Vitamin D3 and COVID-19 Outcomes: An Umbrella Review of Systematic Reviews and Meta-Analyses

Background: The immune system (innate and adaptive) is influenced by vitamin D3, which affects gene expression and inflammatory pathways. An umbrella review was conducted to evaluate the power and accuracy of data connecting vitamin D3 to the outcomes of COVID-19 infection and to appraise the proof provided by published meta-analyses. Methods: MEDLINE, Embase, and the Cochrane Library were searched from database inception to 31 May 2022. Meta-analyses of prospective or retrospective observational studies and randomized trials were included. Evidence of association was graded according to the established criteria: strong, highly suggestive, suggestive, weak, or not significant. Results: From 74 publications, 27 meta-analyses described five associations between vitamin D3 levels and supplementation and COVID-19 outcomes. Low levels of vitamin D3 were significantly associated with severity (highly suggestive evidence; OR = 1.97 [95% CI, 1.55–2.51], p < 0.01; I2 = 77%, p < 0.01) and mortality risk due to COVID-19 disease (OR = 1.83 [95% CI, 1.55–2.16], p < 0.01; I2 = 50%, p < 0.01). Vitamin D3 supplementation, after a diagnosis of COVID-19 infection, was associated with significantly reduced infection severity (e.g., ICU admission) and mortality. Conclusions: This umbrella review of the available evidence suggests that insufficient vitamin D3 may increase COVID-19 infection risk, severity, and mortality, in addition to showing a highly suggestive association between vitamin D3 supplementation and reduced severity and mortality among infected patients.


Introduction
Vitamin D modulates the systemic inflammatory response and may actively protect against respiratory tract infections and other diseases [1]. A recent meta-analysis showed that vitamin D supplementation reduces all-cause mortality [2]. In addition, vitamin D supplementation reduces the risk of acute respiratory infections, despite having a small effect size [3]. The outbreak of coronavirus during the last quarter of 2019 resulted in a global pandemic. The virus responsible for the illness was named severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), and the disease it caused was called coronavirus disease 2019 . COVID-19 infection can range from asymptomatic to mild respiratory tract symptoms to severe pneumonia requiring mechanical ventilation, and may require supportive measures, such as admission to an intensive care unit. The disease has no specific treatment, with options ranging from no intervention to administration of oxygen, steroids, and antivirals.
Multiple systematic reviews and meta-analyses have investigated the correlation between vitamin D3 levels and COVID-19 outcomes. However, the reported associations may not be valid because of inherent biases, such as selective bias, publication bias, or other factors. Additionally, the evidence has not been systematically evaluated; therefore, we

Literature Search
We searched PubMed, Embase, and the Cochrane Database of Systematic Reviews from the beginning of May 2022. The search terms used were ("meta-analysis") AND ("vitamin D3" OR "25-hydroxyvitamin D") AND ("COVID-19"). In addition, we manually screened references to identify eligible articles. A literature search was independently conducted using FP and AG. The differences between the FP and AG were discussed and resolved using AL.

Selection Criteria
Two authors (FP and AG) independently reviewed the full text of potentially eligible articles. Only meta-analyses of epidemiological studies examining the relationship between vitamin D3 and COVID-19 outcomes in adults have been considered. In addition, narrative or systematic reviews without meta-analysis and analyses of the effect of vitamin D3 on other respiratory diseases, conference abstracts, and letters to the editors were excluded. When several meta-analyses from the same authors reported the same health outcomes, we included the meta-analysis with the largest number of studies. In summary, metaanalyses of prospective (observational or randomized) or retrospective studies evaluating the correlation between vitamin levels, according to the cutoff chosen by each author, were analyzed to address three main outcomes: COVID-19 infection risk, infection severity (ICU admissions), and mortality. In addition, meta-analyses with the same criteria as above, exploring the association between vitamin D3 supplementation at infection diagnosis and severe illness (ICU admission or death) in adult patients, were included.

Data Extraction
Data from the included studies were extracted separately by two authors (FP and AG). For each eligible meta-analysis, we extracted the following information: first author, publication year, study design, number of participants and trials, crude or multivariableadjusted summary risk estimates and corresponding 95% CIs (odds ratios [ORs], risk ratios [RRs], or hazard ratios [HRs]), p values of pooled effects, Egger's test measurement, and I 2 with p for significance. Discrepancies were resolved through discussion. We re-examined the estimated risk of an event for each relationship using random effects models. The three measures of association (OR, RR, and HR) were expected to produce comparable results, as the associated risks of the outcomes we studied were likely to be low. To keep things simple, all risk estimates were explained in terms of odds ratios (ORs).

