Albanian Amharic Arabic (Palestinian Territories) العربية Armenian Bosnian Bulgarian Chinese (simplified) 簡體中文 Chinese (traditional) 繁体中文 Croatian Danish English (Philippines) Estonian French German Hausa Hebrew Icelandic Indonesian Italian Japanese Javanese Kazakh Lingala Norwegian Polish Portuguese Romanian Russian Serbian Somali Spanish Swahili Swedish Tagalog Turkish Ukrainian Xhosa Yoruba Zulu
Also have a look at our publication Koeder & Perez-Cueto (2022). Vegan nutrition: a preliminary guide for health professionals.
The following recommendations are general guidelines for your orientation. You do not have to follow them in the minutest detail.
1) Vitamin B12
Choose one of the following options [1–4]:
- 2–5 µg twice per day (from fortified foods or a supplement) [5–12]
- 10–50 µg per day from a supplement [6,10–15]
- 2000–2500 µg per week from a supplement [7,11,12,16–18]
2) Calcium
Consume at least 600 mg of calcium per day [2,19–28]. You can achieve this by choosing at least one of the following options every day. However, in most countries the calcium recommendation (reference values for daily intake) is around 1000 mg. This higher amount may be better at protecting bones. Consuming about two of the following options daily therefore seems advisable.
- 1 glass (~250 ml) of calcium-fortified plant milk, for example, soya milk. The label should state that it contains 120 mg of calcium per 100 ml (just like cow’s milk) [3,23,28–31]. This will provide about 300 mg of calcium.
- Other calcium-fortified foods, for example, calcium-fortified juice, soya yoghurt, rolled oats, or bread, which would also provide about 300 mg of calcium per day (check the label; different products are available in different countries) [23,28,30,32]
- 1 to 2 cups of cooked dark green leafy vegetables:
- pak choi (bok choy)
- kale
- Collard greens/Spring greens
- broccoli raab
- turnip greens
- mustard greens
- broccoli [23,28,31]
- dandelion leaves
- nettle leaves
- Napa cabbage (cooked)
- (Spinach and chard [called silverbeet in Australia and New Zealand] are not good calcium sources, as the bioavailability is low.)
- 2 to 3 cups of raw Napa cabbage
- 1 cup of tofu made with calcium sulfate [23,28–31]
- calcium-rich water/mineral water which should provide at least 300 mg calcium per day – check the label [33,34]
- ½ cup of dried figs + 3 oranges [23]
- 6 nixtamalized corn (maize) tortillas (Ø ~15 cm) (These are available in Mexico and several Central American countries like Guatemala, El Salvador, Honduras, Nicaragua, and Costa Rica.) [35–42]
The official dietary intake recommendations in many countries is about 1000 mg of calcium per day [109].
3) Vitamin D
In summer:
- 15–30 minutes of direct sunshine on your skin every day ... or more sunshine (e.g., 1 or 2 hours) less often (e.g., several times per week). If you live far from the equator, sunshine around midday (about 9 am to 3 pm) is more effective, i.e., your shadow should not be much longer than your height. Avoid excessive sunshine exposure. Avoid sunburn!
or
- take a vitamin D supplement – like in winter. Do not avoid the sun completely even if you take a daily vitamin D supplement. Sunshine has other health benefits apart from stimulating vitamin D synthesis.
In winter (“vitamin D winter”):
- ~25 µg (~1000 IU) vitamin D per day from a supplement [2,3,23,28,43–50]
“Vitamin D winter” is when your body cannot make vitamin D from sunshine, and this depends on where you live on this planet (latitude).
“Vitamin D winter”:
- Between 35° north and 35° south: No “vitamin D winter” at all – you can make vitamin D all year long from sunshine on your skin [51]
- Between 35° and 40° north: December and January
- Between 40° and 50° north: November to February
- North of 50° north: October to March (or longer)
- Between 35° and 40° south: June and July
- Between 40° and 50° south: May to August
- South of 50° south: April to September (or longer)
4) Iodine
Choose one of the following options [2,3,45,52–60]:
- 100–150 µg per day from a supplement
- eat seaweed like nori or wakame, several times per week
- use iodized salt (1 teaspoon contains 40–240 µg of iodine – check the label) [61–63]. Avoid excessive salt intake.
