New Quatrefolic® Educational Videos: MTHFR Polymorphism

New Quatrefolic® Educational Videos: MTHFR Polymorphism

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Approximately half of the global population may carry some form of MTHFR mutation.  MTHFR deficiency may predispose individuals to hyperhomocysteinemia (high blood homocysteine levels) in a dynamic interaction between genetics and nutrition.  Quatrefolic®/, the active form of folate, is recommended to support well-being and reduce health risks in these individuals.

Active Folate and MTHFR Polymorphism

Folate, also known as vitamin B9, is an essential nutrient that plays a crucial role in numerous bodily functions, from cell growth and development to DNA synthesis. However, for individuals with genetic variations in the methylenetetrahydrofolate reductase (MTHFR) enzyme, the benefits of folate can be significantly impaired. 

5,10-methylenetetrahydrofolate reductase (MTHFR) is the key enzyme in the biosynthesis of an active folate form. 

Genetic polymorphisms in the MTHFR gene, such as the C677T and A1298C variants, can reduce the enzyme’s activity, leading to the accumulation of homocysteine in the body. 

Elevated homocysteine levels have been linked to a range of health concerns, including cardiovascular disease, neurological disorders, and pregnancy complications.

This is where the advantages of active folate, such as Quatrefolic®, come into play. 

Watch the video and discover how Quatrefolic®/ can bypass the MTHFR conversion step and deliver a «finished» folate the body can immediately use without any metabolization.

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