Functional

Night blindness results when the vitamin A pool in the eye becomes depleted, and the concentration in the rod cells is lowered. Many countries have a specific term in local languages for this symptom of deficiency. Night blindness that is due to vitamin A deficiency is reversible with increased vitamin A intake or supplementation. In countries where marginal vitamin A status is prevalent, night blindness may occur during pregnancy. Whether this is due to increased demands during pregnancy or lowered serum retinol concentrations because of plasma volume increases is not entirely known.

Although night blindness is typically used as a population indicator of vitamin A status, impaired dark adaptation has been used to evaluate intervention studies (5, 6). Specifically, dark adaptation measured by the pupillary threshold in Nepali women with night blindness improved when liver, fortified rice, amaranth leaves, carrots, or retinyl palmitate were consumed for 6 wk (5). Such improvement may be further enhanced with iron and riboflavin supplementation (6). The vision restoration time or adaptation under dark conditions has also been used to evaluate vitamin A depletion in groups. Zinc supplementation sometimes synergistically improves the vision restoration time (7).

Retinoyl beta-glucuronide hydrolysis test and RBP:prealbumin measurements

Two biochemical methods that have not been widely applied include the retinoyl β-glucuronide (RAG) hydrolysis test (21, 22) and RBP:prealbumin measurements (23). Both of these methods were established in the rat model (21–23) and applied to humans (22–25). The RAG hydrolysis test is a response test in which a dose of RAG is given, and the change in the retinoic acid concentration is measured in the serum. The retinoic acid response is expected to be greater in individuals with poorer vitamin A status. Doses of 25, 50, and 75 mg RAG have been piloted in Indian children aged 3–18 y old (25). Elevated retinoic acid concentrations were observed in children whose serum retinol concentrations were <0.85 μmol/L. The advantages of this test compared with serum retinol concentrations corrected for the degree of infection or inflammation will need to be further investigated. The RBP:prealbumin method is a static measure and may have utility in groups of humans with a high degree of infection or inflammation. Measurements have been done in Zambian children with measles (23), children from Papua New Guinea, and Bangladeshi surgical patients (24). In the Bangladeshi surgical patients, a cutoff ≤0.36 for RBP:prealbumin was associated with vitamin A deficiency defined as <0.07 μmol retinol/g liver (24).

Dose-response tests

The dose-response tests work on the principle that RBP accumulates as vitamin A liver reserves become low. In rats that were fed a vitamin A–deficient diet, apo-RBP accumulated in the liver before serum retinol concentrations decreased, and the liver was depleted (32). Thus, when a challenge dose of retinyl or 3,4-didehydroretinyl ester is administered, the retinol or 3,4-didehydroretinol binds to this accumulated RBP and is rapidly released into the serum. The relative-dose-response (RDR) test was originally applied to a rat model (33). When applied in the field today, 1 mg retinyl ester is administered dissolved in oil (8). Two blood samples are collected (ie, one sample at baseline and another sample 5 h after dosing). The RDR value, which is expressed as a percentage, is calculated as

where A₅ is the serum retinol concentration at 5 h postdosing, and A₀ is the serum retinol concentration at baseline. If the percentage difference is >20%, the individual likely has deficient liver reserves.

Although the RDR test is a useful indicator, the test is somewhat invasive because it requires 2 blood samples from the same individual ≈5 h apart. An accurate RDR value is dependent on correct analysis and consistent retinol recovery from both serum samples. Therefore, the modified RDR (MRDR) test was developed in rats (34–36) and applied to humans in the United States (36, 37) and Indonesia (38). The test was further refined to make it more field friendly by establishing standard test doses and suggesting a range of response times to obtain the blood sample (39). The test works on the same principle as the RDR test, but because the 3,4-didehydroretinol analog is administered instead of retinol, a single blood sample can be taken. HPLC easily separates 3,4-didehydroretinol from retinol in the same sample. Endogenous concentrations of 3,4-didehydroretinol are quite low in humans ,and therefore, the baseline blood sample is not needed. A distinguishing response between depleted and sufficient liver reserves can be measured in ≥4 h and has been validated in rats and piglets against liver vitamin A reserves (34–36, 40) and compared with the RDR test in children (8). After the serum sample is analyzed, the molar ratio of 3,4-didehydroretinol to retinol is calculated, which is sometimes referred to as the MRDR value. A cutoff of 3,4-didehydroretinol to retinol ≥0.060 usually signifies low liver reserves of retinol that can be corrected with vitamin A supplements (15, 41).

The MRDR test has been applied in several countries to evaluate interventions and the prevalence of low liver reserves in surveys. One of the first comparisons was done in preschool-age children in Indonesia (8). In the first group, the distribution of values approached a normal distribution, and most children were vitamin A adequate. A child in the first group who had an MRDR value of 0.18 had just moved into the area. In the second group of children, MRDR values were quite disparate and reached a value of 0.83 in one female subject. An informal dietary interview in the community revealed that the first group of children ate a significant amount of eggs. Eggs provide a highly bioavailable source of preformed retinol and, thus, can make a measurable difference in the vitamin A status of children if consumed regularly.

