Vitamin A equivalency of β-carotene (VEB) is defined as the amount of ingested β-carotene in μg that is absorbed and converted into 1 μg retinol (vitamin A) in the human body. A certain amount of the ingested β-carotene is excreted in the faeces and the remaining part is absorbed, but not all of the absorbed β-carotene will be converted into retinol and enter the lymph, blood and finally the liver and other tissues.
Vitamin A can be obtained from animal-derived foods as preformed vitamin A, or from vegetables and fruits as provitamin A carotenoids, mainly β-carotene, α-carotene and β-cryptoxanthin. In the Western diet, about 20 to 34 % of the habitual intake of vitamin A originates from provitamin A carotenoids( 1 – Reference Waijers and Feskens 3 ). In contrast, the majority of individuals in developing countries require >70 % of provitamin A carotenoids in the diet( 4 ). The effect of food matrices of vegetables and fruits in which β-carotene is incorporated has been found to exert a major influence on measured VEB.
The objective of the present review was to discuss the different estimates for VEB in various types of dietary food matrices. The question is which VEB should be used for humans in general good health.
For this purpose, first, the currently used VEB are described. Second, a brief overview of the main influencing factors on the assessment of VEB is given. Third, the habitual daily intake of dietary vitamin A and β-carotene in humans is described. Fourth, different methods for estimating VEB are discussed to evaluate the reliability of the different studies. The studies are grouped by the different types of dietary food matrices in which β-carotene is incorporated, which are the oil matrix, the complex mixed diet matrix with various vegetables and fruits and the single vegetable or fruit matrix.
Currently used vitamin A equivalency of β-carotene
Currently, two estimates of VEB for the oil matrix and two estimates of VEB in the mixed diet matrix are in use. In the 1967 recommendation of the FAO/WHO, the estimated VEB in the oil matrix was 3·3:1, so 3·3 μg β-carotene dissolved in oil would be required in the diet to produce 1 μg retinol in the human body( 5 ). According to the 1967 and 1988 recommendations of the FAO/WHO( 2 , 5 ), the VEB for a mixed vegetable diet was estimated to be 6:1 and for other provitamin A carotenoids as 12:1. This VEB of 6:1 for a mixed diet is referred to as the retinol equivalents and is used in many food composition tables. The revised food composition tables have used the retinol activity equivalents, which is a VEB of 12:1 for a mixed diet and 24:1 for other provitamin A carotenoids( 1 ). The term ‘retinol activity equivalents’ was introduced by the US Institute of Medicine (IOM)( 1 ). The IOM adopted a two-step process: first, examining VEB in oil, and then examining the absorption of β-carotene in vegetable foods relative to that of β-carotene dissolved in oil. The revised VEB of 12:1 for a mixed plant diet was calculated from the products of 1/2 (the intestinal conversion factor of β-carotene in oil) and 1/6 (the relative absorption of β-carotene in a mixed plant diet). The intestinal conversion factor of β-carotene in oil should be interpreted as 2 μg absorbed β-carotene in the enterocyte that is equivalent to 1 μg retinol in the human body, as has been reported in classical studies( Reference Blomstrand and Werner 6 , Reference Goodman, Huang and Shiratori 7 ).
In the 2004 report of the FAO/WHO, the committee retained the VEB of 6:1 for a mixed diet and emphasised that the conditions that prevent carotenoids from entering enterocytes, such as the food matrix, are more significant than previously thought, and that more data might support an even lower VEB for a mixed diet( 4 ).
Main influencing factors on the assessment of vitamin A equivalency of β-carotene
There are many diet-related and host-related factors that may affect VEB. The main diet-related factors that influence VEB in humans are the food matrix in which β-carotene is incorporated, the amount ingested and the habitual diet type( Reference Yeum and Russell 8 , Reference van Het Hof, West and Weststrate 9 ). The rupture of the food matrix by heating and homogenising promotes the release of β-carotene from plant cells before and during digestion, and therefore it facilitates solubilisation into mixed lipid micelles in the lumen and cellular uptake by intestinal mucosal cells( Reference Castenmiller, West and Linssen 10 ). Cell wall structure in fruits is usually weaker than that in leaves, and therefore VEB for fruits deviates from that for vegetables( Reference De Pee, West and Permaesih 11 ).
VEB may be regarded as constant as long as the consumption of β-carotene is within physiological ranges and the host is in good health. With pharmaceutical doses of β-carotene, serum β-carotene levels increase, and VEB can decrease when an oral dose of β-carotene increases( 2 , Reference Novotny, Harrison and Pawlosky 12 , Reference West and Castenmiller 13 ). The habitual diet type determines the composition of the diet, and therefore various nutrient-to-nutrient interactions affect to a larger extent the absorption of β-carotene. For example, β-carotene absorption can be inhibited by lutein( Reference van Het Hof, Brouwer and West 14 , Reference Van den Berg and Van Vliet 15 ), when a minimum amount of about 5 g dietary fat is consumed simultaneously in a meal to ensure intestinal β-carotene uptake( Reference Roodenburg, Leenen and van Het Hof 16 ). Also, absorption of β-carotene is reduced when dietary fibre content increases. Fibre interacts with bile acids, resulting in decreased absorption of fats and fat-soluble substances such as β-carotene( Reference Hoffmann, Linseisen and Riedl 17 ).
