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Acide folique ou folates : quelle différence ?

Folic acid or folates: what's the difference?

Are you pregnant or trying for a baby? We explain the difference between folic acid and vitamin B9, and why vitamin B9 is so important when planning a pregnancy and during pregnancy.

Contents

La vitamine B9 est la vitamine pour femme enceinte indispensable pendant la grossesse mais également en période de conception.

Did you know?

Dans les fruits et légumes, les folates sont principalement présents sous forme active.

Dietary folates

Les folates (vitamine B9) sont présents dans notre alimentation, notamment dans les légumes à feuilles vertes, les fruits, les légumes secs, le foie et la levure de bière. Cependant, les folates alimentaires sont peu stables, ils résistent mal à la lumière et à la chaleur. Les folates présents à l'état naturel peuvent être perdus jusqu'à 30 % lors de la transformation des aliments, en fonction du type de cuisson utilisée [1]. 
 

La cuisson à la vapeur des fruits et légumes n'entraîne pratiquement aucune perte de folates, contrairement à la cuisson à l'eau.

Dans les fruits et légumes, les folates sont principalement présents sous forme d'équivalent 5-MTHF, soit la forme directement utilisable dans l’organisme, avec une concentration totale de folates allant de 1-2 µg/100 g pour la pêche et la pastèque à une moyenne de 300 µg/100 g pour les épinards [2].

Why this product?

Folates Mama vitamin B9 capsules in methylated form, to support your body during conception and pregnancy.

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Should you supplement with folates?

Il est conseillé de consommer 600 microgrammes de vitamine B9 par jour lors de la grossesse ou de la conception, et il est souvent recommandé de prendre 400 microgrammes sous forme de complément alimentaire, en plus d’un régime alimentaire adapté. Acide folique et grossesse sont ainsi indissociables.

Vérifiez donc que votre complément alimentaire pour tomber enceinte ou votre complément alimentaire grossesse contient bien 400 microgrammes de vitamine B9. Nous verrons par la suite qu'il faut également qu'il soit présent sous forme méthylée. 

Why 5-MTHF?

Il est plus efficace pour améliorer le statut en folates.
Il passe outre la mutation du gène.
Il sera plus susceptible d’être transféré au fœtus.

Comparing the effectiveness of folic acid and 5-MTHF

Folate supplements are generally available in 2 forms: folic acid and 5-MTHF (found as a calcium salt or glucosamine salt). 

The problem? Folic acid is not the same as natural folate.

Folic acid (pteroylmonoglutamate) is the synthetic, oxidised form of folate, which is NOT present in fresh, natural foods. Folic acid has no biological activity unless it is converted into folates.

The bioavailability of 5-MTHF in supplements is identical to or greater than that of folic acid [3].

One study randomly assigned women an equivalent amount of folic acid, 5-MTHF, or a placebo, in order to compare the efficacy of these 2 supplements [4]. Their results show that 5-MTHF may be more effective than folic acid at increasing blood folate levels in women.

Folate concentrations in red blood cells and plasma were higher in women supplemented with 5-MTHF than in women supplemented with folic acid. 

Similarly, two further studies showed that administration of 5-MTHF is more effective than folic acid at improving folate status by increasing folate concentrations in red blood cells [5],[6].

The findings of one study suggest that 5-MTHF is more likely to be transferred to the foetus than folic acid [7]. At the time of delivery, cord 5-MTHF was significantly higher than maternal levels, whereas folic acid showed no significant correlation. These findings suggest that 5-MTHF is actively transported to the foetus, unlike folic acid.

A significant reduction in total plasma homocysteine concentrations, equally across the folic acid and 5-MTHF groups compared with the placebo group, was observed [8]. 

The folate form 5-MTHF helps to lower homocysteine levels in the body. By donating its methyl (M) group, it converts homocysteine into methionine. As a reminder, homocysteine is responsible, among other things, for neural tube defects, and an adequate intake of folates helps to lower homocysteine levels and thereby reduce the risk of neural tube defects. [9].