The application of the MRDR test in a study of the combined treatment of vitamin A supplements and albendazole for deworming children infected with Ascaris lumbricoides showed a significant improvement in the mean (±SD) value of 0.055 ± 0.042 before supplementation to a value of 0.033 ± 0.017 after supplementation (P < 0.0001) (15). This magnitude of difference was not seen with serum retinol concentrations. In another evaluative study of children with helminthic infections, the MRDR test correctly identified children that had received a vitamin A supplement from the local health post (41). MRDR values were 0.021 ± 0.012 and 0.054 ± 0.038 in the children who had and had not received the supplement, respectively. Serum retinol concentrations did not differ between children who had received the supplement and children who had not, and the serum retinol concentrations did not respond to treatment.

The MRDR test has been used in a variety of countries to evaluate population status. It gives more information than serum retinol concentrations alone. For example, in a group of rural lactating women in Ghana, baseline serum retinol concentrations and MRDR values were 1.4 ± 0.5 μmol/L and 0.048 ± 0.037, respectively (18). After treatment with either 210 or 420 μmol retinyl ester, a significant improvement in vitamin A status occurred as assessed by the MRDR test (P < 0.0001), but serum retinol concentrations did not differ (P = 0.87). Furthermore, in an urban group of Ghanaian lactating women, the baseline serum retinol concentration was 1.5 ± 0.6 μmol/L, and the MRDR value was 0.09 ± 0.05 (19), which indicated a much poorer vitamin A status than in the rural women even though serum retinol concentrations were identical. After an intervention with indigenous African green leaves, serum retinol concentrations did not change or differ during the study (P ≥ 0.41), but the MRDR test improved within the intervention group (P = 0.0001). These results contradicted a simulated analysis in which the difference shown in MRDR values was proposed to occur because of underlying different serum retinol concentrations between groups (42).

Even in the United States, vitamin A status can be poor especially in low-income groups. Specifically, in children who qualified for the Special Supplemental Nutrition Program for Women, Infants, and Children, 32% of children were in the uncertain area for MRDR values, which was defined as 0.030–0.060 (43). This result was in contrast to that in children with a generally higher economic status in the United States where the mean MRDR value was 0.019 ± 0.010 in 22 children tested 2–10 h after an oral dose of 3,4-didehydroretinyl acetate (37). Only 2 children tested >0.030 at 4 and 6 h after the dose, which was within the recommended time interval for the test sample to be taken (39). Furthermore, an assessment of low-income pregnant women showed that an alarming 9% were above the international MRDR value cutoff of 0.060 (44). Serum carotenoid concentrations were also analyzed in these low-income women and children. In some cases, serum β-carotene concentrations were not detectable, which indicated that vegetable consumption was likely very low (43, 44).

Although the MRDR test is very useful to evaluate a deficient through normal vitamin A status, as currently applied, it does not have utility in defining the subtoxic and toxic range of liver reserves. Nonetheless, the magnitude of the ratio is related to liver reserves. When data from several piglet studies were combined (40, 45–47), liver reserves <17 μg vitamin A/g liver (0.06 μmol vitamin A/g liver) were exclusively associated with an MRDR value ≥0.060 (Figure 4). Liver reserves from 0.06 to 0.1 μmol vitamin A/g liver were scattered above and below the MRDR cutoff, and liver values >0.1 μmol vitamin A/g liver were almost invariably associated with MRDR values <0.060. From these data by using the MRDR test and data obtained in rats in which the down-regulation of lecithin:retinol acyltransferase, which is responsible for retinol esterification, occurred at the same liver concentration (48), we propose that 0.1 μmol vitamin A/g liver should signify vitamin A deficiency instead of the current cutoff of 0.07 μmol vitamin A/g liver. If liver reserves illicit a biological response to a vitamin A challenge dose, the vitamin A status is not in equilibrium, and the individual should be considered at risk of vitamin A deficiency.

Retinol isotope dilution

The most sensitive biomarker of vitamin A status to liver reserves of vitamin A is isotope dilution testing (31, 49). The most widely used isotope test uses deuterated retinyl acetate as the tracer. ¹³C-retinyl acetate has been used as the tracer in rats (20), rhesus monkeys (50), and humans for the assessment of vitamin A status (51). The difference in practice is the type of equipment used for the analysis. The deuterated retinol test uses conventional gas chromatography–mass spectrometry (GC-MS), whereas the ¹³C-retinol test uses gas chromatography-combustion-isotope ratio mass spectrometry (GCCIRMS). GC-MS analysis requires the formation of the tert-butyldimethylsilyl derivative before injection into the gas chromatograph, whereas the GCCIRMS does not. GC-MS with electron-capture negative chemical ionization detection increased the sensitivity of the method (52, 53), but ¹³C-retinol with GCCIRMS requires a smaller dose to trace total body stores (50, 54).

All methods that calculate total body stores of vitamin A use the same fundamental mass-balance equation (55) as follows:

where a refers to the amount of dose absorbed and stored (experimentally determined to be 0.5–0.8 of the dose administered), b represents baseline reserves of vitamin A, c = a + b = total postdose reserves of vitamin A, and F = R ÷ (R + 1), where R is¹³C:¹²C. Various adaptations of this equation have been used to reflect the unique metabolism of vitamin A (49, 50).