Assessment of Methodological Quality
Two authors carefully assessed the quality of each meta-analysis using the reliable AMSTAR 2 [5] tool. Based on the scores, four grades were assigned to describe methodological quality: high, moderate, low, and critically low. A high score was assigned when there was no or only one minor defect present, and a moderate score was assigned when there was more than one defect.

Grading of the Evidence
Meta-analyses showing nominally significant associations were categorized into 4 evidence groups: strong, highly suggestive, suggestive, and weak [6]. Associations were considered to be supported by strong evidence if all the following criteria were met: the meta-analysis included >1000 cases, a threshold that provides 80% power for hazard ratios ≥ 1.20 (α = 0.05); the random-effects model had a p value ≤10 −6 (under the assumption that the tests of statistical significance of the effect in each meta-analysis were valid); absence of high heterogeneity (I 2 < 50%); 95% prediction intervals excluded the null value; and no evidence of small-study effects and excess significance bias. There was strong evidence associated with meta-analyses containing more than one thousand cases, with a random-effects p-value of 10 −6 or lower. The largest study in the meta-analysis was nominally statistically significant. Meta-analyses with more than 1000 cases and a random-effects p-value of 10 −3 or lower yielded suggestive evidence. All other nominally significant associations were considered weak.

Data Analysis
Sensitivity analysis was performed after excluding studies with a significant risk of bias and low-quality levels. When the p-value was <0.05, the total effects of the pooled metaanalyses were considered significant. I 2 and Q tests were used to evaluate heterogeneity between studies and Egger's test was used to calculate publication bias. p < 0.1 for both heterogeneity and publication bias was considered significant.

Results
This umbrella review identified 74 publications and included 27 meta-analyses (36%) describing five associations. Figure 1 in the Supplement lists the 47 articles (65%) that were excluded and the reasons for their exclusion.   Table 1 describes the characteristics of the 27 eligible meta-analyses , which were published between 2021 and 2022.  The median number of studies included in the meta-analysis was 20. The median sample size in the meta-analysis was 11,901. Overall, 12,767,045 patients were included in these 27 meta-analyses.
Using the AMSTAR 2 method (Table 1), we evaluated the methodological quality of five meta-analyses as high (18.5%) and found that nine (33.3%) were of moderate quality. Two meta-analyses (7.4%) were rated as low-quality, and 11 (40.7%) were rated as critically low-quality.
A description and summary of the association between vitamin D3 levels and supplementation with endpoints are presented in Table 2.
There was considerable heterogeneity among the three associations (those that correlated levels with outcomes: I 2 = 76, 77, and 50%). Neither of the other two associations (vitamin D3 supplementation and outcome) were heterogeneous (I 2 = 0%). There were small-study effects in 6, 7, 10, 4, and 4 studies for each association (50,50,58,44, and 40%, respectively), so grade levels were downgraded for each association. In the largest study, all associations were statistically significant at p < 0.05 for all effect sizes.  Each of the five associations reached statistical significance at p < 0.01, suggesting vitamin D3 supplementation or adequate vitamin D3 levels may protect against COVID-19 risk and unfavorable outcomes.

Susceptibility to Infection
Low levels of vitamin D3 were associated with a significant risk of COVID-19 infection compared to sufficient levels. Twelve meta-analyses evaluated this outcome (AMSTAR 2 quality level was moderate to high in seven papers). Evidence was graded as highly suggestive (OR = 1.72 [95% CI, 1.51-1.97], p < 0.01; I 2 = 76%, p < 0.01; Figure 2).

Susceptibility to Infection
Low levels of vitamin D3 were associated with a significant risk of COVID-19 infection compared to sufficient levels. Twelve meta-analyses evaluated this outcome (AM-STAR 2 quality level was moderate to high in seven papers). Evidence was graded as highly suggestive (OR = 1.72 [95% CI, 1.51-1.97], p < 0.01; I 2 = 76%, p < 0.01; Figure 2).

