Abstract
Background
Transitioning to more sustainable eating habits with less animal-based protein affects not only protein intake but also micronutrient consumption. Given that older adults are already vulnerable to insufficient micronutrient amounts, such dietary changes could further heighten their risk of deficiencies.
Objectives
We simulated how switching toward a more sustainable eating pattern influenced micronutrient intake in older adults.
Methods
Data from the Dutch National Food Consumption Survey 2019–2021 (community-dwelling older adults, n = 607, food intake based on 2-d food diary) were used to simulate 2 flexitarian (40% and 80% meat/fish replacement), pescetarian, vegetarian, and vegan diets. and compared with the estimated average requirement (EAR) or adequate intake based on the Dutch dietary reference values. Nutrient intake was deemed low if >10% of participants fell below the EAR or if the median was below the adequate intake.
Results
In the reference diet, actual micronutrient intake among Dutch older adults was generally adequate, except for riboflavin, vitamin B6, folate, and calcium. Vitamin A and selenium were low in females only. In the simulated flexitarian 40% scenario, no additional nutrients were considered low. In the flexitarian 80%, pescetarian, and vegetarian scenarios, niacin in all, and vitamin A and thiamin in males became low. In the vegan scenario, nearly all micronutrient intakes were low.
Conclusions
Reducing or eliminating animal-based protein sources from the diets of older adults elevates their risk of micronutrient deficiencies.
Keywords: sustainability, micronutrients, simulation study, protein transition, nutrition adequacy
Introduction
A Western eating pattern with relatively high consumption of animal-based protein places a large burden on our planet [1]. Therefore, shifting toward a more sustainable eating pattern (in terms of carbon dioxide emission, land use, and water impact [2]) with fewer animal-based products is advised by institutes such as the WHO [3]. Such a pattern consists of more fruits, vegetables, pulses, whole grains, and nuts, with moderate amounts of fish, eggs, poultry, and dairy, while limiting red meat and cheese [4,5].
Although various studies on protein transition focused on protein adequacy [6], other nutritional aspects should also be considered. Animal-based products are not only rich sources of protein but also provide essential vitamins and minerals [7]. A deficiency in vitamin B12, e.g., is a well-documented risk when adopting a vegan diet [8]. Additionally, the Dutch Health Council emphasizes the importance of monitoring vitamin A, vitamin B2, vitamin B12, as well as the micronutrients calcium, iron, and iodine when transitioning to a more plant-based eating pattern [9].
Micronutrients play a crucial role in the aging process as they are necessary for wound healing, maintaining bone health, synthesis of cells, and muscle functioning [10]. In general, older adults already have insufficient intakes of several micronutrients, such as thiamin, riboflavin, calcium, selenium, and magnesium, largely because of low overall food intake [11]. Special attention should thus be paid to guaranteeing sufficient micronutrient intake when adopting a more sustainable diet to support these essential processes.
A few studies have modeled the impact of transitioning to a more sustainable diet on micronutrient intake [12]. These studies were mainly based on replacing one specific food group (for instance, red meat) or focused on increasing certain products, such as legumes, instead of simulating the most common more sustainable eating patterns, such as flexitarian, vegetarian, pescetarian, or vegan. Even more important, most simulation studies were performed in younger adults or did not stratify their results by age group [12]. Therefore, it is unlikely that these findings can be extrapolated to older adults, who are already at risk of inadequate micronutrient intake from their habitual diets [11].
To evaluate the potential risk of micronutrient deficiencies in older adults when transitioning to a more sustainable eating pattern, we conducted a simulation study. We examined the consequences of shifting to flexitarian, pescetarian, vegetarian, and vegan diets on their micronutrient intake amounts.
Methods
Simulations were made on data of the Dutch National Food Consumption Survey (DNFCS) from the period 2019–2021 [13]. The DNFCS is a cross-sectional periodical survey to assess food intake of the general Dutch population and is conducted by the National Institute for Public Health and The Environment. The database is nationally representative based on age, sex, region, education level, and urbanization level. Besides data on food consumption, self-reported data on sex, age, weight, height, level of education and employment, and lifestyle characteristics were collected.
The DNFCS 2019–2021 included people living at home in the age category 1 to 79 y (n = 3570) but for this study, we only used data of those aged 65 y or older (n = 607).
The study was conducted according to the guidelines of the Helsinki Declaration. The Medical Ethical Committee of the University Medical Centre Utrecht determined that the study did not require full review under the Medical Research Involving Human Subjects Act, as all survey measurements were noninvasive (reference no. 19-145/C). All participants signed an informed consent form at the first home visit.
Dietary intake and nutrition composition
Food intake of all participants in the DNFCS was measured by using 2 nonconsecutive 24-h dietary recalls per participant, making use of GloboDiet [14]. Both recalls were performed with a gap of 2 to 6 wk between them, allowing for a more accurate representation of typical dietary intake. Participants aged >70 y filled in a food diary as a memory aid for the 24-h recall 1 d before the interview. Interviews were conducted throughout the year and both during week and weekend days.
Participants aged 65 to 70 y were interviewed twice by telephone. Those aged 70 y or older received 1 in-home visit and 1 phone interview. However, because of the COVID-19 pandemic, some participants were interviewed twice by telephone instead.
Food consumption was noted on product level and categorized by food consumption occasion (3 meals and 4 in-between moments) category by the participants. The Dutch food composition database (NEVO) was used to calculate intake of micronutrients [15].
Simulations
For the simulations, we used pre-established scenarios [16], including 2 flexitarian scenarios (with either 40% or 80% of meat/fish replaced), a pescetarian scenario (where all meat was replaced but fish remained), a vegetarian scenario (where both meat and fish were replaced), and a vegan scenario (where all animal-based products were replaced). We followed a 2-step approach: we first assessed whether a product is compatible with a scenario; if not, we replaced it randomly by an appropriate alternative.
