Skip to content

Free shipping on orders over $65

Subscribe and save 20%

Refer a friend and get $15 off

  • Free shipping on orders over $65

  • Subscribe and save 20%

  • Refer a friend and get $15 off

Why Do We Need Folate?

What is folate?

Folate is an essential B vitamin sometimes known as vitamin B9, folacin or pteroylmonoglutamic acid. It’s essential to the body so DNA and RNA can be created, and to metabolise amino acids required for cell division[1]. Cells divide for a number of reasons including to replace dead and damaged cells and for growth.

What foods are high in folate?

Folate occurs naturally in a wide variety of foods of both plant and animal origin; great food sources include the following:

  • Spinach
  • Brussel sprouts
  • Cabbage
  • Broccoli
  • Beans and legumes
  • Yeast and beef extracts
  • Oranges and fresh orange juice
  • Wheat bran and other whole grains
  • Poultry
  • Pork
  • Shellfish
  • Liver

Huel products

Some foods are also fortified with additional folic acid. This is used to treat folate-deficiency anaemia, additionally it’s advised as a supplement for women who are trying for a baby[2, 3].

The main role of folate is to function as a coenzyme where it supports the metabolism of energy, DNA and the synthesis of five amino acids including the essential amino acid methionine[4]. As folate is essential in DNA metabolism, it is involved with gene expression and cell differentiation[5]. Folate’s function is closely linked to that of vitamin B12[4].

Recommended intake levels of folate

In the US, the preferred unit of measurement for folate intake is Dietary Folate Equivalent (DFE)[6] and the Daily Values (DVs) are based on this. DFE reflects the higher bioavailability of the folic acid form compared to that of food folates[7]. The following indicates how DFEs are calculated:

    • 1μg of food folate = 1μg DFE
    • 1μg of folic acid in fortified food or as a supplement consumed with food = 1.7μg DFE
    • 1μg of folic acid supplement consumed on an empty stomach = 2μg of DFE

    The DV for folate is 400μg DFE per day[8]. This level provides enough to prevent folate deficiency and for adequate levels of folate in red blood cells. Typical daily intakes in the US are 455μg DFE for females and 602μg DFE for males so by consuming a varied diet, the DV is easily met[9, 10].

    Can you get too much folate?

    Although no adverse effects have been associated with the consumption of large amounts of folate from food, there have been concerns regarding very high intakes of supplementary folic acid. Both the EU and the US have provided a tolerable upper limit recommendation of 1,000μg per day, a level based on intakes from supplementation and fortification[11]. Naturally occurring folate from foods has no tolerable upper limit[11].

    Levels of folic acid significantly higher than the tolerable upper limit are at risk of masking megaloblastic anemia caused by an underlying vitamin B12 deficiency. It is advised for people aged over 50 years or those with a history of bowel cancer not to take folic acid supplements containing more than 200μg per day[12-14].

    Deficiency of folate

    Severe deficiency of either folate or vitamin B12 can lead to megaloblastic anemia a condition that features a low number of large red blood cells called megaloblasts[15]. Symptoms include tiredness, heart palpitations, shortness of breath, sore tongue, change in color of skin or hair, irritability and possibly changes in behavior, especially so in children[16]. There is a complex interaction between folate and vitamin B12, and also with both vitamin B6 and iron to some degree, so that deficiency of one may mask a deficiency of another[4]. Megaloblastic anemia caused by a dietary deficiency or impaired metabolism of vitamin B12 is known as pernicious anemia, whereas megaloblastic anemia caused as a result of folate intake or metabolism is known as folate-deficiency anemia[15].

    Folate deficiency is most commonly a result of inadequate dietary intake[4]. Deficiency can also be due to an increased requirement for folate as a result of the body excreting more than usual or from alcoholism or smoking[4, 17-21]. There are a number of medications that interfere with folate metabolism; these include aspirin, ibuprofen, some anti-epileptic drugs, and some oral contraceptives when taken in large doses[22, 23]. There is also research indicating that the effects of excessive UV light, like tanning beds, can be associated with deficiency[24].

    Additionally, a defect in the enzyme homocysteine methyltransferase or a deficiency of vitamin B12 may lead to a ‘methyl-trap’ of tetrahydrofolate (THF). THF is a derivative of folate that occurs in metabolism. In this condition, THF is converted to methyl-THF, and this cannot be metabolized and leads to subsequent folate deficiency anemia[25].