5) Omega-3 fatty acids
Choose one (or a mix of several) of these options (more or less) every day [19,30,64–69]. The following recommendations are for men – who generally consume more calories. For women a little less is sufficient.
- ~10 walnuts (=20 walnut halves; ~40 g) [64]
- 1–2 teaspoons of linseed oil (flaxseed oil) [64]
- 2 tablespoons of ground linseeds (flaxseeds) [64,70,71]
- 1–2 tablespoons of chia seeds [69,72–74]
- 1–2 tablespoons of hemp seed oil [64]
- ¼ cup of hemp seeds, or 1–2 tablespoons of shelled hemp seeds
- 2–3 tablespoons of rapeseed oil (canola oil) [64]
Optional recommendation:
Use half of the above recommendations – and add a vegan EPA/DHA supplement:
- 200–300 mg EPA/DHA every two or three days (or every day if you like) [64,67–69,75–77]
Current evidence does not clearly indicate that the average vegan would really benefit from EPA/DHA supplements. A benefit (for example, for brain or heart health) is possible but very uncertain.
6) Iron
Eat legumes on a daily basis [26,78,79].
In men, iron deficiency is very uncommon. In premenopausal women, iron deficiency is relatively common (because of blood loss during menstruation).
Additional tips (especially for premenopausal women):
- Consuming vitamin C at the same time as iron-rich foods increases the absorption of iron from plant sources [78,80–83].
- Drinking coffee or tea with meals lowers the absorption of iron from plant sources [80–84].
- Cooking tomato sauce (or other sauces that are slightly acidic) in cast iron cookware will enrich the sauce with iron [83–86].
7) Zinc
Eat legumes, whole grains, and nuts and seeds on a daily basis [2,30,87,88]. They are good sources of zinc.
8) Selenium
Choose (only) one (not both) of the following options [45,89–91]:
- Eat 1 or 2 Brazil nuts per day [92–95]. But do not eat large amounts of Brazil nuts regularly.
- Take a supplement that contains 50–60 µg (not more) of selenium per day [92,95–100].
If you live in the United States, Canada or Venezuela you can ignore these recommendations [101–104]. If you live in Finland (where selenium is added to fertilizer) and you consume plenty of non-organic grains, you can probably ignore these recommendations, too [53].
If you live in any regions in China which have soils extremely high in selenium – do NOT use selenium supplements, and do NOT eat Brazil nuts. If you live in any of the regions of China with extremely low soil selenium levels, do take a selenium supplement (as recommended above) – unless there are local measures being taken to fortify certain foods with selenium (and you eat those foods).
9) Vitamin A (provitamin A)
Eat plenty of dark green leafy vegetables, orange-coloured fruits, and orange-coloured vegetables [3,45,105].
Great beta-carotene (provitamin A) sources are, for example: cooked carrots, carrot juice, pumpkin, orange coloured sweet potatoes, dark green leafy vegetables, orange coloured fruits like mangoes, papayas, and kakis as well as red bell peppers.
10) Protein
Protein is important for healthy muscles and healthy bones.
- Eat legumes, whole grains, nuts and seeds on a daily basis [3,106–108]. Legumes include soya products (tofu, tempeh, soya milk, soya flour, soya mince, etc.), all kinds of beans, lentils, and peas as well as peanuts and peanut butter. Pistachios, hemp seeds, quinoa, and amaranth can also add relevant amounts of protein to your diet.
- Eat enough calories. Most vegans eat enough calories. But if you do not eat enough calories your body will use the protein you eat as calories (for "energy production"), and you might end up with too little protein and you might lose muscle mass.
Healthy vegan lifestyle
References
1. Johnsen, J. B. & Fønnebø, V. Vitamin
B12-mangel ved strengt vegetabilsk kosthold. Hvorfor følger noen et slikt
kosthold, og hva vil de gjøre ved B12-mangel? Abstract.
