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. 2022 Jan 31;1511(1):40–58. doi: 10.1111/nyas.14743

Interventions to improve calcium intake through foods in populations with low intake

Megan W Bourassa 1,, Steven A Abrams 2, José M Belizán 3, Erick Boy 4, Gabriela Cormick 3,5, Carolina Diaz Quijano 6, Sarah Gibson 7, Filomena Gomes 1,8, G Justus Hofmeyr 9,10, Jean Humphrey 11, Klaus Kraemer 11,12, Keith Lividini 4, Lynnette M Neufeld 13, Cristina Palacios 14, Julie Shlisky 1, Prashanth Thankachan 15, Salvador Villalpando 16, Connie M Weaver 17,18
PMCID: PMC9306636  PMID: 35103316

Abstract

Calcium intake remains inadequate in many low‐ and middle‐income countries, especially in Africa and South Asia, where average intakes can be below 400 mg/day. Given the vital role of calcium in bone health, metabolism, and cell signaling, countries with low calcium intake may want to consider food‐based approaches to improve calcium consumption and bioavailability within their population. This is especially true for those with low calcium intake who would benefit the most, including pregnant women (by reducing the risk of preeclampsia) and children (by reducing calcium‐deficiency rickets). Specifically, some animal‐source foods that are naturally high in bioavailable calcium and plant foods that can contribute to calcium intake could be promoted either through policies or educational materials. Some food processing techniques can improve the calcium content in food or increase calcium bioavailability. Staple‐food fortification with calcium can also be a cost‐effective method to increase intake with minimal behavior change required. Lastly, biofortification is currently being investigated to improve calcium content, either through genetic screening and breeding of high‐calcium varieties or through the application of calcium‐rich fertilizers. These mechanisms can be used alone or in combination based on the local context to improve calcium intake within a population.

Keywords: calcium, food fortification, biofortification

Purpose

In March and April 2021, the Nutrition Science Program of the New York Academy of Sciences, in partnership with the Children's Investment Fund Foundation, convened a Calcium Task Force and hosted two virtual meetings. This task force is composed of experts in micronutrients, malnutrition, pediatrics, gynecology and obstetrics, biochemistry, public health, and strategies for supplementation and fortification. During these two virtual meetings, the task force assessed the evidence on global calcium deficiency and its health consequences, useful indicators of calcium status or intake. It also considered potential interventions, such as calcium supplementation for pregnant women to improve pregnancy outcomes and associated implementation challenges, as well as food‐based interventions to improve calcium intake, especially in populations with low dietary intake. The group was also commissioned to identify research gaps and provide guidance for interventions and policies based on the most current available evidence. The following paper, as a consensus viewpoint, describes the task force's discussions and conclusions with regard to population‐wide, food‐based interventions to improve low calcium intake.

Background

Calcium plays integral roles in skeletal structure, smooth muscle contraction, and neuronal signaling. It makes up approximately 1.9% of the total body weight and as such is the fifth most abundant element in the body. However, a recent review found that many countries, especially those in Southeast Asia and South America, have average intakes less than 400 mg/day, well below the recommended intakes, which range between 700 and 1300 mg/day for individuals over 19 years of age. 1 , 2 , 3 Based on these data of low calcium intake and availability, it is difficult for much of the world to obtain adequate calcium from food, and the lowest calcium availability is generally found in low‐income countries in Asia, Africa, and Latin America. 4

This paper includes the conclusions of the task force and considers different food‐based, population‐level approaches that can be used to increase calcium intake and bioavailability. Food‐based approaches to improve calcium intake can reach all members of the population who consume the promoted calcium‐containing food. These include: promoting and facilitating access to foods naturally containing calcium through policies and education; food processing techniques that improve the bioavailability of dietary calcium; fortification of foods with additional calcium; and biofortification of crops to achieve higher calcium density. Considerations for these interventions should include the potential challenges and opportunities that arise from the food systems within which they are embedded as well as consumer preferences, organoleptic properties of calcium‐rich or ‐fortified foods, and issues of bioavailability. Food‐based approaches are also less likely than supplementation to exceed tolerable upper intake levels (ULs) for calcium. The task force concluded that food‐based approaches may be particularly important for reaching especially vulnerable populations, including women who enter pregnancy with low calcium intake and are at risk of preeclampsia, children who are at risk of rickets during rapid growth, and older adults who are at risk of bone fracture. While any population‐level intervention would improve calcium intake of the entire population, women and children are the most vulnerable to low calcium intake and stand to benefit most from such an intervention.

One of the main challenges with studying calcium intake and status in populations is the limited availability of intake data and a lack of acceptable biomarkers of calcium status, which further complicates identifying populations that would most benefit from increased calcium intakes. 3 While nationally representative surveys of calcium intake are not available for all countries, Food and Agriculture Organization of the United Nations’ food balance sheets and household consumption and expenditure surveys can provide indirect evidence on the availability of calcium and household‐level consumption. As a result, information from multiple data sources, including various forms of dietary assessment, target requirements, and health outcomes, should be triangulated to determine when and for whom a calcium intervention is most appropriate.

Promoting the consumption of naturally calcium‐rich foods

In regions where naturally bioavailable calcium‐containing foods are available, affordable, and acceptable, promoting the consumption of these foods may be effective in improving calcium intake. A review of the food balance sheets shows that availability of calcium‐rich foods is insufficient to cover the needs of many low‐ and middle‐income country (LMIC) populations. 5 There are also wide variations in the availability in different regions or intake frequency that can affect the specific recommendations for a particular region. Therefore, assessments of locally available, acceptable, and accessible foods that are rich in bioavailable calcium may be helpful in identifying the most appropriate foods to promote within populations. While a number of foods are naturally high in calcium, there are many necessary considerations, which include biological access (e.g., bioavailability of the calcium), cultural acceptability (e.g., lactose intolerance rates may cause avoidance of dairy foods high in lactose), and economic sustainability (e.g., affordability of the foods recommended). 6 In addition, the promotion of consumption of calcium‐rich foods requires behavioral change and improvement of access to culturally acceptable foods and should, therefore, be considered among long‐term strategies. The cost‐effectiveness of these strategies needs to be evaluated. 7

Promoting the consumption of calcium‐rich foods can be achieved through a number of strategies via policies and education of the public. Policies, such as commodity‐specific (e.g., dairy) vouchers or cash transfers, can be used to help make food more affordable and have been especially effective in increasing the uptake of nutritious foods. 8 , 9 , 10 It may also be possible to increase food availability through agricultural subsidies geared toward increasing production or through improvements to the supply chain that reduce waste. Public education on the health benefits and the importance of calcium in the diet can also be valuable in increasing awareness. This can be done through public health messaging, marketing, or nutrition counseling. The NOURISHING Framework was developed to help countries implement nutrition policies related to food environments and food systems and that incorporate behavior change communication to tackle these issues and promote healthier diets. 11 Hawkes et al. also provide a list of policies that countries associated with development of the framework have implemented. 11

Animal‐source foods

Dairy products, such as milk, cheese, kefir, amasi (sour milk), and yogurt, are some of the richest food sources of naturally occurring calcium and are sources of protein, potassium, and magnesium. 12 Compared with plant‐based foods, as discussed below, bioavailability of calcium is also relatively high in dairy foods. However, the high costs and limited shelf‐life of dairy products make them more unaffordable to many lower‐income households. Despite the overall high costs of dairy foods, when measured in terms of the cost per mg of calcium, dairy products are the least costly source of calcium owing to their relatively high levels of calcium compared with other foods. 13 Lactose intolerance or malabsorption can be another barrier to the consumption of dairy products. It is estimated that two‐thirds of the world's population suffers from some form of lactose maldigestion/malabsorption, especially in South Asia, the Middle East, and in Southern Africa. 14 However, some forms of dairy, including some aged, hard cheeses, yogurt, and other sour milk products, can contain lower levels of lactose and may be well tolerated.

When consumed with bones, small fish and fish meal are also naturally high in calcium, as well as sources of iron and n‐3 fatty acids. An analysis of the nutritional composition of 367 fish species in 43 countries 15 revealed that species from tropical areas contain higher concentrations of calcium (as well as iron and zinc) when compared to temperate and cold areas. Results from animal studies also support the use of small fish in population groups with low intakes of milk and milk products. 16 In one species caught in the Caribbean region, where there is a high prevalence of calcium deficiency, 100 g of the raw, edible portion of the fish provided more than 200 mg of calcium (elemental calcium is implied unless otherwise stated). 15 In an experiment in Bangladesh, the Darkina fish (a small indigenous fish) was selected for its high iron, calcium, and zinc content as a means to increase mineral intake in the diet. These fish were ground into a powder and prepared as a chutney. A 30 g portion was prepared with the usual rice meal and provided 360 mg of calcium, contributing 35% of the recommended dietary intake for pregnant and lactating women. 17 In another study, dried and ground fish, providing 952 mg/day of calcium, were used to treat Nigerian children (6 months to 12.5 years of age) with rickets. 18 Over 24 weeks, the children responded positively to the treatment. There was a decrease in serum alkaline phosphatase and improvements in calcium, 25‐hydroxyvitamin D, and bone mineral density (BMD), and there was no difference between the ground‐fish treatment arms and the limestone treatment arm, which received a similar dose of calcium.

Insects are consumed by as many as 2 billion people around the world and can be naturally high in calcium. 19 , 20 , 21 Insects have been proposed as a sustainable solution to the rising costs of food animal production, food insecurity, population growth, and demand for protein. 21 , 22 In many parts of the world, insects are considered a delicacy. For example, in Zimbabwe, where worms are popular among locals in rural and urban areas, farming of mopane worms has become a multimillion dollar industry. 23 An analysis of six insects considered publicly acceptable in Central Europe found that the Bombyx mori (silk moth caterpillars) had a similar level of calcium to a glass of milk, with approximately 100 mg per 100 g of dry weight. 20 A study in Manipur, India, where aquatic insects are commonly consumed, found all species to be high in calcium (24–96 mg of calcium per 100 g of dry weight), as well as magnesium and protein. 19 The authors noted that the calcium content of these aquatic insects was higher than reported in a separate study of terrestrial insects, which contained just 0.0012–0.126 mg per 100 g of dry weight. 24 Insects also contain phenols and tannins, which have some antinutritive properties, and the bioavailability of calcium and other minerals has not been well studied. 25 Further work is also needed to consider the safety implications specifically of wild‐caught bugs, which may have been exposed to pesticides and other toxins, as well as the allergenicity of insect proteins that are similar to those of mollusks and shellfish, which can lead to severe allergic reactions. 20 , 26

Plant‐source foods

A number of edible plants are also naturally high in calcium, although the quantity and bioavailability are lower than animal‐source foods, especially dairy. The role of calcium and its distribution in plants has been extensively discussed elsewhere. 27 , 28 , 29 , 30 Briefly, plant roots are involved in tightly regulating the amount of calcium that the plant takes up via Ca2+‐permeable cation channels. Once within the cytosol, calcium concentrations are maintained at submicromolar concentrations and generally incorporated into various calcium‐dependent proteins or stored in the vacuoles. From the roots, calcium is transported into shoots and ultimately to leaves, where the majority of calcium is found in plants. The amount of calcium transported into the shoots is dependent on the phytoavailability of calcium in the rhizosphere, the area of the soil surrounding the roots. Fruits, seeds, and tubers often contain less calcium than roots and leaves. 31

As much of the calcium is distributed into the leaves, leafy green vegetables, including kale and spinach, contain calcium. However, the presence of oxalates and phytates in plants can significantly reduce calcium's bioavailability. For example, spinach by weight contains more calcium than kale; but kale has lower oxalate levels, making it a better source of bioavailable calcium per serving than spinach. Other leafy green vegetables with relatively high levels of bioavailable calcium include Chinese spinach, Chinese mustard greens, and bok choy. 32 Table 1 provides several examples of plant‐based sources of calcium, the fractional and total absorption of calcium in one serving, and how they compare with a serving of milk. 12 Cereal grains, especially finger millet and teff, 33 , 34 are relatively high in calcium as well but not as high as dairy sources. Finger millet and teff contain significant concentrations of phytate (679–1419 mg/100 g), which may affect calcium bioavailability. 33 , 34 Some root vegetables, including sweet potatoes, are also natural sources of calcium. In root vegetables, some of the calcium is bound by oxalate, thus reducing its bioavailability.

