ORIGINAL RESEARCH article
Sec. Nutritional Epidemiology
Volume 9 - 2022 | https://doi.org/10.3389/fnut.2022.806566
Priority Micronutrient Density in Foods
- 1Knowledge Leadership, Global Alliance for Improved Nutrition, Washington, DC, United States
- 2Department of Environmental Science and Policy, University of California, Davis, Davis, CA, United States
- 3Knowledge Leadership, Global Alliance for Improved Nutrition, Geneva, Switzerland
Background: Despite concerted efforts to improve diet quality and reduce malnutrition, micronutrient deficiencies remain widespread globally, especially in low- and middle-income countries and among population groups with increased needs, where diets are often inadequate in iron, zinc, folate, vitamin A, calcium, and vitamin B12. There is a need to understand the density of these micronutrients and their bioavailability across diverse foods and the suitability of these foods to help meet requirements for populations with high burdens of micronutrient malnutrition.
Objective: We aimed to identify the top food sources of these commonly lacking micronutrients, which are essential for optimal health, to support efforts to reduce micronutrient malnutrition among various populations globally.
Methods: We built an aggregated global food composition database and calculated recommended nutrient intakes for five population groups with varying requirements. An approach was developed to rate foods according to their density in each and all priority micronutrients for various population groups with different nutrient requirements.
Results: We find that the top sources of priority micronutrients are organs, small fish, dark green leafy vegetables, bivalves, crustaceans, goat, beef, eggs, milk, canned fish with bones, mutton, and lamb. Cheese, goat milk, and pork are also good sources, and to a lesser extent, yogurt, fresh fish, pulses, teff, and canned fish without bones.
Conclusion: The results provide insight into which foods to prioritize to fill common micronutrient gaps and reduce undernutrition.
Food is integral to everyday life, providing essential energy and nutrients for human function. An important aspect of food, among others, is the vitamins and minerals it provides. Yet in many low- and middle-income countries (LMICs) diets are known to be lacking in micronutrients, especially for population groups with increased needs, leading to deficiencies, particularly in iron, zinc, folate, vitamin A, calcium, and vitamin B12 (hereafter referred to as “priority micronutrients”), that can have severe and lasting effects (1–6). For example, more than four in five Indian adolescents have a deficiency in one or more micronutrients (7). Even in high-income countries (HICs) like the United States and United Kingdom, micronutrient deficiencies such as iron deficiency are often common, especially among women of reproductive age (WRA) (3, 8). Globally, current diets are failing to provide adequate density of these essential micronutrients. Furthermore, anthropogenic CO2 emissions are reducing iron and zinc concentrations in crops, which highlights the increasing importance of improving dietary nutrient density (9).
There is an urgent need, therefore, to increase the density of priority micronutrients in diets in countries of all incomes. One efficient and cost-effective strategy for reducing micronutrient deficiencies is food fortification (10). However, there are more than 70,000 compounds in foods (11) bound together in a food matrix, which synergistically impact metabolism, including nutrient absorption, and may have beneficial effects on satiety and the immune system, offering protection from disease, among other potentially important health implications (12–15). Thus, fortifying staple foods with priority micronutrients is important but does not fully replicate inherently nutrient-dense foods and their health effects. Obtaining adequate micronutrients from minimally processed foods may have additional benefits beyond fortification due to the added value of diverse synergistic nutrients within a food matrix (12–14). Moreover, while there is large variation in the health effects of different foods and dietary patterns, energy-dense ultra-processed foods (UPFs) in particular are associated with numerous non-communicable diseases (NCDs) and mortality (16). UPFs make up a large share of calories in most high-income countries and are increasing rapidly in most LMICs (16). Energy-dense ultra-processed foods are generally hyper palatable which can lead to overconsumption and weight gain when they are a predominant component of the food environment (17). Improving overall diet quality, especially the quantity and diversity of minimally processed foods inherently dense in priority micronutrients is crucial to reduce micronutrient malnutrition while minimizing the transition to UPFs and potential associated increase in NCDs.
Our study aims to identify the top food sources of commonly lacking micronutrients, which are essential for optimal health, to support efforts to reduce micronutrient malnutrition among various populations globally, particularly in low- and middle-income countries.
Materials and Methods
Recommended Nutrient Intakes
We calculated recommended intakes for adults ≥25 years of age and groups vulnerable to undernutrition, including children 2–4 years, adolescents, non-pregnant and non-lactating WRA, and pregnant women, from the European Food Safety Authority (EFSA) (18) for vitamin A, folate, calcium, and zinc and from the Institute of Medicine (19) for vitamin B12 and iron. This aligns with the recently proposed harmonized nutrient reference values (20), except for iron, because EFSA values are based on the assumption that the population has iron stores, which is not the case for many people in LMICs. We used recommended nutrient intakes rather than average requirements because we are interested in target values for individuals, not in estimating population level adequacy.