    Absorption of folate takes place in the small intestine, and when in intestinal cells it binds to specific receptor proteins. Inflammatory intestinal diseases, such as Crohn’s disease, coeliac disease, colitis or chronic enteritis, may be associated with a reduced activity of these proteins required for folate absorption so may contribute to folate deficiency[4].

    Folic acid supplementation

    The most common supplementary form is folic acid which, is synthetically derived and used to treat folate-deficiency anemia[26]. As discussed above, caution should be taken to avoid excessive amounts of folic acid supplements.

    Studies have shown that women who are trying to conceive and supplement with additional folic acid have a massive reduction in the risk of babies being born with neural tube defects (NTDs) like spina bifida[27]. The advice is for women to take 400μg of folic acid supplements whilst they are trying for a baby until week 12 of pregnancy[6]. Low blood levels of folate during the early stages of pregnancy have been cited to be the cause of more than 60% of the incidences of NTDs in babies[27-29].

    Another form of folate that’s available as a supplement and an alternative to folic acid is L-methylfolate, also known as L-5-methyltetrahydrofolate, which is often naturally derived. This form has been shown to have comparable activity, bioavailability, and absorption to folic acid and has the advantage of both not interacting with certain drugs and offering some protection against problems regarding vitamin B12 deficiency[30-34].

    MTHFR gene mutation: folate vs. folic acid

    Methylenetetrahydrofolate reductase (MTHFR) is an enzyme produced from the MTHFR gene, which is involved in the metabolism of the amino acid homocysteine via a number of processes that also involves THF, folate and vitamin B12[35]. When homocysteine isn’t metabolised correctly, it can build up in the blood vessels and cause inflammation which can be involved in the disease process of cardiovascular disease (CVD) like heart disease and stroke[36]. A high level of homocysteine, known as hyperhomocysteinemia, is a risk factor for CVD and has also been linked to impaired kidney function[37, 38]. This may happen due to a deficiency in folate or vitamin B12, either as a result of inadequate dietary intake of either vitamin, or from an impaired metabolism from thyroid hormone insufficiency, kidney disease, certain medications or from a genetic origin[39]. High levels of homocysteine may also be associated with increased cancer risk[40-42] and can mask vitamin B12 status[43, 44].

    There are two main variants of a mutation that can occur to the MTHFR gene and these, in more extreme cases, can lead to a build-up of homocysteine in the blood or high levels in the urine known as homocystinuria. The two mutations are the C677T polymorphism and the rarer A1298C, and there are sub-variants of each[45]. People can have a full or partial mutation, and as many as 30 to 40% of North Americans and Europeans have the presence of C677T polymorphism[46]. Not everyone with the full mutation has elevated homocysteine levels, although for women with the MTHFR gene mutation there is the increased risk of NTDs in their children[47].

    People with an MTHFR gene mutation may benefit from a higher than normal intake of dietary folate or from supplementing with L-methylfolate. This is because food-derived folate and L-methylfolate are metabolized in a way that they will not accumulate[48]. Therefore, in people with a low vitamin B12 status - that’s not a result of a poor dietary intake - the advice is to avoid folic acid fortified foods and supplements, in preference for L-methylfolate supplements[49, 50].

    Folate in Huel

    In Huel Powder v3.0, over 20% of the folate is provided by the main ingredients, mainly the oats and flaxseed. In Huel Black Edition, around 12% of the folate is from the main ingredients, mainly the flaxseed, In Huell Ready-to-drink, around 20% of the folate is from the main ingredients, again, mainly the oats, flaxseed and also brown rice flour. The forms of additional folate used in all Huel products are types of L-methylfolate based on the advantages that this form has over folic acid.