Assessing compatibility and alternatives
For the scenarios, we evaluated ∼1600 unique food codes used in the DNFCS to determine their compatibility with each scenario. This assessment was conducted by a dietitian (JB). Assessment of compatibility for each product was added to the ∼40,000 food items consumed in the DNFCS. Foods that did not fit into a scenario (for instance, a hamburger in a vegetarian scenario) were marked as “to be replaced” and categorized into one of the following food groups: meat or fish, bread with meat, savory snacks, sandwich fillings based on meat/fish/egg, soup, minced meat, yogurt/cream/sweet pudding/dessert/ice cream, dairy-based drinks, sweet snacks, or creams. For each food group, ≤12 alternative products were selected by a dietitian (JB and LGMV) based on their similarity to the items being replaced. In cases where fewer suitable alternatives were available, such as soups and snacks, a smaller number of replacements were used (see TABLE 1, TABLE 2).
TABLE 1.
Alternatives used for replacements shown per food group, for vegetarian scenarios (flexitarian 40%/80%, pescetarian, and vegetarian)
| Food group | Replacements |
|---|---|
| Meat or fish1 | Chicken egg |
| Mozzarella cheese | |
| Vegetarian vegetable balls/burgers based on soy2 | |
| Vegetarian schnitzel, enriched with iron and vitamin B12 | |
| Vegetarian vegetable balls/burgers based on soy, enriched with iron and vitamin B12 | |
| Vegetarian vegetable balls/burgers based on soy2 | |
| Vegetarian burger with cheese | |
| Vegetarian vegetable balls/burgers based on soy2 | |
| Vegetarian schnitzel (based on milk) fortified with iron | |
| Gouda cheese 48+ | |
| Sausage roast—vegetarian based on peas2 | |
| Vegetarian meatballs/burgers based on soy/wheat, enriched with iron and vitamin B12 | |
| Sandwich fillings based on meat or fish | Egg salad |
| Gouda cheese 48+ | |
| Peanut butter | |
| Spread sweet average | |
| Hummus | |
| Sausage sandwich—vegetarian enriched with iron and vitamin B12 | |
| Cheese salad | |
| Cream cheese | |
| Chicken egg | |
| Cheese 30+ | |
| Cheese spread | |
| Chocolate sprinkles | |
| Bread with meat | Cheese pastry |
| Baguette cheese-onion | |
| Bread currant | |
| Roll white soft | |
| Minced meat | Lentils green/brown boiled |
| Quorn minced meat2 | |
| Vegetarian minced meat enriched with iron and vitamin B12 | |
| Quorn pieces2 | |
| Minced meat, vegetarian, based on soy2 | |
| Vegetarian meatballs/burgers based on soy/wheat, enriched with iron and vitamin B12 | |
| Soup | Soup clear with vegetables and noodles |
| Soup clear vegetables | |
| Soup thickened vegetables | |
| Soup thickened no filling | |
| Savory snack | Crisp potato |
| Cocktail snacks nibb-it | |
| Cassave crackers | |
| Falafel |
See Appendix 1 for micronutrient content.
Fish is allowed in pescetarian scenario.
Nonfortified option.
TABLE 2.
Alternatives used for replacements shown per food group, for vegan scenario
| Food group | Replacements |
|---|---|
| Meat, fish, meat replacements based on dairy/egg, eggs (dinner), cheese (dinner) | Lentils green/brown boiled |
| Tofu | |
| Falafel | |
| Vegetarian meatballs/burgers based on soy/wheat, enriched with iron and vitamin B12 | |
| Sausage roast—vegetarian based on peas1 | |
| Vegetarian meatballs/burgers based on soy/wheat, enriched with iron and vitamin B12 | |
| Vegetarian meatballs/burgers based on soy/wheat, enriched with iron and vitamin B12 | |
| Strips/pieces vegetarian based on soy/wheat enriched with iron and vitamin B12 | |
| Pieces/chunks vegetarian based on soya/wheat1 | |
| Vegetable balls/burgers vegetarian based on soya1 | |
| Vegetarian meatballs/burgers based on soy/wheat, enriched with iron and vitamin B12 | |
| Vegetarian schnitzel based on soy/wheat, enriched with iron and vitamin B12 | |
| Sandwich fillings based on meat, fish, cheese, eggs (breakfast and lunch) | Peanut butter |
| Sausage luncheon meat vegetarian1 | |
| Hummus naturel | |
| Sesame paste tahin | |
| Sausage luncheon—vegetarian enriched with iron and vitamin B12 | |
| Hummus natural | |
| Bacon pieces vegetarian unprepared1 | |
| Bacon pieces vegetarian unprepared1 | |
| Plant-based alternative to Gouda cheese based on coconut oil1 | |
| Spread sweet averaged | |
| Peanut butter | |
| Sausage luncheon meat vegetarian1 | |
| Bread with meat | Cheese pastry |
| Baguette cheese-onion | |
| Bread currant | |
| Roll white soft | |
| Minced meat | Lentils green/brown boiled |
| Quorn minced meat1 | |
| Vegetarian minced meat enriched with iron and vitamin B12 | |
| Quorn pieces1 | |
| Minced meat, vegetarian, based on soy1 | |
| Vegetarian meatballs/burgers based on soy/wheat, enriched with iron and vitamin B12 | |
| Soup | Soup clear with vegetables and noodles |
| Soup clear vegetables | |
| Soup thickened vegetables | |
| Soup thickened no filling | |
| Savory snack | Crisp potato |
| Cocktail snacks nibb-it | |
| Cassave crackers | |
| Falafel | |
| Drink with dairy | Tea |
| Coffee | |
| Drink soya original Alpro fortified with calcium and vitamins | |
| Water | |
| Milk, yogurt, cream sweet, custard, pudding, desserts, ice cream | Drink soy with sugar, fortified with calcium and vitamins |
| Drink almond unsweeted1 | |
| Rice drink with calcium and vitamins | |
| Drink soy with sugar, fortified with calcium and vitamins | |
| Drink soya chocolate with sugar, fortified calcium and vitamins | |
| Drink oat without sugar fortified with calcium and vitamins | |
| Cream | Cream based on veg oil Alpro cuisine |
| Cream based on veg oil Alpro Cuisine Light | |
| Sweet snacks | Turkish delight |
| Popcorn sweet, popped without oil | |
| Chocolate dark w hazelnuts | |
| Wafer galette |
See Appendix 1 for micronutrient content.