Tidsskrift for den Norske laegeforening
tidsskrift for praktisk medicin, ny raekke 111, 1, 62–64 (1991)
2. Schüpbach, R., Wegmüller, R., Berguerand, C. et al. Micronutrient
status and intake in omnivores, vegetarians and vegans in Switzerland. European journal of nutrition 56, 1, 283–293 (2017)
3. Sobiecki, J. G., Appleby, P. N., Bradbury,
K. E. et al. High compliance with
dietary recommendations in a cohort of meat eaters, fish eaters, vegetarians,
and vegans: results from the European Prospective Investigation into Cancer and
Nutrition-Oxford study. Nutrition
research (New York, N.Y.) 36, 5,
464–477 (2016)
4. Woo, K. S., Kwok, T. C. Y., Celermajer, D.
S. Vegan diet, subnormal vitamin B-12 status and cardiovascular health. Nutrients 6, 8, 3259–3273 (2014)
5. Bor, M. V., Castel-Roberts, K. M. von,
Kauwell, G. P. et al. Daily intake of
4 to 7 microg dietary vitamin B-12 is associated with steady concentrations of
vitamin B-12-related biomarkers in a healthy young population. The American journal of clinical nutrition
91, 3, 571–577 (2010)
6. Carmel R (2006) Cobalamin (Vitamin B12). In Modern nutrition in health and disease.
10th ed., pp. 482–497, [Shils ME, Shike M and Ross AC et al., editors]. Philadelphia: Lippincott Williams & Wilkins
7. Institute of Medicine (IOM) (1998) Dietary reference intakes for Thiamin,
Riboflavin, Niacin, Vitamin B6, Folate, Vitamin B12, Papntothenic Acid, Biotin,
and Choline: A report of the Standing Committee on the Scientific Evaluation of
Dietary Reference Intakes Food and Nutrition Board, Institute of Medicine.
Washington DC: Nat. Acad. Press
8. Luhby AL, Cooperman JM, Donnenfeld AM:
Herrero JM et al. Observations on
transfer of vitamin B12 from mother to fetus and newborn. Am J Dis Child 96,
532–533 (1958)
9. Norris J How recommendations were
formulated. Last updated: August 2013. http://www.veganhealth.org/b12/formula
(accessed June 2017)
10. Haddad, E. H., Berk, L. S., Kettering, J. D. et al. Dietary intake and biochemical,
hematologic, and immune status of vegans compared with nonvegetarians. The American journal of clinical nutrition
70, 3 Suppl, 586 (1999)
11. Heyssel, R. M., Bozian, R. C., Darby, W. J. et al. Vitamin
B12 turnover in man. The assimilation of vitamin B12 from natural foodstuff by
man and estimates of minimal daily dietary requirements. The American journal of clinical nutrition 18, 3, 176–184 (1966)
12. Obeid, R., Fedosov, S. N., Nexo, E. Cobalamin
coenzyme forms are not likely to be superior to cyano- and hydroxyl-cobalamin
in prevention or treatment of cobalamin deficiency. Molecular nutrition & food research 59, 7, 1364–1372 (2015)
13. Adams, J. F., Ross, S. K., Mervyn, L. et al. Absorption of cyanocobalamin,
coenzyme B 12 methylcobalamin, and hydroxocobalamin at different dose levels. Scandinavian journal of gastroenterology
6, 3, 249–252 (1971)
14. Carmel, R. Mandatory fortification of the food
supply with cobalamin: an idea whose time has not yet come. Journal of inherited metabolic disease 34, 1, 67–73 (2011)
15. Deshmukh, U. S., Joglekar, C. V., Lubree, H. G. et al. Effect of physiological doses of
oral vitamin B12 on plasma homocysteine: a randomized, placebo-controlled,
double-blind trial in India. European
journal of clinical nutrition 64, 5,
495–502 (2010)
16. Berlin, H., Berlin, R., Brante, G. Oral treatment
of pernicious anemia with high doses of vitamin B12 without intrinsic factor. Acta medica Scandinavica 184, 4, 247–258 (1968)
17. Donaldson, M. S. Metabolic vitamin B12 status
on a mostly raw vegan diet with follow-up using tablets, nutritional yeast, or
probiotic supplements. Annals of
nutrition & metabolism 44, 5-6,
229–234 (2000)
18. Gomollón, F., Gargallo, C. J., Muñoz, J. F. et al. Oral Cyanocobalamin is Effective
in the Treatment of Vitamin B12 Deficiency in Crohn's Disease. Nutrients 9, 3 (2017)
19. Appleby, P. N. & Key, T. J. The long-term
health of vegetarians and vegans. The
Proceedings of the Nutrition Society 75,
3, 287–293 (2016)
20. Appleby, P., Roddam, A., Allen, N. et al. Comparative fracture risk in
vegetarians and nonvegetarians in EPIC-Oxford. European journal of clinical nutrition 61, 12, 1400–1406 (2007)
21. Dyett, P., Rajaram, S., Haddad, E. H. et al. Evaluation of a validated food
frequency questionnaire for self-defined vegans in the United States. Nutrients 6, 7, 2523–2539 (2014)
22. Fang, A., Li, K., Guo, M. et al. Long-Term Low Intake of Dietary Calcium
and Fracture Risk in Older Adults With Plant-Based Diet: A Longitudinal Study
From the China Health and Nutrition Survey. Journal
of bone and mineral research the official journal of the American Society for
Bone and Mineral Research 31, 11,
2016–2023 (2016)
