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Review

Risk Assessment of Micronutrients Deficiency in Vegetarian or Vegan Children: Not So Obvious

by
Jean-Pierre Chouraqui
Paediatric Nutrition and Gastroenterology, Paediatrics Department, University Hospital of Grenoble-Alpes (CHUGA), Quai Yermoloff, 38700 La Tronche, France
Nutrients 2023, 15(9), 2129; https://doi.org/10.3390/nu15092129
Submission received: 20 March 2023 / Revised: 16 April 2023 / Accepted: 22 April 2023 / Published: 28 April 2023

Abstract

:
Vegetarian diets have gained in popularity worldwide and therefore an increasing number of children may be exposed to the resulting nutritional consequences. Among them, the risk of micronutrient shortfall is particularly of concern. This narrative review aims to assess and discuss the relevance of micronutrient deficiency risk based on the available data. It mainly draws attention to iron, zinc, iodine, and vitamins B12 and D intake. Diets that are more restrictive in animal source foods, such as vegan diets, have a greater likelihood of nutritional deficiencies. However, the actual risk of micronutrient deficiency in vegetarian children is relatively difficult to assert based on the limitations of evidence due to the lack of well-designed studies. The risk of vitamin B12 deficiency must be considered in newborns from vegan or macrobiotic mothers and children with the most restrictive diet, as well as the risk of iron, zinc, and iodine deficiency, possibly by performing the appropriate tests. A lacto-ovo-vegetarian diet exposes a low risk if it uses a very varied diet with a sufficient intake of dairy products. Vegan and macrobiotic diets should be avoided during pregnancy and childhood. There is a need for education and nutrition guidance and the need for supplementation should be assessed individually.

1. Introduction

Micronutrients are vitamins and minerals that are needed in very small amounts for health (mg or μg/day), and that enable the body to produce enzymes, hormones, and other substances which are essential for proper growth and development [1]. Micronutrients are therefore even more crucial during the phases of rapid growth and development in childhood, i.e., the 1000 first days and first years of life and adolescence [2,3,4,5]. Micronutrient deficiencies may lead to deleterious health conditions, and less clinically noticeable disorders such as lower academic performance and an increased risk of diseases [2,3,6,7]. On the other hand, there is increasing evidence that diets during childhood and adolescence can impact health in later adulthood [8]. The World Health Organization’s (WHO) Ambition and Action in Nutrition 2016–2025 aimed to provide a fit-for-purpose nutrition strategy and recalled the resolution WHA 37.18 on prevention and management of micronutrient malnutrition [9].
Micronutrients can only be provided in the diet and their deficiencies in children without underlying disease are food-borne. In general, micronutrients content tends to be denser, more varied, and more bioavailable in animal-source foods (ASF, including meat, fish, eggs, dairy products, and animal-derived ingredients) than in foods of plant origin (FPO) [6,10,11]. ASF are the almost exclusive dietary sources of vitamin B12 and vitamin D, apart from the possible contributions by certain mushrooms and yeasts. ASF is also the source of highly bioavailable vitamin A (retinol), iron, and zinc. Moreover, they provide a daily intake of riboflavin, choline, and vitamin E. Otherwise, vegetable oil and nuts may represent the most prominent sources of vitamin E. Dietary iodine intake depends mainly on that of iodized salt or otherwise from ASF and to a lesser extent from FPO depending then on the iodine content of the local soil and water.
Populations consuming little or no ASF, i.e., a vegetarian diet, are therefore exposed to the risk of deficiency in some or all these nutrients depending on their level of ASF intake [12]. The degree of ASF restriction as well as that of the permitted foods define the different vegetarian patterns [13,14,15]. All patterns include prolonged breastfeeding as much as possible. The lacto-ovo-vegetarian diet (LOV), very often assimilated to a vegetarian diet, is most often practiced, and excludes meat (all types and derived processed products), fish, and seafood but includes dairy products, eggs, and honey, together with a wide variety of plant foods. In addition, lacto-vegetarians also exclude eggs, while pollotarians consume poultry, pescatarians consume fish and seafood, and ovo-vegetarians may consume eggs but not milk. Occasionally and variably flexitarians will eat meat or fish. Veganism is much more restrictive and excludes all ASF, as well as products containing ingredients derived from ASF and all items of animal origin (e.g., wool, silk, leather). A macrobiotic diet is based on cereals, pulses, vegetables, seaweed, and soy products and may include fish.
As a benchmark, it should be acknowledged that in some parts of the world, mainly in Asia, human beings have been able for millennia not only to survive but also to maintain long and healthy lives on diets free from flesh [16,17,18]. Such diet remains part of the cultural and religious tradition in these countries essentially out of respect for all living beings [19]. Furthermore, avoidance of ASF is increasingly popular in industrialized countries due to a growing concern for animal welfare, sustainable development, and health, not to mention the socioeconomic impact of animal product consumption [15,20,21,22,23,24,25,26,27,28]. In households, children’s eating behavior depends on parents purchasing family food, setting an example, and wanting their children to share their beliefs and eating habits [27,29,30]. On the other hand, more and more establishments such as kindergartens, schools, colleges, restaurants, and hospitals are providing vegetarian options at least one or two days a week for educational and environmental reasons. As a result, the question of the risks and benefits of vegetarian diets in childhood arises. Among the risks, those linked to an insufficient intake of micronutrients constitute a particularly important issue. This narrative review aims to assess and discuss the relevance of micronutrient deficiency risk based on the available data.

2. Search Strategy

A comprehensive search of the literature using PubMed, EMBASE, Google Scholar, and the Cochrane Library was conducted from 1980 up to January 2023. The keywords (words or MeSH terms) used were: ‘micronutrients’, ‘vitamin’, ‘mineral’, ‘vegetarian’, or ‘vegan’, ‘pregnancy’, ‘lactation’, ‘breastfeeding’, ‘newborn’, ‘infant’, ‘toddler’, ‘child’, ‘adolescent’, ‘dietary intake’, or ‘deficiencies’. Moreover, a search was undertaken to identify relevant papers referred to in previously identified articles. Original papers, reviews, meta-analyses, position papers, and guidelines published by expert scientific groups or societies were included. Articles in English or with relevant English abstracts and in French were selected. When relevant data were identified in another language, an online translator was used so as not to overlook that information. After reading the title and abstract of the identified articles, duplicate references were removed. Thus, of the 332 publications first selected, 122 are finally cited.

3. Vitamins

3.1. Vitamin Supply from Foods from Plant Origin

FPO may be a significant source of antioxidant vitamins such as vitamin C (ascorbic acid), E (tocopherol), and provitamin A carotenoids, as well as vitamin K (phylloquinone), but also vitamin B1(thiamine), B2 (riboflavin), B3 (niacin, PP), B5 (pantothenic acid), B6 (pyridoxine), B7 (biotin), B9 (folates) [31,32,33,34]. However, the impact of cooking (heating and leaching) and processing on the available vitamin content should not be neglected [34]. Compared to intakes of these vitamins in omnivorous children, those in vegetarians and vegans have been shown either identical or even higher in most studies, especially in vegans [35,36,37,38,39,40,41,42,43,44,45,46,47,48,49]. Lower intake of vitamin B2 has been reported in children following a macrobiotic diet compared to omnivores [35]. No studies assessed the vitamin K or vitamin B5 intake.
On the other hand, the dietary intake of vitamin D is very limited and can only come from infant’s and young child’s formulas and to a lesser extent from some fatty fishes or even less from some mushrooms [50,51,52,53,54]. Compared to the intake in omnivorous children, no study found a difference in vegetarian children [45,46,47], but one found a lower intake in vegan children [41].
The major issue in vegetarian diets is related to the total lack of vitamin B12 in FPO [55]. The only possible plant source of vitamin B12 could be some algae but with a low bioavailability [56,57]

3.2. Vitamin B12 Concern

Vitamin B12 is essential for human metabolism acting as a coenzyme in the conversion of methylmalonyl-CoA to succinyl-CoA in propionate metabolism and the transmethylation of homocysteine to methionine [58]. After reviewing published dietary reference values, the European Food Safety Authority (EFSA) sets an adequate dietary intake of cobalamin of 4.5 μg/d for pregnant women, 5 μg/d for lactating women, 0.5 μg/d for infants under 7 months of age, 1.5 μg/d for infants 7–11 months and children aged 1–6 years, 2.5 μg/d for children 7–10 years old, 3.5 μg/d for teenagers 11–14 years old and 4 μg/d for adolescent 15–17 years old. Symptoms and the long-term prognosis of cobalamin deficiency in children depend on the severity and duration of the deficiency [56]. The diagnosis may be difficult in the mild case and in the absence of specific signs which may lead to a substantial diagnosis delay that can be pejorative in terms of prognosis. Practitioners should be aware of this possibility in infants from vegetarian mothers and children on a vegetarian diet who do not take supplements.