Nonfortified option.
Randomly replacing
Food items that did not fit to an eating pattern (marked “to be replaced,” like fish in a vegetarian scenario) were randomly replaced by one of the alternatives within the same food group in a gram-for-gram way. This was done by changing the original food code in the DNFCS for the new food code that corresponds to the products in TABLE 1, TABLE 2. For instance, a hamburger (food code 1435) does not fit into any eating pattern and could be, depending on a random number, replaced in a vegetarian scenario by the food code of a chicken egg (83). Food codes of items that fitted the eating pattern were left unchanged.
To simulate the models, all separate consumed items in the DNFCS (39,923) were assigned a random number between 0 and 1. This randomization was used to enable the use of multiple alternatives rather than a single fixed option, which would be unrealistic. Replacement options within a category were equally assigned. For instance, in the category “meat or fish,” 12 alternatives were used. The first replacement option (chicken egg) was allocated to the random numbers 0 to 0.083, the second option (Mozzarella cheese) to the random number 0.083 to 0.167, etc. In case of fewer options (2, 3, 4, or 6), all options were equally assigned.
In case of the flexitarian scenario, random number 0 to 0.6 (flexitarian 40%) and 0 to 0.2 (flexitarian 80%) were not replaced. The remaining random numbers (0.6–1.0 for flexitarian 40% and 0.2–1.0 for flexitarian 80%) were equally assigned to the replacement options as described above. R-syntax for replacement is added in Appendix 2.
To make our simulations as realistic as possible, we adhered closely to typical Dutch dietary patterns. Therefore, in the flexitarian, pescetarian, and vegetarian scenarios, we replaced meat and fish (except in the pescetarian scenario) primarily with cheese and processed meat alternatives and only to a small extent with legumes [16,17].
For consumers, both fortified and unfortified processed meat and dairy alternatives are available in supermarkets. To create a realistic balance between these product types in our scenarios, we examined the micronutrient content of 98 meat and dairy alternatives sold in the 2 largest supermarket chains in the Netherlands, Jumbo and Albert Heijn. More than half of the meat replacements for warm meals and nearly all plant-based drinks were fortified (mostly by adding vitamin B12 and vitamin D), whereas meat/cheese replacements on bread were rarely fortified. On the basis of the supermarket inventory, we applied NEVO codes for fortified options in our simulation for more than half of the meat replacements at hot meals (60%) and for nearly all dairy replacements (85%), but only for a small proportion of vegan sandwich fillings (20%). Certain options (for instance, vegetarian vegetable balls/burgers based on soy) were used more often within one category to obtain the right proportion of fortified/nonfortified options (see TABLE 1, TABLE 2). Micronutrient content of all replacements can be seen in Appendix 1.
Reference values
The Dutch guidelines for micronutrients were used to determine which portion of the population had inadequate micronutrient intakes [18]. We applied the sex-specific estimated average requirements (EARs) for vitamins A, B1, B2, niacin, B6, folate, and B12, as well as the minerals copper, iron, and zinc. Because no EARs are available for vitamin E and the minerals calcium, iodine, magnesium, phosphorus, potassium, and selenium, we used adequate intakes instead (see Table 3). Vitamin D intake was reported but not assessed against the EAR as reference values are based on intake with supplementation [18]. Vitamin C was not incorporated in the analyses as it is almost completely derived from products that do not contain protein. Iodine assessment was omitted because of the limited availability of data on iodine content in the NEVO table.
TABLE 3.
Daily requirements of micronutrients for older adults (aged ≥65 y) based on Dutch dietary reference values (2018)
| Estimated average requirements (EAR) | Adequate intake |
|---|---|
| Vitamin A (RAE): ♂: 615 μg; ♀: 525 μg | Vitamin E: ♂: 13 mg; ♀: 11 mg |
| Thiamin: 0.072 mg/MJ | Calcium ♂: 1200 mg1 |
| Riboflavin: 1.3 mg | ♀ <70 y: 1100 mg ♀ ≥70 y: 1200 mg |
| Niacin: 1.3 mg/MJ | Magnesium: ♂: 350 mg; ♀: 300 mg |
| Vit B6: ♂: 1.3 mg; ♀: 1.1 mg | Phosphorus: 550 mg |
| Folate: 200 μg | Potassium: 3.5 g |
| Vit B12: 2.0 μg | Selenium: 70 μg |
| Vit C: ♂: 60 mg; ♀: 50 mg | |
| Copper: 0.7 mg | |
| Iron: 6 mg | |
| Zinc: ♂: 6.4 mg; ♀: 5.7 mg |
RAE = Retinol Activity Equivalents.
Only for age ≥70 y.
Micronutrient intake was evaluated based on the method outlined in the DNFCS [13]. A micronutrient was considered to have a low intake on a population level if >10% of the population did not meet the EAR. However, for nutrients assessed using adequate intake, such conclusions cannot be drawn. Instead, it is generally assumed that intake is sufficient when the median intake (P50) exceeds the adequate intake. When P50 is below the adequate intake, no statement can be made on that micronutrient [19].
Data analyses
All analyses were performed with R (R foundation) (4.2.3). Characteristics of included participants of the DNFCS were described by using means with SDs for normally distributed data, medians with 25th to 75th percentiles for nonnormally distributed data, and counts with percentages for categorical variables. Normality was checked by using qq-plots and stem-and-leaf diagrams.
To compare micronutrient intake with the sex-specific reference values, we used the R package Statistical Program to Assess Habitual Dietary Exposure (SPADE) version 4.1 [20]. SPADE is a package developed by the Dutch National Institute for Public Health and The Environment, especially to analyze the DNFCS. SPADE estimates habitual intake based on repeated short-term dietary assessments, such as the two 24-h recalls used in the DNFCS. It also provides opportunities to stratify data on sex and age and to add weighting factors to make data representative. SPADE provides a distribution of habitual intake on population level expressed in percentiles (for instance, p10, p50, and p90).