Building a Global Food Composition Database
We built a global food composition database (excluding fortified foods), with values for calories, phytate (21), and six priority micronutrients: vitamin A, folate, vitamin B12, calcium, iron, and zinc. Nutrient densities are from USDA FoodData Central (FDC) (22) and national and regional food composition tables (FCTs) from LMICs globally (23): Kenya, Malawi, and Western Africa (Sub-Saharan Africa); Bangladesh, Indonesia, Laos, Vietnam, and ASEAN (South and South-East Asia); Mexico and Colombia (Latin America). These FCTs contained values from analyzed foods. However, for teff, fonio, and small dried fish, we also included values from the literature due to limited availability in FCTs (see Supplementary Material for details).
Foods were aggregated when showing relatively low nutrient density variance (for example, pulses and yogurt) or when likely to be targeted as a food group in policy and programming (for example, DGLVs). Global nutrient values for individual foods were obtained by calculating medians of composite values from the selected FCTs. Composite values were obtained by averaging nutrient values for different cooking methods (and/or raw foods) and/or different cuts of a given food for meat. Global nutrient values for aggregated food groups were obtained by averaging composite values at the regional level and from FDC. Composite values for a given region were obtained by calculating the medians of nutrient values for several individual foods within a food group, available in the selected FCTs corresponding to that region. Standard deviations were calculated for all obtained global nutrient values, as a measure of variability across included FCTs.
We accounted for iron and zinc bioavailability. For iron, foods were classified into one of three levels of iron absorption (20% for ruminant meat, 15% for all other animal-source foods, and 10% for all plant-source foods), based on the proportion of heme to non-heme iron contained (1): 68% heme-iron in ruminant meat, including beef (24–26), goat, and lamb/mutton (26, 27); 39% heme-iron in pork (25, 26, 28–30); 26% heme-iron in chicken (25, 26, 28–30), fish and seafood (25, 28–31), and eggs and dairy (29); and 40% heme-iron in all other meat, including offal (24, 29, 30). Regarding zinc, foods were classified into one of four levels of zinc absorption (44, 35, 30, and 26%), based on the amount of phytate contained in each food in a portion equivalent to one-third of daily mass intake, assuming an energy density of 1.3 kcal/g and considering average requirements for energy for a moderately active WRA (18) (see Supplementary Material for details).
Priority Micronutrient Density Rating
Foods were classified into one of four levels of micronutrient density based on the calories and grams needed to provide one-third (for individual nutrients) or an average of one-third (for the aggregate score) of recommended intakes of vitamin A, folate, vitamin B12, calcium, iron, and zinc. For the aggregate score, the average share of recommended intakes (ASRI) across the six micronutrients (A), for a given quantity of calories and grams (i), of a given food (j), was calculated as:
A similar approach was previously used to identify micronutrient-dense complementary foods for young children (4, 32). Ratings were calculated for different population groups according to the following thresholds for Average Requirements (ARs) of energy for a moderately active individual (18) and hypothetical ARs for mass, assuming an energy density of 1.3 kcal/g [the mean energy density of a minimally processed plant-based, low-fat diet and animal-based, ketogenic diet (33)]:
• Very high: ≤one-sixth of ARs for both energy and mass.
• High: ≤one-third of ARs for both energy and mass and <one-sixth of ARs for either energy or mass.
• Moderate: ≤one-third and >one-sixth of ARs for both energy and mass.
• Low: >one-third of ARs for either energy or mass.
Micronutrient density of milk was classified based solely on ARs for energy, since mass is typically not a limiting factor for liquids. The same energy thresholds as for solid foods were used for very high and low micronutrient density. For high micronutrient density, thresholds were ≤ one-fourth and > one-sixth of ARs for energy. For moderate micronutrient density, thresholds were ≤ one-third and > one-fourth of ARs for energy.
As indicated in the formula for the aggregate score, each micronutrient’s contribution was capped at 100% of recommended intakes, which means that each micronutrient can contribute nothing or up to one-half of the total score (4, 32). To illustrate this, a food containing only two of the six nutrients would provide 100% of recommended intakes of both nutrients, while a food with a perfectly even proportion of recommended intakes across all six nutrients would provide 33.3% of recommended intakes of all six nutrients—each micronutrient thus contributing an equal one-sixth of the total score. This approach ensures that for foods to rate high, they need to be high in at least two micronutrients and that foods with very high densities of individual micronutrients are not rated higher for providing amounts well above recommended intakes or above upper limits.