Table 1.

Food sources of bioavailable calcium 12

Food source Serving size a (g) Calcium content (mg/serving) Estimated absorption efficiency b (%) Absorbable calcium/serving c (mg) Servings needed to equal 1 cup milk
Milk 240 290 32.1 93.1 1.0
Beans, pinto 86 44.7 26.7 11.9 8.1
Beans, red 172 40.5 24.4 9.9 9.7
Beans, white 110 113 21.8 24.7 3.9
Bok choy 85 79 53.8 42.5 2.3
Broccoli 71 35 61.3 21.5 4.5
Cheddar cheese 42 303 32.1 97.2 1.0
Chinese cabbage flower leaves 85 239 39.6 94.7 1.0
Chinese mustard green 85 212 40.2 85.3 1.1
Chinese spinach 85 347 8.36 29 3.3
Kale 85 61 49.3 30.1 3.2
Spinach 85 115 5.1 5.9 16.3
Sugar cookies 15 3 91.9 2.76 34.9
Sweet potatoes 164 44 22.2 9.8 9.8
Rhubarb 120 174 8.54 10.1 9.5
Whole wheat bread 28 20 82.0 16.6 5.8
Wheat bran cereal 28 20 38.0 7.5 12.8
Yogurt 240 300 32.1 96.3 1.0
a

Based on a one‐half cup serving size (∼85 g for green leafy vegetables), except for milk (1 cup or 240 mL) and cheese (42.5 g).

b

Adjusted for load using the equation for milk (fractional absorption = 0.889−0.0964 ln load [23]), then adjusting for the ratio of calcium absorption of the test food relative to milk tested at the same load, the absorptive index.

c

Calculated as calcium content × fractional absorption.

Water

In some places, the naturally occurring calcium in water is high enough that it can contribute to the dietary intake of calcium. Although most tap and bottle waters contain little calcium, waters naturally containing calcium amounts of 300 mg/L have been reported from specific locations in Italy, Spain, the UK, and France. 35 Another study from Poland showed that tap water with around 68–114 mg/L of calcium can contribute to 6–14% of the total calcium intake of young women, and a study in the UK showed that calcium intake in areas of water with 300 mg/L can contribute to 8% of total calcium intake of adolescents. 36 , 37 However, in much of the world, including LMICs, there is very little calcium in drinking water. A study in Argentina shows that the calcium concentration of tap water ranged from 6 to 105 mg/L, while most bottled waters had calcium levels well below 50 mg/L. 38 Groundwater in Brazil showed a mean calcium concentration of 47.6 mg/L, 39 whereas one in Algeria showed concentration above 150 mg/L. 40 Some bottled mineral waters contain even larger amounts, with more than 500 mg/L. 41 One study showed that consumption of calcium‐rich water can provide a quarter of the total calcium daily intake for adult men and women. 42 The ionic nature of calcium in water makes it bioavailable and facilitates absorption as long as the pH is sufficiently low, and absorption is further increased if water intake is spread throughout the day. 35

Utilizing food processing techniques that can increase calcium levels, bioavailability, or shelf‐life

In addition to increasing the consumption of foods naturally rich in calcium, some food‐processing methods incorporate calcium as a functional ingredient, leading to foods with greater calcium content or can improve the bioavailability of calcium in a food. For example in baking, calcium carbonate and calcium phosphate are used to provide structure to breads by retaining the CO2 in the gluten and reduce the stickiness of dough. Calcium chloride, lactate, or carbonate are used in dairy and snack products to add firmness and structure. Dried foods, such as milk powders, can also have a much longer shelf‐life than fresh milk, which can increase availability and accessibility of dairy products.

Reducing phytate levels

Phytate or phytic acid is found in the highest amounts in cereals, legumes, nuts, and oil seeds, where it can account for 60–80% of total phosphorus content, and is found in lower amounts in roots, tubers, fruits, and berries. 43 , 44 It can make up between 1% and nearly 5% of the mass of the seed, fruit, or grain. 45 Phytic acid tightly binds calcium and other divalent cations, such as magnesium, iron, and zinc, and prevents them from being readily absorbed or hydrolyzed in vivo. 46 It has been estimated that a three‐fold increase in phytic acid results in a 25% reduction in calcium absorption. 47 Thus, processing methods that hydrolyze phytate can have a significant impact on calcium bioavailability. While phytate is generally considered an antinutrient because it reduces the bioavailability of minerals and proteins, it is also an antioxidant that is especially important for seed viability.

Phytate can be broken down during food processing through either an enzymatic process, such as the use of phytase (a phytate‐specific phosphatase), or through nonenzymatic processes, such as high temperatures or pH. Enzymatic hydrolysis can occur during fermentation, malting, and sprouting and can help lower the phytate levels in vegetal foods, resulting in more bioavailable calcium and can lead to a longer shelf‐life of the food. 30 , 44 This is especially important in the breadmaking process, as wheat and other cereal grains can contain a significant amount of phytate depending on the level of extraction. However, fermentation with lactic acid, such as during sourdough fermentation, has been shown to help the grain's natural phytase (phytogenic phytase) breakdown of the phytate by as much as 100% with rye, 95–100% with wheat, and 39–47% with oat. 48 The level of phytate reduction was directly correlated with the levels of phytase contained in the cereal and was not directly due to the lactic acid itself, although it creates the favorable conditions to facilitate the enzymatic degradation by lowering the pH.

Fermented foods can play a role in traditional diets and substantially increase calcium content. For example, in Southern Ethiopia, enset or false banana is fermented into kocho, which can increase calcium content 49 and is a major source of calcium for children in the area. 50 Injera, another common Ethiopian food that is made from fermented teff, is another example of improved calcium bioavailability that leads to higher intakes of bioavailable calcium and improved health outcomes. 51 In the mid‐20th century, calcium intake in Ethiopia was estimated to be 1075 mg/day, with relatively low preeclampsia rates. 52 , 53 However, in more recent years, the estimated calcium intakes have decreased in Ethiopia to a mean intake of 501 mg/day for women, possibly due to the increase in maize and wheat flour in the diets and the relatively high cost of teff. 54

Other strategies have also been proposed to reduce phytate in breads, for example, through bifidobacteria, which have higher levels of phytate‐degrading enzymes than typical lactic acid bacteria. 55 Alternatively, a commercially available fungal phytase from Aspergillus niger has been shown to reduce phytate levels in the breadmaking process and improve the overall quality of the bread, with better shape, softer crumbs, and reduced proofing times. 56 These strategies all can result in a bread with lower phytate levels and improved bioavailability of divalent cations, such as calcium.

Germination or soaking seeds in water overnight can also hydrolyze phytate. Germination over 10 days of fava beans resulted in a decrease in phytate levels by 71.2–77.3%, depending on the cultivar, and was concomitant with an increase in phytase activity, which peaked around 6 days. 57 A more recent study found that germination significantly increased the bioavailability of calcium in all legume seeds studied, including lentils, chickpeas, cowpeas, and green gram. 58 Soaking appears to decrease phytate levels but does so to a lesser degree than malting or fermentation in sorghum. 59 However, another study looked at the subsequent bioavailability of iron and zinc after soaking and found it likely did not improve despite the reduction in phytate (calcium was not measured). 60

There are gut bacteria capable of phytase activity, such as Bifidobacterium dentium, Lactobacillus reuteri, and Lactobacillus salivarius, that could break down these compounds. Promoting growth of these bacteria through probiotics can help improve calcium absorption and, as mentioned above, have been proposed for use in the breadmaking process. 61 Finally, phytase could be added to supplements and micronutrient powders to help make calcium and the other divalent cations more available. 62 , 63 , 64 , 65

Nixtamalization

Nixtamalization is a process that refers to soaking boiled corn overnight in a lime solution of calcium hydroxide. 66 After soaking, some of the outer layer of the corn, which can contain aflatoxins, is removed. This is the traditional home process used in Mesoamerica that makes corn dough malleable enough to prepare tortillas, and it results in a 20‐fold increase in calcium content compared with raw maize and increased calcium absorption compared with commercially available tortillas. 67 , 68 , 69 In fact, the nixtamalized tortillas in Guatemala provides diets that are relatively high in calcium and lower rates of preeclampsia. This led to the hypothesis that diets with adequate calcium could reduce the risk of preeclampsia. 52 Work is ongoing to adapt this process to make maize dough from maize for traditional maize dishes in sub‐Saharan Africa (personal communication). Inserting the additional nixtamalization step to increase calcium intake in such setting may face initial acceptability hurdles.

Parboiling rice

In many rice‐consuming communities around the world, slender, long, white grains are the most desired by consumers, but the milling and polishing processes required to achieve the end‐product remove the nutrient‐rich bran layer. It is estimated that 10% milling of raw rice can lead to a loss of 57.2 ± 2.5% of the calcium in unmilled grain. 70 Parboiling is a technique that transfers the nutrients of the bran to the rice grain prior to milling, resulting in greater grain nutrient content. Parboiled rice loses significantly less calcium (48.3 ± 3.2%) than raw rice. 70 However, the product of parboiling rice is a more yellow grain than traditional polished white rice, which is less desirable for consumers in many countries. It was recently shown that parboiling the whole grain could increase calcium content by over 200% in the finished, milled rice. 71 In another study, the soaking water used in parboiling rice was fortified with calcium lactate and iron (ferrous sulfate heptahydrate), resulting in a rice containing nearly 1000 mg of calcium per kg of milled rice. 72 Thus, the consumption of 400 g of this cooked, calcium‐soaked, parboiled rice can provide about 15% of the recommended dietary allowance of calcium.

