MTHFR gene mutation gives directions in creating the enzyme known as the methylenetetrahydrofolate reductase. With this, learning about the MTHFR indicators and vaccines to avoid MTHFR becomes crucial. So, upon getting many calls at our office about MTHFR gene mutation, here are the common questions we get and our answers.
Here’s What You Need to Know About MTHFR Gene Mutation
In this article:
- 1. What ICD9 Code Do You Use for MTHFR Gene Mutation?
- 2. Do Insurance Companies Pay for MTHFR Gene Mutation Test?
- 3. Do You Treat All MTHFR Anomalies the Same Way?
- 4. Can You Expect Side Effects with the Use of Deplin or L-Methyl Folate?
- 5. I Looked Up Deplin and It is Used for Depression and I Don’t Have Depression, Should I Still Take Deplin?
- 6. Are Over the Counter Versions of Methyl Folate Just the Same as the Brand Name Deplin?
- 7. What is an SNP?
- 8. What is the Most Affordable Way to Get MTHFR Gene Mutation Testing?
1. What ICD9 Code do you use for MTHFR Gene Mutation?
Answer: We haven’t found a specific code for MTHFR, but we use 270.4. This is the code that comes up on ICD9Data.com search. Also, there is a second code 270.9, an unspecified disorder of amino-acid metabolism that can be used as well. However, we believe 270.4 is the best code to use.
Next, we change the standard description from ICD9Data.com to MTHFR in our medical record system. We also denote the type and whether it is hetero or homozygous. For example, our coding will be 270.4 MTHFR 677 heterozygous or MTHFR 677/1298 compound heterozygous.
Definition of 270.4 code
Disturbances of Sulphur-Bearing Amino-Acid Metabolism:
- Autosomal recessive inborn error of methionine metabolism usually caused by a deficiency of cystathionine beta-synthase and associated with elevations of homocysteine in plasma and urine; clinical features include a tall, slender habitus, scoliosis, arachnodactyly, muscle weakness, genu varis, thin blond hair, malar flush, lens dislocations, an increased incidence of mental retardation, and a tendency to develop fibrosis of arteries, frequently complicated by cerebrovascular accidents and myocardial infarction.
- Short description: Sulph amino-acid met dis.
- ICD-9-CM 270.4 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
We take out that description and put in MTHFR or MTHFR 677 heterozygous, MTHFR compound heterozygous 677/1298, or MTHFR 1298 homozygous. The detail is useful in the problem list since we treat different variations differently.
2. Do insurance companies pay for the MTHFR Gene Mutation Test?
Answer: Unfortunately, the answer is often no, but that has slowly changed as we are seeing more and more insurance carriers pay for this testing. They certainly should since methylation issues are treatable and treatment can help mitigate or prevent much more expensive problems both immediately and in the future.
3. Do you treat all MTHFR anomalies the same way?
Answer: As for the MTHFR treatment, no. When the 677 variant is present, we have found that L-methyl folate (Deplin) works best. In essence, we then use methyl B12 when the 1298 variant is present.
4. Can you expect side effects with the use of Deplin or L-Methyl Folate?
Answer: Yes, there are several common side effects. Deplin can cause an upset stomach in some people when taken on an empty stomach. If the Deplin dose is too high, it may cause the body to dump excessive amounts of toxins into the system. Also, this can cause side effects. However, these can be reduced or eliminated, in most cases, by using a binding agent to bind up toxic bile being released by the liver or starting at a lower dose and working up to the maintenance dose.
5. I looked up Deplin and it is used for depression. And I don’t have depression, should I still take Deplin?
Answer: If you have an MTHFR 677 anomaly, then you will benefit from L-methyl folate (Deplin). The FDA is fairly simplistic in their thinking, which is one diagnosis, one drug. If you want to use it for something else, then according to the FDA’s way of thinking, you need a different drug name. For example, Zyban (bupropion) is a drug to help with smoking cessation, the exact same medication is used as anti-depressant under several different trade names: Wellbutrin, Voxra, Budeprion, Prexaton, Elontril or Aplenzin.
On the other note, physicians understand that a drug may be used for multiple medical problems, and this is called “off-label prescribing.” Also, FDA has approved Deplin as a medical food that has demonstrated a benefit for the treatment of depression. However, this does not mean Deplin is only useful for depression. The main reason for using Deplin when MTHFR is present is because it helps methylation and indirectly raises glutathione. Low glutathione is the root cause of many chronic illnesses.
6. Are over-the-counter versions of Methyl Folate just the same as the brand name Deplin?
Answer: For the most part, the answer is no, with some exceptions. There are racemic versions of methyl folate being marketed as equivalent to L-methyl folate (Deplin). These are not the same as Deplin. Also, the racemic versions contain both D-methyl folate and L-methyl folate. The D-methyl folate (a non-active form of folic acid) can compete at the binding site making the L-methyl folate less effective. There are some forms of L-methyl folate being marketed OTC.
Definition of racemic: Of, relating to, or constituting a compound or mixture composing of equal amounts of dextrorotatory and levorotatory forms of the same compound and is not optically active.
7. What is an SNP?
A single-nucleotide polymorphism (SNP, pronounced snip; plural snips) is a DNA sequence variation occurring when a single nucleotide – A, T, C or G – in the genome (or other shared sequences) differs between members of a biological species or paired chromosomes in a human.
Aside from this, single nucleotide polymorphism abbreviated as SNP and pronounced snips. This means one nucleotide or setting on the gene has a variation from the normal. For example, in the diagram below, MTHFR 1298C is GT instead of TT. The letters refer to one of the four bases that make up the DNA code. If you feel lost now, then check out the Genetic Science Learning Center below.
Also, the University of Utah Genetic Science Learning Center has an excellent resource that helps you understand this complex genetic nomenclature and the health significance of these SNPs.
8. What is the most affordable way to get MTHFR Gene Mutation Testing?
Answer: If your insurance covers it and that is a big if, that is usually the most affordable way to go, but it requires a physician request. In our office, if patients are not in hurry, a much better solution is through a genetic testing company.
They offer a much broader profile for $99.00. However, two other websites will convert the 23andme data into the form used by physicians for a nominal fee or a donation. Currently, it is taking about two months to get the report back.
For this, we then use Livewello, which charges $20 and you get a nice easy to read a color-coded report with the data presented using nomenclature familiar to physicians, such as MTHFR 677 rather than rs1801133, which referred to as the rsID. The rsID is useful since many databases use this nomenclature for categorizing information on different genetic SNPs. See the NIH SNP database called dbSNP.
Also, the Livewello data comes in report the looks like this. This is just a small portion of the report. Here’s how a color-coded report looks like: green means normal, yellow is heterozygous, and red is homozygous. In the second report, I have highlighted the MTHFR 677 and MTHFR 1298 SNPs, which are both yellow, so this individual is compound heterozygous 677/1298. However, you can see from the report that there are other areas of concern.
After going through the MTHFR Gene Mutation FAQs, here’s a video from BBC News channel to help you learn more about the marvels of gene editing:
To give you more information, below is the table that has the same data copied in spreadsheet format. The links are live and will take you to SNPopedia, which has more detailed information on that SNP.
|Gene & Variation||rsID||Risk Allele||Your Alleles||Results|
|MAO A R297R||rs6323||G||T||-/-|
|MTHFR 03 P39P||rs2066470||A||AG||+/-|
|MTHFR G1793A (R594Q)||rs2274976||T||CT||+/-|
Did we miss anything on our MTHFR Gene Mutation FAQs? Tell us in the comments section below!
Up Next: Methylation Defect Issues
*This article was originally published in 2015