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    Topic review

    Vitamin D

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    Submitted by: Ludmila Máčová


    Vitamin D is a micronutrient with pleiotropic effects in humans. Due to sedentary lifestyles and increasing time spent indoors, a growing body of research is revealing that vitamin D deficiency is a global problem. Despite the routine measurement of vitamin D in clinical laboratories and many years of efforts, methods of vitamin D analysis have yet to be standardized and are burdened with significant difficulties. 

    1. Introduction

    Vitamin D is one of the most frequently discussed nutrients in contemporary public and scientific medicine. Thousands of new scientific papers every year demonstrate that the subject is constantly evolving, and the current severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has further increased interest because vitamin D deficiency has been reported as a risk factor for worse courses of coronavirus disease. Experts from around the world are in agreement that vitamin D deficiency is a global health problem, even in areas with adequate year-round sun exposure. This unfavorable situation is further exacerbated by widespread concerns about the harmfulness of sunlight, the use of sunscreens, and the sedentary lifestyle of current societies with a tendency to spend more time indoors.
    Many questions regarding vitamin D have not yet been satisfactorily answered. In addition to calcium/phosphate balance, vitamin D also regulates many other systems in the human body such as the immune, endocrine, cardiovascular, and nervous systems. The vitamin D receptor (VDR) and the enzymes necessary for vitamin D synthesis (specific hydroxylases, epimerases, etc.) have been observed in more than 35 types of cells throughout the human body [1][2], which indicates the pleiotropic effect of vitamin D. Hence, in addition to its well-described function in maintaining calcium/phosphate metabolism, which has been known since 1920s, studies performed over the past 20 years have demonstrated the beneficial role of vitamin D in numerous widespread diseases, including metabolic [3], cardiovascular [4], immune [4], and neuropsychiatric diseases [5][6], as well as cancer [4], the current coronavirus disease [7][8], and other conditions [9]. Though most studies have highlighted the beneficial effects of vitamin D, some studies on this compound have not observed any effects.
    With the expanding number of published studies, awareness of vitamin D is increasing and the need for laboratory testing is rising. Due to vitamin D’s lipophilic nature, tendency to bind to a protein transporter, and extremely low concentrations, its measurement is accompanied by several analytical complications. Here, we discuss several challenges that accompany current clinical and laboratory testing of vitamin D.

    2. Vitamin D Metabolites and Their Clinical Significance

    2.1. Major Vitamin D Metabolites

    Vitamin D metabolism involves a complex network of metabolic processes with more than 50 structurally similar metabolites [10]. In brief, the major metabolic pathways are based on two sources of vitamin D: cholecalciferol (vitamin D3) is produced in the cutaneous tissue of animals, and ergocalciferol (vitamin D2) is synthesized in plants. Both forms first undergo hydroxylation at position 25 to create calcidiol (25(OH)D), which predominantly occurs in the liver. This step is performed by several enzymes from the cytochrome P450 family with 25-hydroxylase activity. To date, at least six enzymes (sterol 27-hydroxylase—CYP27A1, cytochrome P450 3A4—CYP3A4, vitamin D 25-hydroxylase—CYP2R1, cytochrome P450 2C11—CYP2C11, cytochrome P450 2J1—CYP2J1, and vitamin D3 25-hydroxylase—CYP2D25) that possess 25-hydroxylase activity have been identified, as reviewed by Jenkinson [11]. The need for multiple back-up enzymes indicates that the 25-hydroxylation of vitamin D is absolutely crucial for the normal functioning of the human body.
    The second hydroxylation occurs via the action of vitamin D 1α-hydroxylase (CYP27B1) at position 1 to produce calcitriol (1α,25(OH)2D), which predominantly occurs in the kidney. However, other tissues, including the placenta [12], immune cells, enterocytes, prostate cells, and pancreatic cells [13], are known to express CYP27B1 and thereby be involved in the local production of calcitriol. Calcitriol is the only form of vitamin D that is commonly recognized as biologically active, although it is very likely that other metabolites also have calcemic or non-calcemic effects [14]. However, plasma calcitriol only reaches picogram/milliliter concentrations, and its biological half-life is only calculated in hours, which reflects the activity of 1α-hydroxylase in the kidney.
    Currently, the measurement of total 25(OH)D is considered to be more clinically relevant for monitoring vitamin D supply in patients. Calcidiol is a major derivative of vitamin D, occurs in plasma at concentrations that are thousands of times higher than those of calcitriol, has a biological half-life of dozens of days, and generally better reflects vitamin D saturation in an organism.