Eggshells and fish bones

It is also possible to mix calcium‐rich foods with staple foods, such as flour, to produce a higher calcium food. This has been proposed for calcium‐rich foods like fish bones and eggshell‐fortified foods. Ground tuna bones were used to create a fortified cracker that increased calcium, phosphorus, and protein levels and was tested in Thailand. 73 The study found that up to 30% of the bone mix could be added to the cracker (by weight) without affecting sensory properties, although it did create a more dense and less porous cracker compared with controls. These methods of using otherwise waste products, such as bones, may create a cost‐effective way to fortify foods while reducing waste.

Eggshells also contain a high amount of calcium and with a similar bioavailability to calcium carbonate (∼39%). 74 One gram of eggshells provides approximately 380 mg of calcium and covers half of the calcium needs of a sub‐Saharan African adult female, making eggshell a highly equitable solution to fill the calcium intake gap of rural sub‐Saharan Africa (where village poultry ownership is common). 74 In a study in piglets, eggshell powder added to either the soy‐ or casein‐based diets was more absorbable than purified calcium carbonate, though this difference was only significant in the soy‐based diets. 75 However, the eggshells had no impact on the absorption of magnesium or crude fat digestion, suggesting that the eggshells are not interfering with the absorption of other nutrients.

While Salmonella and other egg‐associated pathogens are a risk to be considered, it has been proposed that eggshells boiled for 10 min when preparing hard‐boiled eggs, with a further 20 min cooking of crushed eggshell in staple foods, would eliminate identified egg‐associated pathogens. 74 In a study done in Tanzania, where the diet is low in energy and micronutrients, especially calcium, zinc, and iron, ground eggshells were used to improve calcium content. In this study, the eggshells were boiled for 20 min and then dried, crushed, and ground to the finest powder particles, reducing the impact on overall meal texture, and added to the mixture of any prepared meal. 74 In one study, eggshell powder was tested as a calcium fortificant for bread, resulting in a better appearance of the crust, the color of the crumb, flavor, and overall acceptability compared with the control bread. 76 The optimal level of calcium was around 200 mg calcium/100 g bread. 77

The acceptability and safety of these approaches as well as the impact on the absorption of other nutrients requires further research. While these methods could reduce waste, behavior modification would be needed to incorporate eggshells and fish bones into the diet and how to prepare the powders if they were to be made in the home.

Implementing calcium food fortification programs

Food fortification is an effective means of increasing micronutrient intakes, including calcium. Staple food fortification is a population‐based approach, which aims to shift intakes of a nutrient among all consumers of a food vehicle. Ideally, fortification is implemented without a change in behavior, unlike supplementation regimes. To realize such population‐level impact, a high proportion of the target population needs to consume the fortified food regularly. Calcium food fortification has been successfully implemented in many, mostly high‐income countries, with demonstrated cost‐effective impacts on health outcomes in some age groups, especially in children and postmenopausal women. 78

Impact of calcium fortification

The UK (and Newfoundland, a former part of the UK) is the only country that currently has mandatory calcium fortification, which is for wheat flour (235–390 mg calcium carbonate (94–156 mg of elemental calcium)/100 g wheat flour) and was implemented in 1943. With this fortification policy, it is estimated that the fortified wheat flour contributes to 13–14% of the total calcium intake in the UK, and without this policy, an additional 10–12% of adolescents would not meet the recommended intake. 37 , 79

For more than 30 years, Denmark had a mandatory calcium fortification policy for wheat and rye flours. In 1985, while this fortification policy was in effect, 7% of women and 6% of men were not meeting their calcium recommendations. However, in 1993–1994, after the fortification program ended, the number of women and men not meeting the daily calcium recommendations increased to 24% and 21%, respectively. 80 As a result, it was estimated that the calcium‐fortified foods contributed to about 30% of the total calcium intake in the diet. While these two examples from the UK and Denmark are in high‐income settings and where dairy is widely consumed and the average calcium intake is higher than in many parts of the word, the policies were effective in raising the calcium intake of the population and preventing inadequate intake, especially in low‐income groups.

For young children, very low calcium intakes, as well as low vitamin D status, can put them at risk for rickets and osteomalacia. In trials of calcium‐fortified foods, children and adolescents receiving the fortified foods had greater gains in height and BMD than children who did not receive these foods. In a randomized, placebo‐controlled trial in Finland, calcium supplemented through cheese (1000 mg/day) over 2 years in adolescent girls (10–12 years old) resulted in a significantly greater percent change in cortical thickness of the tibia over the study period (37.1 mm ± 1.3), when compared with 1000 mg/day calcium with 200 IU vitamin D supplementation (31.7 mm ± 1.3), 1000 mg/day of calcium supplementation alone (29.8 mm ± 1.4), and placebo (31.1 mm ± 1.4). 81 Higher total BMD was also observed in all calcium groups compared with the controls as long as compliance was greater than 50%. Similar results in girls (10 years old) were found in another 2‐year randomized controlled trial in China using fortified milk powders with 300, 600, or 900 mg of calcium with 200 IU of vitamin D in all groups. The high‐calcium group (consuming a total of 1100 mg/day of calcium) showed greater BMD accretion in the hip (2.3%), femoral neck (2.7%), and shaft (2.6%) than those in the low‐calcium group (consuming a total of 655 mg/day of calcium). 82 However, these results were not significant for boys, and more work needs to be done to better understand the effect of sex differences and calcium intake on bone outcomes. It should also be noted that the trials to date have been conducted in just a few settings, including China, the United States, Australia, New Zealand, and Western Europe. 78 While some targeted fortification programs, including calcium, have been successfully implemented in LMICs for children, 83 , 84 , 85 additional work is needed to see if the results with calcium‐fortified foods have similar health impacts on bone density and other health outcomes.

Adequate calcium intake in early pregnancy is important for improving pregnancy outcomes. 86 , 87 As it is very hard to identify women very early in pregnancy, especially in LMICs, a food fortification program that reaches women of reproductive age could help women consume more adequate levels of calcium before they become pregnant. However, the benefits of such a strategy have not yet been tested through fortification. Most of what is known about the impact of calcium in pregnancy is through supplementation trials, whereas food fortification may not reach the same intake levels as supplementation. Work is ongoing to better understand if lower doses of supplementation (500 mg/day) can be as effective as the higher (1–2 g/day) doses currently in use to prevent preeclampsia in pregnant women. 88 If the lower doses can have similar impact, it would be worth investigating whether this level could be achieved in a fortification program without exceeding the UL for any other group in the population and the impact of a calcium fortification program on pregnancy outcomes.

Women of reproductive age and postmenopausal women are another group likely to benefit most from fortification efforts. In a study of 141 postmenopausal Chinese women, daily consumption of cow milk containing 250 mg calcium increased BMD in the hip (2.8%) and femoral neck (2.5%) over 18 months. 89 This is a significant difference from the control group, which decreased BMD in the hip and femoral neck over the study period. However, there were no differences in the BMD of the lumbar spine, where all groups showed a decrease in BMD, and the endline outcomes for calcium‐fortified soymilk (250 mg calcium) were not different from controls. In another study of postpartum women over a 12‐month period in China, consuming 40 g of milk powder/day with either 300, 600, or 900 mg of calcium showed no differences over the study period in the BMD. 90 Interestingly, the previous study of postmenopausal women also saw no significant differences at the 12‐month time point either, and it was only the 18‐month time point that showed significant gains. Longer‐term studies are, therefore, perhaps needed to understand the potential benefits and risks of calcium‐fortified foods. 89

To date, the only study reporting on cost‐effectiveness of calcium with health outcomes assessed the impact of a hypothetical calcium fortification program on bone fractures in postmenopausal women in Germany. This modeling exercise showed that the voluntary fortification of an unspecified food that would provide an additional 800 IU vitamin D (as cholecalciferol) and 200 mg of calcium would prevent 36,705 bone fractures in German women over 65 years old by 2050, with an annual savings of €315 million. 91

Calcium fortification policies

As with all fortification policies, calcium fortification can either be mandatory or voluntary. Mandatory fortification is used as a population‐based approach to address a public health concern and is generally recommended for improving micronutrient intakes. 92 In the case of calcium, the aim is to address inadequate calcium intake to prevent the health consequences of inadequate intake, such as rickets and preeclampsia. Mandatory food fortification requires minimal behavior change and for calcium can be a cost‐effective intervention. 91 By contrast, voluntary fortification relies more on the food manufacturers and consumer demand and access to address the public health issue, and typically many options are available to the consumers. 93 , 94 , 95 In these cases, the equity of availability and affordability must also be considered to ensure that the most at‐risk population groups can benefit from these products, especially if the costs of food fortification are passed on to the consumer. 96 , 97 However, mandating fortification of staple foods (i.e., all commercial production of the specified food must be fortified by law) enhances the potential to realize this benefit and ensures equity.

The food vehicle selected for mandatory food fortification programs should be based on usual intakes in the population of a food that should be consumed regularly by a large proportion of the population and is industrially produced to facilitate effective fortification. In setting the fortificant level, population subgroups with the lowest and highest intakes of the food should be taken into consideration to maximize the potential for impact while minimizing the risks of excess intake. Food selection for voluntary fortification is commonly at the discretion of industry, or may be included in legal documents that allow for (but not obligate) the fortification of certain food types. The WHO provides additional information on how to establish a food fortification program, with specific guidance for calcium. 98 It is also important to monitor coverage of the food fortification program, and the Fortification Assessment Coverage Toolkit (FACT) has been developed by the Global Alliance for Improved Nutrition. 99

While the UK is the only country with a mandatory calcium fortification policy (for wheat flour), several countries have voluntary fortification policies for calcium‐fortified staple foods and are listed in Table 2. Standards generally suggest 1250–2400 mg/kg of product for a variety of calcium salts. 100 The extent and quality of implementation and the population‐level impact of voluntary calcium fortification has not been thoroughly assessed. A recent review of the fortification polices of 15 countries suggests that coverage of fortified staple foods is highly variable, especially with voluntary fortification policies. 7 Limited evaluations of the impact of fortification programs on health outcomes, such as bone density, incidence rate of osteoporotic bone fractures, prevalence of hypertension, population blood pressure, and preeclampsia, have been conducted to date. However, these have assessed the impact of calcium‐fortified dairy products and not staple foods. 101

Table 2.

Staple foods currently fortified with calcium 100

Country Nutrient level in standard (mg/kg)
Maize flour
The United States of America 1375
Zambia 1278
Rice
Belize 650
The United States of America 1650
Wheat flour
Antigua and Barbuda 1250
Bahamas 1250
Bangladesh 53
Barbados 1250
Belize 1250
China 2400
Colombia 1280
Dominica 1250
Grenada 1250
Guyana 1250
Jamaica 1250
Jordan 14.15
Kuwait 2115
Qatar 2115
Saint Kitts and Nevis 1250
Saint Lucia 1250
Saint Vincent and the Grenadines 1250
Saudi Arabia 2115
Suriname 1250
Trinidad and Tobago 1265
United Arab Emirates 2115
The United Kingdom 3125
The United States of America 2112
Zambia 1278

Note: The low values appear to indicate the minimum allowable amount added in the standard.

