ﺑﺎﺯﮔﺸﺖ ﺑﻪ ﺻﻔﺤﻪ ﻗﺒﻠﯽ
خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده : -37 مورد

Vegetarian diets for children

Vegetarian diets for children
Authors:
Michelle Loy, MD, FAAP
Lisa Patel, MD, MESc, FAAP
Section Editor:
Amy B Middleman, MD, MPH, MS Ed
Deputy Editor:
Alison G Hoppin, MD
Literature review current through: Apr 2025. | This topic last updated: Jan 21, 2025.

INTRODUCTION — 

Vegetarian diets are recognized by the 2020-2025 Dietary Guidelines for America as one of three healthy dietary patterns [1]. There is increasing recognition that minimizing animal-based protein, particularly red meats, and maximizing plant-based options for protein provide combined benefits for health and the ability of this planet to continue providing enough food to feed the world's growing population [2]. In the broadest sense, vegetarian diets exclude meat and poultry, although there are a number of subcategories to vegetarianism (table 1).

As more people turn to vegetarian diets due to health, ecologic, and ethical considerations, it is important for clinicians to be equipped to answer questions for their patients and families. Like any diet, vegetarian diets require planning to optimize health, growth, and nutrient intake [3-7].

This topic review will outline the available evidence on vegetarian diets and discuss how to counsel families to ensure a well-planned diet with appropriate caloric and nutrient intake to support optimal growth. A well-planned vegetarian diet offers health benefits, while a poorly planned diet carries risks, particularly for infants, young children, and adolescents.

Overviews of healthy eating for children and adolescents are presented separately. (See "Dietary recommendations for toddlers and preschool and school-age children" and "Healthy eating for adolescents".)

PREVALENCE AND TRENDS — 

Vegetarian diets are becoming increasingly popular in many countries, including among youth [3,8-10].

In the United States, approximately 5 percent of youth 8 to 17 years old describe themselves as vegetarian and 2 percent as vegan [11]. Among adults in the United States, approximately 6 percent follow some form of vegetarian diet and 3 percent follow a vegan diet [12]. When eating away from home, approximately one-half of Americans "sometimes or always" choose vegetarian meals and one-quarter "sometimes or always" choose vegan meals [11,12]. Vegetarian diets were reported by approximately 8 percent of adolescents in the United Kingdom [13] and 8 to 10 percent of adults in Germany, Austria, Italy, and the United Kingdom [14,15].

Interpretation of these surveys is complicated because of variations in definitions for the term "vegetarian" (table 1). Because the types and composition of vegetarian diets have important implications for the growth and development of children and adolescents, it is important for the clinician to discuss with their patients how they define vegetarianism for themselves and, specifically, which foods are included or excluded.

HEALTH CONSIDERATIONS — 

Like any diet, vegetarian diets require planning to optimize health. The typical diet in the United States results in higher-than-needed caloric intake for protein in addition to lower-than-recommended intake for whole grains, fruits, and vegetables [16]. Dietary changes that decrease or eliminate animal-based proteins in favor of plant-forward proteins with increased intake of fresh fruits and vegetables align with recommendations of the US Food and Drug Administration and major nutritional societies [17-19]. Families new to these types of changes should be aware of how to achieve appropriate balance in nutrients to avoid a few important pitfalls, which are outlined below.

Overall diet quality — Surveys of pediatric populations indicate that those who follow a vegetarian diet are more likely to meet general targets for a healthy diet compared with those who do not follow a vegetarian diet. Several studies show that vegan children and adolescents generally have healthier food intake patterns, with the higher intakes of whole grains, vegetables, legumes, and nuts and the lower intakes of sweets and snack foods compared with omnivorous children [20-22]. They also had the highest intakes of vitamin E, vitamin B1, folate, vitamin C, magnesium, iron, and zinc and mean fiber intake, whereas the omnivorous group did not reach the dietary reference value of 14 g/1000 kcal for fiber. Another survey of adolescent schoolchildren in Minnesota compared self-reported dietary intake with the Healthy People 2010 nutritional objectives [23]. Adolescents who identified themselves as vegetarians were more likely than nonvegetarians to meet the objectives for total fat (70 versus 48 percent), saturated fat (65 versus 39 percent), daily servings of vegetables (26 versus 14 percent), and ≥5 servings of fruits or vegetables per day (39 versus 28 percent). The mean calcium intake in both groups was approximately 1100 mg/day, which is less than the recommended 1300 mg/day; only 30 percent of the students, regardless of dietary group, met the recommended target for calcium.

Potential effects on growth — Although children who follow a vegetarian diet tend to be somewhat leaner than their omnivore counterparts, their physical growth is usually within the normal range, provided that meal planning is adequate and sufficient food is made available [24-29]. By contrast, poorly planned or severely restricted diets can lead to nutrient deficiencies that may compromise or delay growth in children [30-32].

For children who have suboptimal growth while following a vegetarian diet, clinicians should review the diet composition and total caloric intake, with particular attention to ensuring sufficient fat content and avoiding excessive fiber. (See 'Energy' below and 'Fiber' below.)

Benefits for cardiovascular and metabolic health — Most available evidence on the benefits of vegetarian diets is for adults and shows an association with lower incidence of obesity, coronary heart disease, hypertension, and type 2 diabetes compared with consumption of a nonvegetarian diet [3,5,33-40]. While there are fewer studies specific for children, several studies show that establishing these patterns in childhood carries benefits into adulthood [6,41-43]. Additionally, studies show that vegetarian children generally have a lower risk of obesity; better lipid profiles; and decreased consumption of cholesterol, added sugars, and saturated fat. These benefits are accompanied by modest decreases in cardiovascular risk factors, including non-high-density lipoprotein cholesterol, blood pressure, and body mass index [5,44]. However, it is difficult to separate the effects of the diet from other characteristics of this population, including associated healthful behaviors (eg, regular exercise, avoidance of tobacco and alcohol products) or socioeconomic privilege. As a consequence, an independent effect of the diet on health outcomes or all-cause mortality has not been shown [45].

Benefits for the gut microbiota — Well-planned vegetarian diets appear to be beneficial to human health by promoting more diverse and stable gut microbiota [46]. The diversity of the microbiota has an important association with body mass index, obesity, and cardiovascular protection. Vegetarians have a microbiota rich in Prevotella and Ruminococcus and depleted in Bacteroides compared with omnivores. Plant fibers increase lactic acid bacteria such as Ruminococcus and Roseburia, which degrade complex carbohydrates into short-chain fatty acids and reduce disease-producing Clostridium and Enterococcus species. Plant fibers encourage the growth of microbiota that produce short-chain fatty acids, which improve immunity against pathogens and regulate intestinal function. Plant polyphenols increase Bifidobacterium and Lactobacillus, both of which have antiinflammatory effects. Thus, plant-based diets may be an effective way to promote a diverse ecosystem of beneficial microbes that support overall health.

OVERVIEW OF NUTRITIONAL COUNSELING

General considerations — Properly planned vegetarian diets can meet all nutrient needs for growth and development. Families new to vegetarian diets may benefit from counseling on energy, protein, iron, calcium, vitamin D, and vitamin B12 (cyanocobalamin) and, to a lesser extent, zinc, long-chain omega-3 fatty acids, and dietary fiber [3,47-50]. Nutritional counseling about these nutrients is detailed in the sections on each nutrient below.

The establishment of healthy eating patterns in childhood reduces the likelihood of developing chronic diseases later in life [51-54]. Thus, vegetarian children, like other children, should follow dietary guidelines that limit total fat, saturated fatty acids, and cholesterol and encourage complex carbohydrates, fiber, and antioxidants (eg, vitamins A and C, carotenoids, and phytochemicals) [1]. At the same time, the greatest risks for inadequate nutrient intake from a vegetarian diet occur during periods of growth. The more restrictive the vegetarian diet, the greater the risk of dietary inadequacy [55-57].

To address this, vegetarian or vegan diets should include a variety of nutrient-rich foods. Examples of foods include cooked legumes, whole-grain breads, enriched cereals, nuts and nut spreads (peanut, tahini, almond, cashew butter), nutlike seeds (soybeans, sunflower seeds, sesame seeds, flaxseeds, chia seeds, pumpkin seeds), avocados, and dried fruits. In addition, if dairy products are included in the vegetarian diet, they are a good source of energy, high-quality protein, calcium, potassium, vitamin B12, magnesium, and vitamin D (if fortified) [58,59].

The United States Department of Agriculture "MyPlate plan" is a tool depicting food groups and portion sizes and may serve as a useful reference guide. Food patterns with vegetarian options are provided for different calorie levels [60]. Similar tools for planning a vegetarian or vegan diet include VegPlate Junior (which meets Italian and United States dietary reference intakes) [61] and the "whole-food plant-based plate for healthy beginnings" from the American College of Lifestyle Medicine [62].

