Vitamin B₂ and its status in Vegetarians and Vegans

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The main goal of this review was to briefly highlight the key points of today’s knowledge about the role and metabolism of vitamin B₂ as well as to compare its status in vegans, vegetarians, and omnivores according to present data. Biologically active forms of water-soluble vitamin B₂ (riboflavin) are represented by flavin mononucleotide (FMN) and flavin adenine diphosphate (FAD), which are coenzymes in the reactions of the electron transport chain and the pyruvate dehydrogenase complex. Riboflavin is also involved in the metabolism of fatty acids, the synthesis of cholesterol and steroid hormones. Riboflavin also participates in the folate cycle. Vitamin B₂ is crucial for the metabolism of other vitamins. FMN is necessary for the formation of the active form of vitamin B₆, while FAD is necessary for the synthesis of niacin. Severe clinical insufficiency of vitamin B₂ is not common. Besides insufficient riboflavin consumption, hypothyroidism can also be a cause of vitamin B₂ deficiency as thyroxine regulates the conversion of riboflavin to its active forms - FMN and FAD. Lack of riboflavin can cause tissue damage; especially of the epithelial, reproductive, and nervous system. The variety of its manifestations is related to the fact that riboflavin deficiency also disrupts the metabolism of vitamins B₆, or PP. Similarly, riboflavin deficiency can also disrupt the folate cycle, increasing the level of homocysteine which damages vascular intima and leads to endothelial dysfunction and atherosclerosis as a result. Rapid urinary excretion of riboflavin makes it safe even if taken in a high dose, changing the urine colour into bright-yellow. This safety of riboflavin makes it unharmful to be used as an oral tracer for monitoring compliance in clinical research. Ultra-high doses of riboflavin (more than 400 mg/day) can cause diarrhoea or polyuria. The content of vitamin B₂ in animal-derived products is higher than in plant-based ones. This also determines its lower intake in vegans and vegetarians compared to omnivores. While there is a shred of evidence that plant-based diets increase the production of bioavailable riboflavin by the gut microbiota, this does not appear to be sufficient to completely compensate for the vegetarians’/vegans’ reduced dietary intake of vitamin B₂, as most of the researches point the fact that vegans and vegetarians are more prone to lack vitamin B₂ than omnivores. At the same time, it should be noted that there exists no universally adopted optimal method for assessing the status of vitamin B₂ in the body. Further research and standardization of methods may ease to assess the prevalence and risks of riboflavin deficiency in various dietary groups.

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作者简介

R. Ranjit

Рeoples’ Friendship University of Russia (RUDN University) named after Patrice Lumumba; State Budgetary Healthcare Centre "Oncological Centre number 1 named after S.S. Yudin" of the Healthcare Department of Moscow City; Melodia Vitae, International

Email: rajesh.ranjit@mail.ru
ORCID iD: 0000-0002-4255-4197

Oncologist, Research Scientist and Assistant, Medical institute, Department of Oncology, Radiology and Nuclear Medicine named after Academician V.P. Kharchenko

俄罗斯联邦, 6 Miklukho-Maklaya st, Moscow, 117198; 18A Zagorodnoye highway, Moscow, 117151

A. Galchenko

Melodia Vitae, International

编辑信件的主要联系方式.
Email: gav.jina@gmail.com
ORCID iD: 0000-0001-7286-5044
SPIN 代码: 3833-9938