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Why is folic acid inferior to the active form 5-MTHF?

The methylation cycle can be partially represented as follows: 

The different forms of folate, including folic acid, are converted to THF by the DHFR enzyme, then this THF is converted into the form 5-MTHF by the MTHFR enzyme, which subsequently allows 5-MTHF to donate its methyl group (M) and convert homocysteine, thereby helping to reduce its levels in the body. All of this requires a great deal of energy, and is not always possible.

There are conditions in which drug treatment causes abnormalities in folate metabolism, impairing their conversion into the active form. This is the case with treatments such as methotrexate, aminopterin, pyrimethamine, and trimethoprim, which inhibit the DHFR (enzyme responsible for converting folic acid into its THF form).  

Under these treatment conditions, folic acid supplementation is ineffective, and 5-MTHF is a good alternative to folic acid as it does not depend on the enzyme that is affected [10].

The conversion of folic acid by DHFR is slow and saturable [11]. This extremely slow rate of conversion means that in the presence of large amounts of folic acid, not all of it will be converted and free folic acid will be present in the body. 

This slow rate of conversion of folic acid to the THF form does not occur with 5-MTHF supplementation, which is already in its usable form. Indeed, a study compared 5-MTHF and folic acid and showed that total folate in the blood is 23% to 55% higher with the 5-MTHF form. For example, 48 hours after the first dose of 5-MTHF, 90% of participants were above the target for folate levels. In contrast, at that same point, 55% of those given folic acid had insufficient levels. Thus, the advantage of 5-MTHF folate is its ability to reliably replenish bodily stores in women with folate insufficiency within a few days [12]. 

The risk of masking the symptoms of a vitamin B12 deficiency can be reduced with 5-MTHF [13].

Dietary folates and folic acid are metabolised into 5-MTHF, which donates its methyl group (M) and reverts to THF. This reaction is carried out by an enzyme dependent on vitamin B12. A low vitamin B12 status, even when folate status is adequate, prevents conversion to THF. 

However, folic acid can be directly metabolised into THF (via the enzyme DHFR). As a result, folic acid does not require vitamin B12 and can mask a deficiency [8]. 

However, since 5-MTHF depends on vitamin B12 for its metabolism, in the event of a vitamin B12 deficiency, 5-MTHF will remain trapped, leading to a folate deficiency. [8].

The practical guide to supplementation during pregnancy

A guide practical and comprehensive to know when and how to supplement.
Discover the essential nutrients (iron, iodine, folates, choline, DHA...), their roles and the best forms for you and your baby

Folic acid or folates: what's the difference?

Les produits Jolly Mama ne contiennent que de la vitamine B9 sous forme active !
 

Notre snack grossesse Vanifique contient des folates issus d’un extrait d’épinard, naturellement riche en 5-méthyltétrahydrofolate, la forme directement active ! Un snack apporte 400 µg de folates. 
 

Baby bumpBump essentials et Bump powder, nos compléments multivitamines pour la conception et la grossesse, apportent 400 µg de folates par jour, sous forme 5-méthyltétrahydrofolate (Quatrefolic). Notre complément alimentaire post partum contient également cette forme.

Genetic mutations affecting folate metabolism

The role of the MTHFR gene 

The MTHFR gene is responsible for producing the enzyme methylenetetrahydrofolate reductase (MTHFR), an enzyme that enables folate metabolism and its conversion into its active form, 5-MTHF. 

Genetic alterations in the genes encoding key enzymes in folate metabolism can affect their activity and reduce folate availability, which may increase folate requirements [14]. 
 

There are two variations of the MTHFR gene: 677C>T and 1298A>C. In the general population, 60 to 70% of individuals carry at least one of these variants [15]. 