If there are concerns about a family's ability to follow through on a well-planned vegetarian diet, families may benefit from a referral to a dietitian to provide more extensive guidance.

Infancy and weaning — Breastfeeding mothers who are vegetarian should ensure adequate intake of vitamin B12, iron, vitamin D, and calcium (table 2). In particular, vitamin B12 content of breast milk reflects maternal vitamin B12 levels and severe deficiency can impair neurologic development in the infant [63]. Vegetarian and vegan mothers should be counseled on B12 supplementation. (See 'Vitamin B12' below.)

If the decision is made to feed an infant a plant-based formula, soy-based formulas are appropriate for full-term infants. Premature infants should be fed human milk if possible but, otherwise, a cow's milk-based premature formula because soy formula is associated with an increased risk of osteopenia [64,65]. Homemade formulas are never appropriate for an infant and should not be utilized [66].

When introducing solids for infants and weaning off of breast milk or formula, it is important to consider that vegetarian foods may have lower caloric density and higher fiber content, filling a smaller stomach without the calories needed for growth. This can be addressed by including higher-fat foods such as nut butters, soy foods, avocados, and oils. Additionally, infants should be offered iron-rich foods such as iron-fortified cereals, beans, dark green leafy vegetables, breads, and peas. Infants weaned to a vegetarian diet also require ongoing attention to ensure that they meet their vitamin B12 needs (0.5 mcg daily) through diet or a supplement.

Older children and adolescents — Understanding and affirming the patient's motivation for a vegetarian diet are valuable steps in counseling. In most cases, the motivation is for ethical or cultural reasons, for planetary or personal health, or for some combination of these.

For adolescents who are new to a vegetarian diet, the change in eating habits should be met with curiosity, both to answer any questions about the implications for health and to identify potential red flags that the change could be related to disordered eating. Adoption of a vegetarian diet during adolescence is not inherently a marker for disordered eating [67-69]. In some cases, ethical or environmental concerns are the key motivations for the dietary choice. In other cases, weight concerns are a primary motivation; this can also be a reasonable and healthy motivation but calls for additional monitoring to ensure that the diet is balanced and eating patterns and growth are appropriate. (See "Healthy eating for adolescents", section on 'Attitudes toward food and body image'.)

Counseling should include information about the nutritional implications of the diet, to set appropriate expectations and encourage the adolescent to make responsible food choices. If the adolescent endorses that their primary goal is to lose weight and/or if the dietary change was related to social or emotional problems, further screening for an eating disorder is appropriate, including a focused history, physical examination and psychological assessments. A patient with body mass index less than the 15th percentile and/or who has other features suggestive of an eating disorder (including disrupted menses or body image disturbances) is a candidate for referral for more intensive medical and psychological care. (See "Eating disorders: Overview of epidemiology, clinical features, and diagnosis" and "Healthy eating for adolescents" and "Healthy eating for adolescents", section on 'Pathologic dietary restriction ("dieting") and body image'.)

Plant-based beverages — For toddlers and preschool-aged children (<5 years), soy milk is an appropriate option in the place of cow-based milk as it has a similar profile in terms of protein, calcium, and vitamin D. Other plant-based beverages (such as oat- or almond-based "milks") should not be used as a primary source of energy and protein, given their lower caloric and protein content.

For school-aged children who avoid cow's milk, counsel families to select plant-based milk options that are fortified with calcium, B12, and vitamin D and do not have added sugar. Specific counseling is important because a wide variety of products are available and consumers may not be aware of the varying nutritional content of the many different plant-based milks. The nutrient profiles of plant-based beverages vary substantially, but they can be relatively low in protein, fat, and other nutrients [70-72]. Even when the beverages are fortified, the plant phytates may reduce the bioavailability of protein and minerals. (See 'Protein' below.)

There is emerging evidence that, in high-quality diets, higher consumption of dairy may have negative health effects. While existing nutritional guidance heavily favors dairy, it is important to recognize that plant-based options in a well-planned vegetarian diet may hold benefits in terms of endometrial and prostate cancer risks in particular, while higher dairy consumption is linked with lower colorectal cancer risk [73].

LABORATORY MONITORING — 

Families or children following well-planned vegetarian or vegan diets do not need routine laboratory monitoring outside of the general guidance in primary care for all children. As examples:

Iron deficiency – Anemia is a relatively common problem in children. Clinicians can help prevent iron deficiency anemia by counseling families about iron-rich foods and ways to improve absorption of iron. In addition, all children should have routine laboratory-based screening for iron deficiency anemia on one occasion for toddlers and adolescent females, with additional screening for those with risk factors including low dietary iron intake. (See "Iron deficiency in infants and children <12 years: Screening, prevention, clinical manifestations, and diagnosis", section on 'Screening recommendations' and "Iron requirements and iron deficiency in adolescents", section on 'Screening'.)

Vitamin D – For patients with low estimated vitamin D intake (eg, those with little or no intake of fortified dairy products or plant-based beverages), check 25-hydroxyvitamin D at baseline, with follow-up testing as needed, depending on the result or to monitor supplementation. If a supplement is added, check the level approximately six months later and, if the result is normal, recheck approximately every two to three years. (See 'Vitamin D' below.)

Vitamin B12 – For patients who follow a vegan diet, supplement empirically with vitamin B12. Measure serum vitamin B12 concentrations if there is a concern for deficiency, eg, question of nonadherence to the supplement or macrocytic anemia. (See 'Vitamin B12' below.)

ENERGY — 

Approximate energy requirements for infants and children are shown in the tables (table 3 and table 4). Some young children who follow a vegetarian or vegan diet may have difficulty meeting their energy needs because of their relatively small stomach capacity and energy needs for growth [24,25,74,75]. A plant-based diet that has a high fiber content and low caloric density may provide a sense of fullness before an adequate amount of energy is ingested. This situation may be a significant problem in young children, who have small stomach capacities.

To meet energy needs, young children typically need three meals and three snacks per day. Both energy-dense and nutrient-dense foods should be included. Foods higher in healthy fats, such as nuts, seeds, nut and seed butters, and avocado, help meet nutrient and energy needs, especially for children who are underweight. The intake of fat should not be restricted in children younger than two years of age. (See "Dietary history and recommended dietary intake in children", section on 'Energy needs'.)

For adolescents who follow a vegetarian or vegan diet, the clinician should monitor growth and body weight to ensure that energy intake is appropriate. Adolescents who are overweight and who adopt a vegetarian diet as a means of weight management also should be monitored for evidence of disordered eating patterns and given anticipatory guidance to emphasize dietary variety and an appropriate energy intake for healthy weight management [76]. (See "Healthy eating for adolescents".)

PROTEIN

Requirements — Protein requirements for infants and children are listed in the tables (table 3 and table 4) [77]. The protein concentration varies among different foods, as shown in these protein foods tables from the MyPlate website.

These estimates are based on proteins from animal sources (meat, dairy, and eggs) or soy protein (eg, tofu), which are more than 90 percent digestible [78,79]. Diets that include these protein sources generally include sufficient protein, as long as the total energy intake is sufficient. This includes semi-vegetarian, pescatarian, or vegetarian diets that include milk, milk products, and/or eggs [80]. Note that the protein content of plant-based beverages is highly variable and generally less compared with cow's milk. (See 'Plant-based beverages' above.)

Proteins from legumes are 80 to 90 percent digestible, while proteins from grains and other plant foods are 70 to 90 percent digestible. Therefore, for vegetarians who rely on these protein sources, the protein requirement may be increased by 20 to 30 percent for children aged two to six years and by 15 to 20 percent for children aged six and older, in comparison with nonvegetarians [78].

Protein type

Definitions – Proteins of plant and animal origin differ in their concentration of essential amino acids, which are necessary for growth and repair.

Complete proteins – Animal proteins (including fish and dairy) and soy protein are considered "complete" because they supply all of the essential amino acids [81,82].

Incomplete proteins – Other plant-based proteins are considered "incomplete" because they supply only some types of essential amino acids.

Complementary proteins – Two types of vegetable proteins are considered "complementary" if the combination supplies all essential amino acids. As an example, grains are low in the essential amino acid lysine and high in methionine, whereas legumes and oily seeds are low in methionine and high in lysine. Together, they combine to make a high-quality protein source.

Clinical implications – In clinical practice, it is rarely necessary to distinguish between these types of protein [83]. For most vegetarian diets, any type of protein can fill the protein requirement because the overall diet will contain ample essential amino acids, either from "complete" proteins or from a variety of "incomplete" proteins (typical intake of legumes or grain proteins).

An exception is a vegan diet that has low protein variety, especially if total protein intake is marginal. In this case, to avoid essential fatty acid deficiency, the protein requirement should be met with either soy protein (a complete protein) or from intentional combinations of complementary proteins (grains plus legumes or seeds). One need not consume complementary proteins at the same time or in the same meal [3,84].