A 1-part model was applied for all nutrients, as dietary supplements were not included. We chose not to include supplements because our aim was to show changes in dietary intake and not to focus on total vitamin adequacy within the population. All data were analyzed stratified by sex. Weighting factors (sociodemographic factors, week/weekend days, season) were used to make data nationally and seasonally representative.
Micronutrient intake was visualized using boxplots, where the box represents the 25th, 50th, and 75th percentiles (p25, p50, and p75), and the whiskers indicate the 10th and 90th percentiles (p10 and p90). Changes of micronutrients for each scenario compared with the original diet were shown by using dot plots.
Results
Of the 607 included participants, 51% were males, median age was 71 in males and 69 in females, and mean BMI was almost 27 kg/m2. Of males, 41% had a high educational level; in females this was 27% (Table 4).
TABLE 4.
Characteristics of participants (aged ≥65 y) included from the Dutch National Food Consumption Survey
| Characteristic | Male |
Female |
|---|---|---|
| n = 311 (51%) | n = 296 (49%) | |
| Age (y) | 71 (68–84) | 69 (67–73) |
| BMI (kg/m2) | 26.9 (±4.5) | 26.8 (±5.4) |
| Education level1 | ||
| Low | 96 (31%) | 132 (45%) |
| Middle | 89 (29%) | 83 (28%) |
| High | 126 (41%) | 81 (27%) |
| Number of food replacements | ||
| Flexitarian 40% | 771 | 596 |
| Flexitarian 80% | 1405 | 1010 |
| Pescetarian | 1355 | 901 |
| Vegetarian | 1709 | 1227 |
| Vegan | 4754 | 4058 |
| Percentage plant-based protein of total protein | ||
| Reference diet | 39.0% (30.7–46.8) | 37.7% (28.0–46.4) |
| Flex 40 | 43.7% (33.9–55.4) | 42.6% (32.6–54.0) |
| Flex 80 | 52.2% (40.5–65.3) | 49.7% (39.2–62.5) |
| Pescetarian | 54.3% (42.1–67.0) | 51.9% (39.2–63.8) |
| Vegetarian | 59.1% (45.2–70.0) | 54.2% (42.9–65.0) |
| Vegan | 99.3% (98.3–99.8) | 99.3% (98.3–99.8) |
| Kcal intake | ||
| Reference diet | 2197 (1955–2463) | 1751 (1545–1969) |
| Flexitarian 40% | 2213 (1979–2472) | 1760 (1552–1979) |
| Flexitarian 80% | 2211 (1970–2474) | 1761 (1550–1984) |
| Pescetarian | 2211 (1971–2499) | 1761 (1547–1987) |
| Vegetarian | 2233 (1984–2509) | 1770 (1555–1998) |
| Vegan | 2180 (1937–2450) | 1747 (1540–1964) |
Data are shown as median (25th–75th percentile), mean (with SD), or as number/percentage. Data (except kcal intake) are based on unweighted data, so no adjustments were done to make this table national representative.
Education level was categorized into low (primary education, lower vocational education, advanced elementary education), middle (intermediate vocational education, higher secondary education), and high (higher vocational education and university).
Of the total of 39,923 consumed items, the least items (n = 1367) were replaced in the flexitarian 40% scenario, and the most (n = 8812) in the vegan scenario. All scenarios included less animal-based protein than the reference scenario, but the goal of 60% plant-based proteins as advised by the Dutch Health Council [9] was only reached in the vegetarian diet (males ∼60%, females ∼55% plant-based protein) and the vegan diet (close to 100% plant-based protein, not fully as some low-protein foods such as cake were not replaced). Daily energy intake increased slightly in the flexitarian, pescetarian, and vegetarian scenario (∼100 kcal) but was stable in the vegan scenario (see Table 4).
Micronutrient intake
In the reference diet, most micronutrients were consumed sufficiently, except riboflavin, vitamin B6, folate (both sexes), and vitamin A in females (Figure 1). Based on adequate intake, most micronutrients were sufficiently consumed, but no statements could be made for calcium and selenium (both sexes) and potassium in females (Figure 2).
FIGURE 1.
Vitamin intake with corresponding EAR cut-off values, stratified by scenario and sex. Vitamin D is not assessed against EAR as this number is based on intake with supplements. EAR, estimated average requirement.
FIGURE 2.
Micronutrient intake with corresponding adequate intake cut-off values, stratified by scenario and sex.
In the flexitarian 40% scenario, intake of most micronutrients decreased, but no additional micronutrients were too low. In the scenarios with higher plant-based proportions (flexitarian 80%, pescetarian, and vegetarian), the intake of nearly all micronutrients decreased. In addition to the previously mentioned micronutrients, the intake of vitamin A (males), thiamin (males), and niacin (both sexes) became too low. Vitamin B6, which was already low in the reference diet, was now low in >50% of all older adults. In contrast, calcium intake (based on adequate intake) became sufficient in males (FIGURE 2, FIGURE 3).
FIGURE 3.
Changes in micronutrient intakes (p50) per simulated diet (flexitarian 40%, vegetarian, and vegan) compared with habitual diet in older males and females.
In the vegan scenario, nearly all micronutrients were low. A sufficient intake was only seen for thiamin, folate (which was low in the reference diet), copper, and iron (all based on EAR) and vitamin E, magnesium, phosphorus (both sexes), and potassium (only in males).
Discussion
This simulation study among older adults demonstrates that a modest reduction in meat and fish is feasible without introducing extra risks of low micronutrient intake. However, removing substantial amounts of meat and fish leads to a decrease in the intake of key nutrients, particularly vitamin A and B vitamins and zinc. A simulated fully vegan scenario showed a risk of inadequate consumption of nearly all analyzed micronutrients.