    2.2. Vitamin D Epimers

    All major metabolites of vitamin D can be irreversibly converted by an epimerase at their C3 position in a reaction that occurs in the liver, bone, or skin cells [15]. The exact source and biological activity of the epimers have not yet been identified, but a higher proportion of C3-epimers (up to 61.1% of the total vitamin D) has been detected in mothers and newborns [16][17]. These observations indicate the importance of epimers in pregnancy and early development. The weak correlation between maternal and neonatal 3-epi-25(OH)D3 suggests that C3-epimers have an endogenous fetal origin rather than a maternal one [18].
    C3-epimers of vitamin D also have plausible roles in inflammatory diseases, as significantly lower concentrations of these alternative serum metabolites have been observed in patients with rheumatoid and reactive arthritis [19]. Other studies have revealed the calcemic regulatory effect of 3-epi-1α,25(OH)2D3, but this effect has been less pronounced than that of its non-epimeric form [20]. However, in some cases, 3-epimers have displayed equal or even stronger activity relative to their non-epimeric counterparts [10][15].
    After the discovery of C3-epimers, an epimer in the C1 position was accidentally revealed during the optimization of a chromatographic method. The co-eluting isobar was identified as 1β,25(OH)2D3 and appeared with a median value of 10.56 pg/mL in the serum of healthy volunteers [21]. The origin of C1-epimers is unclear, but the C1-β-hydroxylation of other compounds is predicted to occur in humans. Similarly, Wang et al. fortuitously identified 4β,25(OH)2D3 as a novel substance that co-eluted with commonly investigated metabolites at concentrations similar to those of 1,25(OH)2D3 [22].

    2.3. Catabolites of Vitamin D

    Vitamin D is inactivated by a multistep pathway catalyzed by vitamin D 24-hydroxylase (CYP24A1). This enzyme has been detected in various target tissues, including the placenta [23], brain [24], kidneys, intestines, and bone [25]. Both 25(OH)D3 and 1,25(OH)2D3 are initially hydroxylated at C24 or C23, followed by C24-oxidation and C23-oxidation pathways that lead to their excretory products, namely calcitroic acid and 1α,25(OH)2D3-26,23-lactone, respectively [26]. Though lactones are primarily catabolic products, and they have biological functions in bone resorption. Interestingly, 24-oxo metabolites were observed to be significantly more potent bone-resorbing agents than lactones, which suggests that conversion to lactones represents a substantial inactivation step, whereas conversion to 24-oxo-derivatives results in less of a reduction in biological activity [27]. The intermediate 24,25(OH)2D3, which occurs in plasma at concentrations on the order of ng/mL, is the most abundant dihydroxy-vitamin D metabolite in the human circulation [28] and appears to have a physiological role in the repair of bone fractures and the development of growth plates without the involvement of the VDR [29].
    The activity of CYP24A1 determines the rate of degradation and thus the amount of bioactive vitamin D. CYP24A1 is tightly regulated by 1α,25(OH)2D3, plasma calcium, and parathormone. However, its activity also increases with age and in some non-physiological conditions [4]. It is of interest that an increased activity of CYP24A1 has been observed in different cancers [30][31][32], and CYP24A1 has been identified as a proto-oncogene [33][34].