VITAMINS AND MINERALS — 

Nutritional counseling is important to ensure that the diet provides adequate vitamins and minerals, especially iron, calcium, vitamin D, and vitamin B12 (cyanocobalamin). If the diet cannot be adjusted to provide recommended amounts of each of these nutrients, supplements should be added to ensure adequate intake. In this case, we suggest a general multivitamin and mineral supplement that contains a broad range of water- and fat-soluble vitamins, minerals, and trace elements to ensure dietary intakes of micronutrients that approximate daily nutrient requirements for age (table 4).

Iron — Children who have rapid growth rates have increased iron needs and are at risk for iron deficiency with or without anemia [85-87]. The recommended dietary allowance (RDA) for iron is 7 mg in children 1 to 3 years old, 10 mg in children 4 to 8 years, 8 mg in children 9 to 13 years, and 11 mg for males and 15 mg for females aged 14 to 18 years. The RDA for pregnant adolescents is 27 mg/day [88]. (See "Iron deficiency in infants and children <12 years: Screening, prevention, clinical manifestations, and diagnosis" and "Iron requirements and iron deficiency in adolescents".)

Potential deficits for a vegetarian diet – Iron deficiency is common among children in the United States and many other countries. Vegetarian and vegan children are potentially at higher risk for iron deficiency because milk and eggs are not good sources of absorbable iron, but the prevalence of iron deficiency varies widely [89]. Risk factors include a diet poor in plant-based iron-rich foods, periods of rapid growth, and menstruation [78,85,90,91]. In a study of 1100 children aged 4 to 18 years, female adolescents who reported being vegetarian were more likely to have low hemoglobin and serum ferritin values compared with their omnivorous peers [85]. One study of 43 lacto-ovovegetarian and 46 omnivorous children aged 4.5 to 9 years found lower serum hepcidin and ferritin levels in the vegetarian children, despite higher dietary intake of vitamin C, compared with the nonvegetarian children [92]. By contrast, a longitudinal study of young children in Toronto found no association between a vegetarian diet and biomarkers of iron deficiency [26].

Children who do not eat meat are at risk for iron deficiency because nonheme iron (from plants) is less readily absorbed compared with heme iron (from meat or fish) [85,88,93,94]. Absorption of heme iron is 15 to 35 percent, compared with 2 to 20 percent for nonheme iron. In addition, the absorption of nonheme iron is reduced greatly by other dietary components, whereas heme iron is little affected (table 5). In particular, tannins and polyphenols in tea and coffee form iron-tannate complexes that greatly reduce nonheme iron absorption [47,85,95]. Phytate found in legumes, nuts, seeds, whole grains, and soy protein also bind with nonheme iron to form insoluble complexes and reduce iron absorption [47,85,96,97]. In one study, absorption of iron from a variety of commonly eaten legumes (dried beans and peas) prepared as soups was only 1 to 2 percent [90].

Nutritional counseling – For children who do not eat meat or fish, important strategies to increase iron absorption include intake of ascorbic acid (vitamin C) at each meal, avoidance of large intakes of tannin-containing teas, and increasing dietary iron content [47,85,87,98].

Iron supplements may be necessary for individuals with laboratory markers for iron deficiency (eg, low mean cell volume and mean corpuscular hemoglobin, microcytic anemia, and/or low ferritin) or those with low iron intake as estimated from a dietary recall. This is most likely for individuals eating restricted vegetarian diets with little or no meat or fish [3,47]. Adolescent girls are at increased risk for iron deficiency after menarche due to menstrual blood loss. (See "Iron deficiency in infants and children <12 years: Screening, prevention, clinical manifestations, and diagnosis" and "Iron requirements and iron deficiency in adolescents".)

Ascorbic acid (vitamin C) is a powerful promoter of nonheme iron absorption because it prevents the formation of less-soluble ferric compounds [90,99-101]. A 75 mg dose of ascorbic acid increases the absorption of nonheme iron three- to fourfold [96]. Because of its mechanism of action, ascorbic acid is effective only when consumed at the same time as the iron-containing food. Important sources of both vitamin C and other facilitators of iron absorption (eg, citric and malic acid) include citrus fruits and strawberries, broccoli, and tomatoes. By increasing absorption of nonheme iron, ascorbic acid helps to counteract the inhibitory effect of phytates in a plant-based diet.

Good plant sources of iron include whole or enriched breads or grains, iron-fortified cereals, legumes, green leafy vegetables, dried fruits, soy products, blackstrap molasses, bulgur, and wheat germ. The widespread fortification of enriched breads, cereals, and pasta products has helped increase iron intake for children.

Calcium — Adequate calcium intake is important throughout life to ensure peak bone mass accumulation, especially during periods of growth. Children with stronger bones may experience fewer fractures and may be more resistant to the development of osteoporosis in later life [102,103]. The recommended intake of calcium is approximately 700 mg for children 1 to 3 years of age, 1000 mg for children 4 to 8 years of age, and 1300 mg for those 9 to 18 years (table 4) [104]. (See "Bone health and calcium requirements in adolescents" and "Dietary recommendations for toddlers and preschool and school-age children", section on 'Dairy products'.)

Potential deficits for a vegetarian diet – For children who consume lactovegetarian or lacto-ovovegetarian diets, most calcium needs can be met by milk and dairy products; these provide approximately 75 percent of the calcium in the average American diet [103,105]. Children who avoid dairy products, such as those following a vegan diet, have more difficulty meeting calcium needs. This is in part because they consume plant foods containing oxalates and phytates and because the calcium contents of typical vegetables, fruit, and cereal grains are relatively low [48,106-108]. Children who avoid dairy products generally require either substantial intake of calcium-fortified foods (eg, several servings daily of calcium-fortified soy milk) or a calcium supplement to meet the age-dependent recommended intake (table 4).

Estimates of calcium needs are imprecise because other dietary constituents also affect calcium balance: Oxalate and phytate decrease calcium absorption, while salt and protein increase calcium excretion [98,103,109]. Foods high in oxalate include spinach, beet greens, Swiss chard, and yams. Thus, the lower protein intake among vegetarians may decrease urinary calcium loss, which improves their net calcium balance and reduces their risk for calcium stone formation compared with omnivores [110]. (See "Kidney stones in adults: Epidemiology and risk factors", section on 'Protein'.)

Nutritional counseling – Vegetarian children who do not drink milk should include at least one calcium-rich or calcium-fortified food with each meal and with several snacks each day. Children who follow a vegan diet can obtain calcium from calcium-fortified foods and beverages (such as fortified soy milk), foods naturally rich in calcium, calcium supplements, or a combination of these:

Calcium-fortified foods include some types of soy milk, soy yogurt, and soy cheese, as well as calcium-precipitated tofu, many types of ready-to-eat cereals and some breakfast bars, pastas, waffles, and juices [111,112]. Calcium bioavailability in most of these sources is equivalent to milk. As an example, one 8-ounce glass of calcium-fortified orange juice provides 300 mg of calcium, equivalent to an 8-ounce glass of milk. In contrast, the bioavailability of calcium in soy milk is only 75 percent of that in cow's milk [113]. Ideally, these foods should also be fortified with vitamin D because vitamin D facilitates the absorption of calcium [114].

Foods that are naturally rich in calcium and low in oxalate include kale, mustard greens, turnip greens, broccoli, bok choy, dried figs, and blackstrap molasses (table 6) [103]. Most of these foods have additional benefits because they provide other important nutrients. However, it is difficult to meet calcium requirements from these foods alone, even with large portions.

Calcium supplements also can be used to provide adequate calcium intake. Consuming calcium supplements at the same time as iron or zinc supplements may interfere with the absorption and utilization of these minerals. (See "Bone health and calcium requirements in adolescents".)

The benefits of using fortified foods to increase calcium intake was demonstrated in a double-blind, placebo-controlled study of prepubertal girls with low spontaneous calcium intake who were randomly assigned to receive food products that were or were not fortified with 850 mg of calcium [115]. Calcium fortification increased mean bone mineral density in all girls, but the increase was greatest in those whose baseline calcium intake was less than 850 mg. The gains in bone mass persisted one year after discontinuation of treatment.

Vitamin D — Normal levels of vitamin D metabolites are necessary for adequate intestinal calcium, phosphate absorption, and bone formation [116-118]. Vitamin D is available through sunlight exposure and dietary intake (figure 1). Dietary intake of 15 mg (600 international units) daily is recommended for children one year and older. (See "Vitamin D insufficiency and deficiency in children and adolescents", section on 'Recommended vitamin D intake'.)

Sunlight exposure is an important source of vitamin D but is often insufficient, especially during the winter, for children with dark skin pigmentation, and for those who use sunscreen or clothing to protect their skin from sun damage. Maintenance of normal serum vitamin D concentrations requires exposure to the sun on hands, arms, and face for 10 to 15 minutes per day for fair-skinned individuals; individuals with dark skin pigmentation require 6 to 10 times as much exposure as a light-skinned individual [119]. (See "Vitamin D insufficiency and deficiency in children and adolescents", section on 'Skin pigmentation and low sun exposure'.)