Risk of Severe Infection (ICU Admission)
Low levels of vitamin D3 were associated with significant risk of severity compared to patients with sufficient levels. Fifteen meta-analyses evaluated this outcome (AMSTAR 2 quality level was moderate to high in seven papers). Evidence was graded as highly suggestive (OR = 1.97 [95% CI, 1.55-2.51], p < 0.01; I 2 = 77%, p < 0.01; Figure 3).

Risk of Severe Infection (ICU Admission)
Low levels of vitamin D3 were associated with significant risk of severity compared to patients with sufficient levels. Fifteen meta-analyses evaluated this outcome (AMSTAR 2 quality level was moderate to high in seven papers). Evidence was graded as highly suggestive (OR = 1.97 [95% CI, 1.55-2.51], p < 0.01; I 2 = 77%, p < 0.01; Figure 3).

Risk of Death
Low levels of vitamin D3 were associated with significant mortality risk compared to patients with sufficient levels. Seventeen meta-analyses evaluated this outcome (AMSTAR 2 quality level was moderate to high in eight papers). Evidence was graded as highly suggestive (OR = 1.83 [95% CI, 1.55-2.16], p < 0.01; I 2 = 50%, p = 0.01; Figure 4).

Risk of Death
Low levels of vitamin D3 were associated with significant mortality risk compared to patients with sufficient levels. Seventeen meta-analyses evaluated this outcome (AM-STAR 2 quality level was moderate to high in eight papers). Evidence was graded as highly suggestive (OR = 1.83 [95% CI, 1.55-2.16], p < 0.01; I 2 = 50%, p = 0.01; Figure 4).

Risk of Death
Low levels of vitamin D3 were associated with significant mortality risk compared to patients with sufficient levels. Seventeen meta-analyses evaluated this outcome (AM-STAR 2 quality level was moderate to high in eight papers). Evidence was graded as highly suggestive (OR = 1.83 [95% CI, 1.55-2.16], p < 0.01; I 2 = 50%, p = 0.01; Figure 4).

Supplementation to Improve Infection Mortality
Vitamin D3 supplementation, after a diagnosis of COVID-19 infection, was associated with significantly reduced infection mortality. Ten meta-analyses evaluated this outcome (AMSTAR 2 quality level was moderate to high in six papers). Evidence was graded as highly suggestive for evidence of publication bias in three meta-analyses (OR = 0.53 [95% CI, 0.42-0.67], p < 0.01; I 2 = 0%, p = 0.88; Figure 6).

Sensitivity Analysis
In studies where the risk of infection and disease severity were correlated with vitamin D3 levels, the strength of association remained unchanged after the exclusion of biased meta-analyses (I 2 85 and 51%). After exclusion of low levels, the meta-analysis association became strong for risk of infection and remained highly suggestive of disease severity (I 2 41 and 75%). For correlation with mortality, the association became strong after excluding papers that retained significant bias and low-quality levels (I 2 0 and 46%). Both Evidence was graded as highly suggestive for evidence of publication bias in two metaanalyses (OR = 0.38 [95% CI, 0.28-0.5], p < 0.01; I 2 = 0%, p = 0.71; Figure 5).

Supplementation to Improve Infection Mortality
Vitamin D3 supplementation, after a diagnosis of COVID-19 infection, was associated with significantly reduced infection mortality. Ten meta-analyses evaluated this outcome (AMSTAR 2 quality level was moderate to high in six papers). Evidence was graded as highly suggestive for evidence of publication bias in three meta-analyses (OR = 0.53 [95% CI, 0.42-0.67], p < 0.01; I 2 = 0%, p = 0.88; Figure 6).

Sensitivity Analysis
In studies where the risk of infection and disease severity were correlated with vitamin D3 levels, the strength of association remained unchanged after the exclusion of biased meta-analyses (I 2 85 and 51%). After exclusion of low levels, the meta-analysis association became strong for risk of infection and remained highly suggestive of disease severity (I 2 41 and 75%). For correlation with mortality, the association became strong after excluding papers that retained significant bias and low-quality levels (I 2 0 and 46%). Both

Sensitivity Analysis
In studies where the risk of infection and disease severity were correlated with vitamin D3 levels, the strength of association remained unchanged after the exclusion of biased meta-analyses (I 2 85 and 51%). After exclusion of low levels, the meta-analysis association became strong for risk of infection and remained highly suggestive of disease severity (I 2 41 and 75%). For correlation with mortality, the association became strong after excluding papers that retained significant bias and low-quality levels (I 2 0 and 46%). Both outcomes explored in supplementation studies maintained an unchanged grade of association (highly suggestive) after excluding studies with significant bias and low-quality levels (I 2 0 and 0%). After considering papers that only calculated adjusted ORs (seven papers), the association between vitamin D3 levels and infection and mortality become strong.

