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Vitamin B2 (Riboflavin)

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Author Information and Affiliations

Last Update: February 1, 2024.

Continuing Education Activity

Riboflavin, also known as vitamin B2, is a water-soluble vitamin that belongs to the vitamin B complex group. Clinicians frequently prescribe riboflavin as part of a combined formulation with other B complex vitamins as a prophylactic supplement to manage and treat vitamin B2 deficiency. Riboflavin deficiency is a rare condition as it is present in various food choices. However, individuals who follow a diet low in meat and milk, which are considered the best sources of riboflavin, and certain specific groups of people, such as pregnant women, children, and athletes, may be more susceptible to this deficiency. Milk and dairy products are rich in riboflavin and vitamin D. Dairy consumption is the primary source of vitamin D in Western diets. This is why riboflavin deficiency is rare among water-soluble vitamins.

The United States Food and Drug Administration (FDA) approved the ophthalmic formulation of riboflavin 5’-phosphate in treating corneal ectasia post-refractive surgery and managing progressive keratoconus. Off-label uses of oral riboflavin include migraine prophylaxis, neonates undergoing phototherapy, and addressing antiretroviral-induced lactic acidosis. This activity aims to elucidate the mechanism of action, adverse event profile, pharmacokinetics, administration, and pertinent interactions for interprofessional healthcare team members involved in treating patients with riboflavin deficiency and related conditions. 

Objectives:

  • Identify manifestations of riboflavin deficiency in diverse patient populations, recognizing signs and symptoms associated with this vitamin B2 insufficiency.
  • Implement timely evaluation and intervention strategies, incorporating evidence-based practices for managing riboflavin deficiency in various clinical scenarios.
  • Apply riboflavin supplementation judiciously, considering patient-specific factors, dosages, and formulation options to optimize therapeutic outcomes.
  • Coordinate care for patients with riboflavin deficiency by collaborating with interprofessional healthcare teams, integrating interventions seamlessly into broader healthcare plans, and ensuring continuity of treatment and follow-up.
Access free multiple choice questions on this topic.

Indications

Riboflavin, also known as vitamin B2, is a water-soluble vitamin that belongs to the vitamin B complex group. Clinicians frequently prescribe riboflavin as part of a combined formulation with other B complex vitamins as a prophylactic supplement to manage and treat vitamin B2 deficiency. Riboflavin deficiency is a rare condition as it is present in various food choices. However, individuals who follow a diet low in meat and milk, which are considered the best sources of riboflavin, and certain specific groups of people, as discussed below, may be more susceptible to this deficiency.[1]

Milk and dairy products are rich in riboflavin and vitamin D. Dairy consumption is the primary source of vitamin D in Western diets. This is why riboflavin deficiency is rare among water-soluble vitamins. However, an increased intake of semi-skimmed milk in developed countries depletes milk's riboflavin content. Although relatively stable, it easily degrades with light exposure. Milk in a glass bottle may contain less riboflavin if exposed to light.

Grain products possess low natural amounts, but fortification practices ensure that certain bread and cereals have become sources of riboflavin. Therefore, according to an article by Morgan KJ et al, high riboflavin levels were found in those who had cereals for breakfast.[2] Fatty fish are also excellent sources of riboflavin, and certain fruits and vegetables, especially dark green vegetables, contain reasonably high concentrations. Vegetarians with access to various fruits and vegetables can avoid deficiency, although intake may be lower than omnivores, and elderly vegetarians are at a higher risk.[3]

FDA-Approved Indication

The United States Food and Drug Administration (FDA) approved the ophthalmic formulation of riboflavin 5’-phosphate in treating corneal ectasia following refractive surgery and managing progressive keratoconus.[4] 

Off-Label Uses

Off-label uses of oral riboflavin include migraine prophylaxis, neonates undergoing phototherapy, and addressing antiretroviral-induced lactic acidosis.[5][6][7][8]

Groups of Individuals at a Higher Risk for Low Riboflavin Intake

Pregnant or lactating women and infants: Pregnancy demands higher riboflavin intake as it crosses the placenta. Therefore, if the maternal status is poor during gestation, the infant will likely have riboflavin deficiency. Breast milk riboflavin concentration may reflect maternal intake and can be improved by supplementation if maternal intake is low.