Potential deficits for a vegetarian diet – Few foods contain vitamin D. The principal dietary source of vitamin D for omnivores, lacto-ovovegetarians, and lactovegetarians is milk fortified with vitamin D (2.5 mg [100 international units] per 8 oz) [120]. Vegetarians who do not consume vitamin D-fortified cow's milk or plant-based beverage are at risk for vitamin D deficiency, which can lead to rickets in young children and osteomalacia in adults [121-124].

Nutritional counseling – For children who do not drink cow's milk (eg, those following a vegan diet), a dietary alternative is fortified soy milk, other fortified alternative milk, or fortified breakfast cereal [114,116]. For children who eat fish (eg, a pescatarian or macrobiotic diet), consuming fatty fish (sardines, salmon, tuna, mackerel) or cod liver oils several times per week can provide sufficient vitamin D. Cheese and egg yolks provide small amounts of vitamin D [116].

To meet the recommended intake for vitamin D, children generally require either substantial intake of these vitamin D-rich foods (eg, several servings daily of fortified cow's milk or soy milk) and some additional vitamin D from sunlight exposure (eg, from participating in outdoor sports or active play). Otherwise, they will require a vitamin D supplement to meet the target, especially if they have risk factors for vitamin D deficiency such as dark skin pigmentation, low sun exposure, or residence in northern latitudes [125-127]. (See "Overview of vitamin D", section on 'Sources'.)

Vitamin B12 — Vitamin B12 (cobalamin) is only found in foods from animal sources (meat, fish, eggs, and dairy products) [48,128]. The RDA for cobalamin is 0.9 mcg for children 1 to 3 years of age, 1.2 mcg for 4 to 8 years, 1.8 mcg for 9 to 13 years, 2.4 mcg for 14 to 18 years, and 2.6 mcg for pregnant adolescents (table 7) [129]. Because substantial amounts of vitamin B12 are stored in the body (primarily in the liver), the deficiency develops gradually. Once vitamin B12 is removed from the diet, deficiency develops within four to six months in infants (eg, the breastfed infant of a mother with vitamin B12 deficiency) or one to two years in adults [129]. Vitamin B12 deficiency in infants can present with tremor, irritability, or spells (apneas, absences, and motor seizures) [63,130,131]. (See "Clinical manifestations and diagnosis of vitamin B12 and folate deficiency".)

Potential deficits for a vegetarian diet – Lacto-ovovegetarians and lactovegetarians can, but do not always, consume sufficient amounts of vitamin B12 from eggs, milk, and milk products. Vegans, whose diets are based entirely on plant food, are at considerable risk for vitamin B12 deficiency [132,133]. For example, in one study, 10 of 25 vegans had vitamin B12 deficiency manifested by macrocytosis (picture 1) and low serum vitamin B12 [134]. In another report, serum vitamin B12 concentrations were determined in 83 volunteer subjects attending an American vegetarian society conference [135]. Among subjects who did not supplement their diets with vitamin B12 or multivitamin tablets, the percentage with serum vitamin B12 levels below the normal range was associated with the degree of dietary restriction:

Vegans – 92 percent

Lactovegetarians – 64 percent

Lacto-ovovegetarians – 47 percent

Semi-vegetarians – 20 percent

Nutritional counseling – For children who eat fish (eg, those following a pescatarian diet), eating fish two to three times per week can provide a good source of vitamin B12. Vegan children and other vegetarians whose diet does not contain significant amounts of meat or fish should consume a regular and reliable source of the vitamin, either in fortified foods or an oral B12 supplement. Commonly used vitamin B12-fortified foods include most ready-to-eat cereals, many meat substitutes, some milk alternatives, and fortified nutritional yeasts [136]. Fortified soy milk is another good source of vitamin B12 for children [137]. Vitamin B12 supplements typically provide 6 to 9 mcg/day [133]. This dose is higher than the RDA to ensure adequate intake and because there are no adverse effects of the higher dose [129]. Of note, only cyanocobalamin is the active form of the vitamin and some listings of vitamin B12 content in foods do not differentiate between this form and its inactive analogs. As examples, much of the vitamin B12 present in spirulina, sea vegetables, tempeh, and miso is inactive and does not contribute to the vitamin B12 requirement [112,138]. Moreover, the inactive forms can compete with active forms for absorption.

Zinc — Recommended intake for zinc is 3 mg/day for children aged 1 to 3 years, 5 mg/day for children aged 4 to 8 years, 8 mg/day for children aged 9 to 13 years, 9 mg/day for adolescent females, and 11 mg/day for adolescent males (table 8).

Potential deficits for a vegetarian diet – Children who do not consume dairy products are at risk of a suboptimal zinc status because of high requirements for growth, although the clinical significance of mild zinc deficiency is unclear. Severe zinc deficiency can be associated with impaired growth, taste, and smell, as well as impaired immunity, with an increased risk of infections, particularly diarrhea and pneumonia. Adult vegetarians do not typically develop zinc deficiency, because they have a compensatory increase in fractional absorption. (See "Zinc deficiency and supplementation in children".)

Zinc is found in foods of both animal and plant origin. Animal sources include oysters, shellfish, liver, meat, poultry, and dairy products [93,139]. The zinc in vegetarian diets has a lower bioavailability because of the high content of phytate and dietary fiber [47,78,140,141]. Certain food preparation techniques, such as the soaking of sprouting beans, grains, and seeds, as well as leavening breads, can mitigate this problem by reducing binding of zinc by phytates, thus increasing zinc bioavailability [3,142,143].

Nutritional counseling – Milk and milk products are the primary source of zinc for children on vegetarian diets who also consume dairy products. For children who do not consume milk (eg, vegans), cereals are the primary source of zinc; secondary sources are meat substitutes (eg, legumes, nuts, and soy products). Plant sources of zinc include whole grains, legumes, wheat germ, and nuts.

Iodine — Iodine is essential for thyroid hormone synthesis, and iodine deficiency during pregnancy or infancy has an adverse effect on child development. Clinically significant iodine deficiency is uncommon in countries with universal salt iodization programs, including the United States. Other food sources include dairy products, eggs, fish, seafood, and fortified bread [144,145]. Plant-based foods typically have low iodine content (with the exception of seaweed). Accordingly, individuals following a vegan diet without iodized salt, fortified bread, or seaweed are at risk for iodine deficiency. In a systematic review of five studies, the median iodine status (as measured by urinary iodine concentrations) was below the threshold for iodine adequacy for all diets and was moderately deficient for all vegan cohorts, three-quarters of vegetarian cohorts, and none of the omnivore cohorts but with a wide range of iodine adequacy within each dietary group [145].

Iodine deficiency, iodine requirements, and iodine supplementation across the lifespan are described separately. (See "Iodine deficiency disorders".)

Omega-3 fatty acids — Dietary requirements for omega-3 fatty acids in infants, children, and adolescents have not been established [146]. However, indirect evidence suggests that they have some health benefits.

Potential deficits for a vegetarian diet – Vegetarian diets generally are rich in omega-6 fatty acids but may be marginal in omega-3 fatty acids unless the diet includes fish, eggs, or generous amounts of algae. Omega-3 fatty acids, which include docosahexaenoic acid (DHA) or eicosapentaenoic acid (EPA), or their precursor alpha-linolenic acid (ALA), are important for cardiovascular health and eye and brain development [49,147,148]. Vegetarians, particularly vegans, have lower blood levels of EPA and DHA compared with nonvegetarians [3,149].

Nutritional counseling – We suggest that vegetarian children include either oily fish or other good sources of omega-3 fatty acids in their diet, such as flaxseed, walnuts, canola oil, and soy. Infant formulas, soy milk, and breakfast bars that are fortified with DHA also are available [3]. For patients who do not consume fish regularly, consider counseling on an algae-based omega-3-supplement [150]. The evidence for benefit of omega-3 fatty acids supplements is based on limited evidence for cardiovascular risk protection in adults, with a low risk of harm [151]. (See "Fish oil: Physiologic effects and administration".)

FIBER — 

Recommended fiber intake is 14 g/1000 kcal energy intake, which translates to approximately 14 g/day for ages 2 to 3 years, 17 to 20 g/day for 4 to 8 years, 22 to 25 g/day for 9 to 13 years, and 25 to 31 g/day for 14 to 18 years [1]. Because these targets are difficult to achieve, somewhat lower targets may be more realistic for children whose diets are not plant based [152].

The optimum level of dietary fiber for infants and children younger than two years of age is not known. For this age group, studies of weaning diets with increased fiber suggested that 5 g/day is beneficial and found no negative effect on the absorption of energy, zinc, and calcium or iron bioavailability [153,154]. However, other studies have shown that growth is poor among infants and toddlers weaned onto very high-fiber, low-calorie diets that often are deficient in vitamins and minerals [155,156]. (See "Dietary recommendations for toddlers and preschool and school-age children", section on 'Fiber'.)