    2.4. Conjugates of Vitamin D

    Conjugation is a mechanism that changes the solubility of compounds, which alters their biological activity and the probability of their elimination from the organism. Sulfation is performed by the enzyme sulfotransferase (SULT), and this process was thoroughly described, inter alia, for steroidal dehydroepiandrosterone and its sulfate [35]. Vitamin D and its metabolites are typically converted by the subtype SULT2A1, and the rate of sulfation is associated with the gene variant encoding the enzyme [36]. 25(OH)D3-3-sulfate, with a mean concentration of 16.7 ng/mL, was identified as the most abundant sulfated form of vitamin D in serum, with levels often exceeding those of unconjugated 25(OH)D3 [37]. Other vitamin D sulfates (25(OH)D2-sulfate and vitamins D2- and D3-sulfate) were detected in human serum (on the order of 0.2–0.6 ng/mL) [38] but not in urine, which raised the hypothesis that these sulfate metabolites serve as 25(OH)D3 reservoirs [36] and are secreted via bile.
    Glucuronidation is another conjugation process for vitamin D and its metabolites, and it is mediated by UDP-glucuronosyltransferases (UGT). The most abundant glucuronide of vitamin D in the circulation is 25(OH)D3-glucuronide, which reaches average concentrations of 1.36–2.4 ng/mL [39][40]. On the contrary, one of the major urinary vitamin D3 metabolites in humans is 24,25(OH)2D3-glucuronide (detected in plasma at extremely low concentrations of up to 120 ng/mL), which corresponds to 52.8 ± 19.3 ng/g creatinine [41].

    2.5. Rare and Predicted Vitamin D Metabolites

    New metabolites of vitamin D are constantly being revealed with the extensive development of advanced analytical technologies that provide the ability to both characterize the exact stereo-chemical structure and detect concentrations in picograms or even femtograms per milliliter. In some cases, such metabolites have been discovered by chance, such as the previously mentioned epimers 1β,25(OH)2D3 and 4β,25(OH)2D3. The biological functions of these substances are yet to be discovered, although some of their hormonal functions have been demonstrated in animal models or in vitro.
    Furthermore, there is a large group of vitamin D metabolites that has not yet been detected in the human circulation; this is strongly predicted to be the case based on the current knowledge of enzymatic and physiological processes. A recently published extensive review by Tuckey et al. provided an illustrative overview [10].

    2.6. Free Vitamin D

    According to the free hormone hypothesis established for steroid and thyroid hormones, only unbound or weakly bound fractions of hormones are considered to be “bioavailable.” Because of the lipophilic character of vitamin D, 85–90% of circulating hormones are tightly bound to a carrier protein (vitamin D binding protein (DBP)), 10–15% are weakly bound to albumin, and less than 0.1% circulates in the unbound form [42][43]. In addition to facilitating circulatory transport, DBP also protects bound vitamin D metabolites from rapid renal excretion. These metabolites are also preferably used by the aforementioned conjugates [36].
    The importance of measuring the free fraction of vitamin D has been re-evaluated several times [44][45]. Studies have shown that the measurement of total vitamin D is not sufficient for evaluating the status of this nutrient in patients, and the determination of free vitamin D has been confirmed to be beneficial, at least under certain conditions [46][47].

    2.7. Vitamin D Supply and Absorption

    Vitamin D supplementation is often necessary due to the insufficient synthesis of vitamin D in the skin after exposure to ultraviolet B radiation. Therefore, a growing body of interest in the absorption and metabolism of orally ingested vitamin D supplements has been observed. Until recently, vitamin D was thought to be absorbed by a simple passive diffusion process, but recent studies revealed that these are more likely mechanisms involving membrane carriers. Both ergocalciferol and cholecalciferol are rapidly absorbed after oral intake, with the maximum level detected 24 h after administration. Plasma concentrations of 25(OH)D also increase, with the highest levels achieved after approximately 7–14 days, depending on the dose of vitamin D administered [48]. Moreover, 25(OH)D has been reported to be better absorbed than the non-hydroxy vitamin D forms—cholecalciferol and ergocalciferol [49].