Our results align closely with a previous simulation study on the DNFCS, which modeled a “no meat/no dairy” diet in adults aged 18 to 69 y (30% replacement, comparable with our flexitarian scenario and 100% replacement, comparable with our vegan scenario) [21]. Similar declines to those observed in our study were noted for zinc, vitamin A, thiamin, and vitamin B12, whereas concentrations of iron and vitamin D increased (no other micronutrients were assessed). In the 30% replacement scenario, these lower intakes did not result in an additional proportion of participants at nutritional risk (except for vitamin A). In their 100% replacement scenario, large groups did become at risk of low intakes. In line with their 30% replacement scenario, our data suggest that substituting a small portion of animal-based products in the diet is feasible without a strong decline in micronutrient intake.
A recent systematic review indicated that only one trial has examined micronutrient intake when transitioning to more sustainable eating patterns [12]. This trial (n = 136; age 20–69 y) assessed micronutrient intake—including vitamin B12, iron, zinc, folate, and iodine—when participants shifted from a 70/30 animal-to-plant protein ratio to 50/50 and 30/70 ratios, primarily by using unprocessed alternatives [22]. Comparable with our results, vitamin B12 significantly decreased by 30% and 55%, zinc declined by approximately 10% to 15%, whereas folate and iron intakes increased in their more plant-based diets.
Observational studies that investigated micronutrient intake among vegetarian and vegan populations were not always in line with our simulated observations. Consistent with our study, these studies show that vegetarian and vegan diets generally provide higher concentrations of folate, similar concentrations of iron, and lower concentrations of vitamins A and B12 compared with omnivorous diets [12]. However, unlike our simulation—which observed significant reductions in several B vitamins—observational studies report similar or even higher intakes of thiamin, riboflavin, niacin, and vitamin B6 in vegetarian and vegan diets [[23], [24], [25]]. These B vitamins are crucial for energy metabolism [26] and for the physical functioning of older adults [27,28]. This discrepancy in vitamin B intake between actual dietary data and our simulation highlights an important limitation of our approach: animal-based products were substituted directly with their plant-based counterparts (often meat analogs), which overlooks the broader differences in dietary habits typically observed between these groups—such as substantially higher intakes of legumes, whole grains, and vegetables [29].
Calcium intake in the reference scenario was low. Shifting dietary patterns toward greater dairy consumption in place of meat—e.g., replacing ham with cheese on sandwiches—reduced the prevalence of inadequate calcium intake. This is particularly relevant for older adults, as calcium is essential for maintaining bone health and preventing osteoporosis, as well as supporting hormonal regulation and vascular function [30]. The relatively high calcium intake observed in our simulations may be explained by the inclusion of cheese products among the substitutes. However, it remains uncertain whether such a shift would occur in everyday practice. Previous studies have reported mixed findings regarding whether individuals following vegetarian diets consume more dairy or cheese than omnivorous diets [31,32].
Iron intake remained high and even increased, with the highest intake observed in the vegan group. That observation replicates those of previous simulation studies [21,33] and of other cohorts that assessed vegan eating patterns [[23], [24], [25]]. In all our scenarios, we included fortified meat replacers as substitutes for meats eaten in a warm meal context. In the Netherlands, fortified meat replacers often contain more iron (±3 to 5 mg/100 g) than their meat counterparts. However, fortification likely varies across countries and products, as there are no European Union regulations on (mandatory) fortification. In the vegan scenario, soy drinks were often introduced as a substitute for dairy drinks. Soy drinks naturally contain ∼1 mg iron per serving of 250 mL [34], whereas dairy drinks do not contain iron, leading to additional increases in the estimated iron intake on a vegan diet. Importantly, iron from plant-based sources, including the fortified meat, consists exclusively of nonheme iron [15], which has a poorer bioavailability [35]. Research showed wide ranges for bioavailability with superior availability of heme iron (15%–35%) [36] compared with nonheme iron (0.7%–22.9%) [37]. Bioavailability of nonheme iron is strongly dependent on an individual iron status [38], which was not available in our data. Therefore, despite the higher intake, it remains unclear whether sufficient iron would be available in more sustainable eating patterns.
Albeit often overlooked, zinc deficiency is one of the most common deficiencies in those with a vegan eating pattern [25]. Our observed decreased intake of zinc while iron remained high might seem remarkable as zinc and iron content in products are correlated with each other, even in plant-based products [39]. However, because processed vegan alternatives are often fortified with iron but not with zinc, this discrepancy is plausible. In the current Western eating pattern, zinc is mainly found in animal-based sources [40]. Plant-based sources of zinc are legumes, such as lentils [15]. For older adults, adequate zinc intake is of importance as it is needed for wound healing, immune function, maintaining bone health, muscle protein synthesis, and taste acuity [41], and zinc fortification or active legume promotion in vegan diets might be considered.
Vitamin B12 intake was lower in each progressively more plant-based scenario, but only fell below thresholds in the vegan scenario. Cohort studies have shown that not only vegan but also those who are following a vegetarian eating pattern are at risk [42]. Plant-based protein alternatives such as nuts, legumes, and soy do not contain any natural source of vitamin B12 [15]. It is therefore commonly advised to use a vitamin B12 supplement when eating vegan [43]. Although meat replacements for warm meals are mostly B12-fortified in the Netherlands, cold-cut replacements are not. In general, the micronutrient profile of meat replacements is not comparable with the pattern of products they aim to replace; meat naturally provides various micronutrients, whereas their replacements are mostly fortified with only iron and vitamin B12. These discrepancies might be considered by food industries and regulatory organizations to better align the nutrient profiles of vegan substitutes with the animal products they replace.
A strength of our modeling approach is the large number of substitutes that we randomly selected from at each replacement, minimizing the risk of single products exerting pronounced effects on micronutrient intakes. In our modeling, we deliberately stayed close to the current eating pattern, as we expect that to be a more realistic population change than diet-wide changes in meal choices. However, this assumption introduces risk to the external validity of our work. In reality, eating a more plant-based diet could be much different than the traditional diet in terms of eating behavior. For instance, it is possible that consuming less animal-based protein will be achieved by eating more mixed meals instead of traditional Dutch meals consisting of a carbohydrate source, vegetables, and a piece of meat or fish, with consequential effects on micronutrient intake. For instance, our observation of dramatically reduced intakes of vitamin A and most B vitamins could be mitigated by an increased consumption of vegetables, legumes, and nuts in a vegan pattern. That idea is supported by cohort studies, showing less pronounced lower micronutrient intakes in vegetarian and vegan diets [24,25]. Thus, our simulation should be interpreted primarily as a reflection of how micronutrient intake might decline when meat and dairy are replaced by processed alternatives, without changes to overall eating patterns.