Potential issues for a vegetarian diet – Vegetarians tend to have a relatively high fiber intake compared with omnivores. In populations following a vegan diet, the average fiber intake is in a healthy range. In a study of 51 adults, average fiber intake among omnivores was 23 g, compared with 37 g among vegetarians and 47 g among vegans [157].

The consumption of a high-fiber diet in childhood promotes regular bowel movements and possibly reduces the risk of developing certain diseases in adulthood. However, during childhood, a diet with very high fiber content can compromise dietary energy intake and reduce the bioavailability of minerals such as iron, calcium, and zinc [3,47,78,158]. A small loss of energy, primarily as fat, and protein may occur with a high intake of dietary fiber. Daily fecal energy loss is estimated to increase by 1 percent for every 6 g increase in dietary fiber. This loss is unlikely to be significant in children who consume adequate energy.

The amount of dietary fiber recommended above, or even fiber intake that exceeds this recommendation, does not have an adverse effect on mineral bioavailability, provided that the dietary mineral intake is adequate. However, mineral bioavailability may be problematic in children who follow strict macrobiotic or vegan diets with low intake of calcium, iron, and zinc.

Nutritional counseling – Most vegetarian children have a healthy intake of fiber. Because a very high-fiber diet can compromise energy intake and mineral absorption, vegetarian children should be monitored to ensure that they have adequate growth and adequate intake of minerals such as iron, calcium, and zinc.

Dietary fiber goals can be met best by eating a variety of fiber-rich fruits, vegetables, cereals, and grain products while consuming adequate energy intake for growth and development [158]. Fiber supplements are not recommended to meet dietary fiber goals.

SOCIETY GUIDELINE LINKS — 

Links to society and government-sponsored guidelines from selected countries and regions around the world are provided separately. (See "Society guideline links: Healthy diet in children and adolescents".)

INFORMATION FOR PATIENTS — 

UpToDate offers two types of patient education materials, "The Basics" and "Beyond the Basics." The Basics patient education pieces are written in plain language, at the 5th to 6th grade reading level, and they answer the four or five key questions a patient might have about a given condition. These articles are best for patients who want a general overview and who prefer short, easy-to-read materials. Beyond the Basics patient education pieces are longer, more sophisticated, and more detailed. These articles are written at the 10th to 12th grade reading level and are best for patients who want in-depth information and are comfortable with some medical jargon.

Here are the patient education articles that are relevant to this topic. We encourage you to print or e-mail these topics to your patients. (You can also locate patient education articles on a variety of subjects by searching on "patient info" and the keyword(s) of interest.)

Basics topic (see "Patient education: Vegetarian or vegan diet (The Basics)")

SUMMARY AND RECOMMENDATIONS

Overview – A well-planned vegetarian diet offers health benefits for children. Vegan diets can also offer benefits but require additional planning to ensure that all nutritional needs are met. In general, a lactovegetarian diet has greater health benefits and fewer health risks than a vegan diet (table 1). (See 'Benefits for cardiovascular and metabolic health' above.)

Counseling

Infants and young children – Breastfeeding mothers who are vegetarian or vegan should be counseled about B12 supplementation. The vitamin B12 content of breast milk reflects maternal vitamin B12 levels, and severe deficiency can impair neurologic development in the infant. When introducing solids and weaning an infant off of formula or breast milk, food choices should be high in fat and iron for the vegetarian child as vegetarian foods can have higher fiber and lower caloric density. Additional nutrients to counsel families about during this period include vitamin D, iron, zinc, folate, and calcium (table 2). Young children can be offered soy milk in the place of dairy, but other types of plant-based beverages are often lower in calories and protein and are not appropriate for periods of rapid growth. (See 'Infancy and weaning' above and 'Plant-based beverages' above.)

Older children and adolescents – Many adolescents are turning to vegetarian diets for ethical or environmental concerns. Some older children or adolescents may choose a vegetarian diet as a means of weight control, and clinicians should be alert for evidence of inappropriate dietary restriction and other disordered eating behaviors. An adolescent whose body mass index is less than the 15th percentile and/or who has features suggestive of an eating disorder (including disrupted menses or body image disturbances) is a candidate for referral for more intensive medical and psychological care. (See 'Older children and adolescents' above.)

Specific nutrients – Nutritional counseling is important to ensure that the diet provides adequate nutrients, especially energy, protein, iron, calcium, vitamin D, and vitamin B12 (cyanocobalamin). If the diet cannot be adjusted to provide recommended amounts of each of these nutrients, supplements should be added to ensure adequate intake.

Iron – Children who do not eat meat or fish are at risk of iron deficiency, especially during periods of rapid growth and in menstruating girls. To enhance the absorption of nonheme iron (from plants), a source of ascorbic acid should be provided at each meal. Teas containing tannin should be limited. Iron supplements may be necessary for some individuals. (See 'Iron' above.)

Calcium and vitamin D – Children who consume little or no dairy products are at risk for calcium and vitamin D deficiencies. Ready-to-eat cereals and alternative plant-based milks (such as soy milk) are good sources of these nutrients, provided that they are adequately fortified. However, the recommended intake for these nutrients is high and requires several servings daily of milk, fortified alternative milk, or fortified cereal. Many children require supplementation to meet their requirements. (See 'Calcium' above and 'Vitamin D' above.)

Vitamin B12 – Children who follow a vegan diet are at risk for vitamin B12 (cobalamin) deficiency because animal products (meat, fish, and dairy products) provide the only dietary source of vitamin B12 (cobalamin) for humans. Individuals following a vegan diet should consume a regular and reliable source of the vitamin, either in fortified foods (soy milk or cereals) or an oral vitamin B12 supplement. (See 'Vitamin B12' above.)

ACKNOWLEDGMENT — 

The UpToDate editorial staff acknowledges Kathleen J Motil, MD, PhD, and Debby Demory-Luce, PhD, RD, LD, who contributed to earlier versions of this topic review.