Calcium salts for food fortification

When considering the form of calcium to be used in food fortification, a number of factors must be considered, including the bioavailability, solubility, sedimentation, acceptability, organoleptic properties, shelf‐life, and cost of the calcium salt. Thus, the choice of calcium salt will be dependent on these properties as well as the properties of the food vehicle being fortified.

There are many calcium salts suitable for human consumption and used by the food industry. These calcium salts have a wide range of elemental calcium content and water solubility, and the most commonly used in fortified foods are listed in Table 3. 76 , 102 Despite the range in physical properties, the fractional absorption of calcium (i.e., the percent of calcium absorbed in the intestine) is fairly similar among the most common salts, including calcium carbonate, tricalcium phosphate, calcium citrate, and calcium citrate malate. In general, calcium salts are fairly water soluble (except for calcium oxalates), but the bioavailability or fractional absorption can be low. Absorption is more dependent on calcium load and other factors, such as foods consumed with the salt, than on the form of the salt itself.

Table 3.

Properties and uses of the most commonly used calcium salts in food fortification 76 , 102

Calcium source Calcium content [%] Solubility [mmol/L] a Fractional absorption b Sensory properties Uses
Calcium carbonate 40 0.14 0.296 ± 0.054 Odorless; white or off‐white; chalky, soapy, or lemony taste Direct food additive; dough strengthener; firming agent; thickener; stabilizer; pH control
Tricalcium phosphate 38 0.97 0.252 ± 0.130 Odorless; sandy or bland taste Food additive to control pH in dough and lard; yeast nutrient in flour; supplement in livestock and poultry feeds
Calcium citrate 21 7.3 0.242 ± 0.049 Odorless; tart, acidic taste Food additive; sequestrant
Calcium citrate malate 30 80 0.363 ± 0.076 Odorless Food additive; sequestrant
a

Solubility in water at neutral pH.

b

Determined in women using isotopic tracer techniques on test loads of 200−300 mg calcium.

Calcium is a relatively bulky nutrient and relatively large amounts are needed in comparison with other nutrients to help meet the calcium requirements of a population, especially where intakes are very low. As a result, a bioavailable salt with high elemental calcium that does not have adverse acceptability or organoleptic properties is needed. 76 Fortunately, most calcium salts are odorless and white, which can help with acceptability and avoid discoloration of foods. Yet, some salts have a tart or acidic flavor that can affect acceptability and the amount that can be used when fortifying foods. Different salts are also used in different types of foods. For example, solid foods, such as cereals and flour, are often fortified with calcium carbonate, while liquids, such as juices, are fortified with different salts depending on the properties of the final food product in terms of pH, flavor, stability, and so on. 103 Acceptability studies have shown that up to 600 mg of calcium citrate malate (or 66 mg of elemental calcium) in 240 mL of orange juice did not reduce acceptability by consumers. 104 Similarly, calcium content in calcium‐fortified tortillas could be increased by nine‐fold with the addition of 114 mg of elemental calcium to a 48 g wheat‐flour tortilla without affecting consumer acceptability. In fact, the calcium carbonate–fortified tortillas were preferred over the unfortified tortillas and the tortillas fortified with either calcium lactate or calcium citrate. 105

Interactions between calcium and the fortified foods or other nutrients should also be considered. Calcium can interact with anthocyanins, contained in some blue, purple, or black foods (e.g., berries and black soybeans), causing a color change. 106 Adding calcium to beverages high in protein, such as soy and nut‐based beverages, can cause sedimentation. 107 However, a soy lecithin coating of the calcium can help avoid this issue. There have also been reports of calcium interfering with iron absorption in supplementation studies, but this was found to be a short‐term issue that is adapted to within a few months. 108 , 109 Some studies have also cited the interactions between calcium and zinc absorption, but longer‐term studies are needed to determine if this effect is limited to the short‐term, as it is for iron. 110 For more information on this, see the paper on supplementation in this special issue. 86

When fortifying foods, it is important to consider the percent of the population at risk of reaching or exceeding the UL with the fortified foods. However, for calcium, the amount that would typically be added to a fortified food would be relatively low due to calcium's effect on organoleptic properties and acceptability when compared with the relatively high UL (2500 mg/day for most adults). Two recent analyses modeled the impact of calcium fortification of water and flour for several countries. 35 , 111 Flour fortification at the level of 156 mg per 100 g of flour would result in less than 2% of individuals (6 months and older) exceeding the UL in the six of the seven countries modeled from five continents. 111 However, in two of these countries, the Lao PDR and Bangladesh, flour consumption is too low to have an impact on calcium intake. In a similar modeling exercise of calcium‐fortified water (500 mg of calcium/L), which included five LMICs and two high‐income countries, the populations from the LMICs had the greatest potential to benefit from fortification, with very few individuals exceeding the UL. 35

Specialized foods

Specialized foods are a form of fortified foods used to target a specific segment of the population, such as pregnant women or young children, for a limited period of time. Unlike staple‐food fortification, these products generally rely on special delivery mechanisms to reach individuals. Several of these specialized foods are available, though these may not be used by the entire population. These include fortified blended foods of partially precooked and milled cereals, soya, beans, and pulses that contain 350–450 mg of calcium as tri‐ or di‐calcium phosphate per 100 g of product, and they have been used in a few settings. 112 , 113 , 114 For example, Super Cereal, a corn‐soy blend, targets pregnant and lactating women and contains 362 mg of calcium per 100 g. 115 Many varieties of micronutrient powders and ready‐to‐use therapeutic foods (RUTFs) also contain 300–800 mg per 100 g food calcium. RUTFs also contain 300–600 mg per 100 g and are used for the treatment of severe acute malnutrition in children. 116

Supporting the production of calcium‐biofortified foods

Biofortification of calcium in various food crops has been suggested as a potentially economic and environmentally advantageous method to increase calcium intake. While calcium content in plants is driven by both environmental and genetic factors, 117 , 118 known strategies for improving the uptake and storage of calcium of food crops like rice require further research into the molecular mechanisms involved and the potential side effects to plant health and productivity. 33 , 119 While there are biological limits on how much calcium can be added to a food via biofortification, and, even with the help of biofortification, some plant foods will remain well below the calcium levels of dairy products. However, it is a potential solution, especially in areas with very low calcium intakes or where plant‐based diets are consumed. 30 A combination of lower‐phytate crops with higher mineral calcium has recently been proposed as a potentially viable path forward to provide bioavailable calcium that can meet the needs of the most vulnerable groups worldwide. 30

Agronomic biofortification

Agronomic biofortification seeks to alter the environment, while conventional breeding and genetic modification take advantage of the genetic properties of the plant that can improve calcium content and bioavailability. The calcium content in the plant is primarily limited by the supply and phytoavailability of calcium within the rhizosphere. 31 Soil properties, such as pH, water content, soil structure, and microbial activity, can also alter the calcium being taken up by the plant. In general, higher soil pH improves calcium availability. 120 , 121 In acidic soils, aluminum cations may inhibit calcium uptake, while sodium inhibits calcium uptake in saline soils. 36 As such, altering the properties of the soil (e.g., increasing the pH) or adding fertilizers containing phytoavailable calcium can improve the uptake of calcium into the plant and accumulation into edible tissues. Common calcium‐containing fertilizers, including lime (CaO and CaCO3), gypsum (CaSO4), calcium phosphate, and calcium nitrate, have been shown to increase the calcium content in tubers and leaves but not always in the fruits and seeds. 31 However, adding lime to the soil can also reduce the bioaccessibility of magnesium to the roots due to carbonate formation and excess calcium in the alkaline soil. 36 Some plants can also alter the rhizosphere to improve the bioavailability of the soil's mineral content, as can some arbuscular mycorrhizal fungi. 122

In one example of agronomic biofortification, durum wheat grown on peat in mineral solutions resulted in a 76% increase in calcium content in the roots and shoots and doubled the calcium content in the grains without toxicity. 123 Similarly, calcium content was increased in mustard and lettuce grown in hydroponic solutions of calcium. 124 This treatment also increased the number of leaves without decreasing biomass.

Calcium fertilizers can help improve soil health, especially in sub‐Saharan Africa. Unfortunately, adding calcium to the soil and leaves does not improve the crop yield, so there is little incentive for a farmer to use these relatively expensive methods to improve calcium content in their crops. 125 There is also concern for negative environmental impacts, so precise application strategies should be used. 31 , 122

Foliar application of calcium can also improve calcium content, though this is most often used to prevent calcium deficiency and can stimulate more uptake of calcium, especially in the leaves. Unfortunately, this is a more expensive approach and is readily washed away by rain. 122 Foliar applications of calcium applied to Rocha pear trees in which the leaves were treated with either Ca(NO3)2 or CaCl2 showed an increase in calcium content in the fruit, both in the epidermis and the central region of the fruit. 126 Importantly, there was no toxicity to the plant and no significant change to the sensory acceptability of the fruit. In another study, sunflower sprouts were treated with CaCl2, which increased calcium as well as total flavonoids and phenolics in the sprouts. 127

Due to the higher costs of manufacturing and distributing calcium fertilizers, agronomic biofortification is recommended in fairly niche areas and as a complement to breeding programs to improve calcium. To date, there are few studies that show a direct link between the application of such fertilizers and the impact on increased intake and health. 128

Conventional plant breeding

Biofortification through conventional plant breeding requires existing and useful genetic variation for targeting a nutrient of interest. For calcium, relatively little is known about the genetic control or physiological mechanisms that can lead to higher calcium content in the grain of staple crops. As a result, this requires additional research to identify crops with high amounts of calcium.