    References

    1. Chan Y-M, et al. Folate. Adv Nutr. 2013; 4(1):123-5.
    2. Board IoMFaN. Dietary Reference Intakes: Thiamin, Riboflavin, Niacin, Vitamin B6, Folate, Vitamin B12, Pantothenic Acid, Biotin, and Choline. Washington, DC: National Academy Press. 1998.
    3. Drugs.com. Folic Acid. Date Accessed: 01/23/2020. [Available from: https://www.drugs.com/monograph/folic-acid.html]
    4. Institute LP. Oregon State University. Folate. Date Accessed: 01/23/2020. [Available from: https://lpi.oregonstate.edu/mic/vitamins/folate]
    5. Mason JB, et al. Folate and carcinogenesis: developing a unifying hypothesis. Adv Enzyme Regul. 2000; 40:127-41.
    6. Dietary Reference Intakes for Thiamin, Riboflavin, Niacin, Vitamin B6, Folate, Vitamin B12, Pantothenic Acid, Biotin, and Choline. The National Academies Collection: Reports funded by National Institutes of Health. Washington (DC)1998.
    7. Bailey LB. Dietary reference intakes for folate: the debut of dietary folate equivalents. Nutr Rev. 1998; 56(10):294-9.
    8. Nutrition F-CfFSaA. U.S. Department of Health and Human Services. A Food Labeling Guide - Guidance for Industry. Date Accessed: 01/23/2020. [Available from: https://www.fda.gov/files/food/published/Food-Labeling-Guide-%28PDF%29.pdf]
    9. Supplements NIoHooD. U.S. Department of Health & Human Services. Folate - Facet Sheet for Health Professionals. Date Accessed: 01/23/2020. [Available from: https://ods.od.nih.gov/factsheets/folate-HealthProfessional/]
    10. Statistics NCfH. Centers for Disease Control and Prevention. What We Eat in America, DHHS-USDA Dietary Survey Integration. Date Accessed: 01/23/2020. [Available from: https://www.cdc.gov/nchs/nhanes/wweia.htm]
    11. Scientific Committee on Food - Scientific Panel on Dietetic Products NaA. Tolerable Upper Intake Levels for Vitamins and Minerals. European Food Safety Authority. 2006.
    12. Association BD. Folic Acid: Food Fact Sheet. Date Accessed: 01/23/2020. [Available from: https://www.bda.uk.com/resource/folic-acid.html]
    13. Morris MS, et al. Folate and vitamin B-12 status in relation to anemia, macrocytosis, and cognitive impairment in older Americans in the age of folic acid fortification. Am J Clin Nutr. 2007; 85(1):193-200.
    14. Morris MS, et al. Circulating unmetabolized folic acid and 5-methyltetrahydrofolate in relation to anemia, macrocytosis, and cognitive test performance in American seniors. Am J Clin Nutr. 2010; 91(6):1733-44.
    15. Nagao T, et al. Diagnosis and treatment of macrocytic anemias in adults. J Gen Fam Med. 2017; 18(5):200-4.
    16. Haslam N, et al. An audit of the investigation and treatment of folic acid deficiency. J R Soc Med. 1998; 91(2):72-3.
    17. Halsted CH, et al. Folate deficiency, methionine metabolism, and alcoholic liver disease. Alcohol. 2002; 27(3):169-72.
    18. Halsted CH, et al. Metabolic interactions of alcohol and folate. J Nutr. 2002; 132(8 Suppl):2367S-72S.
    19. Stark KD, et al. Maternal smoking is associated with decreased 5-methyltetrahydrofolate in cord plasma. Am J Clin Nutr. 2007; 85(3):796-802.
    20. Hutson JR, et al. Folic acid transport to the human fetus is decreased in pregnancies with chronic alcohol exposure. PLoS One. 2012; 7(5):e38057.
    21. Pfeiffer CM, et al. Race-ethnicity is related to biomarkers of iron and iodine status after adjusting for sociodemographic and lifestyle variables in NHANES 2003-2006. J Nutr. 2013; 143(6):977S-85S.
    22. Apeland T, et al. Antiepileptic drugs as independent predictors of plasma total homocysteine levels. Epilepsy Res. 2001; 47(1-2):27-35.
    23. Wilson SM, et al. Oral contraceptive use: impact on folate, vitamin B(6), and vitamin B(1)(2) status. Nutr Rev. 2011; 69(10):572-83.
    24. Borradale D, et al. Exposure to solar ultraviolet radiation is associated with a decreased folate status in women of childbearing age. J Photochem Photobiol B. 2014; 131:90-5.
    25. Hoffbrand AV, et al. The history of folic acid. Br J Haematol. 2001; 113(3):579-89.
    26. Drugs.com. Folic Acid. Date Accessed: 01/23/2020. [Available from: https://www.drugs.com/monograph/folic-acid.html]