Recommended Nutrient Intakes
Recommended nutrient intakes vary by population and, for iron and zinc, bioavailability (Table 1). Among groups with roughly similar ARs for energy, recommended nutrient intakes are generally highest for pregnant women, followed by adults, WRA, and adolescents, but there is variability by nutrient. Notably, recommended folate intake for pregnant women is double than for adults, WRA, and adolescents; recommended iron intake for pregnant women is more than triple than for adults, more than double than for adolescents, and more than 50% higher than for WRA. Recommended intakes for vitamin A, vitamin B12, calcium, and zinc vary less across these groups.
Global Food Composition Database
Table 2 shows the compiled global food composition database of 41 individual and aggregate foods, with values for the six priority micronutrients, energy, phytate, and iron and zinc bioavailability (a version of the global food composition database which includes standard deviations is available in Supplementary Table 1). Interestingly, some food groups showed high nutrient density variance across included foods, such as DGLVs, with spinach, amaranth leaves, and cassava leaves having much higher values than lettuce and cabbage (Supplementary Table 4). Similarly, hard cheese (for example, cheddar and aged goat cheese) and fatty fish (for example, herring and mackerel) were more nutrient-dense than soft cheese (for example, cottage cheese) and lean fish (for example, cod and tilapia), respectively (Supplementary Table 6). Other food groups, such as pulses, presented more equal nutrient density distributions across foods, but there were significant differences across FCTs (Supplementary Tables 2–7). For instance, Sub-Saharan Africa and South/South-East Asia showed much lower values for folate in pulses than Latin America and FDC, which may be due to different varieties, culinary traditions, and cooking methods and times.
Aggregate Micronutrient Density Scores for Women of Reproductive Age
We emphasize the results for WRA in the main text because they are the largest population group, >1.8 billion globally, that is at increased risk for micronutrient malnutrition. The quantity of calories and grams required to provide an average of one-third of recommended intakes for WRA of vitamin A, folate, vitamin B12, calcium, iron, and zinc varies widely by food (Figure 1). Foods with very high aggregate micronutrient density for WRA include organs (liver, spleen, kidney, and heart from beef, goat, lamb, chicken, and pork), small dried fish, DGLVs, bivalves (clams, mussels, and oysters), crustaceans, goat, beef, eggs, milk, canned fish with bones, lamb/mutton, and cheese. Foods with a high aggregate micronutrient density include goat milk and pork. Foods with a moderate aggregate micronutrient density include yogurt, fresh fish (including different species of marine and freshwater fish), pulses, and teff. All other foods included in the analysis scored as having low aggregate micronutrient density for WRA.
Figure 1. Calories and grams needed to provide an average of one-third of recommended intakes of vitamin A, folate, vitamin B12, calcium, iron, and zinc for women of reproductive age. Each micronutrient’s contribution is capped at 100% of recommended intakes. Hypothetical average requirements for mass are based on an energy density of 1.3 kcal/g. AR, average requirement; Vit, vitamin.
Individual Micronutrient Density Scores for Women of Reproductive Age
Bivalves are the only food to contain at least a moderate density of all six micronutrients for WRA—they contained a very high density (hereafter referred to as “top sources”) of all micronutrients except for folate, for which they contain a moderate density (Figure 2). Most animal-source foods and DGLVs were top sources of two or more micronutrients. All foods contained at least a moderate density of at least one of the six micronutrients except for other vegetables; roots, tubers, and plantains; nuts; and refined grain products.
Figure 2. Aggregate and individual micronutrient density scores for women of reproductive age. prod, products; veg, vegetables.
Top iron sources included organs, bivalves, small dried fish, goat, and teff, each providing one-third of recommended iron intakes with less than one-sixth of ARs for energy and hypothetical ARs for mass (Figures 2, 3). Top zinc sources included organs, bivalves, crustaceans, goat, beef, eggs, canned fish with bones, lamb/mutton, cheese, and pork (Figure 2). Top vitamin A sources included liver (including beef, goat, lamb, chicken, and pork liver), small dried fish, DGLVs, bivalves, eggs, cow milk, cheese, and vitamin A-rich fruits and vegetables. Top calcium sources included small dried fish, DGLVs, bivalves, cow milk, canned fish with bones, cheese, goat milk, and yogurt. Top folate sources included liver, DGLVs, eggs, pulses, and quinoa. Finally, top vitamin B12 sources included organs, small dried fish, bivalves, crustaceans, ruminant meat, eggs, milk, cheese, canned fish, pork, yogurt, and fresh fish.