3.2.1. Newborns and Infants

The need for vitamin B12 is increased during pregnancy and lactation in relation to the expansion of tissues and supply to the fetus and the newborn [58,59]. When adhering to vegetarian diets for at least 3 years without supplementation, 22% of pregnant women have been shown to be vitamin B12 deficient [60]. Maternal vitamin B12 deficiency is associated with low birth weight in addition to an increased risk of pregnancy complications [61]. Cobalamin status in the first six months of life depends on maternal cobalamin status during pregnancy [55,62]. The offspring of vitamin B12-deficient mothers are usually asymptomatic at birth but may develop clinical signs at the age of 4–6 months [63]. Symptoms may include megaloblastic anemia, feeding difficulties, failure to thrive, irritability, muscular hypotonia, tremors and seizures, and impaired neurodevelopment which may be irreversible [61,63].
The cobalamin concentration of breast milk reflects maternal cobalamin concentration in blood [56]. The main nutritional deficit of breast milk from vegetarian and vegan mothers is that of vitamin B12 [64,65]. A vegetarian diet in the mother is the main cause (64% of cases) of vitamin B12 deficiency in breastfed infants [66]. In India, the country with the highest prevalence of vegetarians [67], 63.7% of 149 exclusively breastfed infants (3.1 ± 1 mo) had low levels of serum vitamin B12 (<200 pg/mL), but only 21% of them had a vegetarian mother [68]. Symptoms of cobalamin deficiency in breastfed infants are usually manifested between 4 to 8 months of age [56,69,70]. Numerous breastfed infants of vegetarian or vegan mothers have been reported to develop severe vitamin B12 deficiency with anemia, failure to thrive, hypotonia, developmental delay, microcephaly, and cerebral atrophy [69,70,71,72,73].

3.2.2. Children and Adolescents

The reported intakes of vitamin B12 in children are depicted in Figure 1. The more the diet restricts ASF intake and the longer the compliance with this restriction, the lower the intake [35,36,39,40,41,43,46,47,48,49,74,75].
Many studies have confirmed the existence of a vitamin status deficiency in children by showing a low level of serum cobalamin, and/or an increase in plasma methylmalonic acid or homocysteine [35,74,75,76,77,78]. However, others failed to get the same results, probably due to not taking into account possible supplements, or a short duration of the restrictive diet [39,43,63,74,78,79]. Vitamin B12 deficiency develops slowly given that vitamin B12 may be stored in the liver [76]. Overall, the reported prevalence of vitamin B12 deficiency was 62% in pregnant vegetarians, 25–85% in vegetarian children, and 21–41% in vegetarian adolescents [80]. The greater prevalence of deficiency was in vegans and those who had adhered to a vegetarian diet since birth. Nearly 40% of 210 apparently healthy Indian children aged 6–23 months have been shown to be deficient in vitamin B12 (<210 pg/mL), especially since they had not consumed cow’s milk for at least 6 months (OR 2.6, 95% CI 1.4–4.6) [81]. Severe vitamin B12 deficiency in children on a vegan diet and requiring hospitalization was reported in Italy [82]. In a macrobiotic community, 55% of children were vitamin B12-deficient according to their urinary methylmalonic acid [83]. Overall, deficiency symptoms are the same as those described above in infants [69,84]. In the Indian study enrolling 27 young children (6–27 months), anemia was found in 83%, developmental delay or regression in all, and cerebral atrophy was found in the 9 children who underwent neuroimaging [84]. Usually, an appropriate diagnosis of vitamin B12 deficiency is based on the coexistence of megaloblastic anemia with neurological disorders. However, given that folate intake is most of the time high in vegetarians, the pathognomonic haematologic characteristics of vitamin B12 deficiency may be masked [76,85].

4. Minerals

FPO are relatively rich in certain minerals such as potassium and magnesium but have variable content in zinc, copper, and selenium and only contain non-haeme iron with poor bioavailability [10,31,32,86]. Absorption of iron, zinc, and calcium is reduced by phytates and/or oxalates which are quite abundant in unrefined cereals, whole grains, and legumes [76,86,87,88,89]. However, due to its abundance in the human body, calcium is not considered a micronutrient [90,91,92,93,94]. Inadequate intake and/or poor bioavailability of these microminerals are the main cause of deficiency [90].

4.1. Iron

The main role of iron in the body is to ensure the oxygen-carrying capacity of hemoglobin and tissue oxygenation. Current knowledge on iron homeostasis, dietary intake, and prevention of iron deficiency has been recently addressed in this journal [86]. Inadequate intake of bioavailable iron may lead to depletion in body stores and iron deficiency which can be assessed by the measurement of serum ferritin in the absence of inflammation. Children are at particular risk of iron deficiency due to their rapid growth. Iron deficiency will precede the onset of iron deficiency anemia which can lead to poor neurodevelopment. Dietary iron intake and absorption are the main factors driving body iron status alongside blood losses. Most FPO have low iron content which is inorganic iron with low bioavailability (1–12%), without counting the possible iron leaching during cooking [86,88]. Iron bioavailability is moreover hampered by dietary fiber, and phytate but increased by vitamin C. Reported intakes, shown in Figure 2, were generally comparable or even higher in children following a vegetarian, a vegan, or a macrobiotic diet than in those omnivorous [35,36,37,39,40,41,42,44,46,47,48,49,74,95].
However, none of these studies considered iron bioavailability. As a consequence, when assessed, the iron store was shown reduced [35,36,38,39,42,44,48,74]. This is even though it is acknowledged that iron absorption is increased when iron status is deficient which leads to hepcidin suppression [86]. Few studies reported lower hemoglobin concentration [36,38]. Rare cases of iron deficiency anemia due to a vegetarian diet have been reported [41,44,96]. The risk of iron deficiency is increased in the event of an unfavorable socio-economic situation [86].

4.2. Zinc

Zinc provides the prosthetic group of several enzymes to assist in the most major metabolic pathways and is involved in the receptor proteins for vitamins A and D, as well as for thyroid and steroid hormones [87,97]. Worldwide, it has been estimated that 17% of the population may have inadequate zinc intake with a lower percentage in high-income countries than in low-income regions [98]. In this survey, on average 34.8 ± 20% of zinc intake was from ASF. The highest zinc content is found in oysters, shellfish, and red meat, whereas FPO providing the most zinc are whole grains, fortified cereals, pulses, nuts, and seeds [76,97]. However, as for iron, the rich content of phytate, oxalate, or fiber in FPO may interfere with zinc absorption [87,97]. Total dietary phytate and the phytate/zinc molar ratio were shown positively correlated with the risk of inadequate zinc intake (r = 0.62 and 0.92, respectively; p < 0.01) [98]. These considerations were not considered in the studies reported in Figure 3.
The reported intakes of vegetarian or vegan children were similar to that of omnivorous counterparts in most of these studies [37,39,40,42,47,49,95], with similar plasma zinc concentrations [39,47]. However, in three studies, the intake was lower in vegetarian children than in omnivores [36,41,46]. None of these studies reported clinical features of zinc deficiency but some case reports in young vegan children fed with plant milk [96]. The clinical setting of zinc deficiency may range from poor appetite and anorexia, decreased growth velocity, increased susceptibility to infection, diarrhea, depressed mood, and skin rashes at orifices [90].