Another limitation of our study is that dietary intake was self-reported. Although the DNFCS methodology includes multiple quality checks, underreporting or overreporting of intake may still introduce some bias. This is especially relevant for older adults, where memory difficulties can reduce the accuracy of 24-h recall data. On the basis of a previous analysis of this dataset, underreporting in the age group ≥65 y was estimated at 5% in males and 13% in females, which is lower than the 17% estimated for the general DNFCS population [13]. In addition, we used the same underlying data in all our scenarios, so this bias is equal in all scenarios. However, some micronutrient intakes that appear too low might, in reality, be sufficient when accounting for underreporting.
In this study, we showed how micronutrient intake differed for each scenario. Although large differences were sometimes observed between scenarios, no P value testing or differences with 95% confidence intervals were calculated. This was not possible because, after the application of SPADE, only the modeled usual intake distributions for each scenario were available, whereas the individual-level paired data linking observations across scenarios were no longer retained. As a result, standard inferential procedures, such as hypothesis testing and the calculation of P values, could not be performed.
Finally, simulation studies are inherently theoretical, and the feasibility of adopting a different dietary pattern may be limited, particularly among older adults. However, the younger generations that are open to eating flexitarian, pescetarian/vegetarian, or even vegan will one day become the group of older adults. In addition, the WHO does not restrict recommendations to reduce animal-based protein consumption to younger or middle-aged populations [3]. Our findings suggest that if older adults do reduce their animal-based protein intake, careful monitoring of micronutrient consumption is essential, as current intake amounts are already low and may decline further.
In our study, we did not include supplements, as our aim was to examine how micronutrient intake from foods changed across different scenarios. The proportion of the population at risk of inadequate micronutrient intake may therefore be lower in reality, as a large share of the population currently uses vitamin supplements [44,45] and this is even more pronounced in those consuming a vegan eating pattern [46]. In our data, 60% used a supplement (exact content not indicated), so it is likely that inadequate micronutrient intake after including supplements would be lower.
In conclusion, our simulated scenarios suggest that a shift toward more plant-based diets may increase the prevalence of inadequate micronutrient intakes in older adults. Intakes of the nutrients vitamin A, B vitamins, calcium, selenium, and zinc are most at risk when older adults shift to more plant-based dietary patterns. Future research should confirm these findings in real-life settings.
Author contributions
The authors’ responsibilities were as follows – JB, PG, MdvdS, LGMV: designed research; JB, LGMV: analyzed data or performed statistical analysis; JB, LGMV, PG, MdvdS: wrote the paper; MdvdS: had primary responsibility for final content; all authors: read and approved the final manuscript.
Data availability
Data described in the manuscript, code book, and analytic code will be made available upon request. We invite other researchers to contact the corresponding author to collaborate on performing simulations on the DNFCS and to work with our latest syntaxes on this topic.
Declaration of Generative AI and AI-assisted technologies in the writing process
During the preparation of this work, the authors used ChatGPT to improve grammar. After using this tool/service, the authors reviewed and edited the content as needed and take full responsibility for the content of the publication.
Funding
This research was partly funded by the Taskforce for Applied Research (grant number: RAAK.MKB16.012), part of the Netherlands Organization for Scientific Research (NOW), financed by the Dutch Ministry of Education, Culture and Science and by a fund of the Dutch Dairy Association. The funders had no role in the design, analyses, and writing or the decision to submit the manuscript.
Conflict of interest
The author reports no conflicts of interest.
Acknowledgments
We thank Natasha Nalucha Mwala for checking the grammar and spelling.
Footnotes
Supplementary data to this article can be found online at https://doi.org/10.1016/j.cdnut.2026.109446.
Appendix A. Supplementary data
The following are the Supplementary data to this article:
References
- 1.González-García S., Esteve-Llorens X., Moreira M.T., Feijoo G. Carbon footprint and nutritional quality of different human dietary choices. Sci. Total Environ. 2018;644:77–94. doi: 10.1016/j.scitotenv.2018.06.339. [DOI] [PubMed] [Google Scholar]
- 2.Aleksandrowicz L., Green R., Joy E.J., Smith P., Haines A. The impacts of dietary change on greenhouse gas emissions, land use, water use, and health: a systematic review. PLOS ONE. 2016;11(11) doi: 10.1371/journal.pone.0165797. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.World Health Organization . Food & Agriculture Organization; Rome, Italy: 2019. Sustainable healthy diets: guiding principles. ISBN. [Google Scholar]
- 4.Willett W., Rockström J., Loken B., Springmann M., Lang T., Vermeulen S., et al. Food in the anthropocene: the EAT–Lancet Commission on healthy diets from sustainable food systems. Lancet. 2019;393(10170):447–492. doi: 10.1016/S0140-6736(18)31788-4. [DOI] [PubMed] [Google Scholar]