Host-related factors, such as age, pregnancy, health status, immune status and treatment for worms and diarrhoea, can also affect VEB( 18 , Reference Jalal, Nesheim and Agus 19 ). Intestinal helminthic infections are associated with malnutrition, and their effects are possibly mediated through impaired fat absorption and reduced vitamin absorption, particularly vitamin A( 18 , Reference Jalal, Nesheim and Agus 19 ). Micronutrient malabsorption detected during intestinal parasitic infections is not easily explained or investigated, and may be caused by injury to the intestinal mucosa without invasion, mucosal invasion by parasites or bacterial overgrowth in the upper small bowel( Reference Hesham, Edariah and Norhayati 20 ). These host-related factors could have more influence on populations in developing countries than on populations in Western countries, where public health care is well organised and, in general, persons are in good health. Another host-related factor is the recently described polymorphism in the β,β-carotene 15,15′-mono-oxygenase (BCMO1) gene coding for the enzyme that cleaves β-carotene( Reference Leung, Hessel and Meplan 21 , Reference Lietz, Oxley and Leung 22 ). Studies have identified low responders who showed little or no response to plasma β-carotene concentration after a labelled dose of β-carotene( Reference Lin, Dueker and Burri 23 – Reference Wang, Yin and Zhao 25 ). The large inter-individual differences for estimates of VEB might be due to reduced enzymatic activity as a consequence of down-regulated activity of BCMO1 or polymorphisms in the BCMO1 gene. However, in none of the studies discussed below were the genetic polymorphisms analysed, as the importance of BCMO1 was only recently realised; therefore, VEB may be more efficient than currently proposed.
The currently used VEB in a mixed diet and in oil are applicable only for individuals in general good health.
Habitual daily intake of vitamin A and β-carotene in human subjects
A Western type of diet, consumed by most people in developed countries, is relatively high in animal-derived foods (meat and dairy products), processed foods, fats and oils, and refined grains but relatively low in dietary fibres (vegetables, fruits and whole grains)( Reference Fung, Willett and Stampfer 26 , Reference Hu, Rimm and Smith-Warner 27 ). Milk and dairy products contribute 15 to 20 % to total vitamin A intake. In the Western diet, about 66 to 80 % of the habitual intake for vitamin A is preformed vitamin A in the diet, and 20 to 34 % of intake is from provitamin A carotenoids( 1 – Reference Waijers and Feskens 3 ). By assuming that at least 50 % of provitamin A carotenoids are β-carotene, dietary β-carotene contributes for at least 10 to 17 % in the Western diet to daily dietary vitamin A activity.
In contrast, the diet for most people living in developing countries contains only about 12 to 22 % of preformed vitamin A, and consequently, they require 78 to 88 % of provitamin A carotenoids in the diet( 4 ). By assuming that at least 50 % of provitamin A carotenoids are β-carotene, dietary β-carotene contributes for at least 39 to 44 % in the diet to daily dietary vitamin A activity in developing countries. Many people residing in developing countries consume the ‘prudent’ diet type, which is high in fresh fruits and vegetables and whole grains (e.g. rice, maize), and low in meat( Reference Fung, Willett and Stampfer 26 , Reference Hu, Rimm and Smith-Warner 27 ). Overall, adults in the USA and Europe have a total vitamin A intake of 700–1000 μg retinol equivalents/d, and those in Southeast Asia and Africa have a total vitamin A intake of 400–800 μg retinol equivalents/d, which is particularly low in animal sources( 4 ). For populations that are highly dependent for their vitamin A status on the consumption of vegetables and fruits, it is important to have available the correct VEB values in various food matrices to be able to choose vegetables and fruits with the highest β-carotene amount and the highest VEB to maintain or increase their vitamin A status.
Methods
In the past decades, various methods have been used for determination of VEB. Over the years, the chemical analyses of blood, lymph and faeces have been optimised, resulting in higher recoveries of internal standards and better reproducibility within and between samples. Many studies have been performed by measuring serum or plasma β-carotene and retinol levels after a single meal (dose–response) or after a period of depletion and/or repletion. By measuring β-carotene levels in the faeces during a controlled diet, oral–faecal mass balance can be investigated. More recently, progress in the analysis of radio- and stable isotopes in blood has made possible the application of isotopic dilution methods. Extrinsic labelling involves mixing an exact dose of isotopically labelled β-carotene into a food source. The great advantage of using isotope-labelled β-carotene is that only relatively small physiological doses need to be used to follow metabolic pathways such as true absorption and conversion into retinol by discriminating between absorbed and endogenous β-carotene. Table 1 shows the major strengths and major limitations of the methods used to study VEB in human subjects as discussed below.
Table 1 Overview of the methods used to study vitamin A equivalency of β-carotene in human subjects with their major strengths and major limitations
Depletion–repletion method
Studies of depletion and repletion responses using a dark adaptation endpoint have been published by Hume & Krebs( Reference Hume and Krebs 28 ) and Sauberlich et al. ( Reference Sauberlich, Hodges and Wallace 29 ). During consumption of a vitamin A-deficient diet, subjects developed impaired dark adaptation (depletion phase). In the repletion phase of the study, the amount of retinol or β-carotene that was required to reverse the impaired dark adaptation was estimated. Such experiments are not allowed anymore because of medical ethical reasons. Moreover, the method provides only crude estimates because stepwise increased doses of β-carotene are tested. However, these experiments were the first attempts to assess VEB in oil, and they still influence the current recommendations.
Animal models
Animal models may be very useful for studying qualitative problems, but they have limited use for studying quantitative processes that represent the situation in human subjects. There is no validated way to extrapolate animal data to physiological conditions in human subjects. Monkeys, gerbils and preruminant calves convert β-carotene into vitamin A with an efficiency comparable to that of humans. However, in humans, β-carotene is mainly transported in the LDL fraction and many animals, such as ferrets and calves, have a retinyl ester metabolism different from that in humans, resulting in high levels of fasting plasma retinyl esters. Mice, rats, ferrets and chickens efficiently convert β-carotene into vitamin A, but absorb β-carotene intact only when it is provided in the diet at levels much higher than is considered physiological for humans. Not one animal model completely mimics human absorption and metabolism of β-carotene and therefore cannot be used to study the VEB in human subjects( Reference Lee, Boileau and Boileau 30 – Reference Krinsky, Mathews-Roth and Welankiwar 32 ).