4.3. Iodine

Iodine is a mandatory structural and functional element of thyroid hormones and, subsequently, has an important role in the growth, development of neurological, and cognitive functions [99,100]. The iodine concentration, as iodide, in water and foods is highly variable.
The main iodine sources are marine products, eggs, milk, and iodized salt. In meats as well as in FPO the iodine content depends on the richness of the soil of the food production region [90,94]. Adults who consume diets excluding iodine-rich foods have been shown to have an increased risk of iodine deficiency [100,101]. Studies assessing iodine intake in vegetarian children are scarce. A German study found that LOV children had lower intake than omnivores [49]. This was not found in a few Finnish young vegan children who also had similar iodine urine concentration to that of omnivores [47].

4.4. Other Microminerals

Although variably provided by plants, these micromineral intakes have very rarely been evaluated in vegetarian children. Apart from ASF, they may be mainly provided by grains legumes and seeds depending on the soil content [32,102]. Copper intake has been found to be similar or higher in vegetarian children in two studies [37,95]. Canadian LOV adolescents had higher manganese intake than their omnivorous counterparts [37]. Selenium intake in Swedish vegan adolescents were lower than that of omnivorous adolescents [41]. Apart from these few studies, no other study was found in particular regarding the intake of chromium or molybdenum.

5. Discussion and Recommendations

This review emphasizes that the more children are subjected to a diet restricted in ASF (vegan or macrobiotic), the more they are at risk of developing a deficiency in certain micronutrients. All micronutrients, especially vitamin B12 cannot be obtained in an adequate amount from non-ASF. Moreover, some such as carotenoids which can be found as precursors in FPO have a poor conversion to their active form (retinol) and others (e.g., iron and zinc) display low bioavailability. However available data from the studies carried out so far do not formally allow us to find a clear relationship between the diet, which can have diverse patterns, and the intake or the status of micronutrients. There are several reasons for this, some of which represent the limitations of this review, which should be acknowledged.

5.1. Limitations

Many of the reported studies are relatively old, with 53% of them conducted more than 25 years ago [35,36,37,38,39,40,41,77,95], and only a third less than 10 years ago [45,46,47,48,49,74,78]. All are observational studies, frequently enrolling a quite small number of children based on the voluntary participation of the parents. Parents who are likely to be concerned about their own health and that of their child and who are better able to practice a balanced diet and give supplements. The use of such supplements is rarely specified in the calculation of intake. Little information is provided about the duration of a vegetarian or a vegan diet in the various population groups, whereas there is inconsistency in the definition of vegetarianism, leading to a great heterogeneity in the vegetarian spectrum and a great dispersion in the results as shown in the figures. The heterogeneity of the results may also be linked to the use of different modes of assessment of intakes, which may use a food frequency questionnaire or a dietary record on one or three days. Moreover, most of the studies have been conducted in industrialized and high-income countries and neither socioeconomic status nor the environment was considered. Last but not least, very few studies have set the evidence of micronutrient shortfall by performing the appropriate tests in blood or urine samples and thus assessing the child’s micronutrient status.
The nutritional adequacy of a vegetarian diet must be judged individually, given that a vegetarian diet can be composed in many different ways. On the other hand, in addition to the concern about micronutrients, other disadvantages, and risks must be analyzed. Of additional concern are energy, protein, n-3 long chain-polyunsaturated fatty acids, and calcium intake as well as protein quality and bone health.

5.2. Recommendations

From an ethical point of view, the food choice of parents must be respected, whatever the reason. Health professionals must inform parents of the possible risks of an ill-conceived vegetarian diet, but also of the possible benefits in terms of the health of a well-balanced diet. The diet and physical status of pregnant and nursing women and of children or adolescents following a restrictive diet must be carefully monitored and the help of a trained nutritionist may be needed. The main challenge for practitioners is to assess the risk of nutritional deficiency and to determine the need for laboratory tests.
In descending order, the most inappropriate ASF-restrictive diets are the macrobiotic, the vegan, the pescatarian, the lacto-vegetarian, the ovo-vegetarian, the LOV, and the flexitarian diets. A well-balanced LOV diet may be a healthy choice if the potential nutrient deficits are recognized and acted upon. Several dietary guidelines on vegetarian and vegan diets have been developed in this regard [103,104,105,106,107].
Vegan mothers, infants, and children may require supplementation with vitamin B12, iron, and zinc [76,107,108,109,110,111]. Exclusive breastfeeding is recommended for the 1st 4–6 months provided that the mother is supplemented with vitamin B12. Otherwise, an infant formula must be given, followed after the introduction of complementary food by a follow-on-formula, then a young child formula, which should be used as long as possible up to three years of age [112,113]. In cases of refusal of cow milk-based formulae, an alternative is a soya or hydrolyzed rice infant formula [114]. However, industrial or home-made preparations incorrectly named “plant-based milk”, i.e., non-dairy beverages made from a water-based plant extract such as rice, soya, almond, coconut, grains, or other extracts must be strictly avoided because they are not suitable for feeding young children [96].
Complementary feeding should be carefully planned to ensure all critical nutrients are provided in agreement with current nutritional recommendations, and this is quite challenging [26,76,107,108,110,112,115,116,117,118,119]. It should include a wide variety of foods (grains, legumes, pulses, vegetables, fruit, nuts, and seeds). The use of iron- or bio-fortified food should be encouraged [76,86,110]. Apart from taking supplements, it is much more difficult or even impossible for vegans to ensure an adequate intake of vitamin B12 and iron. On the other hand, vitamin D supplementation should be recommended in all children, especially infants and adolescents, whatever their diet [51,53,54].
Parents and adolescents knowledge of nutrition, with which habits and beliefs interfere, determine their food choices according to the availability of certain foods and the subsequent nutrition adequacy of any one particular plant-based diet. This highlights the importance for health professionals to inform and advise families who follow a restrictive diet. Pregnant women, newborns, children, and adolescents with a vegetarian dietary pattern need medical supervision. The underlying problem is the frequent ignorance of the ins and outs of such diets and the solutions to be provided. This is the result of a lack of nutritional education and training in medical schools and postgraduate courses [118,119,120,121,122].

6. Conclusions

Since children’s diets are largely driven by their parents, the prevalence of vegetarian diets during childhood is certainly on the rise parallel in industrialized countries. Maintenance of a vegetarian diet can be challenging. The risk of micronutrient deficiency in vegetarian children is relatively difficult to assert based on the current limitations of evidence due to the lack of well-designed studies. This means the need for more adequately powered trials to better identify any problems, which are not easy to conduct.
However, the risk of vitamin B12 deficiency must be considered in newborns from vegan or macrobiotic mothers and children with severe restrictions of ASF. Iron deficiency needs to be assessed individually in vegan children, as well as that of iodine and zinc. For this, some appropriate tests can be carried out, bearing in mind that the more restrictive the diet in ASF, the greater the risk. A LOV diet exposure is a low risk as long as it uses a very varied diet with a sufficient intake of dairy products and especially specific formula in infants and young children. Most of the deficiencies may be preventable through nutrition guidance and the consumption of a well-planned diet containing diverse foods, as well as food fortification and supplementation, where needed. On the other hand, it would be better to avoid vegan and macrobiotic diets during pregnancy and childhood. However, when it comes to micronutrients, special attention should be paid to vitamin B12, iron, zinc, iodine, and vitamin D.
Parents and teenagers must be informed of the serious consequences of failing to follow the advice and prescriptions regarding supplementation of the diet and the need for medical and dietic regular supervision.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The author declares no conflict of interest.