The MTHFR gene, 677C>T
 

People with a 677C>T genetic mutation have a reduced ability to convert folate into its active form, 5-MTHF. This leads to a decrease in the amount of biologically available 5-MTHF, which generates elevated homocysteine levels and has consequences for health, as it increases the risk of cardiovascular disease, thrombosis and stroke [16], and also presents an increased risk of neural tube defects [17].

In a study published in 2019, looking at infertile couples with a MTHFR gene mutation, researchers showed that treatment with folates in the 5-MTHF form significantly reduced homocysteine levels, demonstrating that consuming folates in their active form compensates for the gene mutation [18].

The MTHFR gene, 1298A>C

Based on current data, this mutation would not cause raised homocysteine levels but does affect the activity of the MTHFR enzyme, which in turn reduces folate levels in their active form (5-MTHF). Furthermore, the 1298(A>C) mutation may also be expected to be a risk factor for neural tube defects, albeit with a lower relative risk than the 677(C>T) mutation [19].

One study highlighted that the 1298A>C mutation could be a cause of Turner syndrome (an exclusively female genetic condition in which only one normal X sex chromosome is present, affecting approximately 1 in 2,000 babies [20]). This mutation is more frequent in the group of patients with Turner syndrome [21].

Is there a risk of excess folic acid?

Ingested folic acid is converted into various forms by the enzyme dihydrofolate reductase (DHFR). The first conversion step is slow; ultimately, folic acid ends up in the form of THF. THF can then be converted into other folates by the enzyme MTHFR, including 5-MTHF, the form normally found in circulation [10]. The capacity of the DHFR enzyme is limited, and when folic acid supplementation is excessive, a large proportion of the ingested folic acid appears in its unmetabolised form in the blood.

Folic acid intakes that exceed the body's capacity to convert it into THF result in the presence of unmetabolised folic acid in the body, which may potentially affect the immune system. Furthermore, some scientists have hypothesised that unmetabolised folic acid could be linked to cognitive decline in older people. These potential negative health consequences are not well understood and warrant further research [22].

In one study, they showed that a high intake of folic acid in pregnant mice leads to intrauterine growth restriction with impaired brain development and poor memory in the offspring [23]. 

Other studies have shown that a high intake of folic acid was associated, among other things, with hepatic degeneration, a reduction in methylation potential (and therefore an accumulation of homocysteine), and disruptions to lipid metabolism. They also suggest that high folic acid consumption disrupts cholesterol balance in the liver [24]. 

The presence of free folic acid can also impair the secretion of folates into breast milk. This free folic acid binds to a receptor at the mammary level in place of the active form of folates (5-MTHF), and does so with 10 times greater affinity. For folate to pass into breast milk, it must dissociate from the receptor, and this dissociation is therefore more efficient with 5-MTHF than with folic acid [25]. 

Should I get a blood folate test?

Another issue related to folic acid concerns binding affinity. Binding affinity refers to the strength with which a substance binds to a receptor. Interestingly, the body appears to prefer folic acid over natural folates. Indeed, folic acid binds more readily to folate receptors than natural forms of folate [26].
 

As a result, folic acid is transported and binds to receptors adequately, but the actual folate does not reach the cells to be used, because folic acid blocks the receptors. This is known as functional folate deficiency. In this case, your laboratory test results will be "normal" or even "elevated", yet symptoms of folate deficiency may still appear. This is because laboratory tests measure blood folate levels, not cellular folate levels [27].

What should I do?

You should have a test to assess your homocysteine levels, as a folate deficiency — even when blood test results appear elevated due to folic acid supplementation — can help reveal a potential functional folate deficiency [27] [28].

Conclusion

Un faible statut en folates est considéré comme l'une des carences nutritionnelles les plus courantes et, bien qu'un apport alimentaire inadéquat en soit la cause principale, des altérations génétiques et des interactions de médicaments avec le métabolisme des folates peuvent contribuer à une moindre disponibilité des folates. 