Research Scientist

俄罗斯联邦

参考

  1. Institute of Medicine. Dietary Reference Intakes for Thiamin, Riboflavin, Niacin, Vitamin B6, Folate, Vitamin B12, Pantothenic Acid, Biotin, and Choline. Washington (DC): National Academies Press (US); 1998.
  2. Ross A.C., Caballero B.H., Cousins R.J. et al. Modern nutrition in health and disease. 11th ed. Wolters Kluwer Health, Lippincott Williams & Wilkins. 2014; 1616 p.
  3. Shah A., Kumar Y., Rohan S., Hazra A.B. Efficient Chemical and Enzymatic Syntheses of FAD Nucleobase Analogues and Their Analysis as Enzyme Cofactors. ChemBioChem. 2023; 24(11):e202300055.
  4. Whitehouse D.G., May B., Moore A.L. Respiratory Chain and ATP Synthase. Reference Module in Biomedical Sciences. Elsevier; 2019.
  5. Patel M.S., Nemeria N.S., Furey W., Jordan F. The Pyruvate Dehydrogenase Complexes: Structure-based Function and Regulation. J Biol Chem. 2014; 289(24):16623.
  6. Moxley M.A., Beard D.A., Bazil J.N. Global Kinetic Analysis of Mammalian E3 Reveals pH-dependent NAD+/NADH Regulation, Physiological Kinetic Reversibility, and Catalytic Optimum. J Biol Chem. 2016; 291(6):2712–2730.
  7. Olfat N., Ashoori M., Saedisomeolia A. Riboflavin is an an-tioxidant: a review update. Br J Nutr. 2022; 128(10):1887–1895.
  8. Curtabbi A., Enríquez J.A. The ins and outs of the flavin mononucleotide cofactor of respiratory complex I. IUBMB Life. 2022; 74(7):629–44.
  9. Dourado D.F.A.R., Swart M., Carvalho A.T.P. Why the Flavin Adenine Dinucleotide (FAD) Cofactor Needs To Be Covalently Linked to Complex II of the Electron-Transport Chain for the Conversion of FADH2 into FAD. Chemistry. 2018; 24(20):5246–52.
  10. Batista A.P., Kletzin A., Pereira M.M. The dihydrolipoamide dehydrogenase from the crenarchaeon Acidianus ambivalens. FEMS Microbiol Lett. 2008; 281(2):147–54.
  11. Zuhra K., Augsburger F., Majtan T., Szabo C. Cystathionine-β-synthase: Molecular Regulation and Pharmacological Inhibition. Biomolecules. 2020; 10(5):697.
  12. D'Souza S.W., Glazier J.D. Homocysteine Metabolism in Pregnancy and Developmental Impacts. Front Cell Dev Biol. 2022; 10:802285.
  13. Munteanu C., Schwartz B. B Vitamins, Glucoronolactone and the Immune System: Bioavailability, Doses and Efficiency. Nutrients. 2023; 16(1):24.
  14. Pinto J., Rivlin R. Handbook of vitamins. 2013; p.191–256.
  15. Argueta E.A., Amoh A.N., Kafle P., Schneider T.L. Unusual non-enzymatic flavin catalysis enhances understanding of flavoenzymes. FEBS Lett. 2015; 589(8):880–884.
  16. Pei J., Pan X., Wei G., Hua Y. Research progress of glutathione peroxidase family (GPX) in redoxidation. Front Pharmacol. 2023; 14:1147414.
  17. Coppo L., Mishra P., Siefert N. et al. A substitution in the glutathione reductase lowers electron leakage and inflammation in modern humans. Sci Adv. 2022; 8(1):eabm1148.
  18. Coates P.M. Encyclopedia of dietary supplements. Informa Healthcare; 2010. 898 p.
  19. Szczuko M., Ziȩtek M., Kulpa D., Seidler T. Riboflavin – Properties, occurrence and its use in medicine. Pteridines. 2019; 30(1):33–47.
  20. Krishnamurthy H.K., Reddy S., Jayaraman V. et al. Effect of Micronutrients on Thyroid Parameters. J Thyroid Res. 2021; 2021:1865483.
  21. Lysne V., Strandler H.S. Riboflavin: a scoping review for Nordic Nutrition Recommendations 2023. Food Nutr Res. 2023; 67:10.29219/fnr.v67.10315.
  22. Galimberti F., Mesinkovska N.A. Skin findings associated with nutritional deficiencies. Cleve Clin J Med. 2016; 83(10):731–739.
  23. Cherng Z.C., Boyles A., Legardeur B. et al. Effects of riboflavin and folic acid supplementation on plasma homocysteine levels in healthy subjects. Am J Med Sci. 2006; 331(2):65–71.