Figure 3. Calories and grams needed to provide one-third of recommended iron intakes for women of reproductive age. Hypothetical average requirements for mass are based on an energy density of 1.3 kcal/g. AR, average requirement; Vit, vitamin.
Aggregate Micronutrient Density Scores for Other Population Groups
Micronutrient density scores may vary depending on the population, given differences in recommended nutrient intakes. The aggregate micronutrient density ratings remained similar for all other groups, with a few exceptions (Figures 4, 5 and Supplementary Figures 1–6). Organs, small dried fish, DGLVs, shellfish, beef, goat, eggs, cow milk, canned fish with bones, and lamb/mutton all remained with a rating of very high aggregate micronutrient density. Cheese rated very high for children 2–4 years, adolescents, WRA, and pregnant women but high for adults. Notably, vitamin A-rich fruits and vegetables and seeds rated high for children 2–4 years but low for all other groups. Canned fish without bones rated moderate for children 2–4 years, adolescents, and adults but low for WRA and pregnant women. Quinoa rated moderate for children 2–4 years and adolescents but low for all other groups. Finally, teff rated low for pregnant women but moderate for all other groups.
Figure 4. Calories and grams needed to provide an average of one-third of recommended intakes of vitamin A, folate, vitamin B12, calcium, iron, and zinc for adults ≥25. Each nutrient’s contribution is capped at 100% of recommended intakes. Hypothetical average requirements for mass are based on an energy density of 1.3 kcal/g. AR, average requirement; Vit, vitamin.
Figure 5. Aggregate and individual micronutrient density scores for adults ≥25. Mod, moderate; prod, products; veg, vegetables.
Individual Micronutrient Density Scores for Other Population Groups
There were many differences in ratings for specific micronutrients depending on the population, especially for iron and folate (Figures 5, 6 and Supplementary Figures 4–6). Organs, bivalves, small dried fish, and goat were the only foods that rated as top iron sources for all population groups. For iron, DGLVs rated low for pregnant women but high for all other groups, while crustaceans rated low for pregnant women, moderate for children 2–4 years and WRA, and high for adolescents and adults. Beef was a top source of iron for children 2–4 years, adolescents, and adults but rated high for WRA and pregnant women. For adults, teff, fonio, sorghum, pulses, and millet were all top iron sources, whereas they all rated low for pregnant women, except for teff and fonio, which rated moderate. Further, quinoa, canned fish with bones, eggs, seeds, and pork also rated high for iron for adults, while they rated moderate (quinoa, canned fish with bones, and eggs) or low (seeds and pork) for WRA and low for pregnant women. In addition, several food groups presented moderate iron density for adults, including fresh fish, canned fish without bones, whole grains, and unrefined grain products, whereas they all rated low for both WRA and pregnant women. Finally, for pregnant women, the only top folate sources were liver and pulses, whereas for adults and WRA top sources also included DGLVs and quinoa, with the addition of eggs for WRA and kidney (including beef, lamb, and pork kidney), fonio, and teff for children 2–4 years and adolescents.
Figure 6. Calories and grams needed to provide one-third of recommended iron intakes for adults ≥25. Hypothetical average requirements for mass are based on an energy density of 1.3 kcal/g. AR, average requirement; Vit, vitamin.
Our analysis has provided ratings of inherent food sources of multiple and individual micronutrients commonly lacking in diets, especially in LMICs, for population groups with increased needs and the broader adult population. In general, animal-source foods and DGLVs are top sources of priority micronutrients. Interestingly, many foods commonly promoted as nutrient-dense, including most fruits and vegetables, nuts and seeds, whole grains and, even animal-source foods like chicken and canned fish without bones, are not particularly dense in bioavailable micronutrients commonly lacking in LMICs. These foods, of course, provide important nutritional benefits beyond these specific nutrients. Indeed, priority micronutrients are just one of many important aspects contributing to overall diet quality, and foods presenting low density in priority micronutrients may be rich in other essential and non-essential beneficial compounds and can contribute to overall energy and protein requirements.