En outre, la carence en folates peut être due à de faibles niveaux de vitamine B12, car cette vitamine sert de cofacteur dans le métabolisme des folates. La carence en folates a été associée à un risque accru de nombreux problèmes de santé tels que l'anomalie du tube neural, les maladies cardiovasculaires, le cancer et les troubles cognitifs. 

La forme 5-MTHF est préférable à l’acide folique dans ses vitamines prénatal, toutefois, il vaut quand même mieux se supplémenter en acide folique que de ne rien prendre du tout !

Source 1 : Folate, folic acid and 5-methyltetrahydrofolate are not the same thing, 2014

Source 2 : Folates in Fruits and Vegetables: Contents, Processing, and Stability, 2016

Source 3 : Office of Dietary Supplements - Folate, 2021

Source 4 : L-5-Methyltetrahydrofolate Supplementation Increases Blood Folate Concentrations, 2018

Source 5 : Red Blood Cell Folate Concentrations Increase More after Supplementation with 5-MTHF..., 2006

Source 6 : 5-Methyltetrahydrofolate is at least as effective as folic acid during lactation, 2006

Source 7 : Distribution of 5-Methyltetrahydrofolate and Folic Acid Levels in Maternal and Cord Blood Serum, 2020

Source 9 : Inhibiting MARSs reduces hyperhomocysteinemia‐associated neural tube and congenital heart defects, 2020

Source 11 : The Extremely Slow and Variable Activity of Dihydrofolate Reductase, 2009

Source 12 : The pharmacokinetic advantage of 5-methyltetrahydrofolate..., 2018

Source 13 : Folic Acid and L-5-Methyltetrahydrofolate: Comparison of Clinical Pharmacokinetics and Pharmacodynamics, 2010

Source 14 : Folate and genetics, 2004

Source 15 : RACGP - MTHFR Genetic Testing: Controversy and Clinical Implications, 2016

Source 16 :Acide folique et grossesse : Des recommandations appliquées, 2014

Source 18 : Impact des mutations du gène MTHFR en médecine, 2019

Source 19 : A second common mutation in the methylenetetrahydrofolate reductase gene, 1998

Source 20 : Turner Syndrome, 2018 (NHS)

Source 21 : Prevalence of the Polymorphism MTHFR A1298C and Not MTHFR C677T..., 2008

Source 22 : Unmetabolized Folic Acid in Plasma and Reduced NK Cell Cytotoxicity, 2006

Source 23 : High Dietary Folate in Pregnant Mice Leads to Pseudo-MTHFR Deficiency..., 2017

Source 24 : High Folic Acid Intake Increases Methylation-Dependent Expression of Lsr..., 2021

Source 25 : Receptor-mediated folate accumulation is regulated by cellular folate content, 1986

Source 26 : Identification of an Intestinal Folate Transporter and the Molecular Basis for Hereditary Folate Malabsorption, 2006

Source 27 : Detection of functional vitamin B12 and folate deficiencies..., 2014

Source 28 : Homocysteine and MTHFR Mutations, 2005

[1] Scaglione, Francesco, et Giscardo Panzavolta. 2014. « Folate, folic acid and 5-methyltetrahydrofolate are not the same thing ». Xenobiotica 44 (5): 480‑88. https://doi.org/10.3109/00498254.2013.845705.

[2] Delchier, Nicolas, Anna-Lena Herbig, Michael Rychlik, et Catherine Renard. 2016. « Folates in Fruits and Vegetables: Contents, Processing, and Stability ». Comprehensive Reviews in Food Science and Food Safety 15 (février). https://doi.org/10.1111/1541-4337.12193.

[3] « Office of Dietary Supplements - Folate ». 2021. https://ods.od.nih.gov/factsheets/Folate-HealthProfessional/.