Abbreviations

ASFanimal food sources
FPOfoods of plant origin
LOVlacto-ovo-vegetarian

References

  1. World Health Organization. Micronutrients. Geneva. 2022. Available online: https://www.who.int/health-topics/micronutrients#tab=tab_1 (accessed on 6 December 2022).
  2. Black, R.E.; Victora, C.G.; Walker, S.P.; Bhutta, Z.A.; Christian, P.; de Onis, M.; Ezzati, M.; Grantham-McGregor, S.; Katz, J.; Martorell, R.; et al. Maternal and Child Nutrition Study Group. Maternal and child undernutrition and overweight in low-income and middle-income countries. Lancet 2013, 382, 427–451, Erratum in Lancet 2013, 382, 396. [Google Scholar] [CrossRef] [PubMed]
  3. Christian, P.; Mullany, L.C.; Hurley, K.M.; Katz, J.; Black, R.E. Nutrition and maternal, neonatal, and child health. Semin. Perinatol. 2015, 39, 361–372, Erratum in Semin. Perinatol 2015, 39, 505. [Google Scholar] [CrossRef] [PubMed]
  4. Mattei, D.; Pietrobelli, A. Micronutrients and Brain Development. Curr. Nutr. Rep. 2019, 8, 99–107. [Google Scholar] [CrossRef]
  5. Inzaghi, E.; Pampanini, V.; Deodati, A.; Cianfarani, S. The Effects of Nutrition on Linear Growth. Nutrients 2022, 14, 1752. [Google Scholar] [CrossRef]
  6. Murphy, S.P.; Allen, L.H. Nutritional importance of animal source foods. J. Nutr. 2003, 133 (Suppl. S2), 3932S–3935S. [Google Scholar] [CrossRef] [PubMed]
  7. Das, J.K.; Salam, R.A.; Mahmood, S.B.; Moin, A.; Kumar, R.; Mukhtar, K.; Lassi, Z.S.; Bhutta, Z.A. Food fortification with multiple micronutrients: Impact on health outcomes in general population. Cochrane Database Syst. Rev 2019, 12, CD011400. [Google Scholar] [CrossRef]
  8. Koletzko, B.; Godfrey, K.M.; Poston, L.; Szajewska, H.; van Goudoever, J.B.; de Waard, M.; Brands, B.; Grivell, R.M.; Deussen, A.R.; Dodd, J.M.; et al. Nutrition During Pregnancy, Lactation and Early Childhood and its Implications for Maternal and Long-Term Child Health: The Early Nutrition Project Recommendations. Ann. Nutr. Metab. 2019, 74, 93–106. [Google Scholar] [CrossRef]
  9. World Health Organization. Ambition and Action in Nutrition 2016–2025. Geneva. 2017. Licence: CC BY-NC-SA 3.0 IGO. Available online: https://apps.who.int/iris/bitstream/handle/10665/255485/9789241512435-eng.pdf?ua=1 (accessed on 6 December 2022).
  10. Allen, L.H. To what extent can food-based approaches improve micronutrient status? Asia. Pac. J. Clin. Nutr. 2008, 17 (Suppl. S1), 103–105. [Google Scholar]
  11. Consalez, F.; Ahern, M.; Andersen, P.; Kjellevold, M. The Effect of the Meat Factor in Animal-Source Foods on Micronutrient Absorption: A Scoping Review. Adv. Nutr. 2022, 13, 2305–2315. [Google Scholar] [CrossRef]
  12. Rudloff, S.; Bührer, C.; Jochum, F.; Kauth, T.; Kersting, M.; Körner, A.; Koletzko, B.; Mihatsch, W.; Prell, C.; Reinehr, T.; et al. Vegetarian diets in childhood and adolescence: Position paper of the nutrition committee, German Society for Paediatric and Adolescent Medicine (DGKJ). Mol. Cell. Pediatr. 2019, 6, 4. [Google Scholar] [CrossRef]
  13. Bettinelli, M.E.; Bezze, E.; Morasca, L.; Plevani, L.; Sorrentino, G.; Morniroli, D.; Giannì, M.; Mosca, F. Knowledge of Health Professionals Regarding Vegetarian Diets from Pregnancy to Adolescence: An Observational Study. Nutrients 2019, 11, 1149. [Google Scholar] [CrossRef]
  14. Kiely, M.E. Risks and benefits of vegan and vegetarian diets in children. Proc. Nutr. Soc. 2021, 80, 159–164. [Google Scholar] [CrossRef]
  15. Bakaloudi, D.R.; Halloran, A.; Rippin, H.L.; Oikonomidou, A.C.; Dardavesis, T.I.; Williams, J.; Wickramasinghe, K.; Breda, J.; Chourdakis, M. Intake and adequacy of the vegan diet. A systematic review of the evidence. Clin. Nutr. 2021, 40, 3503–3521. [Google Scholar] [CrossRef] [PubMed]
  16. Leitzmann, C. Vegetarian nutrition: Past, present, future. Am. J. Clin. Nutr. 2014, 100 (Suppl. S1), 496S–502S. [Google Scholar] [CrossRef] [PubMed]
  17. Appleby, P.N.; Key, T.J. The long-term health of vegetarians and vegans. Proc. Nutr. Soc. 2016, 75, 287–293. [Google Scholar] [CrossRef] [PubMed]
  18. Mann, N.J. A brief history of meat in the human diet and current health implications. Meat. Sci. 2018, 144, 169–179. [Google Scholar] [CrossRef] [PubMed]
  19. Chouraqui, J.P.; Turck, D.; Briend, A.; Darmaun, D.; Bocquet, A.; Feillet, F.; Frelut, M.L.; Girardet, J.P.; Guimber, D.; Hankard, R.; et al. Committee on Nutrition of the French Society of Pediatrics. Religious dietary rules and their potential nutritional and health consequences. Int. J. Epidemiol. 2021, 50, 12–26. [Google Scholar] [CrossRef]
  20. Rosenfeld, D.L.; Burrow, A.L. Vegetarian on purpose: Understanding the motivations of plant-based dieters. Appetite 2017, 116, 456–463. [Google Scholar] [CrossRef]
  21. IPSOS Mori. An Exploration into Diets around the World. 2018. Available online: https://www.ipsos.com/sites/default/files/ct/news/documents/2018-09/an_exploration_into_diets_around_the_world.pdf (accessed on 13 September 2022).
  22. Godfray, H.C.J.; Aveyard, P.; Garnett, T.; Hall, J.W.; Key, T.J.; Lorimer, J.; Pierrehumbert, R.T.; Scarborough, P.; Springmann, M.; Jebb, S.A. Meat consumption, health, and the environment. Science 2018, 361, eaam5324. [Google Scholar] [CrossRef]
  23. Milford, A.B.; Le Mouël, C.; Bodirsky, B.L.; Rolinski, S. Drivers of meat consumption. Appetite 2019, 141, 104313. [Google Scholar] [CrossRef]
  24. Dorard, G.; Mathieu, S. Vegetarian and omnivorous diets: A cross-sectional study of motivation, eating disorders, and body shape perception. Appetite 2021, 156, 104972. [Google Scholar] [CrossRef] [PubMed]
  25. Salter, A.M. The effects of meat consumption on global health. Rev. Sci. Tech. 2018, 37, 47–55. [Google Scholar] [CrossRef] [PubMed]
  26. Baldassarre, M.E.; Panza, R.; Farella, I.; Posa, D.; Capozza, M.; Mauro, A.D.; Laforgia, N. Vegetarian and Vegan Weaning of the Infant: How Common and How Evidence-Based? A Population-Based Survey and Narrative Review. Int. J. Environ. Res. Public Health 2020, 17, 4835. [Google Scholar] [CrossRef]
  27. Bivi, D.; Di Chio, T.; Geri, F.; Morganti, R.; Goggi, S.; Baroni, L.; Mumolo, M.G.; de Bortoli, N.; Peroni, D.G.; Marchi, S.; et al. Raising Children on a Vegan Diet: Parents’ Opinion on Problems in Everyday Life. Nutrients 2021, 13, 1796. [Google Scholar] [CrossRef] [PubMed]
  28. Kim, G.; Oh, J.; Cho, M. Differences between Vegetarians and Omnivores in Food Choice Motivation and Dietarian Identity. Foods 2022, 11, 539. [Google Scholar] [CrossRef]