23. Mangels, A. R. Bone nutrients for vegetarians.
The American journal of clinical
nutrition 100 Suppl 1, 469
(2014)
24. Morales-Torres, J. & Gutiérrez-Ureña, S.
The burden of osteoporosis in Latin America. Osteoporosis international a journal established as result of
cooperation between the European Foundation for Osteoporosis and the National
Osteoporosis Foundation of the USA 15,
8, 625–632 (2004)
25. Nachshon, L. & Katz, Y. [The importance of
"milk bones" to "wisdom bones" - cow milk and bone health -
lessons from milk allergy patients.] Abstract. Harefuah 155, 3, 163
(2016)
26. Rizzo, N. S., Jaceldo-Siegl, K., Sabate, J. et al. Nutrient profiles of vegetarian
and nonvegetarian dietary patterns. Journal
of the Academy of Nutrition and Dietetics 113, 12, 1610–1619 (2013)
27. Thorpe, D. L., Knutsen, S. F., Beeson, W. L. et al. Effects of meat consumption and
vegetarian diet on risk of wrist fracture over 25 years in a cohort of peri-
and postmenopausal women. Public health
nutrition 11, 6, 564–572 (2008)
28. Tucker, K. L. Vegetarian diets and bone
status. The American journal of clinical
nutrition 100 Suppl 1, 329S-35S
(2014)
29. Messina, V. & Messina, M. Soy products as
sources of calcium in the diets of chinese americans. Journal of the American Dietetic Association 110, 12, 1812-3; author reply 1813 (2010)
30. Reid, M. A., Marsh, K. A., Zeuschner, C. L. et al. Meeting
the nutrient reference values on a vegetarian diet. The Medical journal of Australia 199, 4 Suppl, 40 (2013)
31. Weaver, C. M., Proulx, W. R., Heaney, R.
Choices for achieving adequate dietary calcium with a vegetarian diet. The American journal of clinical nutrition
70, 3 Suppl, 543 (1999)
32. de Abajo, Francisco J. de, Rodríguez-Martín,
S., Rodríguez-Miguel, A. et al. Risk
of Ischemic Stroke Associated With Calcium Supplements With or Without Vitamin
D: A Nested Case-Control Study. Journal
of the American Heart Association 6,
5 (2017)
33. Böhmer, H., Müller, H., Resch, K. L. Calcium
supplementation with calcium-rich mineral waters: a systematic review and
meta-analysis of its bioavailability. Osteoporosis
international a journal established as result of cooperation between the
European Foundation for Osteoporosis and the National Osteoporosis Foundation
of the USA 11, 11, 938–943
(2000)
34. Vitoria, I., Maraver, F., Ferreira-Pêgo, C. et al. The calcium concentration of
public drinking waters and bottled mineral waters in Spain and its contribution
to satisfying nutritional needs. Nutricion
hospitalaria 30, 1, 188–199
(2014)
35. Bressani, R., Turcios, J. C., Colmenares de
Ruiz, A. S. et al. Effect of
processing conditions on phytic acid, calcium, iron, and zinc contents of
lime-cooked maize. Journal of
agricultural and food chemistry 52, 5,
1157–1162 (2004)
36. Hambidge, K. M., Krebs, N. F., Westcott, J. L. et al. Absorption of calcium from
tortilla meals prepared from low-phytate maize. The American journal of clinical nutrition 82, 1, 84–87 (2005)
37. Islas-Rubio, A. R., La Barca, A. M. C. de,
Molina-Jacott, L. E. et al.