[4] Henderson, Amanda M, Rika E Aleliunas, Su Peng Loh, Geok Lin Khor, Sarah Harvey-Leeson, Melissa B Glier, David D Kitts, Tim J Green, et Angela M Devlin. 2018. « l-5-Methyltetrahydrofolate Supplementation Increases Blood Folate Concentrations to a Greater Extent than Folic Acid Supplementation in Malaysian Women ». The Journal of Nutrition 148 (6): 885‑90. https://doi.org/10.1093/jn/nxy057.

[5] Lamers, Yvonne, Reinhild Prinz-Langenohl, Susanne Brämswig, et Klaus Pietrzik. 2006. « Red Blood Cell Folate Concentrations Increase More after Supplementation with [6S]-5-Methyltetrahydrofolate than with Folic Acid in Women of Childbearing Age ». The American Journal of Clinical Nutrition 84 (1): 156‑61. https://doi.org/10.1093/ajcn/84.1.156.

[6] Houghton, Lisa A, Kelly L Sherwood, Robert Pawlosky, Shinya Ito, et Deborah L O’Connor. 2006. « [6S]-5-Methyltetrahydrofolate is at least as effective as folic acid in preventing a decline in blood folate concentrations during lactation ». The American Journal of Clinical Nutrition 83 (4): 842‑50. https://doi.org/10.1093/ajcn/83.4.842

[7] Kubo, Yoshinori, Hideoki Fukuoka, Terue Kawabata, Kumiko Shoji, Chisato Mori, Kenichi Sakurai, Masazumi Nishikawa, et al. 2020. « Distribution of 5-Methyltetrahydrofolate and Folic Acid Levels in Maternal and Cord Blood Serum: Longitudinal Evaluation of Japanese Pregnant Women ». Nutrients 12 (6): 1633. https://doi.org/10.3390/nu12061633.

[8] Henderson, Amanda M, Rika E Aleliunas, Su Peng Loh, Geok Lin Khor, Sarah Harvey-Leeson, Melissa B Glier, David D Kitts, Tim J Green, et Angela M Devlin. 2018. « l-5-Methyltetrahydrofolate Supplementation Increases Blood Folate Concentrations to a Greater Extent than Folic Acid Supplementation in Malaysian Women ». The Journal of Nutrition 148 (6): 885‑90. https://doi.org/10.1093/jn/nxy057.

[9] Xinyu Mei et al., « Inhibiting MARSs reduces hyperhomocysteinemia‐associated neural tube and congenital heart defects », EMBO Molecular Medicine 12, no 3 (6 mars 2020): e9469, https://doi.org/10.15252/emmm.201809469.

[10] Scaglione, Francesco, et Giscardo Panzavolta. 2014. « Folate, folic acid and 5-methyltetrahydrofolate are not the same thing ». Xenobiotica 44 (5): 480‑88. https://doi.org/10.3109/00498254.2013.845705.

[11] Bailey, Steven W., et June E. Ayling. 2009. « The Extremely Slow and Variable Activity of Dihydrofolate Reductase in Human Liver and Its Implications for High Folic Acid Intake ». Proceedings of the National Academy of Sciences of the United States of America 106 (36): 15424‑29.https://doi.org/10.1073/pnas.0902072106.

[12] Bailey, Steven W., et June E. Ayling. 2018. « The pharmacokinetic advantage of 5-methyltetrahydrofolate for minimization of the risk for birth defects ». Scientific Reports 8 (mars): 4096. https://doi.org/10.1038/s41598-018-22191-2.

[13] Pietrzik, Klaus, Lynn Bailey, et Barry Shane. 2010. « Folic Acid and L-5-Methyltetrahydrofolate: Comparison of Clinical Pharmacokinetics and Pharmacodynamics ». Clinical Pharmacokinetics 49 (8): 535‑48. https://doi.org/10.2165/11532990-000000000-00000.

[14] Rozen R. (2004). Folate and genetics. J Food Sci 69:S65–7.