Children: Riboflavin deficiency among children is present in many regions of the world where inadequate levels of milk and meat are common in their diets.[1] Riboflavin deficiency among children in the Western world is prevalent in adolescents, especially girls, because of increased metabolic demand. 

Older individuals: With advancing age, an increasing requirement of riboflavin is due to the decreased efficiency of its absorption by the enterocytes.[9]

Athletes: Study results suggest that vigorous exercise may deplete riboflavin due to consuming the nutrients in the metabolic pathways.[10]

Eating disorders: Young women with anorexia nervosa or patients with malignancies and malabsorption syndromes, like celiac disease and short bowel syndrome, have been shown to have low riboflavin levels.[10] Patients with lactose intolerance are likely to have suboptimal intake since dairy products are a good source of riboflavin.

Long-term use of barbiturates: Long-term use of phenobarbital, as well as other barbiturates, can deplete riboflavin due to oxidation.[11]

Prominent Features of Riboflavin Deficiency

Although the clinical features of some vitamin deficiencies are similar and often coexist, the more common signs of riboflavin deficiency include dry, red, fissured, or ulcerated lips, angular cheilitis, dry, atrophic, magenta-red, or blackish tongue, seborrheic dermatitis on the face, hyperpigmentation of the scrotum or vulva, resembling zinc deficiency, conjunctivitis, sore throat, and fatigue.[12][13]

Mechanism of Action

Riboflavin is involved in the metabolism of macronutrients and the production of some other B-complex vitamins. The nutrient participates in redox reactions in the metabolic pathways through cofactors flavin adenine dinucleotide (FAD) and flavin mononucleotide (FMN), derived from riboflavin, by acting as electron carriers.[14] 

Riboflavin plays a principal role in the electron transport chain.[15] Inadequate riboflavin intake would be expected to disturb the intermediate steps of metabolism, with specific functional implications. The conversion of the amino acid tryptophan to niacin requires FAD. Similarly, converting vitamin B6 (pyridoxine) to the coenzyme pyridoxal 5’-phosphate needs FMN.[16] 

Riboflavin is also known as an antioxidant because it regenerates glutathione, a free radical scavenger.[17] Additionally, riboflavin is involved in growth and development, especially during fetal life, reproduction, and lactation.

Pharmacokinetics

Absorption: A small amount of riboflavin is present in foods as free riboflavin, a majority as its derivative flavin adenine dinucleotide (FAD), and a smaller amount as flavin mononucleotide (FMN). Intestinal bacteria also produce a small amount of riboflavin.[18] For the absorption of dietary riboflavin, a prerequisite is converting FAD and FMN to free riboflavin, catalyzed by enzymes called phosphatases in the enterocyte.[19] 

Absorption occurs predominantly in the small intestine through a carrier-mediated transport process by RFVT3 (riboflavin transporter).[20] The absorption of riboflavin is increased by food.

Distribution: Riboflavin is widely distributed between central and peripheral compartments. Riboflavin can cross the blood-brain barrier. RFVT2, encoded by SLC52A2 (solute carrier family 52 member-2), is responsible for the tissue distribution of riboflavin.[21] ABCG2 (ATP-binding cassette G2 transporter) is also responsible for transporting riboflavin into breast milk, CSF, semen, and bile.[15]

Metabolism: Riboflavin is converted to coenzymes within the cytoplasm of most tissues, including the liver, heart, and kidney. Riboflavin is metabolized by flavokinase to form FMN, which is converted to FAD by FMN adenylyltransferase (FMNAT).[22]