Development and evaluation of a nutritionally enhanced multigrain tortilla
snack. Plant foods for human nutrition
(Dordrecht, Netherlands) 69, 2,
128–133 (2014)
38. Monárrez-Espino J, Béjar-Lío GI, Vázquez-Mendoza
G Adecuación de la dieta servida a escolares en albergues indigenistas de la
Sierra Tarahumara, México. Salud Pública
Méx 52, 23–29 (2010)
39. Pappa, M. R., Palomo, P. P. de, Bressani, R.
Effect of lime and wood ash on the nixtamalization of maize and tortilla
chemical and nutritional characteristics. Plant
foods for human nutrition (Dordrecht, Netherlands) 65, 2, 130–135 (2010)
40. Rosado, J. L., López, P., Morales, M. et al. Bioavailability of energy,
nitrogen, fat, zinc, iron and calcium from rural and urban Mexican diets. The British journal of nutrition 68, 1, 45–58 (1992)
41. Rosado, J. L., Díaz, M., Rosas, A. et al. Calcium absorption from corn
tortilla is relatively high and is dependent upon calcium content and liming in
Mexican women. The Journal of nutrition
135, 11, 2578–2581 (2005)
42. Serna-Saldivar, S. O., Amaya Guerra, C. A.,
Herrera Macias, P. et al. Evaluation
of the lime-cooking and tortilla making properties of quality protein maize
hybrids grown in Mexico. Plant foods for
human nutrition (Dordrecht, Netherlands) 63, 3, 119–125 (2008)
43. Holick, M. F. The vitamin D deficiency
pandemic: Approaches for diagnosis, treatment and prevention. Reviews in endocrine & metabolic
disorders (2017)
44. Ho-Pham, L. T., Vu, B. Q., Lai, T. Q. et al. Vegetarianism, bone loss,
fracture and vitamin D: a longitudinal study in Asian vegans and non-vegans. European journal of clinical nutrition 66, 1, 75–82 (2012)
45. Kristensen, N. B., Madsen, M. L., Hansen, T.
H. et al. Intake of macro- and micronutrients
in Danish vegans. Nutrition journal 14, 115 (2015)
46. Outila, T. A., Kärrkkäinen, M. U. M., Seppänen,
R. H. et al. Dietary
Intake of Vitamin D in Premenopausal, Healthy Vegans was Insufficient to
Maintain Concentrations of Serum 25-hydroxyvitamin D and Intact Parathyroid
Hormone Within Normal Ranges During the Winter in Finland. Journal of the American Dietetic Association 100, 4, 434–441 (2000)
47. Plehwe, W. E. & Carey, R. P. L. Spinal
surgery and severe vitamin D deficiency. The
Medical journal of Australia 176, 9,
438–439 (2002)
48. Smith, T. J., Tripkovic, L., Damsgaard, C. T. et al. Estimation of the dietary
requirement for vitamin D in adolescents aged 14-18 y: a dose-response,
double-blind, randomized placebo-controlled trial. The American journal of clinical nutrition 104, 5, 1301–1309 (2016)
49. Ustianowski, A., Shaffer, R., Collin, S. et al. Prevalence and associations of
vitamin D deficiency in foreign-born persons with tuberculosis in London. The Journal of infection 50, 5, 432–437 (2005)
50. Vidailhet, M., Mallet, E., Bocquet, A. et al. Vitamin D: still a topical
matter in children and adolescents. A position paper by the Committee on
Nutrition of the French Society of Paediatrics. Archives de pediatrie organe officiel de la Societe francaise de
pediatrie 19, 3, 316–328 (2012)
51. Jäpelt, R. B. & Jakobsen, J. Vitamin D in
plants: a review of occurrence, analysis, and biosynthesis. Frontiers in plant science 4, 136 (2013)
52. Davidsson, L. Are vegetarians an 'at risk
group' for iodine deficiency? The British
journal of nutrition 81, 1, 3–4
(1999)
53. Elorinne, A.-L., Alfthan, G., Erlund, I. et al. Food and Nutrient Intake and
Nutritional Status of Finnish Vegans and Non-Vegetarians. PloS one 11, 2, e0148235
(2016)
