LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » Anyone test positive for only heterozygous A1298c

 - UBBFriend: Email this page to someone!    
Author Topic: Anyone test positive for only heterozygous A1298c
BuffyFan
LymeNet Contributor
Member # 34679

Icon 1 posted      Profile for BuffyFan     Send New Private Message       Edit/Delete Post   Reply With Quote 
mthfr? if so, did your doc recommend any treatments?
Posts: 287 | From somewhere | Registered: Oct 2011  |  IP: Logged | Report this post to a Moderator
ralphi
LymeNet Contributor
Member # 33834

Icon 1 posted      Profile for ralphi     Send New Private Message       Edit/Delete Post   Reply With Quote 
Me. No treatment yet; we're testing homocystine levels first. From my research so far, I believe hetero 1298 is the least damaging mutation and affects toxin elimination more than anything.

Not so much clotting issues like the other gene. My doc said I can stay on birth conrol pill for now.

Posts: 330 | From TN | Registered: Sep 2011  |  IP: Logged | Report this post to a Moderator
aperture
LymeNet Contributor
Member # 34822

Icon 1 posted      Profile for aperture         Edit/Delete Post   Reply With Quote 
Me too. I am heterozygous A1298C, have normal homocysteine levels, but high B12 and folate. Just waiting for my followup appt to find out what the Dr is gonna do about it.

--------------------
aperture

Posts: 551 | From Louisville, KY | Registered: Nov 2011  |  IP: Logged | Report this post to a Moderator
BuffyFan
LymeNet Contributor
Member # 34679

Icon 1 posted      Profile for BuffyFan     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have normal homocysteine levels too, and normal folate but low serum b12

not sure if I should do anything

Posts: 287 | From somewhere | Registered: Oct 2011  |  IP: Logged | Report this post to a Moderator
dal123
LymeNet Contributor
Member # 6313

Icon 1 posted      Profile for dal123     Send New Private Message       Edit/Delete Post   Reply With Quote 
Don't rely on the homocysteiene for treatment, there is another precursor that many dr's don't test for , but unwed to supplement with Methyl B12 and Methylfolinic acid & Glutathione!!


busy methylating, I hope ! [Smile] )

Posts: 532 | From Texas | Registered: Oct 2004  |  IP: Logged | Report this post to a Moderator
TerryK
Frequent Contributor (5K+ posts)
Member # 8552

Icon 1 posted      Profile for TerryK     Send New Private Message       Edit/Delete Post   Reply With Quote 
Dr. Yasko has written if you have a methylation issue it's like having diabetes and not treating.

Anyone with lyme or other infections needs all the detox help they can get. I do believe it makes sense to treat if you know you have a weakness, especially if you have a chronic illness that puts an extra toxic burden on your body.

The 2 MTHFR tests are just a small part of the methylation cycle. You could have a CBS upregulation or some other mutation that exacerbates the one that you know you have. Best to treat at least what you know for sure is a problem.

I have the same one you have plus others. Here are some of my notes on MTHFR A1298C

Does not impact levels of homocysteine but can cause low levels of BH4. Has been mapped to the SAMe regulatory region of the gene.

Causes an inability to convert BH2 to BH4 and can cause exceedingly low BH4. Low BH4 means more severe parasitic infections, difficulty deactivating viruses, diabetes, hypertension and arteriosclerosis. Serotonin synthesis as well as ammonia detoxification require BH4. Low BH4 will affect dopamine levels. Excess ammonia in the gut may alter gut PH and cause microbial imbalances.

For anethesia - the availability of BH4 helps to determine whether nitric oxide, peroxy nitrite or super oxide are formed as a function of the urea cycle; two molecules of BH4 are required for the formation of nitric oxide, one molecule of BH4 leads to the formation of peroxy nitrite and the absence of BH4 leads to super oxide formation.

Keeping ammonia under control is of paramount importance for people with this mutation as any extra ammonia generated drains stores of BH4 which are probably already low. This will impact serotonin levels and cause fluxes in dopamine (mood swings). Restoring levels of BH4 will help serotonin synthesis maintaining dopamine in a more stable manner and helping with ammonia detoxification.

A number of the mutations in the methylation cycle can cause depleted BH4 not just this one.

Terry
I'm not a doctor

Posts: 6286 | From Oregon | Registered: Jan 2006  |  IP: Logged | Report this post to a Moderator
Razzle
Frequent Contributor (1K+ posts)
Member # 30398

Icon 1 posted      Profile for Razzle     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yes, I too have the hetero mutation for A1298C. I just got some methyl-folate to try. But will have to go very slowly because of the CBS homozygous mutation I have...