Discussion
The most common forms of vitamin D supplementation are cholecalciferol (vitamin D3) and ergocalciferol (vitamin D2), which are the precursors of 1,25(OH) 2 D 3 (the active form of vitamin D). Besides its essential biological functions (classical), such as bone metabolism and calcium and phosphorus homeostasis, vitamin D is also involved in other roles (nonclassical) involving immune modulation, lung and muscle function, cardiovascular health, and infectious disease prevention.
Many reports made in Europe, not among those included in these meta-analyses, based on observations made during the first pandemic wave, have suggested an association between vitamin D deficiency, risk of SARS-CoV-2 infection, incidence and severity of COVID-19, and mortality. Speculative observations related to the higher prevalence of hypovitaminosis D among European countries and the very high prevalence of SARS-CoV-2 and COVID-19 infections, especially in the northern regions, have defined the association between the two events without verifying the causal link or excluding causality. Vitamin D status, risk of infection, and development of severe forms of the disease are complex phenomena dependent on innumerable variables whose complex interdependent relationship cannot be described by their mere sum. Therefore, only studies conducted in large cohorts and/or pooled/umbrella analyses can assume epidemiological relevance.
Here, we present the first umbrella review of published meta-analyses on the association between vitamin D3 and COVID-19. We included 27 published meta-analyses, which comprised five summary risk estimates for the association vitamin D3 insufficiency (<30 ng/mL) and supplementation have with COVID-19 outcomes. We found a significant effect size that supported all the statistically significant associations in the primary and sensitivity analyses. There is highly suggestive evidence for an association between low vitamin D3 levels and COVID-19 incidence and disease severity (ICU admission). Furthermore, suggestive evidence exists for positive associations between insufficient vitamin D3 levels and mortality in infected patients (83% increased risk compared with normally replete patients). However, we did not analyze continuous vitamin D3 level/effect associations due to data limitations. Furthermore, after exclusion of biased or low-quality meta-analyses, or those that included unadjusted (crude) ORs, the association with mortality became strong. Finally, we found positive, highly suggestive evidence of an association between vitamin D administration and risk of death reduction.
Vitamin D regulates other cellular functions, in addition to calcium and bone homeostasis. The vitamin D receptor is universally expressed in nucleated cells. A large amount of epidemiological data indicate that the risks of cancer and infectious, autoimmune, and vascular diseases are higher when 25-hydroxyvitamin D (25[OH]D) levels are <20 ng/mL, and that risks decrease with higher 25(OH)D concentrations [34]. However, no convincing randomized trial data has shown that vitamin D supplements can decrease cancer risk or prognosis, decrease the risk or severity of infections or autoimmune diseases, or decrease cardiovascular risks or metabolic diseases. Subjects with normal vitamin D3 levels may be healthier and less prone to many diseases, as well as to COVID-19 infection and potential consequences (e.g., intubation). In particular, in COVID-19 patients, a meta-analysis showed that patients with sufficient vitamin D had significantly lower levels of interleukin-6, C-reactive protein, ferritin, lactate dehydrogenase, fibrinogen, and D-dimer compared to those in the vitamin D deficient group [35].
It is highly plausible that the proposed biological mechanisms explain the observed associations. Several genes involved in the immune system (innate and adaptive immunity) and the downstream inflammatory cascade are influenced by vitamin D, which affects the susceptibility to and severity of infectious diseases. Patients with COVID-19 may benefit from vitamin D supplementation as a preventive and therapeutic agent. Vitamin D binds to its receptor and affects two main pathways: (a) it inhibits pro-inflammatory cytokines, interfering with the TNF-induced NFkB1 pathway, and (b) it activates the Jak-Stat pathway by inducing the expression of interferon-stimulating genes [36][37][38].