54. Fields, C., Dourson, M., Borak, J.
Iodine-deficient vegetarians: a hypothetical perchlorate-susceptible
population? Regulatory toxicology and
pharmacology RTP 42, 1, 37–46
(2005)
55. Krajcovicová-Kudlácková, M., Bucková, K.,
Klimes, I. et al. Iodine deficiency
in vegetarians and vegans. Annals of
nutrition & metabolism 47, 5,
183–185 (2003)
56. Leung, A. M., Lamar, A., He, X. et al. Iodine status and thyroid
function of Boston-area vegetarians and vegans. The Journal of clinical endocrinology and metabolism 96, 8, E1303-7 (2011)
57. Lightowler, H. J. & Davies, G. J.
Assessment of iodine intake in vegans: weighed dietary record vs duplicate
portion technique. European journal of
clinical nutrition 56, 8,
765–770 (2002)
58. Lightowler, H. J. & Davies, G. J. Iodine
intake and iodine deficiency in vegans as assessed by the duplicate-portion
technique and urinary iodine excretion. The
British journal of nutrition 80, 6,
529–535 (1998)
59. Kanaka, C., Schütz, B., Zuppinger, K. A. Risks
of alternative nutrition in infancy: a case report of severe iodine and
carnitine deficiency. European journal of
pediatrics 151, 10, 786–788
(1992)
60. Remer, T., Neubert, A., Manz, F. Increased
risk of iodine deficiency with vegetarian nutrition. The British journal of nutrition 81, 1, 45–49 (1999)
61. García-Casal, M. N., Landaeta, M., Adrianza de
Baptista, G. et al. Valores de
referencia de hierro, yodo, zinc, selenio, cobre, molibdeno, vitamina C,
vitamina E, vitamina K, carotenoides y polifenoles para la población
venezolana. Archivos latinoamericanos de nutricion 63, 4,
338–361 (2013)
62. Rohner, F., Zimmermann, M., Jooste, P. et al. Biomarkers
of nutrition for development--iodine review. The Journal of nutrition 144,
8, 1322S-1342S (2014)
63. Zimmermann, M. B. & Andersson, M.
Assessment of iodine nutrition in populations: past, present, and future. Nutrition reviews 70, 10, 553–570 (2012)
64. Davis, B. C. & Kris-Etherton, P. M.
Achieving optimal essential fatty acid status in vegetarians: current knowledge
and practical implications. The American
journal of clinical nutrition 78, 3
Suppl, 640 (2003)
65. Domenichiello, A. F., Chen, C. T., Trepanier,
M.-O. et al. Whole
body synthesis rates of DHA from α-linolenic acid are greater than brain DHA
accretion and uptake rates in adult rats. Journal
of lipid research 55, 1, 62–74
(2014)
66. Fayet-Moore, F., Baghurst, K., Meyer, B. J.
Four Models Including Fish, Seafood, Red Meat and Enriched Foods to Achieve
Australian Dietary Recommendations for n-3 LCPUFA for All Life-Stages. Nutrients 7, 10, 8602–8614 (2015)
67. Harris, W. S. Achieving optimal n-3 fatty acid
status: the vegetarian's challenge… or not. The
American journal of clinical nutrition 100
Suppl 1, 449S-52S (2014)
68. Sanders, T. A. B. DHA status of vegetarians. Prostaglandins, leukotrienes, and essential
fatty acids 81, 2-3, 137–141
(2009)