Elimination: The elimination half-life of riboflavin is approximately 1 h. Riboflavin is primarily excreted unchanged in the urine. Elimination in bile is <1%.[6]

Administration

Available Dosage Forms and Strengths

Riboflavin is also available as single-ingredient oral tablets of 25 mg, 50 mg, and 100 mg and oral capsules of 400 mg strengths. Riboflavin is often available in conjugation with other water-soluble multivitamins. Riboflavin 5’-phosphate is available as a 0.146% ophthalmic solution formulation.[4]

Adult Dosage

Recommended daily allowance for riboflavin:

  • Adults (aged 19 to 70): The dosage for women is 0.9 to 1.1 mg/d, and for men, it is 1.1 to 1.3 mg/d. These values are based on clinical evidence of deficiency in intake of less than 0.6 mg/d. The recommended daily allowance increases from 1.4 to 1.6 mg/d during pregnancy and lactation.
  • Adolescents (aged 10 to 18): The dosage is 0.9 to 1.3 mg/d.
  • Children (aged 1 to 9): The dosage is 0.5 to 0.6 mg/d.
  • Infants (aged 0 to 12 months): The dosage is 0.3 to 0.4 mg/d.[15]

The dose for supplementation is generally 50 to 100 mg daily.[23] Apart from supplementation in deficiency, it is also prescribed in some clinical situations as follows: 

Corneal Ectasia Following Refractory Surgery and Progressive Keratoconus

Riboflavin is available for topical ophthalmic use as riboflavin 5’-phosphate ophthalmic solution (0.146%) and riboflavin 5’-phosphate in 20% dextran solution (0.146%). These ophthalmic formulations are photo enhancers used in corneal collagen cross-linking to manage keratoconus and corneal ectasia after refractive surgery. Riboflavin-5'-phosphate induces the formation of singlet oxygen, which enables cross-linking. The corneal cross-linking system (KXL) leads to rapid cross-linking between collagen fibers.[24][25][26]

Migraine Prophylaxis

Riboflavin is effective for the prophylaxis of migraines. The American Academy of Neurology (AAN) and American Headache Society guidelines endorse the use. The usual dose for migraine prophylaxis is 400 mg daily.[6][5]

Neonates Undergoing Phototherapy

The management of hyperbilirubinemia in the neonatal period is often done with phototherapy. However, phototherapy has been shown to degrade riboflavin and cause a deficiency in newborns. A prophylactic daily oral dose of riboflavin prevents the development of the deficiency.[7]

Antiretroviral-Induced Lactic Acidosis

This rare syndrome results from a group of antiretroviral drugs used to treat HIV infection called nonnucleoside reverse transcriptase inhibitors (NNRTI). Discontinuation of the drug and treatment with riboflavin causes its reversal.[8]

Specific Patient Populations

Hepatic impairment: No dose adjustment is required. 

Renal impairment: No dose adjustment is necessary.[27]

Pregnancy considerations: Riboflavin requirements increase during pregnancy. Low consumption of dairy products during pregnancy is associated with riboflavin deficiency.[28] Riboflavin deficiency is a possible risk factor for preeclampsia.[29]

Breastfeeding considerations: Riboflavin requirement is increased during lactation. Maternal deficiency of riboflavin may predispose the infant to riboflavin deficiency.[30] Dairy products and meat are required to provide adequate riboflavin for the mother and infant.[30]

Pediatric patients: Rare inborn errors of metabolism, such as glutaric acidemia type 1 or multiple acyl-coenzyme A (CoA) dehydrogenase deficiencies (MADD), in which there is a defect in the formation of riboflavin-dependent enzymes, or Brown-Vialetto-Van Laere syndrome, in which there is a defect in a riboflavin transporter may respond to high-dose riboflavin therapy.[31]

Older patients: Older patients with acute illness often have suboptimal riboflavin status, and supplementation with riboflavin and other nutrients is recommended.[32]

Adverse Effects

Riboflavin is relatively safe to administer as it has limited water solubility, and enterocytes do not absorb the excess. However, caution is necessary when administering large doses to pregnant women. Riboflavin may cause benign urine discoloration.