More specifically, 1,25(OH) 2 D has antimicrobial activity, as it can induce the expression of cathelicidin and β-defensin 2 proteins with both direct and indirect antimicrobial efficacy (through stimulation of chemotaxis of cells of the immune system, inducing the expression of pro-inflammatory cytokines, resulting in the removal of infected cells in the respiratory tract). The expression of β-defensin [39] is stimulated by vitamin D through the induction of nucleotide-binding oligomerization domain-containing protein 2 (NOD2) 2. Furthermore, 1,25(OH) 2 D inhibits the expression of hepcidin and, therefore, determines the elimination of the hepcidin-mediated block of iron export dependent on ferroportin, resulting in increased efflux of iron from the infected cell and, consequently, the reduction in the availability of this element for microbial growth [40]. Indeed, vitamin D has multiple antimicrobial effects, including stimulation of the barrier function of the intestine [41] and alveolar epithelia [42], production of reactive oxygen species (ROS) [43], neutrophil function [44], and phagocytic and autophagocytic activities (through the induction of the key effectors of autophagy, LC3, beclin 1, and PI3Kγ3) of macrophages [45]. Both the induction of cathelicidin and defensins and stimulation of one of the pro-autophagic pathways in antigen-presenting cells have an important antiviral effect, inhibit virus replication [46], and aid in the clearance of virus particles [47]. In the context of adaptive immunity, calcitriol limits the activation of T lymphocytes [48], induces the expression of regulatory phenotypes (Tregs) that mediate immune tolerance, and limits abnormal immune responses and phenotypic shifts from T helper Th1/Th17 to Th2 (from pro-inflammatory to regulatory) [49]. The effectiveness of vitamin D is a function of the activity of its receptor, VDR. Single nucleotide polymorphisms (SNPs) in the VDR gene affect protein responsiveness and have been associated with numerous immune dysfunctions. Compared to the CT and CC genotypes, the TT genotype of the FokI polymorphism has been associated with a greater risk of respiratory syncytial virus (SCV) infections [50].
The attack/replication sequence into human cells explains another possible therapeutic role of vitamin D. Through its spike protein, SARS-CoV-2 enters the human body via its cognate angiotensin, converting enzyme-2 (ACE-2) receptor on the cells of the lungs and other organs [51]. As soon as the viral RNA enters the host cell, it replicates continuously, using the host's polymerase system. This leads to severe pathological changes and, finally, cell death. The virus uses multiple mechanisms to evade the host immune system, including excessive stimulation of the renin-angiotensin system (RAS) [52]. SARS-CoV-2 interferes with and modulates the RAS system, resulting in an excess of angiotensin II being generated, activating the cytokine storm, and downregulating the host's immune system. Dysfunctional immune responses in some COVID-19 cases lead to overproduction of pro-inflammatory cytokines in circulation that trigger acute respiratory distress syndrome (ARDS) and eventually death. Vitamin D has been hypothesized to play a role in acute respiratory distress syndrome (ARDS). ACE2, which, as previously reported, serves as the docking site for viral protein S, converts angiotensin II (Ang-II) to angiotensin 1-7 [Ang(1-7)]. The latter has vasodilator, anti-inflammatory, and protective effects against organ damage actions [53]. Following binding to protein S, the ACE2-viral particle complex is internalized and, therefore, the enzymatic activity of ACE2 is downregulated. Downregulation of ACE2 is associated with an abnormal inflammatory response that can cause tissue damage, leading to further downregulation of ACE2. This process can result in acute respiratory distress syndrome (ARDS) [54,55]. Vitamin D has a protective role against ARDS, given the ability to inhibit the expression of renin and the activity of the ACE/Ang-II/AT1R axis and to stimulate, instead, the ACE2/Ang-(1-7)/MasG (G proteinassociated Mas receptor). Thus, vitamin D acts as a negative endocrine modulator of the renin-angiotensin-aldosterone system (RAAS) [56][57][58].
An abnormal inflammatory response resulting from SARS-CoV-2 infection is responsible for the development of COVID-19 and, in some cases, for manifestations of increasing severity. The so-called "cytokine storm", characterized by the massive and sustained release of pro-inflammatory cytokines (IL-1, IL-6, TNFα, and IFNγ), is responsible for the symptoms and organ damage (particularly affecting the lungs and heart). In severe COVID-19 cases, IL-6 levels were 2.9 times higher than in cases with less severe disease. This evidence supports the role of vitamin D in reducing cytokine storms by inducing anti-inflammatory mediators (IL-10, IL-4, and TGFβ). Furthermore, 1,25(OH) 2 D can reduce the hyperinflammatory response and, therefore, the manifestations of COVID-19 by enhancing the expression of anti-inflammatory and regulatory phenotypes Th2 and T-reg at the expense of pro-inflammatory Th1/Th17, which is also more prominently involved in the cytokine storm [59].