  29. Larsen, J.K.; Hermans, R.C.; Sleddens, E.F.; Engels, R.C.; Fisher, J.O.; Kremers, S.P. How parental dietary behavior and food parenting practices affect children’s dietary behavior. Interacting sources of influence? Appetite 2015, 89, 246–257. [Google Scholar] [CrossRef]
  30. Eurispes. Quanti Sono i Vegani in Italia? 2022. Available online: https://www.veganok.com/vegani-in-italia/ (accessed on 13 September 2022).
  31. Clarys, P.; Deliens, T.; Huybrechts, I.; Deriemaeker, P.; Vanaelst, B.; De Keyzer, W.; Hebbelinck, M.; Mullie, P. Comparison of nutritional quality of the vegan, vegetarian, semi-vegetarian, pesco-vegetarian and omnivorous diet. Nutrients 2014, 6, 1318–1332. [Google Scholar] [CrossRef]
  32. Rauma, A.L.; Mykkänen, H. Antioxidant status in vegetarians versus omnivores. Nutrition 2000, 16, 111–119. [Google Scholar] [CrossRef] [PubMed]
  33. Meléndez-Martínez, A.J. An Overview of Carotenoids, Apocarotenoids, and Vitamin A in Agro-Food, Nutrition, Health, and Disease. Mol. Nutr. Food. Res. 2019, 63, e1801045, Erratum in: Mol. Nutr. Food Res. 2020, 64, e2070024. [Google Scholar] [CrossRef]
  34. Hrubša, M.; Siatka, T.; Nejmanová, I.; Vopršalová, M.; Kujovská Krčmová, L.; Matoušová, K.; Javorská, L.; Macáková, K.; Mercolini, L.; Remião, F.; et al. Biological Properties of Vitamins of the B-Complex, Part 1: Vitamins B1, B2, B3, and B5. Nutrients 2022, 14, 484. [Google Scholar] [CrossRef]
  35. Dagnelie, P.C.; van Staveren, W.A. Macrobiotic nutrition and child health: Results of a population-based, mixed-longitudinal cohort study in The Netherlands. Am. J. Clin. Nutr. 1994, 59 (Suppl. S5), 1187S–1196S. [Google Scholar] [CrossRef]
  36. Nathan, I.; Hackett, A.F.; Kirby, S. The dietary intake of a group of vegetarian children aged 7–11 years compared with matched omnivores. Br. J. Nutr. 1996, 75, 533–544. [Google Scholar] [CrossRef] [PubMed]
  37. Donovan, U.M.; Gibson, R.S. Dietary intakes of adolescent females consuming vegetarian, semi–vegetarian, and omnivorous diets. J. Adolesc. Health 1996, 18, 292–300. [Google Scholar] [CrossRef]
  38. Krajcovicová-Kudlácková, M.; Simoncic, R.; Béderová, A.; Grancicová, E.; Magálová, T. Influence of vegetarian and mixed nutrition on selected haematological and biochemical parameters in children. Nahrung 1997, 41, 311–314. [Google Scholar] [CrossRef] [PubMed]
  39. Thane, C.W.; Bates, C.J. Dietary intakes and nutrient status of vegetarian preschool children from a British national survey. J. Hum. Nutr. Diet. 2000, 13, 149–162. [Google Scholar] [CrossRef]
  40. Perry, C.L.; McGuire, M.T.; Neumark-Sztainer, D.; Story, M. Adolescent vegetarians: How well do their dietary patterns meet the healthy people 2010 objectives? Arch. Pediatr. Adolesc. Med. 2002, 156, 431–437. [Google Scholar] [CrossRef]
  41. Larsson, C.L.; Johansson, G.K. Dietary intake and nutritional status of young vegans and omnivores in Sweden. Am. J. Clin. Nutr. 2002, 76, 100–106. [Google Scholar] [CrossRef] [PubMed]
  42. Yen, C.E.; Yen, C.H.; Huang, M.C.; Cheng, C.H.; Huang, Y.C. Dietary intake and nutritional status of vegetarian and omnivorous preschool children and their parents in Taiwan. Nutr. Res. 2008, 28, 430–436. [Google Scholar] [CrossRef] [PubMed]
  43. Yen, C.E.; Yen, C.H.; Cheng, C.H.; Huang, Y.C. Vitamin B-12 status is not associated with plasma homocysteine in parents and their preschool children: Lacto-ovo, lacto, and ovo vegetarians and omnivores. J. Am. Coll. Nutr. 2010, 29, 7–13. [Google Scholar] [CrossRef]
  44. Gorczyca, D.; Prescha, A.; Szeremeta, K.; Jankowski, A. Iron status and dietary iron intake of vegetarian children from Poland. Ann. Nutr. Metab. 2013, 62, 291–297. [Google Scholar] [CrossRef]
  45. Ambroszkiewicz, J.; Chełchowska, M.; Szamotulska, K.; Rowicka, G.; Klemarczyk, W.; Strucińska, M.; Gajewska, J. Bone status and adipokine levels in children on vegetarian and omnivorous diets. Clin. Nutr. 2019, 38, 730–737. [Google Scholar] [CrossRef] [PubMed]
  46. Segovia-Siapco, G.; Sabaté, J. Health and sustainability outcomes of vegetarian dietary patterns: A revisit of the EPIC-Oxford and the Adventist Health Study-2 cohorts. Eur. J. Clin. Nutr. 2019, 72 (Suppl. S1), 60–70, Erratum in Eur. J. Clin. Nutr 2019, 73, 968. [Google Scholar] [CrossRef] [PubMed]
  47. Hovinen, T.; Korkalo, L.; Freese, R.; Skaffari, E.; Isohanni, P.; Niemi, M.; Nevalainen, J.; Gylling, H.; Zamboni, N.; Erkkola, M.; et al. Vegan diet in young children remodels metabolism and challenges the statuses of essential nutrients. EMBO. Mol. Med. 2021, 13, e13492. [Google Scholar] [CrossRef]
  48. Alexy, U.; Fischer, M.; Weder, S.; Längler, A.; Michalsen, A.; Sputtek, A.; Keller, M. Nutrient Intake and Status of German Children and Adolescents Consuming Vegetarian, Vegan or Omnivore Diets: Results of the VeChi Youth Study. Nutrients 2021, 13, 1707. [Google Scholar] [CrossRef] [PubMed]
  49. Weder, S.; Keller, M.; Fischer, M.; Becker, K.; Alexy, U. Intake of micronutrients and fatty acids of vegetarian, vegan, and omnivorous children (1–3 years) in Germany (VeChi Diet Study). Eur. J. Nutr. 2022, 61, 1507–1520. [Google Scholar] [CrossRef]
  50. Braegger, C.; Campoy, C.; Colomb, V.; Decsi, T.; Domellof, M.; Fewtrell, M.; Hojsak, I.; Mihatsch, W.; Molgaard, C.; Shamir, R.; et al. ESPGHAN Committee on Nutrition. Vitamin D in the healthy European paediatric population. J. Pediatr. Gastroenterol. Nutr. 2013, 56, 692–701. [Google Scholar] [CrossRef] [PubMed]
  51. Saggese, G.; Vierucci, F.; Prodam, F.; Cardinale, F.; Cetin, I.; Chiappini, E.; De’ Angelis, G.L.; Massari, M.; Miraglia Del Giudice, E.; Miraglia Del Giudice, M.; et al. Vitamin D in pediatric age: Consensus of the Italian Pediatric Society and the Italian Society of Preventive and Social Pediatrics, jointly with the Italian Federation of Pediatricians. Ital. J. Pediatr. 2018, 44, 51. [Google Scholar] [CrossRef] [PubMed]
  52. Liu, Z.; Huang, S.; Yuan, X.; Wang, Y.; Liu, Y.; Zhou, J. The role of vitamin D deficiency in the development of paediatric diseases. Ann. Med. 2023, 55, 127–135. [Google Scholar] [CrossRef]
  53. Jullien, S. Vitamin D prophylaxis in infancy. BMC Pediatr. 2021, 21 (Suppl. S1), 319. [Google Scholar] [CrossRef]
  54. Bacchetta, J.; Edouard, T.; Laverny, G.; Bernardor, J.; Bertholet-Thomas, A.; Castanet, M.; Garnier, C.; Gennero, I.; Harambat, J.; Lapillonne, A.; et al. Vitamin D and calcium intakes in general pediatric populations: A French expert consensus paper. Arch. Pediatr. 2022, 29, 312–325. [Google Scholar] [CrossRef]