Drug-Drug Interactions

  • Tricyclic antidepressants and tetracyclines can interfere with riboflavin utilization.[15]
  • Chronic alcohol exposure impairs intestinal absorption and renal reabsorption of riboflavin.[33]

Contraindications

No absolute contraindications to riboflavin intake are apparent. In patients with prior hypersensitivity reactions, riboflavin should be avoided due to the risk of anaphylaxis.[34]

Monitoring

Blood levels and urinary excretion are not sensitive markers of riboflavin deficiency, and the preferred method for assessing riboflavin status is stimulation of the FAD-dependent erythrocyte glutathione reductase. The results express an activation coefficient-EGRAC (erythrocyte glutathione reductase activity coefficient) such that the poorer the riboflavin status, the higher the activation coefficient.[9] An EGRAC above 1.3 indicates riboflavin deficiency.[27] The recommendation is to monitor the healing of epithelial defects when using ophthalmic riboflavin formulation.[35]

Toxicity

No observable toxicities with intakes of riboflavin are from food sources many times the recommended daily allowance. Riboflavin has high water solubility and limited absorption. No adverse effects are from high riboflavin intakes from foods or supplements up to 400 mg daily for at least 3 months. The Food and Nutrition Board has not established the upper limit for riboflavin as it has a good safety profile. High-dose riboflavin does not cause toxicity as excess riboflavin is excreted in the urine.[36]

Enhancing Healthcare Team Outcomes

The body does not store riboflavin in large amounts; only small reserves exist in the liver, heart, and kidneys. Most people obtain riboflavin from their diet. Those on restricted diet plans and many individuals who do not consume dairy are prone to developing riboflavin deficiency. Other risk factors for riboflavin deficiency include pregnancy, poverty, old age, depression, breastfeeding, phototherapy, and poor cognition. Riboflavin deficiency can present with many clinical features, leading to poor quality of life.

Given these facts, an interprofessional team approach that includes clinicians, pharmacists, nurses, and dieticians is required to prevent or correct this nutritional deficiency. Pharmacists play a relevant role in patient education. They are often the first-line professionals to see patients and can also recommend dosing to the prescribing clinician based on the indication. Nutritionists should emphasize the importance of adequate nutrition, exercise, and healthy weight.

For outpatients, a dietitian or nurse educator should be consulted to teach patients about rich riboflavin foods. The nurse also plays a critical role in educating pregnant mothers on the possibility of riboflavin deficiency when breastfeeding and the need to take supplements. Inborn errors of metabolism, such as Brown-Vialetto-Van Laere syndrome, require coordination between pediatricians and clinical geneticists. 

An ophthalmologist consultation is required to use riboflavin 5’-phosphate for keratoconus appropriately. Treatment by nurses who look after newborns who receive phototherapy for hyperbilirubinemia should be aware that this treatment can also cause riboflavin breakdown and the need for supplements.

Most cases of riboflavin deficiency are preventable by a proactive, interprofessional team approach between clinicians, nutritionists, specialists, pharmacists, and dieticians, which can optimize the treatment outcomes related to riboflavin supplementation. This approach can also decrease healthcare costs and improve nutrition status.[15][37][38] Working as an interprofessional team can adequately address the remediation of vitamin B2 deficiencies.