- 5.Rockström J., Thilsted S.H., Willett W.C., Gordon L.J., Herrero M., Hicks C.C., et al. The EAT–Lancet Commission on healthy, sustainable, and just food systems. Lancet. 2025;406(10512):1625–1700. doi: 10.1016/S0140-6736(25)01201-2. [DOI] [PubMed] [Google Scholar]
- 6.Soh B.X.P., Smith N.W., von Hurst P.R., McNabb W.C. Evaluation of protein adequacy from plant-based dietary scenarios in simulation studies: a narrative review. J. Nutr. 2024;154(2):300–313. doi: 10.1016/j.tjnut.2023.11.018. [DOI] [PubMed] [Google Scholar]
- 7.Murphy S.P., Allen L.H. Nutritional importance of animal source foods. J. Nutr. 2003;133(11):3932S–3935S. doi: 10.1093/jn/133.11.3932S. [DOI] [PubMed] [Google Scholar]
- 8.Beal T., Ortenzi F., Fanzo J. Estimated micronutrient shortfalls of the EAT–Lancet planetary health diet. Lancet Planetary Health. 2023;7(3):e233–e237. doi: 10.1016/S2542-5196(23)00006-2. [DOI] [PubMed] [Google Scholar]
- 9.Health Council of the Netherlands . 2023 Dec 13. A healthy protein transition. Health Council of the Netherlands: The Hague. Report No.: 2023/19e. [Google Scholar]
- 10.Marian M., Sacks G. Micronutrients and older adults. Nutr. Clin. Pract. 2009;24(2):179–195. doi: 10.1177/0884533609332177. [DOI] [PubMed] [Google Scholar]
- 11.ter Borg S., Verlaan S., Hemsworth J., Mijnarends D.M., Schols J.M., Luiking Y.C., et al. Micronutrient intakes and potential inadequacies of community-dwelling older adults: a systematic review. Br. J. Nutr. 2015;113(8):1195–1206. doi: 10.1017/S0007114515000203. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Leonard U.M., Leydon C.L., Arranz E., Kiely M.E. Impact of consuming an environmentally protective diet on micronutrients: a systematic literature review. Am. J. Clin. Nutr. 2024;119:927–948. doi: 10.1016/j.ajcnut.2024.01.014. [DOI] [PubMed] [Google Scholar]
- 13.Van Rossum C., Sanderman-Nawijn E., Brants H., Dinnissen C., Jansen-van der Vliet M, Beukers M, et al. The diet of the Dutch: results of the Dutch National Food Consumption Survey 2019-2021 on food consumption and evaluation with dietary guidelines. RIVM Off. Rep. 2023 doi: 10.21945/RIVM-2022-0190. 2022–0190. [DOI] [Google Scholar]
- 14.Slimani N., Casagrande C., Nicolas G., Freisling H., Huybrechts I., Ocké M., et al. The standardized computerized 24-h dietary recall method EPIC-Soft adapted for pan-European dietary monitoring. Eur. J. Clin. Nutr. 2011;65(1):S5–S15. doi: 10.1038/ejcn.2011.83. [DOI] [PubMed] [Google Scholar]
- 15.RIVM . Bilthoven; The Netherlands: 2023. NEVO-online. [Google Scholar]
- 16.Borkent J.W., Grootswagers P., Linschooten J., Roodenburg A.J.C., Ocke M., de van der Schueren M.A.E. A vegan dietary pattern is associated with high prevalence of inadequate protein intake in older adults; a simulation study. J. Nutr. Health Aging. 2024;28(10) doi: 10.1016/j.jnha.2024.100361. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Bradbury K.E., Tong T.Y., Key T.J. Dietary intake of high-protein foods and other major foods in meat-eaters, poultry-eaters, fish-eaters, vegetarians, and vegans in UK Biobank. Nutrients. 2017;9(12):1317. doi: 10.3390/nu9121317. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Health Council of the Netherlands An evaluation of the EFSA’s dietary reference values. Health Council of the Netherlands: The Hague. 2018 Contract No.: 2018/19A. [Google Scholar]
- 19.Murphy S.P., Poos M.I. Dietary reference intakes: summary of applications in dietary assessment. Public Health Nutr. 2002;5(6a):843–849. doi: 10.1079/PHN2002389. [DOI] [PubMed] [Google Scholar]
- 20.Dekkers A.L., Verkaik-Kloosterman J., van Rossum C.T., Ocké M.C. SPADE, a new statistical program to estimate habitual dietary intake from multiple food sources and dietary supplements. J. Nutr. 2014;144(12):2083–2091. doi: 10.3945/jn.114.191288. [DOI] [PubMed] [Google Scholar]
- 21.Seves S.M., Verkaik-Kloosterman J., Biesbroek S., Temme E.H. Are more environmentally sustainable diets with less meat and dairy nutritionally adequate? Public Health Nutr. 2017;20(11):2050–2062. doi: 10.1017/S1368980017000763. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Pellinen T., Päivärinta E., Isotalo J., Lehtovirta M., Itkonen S.T., Korkalo L., et al. Replacing dietary animal-source proteins with plant-source proteins changes dietary intake and status of vitamins and minerals in healthy adults: a 12-week randomized controlled trial. Eur. J. Nutr. 2022;61:1391–1404. doi: 10.1007/s00394-021-02729-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Storz M.A., Müller A., Niederreiter L., Zimmermann-Klemd A.M., Suarez-Alvarez M., Kowarschik S., et al. A cross-sectional study of nutritional status in healthy, young, physically-active German omnivores, vegetarians and vegans reveals adequate vitamin B12 status in supplemented vegans. Ann. Med. 2023;55(2) doi: 10.1080/07853890.2023.2269969. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Davey G.K., Spencer E.A., Appleby P.N., Allen N.E., Knox K.H., Key T.J. EPIC–Oxford: lifestyle characteristics and nutrient intakes in a cohort of 33 883 meat-eaters and 31 546 non meat-eaters in the UK. Public Health Nutr. 2003;6(3):259–269. doi: 10.1079/PHN2002430. [DOI] [PubMed] [Google Scholar]
- 25.Schüpbach R., Wegmüller R., Berguerand C., Bui M., Herter-Aeberli I. Micronutrient status and intake in omnivores, vegetarians and vegans in Switzerland. Eur. J. Nutr. 2017;56:283–293. doi: 10.1007/s00394-015-1079-7. [DOI] [PubMed] [Google Scholar]
- 26.Penberthy W.T., Kirkland J.B. Elsevier; 2020. Niacin. Present Knowledge in Nutrition; pp. 209–224. [Google Scholar]