  55. Chittaranjan, Y. Vitamin B12: An intergenerational story. Nestle. Nutr. Inst. Workshop Ser. 2020, 93, 91–102. [Google Scholar] [CrossRef] [PubMed]
  56. Bjørke-Monsen, A.L.; Ueland, P.M. Cobalamin status in children. J. Inherit. Metab. Dis. 2011, 34, 111–119. [Google Scholar] [CrossRef] [PubMed]
  57. Watanabe, F.; Yabuta, Y.; Tanioka, Y.; Bito, T. Biologically active vitamin B12 compounds in foods for preventing deficiency among vegetarians and elderly subjects. J. Agric. Food Chem. 2013, 61, 6769–6775. [Google Scholar] [CrossRef] [PubMed]
  58. EFSA NDA Panel (EFSA Panel on Dietetic Products, Nutrition and Allergies). Scientific Opinion on Dietary Reference Values for cobalamin (vitamin B12). EFSA J. 2015, 13, 4150. [Google Scholar] [CrossRef]
  59. Rizzo, G.; Laganà, A.S.; Rapisarda, A.M.; La Ferrera, G.M.; Buscema, M.; Rossetti, P.; Nigro, A.; Muscia, V.; Valenti, G.; Sapia, F.; et al. Vitamin B12 among vegetarians: Status, assessment and supplementation. Nutrients 2016, 8, 767. [Google Scholar] [CrossRef]
  60. Koebnick, C.; Hoffmann, I.; Dagnelie, P.C.; Heins, U.A.; Wickramasinghe, S.N.; Ratnayaka, I.D.; Gruendel, S.; Lindemans, J.; Leitzmann, C. Long-term ovo-lacto vegetarian diet impairs vitamin B-12 status in pregnant women. J. Nutr. 2004, 134, 3319–3326. [Google Scholar] [CrossRef]
  61. Finkelstein, J.L.; Layden, A.J.; Stover, P.J. Vitamin B-12 and Perinatal Health. Adv. Nutr. 2015, 6, 552–563. [Google Scholar] [CrossRef]
  62. Varsi, K.; Ueland, P.M.; Torsvik, I.K.; Bjørke-Monsen, A.L. Maternal Serum Cobalamin at 18 Weeks of Pregnancy Predicts Infant Cobalamin Status at 6 Months-A Prospective, Observational Study. J. Nutr. 2018, 148, 738–745. [Google Scholar] [CrossRef]
  63. Reischl-Hajiabadi, A.T.; Garbade, S.F.; Feyh, P.; Weiss, K.H.; Mütze, U.; Kölker, S.; Hoffmann, G.F.; Gramer, G. Maternal vitamin B12 deficiency detected by newborn screening—Evaluation of causes and characteristics. Nutrients 2022, 14, 3767. [Google Scholar] [CrossRef]
  64. Perrin, M.T.; Pawlak, R.; Dean, L.L.; Christis, A.; Friend, L. A cross-sectional study of fatty acids and brain-derived neurotrophic factor (BDNF) in human milk from lactating women following vegan, vegetarian, and omnivore diets. Eur. J. Nutr. 2019, 58, 2401–2410. [Google Scholar] [CrossRef]
  65. Karcz, K.; Królak-Olejnik, B. Vegan or vegetarian diet and breast milk composition—A systematic review. Crit. Rev. Food Sci. Nutr. 2021, 61, 1081–1098. [Google Scholar] [CrossRef]
  66. Mathey, C.; Di Marco, J.N.; Poujol, A.; Cournelle, M.A.; Brevaut, V.; Livet, M.O.; Chabrol, B.; Michel, G. Stagnation pondérale et régression psychomotrice révélant une carence en vitamine B12 chez 3 nourrissons [Failure to thrive and psychomotor regression revealing vitamin B12 deficiency in 3 infants]. Arch. Pediatr. 2007, 14, 467–471. [Google Scholar] [CrossRef]
  67. Sahgal, N.; Evans, J.; Salazar, A.M.; Starr, K.J.; Corichi, M. Religion in India: Tolerance and Segregation. 10: Religion and Food. Pew Research Center 2021. Available online: https://www.pewresearch.org/religion/2021/06/29/religion-and-food/ (accessed on 13 February 2023).
  68. Kadiyala, A.; Palani, A.; Rajendraprasath, S.; Venkatramanan, P. Prevalence of vitamin B12 deficiency among exclusively breast fed term infants in South India. J. Trop. Pediatr. 2021, 67, fmaa114. [Google Scholar] [CrossRef]
  69. Dubaj, C.; Czyż, K.; Furmaga-Jabłońska, W. Vitamin B12 deficiency as a cause of severe neurological symptoms in breast fed infant—A case report. Ital. J. Pediatr. 2020, 46, 40. [Google Scholar] [CrossRef]
  70. Honzik, T.; Adamovicova, M.; Smolka, V.; Magner, M.; Hruba, E.; Zeman, J. Clinical presentation and metabolic consequences in 40 breastfed infants with nutritional vitamin B12 deficiency--what have we learned? Eur. J. Paediatr. Neurol. 2010, 14, 488–495. [Google Scholar] [CrossRef] [PubMed]
  71. Kocaoglu, C.; Akin, F.; Caksen, H.; Böke, S.B.; Arslan, S.; Aygün, S. Cerebral atrophy in a vitamin B12-deficient infant of a vegetarian mother. J. Health Popul. Nutr. 2014, 32, 367–371. [Google Scholar] [PubMed]
  72. Reghu, A.; Hosdurga, S.; Sandhu, B.; Spray, C. Vitamin B12 deficiency presenting as oedema in infants of vegetarian mothers. Eur. J. Pediatr. 2005, 164, 257–258. [Google Scholar] [CrossRef]
  73. von Schenck, U.; Bender-Götze, C.; Koletzko, B. Persistence of neurological damage induced by dietary vitamin B-12 deficiency in infancy. Arch. Dis. Child. 1997, 77, 137–139. [Google Scholar] [CrossRef] [PubMed]
  74. Ambroszkiewicz, J.; Klemarczyk, W.; Mazur, J.; Gajewska, J.; Rowicka, G.; Strucińska, M.; Chełchowska, M. Serum Hepcidin and Soluble Transferrin Receptor in the Assessment of Iron Metabolism in Children on a Vegetarian Diet. Biol. Trace. Elem. Res. 2017, 180, 182–190. [Google Scholar] [CrossRef] [PubMed]
  75. Rush, E.C.; Chhichhia, P.; Hinckson, E.; Nabiryo, C. Dietary patterns and vitamin B(12) status of migrant Indian preadolescent girls. Eur. J. Clin. Nutr 2009, 63, 585–587. [Google Scholar] [CrossRef]
  76. Agnoli, C.; Baroni, L.; Bertini, I.; Ciappellano, S.; Fabbri, A.; Papa, M.; Pellegrini, N.; Sbarbati, R.; Scarino, M.L.; Siani, V.; et al. Position paper on vegetarian diets from the working group of the Italian Society of Human Nutrition. Nutr. Metab. Cardiovasc. Dis. 2017, 27, 1037–1052. [Google Scholar] [CrossRef] [PubMed]
  77. Schneede, J.; Dagnelie, P.C.; van Staveren, W.A.; Vollset, S.E.; Refsum, H.; Ueland, P.M. Methylmalonic acid and homocysteine in plasma as indicators of functional cobalamin deficiency in infants on macrobiotic diets. Pediatr. Res. 1994, 36, 194–201. [Google Scholar] [CrossRef] [PubMed]
  78. Světnička, M.; Sigal, A.; Selinger, E.; Heniková, M.; El-Lababidi, E.; Gojda, J. Cross-Sectional Study of the Prevalence of Cobalamin Deficiency and Vitamin B12 Supplementation Habits among Vegetarian and Vegan Children in the Czech Republic. Nutrients 2022, 14, 535. [Google Scholar] [CrossRef] [PubMed]
  79. Leung, S.S.; Lee, R.H.; Sung, R.Y.; Luo, H.Y.; Kam, C.W.; Yuen, M.P.; Hjelm, M.; Lee, S.H. Growth and nutrition of Chinese vegetarian children in Hong Kong. J. Paediatr. Child. Health 2001, 37, 247–253. [Google Scholar] [CrossRef]
  80. Pawlak, R.; Parrott, S.J.; Raj, S.; Cullum-Dugan, D.; Lucus, D. How prevalent is vitamin B(12) deficiency among vegetarians? Nutr. Rev. 2013, 71, 110–117. [Google Scholar] [CrossRef]
  81. Kalyan, G.B.; Mittal, M.; Jain, R. Compromised vitamin B12 status of Indian infants and toddlers. Food. Nutr. Bull. 2020, 41, 430–437. [Google Scholar] [CrossRef]
