Tuesday, September 1, 2015

MTHFR Gene can cause a lack of B12 absorption

The MTHFR is a genetic mutation that causes a B12 malabsorption.  It can also be related to breast cancer, autism, and chronic fatigue.  When someone has the MTHFR gene, blood testing will show normal or high levels of B12 in the blood because the mutation does not allow the B12 to be absorbed in the tissues, but it remains in the blood.  the same occurs with the nutrient, folic acid.  It doesn't absorb the B12, it also prevents the body form detoxifying substances.  The solution is to eliminate all synthetic forms of B12 and folic acid, use the methyl forms of these vitamins, such as methylcobalamin B12 and methylletrafolate.

The MTHFR is a gene variant that is found in 40% of the population, which is 1 in 3 of the population.

The MTHFR gene is discovered through a simple blood test.  I worked with a family who discovered the gene variant in their son, then discovered it in several other family members as well.  Through the discovery, they were able to make positive changes in future generations!

1 comment:

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