These findings have implications for how to address important micronutrient gaps in the general population through food-based interventions. They are particularly relevant for populations with increased nutrient needs, such as pregnant women and WRA. We show that pregnant women and WRA need particularly nutrient dense foods to meet requirements and our analysis helps identify foods to prioritize. Programs and policies seeking to address undernutrition through dietary interventions in the most vulnerable populations could be improved by promoting specific foods containing the highest densities in bioavailable micronutrients commonly lacking, such as organs, small dried fish, DGLVs, and bivalves. For instance, policy makers and program managers could incentivize production of these foods to increase their availability and affordability, as well as adopt social protection policies and provide cash transfers to low-income households to purchase nutrient-dense foods. In addition, they could establish nutrition education programs within schools and the public health system and implement social and behavior change communication campaigns through mass media, to sensitize the general population or targeted groups on the importance of regularly consuming these foods within the context of a broader healthy diet. Similar policy and program implications have been identified in a related analysis that focused specifically on young children during the complementary feeding period in South and Southeast Asia and which found that organs, eggs, and bivalves had the highest densities of bioavailable micronutrients commonly lacking (34).
These findings also have important implications for vegetarian populations, since animal flesh foods are dense in priority micronutrients. In addition to DGLVs, both eggs and dairy foods are excellent sources of priority micronutrients for lacto-ovo vegetarians. Fortunately, eggs and dairy foods are among the more affordable animal-source foods per unit priority nutrient density, although not as affordable as organs and small fish, and they are still often inaccessible or unaffordable for people with limited resources (32, 35). Importantly, DGLVs and pulses are accessible and affordable sources of several priority micronutrients in most populations (32, 35). Further, traditional grains, including teff, quinoa, fonio, and millet, are at least moderately dense in iron, zinc, and folate and can also make significant contributions to nutrient adequacy. Lacto-ovo vegetarian diets rich in eggs, dairy, DGLVs, pulses, and traditional grains can provide adequate amounts of all six priority micronutrients. Carefully constructed vegan diets could provide adequate amounts of all six priority micronutrients for the general population, except vitamin B12, which would need to be consumed through fortified foods or supplements. However, population groups with increased nutritional requirements, such as pregnant women and children during the complementary feeding period, following a vegan diet likely also need fortification or supplementation for other micronutrients, such as iron, in addition to vitamin B12.
Importantly, to the extent possible, the pursuit of dietary nutrient adequacy for the global population should not come at the expense of increased environmental destruction. There may be some inevitable trade-offs between achieving micronutrient adequacy and minimizing the environmental impact of diets, but there is great potential to improve the sustainability of all types of foods using productive regenerative practices suitable to local ecosystems (36–38). Particular attention could be given to nutrient dense foods with the greatest potential for sustainable production. For example, seaweeds, bivalves, and small fish are generally highly nutrient dense and sustainable to produce (39). While there may be nutritional advantages of obtaining nutrients through foods (12–14), the very high iron requirements of more than 1.8 billion WRA globally might be challenging to achieve sustainably through foods alone and thus supplementation should be considered. Finally, plant-source foods generally have lower negative environmental impact than animal-source foods per unit protein, energy, or mass based on current production practices and existing metrics used to quantify environmental impact (40). However, this generalization may not hold when considering the higher bioavailable nutrient density of many animal-source foods as shown in the present analysis and others (34, 36), or when considering regenerative production practices and metrics that holistically quantify their environmental impacts (37, 38, 41).
Our study has several strengths. The methods are transparent and based on publicly available data, as has been recommended (42, 43). The food composition data is comprehensive and representative of diets in diverse contexts globally, unlike existing nutrient profiling systems, which are based solely on national food composition data, typically USDA FDC (42, 43), and we adjusted for differences in bioavailability of iron and zinc across foods. Similarly, recommended intakes are based on dietary reference values that are appropriate for global populations, including LMICs, and were calculated for the general adult population as well as groups with increased needs. Our ratings prioritize foods that are optimal sources of micronutrients known to be commonly lacking and causing significant health burdens in LMICs, in alignment with the recommendation to focus nutrient profiling models for LMICs on nutrient density of beneficial nutrients, rather than nutrients to limit (42). Lastly, the results are organized in clear and simple visualizations which are easily interpretable by non-technical audiences, including decision makers.
We focused on inherent priority micronutrient density and bioavailability and did not include fortified foods or address the overall role of food and diets in nutrient adequacy, infectious diseases, and NCDs and their broader impact on the global burden of disease (44). Other essential vitamins and minerals, including vitamin C, vitamin E, riboflavin, thiamin, niacin, potassium, and magnesium, can also be lacking in diets, but data is limited on how widespread these inadequacies are and their public health significance (1). Moreover, adequate calories (45), protein (46), and essential amino acids (47) and fatty acids (especially n-3 fatty acids) (48) are also often lacking and critically important for health. Furthermore, there are countless “non-essential” but nonetheless potentially beneficial compounds including fiber, phytonutrients, and bioactive compounds in plant and animal-source foods which play an important role in health and disease (12–14, 44). Finally, there are numerous compounds that are associated with increased risk of disease when consumed in excess, including sugar, sodium, trans fat, cosmetic additives, and contamination and biological hazards in unsafe food, among others, for which the type and level of processing often plays an important role (49–51).