When treating riboflavin deficiency, the outcomes are good. The majority of symptoms improve within a few weeks or months. However, those who develop neurological abnormalities may have residual deficits that last for an extended period.[39] 

Review Questions

Image

Figure

Seborrheic Dermatitis Contributed by S bhimji, MD

References

1.
Oppenheimer SJ, Bull R, Thurnham DI. Riboflavin deficiency in Madang infants. P N G Med J. 1983 Mar;26(1):17-20. [PubMed: 6585094]
2.
Morgan KJ, Zabik ME, Leveille GA. The role of breakfast in nutrient intake of 5- to 12-year-old children. Am J Clin Nutr. 1981 Jul;34(7):1418-27. [PubMed: 6266245]
3.
Woo J, Kwok T, Ho SC, Sham A, Lau E. Nutritional status of elderly Chinese vegetarians. Age Ageing. 1998 Jul;27(4):455-61. [PubMed: 9884002]
4.
Belin MW, Lim L, Rajpal RK, Hafezi F, Gomes JAP, Cochener B. Corneal Cross-Linking: Current USA Status: Report From the Cornea Society. Cornea. 2018 Oct;37(10):1218-1225. [PubMed: 30067537]
5.
Holland S, Silberstein SD, Freitag F, Dodick DW, Argoff C, Ashman E., Quality Standards Subcommittee of the American Academy of Neurology and the American Headache Society. Evidence-based guideline update: NSAIDs and other complementary treatments for episodic migraine prevention in adults: report of the Quality Standards Subcommittee of the American Academy of Neurology and the American Headache Society. Neurology. 2012 Apr 24;78(17):1346-53. [PMC free article: PMC3335449] [PubMed: 22529203]
6.
Thompson DF, Saluja HS. Prophylaxis of migraine headaches with riboflavin: A systematic review. J Clin Pharm Ther. 2017 Aug;42(4):394-403. [PubMed: 28485121]
7.
Tan KL, Chow MT, Karim SM. Effect of phototherapy on neonatal riboflavin status. J Pediatr. 1978 Sep;93(3):494-7. [PubMed: 690775]
8.
Posteraro AF, Mauriello M, Winter SM. Riboflavin treatment of antiretroviral induced lactic acidosis and hepatic steatosis. Conn Med. 2001 Jul;65(7):387-90. [PubMed: 11508132]
9.
Boisvert WA, Mendoza I, Castañeda C, De Portocarrero L, Solomons NW, Gershoff SN, Russell RM. Riboflavin requirement of healthy elderly humans and its relationship to macronutrient composition of the diet. J Nutr. 1993 May;123(5):915-25. [PubMed: 8487103]
10.
Belko AZ, Obarzanek E, Roach R, Rotter M, Urban G, Weinberg S, Roe DA. Effects of aerobic exercise and weight loss on riboflavin requirements of moderately obese, marginally deficient young women. Am J Clin Nutr. 1984 Sep;40(3):553-61. [PubMed: 6475825]
11.
Husebye ESN, Riedel B, Bjørke-Monsen AL, Spigset O, Daltveit AK, Gilhus NE, Bjørk MH. Vitamin B status and association with antiseizure medication in pregnant women with epilepsy. Epilepsia. 2021 Dec;62(12):2968-2980. [PubMed: 34590314]
12.
Barthelemy H, Chouvet B, Cambazard F. Skin and mucosal manifestations in vitamin deficiency. J Am Acad Dermatol. 1986 Dec;15(6):1263-74. [PubMed: 2948974]
13.
Blanck HM, Bowman BA, Serdula MK, Khan LK, Kohn W, Woodruff BA., Bhutanese Refugee Investigation Group. Angular stomatitis and riboflavin status among adolescent Bhutanese refugees living in southeastern Nepal. Am J Clin Nutr. 2002 Aug;76(2):430-5. [PubMed: 12145018]
14.