  1. United States Department of Agriculture and United States Department of Health and Human Services. Dietary Guidelines for Americans, 2020-2025. 9th ed. 2020. Available at: https://www.dietaryguidelines.gov/ (Accessed on October 23, 2024).
  2. Willett W, Rockström J, Loken B, et al. Food in the Anthropocene: the EAT-Lancet Commission on healthy diets from sustainable food systems. Lancet 2019; 393:447.
  3. Melina V, Craig W, Levin S. Position of the Academy of Nutrition and Dietetics: Vegetarian Diets. J Acad Nutr Diet 2016; 116:1970.
  4. Appleby PN, Key TJ. The long-term health of vegetarians and vegans. Proc Nutr Soc 2016; 75:287.
  5. Crowe FL, Appleby PN, Travis RC, Key TJ. Risk of hospitalization or death from ischemic heart disease among British vegetarians and nonvegetarians: results from the EPIC-Oxford cohort study. Am J Clin Nutr 2013; 97:597.
  6. Orlich MJ, Singh PN, Sabaté J, et al. Vegetarian dietary patterns and mortality in Adventist Health Study 2. JAMA Intern Med 2013; 173:1230.
  7. Mullee A, Vermeire L, Vanaelst B, et al. Vegetarianism and meat consumption: A comparison of attitudes and beliefs between vegetarian, semi-vegetarian, and omnivorous subjects in Belgium. Appetite 2017; 114:299.
  8. Schürmann S, Kersting M, Alexy U. Vegetarian diets in children: a systematic review. Eur J Nutr 2017; 56:1797.
  9. Karlsen MC, Rogers G, Miki A, et al. Theoretical Food and Nutrient Composition of Whole-Food Plant-Based and Vegan Diets Compared to Current Dietary Recommendations. Nutrients 2019; 11.
  10. Alcorta A, Porta A, Tárrega A, et al. Foods for Plant-Based Diets: Challenges and Innovations. Foods 2021; 10.
  11. Stahler C, Manels R. Vegetarian Resource Group. How many youth in the U.S. are vegan? How many teens eat vegetarian when eating out? 2021. Available at: https://www.vrg.org/nutshell/Yougov2021youthteenwriteup.pdf (Accessed on March 24, 2021).
  12. Stahler C. Vegetarian Resource Group. How many adults in the U.S. are vegan? How many adults eat vegetarian when eating out? 2020. Available at: https://www.vrg.org/journal/vj2020issue4/2020_issue4_poll_results.php (Accessed on March 24, 2021).
  13. Vegetarian Society, UK. Trends in vegetarianism among adults and young people. Vegetarian Society, Altrincham, United Kingdom 1991.
  14. Sawe BE. World Atlas. Countries With The Highest Rates Of Vegetarianism. 2016. Available at: http://www.worldatlas.com/articles/countries-with-the-highest-rates-of-vegetarianism.html (Accessed on July 18, 2017).
  15. VEBU Vegetarierbund Deutschland. Anzahl der veganer und vegetarier in Deutschland, 2016. https://vebu.de/veggie-fakten/entwicklung-in-zahlen/anzahl-veganer-und-vegetarier-in-deutschland/ (Accessed on July 18, 2017).
  16. Grotto D, Zied E. The Standard American Diet and its relationship to the health status of Americans. Nutr Clin Pract 2010; 25:603.
  17. United States Department of Agriculture. MyPlate. Available at: https://www.myplate.gov/ (Accessed on October 21, 2024).
  18. Craig WJ, Mangels AR, American Dietetic Association. Position of the American Dietetic Association: vegetarian diets. J Am Diet Assoc 2009; 109:1266.
  19. American Academy of Pediatrics. Nutritional aspects of vegetarian diets. In: Pediatric Nutrition, 8th Ed, Kleinman RE, Greer, FR (Eds), American Academy of Pediatrics, Itasca, IL 2020. p.293.
  20. Weder S, Keller M, Fischer M, et al. 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.
  21. Alexy U, Fischer M, Weder S, et al. Food group intake of children and adolescents (6-18 years) on a vegetarian, vegan or omnivore diet: results of the VeChi Youth Study. Br J Nutr 2022; 128:851.
  22. Weder S, Hoffmann M, Becker K, et al. Energy, Macronutrient Intake, and Anthropometrics of Vegetarian, Vegan, and Omnivorous Children (1⁻3 Years) in Germany (VeChi Diet Study). Nutrients 2019; 11.
  23. Perry CL, McGuire MT, 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.
  24. Hebbelinck M, Clarys P, De Malsche A. Growth, development, and physical fitness of Flemish vegetarian children, adolescents, and young adults. Am J Clin Nutr 1999; 70:579S.
  25. Nathan I, Hackett AF, Kirby S. A longitudinal study of the growth of matched pairs of vegetarian and omnivorous children, aged 7-11 years, in the north-west of England. Eur J Clin Nutr 1997; 51:20.
  26. Elliott LJ, Keown-Stoneman CDG, Birken CS, et al. Vegetarian Diet, Growth, and Nutrition in Early Childhood: A Longitudinal Cohort Study. Pediatrics 2022; 149.
  27. Sabaté J, Lindsted KD, Harris RD, Sanchez A. Attained height of lacto-ovo vegetarian children and adolescents. Eur J Clin Nutr 1991; 45:51.
  28. Sanders TA. Growth and development of British vegan children. Am J Clin Nutr 1988; 48:822.
  29. O'Connell JM, Dibley MJ, Sierra J, et al. Growth of vegetarian children: The Farm Study. Pediatrics 1989; 84:475.
  30. Van Dusseldorp M, Arts IC, Bergsma JS, et al. Catch-up growth in children fed a macrobiotic diet in early childhood. J Nutr 1996; 126:2977.
  31. Desmond MA, Fewtrell MS, Wells JCK. Plant-Based Diets in Children: Secular Trends, Health Outcomes, and a Roadmap for Urgent Practice Recommendations and Research-A Systematic Review. Nutrients 2024; 16.
  32. Desmond MA, Sobiecki JG, Jaworski M, et al. Growth, body composition, and cardiovascular and nutritional risk of 5- to 10-y-old children consuming vegetarian, vegan, or omnivore diets. Am J Clin Nutr 2021; 113:1565.
  33. Dominique Ashen M. Vegetarian diets in cardiovascular prevention. Curr Treat Options Cardiovasc Med 2013; 15:735.
  34. Sabaté J, Wien M. Vegetarian diets and childhood obesity prevention. Am J Clin Nutr 2010; 91:1525S.
  35. Sabaté J, Wien M. A perspective on vegetarian dietary patterns and risk of metabolic syndrome. Br J Nutr 2015; 113 Suppl 2:S136.
  36. Appel LJ. The Effects of Dietary Factors on Blood Pressure. Cardiol Clin 2017; 35:197.
  37. Yokoyama Y, Barnard ND, Levin SM, Watanabe M. Vegetarian diets and glycemic control in diabetes: a systematic review and meta-analysis. Cardiovasc Diagn Ther 2014; 4:373.
  38. Dinu M, Abbate R, Gensini GF, et al. Vegetarian, vegan diets and multiple health outcomes: A systematic review with meta-analysis of observational studies. Crit Rev Food Sci Nutr 2017; 57:3640.
  39. Barnard ND, Levin SM, Yokoyama Y. A systematic review and meta-analysis of changes in body weight in clinical trials of vegetarian diets. J Acad Nutr Diet 2015; 115:954.
  40. Qian F, Liu G, Hu FB, et al. Association Between Plant-Based Dietary Patterns and Risk of Type 2 Diabetes: A Systematic Review and Meta-analysis. JAMA Intern Med 2019; 179:1335.
  41. Rizzo NS, Sabaté J, Jaceldo-Siegl K, Fraser GE. Vegetarian dietary patterns are associated with a lower risk of metabolic syndrome: the adventist health study 2. Diabetes Care 2011; 34:1225.
  42. Wang F, Zheng J, Yang B, et al. Effects of Vegetarian Diets on Blood Lipids: A Systematic Review and Meta-Analysis of Randomized Controlled Trials. J Am Heart Assoc 2015; 4:e002408.
  43. Tonstad S, Stewart K, Oda K, et al. Vegetarian diets and incidence of diabetes in the Adventist Health Study-2. Nutr Metab Cardiovasc Dis 2013; 23:292.
  44. Nebl J, Schuchardt JP, Wasserfurth P, et al. Characterization, dietary habits and nutritional intake of omnivorous, lacto-ovo vegetarian and vegan runners - a pilot study. BMC Nutr 2019; 5:51.
  45. Mihrshahi S, Ding D, Gale J, et al. Vegetarian diet and all-cause mortality: Evidence from a large population-based Australian cohort - the 45 and Up Study. Prev Med 2017; 97:1.
  46. Tomova A, Bukovsky I, Rembert E, et al. The Effects of Vegetarian and Vegan Diets on Gut Microbiota. Front Nutr 2019; 6:47.
  47. Gibson RS, Heath AL, Szymlek-Gay EA. Is iron and zinc nutrition a concern for vegetarian infants and young children in industrialized countries? Am J Clin Nutr 2014; 100 Suppl 1:459S.
  48. Tucker KL. Vegetarian diets and bone status. Am J Clin Nutr 2014; 100 Suppl 1:329S.
  49. Saunders AV, Davis BC, Garg ML. Omega-3 polyunsaturated fatty acids and vegetarian diets. Med J Aust 2013; 199:S22.
  50. Craig WJ, Mangels AR, Fresán U, et al. The Safe and Effective Use of Plant-Based Diets with Guidelines for Health Professionals. Nutrients 2021; 13.
  51. Mikkilä V, Räsänen L, Raitakari OT, et al. Major dietary patterns and cardiovascular risk factors from childhood to adulthood. The Cardiovascular Risk in Young Finns Study. Br J Nutr 2007; 98:218.
