually used a prediction interval for study means, not for individuals, so the 600 IU figure only predicts that 97.5% of future study averages exceed about 50 nmol/L, not that 97.5% of people do.[1]
Using the eight trials that reported both mean and standard deviation, the authors reconstructed the lower tail (about the 2.5th percentile) of individual 25(OH)D values at each dose by subtracting two standard deviations from the mean. Regressing these reconstructed 2.5th percentiles on vitamin D intake showed that 600 IU/day would give 97.5% of individuals a level above only about 26.8 nmol/L, not 50 nmol/L.[1]
Extrapolating the same regression, the intake needed so that 97.5% of individuals reach at least 50 nmol/L is estimated at roughly 8900 IU/day, well above both the current RDA (600 IU) and the IOM’s tolerable upper intake level of 4000 IU/day. The authors stress that this estimate lies outside the range of doses actually studied, so it should be interpreted cautiously, but it clearly implies the true requirement is far above 600 IU/day.[1]
The authors point to Canadian data, where background diet provides about 232 IU/day, showing that even with supplements of 400 IU or more (total ≥632 IU/day), 10–15% of adults still have 25(OH)D below 50 nmol/L. If the RDA were correctly set for 97.5% coverage, fewer than 2.5% should fall below this threshold, so these observations empirically support the claim that the current RDA is too low.[1]
Because the misinterpretation leads to underestimation of vitamin D needs, the authors conclude that the vitamin D RDA should be revisited so that public health guidance and clinical decisions are based on requirements of individuals rather than study averages. They argue that without such correction, goals related to bone health and prevention of vitamin D–related disease cannot be reliably met.[1]
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https://pmc.ncbi.nlm.nih.gov/articles/PMC4210929/
The reanalysis paper suggests that, to get about 97.5% of people to at least 20 ng/mL (50 nmol/L), an intake around 8,900 IU/day would be needed, which is far above current official recommendations. However, major medical bodies still advise much lower routine doses and treat such high intakes as above the usual safe upper limit.[1][2][3][4][5]
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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.
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You need Magnesium w/ Vitamin D....and vitamin K?
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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
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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.
All relevant ethical guidelines have been followed; any necessary IRB and/or ethics committee approvals have been obtained and details of the IRB/oversight body are included in the manuscript.
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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.
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