69. Saunders, A. V., Davis, B. C., Garg, M. L.
Omega-3 polyunsaturated fatty acids and vegetarian diets. Med J Aust 1, 2, 22–26
(2012)
70. Demark-Wahnefried, W., Polascik, T. J.,
George, S. L. et al. Flaxseed supplementation
(not dietary fat restriction) reduces prostate cancer proliferation rates in
men presurgery. Cancer epidemiology,
biomarkers & prevention a publication of the American Association for
Cancer Research, cosponsored by the American Society of Preventive Oncology
17, 12, 3577–3587 (2008)
71. Hackshaw-McGeagh, L. E., Perry, R. E., Leach,
V. A. et al. A systematic review of
dietary, nutritional, and physical activity interventions for the prevention of
prostate cancer progression and mortality. Cancer
causes & control CCC 26, 11,
1521–1550 (2015)
72. EFSA Opinion on the safety of ‘Chia seeds
(Salvia hispanica L.) and ground whole Chia seeds’ as a food ingredient. EFSA Journal 7, 4, 996 (2009)
73. Mohd Ali, N., Yeap, S. K., Ho, W. Y. et al. The promising future of chia,
Salvia hispanica L. Journal of
biomedicine & biotechnology 2012,
171956 (2012)
74. Ullah, R., Nadeem, M., Khalique, A. et al. Nutritional and therapeutic
perspectives of Chia (Salvia hispanica L.): a review. Journal of food science and technology 53, 4, 1750–1758 (2016)
75. Cottin, S. C., Sanders, T. A., Hall, W. L. The
differential effects of EPA and DHA on cardiovascular risk factors. The Proceedings of the Nutrition Society
70, 2, 215–231 (2011)
76. Geppert, J., Kraft, V., Demmelmair, H. et al. Microalgal docosahexaenoic acid
decreases plasma triacylglycerol in normolipidaemic vegetarians: a randomised
trial. The British journal of nutrition
95, 4, 779–786 (2006)
77. Sarter, B., Kelsey, K. S., Schwartz, T. A. et al. Blood docosahexaenoic acid and
eicosapentaenoic acid in vegans: Associations with age and gender and effects
of an algal-derived omega-3 fatty acid supplement. Clinical nutrition (Edinburgh, Scotland) 34, 2, 212–218 (2015)
78. Waldmann, A., Koschizke, J. W., Leitzmann, C. et al. Dietary
iron intake and iron status of German female vegans: results of the German
vegan study. Annals of nutrition &
metabolism 48, 2, 103–108 (2004)
79. Gorczyca, D., Prescha, A., Szeremeta, K. et al. Iron status and dietary iron
intake of vegetarian children from Poland. Annals
of nutrition & metabolism 62, 4,
291–297 (2013)
80. Craig, W. J. Iron status of vegetarians. The American journal of clinical nutrition
59, 5 Suppl, 1233 (1994)
81. Gibson, R. S., Heath, A.-L. M., Szymlek-Gay,
E. A. Is iron and zinc nutrition a concern for vegetarian infants and young
children in industrialized countries? The
American journal of clinical nutrition 100
Suppl 1, 459S-68S (2014)
82. Hurrell, R. & Egli, I. Iron
bioavailability and dietary reference values. The American journal of clinical nutrition 91, 5, 1461S-1467S (2010)
83. Hunt, J. R. Moving toward a plant-based diet:
are iron and zinc at risk? Nutrition
reviews 60, 5 Pt 1, 127–134
(2002)
84. Hunt, J. R. Bioavailability of iron, zinc, and
other trace minerals from vegetarian diets. The
American journal of clinical nutrition 78,
3 Suppl, 633 (2003)
85. Quintaes, K. D., Amaya-Farfan, J., Tomazini,
F. M. et al. Mineral Migration and
Influence of Meal Preparation in Iron Cookware on the Iron Nutritional Status
of Vegetarian Students. Ecology of Food
and Nutrition 46, 2, 125–141
(2007)
86. Sanders TAB (2012) Vegetarian diets. In Human nutrition. 12th ed., pp. 355–363,
[Geissler CA and Powers HJ, editors]. Edinburgh: Churchill Livingstone Elsevier
87. Ball, M. J. & Ackland, M. L. Zinc intake
and status in Australian vegetarians. The
British journal of nutrition 83, 1,
27–33 (2000)
88. Saunders, A. V., Craig, W. J., Baines, S. K.
Zinc and vegetarian diets. Med J Aust 1, 2, 17–21 (2012)
89. Hildbrand SM (2015) Bedeutung des
Jod/Selen-Quotienten und des Ferritins für das Auftreten einer
Autoimmunthyreoiditis (AIT) bei omnivor, lakto-vegetarisch und vegan sich
ernährenden Personen: Eine epidemiologische klinische Querschnittstudie.