Our analysis has important limitations. First, there are large differences in nutrient densities across food composition databases, which may reflect differences in varieties, production methods, soil conditions, fertilizer use, animal feed quality, culinary traditions, and/or technical and analytical quality of the underlying databases. Moreover, mineral densities have even been shown to vary geospatially within individual countries (52). Since the exact nutrient densities of any given food and context are unknown, we chose to use aggregate values to smooth out these variations, which contributes to the added value of our global food composition database. Second, in addition to significant differences across FCTs, there is sometimes high nutrient-density variance across foods within food groups, meaning that the ranking of a food group as a whole might not reflect the micronutrient density of the most (or least) nutrient-dense foods included. However, we chose to maintain these levels of aggregation because our selected food groups are more likely to be targeted in programming and policies than individual foods and match more closely with food groups in upcoming global diet quality monitoring data (53, 54). Third, country and regional FCTs only included a limited set of commonly consumed foods, which limited the breadth of foods included in our aggregated food composition database. For instance, we were unable to analyze many nutrient-dense wild or indigenous vegetables, nuts, seeds, pulses, and insects, or novel foods like ground eggshells. Fourth, while we adjusted for bioavailability of iron and zinc, actual bioavailability depends on the genetics and micronutrient status of the individual and their overall diet, including a broad set of enhancers and inhibitors. Finally, ratings are sensitive to categorical thresholds for quantities of calories and grams, which requires some attention when interpreting results, since foods near the thresholds could have been rated differently with only small changes in nutrient densities. Some of the differences in ratings across population groups could thus be due to small differences in nutrient densities for foods near thresholds.
These ratings are most applicable for populations in LMICs suffering from widespread micronutrient deficiencies. However, for population groups with increased needs in HICs, such as pregnant women and WRA, who may often be deficient in micronutrients such as iron, zinc, and folate, these results can also help identify relevant foods to prioritize. Importantly, diets should consist of a variety of foods with varying nutrient densities. Even adding just small amounts of particularly nutrient dense animal-source foods (for example, organs, small fish, and bivalves) to largely plant-based diets would go a long way toward ensuring adequacy of micronutrients commonly lacking. Future analyses should focus on understanding how to use these findings to improve food, agriculture, and nutrition policies and programs, which tend to focus on specific foods or food groups. Researchers could build on this work by incorporating additional foods and food groups, including eggshells (55) and wild or indigenous vegetables, nuts, seeds, pulses, and insects (56), many of which contain very high nutrient densities (57). Moreover, these ratings could be paired with broader diet quality metrics (54) and included as an additional way to assess food affordability, for example, by expanding on existing approaches (32, 35), as has been done for other nutrient profiling systems (58). Finally, these ratings could also be used to provide more nutritionally relevant indicators of the environmental impact of foods, for example, by quantifying impact in terms of nutrient density.
Data Availability Statement
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s.
TB and FO designed the study, conducted the analyses, and wrote the manuscript. Both authors contributed to the article and approved the submitted version.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
We thank Lynnette M. Neufeld, Saul S. Morris, Stella Nordhagen, Gina L. Kennedy, and Christina Nyhus Dhillon for their feedback on draft versions of the manuscript.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fnut.2022.806566/full#supplementary-material
ARs, average requirements; DGLVs, dark green leafy vegetables; EFSA, European Food Safety Authority; FCTs, food composition tables; FDC, FoodData Central; HICs, high-income countries; LMICs, low- and middle-income countries; NCDs, non-communicable diseases; UPFs, ultra-processed foods; WRA, women of reproductive age.