BuffyFan,

Yes, you should at the very least be supplementing Vitamin B12. Low serum Vitamin B12 is linked to a lot of neurological issues, some of which can become permanent if the B12 level stays low chronically.

TerryK,

Thanks for your obviously well-researched information - it is much appreciated.

I take yucca root powder every morning to help with the ammonia, and the difference is amazing even with only 1/8 teaspoon of the yucca root! Of course, I'm also on a low protein diet to help with the ammonia...

--------------------
-Razzle
Lyme IgM IGeneX Pos. 18+++, 23-25+, 30++, 31+, 34++, 39 IND, 83-93 IND; IgG IGeneX Neg. 30+, 39 IND; Mayo/CDC Pos. IgM 23+, 39+; IgG Mayo/CDC Neg. band 41+; Bart. (clinical dx; Fry Labs neg. for all coinfections), sx >30 yrs.

Posts: 4166 | From WA | Registered: Feb 2011  |  IP: Logged | Report this post to a Moderator
sk8ter
LymeNet Contributor
Member # 8671

Icon 1 posted      Profile for sk8ter     Send New Private Message       Edit/Delete Post   Reply With Quote 
razzle what test did you take to check your CBS?? Did you have the Dr. Yasko test?
Posts: 871 | From orange county, ca. | Registered: Jan 2006  |  IP: Logged | Report this post to a Moderator
sk8ter
LymeNet Contributor
Member # 8671

Icon 1 posted      Profile for sk8ter     Send New Private Message       Edit/Delete Post   Reply With Quote 
Please go to MTHFR.net...That doctor has the most information on these mutations and the correct treatment for them since he has two mutations along with his family.
Posts: 871 | From orange county, ca. | Registered: Jan 2006  |  IP: Logged | Report this post to a Moderator
BuffyFan
LymeNet Contributor
Member # 34679

Icon 1 posted      Profile for BuffyFan     Send New Private Message       Edit/Delete Post   Reply With Quote 
thank you everyone!please post if you find out anything else. I had a a hard time researching, and mostly came up with women who have had lots of miscarriages and hoping to get pregnant again.

Razzle, I will take B12, thanks! You said you take yucca root powder what exactly is the difference you are feeling? oh and did you get your ammonia levels tested(or did you just know it was high because of the mutation?)

sk8ter, I have gone to that site, but I thought I read he didn't recommend treatment for this particular mutation?? or maybe I read it wrong??

I really find this all very interesting..I have suffered with insomnia since I was a kid and now all of a sudden I am having high blood pressure.

Posts: 287 | From somewhere | Registered: Oct 2011  |  IP: Logged | Report this post to a Moderator
BuffyFan
LymeNet Contributor
Member # 34679

Icon 1 posted      Profile for BuffyFan     Send New Private Message       Edit/Delete Post   Reply With Quote 
Terry, thanks for your post, you made it a lot easier to understand. [Smile]
Posts: 287 | From somewhere | Registered: Oct 2011  |  IP: Logged | Report this post to a Moderator
sk8ter
LymeNet Contributor
Member # 8671

Icon 1 posted      Profile for sk8ter     Send New Private Message       Edit/Delete Post   Reply With Quote 
i do think he does for all mutations...
Posts: 871 | From orange county, ca. | Registered: Jan 2006  |  IP: Logged | Report this post to a Moderator
Razzle
Frequent Contributor (1K+ posts)
Member # 30398

Icon 1 posted      Profile for Razzle     Send New Private Message       Edit/Delete Post   Reply With Quote 
Sk8ter,

Yes, I had the Yasko methylation test panel.

BuffyFan,

I did not have ammonia tested. But my sweat smelled like cat pee and that has now disappeared since I started taking the yucca.

I was on a low protein diet before I started the yucca, but still had the cat-pee smelling sweat. After starting the yucca, I no longer smell the strong eye-watering ammonia smell.

That's really the only concrete difference I notice, but it may also be affecting me in other ways (more subtle) that I'm just not aware of as of yet.

--------------------
-Razzle
Lyme IgM IGeneX Pos. 18+++, 23-25+, 30++, 31+, 34++, 39 IND, 83-93 IND; IgG IGeneX Neg. 30+, 39 IND; Mayo/CDC Pos. IgM 23+, 39+; IgG Mayo/CDC Neg. band 41+; Bart. (clinical dx; Fry Labs neg. for all coinfections), sx >30 yrs.

Posts: 4166 | From WA | Registered: Feb 2011  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.