[15] Practitioners, The Royal Australian College of General. 2016 « RACGP - MTHFR Genetic Testing: Controversy and Clinical Implications ». 

[16] POIRIER Ysaura. “Acide folique et grossesse : Des recommandations appliquées, des malformations évitées.”. 2014.

[17] « Office of Dietary Supplements - Folate ». 2021. https://ods.od.nih.gov/factsheets/Folate-HealthProfessional/.

[18] CLEMENT Arthur. “Impact des mutations du gène MTHFR en médecine (fertilité notamment) et intérêt de la prise en charge thérapeutique”. 2019.

[19] Put, N M van der, F Gabreëls, E M Stevens, J A Smeitink, F J Trijbels, T K Eskes, L P van den Heuvel, et H J Blom. 1998. « A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects? » American Journal of Human Genetics62 (5): 1044‑51.

[20] « Turner Syndrome ». 2018. Nhs.Uk.

[21] Oliveira, Kelly Cristina de, Bianca Bianco, Ieda T. N. Verreschi, Alexis Dourado Guedes, Bianca Borsato Galera, Marcial Francis Galera, Caio P. Barbosa, et Monica Vannucci Nunes Lipay. 2008. « Prevalence of the Polymorphism MTHFR A1298C and Not MTHFR C677T Is Related to Chromosomal Aneuploidy in Brazilian Turner Syndrome Patients ». Arquivos Brasileiros de Endocrinologia & Metabologia 52 (novembre): 1374‑81.https://doi.org/10.1590/S0004-27302008000800028.

[22] Troen, Aron M., Breeana Mitchell, Bess Sorensen, Mark H. Wener, Abbey Johnston, Brent Wood, Jacob Selhub, et al. 2006. « Unmetabolized Folic Acid in Plasma Is Associated with Reduced Natural Killer Cell Cytotoxicity among Postmenopausal Women ». The Journal of Nutrition 136 (1): 189‑94. https://doi.org/10.1093/jn/136.1.189.

[23] Bahous, Renata H, Nafisa M Jadavji, Liyuan Deng, Marta Cosín-Tomás, Jessica Lu, Olga Malysheva, Kit-Yi Leung, et al. 2017. « High Dietary Folate in Pregnant Mice Leads to Pseudo-MTHFR Deficiency and Altered Methyl Metabolism, with Embryonic Growth Delay and Short-Term Memory Impairment in Offspring ». Human Molecular Genetics 26 (5): 888‑900. https://doi.org/10.1093/hmg/ddx004.

[24] Leclerc, Daniel, Jaroslav Jelinek, Karen E. Christensen, Jean-Pierre J. Issa, et Rima Rozen. 2021. « High Folic Acid Intake Increases Methylation-Dependent Expression of Lsr and Dysregulates Hepatic Cholesterol Homeostasis ». The Journal of Nutritional Biochemistry 88 (février): 108554. https://doi.org/10.1016/j.jnutbio.2020.108554.

[25] Kamen, B A, et A Capdevila. 1986. « Receptor-mediated folate accumulation is regulated by the cellular folate content. » Proceedings of the National Academy of Sciences of the United States of America 83 (16): 5983‑87.

[26] Andong Qiu et al., « Identification of an Intestinal Folate Transporter and the Molecular Basis for Hereditary Folate Malabsorption », Cell 127, no 5 (1 décembre 2006): 917‑28, https://doi.org/10.1016/j.cell.2006.09.041.

[27] Alpaslan Cosar et Osman Metin Ipcioglu, « Detection of functional vitamin B12 and folate deficiencies, while serum levels are normal », Blood Transfusion 12, no Suppl 1 (janvier 2014): s164, https://doi.org/10.2450/2013.0040-13.

[28] Elizabeth A. Varga et al., « Homocysteine and MTHFR Mutations », Circulation 111, no 19 (17 mai 2005): e289‑93, https://doi.org/10.1161/01.CIR.0000165142.37711.E7.

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