  82. Ferrara, P.; Corsello, G.; Quattrocchi, E.; Dell’Aquila, L.; Ehrich, J.; Giardino, I.; Pettoello-Mantovani, M. Caring for Infants and Children Following Alternative Dietary Patterns. J. Pediatr. 2017, 187, 339–340.e1. [Google Scholar] [CrossRef]
  83. Miller, D.R.; Specker, B.L.; Ho, M.L.; Norman, E.J. Vitamin B-12 status in a macrobiotic community. Am. J. Clin. Nutr. 1991, 53, 524–529. [Google Scholar] [CrossRef]
  84. Goraya, J.S.; Kaur, S.; Mehra, B. Neurology of Nutritional Vitamin B12 Deficiency in Infants: Case Series from India and Literature Review. J. Child. Neurol. 2015, 30, 1387–1831. [Google Scholar] [CrossRef]
  85. Johnson, M.A. If high folic acid aggravates vitamin B12 deficiency what should be done about it? Nutr. Rev. 2007, 65, 451–458. [Google Scholar] [CrossRef]
  86. Chouraqui, J.P. Dietary Approaches to Iron Deficiency Prevention in Childhood-A Critical Public Health Issue. Nutrients 2022, 14, 1604. [Google Scholar] [CrossRef]
  87. Willoughby, J.L.; Bowen, C.N. Zinc deficiency and toxicity in pediatric practice. Curr. Opin. Pediatr. 2014, 26, 579–584. [Google Scholar] [CrossRef]
  88. Platel, K.; Srinivasan, K. Bioavailability of Micronutrients from Plant Foods: An Update. Crit. Rev. Food Sci. Nutr. 2016, 56, 1608–1619. [Google Scholar] [CrossRef] [PubMed]
  89. Craig, W.J.; Mangels, A.R.; Fresán, U.; Marsh, K.; Miles, F.L.; Saunders, A.V.; Haddad, E.H.; Heskey, C.E.; Johnston, P.; Larson-Meyer, E.; et al. The Safe and Effective Use of Plant-Based Diets with Guidelines for Health Professionals. Nutrients 2021, 13, 4144. [Google Scholar] [CrossRef]
  90. Krebs, N.F.; Hambidge, K.M. Trace elements. In Nutrition in Pediatrics, 5th ed.; Duggan, C., Watkins, J.B., Koletzko, B., Walker, W.A., Eds.; Peoples Medical Publishing House: Shelton, CT, USA, 2016; Volume 1, pp. 95–116. [Google Scholar]
  91. Institute of Medicine. Dietary Reference Intakes for Vitamin A, Vitamin K, Arsenic, Boron, Chromium, Copper, Iodine, Iron, Manganese, Molybdenum, Nickel, Silicon, Vanadium, and Zinc; The National Academies Press: Washington, DC, USA, 2001. [Google Scholar] [CrossRef]
  92. Mensink, G.B.; Fletcher, R.; Gurinovic, M.; Huybrechts, I.; Lafay, L.; Serra-Majem, L.; Szponar, L.; Tetens, I.; Verkaik-Kloosterman, J.; Baka, A.; et al. Mapping low intake of micronutrients across Europe. Br. J. Nutr. 2013, 110, 755–773. [Google Scholar] [CrossRef]
  93. Weikert, C.; Trefflich, I.; Menzel, J.; Obeid, R.; Longree, A.; Dierkes, J.; Meyer, K.; Herter-Aeberli, I.; Mai, K.; Stangl, G.I.; et al. Vitamin and Mineral Status in a Vegan Diet. Dtsch. Arztebl. Int. 2020, 117, 575–582. [Google Scholar] [CrossRef]
  94. Morris, A.L.; Mohiuddin, S.S. Biochemistry, Nutrients; StatPearls Publishing: Treasure Island, FL, USA, 2022. Available online: https://www.ncbi.nlm.nih.gov/books/NBK554545/ (accessed on 8 March 2023).
  95. Taylor, A.; Redworth, E.W.; Morgan, J.B. Influence of diet on iron, copper, and zinc status in children under 24 months of age. Biol. Trace. Elem. Res. 2004, 97, 197–214. [Google Scholar] [CrossRef] [PubMed]
  96. Le Louer, B.; Lemale, J.; Garcette, K.; Orzechowski, C.; Chalvon, A.; Girardet, J.P.; Tounian, P. Conséquences nutritionnelles de l’utilisation de boissons végétales inadaptées chez les nourrissons de moins d’un an [Severe nutritional deficiencies in young infants with inappropriate plant milk consumption]. Arch. Pediatr. 2014, 21, 483–488. [Google Scholar] [CrossRef]
  97. Maywald, M.; Rink, L. Zinc in Human Health and Infectious Diseases. Biomolecules 2022, 12, 1748. [Google Scholar] [CrossRef]
  98. Wessells, K.R.; Brown, K.H. Estimating the global prevalence of zinc deficiency: Results based on zinc availability in national food supplies and the prevalence of stunting. PLoS ONE 2012, 7, e50568. [Google Scholar] [CrossRef] [PubMed]
  99. EFSA NDA Panel (EFSA Panel on Panel on Dietetic Products Nutrition and Allergies). Scientific Opinion on Dietary Reference Values for iodine. EFSA J. 2014, 12, 3660. [Google Scholar] [CrossRef]
  100. Eveleigh, E.R.; Coneyworth, L.J.; Avery, A.; Welham, S.J.M. Vegans, Vegetarians, and Omnivores: How Does Dietary Choice Influence Iodine Intake? A Systematic Review. Nutrients 2020, 12, 1606. [Google Scholar] [CrossRef]
  101. Groufh-Jacobsen, S.; Hess, S.Y.; Aakre, I.; Folven Gjengedal, E.L.; Blandhoel Pettersen, K.; Henjum, S. Vegans, Vegetarians and Pescatarians Are at Risk of Iodine Deficiency in Norway. Nutrients 2020, 12, 3555. [Google Scholar] [CrossRef] [PubMed]
  102. Comerford, K.B.; Miller, G.D.; Reinhardt Kapsak, W.; Brown, K.A. The Complementary Roles for Plant-Source and Animal-Source Foods in Sustainable Healthy Diets. Nutrients 2021, 13, 3469. [Google Scholar] [CrossRef] [PubMed]
  103. Messina, V.; Mangels, A.R. Considerations in planning vegan diets: Children. J. Am. Diet. Assoc. 2001, 101, 661–669. [Google Scholar] [CrossRef] [PubMed]
  104. Richter, M.; Boeing, H.; Grünewald-Funk, D.; Heseker, H.; Kroke, A.; Leschik-Bonnet, E.; Oberritter, H.; Strohm, D.; Watzl, B. Vegan diet. Position of the German Nutrition Society (DGE). Ernähr. Umsch. 2016, 63, 92–102, Erratum in Ernähr. Umsch. 2016, 63, M262. [Google Scholar] [CrossRef]
  105. Menal-Puey, S.; Marques-Lopes, I. Development of a food guide for the vegetarians of Spain. J. Acad. Nutr. Diet. 2017, 117, 1509–1516. [Google Scholar] [CrossRef]
  106. Federal Commission for Nutrition (FCN). Vegan Diets: Review of Nutritional Benefits and Risks. Expert Report of the FCN. Bern: Federal Food Safety and Veterinary Office. 2018. Available online: https://www.blv.admin.ch/blv/en/home/das-blv/organisation/kommissionen/eek/vor-und-nachteile-vegane-ernaehrung.html (accessed on 13 February 2023).
  107. Dietary Guidelines Advisory Committee. Scientific Report of the 2020 Dietary Guidelines Advisory Committee: Advisory Report to the Secretary of Agriculture and the Secretary of Health and Human Services; U.S. Department of Agriculture, Agricultural Research Service: Washington, DC, USA, 2020. Available online: https://www.dietaryguidelines.gov/sites/default/files/2020-07/ScientificReport_of_the_2020DietaryGuidelinesAdvisoryCommittee_first-print.pdf (accessed on 13 February 2023).
  108. Van Winckel, M.; Vande Velde, S.; De Bruyne, R.; Van Biervliet, S. Clinical practice: Vegetarian infant and child nutrition. Eur. J. Pediatr. 2011, 170, 1489–1494. [Google Scholar] [CrossRef]