In vitro models
Results from in vitro models cannot be translated to the human situation, but can provide some predictions. For example, the available time for food processing can be influenced by various food matrices and different levels of enzymes and pH simulating infant or adult situations, as these factors influence the transit time and competition for absorption( Reference Yeum and Russell 8 , Reference van Het Hof, West and Weststrate 9 ). An in vitro gastrointestinal model can precisely measure the bioaccessible fraction, which is available for absorption by measuring β-carotene in mixed micelles in different prepared meals of vegetable foods. Measurements in isolated human intestinal epithelial cells provide estimates of the conversion of β-carotene into retinol under various conditions.
Mass balance method
In the mass balance method, the apparent β-carotene absorption is estimated as the difference between controlled β-carotene intake and faecal β-carotene excretion over a period of time. On the one hand, data obtained from the oral–faecal mass balance method might be overestimated because of (bacterial) degradation of carotenoids in the gut and incomplete faecal collection. On the other hand, endogenously secreted carotenoids may be excreted in the faeces, thus leading to underestimation of the absorption of dietary carotenoids. Faecal collection studies in ileostomy subjects have the advantage of excluding the possible effect of bacterial degradation or even synthesis of β-carotene in the colon, resulting in less overestimation of absorption in human subjects with an intact gut( Reference Van Loo-Bouwman, Naber and van Breemen 33 – Reference Livny, Reifen and Levy 37 ). In spite of these limitations, oral–faecal mass balance studies may yield reasonable measurements of apparent intestinal β-carotene absorption. Together with the assumption of the FAO/WHO and IOM that half the absorbed amount of β-carotene in the intestine is converted into retinol, an acceptable estimate of VEB can be obtained using the mass balance method( Reference Van Loo-Bouwman, Naber and van Breemen 33 ).
Dose–response method
Many dose–response studies have been conducted with β-carotene by measuring the blood level response over time after consuming a certain amount of β-carotene (for a review, see Swanson et al. ( Reference Swanson, Wang and Goodman 38 )). The most commonly applied methods have included the measurement of the increase in serum or plasma β-carotene levels following chronic intervention, and the calculation of the AUC using the curves of total responses v. time following a single dose of β-carotene( Reference Parker, Swanson and You 39 ). The concentration of β-carotene in serum or plasma represents a balance between intestinal absorption, breakdown, tissue uptake and release from body stores. The disadvantage of these studies is the homeostatic control of serum or plasma retinol concentrations. However, change from baseline serum or plasma β-carotene concentration can be useful as an endpoint to estimate the relative absorption of β-carotene in human subjects, provided such studies are sufficiently long to result in a new steady-state condition. Only dose–response studies with an (isotopic) reference dose can directly measure a VEB.
Retinyl ester response method
As the liver does not secrete retinyl esters, except when its storage capacity is saturated, newly absorbed and converted β-carotene can be measured by determining retinyl esters in chylomicrons. The advantage of the retinyl ester response method over the serum/plasma response method is that it accounts for intestinal conversion of β-carotene into retinyl esters. Consequently, it is theoretically possible to assess the VEB by measuring the retinyl ester response in postprandial blood. However, in practice, this is generally not feasible because of the low instantaneous concentration of chylomicron retinyl esters, the relatively low sensitivity of direct determination of retinyl ester concentration by HPLC, and the presence of large quantities of other lipids in extracted plasma or serum. In some studies, postprandial chylomicron β-carotene or retinyl ester response has been measured with a single oral dose of β-carotene( Reference O'Neill and Thurnham 40 – Reference Johnson and Russell 42 ). Also, two earlier lymph recovery studies were carried out in subjects with lymph cannulation( Reference Blomstrand and Werner 6 , Reference Goodman, Huang and Shiratori 7 ).
Interpretation of postprandial response curves of β-carotene and retinol esters in TAG-rich lipoprotein (TRL) data is limited by the lack of means to control for inter-individual variations in in vivo chylomicron clearance kinetics or variations in chylomicron recovery during the preparation and analysis of TRL. Consequently, use of this approach is generally restricted to comparative (between-treatment) studies, because it does not directly measure the VEB.
Retinyl ester response method with isotopes
Edwards et al. ( Reference Edwards, You and Swanson 43 , Reference Edwards, Nguyen and You 44 ) adapted the TRL response model and co-administered [2H4]retinyl acetate as an extrinsically isotope-labelled reference standard. This extrinsic reference dose controls for variations in chylomicron kinetics in vivo and for retinyl ester recovery during the preparation and analysis of TRL. The sensitivity and reproducibility of the detection of β-carotene in the plasma chylomicron fraction should be optimised before this approach can deliver reliable estimates of VEB( Reference van Lieshout, West and van Breemen 45 ).
Extrinsic radioisotopic labelling method
The radioisotope tracer method requires a compartment model to interpret the increasing tracer curves after ingesting a single dose or constant infusion by assuming that the body is in endogenous constant steady state. Isotopic tracer techniques can provide accurate estimates of VEB with high precision, thus enabling studies with a limited number of subjects. The isotopic enrichment of labelled β-carotene in serum or plasma is corrected for the amount of labelled β-carotene consumed after some hours or days. By using isotope-labelled β-carotene, the measurement can distinguish between recently absorbed and endogenous β-carotene. Radioisotopes have been used only occasionally( Reference Blomstrand and Werner 6 , Reference Goodman, Huang and Shiratori 7 , Reference Dueker, Lin and Buchholz 46 , Reference Ho, de Moura and Kim 47 ) because of potential radiation damage.