    2.8. Physiological and Clinical Significance of Vitamin D Metabolites—A Review

    Even though over 50 different vitamin D metabolites have been described so far, which enables us to speak of a whole vitamin D metabolome, only 1α,25(OH)2D has been generally recognized as biologically active. By consensus, the determination of total 25(OH)D has been used to evaluate the vitamin D supply. The physiological effects of other metabolites are only considered potential, as their roles in vivo remain unrecognized. C-3 epimers of vitamin D are the exception for which a weak calcemic and immunomodulatory effect has been demonstrated and whose ratio to total circulating vitamin D is a promising tool for predicting disease status such as type 1 diabetes, rheumatoid arthritis, and Alzheimer disease [50]. The 24,25(OH)2D to total 25(OH)D ratio is used as a marker for vitamin D catabolism and as a predictor of response to vitamin D supplementation [51]. Relatively high serum levels of 25(OH)D-3-sulfate and the ability to be converted to unconjugated 25(OH)D suggest its role as a reservoir of unconjugated forms. On the contrary, conjugated glucuronides, which predominate in urine, serve to monitor vitamin D excretion. In addition, the determination of a number of vitamin D metabolites may be useful in identifying possible genetic polymorphisms and variations, especially when the mutation does not cause a disease or an apparent phenotype [10].

    3. Vitamin D Determination

    Though the measurement of vitamin D is predominantly performed on blood samples obtained by venipuncture in clinical practice (for diagnostic/therapeutic purposes), for research purposes, vitamin D is measured in other biological matrices, such as urine [41], tissues [52][53], tissue culture cells, umbilical cord blood [54][55][56], finger-prick blood [57], amniotic fluid [58][59], breastmilk [38], and synovial fluid [19]. Table 1 lists vitamin D metabolites that have been detected in different biological matrices in a wide concentration range from a few picograms to dozens of nanograms per milliliter of liquid sample.
    Table 1. Normal ranges of vitamin D metabolites in various biological matrices.
    Matrix Analyte Method Average Concentration Reference
    AF 25(OH)D3 LC–MS/MS 0.4–3.2 ng/mL [59]
    24,25(OH)2D3 RIA 0.017–0.225 ng/mL [58]
    1,25(OH)2D3 RIA 4.3–24.3 ng/mL [58]
    Breast milk D3-S LC–MS/MS 99.28–109.52 pg/mL [38]
    25(OH)D3 LC–MS/MS 32.04–37.56 pg/mL [38]
    CSF Total 25(OH)D RIA 2.0–24.8 ng/mL [60]
    Total 24,25(OH)2D RIA 0.3–4.6 ng/mL [60]
    Total 1,25(OH)2D RIA 2.2–39 pg/mL [60]
    Serum/plasma 25(OH)D3 LC–MS/MS 30–80 ng/mL [61]
    25(OH)D2 LC–MS/MS 0.62–5.63 ng/mL [62]
    3-epi-25(OH)D3 (infant) LC–MS/MS 0–92 ng/mL [63]
    3-epi-25(OH)D3 (pediatric) LC–MS/MS 0–3 ng/mL [63]
    3-epi-25(OH)D3 (adult) LC–MS/MS 0–9 ng/mL [63]
    24,25-(OH)2D3 LC–MS/MS 2–8 ng/mL [61]
    1α,25(OH)2D3 LC–MS/MS 31–72 pg/mL [21]
    1β,25(OH)2D3 LC–MS/MS 3–19 pg/mL [21]
    D2-S LC–MS/MS 0.192–0.203 ng/mL [38]
    D3-S LC–MS/MS 0.267–0.296 ng/mL [38]
    25(OH)D2-S LC–MS/MS 0.566–0.613 ng/mL [38]
    25(OH)D3-S LC–MS/MS 4.115–4.200 ng/mL [38]
    Synovial fluid 3epi-25(OH)D3 LC–MS/MS 0.832–1.59 ng/mL [19]
    Umbilical cord blood 25(OH)D RIA 6.1–12.7 ng/mL [56]
    24,25(OH)2D3 RIA 0.14–1.66 ng/mL [58]
    1,25(OH)2D3 RIA 10.65–47.78 pg/mL [58]
    Urine 25(OH)D3 LC–MS/MS 3.6–25.2 ng/g creatinine [41]
    24,25(OH)2D3 LC–MS/MS 11.7–83.2 ng/g creatinine [41]
    Due to the vitamin’s extremely low circulating concentrations, lipophilic properties, VDBP binding, and other matrix interactions, the measurement of vitamin D in biological samples requires pre-analytical treatment to reduce the adverse effects of the matrix. Different methods and conditions are used for sample preparation prior to vitamin D analysis, but the most common techniques are protein precipitation (PP), liquid–liquid extraction (LLE), solid-phase extraction (SPE), or their combination, as summarized in Table 2.
    Table 2. Variations in vitamin D extraction.
    Matrix (Amount/Assay) PP Extraction Method Stationary Phase Reference
    Plasma and urine MeCN SPE Sep-Pak C18 cartridges   NP Silica [64] *
    Plasma (0.5 mL) EtOH n-hexane/CH2Cl2 (90:10, v/v) HPLC–UV/VIS C18 [65]
    Serum (0.5 mL) EtOH isopropanol/MeOH (1:9, v/v) n-hexane HPLC–UV/VIS C18 [66]
    Animal/human plasma (1.5 mL) EtOH + MeOH
    KOH +ASC
    heptane HPLC–UV/VIS C30 [67]
    Serum (0.25 mL) EtOH n-hexane Sephadex LH-20 fractionation ID-LC–MS/MS C4 and C18 (CN resp.) [68]
    Serum (ca. 2 g) EtOH hexane/EA (50:50, v/v) ID-LC–MS/MS CN [69]
    Plasma (0.2 mL) EtOH n-hexane HPLC–UV/VIS C18 and C30 [70]
    Serum (0.1 mL) EtOH MTBE LC–MS/MS F5 [71]
    Serum (50 µL)   SLE–TICE (AC Extraction Plate) LC–MS/MS F5 [72]
    Dried blood spot (ca. 6 µL) MeOH   LC–MS/MS (deriv. by DAPTAD) F5 [73]
    Dried blood spot (ca. 3 µL) MeCN EA/CH2Cl2 (1/3, v/v) LC–MS/MS (deriv. by INC) F5 [57]
    In the last two decades, the determination of circulating vitamin D has become a standard routine examination in biochemical laboratories. In general, vitamin D measurement methods can be divided into two main approaches: methods based on immunoassays (CLIA, ECLIA, RIA, and ELISA) and chromatographic methods (HPLC and LC–MS).