While biofortification through breeding is still in the early stages of understanding the genes involved in calcium regulation, there are several potentially good starting points to explore plant breeding to increase calcium content. Currently, finger millet is known to have relatively large amounts of calcium at 344 mg/100 g of dry weight compared with pearl millet, which contains 42 mg/100 g of dry weight, and other cereal grains. 33 Finger millet also has high grain yield potential and environmental sustainability, 33 as well as many accessions in gene banks from around the world, 129 which makes this form of millet a good starting point for conventional breeding programs. Other cereals, such as wheat, have fairly high calcium values, and their genetic variability could be explored. Legumes also provide some potential based on their genetic variability, especially in the wild lines that contain up to nine times higher amounts of calcium than the cultivated versions. 130 Use of lower‐phytate corn can help improve the fractional absorption of calcium in corn by about 30%. 131 However, any alteration of phytate content in the originating plant must be considered for its potential effects on yield, either direct 132 or indirect. 119

Transgenic modification

The major genetic targets for transgenic modifications to increase calcium in plants are overexpression of calcium transport proteins, calcium channels, and other calcium‐binding proteins. Most of the research to date has focused on cation exchanger 1 (CAX1), which exchanges Ca2+ and H+ and can thereby increase calcium content. 133 Ensuring the health of the plant can also be a challenge because the overexpression of some of these genes has resulted in defects in the plants that could lead to mineral imbalances and growth defects. 134

Other opportunities remain for genetic modification of plants, such as lowering phytic acid levels, which could increase the bioavailability of micronutrients, including calcium. 135 , 136 Calcium‐dependent protein kinases could be a future target that can increase a plant's stress resistance. This may prove especially important for climate change and improving the drought resistance of plants. This has been done for potatoes and rice to enhance their tolerance to drought, stress, and diseases. 137 , 138 It will also be important to monitor the heavy metal uptake in transgenic plants as it may be possible for ions similar to calcium, such as cadmium, to be transported into the plants along with the calcium, and increasing calcium uptake could lead to higher levels of these toxic ions. 139

Interactions with other food components

Several food components may affect the absorption of calcium present in many foods. Oxalates and phytates (described above) are plant components that create insoluble salts with calcium, resulting in reduced bioavailability. 32 Oxalate salts are found in strawberries, spinach, rhubarb, beets, nuts, wheat bran, chocolate, tea, and coffee. 140 In particular, calcium oxalate crystals are insoluble at the intestinal pH. 141 However, some gut bacteria can break down the oxalates, including Oxalobacter formigenes, Lactobacillus, and Bifidobacterium. These bacteria have been proposed for use in the form of probiotics for oxalate degradation. 140 However, this is under investigation, and the effect on increasing calcium absorption is rather small, that is, <5%. 47 , 142

Sodium consumption can increase the elimination of calcium through urinary excretion (calcinuria). 143 As the amount of sodium consumed is on the rise, largely due to the increased consumption of processed foods, including bread, this is an especially important consideration. As a result, reducing sodium consumption can improve the retention of calcium.

Vitamin D can help promote the absorption of calcium depending on age and health/vitamin D status. Vitamin D status influences active calcium absorption through vitamin D– and parathyroid hormone–dependent upregulation of transport proteins, which takes longer than can be accomplished to influence coingested calcium. 144 Nevertheless, combining calcium with vitamin D can assist with adherence to taking both nutrients through supplementation. A recent study using isotopic techniques has shown that vitamin D3 supplementation in the short term causes positive bone mineral balance, leading to better calcium deposition into the bone. 145

Based on animal models, lactose may also help in the passive absorption of calcium. But calcium absorption from various dairy products that differ widely in lactose content is similar in humans. 146 Milk proteins, such as casein phosphopeptides, 12 can also promote calcium absorption, but the effect is modest. 147 Some amino acids (i.e., lysine and arginine) can help convert calcium into a more soluble form in the lumen. 148

Prebiotic fibers can increase calcium absorption and retention in children and adults. 149 , 150 , 151 , 152 , 153 In one study, adolescents consumed short‐ and long‐chain inulin‐like fructans, which increased calcium absorption and BMD, and this effect was influenced by the genotype of a vitamin D receptor gene, Fok1. 152 Soluble corn fiber (10 and 20 g/day) was also shown to increase calcium retention in postmenopausal women and improved calcium balance by 50 mg/day. 153 Similar results were found in adolescents as well. 150 , 151 It is thought that the soluble corn fiber is fermented by one group of bacteria and the metabolites are fermented further by a second group of bacteria, which in turn results in increased calcium absorption. 151

There have been concerns raised over the interactions of calcium with other divalent cations, such as iron and zinc. Short‐term supplementation studies showed that increasing calcium can interfere with the intestinal absorption of iron, but this does not appear to have any long‐term effects on iron status. A recent systematic review suggests the short‐term effect is small, but more work is needed to better understand the effect. 154 This is described in more detail in the supplementation article in this special issue. 86 With respect to foods, the quantities of micronutrients consumed at any one time are likely to be smaller and thus have a less of an impact on absorption.

Remaining research questions

There are a number of unanswered research questions that would better inform polices and interventions for food‐based approaches to improve calcium intake. One such issue that remains unknown, especially for calcium, is the potential impact of calcium interventions on the burden of disease. It would be helpful to have a validated indicator of impact for modeling interventions, whether this is in terms of disability adjusted life years or lives saved from maternal and perinatal mortality.

The effectiveness and cost‐effectiveness of the various calcium interventions discussed here are also largely unknown and would be useful in advocating for interventions, such as fortification or the impact of water fortification on infrastructure. However, it is also unclear whether the costs of agronomic biofortification can be overcome to increase the calcium intake in a meaningful way among those most vulnerable, and if fertilizer formulations can be optimized to reduce costs.

Also, there is a need to better understand which foods and staples are amenable to conventional or transgenic calcium biofortification and if there is an ideal “basket” of foods that can be biofortified/fortified to reach all vulnerable populations. Investments are needed to characterize the genes involved in the acquisition and mobilization of calcium and other nutrients among millets, other cereals, and legumes in order to identify future candidates for biofortification. High‐quality reference genomes must be created in order to apply the increased capabilities of next‐generation sequencing platforms that will enable doing so at increasingly faster speeds.

There are also remaining needs in overcoming the impacts of antinutrients, such as phytates in whole grain flours, in conventional or transgenic biofortification methods and/or food processing methods, by using phytase to increase calcium absorption. The answer could lie in traditional practices and crops that had relatively high levels of calcium, such as millet and other ancient grains. 155 Lastly, the elevated CO2 from climate change is likely to decrease nutritional quality, which may impact the calcium content of crops and is expected to affect the availability and affordability of foods, including those rich in calcium. 156 The effects of climate change are also expected to result in a decline of small local fish, which are a natural source of calcium for some populations. 15 Determining how climate‐related challenges will impact calcium intake and developing solutions will be an important step in providing adequate dietary calcium in the future.

These research gaps would also help inform which policy levers would be available to increase local supplies of natural calcium‐source foods to reach vulnerable populations if increasing scale is a viable option (e.g., production subsidies, trade policies, etc.).

Conclusions

Calcium intake in many LMICs remains well below the recommended levels. To help improve calcium intake, there are a number of interventions that can be implemented. These include promoting the consumption of foods naturally high in calcium, using food processing techniques that can improve calcium content or bioavailability, staple food fortification, and biofortification to produce higher calcium‐containing crops. These interventions are available to policy makers interested in improving calcium intake. Monitoring and evaluation of the coverage and health impacts of such interventions is strongly encouraged. Addressing some of the research gaps will also help optimize interventions and should lead to greater understanding of the health impacts of improving calcium intake.

Competing interests

The authors declare no competing interests.

Peer review

The peer review history for this article is available at: https://publons.com/publon/10.1111/nyas.14743

Acknowledgments

We gratefully acknowledge Christine Stewart for her critical review and comments on this paper. The meetings of the Calcium Task Force, the development of this paper, and its open access were supported by funding from the Children's Investment Fund Foundation to the Nutrition Science Program of the New York Academy of Sciences.