Extrinsic stable isotope labelling method
In the past two decades, the availability of stable isotope-labelled compounds increased and, their analyses were improved. The use of stable isotopes in research is safe for human subjects and accepted by institutional review boards. The stable isotope tracer dilution method consists of administering an oral single or multiple doses, collection of a blood sample, measurement of the plasma or serum isotopic ratio of tracer:tracee (unlabelled vitamin A), and the use of a prediction equation for calculation of the bioavailability of β-carotene or VEB. Isotopic dilution techniques can also be used to estimate the total amount of vitamin A in the body, which has been described in the review of Furr et al. ( Reference Furr, Green and Haskell 48 ).
Presently, over thirty studies have been conducted using stable isotope tracer techniques for studying the bioavailability of β-carotene and VEB in human subjects. Because of their design, some studies could only provide qualitative data, and some other studies were performed with a limited number of subjects. Since the early 1990 s, it was possible to follow absorption and biokinetics of labelled β-carotene or retinol after a single dose( Reference Parker, Swanson and Marmor 49 – Reference Novotny, Dueker and Zech 51 ). Over 20 years ago, Parker et al. ( Reference Parker, Swanson and Marmor 49 ) pointed out the necessity of stable isotope tracer methods for studying VEB in human subjects. The commonly used assumption is that the absorbed labelled β-carotene and retinyl palmitate are secreted and cleared with approximately the same kinetics as the unlabelled carotenoids and retinyl esters in the diet. Interpretation of data and mathematics from single-dose labelling studies are more complicated than those from multiple-dose labelling studies in which a plateau of isotopic enrichment is measured far above the threshold limit( Reference van Lieshout, West and van Breemen 45 ).
Intrinsic isotopic labelling method
Intrinsically labelled vegetables can be produced by irrigating with 2H-labelled water or by supplying 13CO2 in a closed atmosphere( Reference Grusak 52 ). The advantage of the use of intrinsically labelled vegetables is that it is not necessary to assume that the labelled compound behaves in the same way as the unlabelled compound. To date, the following intrinsically isotope-labelled vegetables have been produced: biofortified yellow maize( Reference Muzhingi, Gadaga and Siwela 53 ); biofortified ‘Golden Rice’( Reference Tang, Hu and Yin 54 , Reference Tang, Qin and Dolnikowski 55 ); carrot( Reference Ghavami, Coward and Bluck 56 – Reference Putzbach, Krucker and Albert 58 ); spinach( Reference Tang, Hu and Yin 54 , Reference Tang, Qin and Dolnikowski 57 – Reference Lienau, Glaser and Tang 59 ); collard greens( Reference Lienau, Glaser and Tang 59 ); kale( Reference Novotny, Kurilich and Britz 60 , Reference Kurilich, Britz and Clevidence 61 ); tomato( Reference Tang, Ferreira and Grusak 62 ). Because these specially produced vegetables are very expensive, few subjects could participate and only one simple single meal was measured. With this intrinsic labelling method, accurate data of VEB can be expected for specific vegetables and for human subjects with diverse nutritional status. However, data of VEB for a complex mixed diet with various vegetables and fruits are not yet available using the intrinsic labelling method.
Summary of studies
By comparing data from the aforementioned studies, the method and the three main factors that influence VEB in humans (the food matrix, the amount ingested and the habitual diet type) should be mentioned. The present review focuses on the influence of the food matrix on VEB and distinguishes the results by the different types of dietary food matrices of β-carotene, which are the oil matrix, the complex mixed diet matrix with various vegetables and fruits and the single vegetable or fruit matrix.
The majority of the data that the IOM reconsidered in 2001 were obtained from children and adults in developing countries with an inadequate nutritional status and their own habitual dietary patterns. The minority of the studies that IOM reviewed were obtained from subjects in developed countries with an adequate nutritional status, consuming a Western diet. Additional studies, especially those using stable isotopes, have been published since then (see Tables 2–4).
Table 2 Overview of the studies with unlabelled and extrinsically isotope-labelled β-carotene in oil to quantify vitamin A equivalency of β-carotene in oil
NA, not available; TRL, TAG-rich lipoprotein.
* The ‘prudent’ diet type is high in fresh fruits and vegetables and whole grains (e.g. rice, maize), and low in meat.
Table 3 Overview of the studies with unlabelled β-carotene in a mixed diet from multiple vegetables and fruits to quantify vitamin A equivalency of β-carotene in a mixed plant diet
NA, not available.
* The ‘prudent’ diet type is high in fresh fruits and vegetables and whole grains (e.g. rice, maize), and low in meat.
† Due to the relatively high weight of total 72 h faecal collection.
Table 4 Overview of the studies with unlabelled or extrinsically isotope-labelled or intrinsically isotope-labelled β-carotene in a diet from a single vegetable or fruit to quantify vitamin A equivalency of β-carotene in a single vegetable or fruit
TRL, TAG-rich lipoprotein; NA, not available.
* The ‘prudent’ diet type is high in fresh fruits and vegetables and whole grains (e.g. rice, maize), and low in meat.