    3.1. Immunoassays

    Due to the advantages of automation and rapid results, immunoanalytical methods are the most frequently used techniques for vitamin D measurement in clinical laboratories. The disadvantages of these methods are the non-specificity of the used antibodies and significant interference. As a result of these limitations, most of these methods are not able to quantify individual forms of vitamin D. The cross-reactivity between similar metabolites can be a source of inaccuracies that lower the specificity of the method. It follows that the quality of the used antibody defines the quality of the assay. Furthermore, some of these methods designed for vitamin D measurement are based on the use of DBP, which binds a number of vitamin D metabolites with different affinities. A comparison of different methods used in different laboratories showed that assays produced significantly dissimilar results, indicating that the measurement of vitamin D supply is a function of the laboratory [74].

    3.2. Chromatographic Methods

    The general advantage of chromatographic methods is their ability to efficiently separate and quantify structurally similar metabolites. However, these techniques are also burdened with certain limitations and have their own drawbacks, especially the complex technical equipment and the time-consuming preparation and evaluation of samples.
    Initially, chromatographic methods for vitamin D measurement combined thin-layer chromatography (TLC) with gas chromatography (GC) [75]. Several years later, high-performance liquid chromatography with ultraviolet detection (HPLC–UV/VIS) was introduced [76]. Currently, with the advanced development of analytical methods, LC–MS/MS is accepted as an alternative method, especially in research laboratories. Though a number of promising approaches for vitamin D measurement have been reported, this challenge remains unresolved. An overview of available mass spectrometry assays, in which the authors compared techniques such as the type of chromatographic column, mobile phases, type of ionization, and use of derivatization, was recently published [77].
    Due to the picogram (in mL) amounts of some vitamin D analytes, derivatization techniques are often employed to increase the ionization efficiency and analytical sensitivity of the methods. In general, three types of approaches are currently used to improve the ionization of vitamin D metabolites. A significant group comprises methodologies that use Cookson-type reagents (also known as dienophiles), which include 1,2,4-triazoline-3,5-dione (TAD), 4-phenyl-1,2,4-triazole-3,5-dione (PTAD), substituted TAD (DMEQ-TAD, DAPTAD, Ampliflex Diene, and SecoSET. Several dienophiles improve sensitivity by 10–100-fold and enable detection at the picogram/microliter range in 25 microliter samples. However, an important feature of tagging with a dienophile is that two adduct peaks are formed when the reagent attacks the molecule from either plane of the cis-triene [78]. Another type of method involves 2-nitrosopyridine (PyrNO) and other functionalized nitroso compounds that improve ionization and lead to even higher sensitivity than PTAD [79]. Both previously mentioned derivatization techniques target the s-cis-diene structure of the vitamin D molecule to create Diels–Alder adducts. The last type of approach involves the acylation of the C3-hydroxyl of the vitamin D molecule with isonicotinoyl chloride (INC) [57]. Using this derivatization method, the authors observed no isomer interference and an improvement in the detection sensitivity of 200–1000-fold, which enabled the quantification of the most challenging metabolites at concentrations as low as 1 ng/mL, even in finger-prick blood samples (3 µL of plasma).