References

  • 1. Balk, E.M. , Adam G.P., Langberg V.N., et al. 2017. Global dietary calcium intake among adults: a systematic review. Osteoporos. Int. 28: 3315–3324. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2. Ross, A. , Manson J.A.E., Abrams S.A., et al. 2011. The 2011 report on dietary reference intakes for calcium and vitamin D from the Institute of Medicine: what clinicians need to know. J. Clin. Endocrinol. Metab. 96: 53–58. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3. La, V.S. , Marchelli R., Martin A., et al. 2015. Scientific opinion on dietary reference values for calcium. EFSA J. 13: 4101. [Google Scholar]
  • 4. Beal, T. , Massiot E., Arsenault J.E., et al. 2017. Global trends in dietary micronutrient supplies and estimated prevalence of inadequate intakes. PLoS One 12: e0175554. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5. Kumssa, D.B. , Joy E.J.M., Ander E.L., et al. 2015. Dietary calcium and zinc deficiency risks are decreasing but remain prevalent. Sci. Rep. 5: 10974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6. Jansson‐Knodell, C.L. , Krajicek E.J., Savaiano D.A., et al. 2020. Lactose intolerance: a concise review to skim the surface. Mayo Clin. Proc. 95: 1499–1505. [DOI] [PubMed] [Google Scholar]
  • 7. Cormick, G. , Betrán A.P., Metz F., et al. 2020. Regulatory and policy‐related aspects of calcium fortification of foods — implications for implementing national strategies of calcium fortification. Nutrients 12: 1022. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Drewnowski, A. , Monterrosa E.C., De Pee S., et al. 2020. Shaping physical, economic, and policy components of the food environment to create sustainable healthy diets. Food Nutr. Bull. 41: S74–S86. [DOI] [PubMed] [Google Scholar]
  • 9. Hidrobo, M. , Hoddinott J., Peterman A., et al. 2014. Cash, food, or vouchers? Evidence from a randomized experiment in northern Ecuador. J. Dev. Econ. 107: 144–156. [Google Scholar]
  • 10. Yen, S.T. 2010. The effects of SNAP and WIC programs on nutrient intakes of children. Food Policy 35: 576–583. [Google Scholar]
  • 11. Hawkes, C. , Jewell J. & Allen K.. 2013. A food policy package for healthy diets and the prevention of obesity and diet‐related non‐communicable diseases: the NOURISHING framework. Obes. Rev. 14: 159–168. [DOI] [PubMed] [Google Scholar]
  • 12. Weaver, C.M. & Heaney R.P.. 2006. Food sources, supplements, and bioavailability. In Calcium in Human Health. Weaver C.M. & Heaney R.P., Eds.: 129–142. Springer. [Google Scholar]
  • 13. Hess, J.M. , Cifelli C.J., Agarwal S., et al. 2019. Comparing the cost of essential nutrients from different food sources in the American diet using NHANES 2011–2014. Nutr. J. 18: 68. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14. Storhaug, C.L. , Fosse S.K. & Fadnes L.T.. 2017. Country, regional, and global estimates for lactose malabsorption in adults: a systematic review and meta‐analysis. Lancet Gastroenterol. Hepatol. 2: 738–746. [DOI] [PubMed] [Google Scholar]
  • 15. Hicks, C.C. , Cohen P.J., Graham N.A.J., et al. 2019. Harnessing global fisheries to tackle micronutrient deficiencies. Nature 574: 95–98. [DOI] [PubMed] [Google Scholar]
  • 16. Larsen, T. , Thilsted S.H., Kongsbak K., et al. 2000. Whole small fish as a rich calcium source. Br. J. Nutr. 83: 191–196. [PubMed] [Google Scholar]
  • 17. Bogard, J.R. , Hother A.L., Saha M., et al. 2015. Inclusion of small indigenous fish improves nutritional quality during the first 1000 days. Food Nutr. Bull. 36: 276–289. [DOI] [PubMed] [Google Scholar]
  • 18. Thacher, T.D. , Bommersbach T.J., Pettifor J.M., et al. 2015. Comparison of limestone and ground fish for treatment of nutritional rickets in children in Nigeria. J. Pediatr. 167: 148–154.e1. [DOI] [PubMed] [Google Scholar]
  • 19. Shantibala, T. , Lokeshwari R.K. & Debaraj H.. 2014. Nutritional and antinutritional composition of the five species of aquatic edible insects consumed in Manipur, India. J. Insect Sci. 14: 14. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20. Adámková, A. , Kouřimská L., Borkovcová M., et al. 2014. Calcium in edible insects and its use in human nutrition. Potravinárstvo 8: 233–238. [Google Scholar]
  • 21. Food and Agriculture Organization of the United Nations . 2013. Edible insects–future prospects for food and feed security. Rome: FAO. [Google Scholar]
  • 22. Williams, J.P. , Williams J.R., Kirabo A., et al. 2016. Nutrient content and health benefits of insects. In Insects as Sustainable Food Ingredients. Dossey A.T., Morales‐Ramos J.A. & Rojas M.G, Eds.: 61–84. [Google Scholar]
  • 23. Associated Press . 2013. Worms! A look at Zimbabwe's favorite snack: mopane worms. Daily News. [Google Scholar]
  • 24. Adeduntan, S.A. 2005. Foraging in Akure Forest Reserve Ondo State, Nigeria. J. Food Technol. 3: 563–567. [Google Scholar]
  • 25. Ojha, S. , Bekhit A., Grune T., et al. 2021. Bioavailability of nutrients from edible insects. Curr. Opin. Food Sci. 41: 240–248. [Google Scholar]
  • 26. EFSA Scientific Committee . 2015. Risk profile related to production and consumption of insects as food and feed. EFSA J. 13: 4257. [Google Scholar]
  • 27. White, P.J. & Broadley M.R.. 2001. Chloride in soils and its uptake and movement within the plant: a review. Ann. Bot. 88: 967–988. [Google Scholar]
  • 28. White, P.J. 2001. The pathways of calcium movement to the xylem. J. Exp. Bot. 52: 891–899. [DOI] [PubMed] [Google Scholar]
  • 29. White, P.J. & Broadley M.R.. 2003. Calcium in plants. Ann. Bot. 92: 487–511. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30. Knez, M. & Stangoulis J.C.R.. 2021. Calcium biofortification of crops–challenges and projected benefits. Front. Plant Sci. 12: 669053. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31. White, P.J. & Broadley M.R.. 2009. Biofortification of crops with seven mineral elements often lacking in human diets–iron, zinc, copper, calcium, magnesium, selenium and iodine. New Phytol. 182: 49–84. [DOI] [PubMed] [Google Scholar]
  • 32. Weaver, C.M. & Plawecki K.L.. 1994. Dietary calcium: adequacy of a vegetarian diet. Am. J. Clin. Nutr. 59: 1238S–1241S. [DOI] [PubMed] [Google Scholar]
  • 33. Puranik, S. , Kam J., Sahu P.P., et al. 2017. Harnessing finger millet to combat calcium deficiency in humans: challenges and prospects. Front. Plant Sci. 8: 1311. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34. Food and Agriculture Organization of the United Nations & iZiNCG . 2018. Global Food Composition Database for Phytate Version 1.0 ‐ PhyFoodComp. Rome. [Google Scholar]
  • 35. Cormick, G. , Gibbons L. & Belizán J.M.. 2020. Impact of water fortification with calcium on calcium intake in different countries: a simulation study. Public Health Nutr. 1–14. 10.1017/S1368980020002232 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36. Januszko, O. , Madej D., Postaleniec E., et al. 2012. [Minerals intake from drinking water by young women]. Rocz. Państwowego Zakładu Hig. 63: 43–50. [PubMed] [Google Scholar]
  • 37. Moynihan, P. , Adamson A., Rugg A., et al. 1996. Dietary sources of calcium and the contribution of flour fortification to total calcium intake in the diets of Northumbrian adolescents. Br. J. Nutr. 75: 495–505. [DOI] [PubMed] [Google Scholar]
  • 38. Cormick, G. , Lombarte M., Minckas N., et al. 2020. Contribution of calcium in drinking water from a South American country to dietary calcium intake. BMC Res. Notes 13: 465. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39. de Souza, C.F.M. , Lima J.F., Adriano M.S.P.F., et al. 2013. Assessment of groundwater quality in a region of endemic fluorosis in the northeast of Brazil. Environ. Monit. Assess. 185: 4735–4743. [DOI] [PubMed] [Google Scholar]
  • 40. Djellouli, H.M. , Taleb S., Harrache‐Chettouh D., et al. 2005. Qualité physico‐chimique des eaux de boisson du Sud algérien: étude de l'excès en sels minéraux. Cah. d’études Rech. Francoph. 15: 109–112. [PubMed] [Google Scholar]
  • 41. Ensinger . Accessed August 23, 2021. https://www.ensinger.de/mineralien‐check/.
  • 42. Galan, P. , Arnaud M.J., Czernichow S., et al. 2002. Contribution of mineral waters to dietary calcium and magnesium intake in a French adult population. J. Am. Diet. Assoc. 102: 1658–1662. [DOI] [PubMed] [Google Scholar]
  • 43. Skoglund, E. , Carlsson N.‐G. & Sandberg A.‐S.. 2009. Phytate. In HEALTHGRAIN Methods: Analysis of Bioactive Components in Small Grain Cereals. Shewry P. & Ward J.L., Eds.: 129–139. [Google Scholar]
  • 44. Afinah, S. , Yazid A.M., Anis Shobirin M.H., et al. 2010. Review Article Phytase: application in food industry. Int. Food Res. J. 17: 13–21. [Google Scholar]
  • 45. Lott, J.N.A. , Ockenden I., Raboy V., et al. 2001. A global estimate of phytic acid and phosphorus in crop grains, seeds, and fruits. In Food Phytates. Reddy N.R. & Sathe S.K., Eds.: 23–40. CRC Press. [Google Scholar]
  • 46. Stevenson, L. , Phillips F., O'sullivan K., et al. 2012. Wheat bran: its composition and benefits to health, a European perspective. Int. J. Food Sci. Nutr. 63: 1001–1013. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47. Hanes, D.A. , Weaver C.M., Heaney R.P., et al. 1999. Absorption of calcium oxalate does not require dissociation in rats. J. Nutr. 129: 170–173. [DOI] [PubMed] [Google Scholar]
  • 48. Reale, A. , Konietzny U., Coppola R., et al. 2007. The importance of lactic acid bacteria for phytate degradation during cereal dough fermentation. J. Agric. Food Chem. 55: 2993–2997. [DOI] [PubMed] [Google Scholar]
  • 49. Abebe, Y. , Bogale A., Hambidge K.M., et al. 2007. Phytate, zinc, iron and calcium content of selected raw and prepared foods consumed in rural Sidama, Southern Ethiopia, and implications for bioavailability. J. Food Compos. Anal. 20: 161–168. [Google Scholar]
  • 50. Tezera, F. , Whiting S.J. & Gebremedhin S.. 2017. Dietary calcium intake and sunlight exposure among children aged 6–23 months in Dale Woreda, Southern Ethiopia. Afr. J. Food Agric. Nutr. Dev. 17: 12427–12440. [Google Scholar]
  • 51. Shumoy, H. , Lauwens S., Gabaza M., et al. 2017. Traditional fermentation of tef injera: impact on in vitro iron and zinc dialysability. Food Res. Int. 102: 93–100. [DOI] [PubMed] [Google Scholar]
  • 52. Belizan, J.M. & Villar J.. 1980. The relationship between calcium intake and edema‐, proteinuria‐, and hypertension‐gestosis: an hypothesis. Am. J. Clin. Nutr. 33: 2202–2210. [DOI] [PubMed] [Google Scholar]
  • 53. Hamlin, R.H.J. 1962. Prevention of pre‐eclampsia. Lancet 279: 864–865. [Google Scholar]
  • 54. Tesfaye, B. , Sinclair K., Wuehler S.E., et al. 2019. Applying international guidelines for calcium supplementation to prevent pre‐eclampsia: simulation of recommended dosages suggests risk of excess intake in Ethiopia. Public Health Nutr. 22: 531–541. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55. Palacios, M.C. , Haros M., Sanz Y., et al. 2008. Phytate degradation by Bifidobacterium on whole wheat fermentation. Eur. Food Res. Technol. 226: 825–831. [Google Scholar]