  24. Guthikonda S., Haynes W.G. Homocysteine: role and implications in atherosclerosis. Curr Atheroscler Rep. 2006; 8(2):100–106.
  25. Ramanujam V.M., Anderson K.E., Grady J.J. et al. Riboflavin as an oral tracer for monitoring compliance in clinical research. Open Biomark J. 2011; 2011(4):1–7.
  26. Mahabadi N., Bhusal A., Banks S.W. Riboflavin Deficiency. British Medical Journal. Treasure Island (FL): StatPearls Publishing; 2022.
  27. Ramanujam V.M.S., Nayeem F., Anderson K.E. et al. Riboflavin as an independent and accurate biomarker for adherence in a randomized double-blind and placebo-controlled clinical trial. Biomarkers. 2017; 22(6):516.
  28. Silberstein SD, Goadsby PJ. Migraine: preventive treatment. Cephalalgia. 2002; 22(7):491–512.
  29. Ramanujam V.M.S., Anderson K.E., Grady J.J. et al. Riboflavin as an oral tracer for monitoring compliance in clinical research. Open Biomark J. 2011; 2011(4):7.
  30. State sanitary and epidemiological regulation of the Russian Federation. Food hygiene and balanced diet. Guidelines 2.3.1.0253-21. Norms of physiological needs for energy and nutrients for various groups of the population of the Russian Federation. Moscow. 2021, Jul.
  31. D-A-CH (German Society for Nutrition, Austrian Society for Nutrition S.S. for N. Reference values for nutrient intake. Bonn, Germany. 2015.
  32. Nordic Council of Ministers. Nordic Nutrition Recommen-dations. Integrating nutrition and physical activity. Copen-hagen, Denmark. 2014, Mar.
  33. WHO/FAO (World Health Organization/Food and Agriculture Organization of the United Nations). Vitamin and mineral requirements in human nutrition: report of a joint FAO/WHO expert consultation. Bangkok, Thailand. 2004.
  34. Afssa (Agence francaise de securite sanitaire des aliments). Apports nutritionnels conseilles pour la population francaise. Paris, France. 2001.
  35. Health Council of the Netherlands. Dietary reference intakes: calcium, vitamin D, thiamin, riboflavin, niacin, pantothenic acid, and biotin. 2000.
  36. SCF (Scientific Committee for Food). Nutrient and energy intakes for the European Community. Reports of the Scientific Committee for Food, 31st Series. Luxembourg. 1993.
  37. DH (Department of Health). Dietary reference values for food energy and nutrients for the United Kingdom. Report of the Panel on Dietary Reference Values of the Committee on Medical Aspects of Food Policy. London, UK. 1991.
  38. McCormick D.B. Riboflavin. In: Erdman J.W., MacDonald I.A., Zeisel S.H., editors. Present Knowledge in Nutrition. 10th ed. Washington, DC: Wiley-Blackwell; 2012. p. 280–92.
  39. Said H.M., Ross A.C. Modern nutrition in health and disease. 11th ed. Ross A.C., Caballero B., Cousins R.J., Tucker K.L., Ziegler T.R., editors. Baltimore, MD: Wolters Kluwer Health Adis (ESP); 2014. 325–330 p.
  40. Pinto J.T., Zempleni J. Riboflavin. Adv Nutr. 2016; 7(5):975.
  41. Arumugam M., Raes J., Pelletier E. et al. Enterotypes of the human gut microbiome. Nature. 2011; 473(7346):174–80.
  42. Tomova A., Bukovsky I., Rembert E. et al. The Effects of Vegetarian and Vegan Diets on Gut Microbiota. Front Nutr. 2019; 6:47.
  43. Hossain K.S., Amarasena S., Mayengbam S. B Vitamins and Their Roles in Gut Health. Microorganisms. 2022; 10(6):1168.
  44. Yoshii K., Hosomi K., Sawane K., Kunisawa J. Metabolism of Dietary and Microbial Vitamin B Family in the Regulation of Host Immunity. Front Nutr. 2019; 6:48.
  45. U.S. Department of Agriculture, Agricultural Research Service. 2019.
  46. Federal Register. Food Labeling: Revision of the Nutrition and Supplement Facts Labels. 2016.
  47. Janelle K.C., Barr S.I. Nutrient Intakes and Eating Behavior scores of Vegetarian and Nonvegetarian Women. J Am Diet Assoc. 1995; 95(2):180–189.