    3.3. Standardization

    The Vitamin D External Quality Assessment Scheme (DEQAS) was launched in London in 1989 with the aim of ensuring the analytical reliability of assays. The initial focus was 25(OH)D, followed by the inclusion of 1,25(OH)2D in 1992. A pilot scheme for 24,25(OH)2D was launched in 2015, and the evaluation of results of free 25(OH)D were added in October 2019.
    To standardize the laboratory measurement of vitamin D status, the US National Institutes of Health (NIH) Office of Dietary Supplements established the Vitamin D Standardization Program (VDSP) in 2010. Since then, the VDSP, in cooperation with the National Institute of Standards and Technology (NIST), Ghent University Reference Measurement Procedures, and the United States Centers for Disease Control and Prevention (CDC), has developed a reference measurement system to establish the international standardization of 25(OH)D measurement [68][69][80]. In 2015, the NIST developed a reference measurement procedure for the determination of (24R),25(OH)2D3 in human serum using isotope-dilution LC–MS/MS [81].
    For the validation of in-house methods, the NIST released Standard Reference Materials® (SRMs) with NIST-certified values. SRMs can be used as “trueness” controls of vitamin D assays, e.g., SRM 972a, or as calibrators (SRM 2972). The VDSP has also developed protocols for calibrating previous measurements of 25(OH)D to the current gold standard reference measurement procedures [82][83]. Due to the considerable difference in results before and after standardization, experts from the VDSP strongly recommend suspending the publication of meta-analyses based on unstandardized 25(OH)D data [84].
    Since October 2012, the NIST and VDSP have worked closely with the DEQAS by using the reference measurement procedure to analyze quarterly serum sample sets and assign an accuracy-based target value for total serum 25(OH)D. In 2017, the DEQAS switched to CDC for target value assessment [85].
    According to the recent reports of the DEQAS, over 1000 participants from 56 countries were involved in this external quality testing, in which 30 different methods or their variants were used. Despite 10 years of standardization efforts, the measurement of vitamin D still faces problems with cross-reactivity and matrix effects, e.g., the presence of triglycerides [86] or biotin [87]. In 2018, the difference between results from the NIST and tested participants still varied by up to 23.7%. However, the bias of LC–MS/MS methods was much lower than that of antibody-based 25(OH)D methods [87].
    The US NIST and the NIH also established the Vitamin D Metabolites Quality Assurance Program (VitDQAP), which was used to perform an inter-laboratory comparison of vitamin D evaluation methods in human serum and plasma and to assess measurements made via in-house methods. This program was concluded in 2015, and since 2017, some of the VitDQAP functions have been served through the NIST Health Assessment Measurements Quality Assurance Program (HAMQAP) [88].
    Other systems for the external quality assessment of vitamin D measurement—such as the German Reference Institute for Bioanalytics (RfB) or the Czech equivalent, SEKK—are used in Europe. According to the latest published report (August 2020), luminescence methods are still the most frequently used to determine both total 25(OH)D and 25(OH)D3 alone. The coefficient of variation between laboratories was found to range from 5 to 35% in individual groups, depending on the used analytical method [89].

    The entry is from 10.3390/nu13061758


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