Folate
is the name given to a water soluble b-vitamin and is also known as B9. Folic
acid refers to the oxidized synthetic compound used in dietary supplements and
food fortification, whereas folate refers to the natural substance which is
derived from eating folate rich food.
To make new cells, an
existing cell divides in two. But first it copies its DNA so the new cells will
each have a complete set of genetic instructions. Folate is a vital component
in this cell replication, and understandably an important nutrient to
developing a new life, as well as sustaining your own cell life!
The history
of folate dates back to 1931 when chemists concluded that anaemia was caused by
a dietary deficiency of the vitamin, based on their discovery of it in folate
rich foods. Pharmaceutical and supplement companies moved quickly to
counterfeit this vitamin. Folic acid was created in a lab in the early 1940s
and today has largely replaced natural folate consumption as part of pregnancy support.
In
the US and also in other countries like Australia this was taken one step
further in the late 1990s through mandatory food fortification. Government
intervention in this areas was due to what scientists deemed as overwhelming
evidence that folic acid would protect babies and as part of preconception
plans to ensure that that development of
neural tube defects (NTD) in new-borns was eliminated.
http://www.pinterest.com/pin/498421883731034732/
The
body recognises the natural form of folate which can enter the methylation
cycle, a cycle of donation of methyl groups which enables us to carry on
living, so pretty important. However in order to complete this cycle we need specific
enzymes to break down substances in a
multi step process. This is also the case for many things we ingest;
they need converting many times before the body can use them. Folate is such an important nutrient for fertility
and sustaining life! The folate you eat has to be converted via many steps to
the active folate 5-MTHFR
The low activity of this
enzyme in the human liver, combined with a high intake of folic acid, may
result in unnatural levels of unmetabolized folic acid entering the bodies
systems.
Several
studies have reported the presence of Unmetabolized folic acid in the blood
following the consumption of folic acid supplements or fortified foods. Human
exposure to folic acid was non-existent until its chemical synthesis in 1940s.
Risks associated with excessive folic acid intake
While
the incidence of NTDs in the United States been significantly reduced since
folic acid fortification began, (as up
to 60% people can process folic acid) there has been concern about the safety
of chronic intake of high levels of folic acid from fortified foods, beverages
and dietary supplements. In recent years this has been increasingly studied in
terms of how we are made and our genetic make up. Genetics is the reason why some
people can smoke and drink like a trouper and live to a ripe old age and some
people develop chronic diseases when they live a wholesome life and fade away
in such a short time.
It’s
all in your genetics Chromosomes are organized into short segments of DNA
called genes. If you imagine the chromosome as the bookshelf then your DNA as a
cookbook in a shelf, and your genes are the recipes. Written in the DNA
alphabet - A, T, C, and G, which are the DNA bases - the recipes tell your
cells how to function and what traits to express. For example, if you have blue
eyes it is because the genes you inherited from your parents are instructing
your eye cells to make blue eyes!
To make new cells, an
existing cell divides in two. But first it copies its DNA so the new cells will
each have a complete set of genetic instructions. Cells sometimes make mistakes
during the copying process – a bit like typos. These typos lead to variations
in the DNA sequence at particular locations, called single nucleotide
polymorphisms, or SNPs (this is where
the DNA bases have paired with the wrong base. One I want to look at that has
been widely studied as to implications around folate and currently has a total of 34
mutations is a more widely known SNP called MTHFR.
The MTHFR gene sits on Chromosome 1. There are two
key variants we test for.
·
MTHFR C677T so the 677 position
·
MTHFR A1298C – on the
1298 position
If you
get a mixture of the Gene bases and one bases is wrong you may be ‘Heterozygous’
= 1 copy of the gene from either parent.
Or if you pair wrongly with both base pairs you are then deemed ‘Homozygous’
= 1 copy of the gene from each parent
MTHFR
C677T Heterozygous = 40% loss of function
MTHFR C677T Homozygous = 70% loss of function
MTHFR
A1298C Heterozygous = 20% loss of function (research on this SNP is limited)
MTHFR A1298C Homozygous = between 50-70%
MTHFR C677T & MTHFR A1298C heterozygous =
compound heterozygous = 50% loss of function in this SNP
Or if you pair wrongly with both base pairs you are then deemed ‘Homozygous’ = 1 copy of the gene from each parent
MTHFR C677T Homozygous = 70% loss of function
MTHFR A1298C Homozygous = between 50-70%
No comments:
Post a Comment