1. Beal T, Massiot E, Arsenault JE, Smith MR, Hijmans RJ. Global trends in dietary micronutrient supplies and estimated prevalence of inadequate intakes. PLoS One. (2017) 12:e0175554. doi: 10.1371/journal.pone.0175554
3. WHO. Vitamin and Mineral Nutrition Information System (VMNIS). (2021). Available online at: https://www.who.int/teams/nutrition-and-food-safety/databases/vitamin-and-mineral-nutrition-information-system (accessed June 13, 2021)
4. Beal T, White JM, Arsenault JE, Okronipa H, Hinnouho G-M, Torlesse H, et al. Micronutrient gaps during the complementary feeding period in South Asia: a comprehensive nutrient gap assessment. Nutr Rev. (2021) 79(Suppl. 1):26–34. doi: 10.1093/nutrit/nuaa144
5. White JM, Beal T, Chimanya K, Arsenault JE, Okronipa H, Hinnouho G-M, et al. Micronutrient gaps during the complementary feeding period in Eastern and Southern Africa: a comprehensive nutrient gap assessment. Nutr Rev. (2021) 79(Suppl. 1):16–25. doi: 10.1093/nutrit/nuaa142
6. Black RE, Victora CG, Walker SP, Bhutta ZA, Christian P, de Onis M, et al. Maternal and child undernutrition and overweight in low-income and middle-income countries. Lancet. (2013) 382:427–51. doi: 10.1016/S0140-6736(13)60937-X
10. Osendarp SJM, Martinez H, Garrett GS, Neufeld LM, De-Regil LM, Vossenaar M, et al. Large-scale food fortification and biofortification in low- and middle-income countries: a review of programs, trends, challenges, and evidence gaps. Food Nutr Bull. (2018) 39:315–31. doi: 10.1177/0379572118774229
11. FooDB. Listing Compounds. (2021). Available online at: https://foodb.ca/compounds (accessed June 13, 2021)
16. Lane MM, Davis JA, Beattie S, Gómez-Donoso C, Loughman A, O’Neil A, et al. Ultraprocessed food and chronic noncommunicable diseases: a systematic review and meta-analysis of 43 observational studies. Obes Rev. (2021) 22:e13146. doi: 10.1111/obr.13146
17. Hall KD, Ayuketah A, Brychta R, Cai H, Cassimatis T, Chen KY, et al. Ultra-Processed diets cause excess calorie intake and weight gain: an inpatient randomized controlled trial of ad libitum food intake. Cell Metab. (2019) 30:67–77.e3. doi: 10.1016/j.cmet.2019.05.008
19. Institute of Medicine Committee to Review Dietary Reference Intakes for Vitamin D and Calcium. Dietary Reference Intakes for Calcium and Vitamin D. Ross AC, Taylor CL, Yaktine AL, Del Valle HB editors. Washington, DC: National Academies Press (2011).
22. U.S. Department Of Agriculture (USDA), Agricultural Research Service. USDA FoodData Central. (2021). Available online at: https://fdc.nal.usda.gov/ (accessed June 18, 2021).
23. FAO. INFOODS: FAO/INFOODS Databases. (2021). Available online at: http://www.fao.org/infoods/infoods/tables-and-databases/faoinfoods-databases/en/ (accessed June 18, 2021)
24. Valenzuela C, López de Romaña D, Olivares M, Morales MS, Pizarro F. Total iron and heme iron content and their distribution in beef meat and viscera. Biol Trace Elem Res. (2009) 132:103–11. doi: 10.1007/s12011-009-8400-3
25. Balder HF, Vogel J, Jansen MCJF, Weijenberg MP, van den Brandt PA, Westenbrink S, et al. Heme and chlorophyll intake and risk of colorectal cancer in the Netherlands cohort study. Cancer Epidemiol Biomarkers Prev. (2006) 15:717–25. doi: 10.1158/1055-9965.EPI-05-0772
27. Pourkhalili A, Mirlohi M, Rahimi E. Heme iron content in lamb meat is differentially altered upon boiling, grilling, or frying as assessed by four distinct analytical methods. Sci World J. (2013) 2013:e374030. doi: 10.1155/2013/374030
29. Ronco A, Espinosa E, Calderon J. A Case-Control Study on Heme/Non-heme Iron and Breast Cancer Risk 1 MedDocs Publishers of Creative Commons Attribution 4.0 International License Annals of Clinical Nutrition. Reno, NV: MedDocs Publishers LLC (2018).