Prentice AM, Bates CJ. A biochemical evaluation of the erythrocyte glutathione reductase (EC 1.6.4.2) test for riboflavin status. 1. Rate and specificity of response in acute deficiency. Br J Nutr. 1981 Jan;45(1):37-52. [PubMed: 7470436]
15.
Pinto JT, Zempleni J. Riboflavin. Adv Nutr. 2016 Sep;7(5):973-5. [PMC free article: PMC5015041] [PubMed: 27633112]
16.
Jarrett H, McNulty H, Hughes CF, Pentieva K, Strain JJ, McCann A, McAnena L, Cunningham C, Molloy AM, Flynn A, Hopkins SM, Horigan G, O'Connor C, Walton J, McNulty BA, Gibney MJ, Lamers Y, Ward M. Vitamin B-6 and riboflavin, their metabolic interaction, and relationship with MTHFR genotype in adults aged 18-102 years. Am J Clin Nutr. 2022 Dec 19;116(6):1767-1778. [PMC free article: PMC9761749] [PubMed: 36264281]
17.
Ashoori M, Saedisomeolia A. Riboflavin (vitamin B₂) and oxidative stress: a review. Br J Nutr. 2014 Jun 14;111(11):1985-91. [PubMed: 24650639]
18.
IINUMA S. Synthesis of riboflavin by intestinal bacteria. J Vitaminol (Kyoto). 1955 Feb 10;1(2):6-13. [PubMed: 13264325]
19.
Daniel H, Binninger E, Rehner G. Hydrolysis of FMN and FAD by alkaline phosphatase of the intestinal brush-border membrane. Int J Vitam Nutr Res. 1983;53(1):109-14. [PubMed: 6853053]
20.
Jin C, Yonezawa A. Recent advances in riboflavin transporter RFVT and its genetic disease. Pharmacol Ther. 2022 May;233:108023. [PubMed: 34662687]
21.
Zhang L, Li M, Cui Z, Chai D, Guan Y, Chen C, Wang W. Systematic analysis of the role of SLC52A2 in multiple human cancers. Cancer Cell Int. 2022 Jan 06;22(1):8. [PMC free article: PMC8739691] [PubMed: 34991609]
22.
Hirano G, Izumi H, Yasuniwa Y, Shimajiri S, Ke-Yong W, Sasagiri Y, Kusaba H, Matsumoto K, Hasegawa T, Akimoto M, Akashi K, Kohno K. Involvement of riboflavin kinase expression in cellular sensitivity against cisplatin. Int J Oncol. 2011 Apr;38(4):893-902. [PubMed: 21308351]
23.
Bourgonje AR, Otten AT, Sadaghian Sadabad M, von Martels JZH, Bulthuis MLC, Faber KN, van Goor H, Dijkstra G, Harmsen HJM. The effect of riboflavin supplementation on the systemic redox status in healthy volunteers: A post-hoc analysis of the RIBOGUT trial. Free Radic Biol Med. 2022 Sep;190:169-178. [PubMed: 35973668]
24.
Gore DM, Leucci MT, Koay SY, Kopsachilis N, Nicolae MN, Malandrakis MI, Anand V, Allan BD. Accelerated Pulsed High-Fluence Corneal Cross-Linking for Progressive Keratoconus. Am J Ophthalmol. 2021 Jan;221:9-16. [PubMed: 32818448]
25.
Ostacolo C, Caruso C, Tronino D, Troisi S, Laneri S, Pacente L, Del Prete A, Sacchi A. Enhancement of corneal permeation of riboflavin-5'-phosphate through vitamin E TPGS: a promising approach in corneal trans-epithelial cross linking treatment. Int J Pharm. 2013 Jan 20;440(2):148-53. [PubMed: 23046664]
26.
Woo JH, Iyer JV, Lim L, Hla MH, Mehta JS, Chan CM, Tan DT. Conventional Versus Accelerated Collagen Cross-Linking for Keratoconus: A Comparison of Visual, Refractive, Topographic and Biomechanical Outcomes. Open Ophthalmol J. 2017;11:262-272. [PMC free article: PMC5633701] [PubMed: 29081866]
27.
Clase CM, Ki V, Holden RM. Water-soluble vitamins in people with low glomerular filtration rate or on dialysis: a review. Semin Dial. 2013 Sep-Oct;26(5):546-67. [PMC free article: PMC4285924] [PubMed: 23859229]