  109. Melina, V.; Craig, W.; Levin, S. Position of the Academy of Nutrition and Dietetics: Vegetarian Diets. J. Acad. Nutr. Diet. 2016, 116, 1970–1980. [Google Scholar] [CrossRef]
  110. Baroni, L.; Goggi, S.; Battaglino, R.; Berveglieri, M.; Fasan, I.; Filippin, D.; Griffith, P.; Rizzo, G.; Tomasini, C.; Tosatti, M.A.; et al. Vegan Nutrition for Mothers and Children: Practical Tools for Healthcare Providers. Nutrients 2018, 11, 5. [Google Scholar] [CrossRef]
  111. Müller, P. Vegan diet in young children. Nestle. Nutr. Inst. Workshop Ser. 2020, 93, 103–110. [Google Scholar] [CrossRef] [PubMed]
  112. Fewtrell, M.; Bronsky, J.; Campoy, C.; Domellöf, M.; Embleton, N.; Fidler Mis, N.; Hojsak, I.; Hulst, J.M.; Indrio, F.; Lapillonne, A.; et al. Complementary Feeding: A Position Paper by the European Society for Paediatric Gastroenterology, Hepatology, and Nutrition (ESPGHAN) Committee on Nutrition. J. Pediatr. Gastroenterol. Nutr 2017, 64, 119–132. [Google Scholar] [CrossRef] [PubMed]
  113. Chouraqui, J.P.; Turck, D.; Tavoularis, G.; Ferry, C.; Dupont, C. The Role of Young Child Formula in Ensuring a Balanced Diet in Young Children (1–3 Years Old). Nutrients 2019, 11, 2213. [Google Scholar] [CrossRef]
  114. Bocquet, A.; Dupont, C.; Chouraqui, J.P.; Darmaun, D.; Feillet, F.; Frelut, M.L.; Girardet, J.P.; Hankard, R.; Lapillonne, A.; Rozé, J.C.; et al. Committee on Nutrition of the French Society of Pediatrics (CNSFP). Efficacy and safety of hydrolyzed rice-protein formulas for the treatment of cow’s milk protein allergy. Arch. Pediatr. 2019, 26, 238–246. [Google Scholar] [CrossRef]
  115. Amit, M. Vegetarian diets in children and adolescents. Paediatr. Child Health 2010, 15, 303–314. [Google Scholar]
  116. National Health and Medical Research Council. Eat for health—Australian dietary guidelines. 2013; 212p. Available online: https://www.eatforhealth.gov.au/sites/default/files/content/n55_australian_dietary_guidelines.pdf (accessed on 13 February 2023).
  117. Gomes Silva, S.C.; Pinho, J.P.; Borges, C.; Teixeira Santos, C.; Santos, A.; Graça, A. Guidelines for a healthy vegetarian diet. In National Programme for the Promotion of a Healthy Diet; Direção-Geral da Saúde: Lisbon, Portugal, 2015; 45p, Available online: https://nutrimento.pt/activeapp/wp–content/uploads/2015/12/Guidelines-for-a-healthy-vegetarian-diet.pdf (accessed on 13 February 2023).
  118. Patel, P.; Kassam, S. Evaluating nutrition education interventions for medical students: A rapid review. J. Hum. Nutr. Diet. 2022, 35, 861–871. [Google Scholar] [CrossRef] [PubMed]
  119. STAGE (Strategic Technical Advisory Group of Experts); Duke, T.; AlBuhairan, F.S.; Agarwal, K.; Arora, N.K.; Arulkumaran, S.; Bhutta, Z.A.; Binka, F.; Castro, A.; Claeson, M.; et al. World Health Organization and knowledge translation in maternal, newborn, child and adolescent health and nutrition. Arch. Dis. Child. 2022, 107, 644–649. [Google Scholar] [CrossRef]
  120. Kushner, R.F.; Van Horn, L.; Rock, C.L.; Edwards, M.S.; Bales, C.W.; Kohlmeier, M.; Akabas, S.R. Nutrition education in medical school: A time of opportunity. Am. J. Clin. Nutr. 2014, 99 (Suppl. S5), 1167S–1173S. [Google Scholar] [CrossRef]
  121. Bassin, S.R.; Al-Nimr, R.I.; Allen, K.; Ogrinc, G. The state of nutrition in medical education in the United States. Nutr. Rev. 2020, 78, 764–780. [Google Scholar] [CrossRef]
  122. Villette, C.; Vasseur, P.; Lapidus, N.; Debin, M.; Hanslik, T.; Blanchon, T.; Steichen, O.; Rossignol, L. Vegetarian and Vegan Diets: Beliefs and Attitudes of General Practitioners and Pediatricians in France. Nutrients 2022, 14, 3101. [Google Scholar] [CrossRef]
Figure 1. Bar chart to present the reported vitamin B12 intake in lacto-ovo-vegetarian (LOV), vegan or macrobiotic children compared to omnivorous counterparts [35,36,39,40,41,43,46,47,48,49,74,75]. The dark-colored bars display the mean with SD, when available, whereas the light-colored bars display the median value.
Figure 1. Bar chart to present the reported vitamin B12 intake in lacto-ovo-vegetarian (LOV), vegan or macrobiotic children compared to omnivorous counterparts [35,36,39,40,41,43,46,47,48,49,74,75]. The dark-colored bars display the mean with SD, when available, whereas the light-colored bars display the median value.
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Figure 2. Bar chart presenting the reported iron intake in lacto-ovo-vegetarian (LOV) and vegan children compared to omnivorous counterparts [35,36,37,39,40,41,42,44,46,47,48,49,74,95]. The dark-colored bars display the mean with SD, when available, whereas the light-colored bars display the median value.
Figure 2. Bar chart presenting the reported iron intake in lacto-ovo-vegetarian (LOV) and vegan children compared to omnivorous counterparts [35,36,37,39,40,41,42,44,46,47,48,49,74,95]. The dark-colored bars display the mean with SD, when available, whereas the light-colored bars display the median value.
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Figure 3. Bar chart to present the reported zinc intake in lacto-ovo-vegetarian (LOV)and vegan children compared to omnivorous counterparts [36,37,39,40,41,42,46,47,48,49,95]. The dark-colored bars display the mean with SD, when available, whereas the light-colored bars display the median value.
Figure 3. Bar chart to present the reported zinc intake in lacto-ovo-vegetarian (LOV)and vegan children compared to omnivorous counterparts [36,37,39,40,41,42,46,47,48,49,95]. The dark-colored bars display the mean with SD, when available, whereas the light-colored bars display the median value.
Nutrients 15 02129 g003
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MDPI and ACS Style

Chouraqui, J.-P. Risk Assessment of Micronutrients Deficiency in Vegetarian or Vegan Children: Not So Obvious. Nutrients 2023, 15, 2129. https://doi.org/10.3390/nu15092129

AMA Style

Chouraqui J-P. Risk Assessment of Micronutrients Deficiency in Vegetarian or Vegan Children: Not So Obvious. Nutrients. 2023; 15(9):2129. https://doi.org/10.3390/nu15092129

Chicago/Turabian Style

Chouraqui, Jean-Pierre. 2023. "Risk Assessment of Micronutrients Deficiency in Vegetarian or Vegan Children: Not So Obvious" Nutrients 15, no. 9: 2129. https://doi.org/10.3390/nu15092129

APA Style

Chouraqui, J. -P. (2023). Risk Assessment of Micronutrients Deficiency in Vegetarian or Vegan Children: Not So Obvious. Nutrients, 15(9), 2129. https://doi.org/10.3390/nu15092129

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