Tools
Vitamin B2 (Riboflavin)
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
Register For Free And Read The Full Article
Search engine and full access to all medical articles- 10 free questions in your specialty
- Free CME/CE Activities
- Free daily question in your email
- Save favorite articles to your dashboard
- Emails offering discounts
Learn more about a Subscription to StatPearls Point-of-Care
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]
Media
(Click Image to Enlarge)
Seborrheic Dermatitis
Contributed by S bhimji, MD
References
Oppenheimer SJ, Bull R, Thurnham DI. Riboflavin deficiency in Madang infants. Papua and New Guinea medical journal. 1983 Mar:26(1):17-20 [PubMed PMID: 6585094]
Morgan KJ, Zabik ME, Leveille GA. The role of breakfast in nutrient intake of 5- to 12-year-old children. The American journal of clinical nutrition. 1981 Jul:34(7):1418-27 [PubMed PMID: 6266245]
Woo J, Kwok T, Ho SC, Sham A, Lau E. Nutritional status of elderly Chinese vegetarians. Age and ageing. 1998 Jul:27(4):455-61 [PubMed PMID: 9884002]
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. doi: 10.1097/ICO.0000000000001707. Epub [PubMed PMID: 30067537]
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. doi: 10.1212/WNL.0b013e3182535d0c. Epub [PubMed PMID: 22529203]
Level 2 (mid-level) evidenceThompson DF, Saluja HS. Prophylaxis of migraine headaches with riboflavin: A systematic review. Journal of clinical pharmacy and therapeutics. 2017 Aug:42(4):394-403. doi: 10.1111/jcpt.12548. Epub 2017 May 8 [PubMed PMID: 28485121]
Level 1 (high-level) evidenceTan KL, Chow MT, Karim SM. Effect of phototherapy on neonatal riboflavin status. The Journal of pediatrics. 1978 Sep:93(3):494-7 [PubMed PMID: 690775]
Posteraro AF 3rd, Mauriello M, Winter SM. Riboflavin treatment of antiretroviral induced lactic acidosis and hepatic steatosis. Connecticut medicine. 2001 Jul:65(7):387-90 [PubMed PMID: 11508132]
Level 3 (low-level) evidenceBoisvert 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. The Journal of nutrition. 1993 May:123(5):915-25 [PubMed PMID: 8487103]
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. The American journal of clinical nutrition. 1984 Sep:40(3):553-61 [PubMed PMID: 6475825]
Level 1 (high-level) evidenceHusebye 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. doi: 10.1111/epi.17076. Epub 2021 Sep 30 [PubMed PMID: 34590314]
Barthelemy H, Chouvet B, Cambazard F. Skin and mucosal manifestations in vitamin deficiency. Journal of the American Academy of Dermatology. 1986 Dec:15(6):1263-74 [PubMed PMID: 2948974]
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. The American journal of clinical nutrition. 2002 Aug:76(2):430-5 [PubMed PMID: 12145018]
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. The British journal of nutrition. 1981 Jan:45(1):37-52 [PubMed PMID: 7470436]
Level 3 (low-level) evidencePinto JT, Zempleni J. Riboflavin. Advances in nutrition (Bethesda, Md.). 2016 Sep:7(5):973-5. doi: 10.3945/an.116.012716. Epub 2016 Sep 15 [PubMed PMID: 27633112]
Level 3 (low-level) evidenceJarrett 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. The American journal of clinical nutrition. 2022 Dec 19:116(6):1767-1778. doi: 10.1093/ajcn/nqac240. Epub [PubMed PMID: 36264281]
Ashoori M, Saedisomeolia A. Riboflavin (vitamin B₂) and oxidative stress: a review. The British journal of nutrition. 2014 Jun 14:111(11):1985-91. doi: 10.1017/S0007114514000178. Epub 2014 Mar 20 [PubMed PMID: 24650639]
IINUMA S. Synthesis of riboflavin by intestinal bacteria. The Journal of vitaminology. 1955 Feb 10:1(2):6-13 [PubMed PMID: 13264325]
Daniel H, Binninger E, Rehner G. Hydrolysis of FMN and FAD by alkaline phosphatase of the intestinal brush-border membrane. International journal for vitamin and nutrition research. Internationale Zeitschrift fur Vitamin- und Ernahrungsforschung. Journal international de vitaminologie et de nutrition. 1983:53(1):109-14 [PubMed PMID: 6853053]
Level 3 (low-level) evidenceJin C, Yonezawa A. Recent advances in riboflavin transporter RFVT and its genetic disease. Pharmacology & therapeutics. 2022 May:233():108023. doi: 10.1016/j.pharmthera.2021.108023. Epub 2021 Oct 15 [PubMed PMID: 34662687]