  48. Sobiecki J.G., Appleby P.N., Bradbury K.E., Key T.J. 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. Nutr Res. 2016; 36(5):464–477.
  49. Larsson C.L., Johansson G.K. Dietary intake and nutritional status of young vegans and omnivores in Sweden. Am J Clin Nutr. 2002; 76(1):100–106.
  50. Elorinne A.L., Alfthan G., Erlund I. et al. Food and nutrient intake and nutritional status of Finnish vegans and non-vegetarians. PLoS One. 2016; 11(2):e0148235.
  51. Davey G.K., Spencer E.A., Appleby P.N. et al. 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):259–268.
  52. Weikert C., Trefflich I., Menzel J. et al. Vitamin and Mineral Status in a Vegan Diet. Dtsch Arztebl Int. 2020; 117(35–36):575–582.
  53. Kristensen N.B., Madsen M.L., Hansen T.H., et al. Intake of macro- and micronutrients in Danish vegans. Nutr J. 2015; 14:115.
  54. Allès B., Baudry J., Méjean C. et al. Comparison of Sociodemographic and Nutritional Characteristics between Self-Reported Vegetarians, Vegans, and Meat-Eaters from the NutriNet-Santé Study. Nutrients. 2017; 9(9):1023.
  55. Fallon N., Dillon S.A. Low Intakes of Iodine and Selenium Amongst Vegan and Vegetarian Women Highlight a Potential Nutritional Vulnerability. Front Nutr. 2020; 7:72.
  56. Haddad E.H., Berk L.S., Kettering J.D., et al. Dietary intake and biochemical, hematologic, and immune status of vegans compared with nonvegetarians. Am J Clin Nutr. 1999; 70(3 Suppl):586S–593S.
  57. Draper A., Lewis J., Malhotra N., Wheeler L.E. The energy and nutrient intakes of different types of vegetarian: a case for supplements? Br J Nutr. 1993; 69(1):3–19.
  58. Schüpbach R., Wegmüller R., Berguerand C., et al. Micronutrient status and intake in omnivores, vegetarians and vegans in Switzerland. Eur J Nutr. 2017; 56(1):283–293.
  59. Millet P., Guilland J.C., Fuchs F., Klepping J. Nutrient intake and vitamin status of healthy French vegetarians and nonvegetarians. Am J Clin Nutr. 1989; 50(4):718–727.
  60. Shultz T.D., Leklem J.E. Vitamin B-6 status and bioavailability in vegetarian women. Am J Clin Nutr. 1987; 46(4):647–651.
  61. Majchrzak D., Singer I., Männer M., et al. B-vitamin status and concentrations of homocysteine in Austrian omnivores, vegetarians and vegans. Ann Nutr Metab. 2007; 50(6):485–491.
  62. Gorbachev D.O., Sazonova O. V, Gilmiyarova F.N., et al. Characteristics of the nutritional status of vegetarians. Profil Meditsina. 2018; 21(3):51–56.
  63. Kowalska K., Brodowski J., Pokorska-Niewiada K., Szczuko M. The Change in the Content of Nutrients in Diets Eliminating Products of Animal Origin in Comparison to a Regular Diet from the Area of Middle-Eastern Europe. Nutrients. 2020; 12(10):2986.
  64. Alexy U., Fischer M., Weder S., et al. Nutrient intake and status of german children and adolescents consuming vegetarian, vegan or omnivore diets: Results of the vechi youth study. Nutrients. 2021; 13(5):1707.
  65. Vudhivai N., Ali A., Pongpaew P., et al. Vitamin B1, B₂ and B6 status of vegetarians. J Med Assoc Thail. 1991; 74(10):465–470.

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2. Figure 1. Structures of different forms of riboflavin

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3. Figure 2. Some of the physiological roles of vitamin B₂: PDC = Pyruvate dehydrogenase complex; DLT = Dihydrolipoyl transacetylase; TPP = Thiamine pyrophosphate; DLD = Dihydrolipoyl dehydrogenase

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4. Figure 3. Involvement of riboflavin in the metabolism of some other vitamins

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