28.
Higgins KA, Bi X, Davis BJ, Barraj LM, Scrafford CG, Murphy MM. Adequacy of total usual micronutrient intakes among pregnant women in the United States by level of dairy consumption, NHANES 2003-2016. Nutr Health. 2022 Dec;28(4):621-631. [PMC free article: PMC9716399] [PubMed: 35132897]
29.
Wacker J, Frühauf J, Schulz M, Chiwora FM, Volz J, Becker K. Riboflavin deficiency and preeclampsia. Obstet Gynecol. 2000 Jul;96(1):38-44. [PubMed: 10862839]
30.
Allen LH. B vitamins in breast milk: relative importance of maternal status and intake, and effects on infant status and function. Adv Nutr. 2012 May 01;3(3):362-9. [PMC free article: PMC3649471] [PubMed: 22585913]
31.
Chaya S, Zampoli M, Gray D, Booth J, Riordan G, Ndondo A, Fieggen K, Rusch J, van der Watt G, Pillay K, van der Westhuizen F, Menezes M, Wilmshurst J. The First Case of Riboflavin Transporter Deficiency in sub-Saharan Africa. Semin Pediatr Neurol. 2018 Jul;26:10-14. [PubMed: 29961494]
32.
Gariballa S, Forster S, Powers H. Riboflavin status in acutely ill patients and response to dietary supplements. JPEN J Parenter Enteral Nutr. 2009 Nov-Dec;33(6):656-61. [PubMed: 19644132]
33.
Subramanian VS, Subramanya SB, Ghosal A, Said HM. Chronic alcohol feeding inhibits physiological and molecular parameters of intestinal and renal riboflavin transport. Am J Physiol Cell Physiol. 2013 Sep;305(5):C539-46. [PMC free article: PMC3761153] [PubMed: 23804199]
34.
Ou LS, Kuo ML, Huang JL. Anaphylaxis to riboflavin (vitamin B2). Ann Allergy Asthma Immunol. 2001 Nov;87(5):430-3. [PubMed: 11730188]
35.
Beckman KA. Epithelium-on Corneal Collagen Cross-Linking with Hypotonic Riboflavin Solution in Progressive Keratoconus. Clin Ophthalmol. 2021;15:2921-2932. [PMC free article: PMC8273905] [PubMed: 34262252]
36.
Suwannasom N, Kao I, Pruß A, Georgieva R, Bäumler H. Riboflavin: The Health Benefits of a Forgotten Natural Vitamin. Int J Mol Sci. 2020 Jan 31;21(3) [PMC free article: PMC7037471] [PubMed: 32023913]
37.
Chan M, Kelly J, Batterham M, Tapsell L. A high prevalence of abnormal nutrition parameters found in predialysis end-stage kidney disease: is it a result of uremia or poor eating habits? J Ren Nutr. 2014 Sep;24(5):292-302. [PubMed: 25023456]
38.
Barile M, Giancaspero TA, Brizio C, Panebianco C, Indiveri C, Galluccio M, Vergani L, Eberini I, Gianazza E. Biosynthesis of flavin cofactors in man: implications in health and disease. Curr Pharm Des. 2013;19(14):2649-75. [PubMed: 23116402]
39.
Dror DK, Allen LH. Dairy product intake in children and adolescents in developed countries: trends, nutritional contribution, and a review of association with health outcomes. Nutr Rev. 2014 Feb;72(2):68-81. [PubMed: 24330063]

Disclosure: Basil Peechakara declares no relevant financial relationships with ineligible companies.

Disclosure: Reddog Sina declares no relevant financial relationships with ineligible companies.

Disclosure: Mohit Gupta declares no relevant financial relationships with ineligible companies.

Copyright © 2024, StatPearls Publishing LLC.

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