The results of this study suggest a positive association between vitamin D3 supplementation and the severity and mortality of COVID-19 (a reduction in events by approximately 60% and 50%, respectively), as described by Albergamo et al. [60]. However, its dosage and timing are yet to be determined. A recent randomized trial found that the administration of vitamin D did not affect the severity of COVID-19 [61]. In this trial, a single dose of 200 000 IU vitamin D was administered to hospitalized patients with moderate or severe disease. Whether high-dose bolus or continuous low-dose administration is the preferred regimen remains unclear. In addition, whether patients with only true deficiency (<20 ng/mL) or the whole COVID-19 population should be treated with cholecalciferol is still unknown. Current recommendations suggest treating patients with vitamin D3 insufficiency with daily doses of 400-800 units for up to 3 months [62]. Only those with severe vitamin D3 deficiency (<10 ng/mL) may be offered higher doses; however, in general, higher monthly doses can increase the risk of falls in older adults [63]. NICE has proposed specific guidelines related to vitamin D3 administration during the COVID-19 pandemic. In this document, all adults (including women who are pregnant or breastfeeding), young people, and children older than 4 years should consider taking a daily supplement containing 400 units of vitamin D between October and early March because people do not produce enough vitamin D from sunlight in these months [64].
Other micronutrients or vitamin D agents may also play a role in this disease. In particular, compounds such as vitamin C and zinc may play a role; however, Beran et al. [27] found that vitamin C and zinc might not reduce the mortality or severity of COVID-19.
This study has several limitations. First, we must acknowledge that most of the studies examined were retrospective in nature, and a few made adjustments for common variables (e.g., age and pre-existing chronic diseases). In addition, few randomized controlled trials that are capable of managing confounding factors due to their design are available for supplementation. Additionally, many of the included studies showed publication bias based on Egger's test and a moderate to low quality according to the AMSTAR 2 checklist, leading to the recommendation that researchers follow methodology guidelines to ensure the methodological quality of future meta-analyses. This resulted in the evidence for two associations being downgraded from strong to highly suggestive. When studies with intrinsic bias or low quality were excluded, vitamin D3 levels strongly correlated with COVID-19 mortality. Furthermore, we were unable to perform subgroup analyses due to the absence of data (e.g., sex, age, previous use of vitamin D3, comorbidities, and country of origin).
The following considerations can be made based on the results of these studies. Even if further controlled studies are needed, vitamin D appears to be more effective against COVID-19 (both due to the speed of negativization and the benign evolution of the disease in case of infection) if administered prior to the manifested infection, especially in elderly, frail, and institutionalized subjects. The minimum optimal plasma target of 25(OH)D to be reached in the preventive setting would be ≥30 ng/mL, for which it is necessary to administer high doses of cholecalciferol, also in relation to the basal levels of the patient, up to 4000 IU/day [37,65,66]. With the preventive administration of oral cholecalciferol (up to 4000 IU/day), the use of vitamin D, which, even at high doses, does not present substantial side effects, is useful for correcting a situation of specific general deficiency in the population, especially in winter, regardless of SARS-CoV-2 infection [67]. Additionally, higher parenteral doses of vitamin D3 could have an effect on the final outcome, as bypassing liver vitamin D3 will also be available to CYP11A1 for metabolism in organs expressing this enzyme [68]. In addition to targeting COVID-19 through both nuclear receptor-dependent and-independent mechanisms, new CYP11A1-derived active forms of vitamin D and lumisterol can be used as antiviral drugs and supplements to prevent and attenuate it [69].

Conclusions
In conclusion, the results of the present study support and reaffirm the recommendation for vitamin D3 supplementation as helpful in preventing COVID-19 (particularly for elderly or frail people, housebound individuals, or individuals living in nursing homes and who spend a great deal of their time indoors due to COVID-19), while emphasizing its potential anti-inflammatory and immunomodulatory properties to lessen the severity and mortality of infected individuals. Additionally, this evidence supports the possibility of monitoring vitamin D3 levels, especially in high-risk populations. However, additional research is necessary to determine the optimal dose, timing, and duration of vitamin D3 therapy for infected patients.