  52. Banfield EC, Liu Y, Davis JS, et al. Poor Adherence to US Dietary Guidelines for Children and Adolescents in the National Health and Nutrition Examination Survey Population. J Acad Nutr Diet 2016; 116:21.
  53. Funtikova AN, Navarro E, Bawaked RA, et al. Impact of diet on cardiometabolic health in children and adolescents. Nutr J 2015; 14:118.
  54. Appel LJ, Lichtenstein AH, Callahan EA, et al. Reducing Sodium Intake in Children: A Public Health Investment. J Clin Hypertens (Greenwich) 2015; 17:657.
  55. Phillips F. Vegetarian nutrition. Nutr Bull 2005; 30:132.
  56. 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.
  57. Kiely ME. Risks and benefits of vegan and vegetarian diets in children. Proc Nutr Soc 2021; 80:159.
  58. Weaver CM. Should dairy be recommended as part of a healthy vegetarian diet? Point. Am J Clin Nutr 2009; 89:1634S.
  59. Weaver CM. How sound is the science behind the dietary recommendations for dairy? Am J Clin Nutr 2014; 99:1217S.
  60. United States Department of Agriculture, MyPlate. Available at: https://www.myplate.gov/ (Accessed on January 20, 2021).
  61. Baroni L, Goggi S, Battino M. Planning Well-Balanced Vegetarian Diets in Infants, Children, and Adolescents: The VegPlate Junior. J Acad Nutr Diet 2019; 119:1067.
  62. American College of Lifestyle Medicine, Lifestyle Medicine Patient Handouts. Available at: https://lifestylemedicine.org/project/patient-resources/ (Accessed on October 22, 2024).
  63. Mütze U, Gleich F, Haas D, et al. Vitamin B12 Deficiency Newborn Screening. Pediatrics 2024; 154.
  64. Young L, Embleton ND, McGuire W. Nutrient-enriched formula versus standard formula for preterm infants following hospital discharge. Cochrane Database Syst Rev 2016; 12:CD004696.
  65. Kulkarni PB, Dorand RD, Bridger WM, et al. Rickets in premature infants fed different formulas. South Med J 1984; 77:13.
  66. US Food and Drug Administration: FDA Advises Parents and Caregivers to Not Make or Feed Homemade Infant Formula to Infants (February 2021). Available at: https://www.fda.gov/food/alerts-advisories-safety-information/fda-advises-parents-and-caregivers-not-make-or-feed-homemade-infant-formula-infants (Accessed on August 20, 2021).
  67. McLean CP, Kulkarni J, Sharp G. Disordered eating and the meat-avoidance spectrum: a systematic review and clinical implications. Eat Weight Disord 2022; 27:2347.
  68. Sergentanis TN, Chelmi ME, Liampas A, et al. Vegetarian Diets and Eating Disorders in Adolescents and Young Adults: A Systematic Review. Children (Basel) 2020; 8.
  69. Timko CA, Hormes JM, Chubski J. Will the real vegetarian please stand up? An investigation of dietary restraint and eating disorder symptoms in vegetarians versus non-vegetarians. Appetite 2012; 58:982.
  70. Healthy Eating Research. Consensus Statement: Healthy Beverage Consumption in Early Childhood, Recommendations from Key National Health and Nutrition Organizations. 2019. Available at: https://healthyeatingresearch.org/wp-content/uploads/2019/09/HER-HealthyBeverage-ConsensusStatement.pdf (Accessed on August 27, 2021).
  71. Verduci E, D'Elios S, Cerrato L, et al. Cow's Milk Substitutes for Children: Nutritional Aspects of Milk from Different Mammalian Species, Special Formula and Plant-Based Beverages. Nutrients 2019; 11.
  72. Bodnar LM, Jimenez EY, Baker SS. Plant-Based Beverages in the Diets of Infants and Young Children. JAMA Pediatr 2021; 175:555.
  73. Willett WC, Ludwig DS. Milk and Health. N Engl J Med 2020; 382:644.
  74. Sanders TA, Manning J. The growth and development of vegan children. J Hum Nutr Diet 1992; 5:11.
  75. Larsson CL, Johansson GK. Young Swedish vegans have different sources of nutrients than young omnivores. J Am Diet Assoc 2005; 105:1438.
  76. Renda M, Fischer P. Vegetarian diets in children and adolescents. Pediatr Rev 2009; 30:e1.
  77. Institute of Medicine, Food and Nutrition Board. Dietary reference intakes for energy, carbohydrate, fiber, fat, fatty acids, cholesterol, protein, and amino acids. National Academies Press, Washington DC, 2005. Available at: http://www.nap.edu/catalog.php?record_id=10490 (Accessed on February 14, 2019).
  78. Messina V, Mangels AR. Considerations in planning vegan diets: children. J Am Diet Assoc 2001; 101:661.
  79. Johnston PK, Sabate J. Nutritional implications of vegetarian diets. In: Modern Nutrition in Health and Disease, 10th ed, Shils ME, Shike M, Ross AC, et al (Eds), Lippincott Williams & Wilkins, 2006. p.1641.
  80. Jacobs C, Dwyer JT. Vegetarian children: appropriate and inappropriate diets. Am J Clin Nutr 1988; 48:811.
  81. Hughes GJ, Ryan DJ, Mukherjea R, Schasteen CS. Protein digestibility-corrected amino acid scores (PDCAAS) for soy protein isolates and concentrate: criteria for evaluation. J Agric Food Chem 2011; 59:12707.
  82. Rizzo G, Baroni L. Soy, Soy Foods and Their Role in Vegetarian Diets. Nutrients 2018; 10.
  83. Gardner CD, Hartle JC, Garrett RD, et al. Maximizing the intersection of human health and the health of the environment with regard to the amount and type of protein produced and consumed in the United States. Nutr Rev 2019; 77:197.
  84. Young VR, Pellett PL. Plant proteins in relation to human protein and amino acid nutrition. Am J Clin Nutr 1994; 59:1203S.
  85. Thane CW, Bates CJ, Prentice A. Risk factors for low iron intake and poor iron status in a national sample of British young people aged 4-18 years. Public Health Nutr 2003; 6:485.
  86. Domellöf M, Braegger C, Campoy C, et al. Iron requirements of infants and toddlers. J Pediatr Gastroenterol Nutr 2014; 58:119.
  87. Clénin GE. The treatment of iron deficiency without anaemia (in otherwise healthy persons). Swiss Med Wkly 2017; 147:w14434.
  88. Institute of Medicine, Food and Nutrition Board. Dietary reference intakes for vitamin A, vitamin K, arsenic, boron, chromium, copper, iodine, iron, manganese, molybdenum, nickel, silicon, vanadium, and zinc. Available at: http://www.nap.edu/catalog.php?record_id=10026 (Accessed on December 02, 2010).
  89. Pawlak R, Bell K. Iron Status of Vegetarian Children: A Review of Literature. Ann Nutr Metab 2017; 70:88.
  90. Craig WJ. Iron status of vegetarians. Am J Clin Nutr 1994; 59:1233S.
  91. 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.
  92. Ambroszkiewicz J, Klemarczyk W, Mazur J, et al. 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.
  93. Murphy SP, Allen LH. Nutritional importance of animal source foods. J Nutr 2003; 133:3932S.
  94. Haider LM, Schwingshackl L, Hoffmann G, Ekmekcioglu C. The effect of vegetarian diets on iron status in adults: A systematic review and meta-analysis. Crit Rev Food Sci Nutr 2018; 58:1359.
  95. Anderson GJ, Frazer DM. Current understanding of iron homeostasis. Am J Clin Nutr 2017; 106:1559S.
  96. Hallberg L, Hulthén L. Prediction of dietary iron absorption: an algorithm for calculating absorption and bioavailability of dietary iron. Am J Clin Nutr 2000; 71:1147.
  97. Hunt JR. Bioavailability of iron, zinc, and other trace minerals from vegetarian diets. Am J Clin Nutr 2003; 78:633S.
  98. Chiplonkar SA, Tupe R. Development of a diet quality index with special reference to micronutrient adequacy for adolescent girls consuming a lacto-vegetarian diet. J Am Diet Assoc 2010; 110:926.
  99. Hallberg L, Brune M, Rossander L. Effect of ascorbic acid on iron absorption from different types of meals. Studies with ascorbic-acid-rich foods and synthetic ascorbic acid given in different amounts with different meals. Hum Nutr Appl Nutr 1986; 40:97.
  100. Siegenberg D, Baynes RD, Bothwell TH, et al. Ascorbic acid prevents the dose-dependent inhibitory effects of polyphenols and phytates on nonheme-iron absorption. Am J Clin Nutr 1991; 53:537.
  101. Sandström B. Micronutrient interactions: effects on absorption and bioavailability. Br J Nutr 2001; 85 Suppl 2:S181.
  102. Matkovic V, Fontana D, Tominac C, et al. Factors that influence peak bone mass formation: a study of calcium balance and the inheritance of bone mass in adolescent females. Am J Clin Nutr 1990; 52:878.
  103. Weaver CM, Proulx WR, Heaney R. Choices for achieving adequate dietary calcium with a vegetarian diet. Am J Clin Nutr 1999; 70:543S.
  104. Greer FR, Krebs NF, American Academy of Pediatrics Committee on Nutrition. Optimizing bone health and calcium intakes of infants, children, and adolescents. Pediatrics 2006; 117:578.
  105. Donovan UM, Gibson RS. Dietary intakes of adolescent females consuming vegetarian, semi-vegetarian, and omnivorous diets. J Adolesc Health 1996; 18:292.