Oil matrix: β-carotene dissolved in oil
Overall, eighteen studies are presented in Table 2, of which four( Reference Hume and Krebs 28 , Reference Sauberlich, Hodges and Wallace 29 , Reference Li, Nugroho and Rochford 63 , Reference Liu, Zhou and Sanchez 64 ) measured the VEB in oil with unlabelled β-carotene and fourteen( Reference Wang, Yin and Zhao 25 , Reference Van Loo-Bouwman, Naber and van Breemen 33 , Reference Tang, Hu and Yin 54 , Reference Tang, Qin and Dolnikowski 65 – Reference Van Loo-Bouwman, West and van Breemen 73 ) with labelled β-carotene. Of these studies, two had a depletion–repletion study design( Reference Hume and Krebs 28 , Reference Sauberlich, Hodges and Wallace 29 ). In the Sheffield experiment during the Second World War, Hume & Krebs( Reference Hume and Krebs 28 ) compared the amount of β-carotene with the amount of retinol required to reverse and prevent abnormal dark adaptation. Only two subjects achieved abnormal dark adaptation or correction of abnormal dark adaptation with β-carotene. Data for these two responding subjects suggested a VEB of 3·8:1 based on the observation that 390 μg retinol or 1500 μg β-carotene reversed abnormal dark adaptation. Many years later, a study with six subjects was performed with a validated method to confirm impaired visual function in response to vitamin A depletion( Reference Sauberlich, Hodges and Wallace 29 ). The VEB was determined to be 2:1, meaning that 600 μg retinol/d or 1200 μg β-carotene/d corrected dark adaptation. This latter study was considered by the IOM to be the more reliable VEB for β-carotene dissolved in oil( 1 ).
Furthermore, two other studies have measured the VEB in oil with a dose–response study design by calculating the AUC for retinyl palmitate in the TRL fraction( Reference Li, Nugroho and Rochford 63 , Reference Liu, Zhou and Sanchez 64 ). Both studies were designed to measure the VEB in biofortified maize porridge and biofortified cassava porridge. Also, the VEB of the reference dose of β-carotene in oil was measured, resulting in 2·3:1 and 2·1:1. However, although these results were obtained from a small group of subjects, they confirm the IOM recommendation of 2:1 for VEB in oil( 1 ).
The fourteen reported VEB measured with labelled β-carotene in oil, presented in Table 2, have a wide range from 2·0:1( Reference Tang, Hu and Yin 54 ) (healthy children) to 55:1( Reference Tang, Qin and Dolnikowski 65 ) (in one female adult after a pharmaceutical dose of 126 mg β-carotene). In this latter study, a VEB of 3·8:1 was obtained after a labelled dose of 6 mg β-carotene given to the same female subject over 21 d( Reference Tang, Qin and Dolnikowski 65 ). In another study in one male adult, the VEB was 15·9:1 after a very high dose of 16·2 mg β-carotene over 23 d( Reference Hickenbottom, Lemke and Dueker 69 ). These large variations in VEB stress the importance of carrying out experiments to measure VEB using physiological doses of β-carotene.
In four labelling studies that were performed in school children, a VEB ranging from 2·0:1 to 3·2:1 was reported. In two studies in children with adequate vitamin A status in Indonesia, low retinol diets containing daily amounts of [13C10]β-carotene and [13C10]retinol were consumed( Reference van Lieshout and West 66 , Reference van Lieshout, West, Wang and van Lieshout 67 ). From measurements in plasma of the plateau enrichment of retinol with [13C10]retinol and [13C5]retinol, the VEB in oil was found on average to be 2·4:1 in a 10-week study( Reference van Lieshout and West 66 )and 2·7:1 in a 3-week study( Reference van Lieshout, West, Wang and van Lieshout 67 ). The other two studies with children were performed in China( Reference Tang, Hu and Yin 54 , Reference Li, Wang and Wu 72 ). In one study in China carried out on twenty-three healthy children over 21 d, the VEB was quantified as 2·0:1( Reference Tang, Hu and Yin 54 ). The other study in China carried out over 28 d reported a VEB of 2·9:1 for a group of eight healthy children and a VEB of 3·2:1 for a group of eight vitamin A-deficient children( Reference Li, Wang and Wu 72 ).
In six labelling studies that were performed in adults, VEB values ranging from 3·4:1 to 9·1:1 were reported, which are less efficient than the reported VEB values for school children. Of these studies, two used a single dose of stable isotope-labelled [2H8]β-carotene in ‘corn’ oil with [2H8]retinol as a reference dose in well-nourished adults aged 55–60 years over 56 d with a low β-carotene diet( Reference Tang, Qin and Dolnikowski 70 , Reference Wang, Yin and Zhao 25 ). The average VEB was 9·1:1 in twenty-two adults in the USA( Reference Tang, Qin and Dolnikowski 70 ) and 9·1:1 in eleven rural Chinese adults with a diet of limited amounts of animal foods( Reference Wang, Yin and Zhao 25 ). Haskell et al. ( Reference Haskell, Jamil and Hassan 71 ) reported an estimated VEB in oil of 6·3:1 for synthetic β-carotene in fourteen young men in Bangladesh. In one short-term study, the VEB was quantified to be 5·7:1 in red palm oil after 8·5 h of a [2H8]retinyl acetate dose administered to twelve adults( Reference You, Parker and Swanson 68 ). In two diet-controlled studies conducted in The Netherlands, a VEB of 3·4:1 was quantified in twenty-four healthy young adults( Reference Van Loo-Bouwman, West and van Breemen 73 ) and a VEB of 3·6:1 in seventeen ileostomy subjects( Reference Van Loo-Bouwman, Naber and van Breemen 33 ) using the same dual-isotope dilution technique as used by van Lieshout et al. ( Reference van Lieshout and West 66 , Reference van Lieshout, West, Wang and van Lieshout 67 ).
In conclusion, at low physiological doses, a VEB in oil of approximately 3:1 was obtained; however, at very high doses, the VEB decreases, as already mentioned in the introduction.