Paired-isotope dilution tests to evaluate baseline and follow-up liver reserves have been used to determine changes in total-body vitamin A reserves in response to an intervention (56, 57). Examples of this included the estimation of relative vitamin A equivalency factors (58) and assessment of the effect of different intakes of vitamin A on calculations of total body reserves (59) and effects of supplementation on liver stores (53, 60). Vitamin A supplementation and abrupt changes in dietary intakes may result in the exaggeration of liver reserves or affect value estimates with the test (53, 59). With the use of a graded supplementation strategy, paired-isotope dilution testing predicted that higher intakes of vitamin A were needed to maintain a higher total-body vitamin A pool size (60). Thus, vitamin A utilization and requirements vary based on the amount of vitamin A contained in the body.

The ¹³C-retinol dilution test has been validated in rats against liver reserves with an r = 0.98 (20). When the atom percentage excess was evaluated at 3 different intakes of vitamin A supplementation at 4 time intervals after isotope dosage, none of the relations overlapped, which showed the robustness of the test to assess differences in liver vitamin A reserves. This test required very small doses of the isotope tracer, and thus, vitamin A trafficking was not perturbed. After the rat study, the test was applied to rhesus monkeys (50) that were known to have hypervitaminosis A based on liver-reserve analysis in monkeys from the same colony (61). Measured compared with predicted liver reserves in these monkeys revealed a linear relation, and all monkeys were diagnosed as having hypervitaminosis A by the predicted values (50). The ¹³C-retinol dilution test has been applied to humans.

A recent application of ¹³C-retinol analysis by GCCIRMS was to evaluate the compliance to a high vegetable intake (62). Plant foods have different enrichments of ¹³C depending on whether they are C4 or C3 plants, the former which contains higher amounts of ¹³C (63). Most vegetables consumed in the United States are C3 plants and therefore have less ¹³C than C4 plants such as maize. The shift in natural abundance of ¹³C in retinol was used as a biomarker of the formation of retinol from the β-carotene consumed in the diet. The provided diet was high in pumpkin, carrots, and spinach, which are all C3 plants. Indeed, the group that received more vegetables during the intervention had a lower enrichment of ¹³C in the purified retinol from their serum (62).

Although isotope dilution testing is usually too expensive to consider as a means to evaluate a program, an evaluation of a sugar-fortification program was performed in a small group of Nicaraguan children (64). The baseline mean liver retinol concentration was 0.57 μmol retinol/g liver, which was well above what is currently considered deficient (0.07 μmol retinol/g liver). All children had serum retinol concentrations between 0.74 and 1.31 μmol/L. One year after the sugar fortification was implemented, the estimated liver reserve concentration increased to an average of 1.2 μmol retinol/g liver. In 9 of 21 children, liver vitamin A concentrations were calculated to be >1.05 μmol vitamin A/g liver after fortification, which was defined as toxic in 1990 (65). Because many foods are being considered for fortification, this sensitive methodology may have to be used because no other method except a liver biopsy is able to diagnose hypervitaminosis A.

Considering the validation in monkeys and these results in children, an isotope methodology can be useful in defining the hypervitaminotic range of liver reserves. Specifically, liver reserves >10 μmol vitamin A/g were quantified (50). Thus, a question mark that vitamin A experts published in 2004 in relation to the upper useful limit for isotope dilution can now be replaced with the value of 10 μmol vitamin A/g liver (Figure 3) in 2010. However, a paucity of data exists in humans regarding the ramifications of a subtoxic or toxic vitamin A status. In 1990, excessive liver reserves were defined as 0.70–1.05 μmol vitamin A/g liver, and toxic status was defined as ≥1.05 μmol vitamin A/g in humans (65). However, after fortification of sugar with vitamin A in Nicaragua, many of the children had liver reserves greater than this range. The liver vitamin A concentration at which ill health in humans occurs needs to be examined more carefully. Are there ramifications of having a liver reserve that hovers at ≈1 μmol vitamin A/g liver, or is the human body able to sequester this concentration in the liver? Considering the degree of fortification in some developing countries, the improvements in the stability of fortificants used in formulations and the high consumption of some of these fortified foods, an additional examination of toxicity or hypervitaminosis A needs to occur. For example, in the study performed in hypervitaminotic rhesus monkeys, lactate dehydrogenase, aspartate aminotransferase, and serum albumin were elevated in 50%, 19%, and 44% of the monkeys, respectively (50). Elevations of these enzymes are markers of liver disease or malfunction (66) and may be a vitamin A–toxicity outcome (67, 68). The key questions are as follows: Should we be concerned about vitamin A toxicity in countries with a high degree of fortification? Or is the alleviation of vitamin A deficiency more important than the potential ramifications from hypervitaminosis A?

The author has been working on vitamin A assessment methodology for most of her research career and received no financial gain from these activities apart from research grants, travel reimbursement, and speaker honoraria.