Dissertation zum Erwerb des Doktorgrades der Medizin,
Ludwig-Maximilians-Universität
90. Hoeflich, J., Hollenbach, B., Behrends, T. et al. The
choice of biomarkers determines the selenium status in young German vegans and
vegetarians. The British journal of
nutrition 104, 11, 1601–1604
(2010)
91. Lightowler, H. J. & Davies, G. J.
Micronutrient intakes in a group of UK vegans and the contribution of
self-selected dietary supplements. The
journal of the Royal Society for the Promotion of Health 120, 2, 117–124 (2000)
92. Thomson, C. D., Chisholm, A., McLachlan, S. K. et al. Brazil
nuts: an effective way to improve selenium status. The American journal of clinical nutrition 87, 2, 379–384 (2008)
93. Colpo, E., Vilanova, C. D. d. A., Brenner
Reetz, L. G. et al. A single
consumption of high amounts of the Brazil nuts improves lipid profile of
healthy volunteers. Journal of nutrition
and metabolism 2013,
11348568653185 (2013)
94. Martens, I. B. G., Cardoso, B. R., Hare, D. J. et al. Selenium status in preschool
children receiving a Brazil nut-enriched diet. Nutrition (Burbank, Los Angeles County, Calif.) 31, 11-12, 1339–1343 (2015)
95. Dumont, E., Vanhaecke, F., Cornelis, R.
Selenium speciation from food source to metabolites: a critical review. Analytical and bioanalytical chemistry 385, 7, 1304–1323 (2006)
96. Benstoem, C., Goetzenich, A., Kraemer, S. et al. Selenium and its supplementation
in cardiovascular disease--what do we know? Nutrients
7, 5, 3094–3118 (2015)
97. Ogawa-Wong, A. N., Berry, M. J., Seale, L. A.
Selenium and Metabolic Disorders: An Emphasis on Type 2 Diabetes Risk. Nutrients 8, 2, 80 (2016)
98. Thomson, C. D. Assessment of requirements for
selenium and adequacy of selenium status: a review. European journal of clinical nutrition 58, 3, 391–402 (2004)
99. Wrobel, J. K., Power, R., Toborek, M.
Biological activity of selenium: Revisited. IUBMB
life 68, 2, 97–105 (2016)
100. Xia, Y., Hill, K. E., Byrne, D. W. et al. Effectiveness of selenium
supplements in a low-selenium area of China. The American journal of clinical nutrition 81, 4, 829–834 (2005)
101. Combs, G. F. Selenium in global food
systems. The British journal of nutrition
85, 5, 517–547 (2001)
102. Combs Jr GF & Combs SB (1986) The role of selenium in nutrition.
Orlando: Academic Press
103. Mondragón, M. C. & Jaffé, W. G. Consumo
de selenio en la ciudad de Caracas en comparación con el de otras ciudades del
mundo. Abstract. Archivos
latinoamericanos de nutricion 26, 3,
343–352 (1976)
104. Surai PF (2006) Selenium in nutrition and health. Nottingham: Nottingham University
Press
105. Pan American Health Organization (PAHO)
Nutritional situation in the Americas. Epidemiological
bulletin 15, 3, 1–6 (1994)
106. Lousuebsakul-Matthews, V., Thorpe, D. L.,
Knutsen, R. et al. Legumes and meat
analogues consumption are associated with hip fracture risk independently of
meat intake among Caucasian men and women: the Adventist Health Study-2. Public health nutrition 17, 10, 2333–2343 (2014)
107. Shams-White, M. M., Chung, M., Du, M. et al. Dietary protein and bone health:
a systematic review and meta-analysis from the National Osteoporosis
Foundation. The American journal of
clinical nutrition 105, 6,
1528–1543 (2017)
108. Marsh, K. A., Munn, E. A., Baines, S. K.
Protein and vegetarian diets. Med J Aust
1, 2, 7–10 (2012)
109. Torfadóttir, J. E., Uusi-Rasi, K.: Calcium - a scoping review for Nordic Nutrition Recommendations 2023. Food Nutr Res. 2023 Dec 19:67. doi: 10.29219/fnr.v67.10303. eCollection 2023 (2023)