Vegetable matrix: β-carotene in a diet with multiple vegetables and fruits
Table 3 presents five diet-controlled studies with a duration of 2 to 10 weeks with multiple vegetables and fruits. The study design of the study in school children in Indonesia( Reference De Pee, West and Permaesih 11 ) and of the study in breast-feeding women in Vietnam( Reference Khan, West and de Pee 74 ) were similar and comprised four dietary groups: low-retinol, low-carotenoid (negative control); dark-green leafy vegetables (also carrots in the Indonesian study); yellow and orange fruits; a retinol-containing diet (positive control). The increase in serum retinol concentrations was measured over the 9 to 10 weeks, mainly the diet-controlled period. For the dark-green leafy vegetables, the VEB was estimated to be 26:1 in the Indonesian study( Reference De Pee, West and Permaesih 11 ) and 28:1 in the Vietnamese study( Reference Khan, West and de Pee 74 ), while for the fruits, it was 12:1 in both studies. In an intervention study in Chinese kindergarten school children, a VEB of 27:1 was calculated for a diet with green and yellow vegetables( Reference Tang, Gu and Hu 75 ). In two completely diet-controlled studies in The Netherlands with a diet containing β-carotene-rich vegetables, a VEB of 15·7:1 was obtained in twenty-four healthy young adults( Reference Van Loo-Bouwman, West and van Breemen 73 ) and a VEB of 12·5:1 in seventeen ileostomy subjects( Reference Van Loo-Bouwman, Naber and van Breemen 33 ). The same two studies crossed-over with another controlled diet for 2 to 3 weeks. That diet contained β-carotene-poor vegetables and fruits with consumption of food items fortified with β-carotene and/or β-carotene supplements, such as those regularly consumed in industrialised societies. For this complex β-carotene supplemented and vegetable matrix, the VEB was found to be 5·4:1( Reference Van Loo-Bouwman, West and van Breemen 73 ) and 6·7:1( Reference Van Loo-Bouwman, Naber and van Breemen 33 ).
In conclusion, the seven reported VEB for a diet with multiple vegetables are lower than the IOM recommendation of 12:1 for VEB in a mixed plant diet. For the fruit matrix, the VEB of 12:1 is realistic.
Vegetable matrix: β-carotene in a single vegetable or fruit matrix
Of the thirteen studies presented in Table 4, three were performed with a single unlabelled vegetable by measuring the TRL response over 9 h in women. A study with maize porridge determined a VEB of 6·48:1( Reference Li, Nugroho and Rochford 63 ). A study with biofortified cassava porridge in Colombia reported a VEB of 2·80:1( Reference Liu, Zhou and Sanchez 64 ). Another study with biofortified cassava porridge in the USA determined a VEB of 4·2:1 when provided with added oil and a VEB of 4·5:1 when provided without added oil( Reference La Frano, Woodhouse and Burnett 76 ).
Overall, three β-carotene-labelled studies, which used [2H4] retinyl acetate as the reference dose, are presented in Table 4. Parker et al. ( Reference Parker, Swanson and You 39 ) reported a VEB of 13:1 for raw carrot in one adult. Edwards et al. ( Reference Edwards, You and Swanson 43 ) estimated a VEB of 23:1 for raw carrot as well as raw spinach in three adults. A study with daily supplementation of Indian spinach and sweet potato in fourteen Bangladeshi men for 60 d quantified VEB values of 9·5:1 and 13·4:1, respectively( Reference Haskell, Jamil and Hassan 71 ).
In total, seven studies have been published, which quantified the VEB for intrinsically labelled spinach, carrot, maize or Golden Rice (see Table 4). Tang et al. ( Reference Tang, Qin and Dolnikowski 57 ) produced two 2H-labelled vegetables and quantified a VEB of 21:1 for spinach and a VEB of 15:1 for carrot over 36 d compared with [13C8]retinyl acetate as the reference dose. In two Chinese studies with 2H10-labelled spinach, a VEB of 9·0:1 was presented for male adults( Reference Wang, Wang and Wang 77 ), 10·1:1 for healthy school children and 10·3:1 for vitamin A-deficient school children( Reference Li, Wang and Wu 72 ). A 72 h short-term study in the UK in four adults provided an approximate VEB of 77:1 for raw carrot and a VEB of 11·6:1 for the same intrinsically isotope-labelled carrot, but consumed after stir-frying in groundnut oil( Reference Ghavami, Coward and Bluck 56 ). Muzhingi et al. ( Reference Muzhingi, Gadaga and Siwela 53 ) produced 2H-labelled yellow maize β-carotene and determined a VEB of 3·2:1 in eight men. In two studies by Tang et al. ( Reference Tang, Hu and Yin 54 , Reference Tang, Qin and Dolnikowski 55 ), different measured VEB have been reported using intrinsically labelled Golden Rice with high levels of β-carotene that could be explained by the target group and duration of measuring the AUC. The first study( Reference Tang, Qin and Dolnikowski 55 ) determined a VEB of 3·8:1 in five adults in the USA measured over 36 d and the second study( Reference Tang, Hu and Yin 54 ) obtained a VEB of 2·3:1 for twenty-three healthy children in China measured over 21 d. The latter study in twenty-two other healthy Chinese children, a VEB of 7·5:1 was reported for intrinsically labelled spinach( Reference Tang, Hu and Yin 54 ).
In conclusion, the type of the vegetable matrix plays a dominant role in determining the VEB as demonstrated by the VEB reported above. The intrinsic labelling method is very helpful to quantify the values of major vegetables consumed, but it is very time-consuming and expensive and will not directly quantify a value for a mixed vegetable diet.
Discussion
Discussing the methods
In summary, dose–response methods cannot discriminate between absorbed and endogenous β-carotene, while the isotopic labelling methods can discriminate between absorbed and endogenic β-carotene. In small physiological doses, isotopically labelled β-carotene is measurable in blood. Intrinsic isotopic labelling methods provide reliable data on VEB in various plant sources of β-carotene. Stable isotope labelling methods measure the proportion of β-carotene ingested, which is absorbed and converted into vitamin A, but cannot distinguish between the degree of absorption and the degree of conversion. There are methods to measure VEB directly without steps in between. Therefore, in many studies, the absorption of β-carotene from various food matrices is compared with β-carotene in oil. Depletion–repletion studies can provide the VEB dissolved in oil.