Level 3 (low-level) evidenceZhang 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 international. 2022 Jan 6:22(1):8. doi: 10.1186/s12935-021-02432-7. Epub 2022 Jan 6 [PubMed PMID: 34991609]
Level 1 (high-level) evidenceHirano 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. International journal of oncology. 2011 Apr:38(4):893-902. doi: 10.3892/ijo.2011.938. Epub 2011 Feb 9 [PubMed PMID: 21308351]
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 radical biology & medicine. 2022 Sep:190():169-178. doi: 10.1016/j.freeradbiomed.2022.08.008. Epub 2022 Aug 13 [PubMed PMID: 35973668]
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. American journal of ophthalmology. 2021 Jan:221():9-16. doi: 10.1016/j.ajo.2020.08.021. Epub 2020 Aug 18 [PubMed PMID: 32818448]
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. International journal of pharmaceutics. 2013 Jan 20:440(2):148-53. doi: 10.1016/j.ijpharm.2012.09.051. Epub 2012 Oct 6 [PubMed PMID: 23046664]
Level 3 (low-level) evidenceWoo 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. The open ophthalmology journal. 2017:11():262-272. doi: 10.2174/1874364101711010262. Epub 2017 Aug 29 [PubMed PMID: 29081866]
Clase CM, Ki V, Holden RM. Water-soluble vitamins in people with low glomerular filtration rate or on dialysis: a review. Seminars in dialysis. 2013 Sep-Oct:26(5):546-67. doi: 10.1111/sdi.12099. Epub 2013 Jul 17 [PubMed PMID: 23859229]
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. Nutrition and health. 2022 Dec:28(4):621-631. doi: 10.1177/02601060211072325. Epub 2022 Feb 8 [PubMed PMID: 35132897]
Wacker J, Frühauf J, Schulz M, Chiwora FM, Volz J, Becker K. Riboflavin deficiency and preeclampsia. Obstetrics and gynecology. 2000 Jul:96(1):38-44 [PubMed PMID: 10862839]
Allen LH. B vitamins in breast milk: relative importance of maternal status and intake, and effects on infant status and function. Advances in nutrition (Bethesda, Md.). 2012 May 1:3(3):362-9. doi: 10.3945/an.111.001172. Epub 2012 May 1 [PubMed PMID: 22585913]
Level 3 (low-level) evidenceChaya 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. Seminars in pediatric neurology. 2018 Jul:26():10-14. doi: 10.1016/j.spen.2017.03.002. Epub 2017 Apr 4 [PubMed PMID: 29961494]
Level 3 (low-level) evidenceGariballa S, Forster S, Powers H. Riboflavin status in acutely ill patients and response to dietary supplements. JPEN. Journal of parenteral and enteral nutrition. 2009 Nov-Dec:33(6):656-61. doi: 10.1177/0148607109336602. Epub 2009 Jul 30 [PubMed PMID: 19644132]
Level 1 (high-level) evidenceSubramanian VS, Subramanya SB, Ghosal A, Said HM. Chronic alcohol feeding inhibits physiological and molecular parameters of intestinal and renal riboflavin transport. American journal of physiology. Cell physiology. 2013 Sep:305(5):C539-46. doi: 10.1152/ajpcell.00089.2013. Epub 2013 Jun 26 [PubMed PMID: 23804199]
Level 3 (low-level) evidenceOu LS, Kuo ML, Huang JL. Anaphylaxis to riboflavin (vitamin B2). Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology. 2001 Nov:87(5):430-3 [PubMed PMID: 11730188]
Beckman KA. Epithelium-on Corneal Collagen Cross-Linking with Hypotonic Riboflavin Solution in Progressive Keratoconus. Clinical ophthalmology (Auckland, N.Z.). 2021:15():2921-2932. doi: 10.2147/OPTH.S318317. Epub 2021 Jul 7 [PubMed PMID: 34262252]
Suwannasom N, Kao I, Pruß A, Georgieva R, Bäumler H. Riboflavin: The Health Benefits of a Forgotten Natural Vitamin. International journal of molecular sciences. 2020 Jan 31:21(3):. doi: 10.3390/ijms21030950. Epub 2020 Jan 31 [PubMed PMID: 32023913]
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? Journal of renal nutrition : the official journal of the Council on Renal Nutrition of the National Kidney Foundation. 2014 Sep:24(5):292-302. doi: 10.1053/j.jrn.2014.03.008. Epub 2014 Jul 10 [PubMed PMID: 25023456]
Level 2 (mid-level) evidenceBarile 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. Current pharmaceutical design. 2013:19(14):2649-75 [PubMed PMID: 23116402]
Level 3 (low-level) evidenceDror DK, Allen LH. Dairy product intake in children and adolescents in developed countries: trends, nutritional contribution, and a review of association with health outcomes. Nutrition reviews. 2014 Feb:72(2):68-81. doi: 10.1111/nure.12078. Epub 2013 Dec 13 [PubMed PMID: 24330063]
Level 3 (low-level) evidence