30. Kongkachuichai R, Napatthalung P, Charoensiri R. Heme and nonheme iron content of animal products commonly consumed in Thailand. J Food Composit Anal. (2002) 15:389–98. doi: 10.1006/jfca.2002.1080
31. Taniguchi CN, Dobbs J, Dunn MA. Heme iron, non-heme iron, and mineral content of blood clams (Anadara spp.) compared to Manila clams (V. philippinarum), Pacific oysters (C. gigas), and beef liver (B. taurus). J Food Composit Anal. (2017) 57:49–55. doi: 10.1016/j.jfca.2016.12.018
32. Ryckman T, Beal T, Nordhagen S, Chimanya K, Matji J. Affordability of nutritious foods for complementary feeding in Eastern and Southern Africa. Nutr Rev. (2021) 79(Suppl. 1):35–51. doi: 10.1093/nutrit/nuaa137
33. Hall KD, Guo J, Courville AB, Boring J, Brychta R, Chen KY, et al. Effect of a plant-based, low-fat diet versus an animal-based, ketogenic diet on ad libitum energy intake. Nat Med. (2021) 27:344–53. doi: 10.1038/s41591-020-01209-1
34. Ortenzi F, Beal T. Priority micronutrient density of foods for complementary feeding of young children (6–23 months) in South and Southeast Asia. Front Nutr. (2021) 8:785227. doi: 10.3389/fnut.2021.785227
41. Fenster TLD, LaCanne CE, Pecenka JR, Schmid RB, Bredeson MM, Busenitz KM, et al. Defining and validating regenerative farm systems using a composite of ranked agricultural practices. F1000Res. (2021) 10:115. doi: 10.12688/f1000research.28450.1
42. Miller GD, Drewnowski A, Fulgoni V, Heaney RP, King J, Kennedy E. It is time for a positive approach to dietary guidance using nutrient density as a basic principle. J Nutr. (2009) 139:1198–202. doi: 10.3945/jn.108.100842
44. Afshin A, Sur PJ, Fay KA, Cornaby L, Ferrara G, Salama JS, et al. Health effects of dietary risks in 195 countries, 1990–2017: a systematic analysis for the global burden of disease study 2017. Lancet. (2019) 393:1958–72. doi: 10.1016/S0140-6736(19)30041-8
46. Wu G, Fanzo J, Miller DD, Pingali P, Post M, Steiner JL, et al. Production and supply of high-quality food protein for human consumption: sustainability, challenges, and innovations. Ann N Y Acad Sci. (2014) 1321:1–19. doi: 10.1111/nyas.12500
47. Semba RD, Shardell M, Sakr Ashour FA, Moaddel R, Trehan I, Maleta KM, et al. Child stunting is associated with low circulating essential amino acids. EBioMedicine. (2016) 6:246–52. doi: 10.1016/j.ebiom.2016.02.030
51. Monteiro CA, Cannon G, Levy RB, Moubarac J-C, Louzada ML, Rauber F, et al. Ultra-processed foods: what they are and how to identify them. Public Health Nutr. (2019) 22:936–41. doi: 10.1017/S1368980018003762
52. Gashu D, Nalivata PC, Amede T, Ander EL, Bailey EH, Botoman L, et al. The nutritional quality of cereals varies geospatially in Ethiopia and Malawi. Nature. (2021) 594:71–6. doi: 10.1038/s41586-021-03559-3
53. Herforth AW, Wiesmann D, Martínez-Steele E, Andrade G, Monteiro CA. Introducing a suite of low-burden diet quality indicators that reflect healthy diet patterns at population level. Curr Dev Nutr. (2020) 4:nzaa168. doi: 10.1093/cdn/nzaa168
54. Herforth A, Beal T, Rzepa A. Global Diet Quality Project Aims to Bridge Data Gap. Gallup.com. (2020). Available online at: https://news.gallup.com/opinion/gallup/321968/global-diet-quality-project-aims-bridge-data-gap.aspx (accessed June 29, 2021).
55. Bartter J, Diffey H, Yeung YH, O’Leary F, Häsler B, Maulaga W, et al. Use of chicken eggshell to improve dietary calcium intake in rural sub-Saharan Africa. Matern Child Nutr. (2018) 14:e12649. doi: 10.1111/mcn.12649
56. Smith MR, Stull VJ, Patz JA, Myers SS. Nutritional and environmental benefits of increasing insect consumption in Africa and Asia. Environ Res Lett. (2021) 16:065001. doi: 10.1088/1748-9326/abf06c
58. Drewnowski A, Smith J, Fulgoni VL. The new hybrid nutrient density score NRFh 4:3:3 tested in relation to affordable nutrient density and healthy eating index 2015: analyses of NHANES data 2013–16. Nutrients. (2021) 13:1734. doi: 10.3390/nu13051734
Keywords: nutrient density, micronutrient deficiencies, animal-source foods, organs, shellfish, fish, dark green leafy vegetables, ruminant meat
Citation: Beal T and Ortenzi F (2022) Priority Micronutrient Density in Foods. Front. Nutr. 9:806566. doi: 10.3389/fnut.2022.806566
Received: 01 November 2021; Accepted: 15 February 2022;
Published: 07 March 2022.
Edited by:Donato Angelino, University of Teramo, Italy
Reviewed by:Robyn Gwen Alders, Chatham House, United Kingdom
Little Flower Augustine, National Institute of Nutrition, India
Copyright © 2022 Beal and Ortenzi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Ty Beal, email@example.com