In conclusion, as much data as possible should be collected to identify the impact of the three main factors that influence VEB in healthy human subjects: the amount ingested; the habitual diet type; the food matrix in which β-carotene is incorporated. Furthermore, the known polymorphisms in the BCMO1 gene( Reference Leung, Hessel and Meplan 21 , Reference Lietz, Oxley and Leung 22 ) should be measured in the participants for clarification of possible variations in estimates for VEB. Stable isotope labelling studies appear to be the best approach to collect data for large groups (healthy or specific disease) by collection of blood samples after a controlled meal or diet. Validation studies of stable isotope labelling methods are necessary to estimate and understand the reproducibility of data.
Next, we suggest the most appropriate VEB for a Western diet and a ‘prudent’ diet based on current evidence.
Applicability of vitamin A equivalency of β-carotene in an oil matrix for a Western diet and for a ‘prudent’ diet
The current recommendation of the FAO/WHO is 3·3:1 and that of the IOM is 2:1 for VEB in oil. Fortified foods and dietary supplements are available, which contain physiological doses of β-carotene in oil( 2 , 4 ) to complete an inadequate diet pattern. In four studies with unlabelled β-carotene, the IOM recommendation of 2:1 for VEB in oil has been confirmed( Reference Hume and Krebs 28 , Reference Sauberlich, Hodges and Wallace 29 , Reference Li, Nugroho and Rochford 63 , Reference Liu, Zhou and Sanchez 64 ). In seven studies with labelled compounds, a VEB in oil ranging from 3·4:1 to 9·1:1 has been reported in adults, which was less efficient than that reported by the four studies for VEB in oil of 2·0:1 to 3·2:1 in school children. As has already been established( Reference Novotny, Harrison and Pawlosky 12 , Reference Tang, Qin and Dolnikowski 65 ), the studies using higher amounts of ingested β-carotene resulted in higher reported VEB. By only considering the studies with amounts of ingested β-carotene that were lower than 6 mg, a VEB in oil for a Western diet ranged from 2·3:1 to 5·7:1 and for a ‘prudent’ diet from 2:1 to 6·3:1. Furthermore, by only considering the studies with amounts of ingested β-carotene that were lower than 2 mg, a VEB in oil for a Western diet ranged from 2·3:1 to 3·6:1 and for a ‘prudent’ diet from 2:1 to 3·8:1.
For humans consuming β-carotene dissolved in oil, a VEB between 2:1 and 4:1 is feasible in a Western diet as well as in a ‘prudent’ diet. The down-regulation mechanism of the expression of BCMO1 by high doses and genetic polymorphisms in the BCMO1 gene might explain the observed variations in VEB in oil.
Applicability of vitamin A equivalency of β-carotene in the plant matrix for a Western diet and for a ‘prudent’ diet
The current recommendation of the FAO/WHO is 6:1 and that of the IOM is 12:1 for VEB in a mixed diet. Only five studies directly investigated the mixed plant matrix with multiple vegetables, of which three studies reported a VEB of 26:1( Reference De Pee, West and Permaesih 11 ), 27:1( Reference Tang, Gu and Hu 75 ) and 28:1( Reference Khan, West and de Pee 74 ) using a ‘prudent’ diet, and two studies reported a VEB of 15·7:1( Reference Van Loo-Bouwman, West and van Breemen 73 ) and 12·5:1( Reference Van Loo-Bouwman, Naber and van Breemen 33 ) using a Western diet. These three studies were performed in developing countries in children( Reference De Pee, West and Permaesih 11 , Reference Tang, Gu and Hu 75 ) and breast-feeding women( Reference Khan, West and de Pee 74 ), where the subjects may have different health status and nutritional needs from those of healthy adults participating in the two studies with the Western diet( Reference Van Loo-Bouwman, Naber and van Breemen 33 , Reference Van Loo-Bouwman, West and van Breemen 73 ).
To determine which VEB should be used for humans in general good health, all studies with single vegetables and single fruits were considered. Only two studies investigated the fruit matrix and both reported a VEB of 12:1( Reference De Pee, West and Permaesih 11 , Reference Khan, West and de Pee 74 ). In two studies using a fortified Western diet a VEB of 5·4:1 and 6·7:1 was obtained, respectively( Reference Van Loo-Bouwman, Naber and van Breemen 33 , Reference Van Loo-Bouwman, West and van Breemen 73 ). The results of the latter two studies reflect a combination of VEB in oil and VEB in a mixed plant matrix.
The overall VEB of approximately 9:1 for spinach (range 7·5:1–10·3:1) is assumed on the basis of four studies( Reference Grusak 52 , Reference Hickenbottom, Lemke and Dueker 69 , Reference Tang, Qin and Dolnikowski 70 , Reference Khan, West and de Pee 74 ), and excludes two studies with a reported VEB of 23:1( Reference Edwards, You and Swanson 43 ) and 21:1( Reference Tang, Qin and Dolnikowski 57 ) with non-physiological doses of 6 and 11 mg β-carotene, respectively. The overall VEB of approximately 13:1 for carrot (range 11·6:1–14·8:1) is assumed on the basis of three studies( Reference Parker, Swanson and You 39 , Reference Ghavami, Coward and Bluck 56 , Reference Tang, Qin and Dolnikowski 57 ) and excludes the reported VEB of 77:1 in raw carrots( Reference Ghavami, Coward and Bluck 56 ), which were very minimally processed before ingestion. Only one study was performed with sweet potato, which reported a VEB of 13:1( Reference Haskell, Jamil and Hassan 71 ). The overall VEB for three biofortified crops are approximately 4:1 for cassava( Reference Liu, Zhou and Sanchez 64 , Reference Khan, West and de Pee 74 ), approximately 3:1 to approximately 6:1 for yellow maize( Reference Muzhingi, Gadaga and Siwela 53 , Reference Li, Nugroho and Rochford 63 ) and approximately 2·5:1 to approximately 4:1 for Golden Rice( Reference Tang, Hu and Yin 54 , Reference Tang, Qin and Dolnikowski 55 ). A β-carotene-rich alga is available as a food supplement and has a VEB that is similar to that of biofortified crops, namely 4·5:1( Reference Wang, Wang and Wang 78 ). Specially bred cassava, maize and Golden Rice are intended to be consumed in developing countries. Currently, spinach, carrots and sweet potato are widely available for consumption.