  • 56. Greiner, R. & Konietzny U.. 2006. Phytase for food application. Food Technol. Biotechnol. 44: 125–140. [Google Scholar]
  • 57. Eskin, N.A.M. & Wiebe S.. 1983. Changes in phytase activity and phytate during germination of two fababean cultivars. J. Food Sci. 48: 270–271. [Google Scholar]
  • 58. Ghavidel, R.A. & Prakash J.. 2007. The impact of germination and dehulling on nutrients, antinutrients, in vitro iron and calcium bioavailability and in vitro starch and protein digestibility of some legume seeds. LWT ‐ Food Sci. Technol. 40: 1292–1299. [Google Scholar]
  • 59. Mahgoub, S.E.O. & Elhag S.A.. 1998. Effect of milling, soaking, malting, heat‐treatment and fermentation on phytate level of four Sudanese sorghum cultivars. Food Chem. 61: 77–80. [Google Scholar]
  • 60. Lestienne, I. , Icard‐Vernière C., Mouquet C., et al. 2005. Effects of soaking whole cereal and legume seeds on iron, zinc and phytate contents. Food Chem. 89: 421–425. [Google Scholar]
  • 61. Palacios, M.C. , Haros M., Sanz Y., et al. 2008. Selection of lactic acid bacteria with high phytate degrading activity for application in whole wheat breadmaking. LWT‐Food Sci. Technol. 41: 82–92. [Google Scholar]
  • 62. Monnard, A. , Moretti D., Zeder C., et al. 2017. The effect of lipids, a lipid‐rich ready‐to‐use therapeutic food, or a phytase on iron absorption from maize‐based meals fortified with micronutrient powders. Am. J. Clin. Nutr. 105: 1521–1527. [DOI] [PubMed] [Google Scholar]
  • 63. Zyba, S.J. , Wegmüller R., Woodhouse L.R., et al. 2019. Effect of exogenous phytase added to small‐quantity lipid‐based nutrient supplements (SQ‐LNS) on the fractional and total absorption of zinc from a millet‐based porridge consumed with SQ‐LNS in young Gambian children: a randomized controlled trial. Am. J. Clin. Nutr. 110: 1465–1475. [DOI] [PubMed] [Google Scholar]
  • 64. Troesch, B. , Egli I., Zeder C., et al. 2009. Optimization of a phytase‐containing micronutrient powder with low amounts of highly bioavailable iron for in‐home fortification of complementary foods. Am. J. Clin. Nutr. 89: 539–544. [DOI] [PubMed] [Google Scholar]
  • 65. Troesch, B. , Jing H., Laillou A., et al. 2013. Absorption studies show that phytase from Aspergillus niger significantly increases iron and zinc bioavailability from phytate‐rich foods. Food Nutr. Bull. 34: S90–S101. [DOI] [PubMed] [Google Scholar]
  • 66. Rosado, J.L. , Cassís L., Solano L., et al. 2005. Nutrient addition to corn masa flour: effect on corn flour stability, nutrient loss, and acceptability of fortified corn tortillas. Food Nutr. Bull. 26: 266–272. [DOI] [PubMed] [Google Scholar]
  • 67. Solomons, N.W. 1997. Micronutrients and urban life‐style: lessons from Guatemala. Arch. Latinoam. Nutr. 47: 44–49. [PubMed] [Google Scholar]
  • 68. Espejel‐García, M.V. , Mora‐Flores J.S., García‐Salazar J.A., et al. 2016. Characterization of tortilla consumers in Estado de México. Agric. Soc. y Desarro 13: 371–384. [Google Scholar]
  • 69. Gomez‐Aldapa, G. , Martinez‐Bustos F., Figueroa C., et al. 1999. A comparison of the quality of whole corn tortillas made from instant corn flours by traditional or extrusion processing. Int. J. Food Sci. Technol. 34: 391–399. [Google Scholar]
  • 70. Doesthale, Y.G. , Devara S., Rao S., et al. 1979. Effect of milling on mineral and trace element composition of raw and parboiled rice. J. Sci. Food Agric. 30: 40–46. [DOI] [PubMed] [Google Scholar]
  • 71. Rahman, H. , Carey M., Hossain M., et al. 2019. Modifying the parboiling of rice to remove inorganic arsenic, while fortifying with calcium. Environ. Sci. Technol. 53: 5249–5255. [DOI] [PubMed] [Google Scholar]
  • 72. Jannasch, A. & Wang Y.J.. 2020. Development of a limited‐water soaking method on the fortification of rice with calcium and iron by parboiling. J. Cereal Sci. 94: 103014. [Google Scholar]
  • 73. Benjakul, S. & Karnjanapratum S.. 2018. Characteristics and nutritional value of whole wheat cracker fortified with tuna bone bio‐calcium powder. Food Chem. 259: 181–187. [DOI] [PubMed] [Google Scholar]
  • 74. Bartter, J. , Diffey H., Yeung Y.H., et al. 2018. Use of chicken eggshell to improve dietary calcium intake in rural sub‐Saharan Africa. Matern. Child Nutr. 14: e12649. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 75. Schaafsma, A. & Beelen G.M.. 1999. Eggshell powder, a comparable or better source of calcium than purified calcium carbonate: piglet studies. J. Sci. Food Agric. 79: 1596–1600. [Google Scholar]
  • 76. Palacios, C. , Cormick G., Hofmeyr G.J., et al. 2021. Calcium‐fortified foods in public health programs: considerations for implementation. Ann. N.Y. Acad. Sci. 1485: 3–21. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77. Bradauskiene, V. , Montrimaite K. & Moscenkova E.. 2017. Facilities of bread enrichment with calcium by using eggshell powder. 91–95.
  • 78. Cormick, G. , Betran A.P., Romero I.B., et al. 2021. Effect of calcium fortified foods on health outcomes: a systematic review and meta‐analysis. Nutrients 13: 316. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 79. Department for Environment Food & Rural Affairs of the UK . 1998. Bread and Flour Regulations. London. [Google Scholar]
  • 80. Osler, M. & Heitmann B.L.. 1998. Food patterns, flour fortification, and intakes of calcium and vitamin D: a longitudinal study of Danish adults. J. Epidemiol. Community Health 52: 161–165. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 81. Cheng, S. , Lyytikäinen A., Kröger H., et al. 2005. Effects of calcium, dairy product, and vitamin D supplementation on bone mass accrual and body composition in 10–12‐y‐old girls: a 2‐y randomized trial. Am. J. Clin. Nutr. 82: 1115–1126. [DOI] [PubMed] [Google Scholar]
  • 82. Zhe‐qing, Z. , Ma X. M., Z.W. Huang, et al. 2014. Effects of milk salt supplementation on bone mineral gain in pubertal Chinese adolescents: a 2‐year randomized, double‐blind, controlled, dose–response trial. Bone 65: 69–76. [DOI] [PubMed] [Google Scholar]
  • 83. de Romaña, G.L. 2000. Experience with complementary feeding in the FONCODES Project. Food Nutr. Bull. 21: 43–48. [Google Scholar]
  • 84. van Stuijvenberg, M.E. 2005. Using the school of feeding system as a vehicle for micronutrient fortification: experience from South Africa. Food Nutr. Bull. 26: S213–S219. [DOI] [PubMed] [Google Scholar]
  • 85. Tartanac, F. 2000. Incaparina and other Incaparina‐based foods: experience in INCAP in Central America. Food Nutr. Bull. 21: 49–54. [Google Scholar]
  • 86. Gomes, F. , Ashorn P., Askari S., et al. 2022. Calcium supplementation for the prevention of hypertensive disorders of pregnancy: current evidence and programmatic considerations. Ann. N.Y. Acad. Sci. 10.1111/nyas.14733 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 87. Hofmeyr, G.J. , Betrán A.P., Singata‐Madliki M., et al. 2019. Prepregnancy and early pregnancy calcium supplementation among women at high risk of pre‐eclampsia: a multicentre, double‐blind, randomised, placebo‐controlled trial. Lancet 393: 330–339. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 88. Fawzi, W. 2020. ClinicalTrials.gov 2020 Accessed December 4, 2021. https://clinicaltrials.gov/ct2/show/NCT03350516.
  • 89. Gui, J.‐C. , Brašić J.R., Liu X.‐D., et al. 2012. Bone mineral density in postmenopausal Chinese women treated with calcium fortification in soymilk and cow's milk. Osteoporos. Int. 23: 1563–1570. [DOI] [PubMed] [Google Scholar]
  • 90. Zhang, Z.‐Q. , Chen Y.‐M., Wang R.‐Q., et al. 2016. The effects of different levels of calcium supplementation on the bone mineral status of postpartum lactating Chinese women: a 12‐month randomised, double‐blinded, controlled trial. Br. J. Nutr. 115: 24–31. [DOI] [PubMed] [Google Scholar]
  • 91. Sandmann, A. , Amling M., Barvencik F., et al. 2017. Economic evaluation of vitamin D and calcium food fortification for fracture prevention in Germany. Public Health Nutr. 20: 1874–1883. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 92. Mannar, M.G.V. & Hurrell R.F.. 2018.. Food Fortification in a Globalized World. Academic Press. [Google Scholar]
  • 93. Wagner, K.‐H. , Blauensteiner D., Schmid I., et al. 2005. The role of fortified foods–situation in Austria. In Diet Diversification and Health Promotion. Elmadfa I., Ed.: 84–90. Karger Publishers. [DOI] [PubMed] [Google Scholar]
  • 94. Sacco, J.E. , Dodd K.W., Kirkpatrick S.I., et al. 2013. Voluntary food fortification in the United States: potential for excessive intakes. Eur. J. Clin. Nutr. 67: 592–597. [DOI] [PubMed] [Google Scholar]
  • 95. Sicińska, E. , Pietruszka B., Januszko O., et al. 2020. Intake of vitamins and minerals from voluntarily fortified foods and/or dietary supplements in school adolescents in Central‐Eastern Poland. Front. Public Health 8: 504015. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 96. Das, J.K. , Salam R.A., Kumar R., et al. 2013. Micronutrient fortification of food and its impact on woman and child health: a systematic review. Syst. Rev. 2: 67. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 97. Eichler, K. , Hess S., Twerenbold C., et al. 2019. Health effects of micronutrient fortified dairy products and cereal food for children and adolescents: a systematic review. PLoS One 14: e0210899. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 98. Allen, L.H. , de Benoist B., Dary O., et al. 2006. Guidelines on Food Fortification with Micronutrients. WHO. [Google Scholar]
  • 99. Friesen, V.M. , Aaron G.J., Myatt M., et al. 2017. Assessing coverage of population‐based and targeted fortification programs with the use of the Fortification Assessment Coverage Toolkit (FACT): background, toolkit development, and supplement overview. J. Nutr. 147: 981S–983S. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 100.Global Fortification Data Exchange. Accessed May 13, 2021. https://fortificationdata.org/.
  • 101. Whiting, S.J. , Kohrt W.M., Warren M.P., et al. 2016. Food fortification for bone health in adulthood: a scoping review. Eur. J. Clin. Nutr. 70: 1099–1105. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 102. Weaver, C.M. 1998. Calcium in food fortification strategies. Int. Dairy J. 8: 443–449. [Google Scholar]
  • 103. Palacios, C. , Hofmeyr G.J., Cormick G., et al. 2021. Current calcium fortification experiences: a review. Ann. N.Y. Acad. Sci. 1484: 55–73. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 104. Assmann, S. , Medeiros D.M. & Chambers E.. 2003. Fortification with calcium citrate malate may not influence the sensory properties of an orange flavored beverage. J. Food Qual. 26: 395–407. [Google Scholar]
  • 105. Romanchik‐Cerpovicz, J.E. & McKemie R.J.. 2007. Fortification of all‐purpose wheat‐flour tortillas with calcium lactate, calcium carbonate, or calcium citrate is acceptable. J. Am. Diet. Assoc. 107: 506–509. [DOI] [PubMed] [Google Scholar]
  • 106. Cortez, R. , Luna‐Vital D.A., Margulis D., et al. 2017. Natural pigments: stabilization methods of anthocyanins for food applications. Compr. Rev. Food Sci. Food Saf. 16: 180–198. [DOI] [PubMed] [Google Scholar]