- 27.Struijk E.A., Lana A., Guallar-Castillón P., Rodríguez-Artalejo F., Lopez-Garcia E. Intake of B vitamins and impairment in physical function in older adults. Clin. Nutr. 2018;37(4):1271–1278. doi: 10.1016/j.clnu.2017.05.016. [DOI] [PubMed] [Google Scholar]
- 28.Grootswagers P., Mensink M., Berendsen A.A., Deen C.P., Kema I.P., Bakker S.J., et al. Vitamin B-6 intake is related to physical performance in European older adults: results of the new dietary strategies addressing the specific needs of the elderly population for healthy aging in Europe (NU-AGE) study. Am. J. Clin. Nutr. 2021;113(4):781–789. doi: 10.1093/ajcn/nqaa368. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Bowman S.A. A vegetarian-style dietary pattern is associated with lower energy, saturated fat, and sodium intakes; and higher whole grains, legumes, nuts, and soy intakes by adults: National Health and Nutrition Examination Surveys 2013–2016. Nutrients. 2020;12(9):2668. doi: 10.3390/nu12092668. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Li K., Wang X.-F., Li D.-Y., Chen Y.-C., Zhao L.-J., Liu X.-G., et al. The good, the bad, and the ugly of calcium supplementation: a review of calcium intake on human health. Clin. Interv. Aging. 2018;13:2443–2452. doi: 10.2147/CIA.S157523. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Clarys P., Deliens T., Huybrechts I., Deriemaeker P., Vanaelst B., De Keyzer W W., et al. Comparison of nutritional quality of the vegan, vegetarian, semi-vegetarian, pesco-vegetarian and omnivorous diet. Nutrients. 2014;6(3):1318–1332. doi: 10.3390/nu6031318. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Rizzo N.S., Jaceldo-Siegl K., Sabate J., Fraser G.E. Nutrient profiles of vegetarian and nonvegetarian dietary patterns. J. Acad. Nutr. Diet. 2013;113(12):1610–1619. doi: 10.1016/j.jand.2013.06.349. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Lawrence A.S., Huang H., Johnson B.J., Wycherley T.P. Impact of a switch to plant-based foods that visually and functionally mimic animal-source meat and dairy milk for the Australian population—a dietary modelling study. Nutrients. 2023;15(8):1825. doi: 10.3390/nu15081825. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Stöckl M., Pferdmenges L.E., Brühl L., Greiner R., Hüsken A., Krüger R., et al. Characterization of the nutritional profile of three plant-based drinks. J. Food Composition Anal. 2024;135 [Google Scholar]
- 35.Sandberg A.-S. Bioavailability of minerals in legumes. Br. J. Nutr. 2002;88(S3):281–285. doi: 10.1079/BJN/2002718. [DOI] [PubMed] [Google Scholar]
- 36.Hurrell R., Egli I. Iron bioavailability and dietary reference values. Am. J. Clin. Nutr. 2010;91(5):1461S–1467S. doi: 10.3945/ajcn.2010.28674F. [DOI] [PubMed] [Google Scholar]
- 37.Collings R., Harvey L.J., Hooper L., Hurst R., Brown T.J., Ansett J., et al. The absorption of iron from whole diets: a systematic review. Am. J. Clin. Nutr. 2013;98(1):65–81. doi: 10.3945/ajcn.112.050609. [DOI] [PubMed] [Google Scholar]
- 38.van Wonderen D., Melse-Boonstra A., Gerdessen J.C. Iron bioavailability should be considered when modeling omnivorous, vegetarian, and vegan diets. J. Nutr. 2023;153(7):2125–2132. doi: 10.1016/j.tjnut.2023.05.011. [DOI] [PubMed] [Google Scholar]
- 39.Lim K.H., Riddell L.J., Nowson C.A., Booth A.O., Szymlek-Gay E.A. Iron and zinc nutrition in the economically-developed world: a review. Nutrients. 2013;5(8):3184–3211. doi: 10.3390/nu5083184. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Olza J., Aranceta-Bartrina J., González-Gross M., Ortega R.M., Serra-Majem L., Varela-Moreiras G., et al. Reported dietary intake and food sources of zinc, selenium, and vitamins A, E and C in the Spanish population: findings from the ANIBES study. Nutrients. 2017;9(7):697. doi: 10.3390/nu9070697. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Abeywickrama H.M., Uchiyama M., Sumiyoshi T., Okuda A., Koyama Y. The role of zinc on nutritional status, sarcopenia, and frailty in older adults: a scoping review. Nutr. Rev. 2024;82(7):988–1011. doi: 10.1093/nutrit/nuad094. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Pawlak R., Parrott S.J., Raj S., Cullum-Dugan D., Lucus D. How prevalent is vitamin B12 deficiency among vegetarians? Nutr. Rev. 2013;71(2):110–117. doi: 10.1111/nure.12001. [DOI] [PubMed] [Google Scholar]
- 43.Fernandes S., Oliveira L., Pereira A., Costa M.d.C., Raposo A., Saraiva A., et al. Exploring vitamin B12 supplementation in the vegan population: a scoping review of the evidence. Nutrients. 2024;16(10):1442. doi: 10.3390/nu16101442. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Mishra S., Stierman B., Gahche J.J., Potischman N. NCHS Data Brief; 2021. Dietary supplement use among adults: United States, 2017–2018; pp. 1–8. [PubMed] [Google Scholar]
- 45.Li K., Kaaks R., Linseisen J., Rohrmann S. Consistency of vitamin and/or mineral supplement use and demographic, lifestyle and health-status predictors: findings from the European prospective investigation into cancer and nutrition (EPIC)-Heidelberg cohort. Br. J. Nutr. 2010;104(7):1058–1064. doi: 10.1017/S0007114510001728. [DOI] [PubMed] [Google Scholar]
- 46.Janko R.K., Haussmann I., Patel A. Vitamin B12 status in vegan and vegetarian seventh-day adventists: a systematic review and meta-analysis of serum levels and dietary intake. Am. J. Health Promot. 2025;39(1):162–171. doi: 10.1177/08901171241273330. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
Data described in the manuscript, code book, and analytic code will be made available upon request. We invite other researchers to contact the corresponding author to collaborate on performing simulations on the DNFCS and to work with our latest syntaxes on this topic.