So, for the Western diet including a variety of fruits, leafy vegetables such as spinach, and root vegetables such as carrots and sweet potato, a VEB for a mixed diet of 9:1 to 16:1 is feasible.
For a ‘prudent’ diet including a variety of commonly consumed and specially bred vegetables, a VEB for a mixed diet could range from 4:1 to 28:1. These VEB values were obtained from human subjects in apparently normal health in developing countries. Data are not available on VEB in a mixed diet applicable to malnourished children or pregnant women. Furthermore, less favourable host-related factors, such as parasites and gastrointestinal infections, should be taken into account. In addition, individuals in developing countries have a diet relatively low in animal-derived foods, and their diet should contain as much as possible carotenoid-rich vegetables and fruits to maintain or gain adequate vitamin A status.
In conclusion, the proposed range for VEB in a mixed diet of 9:1 to 16:1 includes the IOM VEB of 12:1 and is realistic for a Western diet and Western conditions. For a ‘prudent’ diet including a variety of commonly consumed vegetables, a VEB in a mixed diet could range from 9:1 to 28:1. Large inter-individual variations in the estimates of VEB are reported, possibly due to genetic polymorphisms in the BCMO1 gene and the degree of regulation of the expression of BCMO1 in response to vitamin A status.
Different reported vitamin A equivalency of β-carotene in children and in adults
A closer examination of some studies suggests that there is an indication that children can convert β-carotene into retinol more effectively than adults, as shown by a lower VEB in children than in adults. For instance, four studies used the same dual-isotope dilution technique and quantified a VEB in oil of 2·4:1 and 2·7:1 in children( Reference van Lieshout and West 66 , Reference van Lieshout, West, Wang and van Lieshout 67 ) and a VEB in oil of 3·4:1 and 3·6:1 in adults( Reference Van Loo-Bouwman, Naber and van Breemen 33 , Reference Van Loo-Bouwman, West and van Breemen 73 ). Furthermore, two studies with intrinsically labelled Golden Rice used the single dose–response method and quantified a VEB of 2·3:1 in children( Reference Tang, Hu and Yin 54 ) and a VEB of 3·8:1 in adults( Reference Tang, Qin and Dolnikowski 55 ). As another example, two studies with intrinsically labelled spinach by Tang et al. ( Reference Tang, Qin and Dolnikowski 57 ) used the single dose–response method and quantified a VEB of 7·5:1 in children( Reference Tang, Hu and Yin 54 ) and a VEB of 20·9:1 in adults. However, these different measured VEB values could be explained by the provided doses 1·4 and 11 mg in children and adults, respectively. The VEB of 7·5:1 for spinach in children( Reference Tang, Hu and Yin 54 ) could also be compared with the estimated VEB of 9·5:1 for spinach in adults( Reference Haskell, Jamil and Hassan 71 ) obtained with a multiple dose–response method with a reference dose of labelled retinyl acetate. However, other host-related factors (e.g. health status, immune status, treatment for worms and diarrhoea, BCMO1 expression) could explain the differences in VEB. However, two studies using the same method indicated that the VEB in children is not always higher than that in adults; those studies with intrinsically labelled spinach used the single dose–response method and reported a VEB of 10·1:1 in children( Reference Li, Wang and Wu 72 ) and a VEB of 9·0:1 in adults( Reference Wang, Wang and Wang 77 ). When more studies are performed in children, more precise data will be available for determining whether there should be separate VEB values for children and adults.
Future studies
Studies with isotope-labelled β-carotene in fruits and vegetables in habitual diets, such as the Western diet, measured over a long period have not yet been performed. The intrinsic labelling method could be used to compare labelled β-carotene in plant sources with labelled β-carotene in oil in a common diet to provide an estimate of VEB in a complex mixed total diet. However, as has already been mentioned, the preparations will be very time-consuming and expensive, and a representative target group should be recruited. There is a need for more studies to be carried out in populations in developing countries as well as in Western populations to see whether and to what extent the VEB is influenced by nutritional status, age and other factors that might differ between developed and developing countries, such as genetic variability and polymorphisms in the BCMO1 gene across different ethnic groups.
Future isotopic labelling studies should be carried out to obtain more accurate and precise data for various factors influencing the VEB. Populations in developing countries should consume carotenoid-rich vegetables, which are processed whenever possible for optimal disruption of the food matrix to release β-carotene.
Acknowledgements
We thank Richard B. van Breemen for his critical review of the manuscript.
The present review was funded by the Dutch Dairy Association. The Dutch Dairy Association had no role in the design, analysis or writing of this article.
C. A. V. L.-B. conducted the research, collected the data and wrote the manuscript. T. H. J. N. and G. S. contributed to the interpretation of the study results and the discussion. All authors read and approved the final manuscript.
The authors had no conflicts of interest.