  106. Mangels AR. Bone nutrients for vegetarians. Am J Clin Nutr 2014; 100 Suppl 1:469S.
  107. Movassagh EZ, Vatanparast H. Current Evidence on the Association of Dietary Patterns and Bone Health: A Scoping Review. Adv Nutr 2017; 8:1.
  108. National Institutes of Health. Calcium: Fact Sheet for Health Professionals. 2018. Available at: https://ods.od.nih.gov/factsheets/Calcium-HealthProfessional/ (Accessed on May 09, 2019).
  109. Heaney RP. Protein intake and the calcium economy. J Am Diet Assoc 1993; 93:1259.
  110. Breslau NA, Brinkley L, Hill KD, Pak CY. Relationship of animal protein-rich diet to kidney stone formation and calcium metabolism. J Clin Endocrinol Metab 1988; 66:140.
  111. Messina V, Melina V, Mangels AR. A new food guide for North American vegetarians. J Am Diet Assoc 2003; 103:771.
  112. Haddad EH. Meeting the RDAs with a vegetarian diet. Top Clin Nutr 1995; 10:7.
  113. Heaney RP, Dowell MS, Rafferty K, Bierman J. Bioavailability of the calcium in fortified soy imitation milk, with some observations on method. Am J Clin Nutr 2000; 71:1166.
  114. Haddad EH. Development of a vegetarian food guide. Am J Clin Nutr 1994; 59:1248S.
  115. Bonjour JP, Carrie AL, Ferrari S, et al. Calcium-enriched foods and bone mass growth in prepubertal girls: a randomized, double-blind, placebo-controlled trial. J Clin Invest 1997; 99:1287.
  116. National Institutes of Health. Vitamin D: Fact Sheet for Health Professionals. 2008. Available at: http://ods.od.nih.gov/factsheets/vitamind.asp (Accessed on October 10, 2015).
  117. Ross AC, Taylor Cl, Yaktine AL, Del Valle HB. Institute of Medicine/National Academies Press/Food and Nutrition Board. Dietary Reference Intakes of Calcium and Vitamin D. 2010. Available at: http://books.nap.edu/openbook.php?record_id=13050 (Accessed on December 02, 2010).
  118. Elsori DH, Hammoud MS. Vitamin D deficiency in mothers, neonates and children. J Steroid Biochem Mol Biol 2018; 175:195.
  119. Hollis BW. Circulating 25-hydroxyvitamin D levels indicative of vitamin D sufficiency: implications for establishing a new effective dietary intake recommendation for vitamin D. J Nutr 2005; 135:317.
  120. Venti CA, Johnston CS. Modified food guide pyramid for lactovegetarians and vegans. J Nutr 2002; 132:1050.
  121. Bergstrom WH. When you see rickets, consider calcium deficiency. J Pediatr 1998; 133:722.
  122. Hellebostad M, Markestad T, Seeger Halvorsen K. Vitamin D deficiency rickets and vitamin B12 deficiency in vegetarian children. Acta Paediatr Scand 1985; 74:191.
  123. Parsons TJ, van Dusseldorp M, van der Vliet M, et al. Reduced bone mass in Dutch adolescents fed a macrobiotic diet in early life. J Bone Miner Res 1997; 12:1486.
  124. Elorinne AL, Alfthan G, Erlund I, et al. Food and Nutrient Intake and Nutritional Status of Finnish Vegans and Non-Vegetarians. PLoS One 2016; 11:e0148235.
  125. Laskowska-Klita T, Chełchowska M, Ambroszkiewicz J, et al. The effect of vegetarian diet on selected essential nutrients in children. Med Wieku Rozwoj 2011; 15:318.
  126. Baroni L, Goggi S, Battaglino R, et al. Vegan Nutrition for Mothers and Children: Practical Tools for Healthcare Providers. Nutrients 2018; 11.
  127. Demay MB, Pittas AG, Bikle DD, et al. Vitamin D for the Prevention of Disease: An Endocrine Society Clinical Practice Guideline. J Clin Endocrinol Metab 2024; 109:1907.
  128. Herrmann W, Geisel J. Vegetarian lifestyle and monitoring of vitamin B-12 status. Clin Chim Acta 2002; 326:47.
  129. Institute of Medicine, Food and Nutrition Board. Dietary reference intakes for thiamin, riboflavin, niacin, vitamin B6, folate, vitamin B12, pantothenic acid, biotin, and choline, National Academy Press, Washington DC, 1998. Available at: http://www.nap.edu/catalog.php?record_id=6015 (Accessed on February 14, 2019).
  130. Irevall T, Axelsson I, Naumburg E. B12 deficiency is common in infants and is accompanied by serious neurological symptoms. Acta Paediatr 2017; 106:101.
  131. Ljungblad UW, Astrup H, Mørkrid L, et al. Breastfed Infants With Spells, Tremor, or Irritability: Rule Out Vitamin B12 Deficiency. Pediatr Neurol 2022; 131:4.
  132. Allen LH. Causes of vitamin B12 and folate deficiency. Food Nutr Bull 2008; 29:S20.
  133. Pawlak R, Lester SE, Babatunde T. The prevalence of cobalamin deficiency among vegetarians assessed by serum vitamin B12: a review of literature. Eur J Clin Nutr 2014; 68:541.
  134. Haddad EH, Berk LS, Kettering JD, et al. Dietary intake and biochemical, hematologic, and immune status of vegans compared with nonvegetarians. Am J Clin Nutr 1999; 70:586S.
  135. Dong A, Scott SC. Serum vitamin B12 and blood cell values in vegetarians. Ann Nutr Metab 1982; 26:209.
  136. Haddad EH, Tanzman JS. What do vegetarians in the United States eat? Am J Clin Nutr 2003; 78:626S.
  137. Burke KI. The use of soy foods in a vegetarian diet. Top Clin Nutr 1995; 10:37.
  138. Dagnelie PC, van Staveren WA, van den Berg H. Vitamin B-12 from algae appears not to be bioavailable. Am J Clin Nutr 1991; 53:695.
  139. Anderson GH, Zlotkin SH. Developing and implementing food-based dietary guidance for fat in the diets of children. Am J Clin Nutr 2000; 72:1404S.
  140. Hunt JR. Moving toward a plant-based diet: are iron and zinc at risk? Nutr Rev 2002; 60:127.
  141. Foster M, Samman S. Vegetarian diets across the lifecycle: impact on zinc intake and status. Adv Food Nutr Res 2015; 74:93.
  142. Harland BF, Morris ER. Phytate: a good or a bad food component? Nutr Res 1995; 15:733.
  143. Gibson RS, Hotz C. Dietary diversification/modification strategies to enhance micronutrient content and bioavailability of diets in developing countries. Br J Nutr 2001; 85 Suppl 2:S159.
  144. Zimmermann MB. Iodine deficiency in industrialized countries. Clin Endocrinol (Oxf) 2011; 75:287.
  145. Eveleigh ER, Coneyworth L, Welham SJM. Systematic review and meta-analysis of iodine nutrition in modern vegan and vegetarian diets. Br J Nutr 2023; 130:1580.
  146. Koletzko B, Beblo S, Demmelmair H, Hanebutt FL. Omega-3 LC-PUFA supply and neurological outcomes in children with phenylketonuria (PKU). J Pediatr Gastroenterol Nutr 2009; 48 Suppl 1:S2.
  147. Stonehouse W. Does consumption of LC omega-3 PUFA enhance cognitive performance in healthy school-aged children and throughout adulthood? Evidence from clinical trials. Nutrients 2014; 6:2730.
  148. Koletzko B, Lien E, Agostoni C, et al. The roles of long-chain polyunsaturated fatty acids in pregnancy, lactation and infancy: review of current knowledge and consensus recommendations. J Perinat Med 2008; 36:5.
  149. Rosell MS, Lloyd-Wright Z, Appleby PN, et al. Long-chain n-3 polyunsaturated fatty acids in plasma in British meat-eating, vegetarian, and vegan men. Am J Clin Nutr 2005; 82:327.
  150. Lane KE, Wilson M, Hellon TG, Davies IG. Bioavailability and conversion of plant based sources of omega-3 fatty acids - a scoping review to update supplementation options for vegetarians and vegans. Crit Rev Food Sci Nutr 2022; 62:4982.
  151. Hu Y, Hu FB, Manson JE. Marine Omega-3 Supplementation and Cardiovascular Disease: An Updated Meta-Analysis of 13 Randomized Controlled Trials Involving 127 477 Participants. J Am Heart Assoc 2019; 8:e013543.
  152. Williams CL, Bollella M, Wynder EL. A new recommendation for dietary fiber in childhood. Pediatrics 1995; 96:985.
  153. Agostoni C, Riva E, Giovannini M. Dietary fiber in weaning foods of young children. Pediatrics 1995; 96:1002.
  154. Davidsson L, Mackenzie J, Kastenmayer P, et al. Dietary fiber in weaning cereals: a study of the effect on stool characteristics and absorption of energy, nitrogen, and minerals in healthy infants. J Pediatr Gastroenterol Nutr 1996; 22:167.
  155. Dagnelie PC, van Dusseldorp M, van Staveren WA, Hautvast JG. Effects of macrobiotic diets on linear growth in infants and children until 10 years of age. Eur J Clin Nutr 1994; 48 Suppl 1:S103.
  156. Dagnelie PC, van Staveren WA. Macrobiotic nutrition and child health: results of a population-based, mixed-longitudinal cohort study in The Netherlands. Am J Clin Nutr 1994; 59:1187S.
  157. Davies GJ, Crowder M, Dickerson JW. Dietary fibre intakes of individuals with different eating patterns. Hum Nutr Appl Nutr 1985; 39:139.
  158. Williams CL, Bollella M. Is a high-fiber diet safe for children? Pediatrics 1995; 96:1014.
Topic 5353 Version 38.0

References