    27. Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. MRC Vitamin Study Research Group. Lancet. 1991; 338(8760):131-7.
    28. Czeizel AE, et al. Prevention of the first occurrence of neural-tube defects by periconceptional vitamin supplementation. N Engl J Med. 1992; 327(26):1832-5.
    29. Force USPST, et al. Folic Acid Supplementation for the Prevention of Neural Tube Defects: US Preventive Services Task Force Recommendation Statement. JAMA. 2017; 317(2):183-9.
    30. Bailey SW, et al. The extremely slow and variable activity of dihydrofolate reductase in human liver and its implications for high folic acid intake. Proc Natl Acad Sci U S A. 2009; 106(36):15424-9.
    31. Litynski P, et al. Effect of low doses of 5-methyltetrahydrofolate and folic acid on plasma homocysteine in healthy subjects with or without the 677C-->T polymorphism of methylenetetrahydrofolate reductase. Eur J Clin Invest. 2002; 32(9):662-8.
    32. Pietrzik K, et al. Folic acid and L-5-methyltetrahydrofolate: comparison of clinical pharmacokinetics and pharmacodynamics. Clin Pharmacokinet. 2010; 49(8):535-48.
    33. Smulders YM, et al. Cellular folate vitamer distribution during and after correction of vitamin B12 deficiency: a case for the methylfolate trap. Br J Haematol. 2006; 132(5):623-9.
    34. Willems FF, et al. Pharmacokinetic study on the utilisation of 5-methyltetrahydrofolate and folic acid in patients with coronary artery disease. Br J Pharmacol. 2004; 141(5):825-30.
    35. Varga EA, et al. Cardiology patient pages. Homocysteine and MTHFR mutations: relation to thrombosis and coronary artery disease. Circulation. 2005; 111(19):e289-93.
    36. Cattaneo M. Hyperhomocysteinemia, atherosclerosis and thrombosis. Thromb Haemost. 1999; 81(2):165-76.
    37. Jager A, et al. Serum homocysteine levels are associated with the development of (micro)albuminuria: the Hoorn study. Arterioscler Thromb Vasc Biol. 2001; 21(1):74-81.
    38. Moake JL. Professional Version. Hyperhomocysteinemia. Date Accessed: 01/23/2020. [Available from: https://www.msdmanuals.com/en-gb/professional/hematology-and-oncology/thrombotic-disorders/hyperhomocysteinemia]
    39. Ganguly P, et al. Role of homocysteine in the development of cardiovascular disease. Nutr J. 2015; 14:6-.
    40. Cole BF, et al. Folic acid for the prevention of colorectal adenomas: a randomized clinical trial. JAMA. 2007; 297(21):2351-9.
    41. Ebbing M, et al. Cancer incidence and mortality after treatment with folic acid and vitamin B12. JAMA. 2009; 302(19):2119-26.
    42. Rees JR, et al. Unmetabolized Folic Acid, Tetrahydrofolate, and Colorectal Adenoma Risk. Cancer Prev Res (Phila). 2017; 10(8):451-8.
    43. Reynolds EH. Benefits and risks of folic acid to the nervous system. J Neurol Neurosurg Psychiatry. 2002; 72(5):567-71.
    44. Selhub J, et al. In vitamin B12 deficiency, higher serum folate is associated with increased total homocysteine and methylmalonic acid concentrations. Proc Natl Acad Sci U S A. 2007; 104(50):19995-20000.
    45. Center GaRDI. U.S. Department of Health & human Services. MTHFR gene variant. Date Accessed: 01/23/2020. [Available from: https://rarediseases.info.nih.gov/diseases/10953/mthfr-gene-mutation]
    46. Dean L. Methylenetetrahydrofolate Reductase Deficiency. In: Pratt V, et al., editors. Medical Genetics Summaries. Bethesda (MD)2012.
    47. Botto LD, et al. 5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HuGE review. Am J Epidemiol. 2000; 151(9):862-77.
    48. Scaglione F, et al. Folate, folic acid and 5-methyltetrahydrofolate are not the same thing. Xenobiotica; the fate of foreign compounds in biological systems. 2014; 44(5):480-8.
    49. Pfeiffer CM, et al. Unmetabolized folic acid is detected in nearly all serum samples from US children, adolescents, and adults. J Nutr. 2015; 145(3):520-31.
    50. Arnarson A. Healthline. Folic Acid vs. Folate — What’s the Difference? Date Accessed: 01/23/2020. [Available from: https://www.healthline.com/nutrition/folic-acid-vs-folate]

    Your Cart

    Oops! Your cart is empty

    Shop All

    Nutritionally Complete Powders

    Ready-to-drink Meals

    Greens & Superfoods

    High-Protein Snacks

    Vitamin & Energy Drinks

    Hot Meals

    Secure Checkout