  • 107. Hirotsuka, M. , Taniguchi H., Narita H., et al. 1984. Calcium fortification of soy milk with calcium‐lecithin liposome system. J. Food Sci. 49: 1111–1112. [Google Scholar]
  • 108. Yan, L. , Prentice A., Dibba B., et al. 1996. The effect of long‐term calcium supplementation on indices of iron, zinc and magnesium status in lactating Gambian women. Br. J. Nutr. 76: 821–831. [DOI] [PubMed] [Google Scholar]
  • 109. Mølgaard, C. , Kæstel P. & Michaelsen K.F.. 2005. Long‐term calcium supplementation does not affect the iron status of 12–14‐y‐old girls–. Am. J. Clin. Nutr. 82: 98–102. [DOI] [PubMed] [Google Scholar]
  • 110. Wood, R.J. & Zheng J.J.. 1997. High dietary calcium intakes reduce zinc absorption and balance in humans. Am. J. Clin. Nutr. 65: 1803–1809. [DOI] [PubMed] [Google Scholar]
  • 111. Cormick, G. , Betran A.P., Romero I.B., et al. 2021. Impact of flour fortification with calcium on calcium intake: a simulation study in seven countries. Ann. N.Y. Acad. Sci. 1493: 59–74. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 112. Ruel, M.T. , Menon P., Loechl C., et al. 2004. Donated fortified cereal blends improve the nutrient density of traditional complementary foods in Haiti, but iron and zinc gaps remain for infants. Food Nutr. Bull. 25: 361–376. [DOI] [PubMed] [Google Scholar]
  • 113. Rogers, B.L. , Wilner L.B., Maganga G., et al. 2017. Program changes are effective and cost‐effective in increasing the amount of oil used in preparing corn soy blend porridge for treatment of moderate acute malnutrition in Malawi. Matern. Child Nutr. 13: e12393. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 114. Chanadang, S. , Chambers E.I.V., Kayanda R., et al. 2018. Novel fortified blended foods: preference testing with infants and young children in Tanzania and descriptive sensory analysis. J. Food Sci. 83: 2343–2350. [DOI] [PubMed] [Google Scholar]
  • 115. World Food Programme . 2013. Super Cereal .
  • 116. World Health Organization, World Food Programme , Standing Committee on Nutrition , et al. 2007. WHO/WFP/SCN and UNICEF Joint Statement on Community‐Based Management of Severe Acute Malnutrition.
  • 117. Singh, M.K. & Prasad S.K.. 2014. Agronomic aspects of zinc biofortification in rice (Oryza sativa L.). Proc. Natl. Acad. Sci. India Sect. B Biol. Sci. 84: 613–623. [Google Scholar]
  • 118. Singh, U. , Praharaj C.S., Chaturvedi S.K., et al. 2016. Biofortification: introduction, approaches, limitations, and challenges. In Biofortification of Food Crops. Singh U., Praharaj C.S., Singh S.S., & Singh N.P., Eds.: 3–18. Springer. [Google Scholar]
  • 119. Yang, J. , Punshon T., Lou Guerinot M., et al. 2012. Plant calcium content: ready to remodel. Nutrients 4: 1120–1136. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 120. Brady, N. & Weil R.. 1996. The Nature and Properties of Soil. [Google Scholar]
  • 121. Yan, F. , Schubert S. & Mengel K.. 1992. Effect of low root medium pH on net proton release, root respiration, and root growth of corn (Zea mays L.) and broad bean (Vicia faba L.). Plant Physiol. 99: 415–421. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 122. De Valença, A.W. , Bake A., Brouwer I.D., et al. 2017. Agronomic biofortification of crops to fight hidden hunger in sub‐Saharan Africa. Glob. Food Sec. 12: 8–14. [Google Scholar]
  • 123. Pataco, I.M. , Lidon F.C., Ramos I., et al. 2017. Biofortification of durum wheat (Triticum turgidum L. ssp. durum (Desf.) Husnot) grains with nutrients. J. Plant Interact. 12: 39–50. [Google Scholar]
  • 124. Gustiar, F. , Munandar M., Ningsih S.W., et al. 2020. Biofortification of calcium on mustard (Brassica juncea L.) and lettuce (Lactuca sativa) cultivated in floating hydroponic system. Bul. Agroteknologi 1: 27–36. [Google Scholar]
  • 125. Gómez‐Galera, S. , Rojas E., Sudhakar D., et al. 2010. Critical evaluation of strategies for mineral fortification of staple food crops. Transgenic Res. 19: 165–180. [DOI] [PubMed] [Google Scholar]
  • 126. Pessoa, C.C. , Lidon F.C., Coelho A.R.F., et al. 2021. Calcium biofortification of Rocha pears, tissues accumulation and physicochemical implications in fresh and heat‐treated fruits. Sci. Hortic. 277: 109834. [Google Scholar]
  • 127. Nagarajan, S. , Haldipur A.C. & Uma Bharathi S.T.. 2018. Agronomic biofortification of sprouts: a low cost intervention for addressing double burden of malnutrition .
  • 128. Joy, E.J.M. , Ander E.L., Young S.D., et al. 2014. Dietary mineral supplies in Africa. Physiol. Plant. 151: 208–229. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 129. Vetriventhan, M. , Upadhyaya H.D., Dwivedi S.L., et al. 2015. Finger and foxtail millets. In Genetic and genomic resources for grain cereals improvement. Singh M. & Upadhyaya H.D., Eds.: 291–319. [Google Scholar]
  • 130. Rehman, H.M. , Cooper J.W., Lam H.M., et al. 2019. Legume biofortification is an underexploited strategy for combatting hidden hunger. Plant Cell Environ. 42: 52–70. [DOI] [PubMed] [Google Scholar]
  • 131. Hambidge, K.M. , Krebs N.F., Westcott J.L., et al. 2005. Absorption of calcium from tortilla meals prepared from low‐phytate maize. Am. J. Clin. Nutr. 82: 84–87. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 132. Raboy, V. 2020. Low phytic acid crops: observations based on four decades of research. Plants 9: 140. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 133. Kumar, A. , Singh U.M., Manohar M., et al. 2015. Calcium transport from source to sink: understanding the mechanism(s) of acquisition, translocation, and accumulation for crop biofortification. Acta Physiol. Plant 37: 1–14. [Google Scholar]
  • 134. Hirschi, K.D. 1999. Expression of Arabidopsis CAX1 in tobacco: altered calcium homeostasis and increased stress sensitivity. Plant Cell 11: 2113–2122. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 135. Gupta, R.K. , Gangoliya S.S. & Singh N.K.. 2015. Reduction of phytic acid and enhancement of bioavailable micronutrients in food grains. J. Food Sci. Technol. 52: 676–684. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 136. Morris, J. , Hawthorne K.M., Hotze T., et al. 2008. Nutritional impact of elevated calcium transport activity in carrots. Proc. Natl. Acad. Sci. USA 105: 1431–1435. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 137. Bundó, M. & Coca M.. 2017. Calcium‐dependent protein kinase OsCPK10 mediates both drought tolerance and blast disease resistance in rice plants. J. Exp. Bot. 68: 2963–2975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 138. Nie, L.Z. , Yu X.X., Ma Y.H., et al. 2018. Enhanced drought and osmotic stress tolerance in transgenic potato plants expressing AtCDPK1, a calcium‐dependent protein kinase. Russ. J. Plant Physiol. 65: 865–873. [Google Scholar]
  • 139. Huang, D. , Gong X., Liu Y., et al. 2017. Effects of calcium at toxic concentrations of cadmium in plants. Planta 245: 863–873. [DOI] [PubMed] [Google Scholar]
  • 140. Abratt, V.R. & Reid S.J.. 2010. Oxalate‐degrading bacteria of the human gut as probiotics in the management of kidney stone disease. Adv. Appl. Microbiol. 72: 63–87. [DOI] [PubMed] [Google Scholar]
  • 141. Mohan, V.R. , Tresina P.S. & Daffodil E.D.. 2016. Antinutritional factors in legume seeds: characteristics and determination. 10.1016/B978-0-12-384947-2.00036-2. [DOI]
  • 142. Hanes, D.A. , Weaver C.M. & Wastney M.E.. 1999. Calcium and oxalic acid kinetics differ in rats. J. Nutr. 129: 165–169. [DOI] [PubMed] [Google Scholar]
  • 143. Teucher, B. , Dainty J.R., Spinks C.A., et al. 2008. Sodium and bone health: impact of moderately high and low salt intakes on calcium metabolism in postmenopausal women. J. Bone Miner. Res. 23: 1477–1485. [DOI] [PubMed] [Google Scholar]
  • 144. Christakos, S. , Dhawan P., Porta A., et al. 2011. Vitamin D and intestinal calcium absorption. Mol. Cell. Endocrinol. 347: 25–29. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 145. Rangarajan, R. , Mondal S., Thankachan P., et al. 2018. Assessing bone mineral changes in response to vitamin D supplementation using natural variability in stable isotopes of calcium in urine. Sci. Rep. 8: 4–11. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 146. Nickel, K.P. , Martin B.R., Smith D.L., et al. 1996. Calcium bioavailability from bovine milk and dairy products in premenopausal women using intrinsic and extrinsic labeling techniques. J. Nutr. 126: 1406–1411. [DOI] [PubMed] [Google Scholar]
  • 147. Mykkänen, H.M. & Wasserman R.H.. 1980. Enhanced absorption of calcium by casein phosphopeptides in rachitic and normal chicks. J. Nutr. 110: 2141–2148. [DOI] [PubMed] [Google Scholar]
  • 148. Wasserman, R.H. , Comar C.L. & Nold M.M.. 1956. The influence of amino acids and other organic compounds on the gatrointestinal absorption of calcium45 and strontium89 in the rat: two figures. J. Nutr. 59: 371–383. [DOI] [PubMed] [Google Scholar]
  • 149. Whisner, C.M. , Martin B.R., Schoterman M.H.C., et al. 2013. Galacto‐oligosaccharides increase calcium absorption and gut bifidobacteria in young girls: a double‐blind cross‐over trial. Br. J. Nutr. 110: 1292–1303. [DOI] [PubMed] [Google Scholar]
  • 150. Whisner, C.M. , Martin B.R., Nakatsu C.H., et al. 2014. Soluble maize fibre affects short‐term calcium absorption in adolescent boys and girls: a randomised controlled trial using dual stable isotopic tracers. Br. J. Nutr. 112: 446–456. [DOI] [PubMed] [Google Scholar]
  • 151. Whisner, C.M. , Martin B.R., Nakatsu C.H., et al. 2016. Soluble corn fiber increases calcium absorption associated with shifts in the gut microbiome: a randomized dose–response trial in free‐living pubertal females. J. Nutr. 146: 1298–1306. [DOI] [PubMed] [Google Scholar]
  • 152. Abrams, S.A. , Griffin I.J., Hawthorne K.M., et al. 2005. A combination of prebiotic short‐ and long‐chain inulin‐type fructans enhances calcium absorption and bone mineralization in young adolescents. Am. J. Clin. Nutr. 82: 471–476. [DOI] [PubMed] [Google Scholar]
  • 153. Jakeman, S.A. , Henry C.N., Martin B.R., et al. 2016. Soluble corn fiber increases bone calcium retention in postmenopausal women in a dose‐dependent manner: a randomized crossover trial. Am. J. Clin. Nutr. 104: 837–843. [DOI] [PubMed] [Google Scholar]
  • 154. Abioye, A.I. , Okuneye T.A., Odesanya A.‐M.O., et al. 2021. Calcium intake and iron status in human studies: a systematic review and dose–response meta‐analysis of randomized trials and crossover studies. J. Nutr. 151: 1084–1101. [DOI] [PubMed] [Google Scholar]
  • 155. Jacob, M.C.M. , Feitosa I.S., de Araujo J.Y.M., et al. 2021. Rapid ethnonutrition assessment method is useful to prototype dietary assessments with a focus on local biodiverse food plants. Ecol. Food Nutr. 60: 334–350. [DOI] [PubMed] [Google Scholar]
  • 156. Nelson, G. , Bogard J., Lividini K., et al. 2018. Income growth and climate change effects on global nutrition security to mid‐century. Nat. Sustain. 1: 773–781. [Google Scholar]

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