Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Ttg Still Positive After 6 Mos.


greenbeanie

Recommended Posts

greenbeanie Enthusiast

How long does it normally take for a young child's tTG to go down to normal? My daughter is 4 1/2. Her tTG was 65 at diagnosis and was still positive at 9 after six months (with anything over 4 considered positive). Obviously we're happy it decreased significantly, but the doctor expected it to be negative by now, and of course that's what we were hoping too. I know that super-high levels often take longer than six months to become normal, but hers wasn't super-high to start. On the other hand, we suspect that she's had celiac since infancy and was undiagnosed for most of her life, so even though she's young she may have had it for quite a while. She was not eating much gluten at the time of her original level of 65 - just one small serving per day for the month before testing, and only a few servings per week before that.

My initial response was to be quite discouraged by today's results, but maybe I'm overreacting. Our house was totally gluten-free for the entire six months between tests, we've replaced all the appropriate kitchen stuff, we cook almost everything from scratch and only eat a few processed foods from dedicated facilities, all toiletries are gluten free, etc. She does attend daycare, but they have been outstanding at reducing the potential for cc and switched to all gluten-free art supplies, serve only gluten-free snacks, make sure her lunch space is clean, have the whole class wash hands frequently, and basically do everything reasonably possible to keep a celiac preschooler safe.

Does it sound like it could just be normal for her tests to take longer than six months to become negative, or is it a sign of ongoing gluten exposure? We have been extremely strict about her diet. The only somewhat-risky thing we did was to try very small amount of gluten free oats a few times after the first five months. She had no apparent reaction to the oats (and always had obvious symptoms from wheat before), but maybe that little bit could be just enough to keep the numbers positive? We're going to test again after three more months oat-free, then do an oat challenge if her tTG has become negative by then.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



blmoreschi Apprentice

I thought the TtG was supposed to be under 20, not 4?

 

No matter which is right, you must be doing a great job to get it down that much in 6 months! And I don't think the oats would affect that if they are gluten-free oats. I think some Celiacs just can't tolerate oats, but they do not have gluten in them and so therefore should not affect the tTG number.

greenbeanie Enthusiast

Thanks for the encouragement. This lab's reference range shows anything over 4 as positive, but I know other labs use different ranges. I'm not sure if that reflects an actual difference in the labs' measurement methods or is just a matter of their reporting criteria.

Our pediatric GI clearly thinks that for the small percentage of celiacs who are sensitive to pure oats, the oats can cause a rise in tTG (not just symptoms that mimic gluten exposure). Does anyone know if there is firm data on this yet? I know there have been mixed views on oats for a long time.

nvsmom Community Regular

The tTG tests are slow to come down.  Did they test the DGP (deaminated gliadin peptides) as that one is a better test for checking how gluten-free you are - it tends to go up and down faster. How about the EMA IgA? That one shows advanced damage and usually comes down before the tTG tests too.

 

The tTG IgA can also be elevated from other health problems like thyroiditis, diabetes, chronic liver disease, crohn's, colitis, and infections. When those are a factor, they will often keep the tTG elevated at a low level.

 

Or it could just be taking a long time to come down. i was gluten-free for over a year and my ttG was still abnormal. It finally almost touched normal when I was on some mild steroids for another health issue. It can take a long time to normalize.

 

I would request the DGP and EMA tests as well the next time the doctor wants to check it. That could give you a better idea of whether it is cc or just a slower recovery.

 

Best wishes.

greenbeanie Enthusiast

Thanks, Nicole. She had both DGP tests run at the time of diagnosis (but not EMA), and I had thought they were running all three again for the follow-up, but it turns out they didn't. I'm sure the move to electronic medical records has advantages for efficiency, but it's annoying that patients never get to see their actual lab slips anymore! I'll try to get them to do the whole panel next time. She doesn't seem to have symptoms of any other diseases and had a normal metabolic panel and CBC last summer, but we'll look more into the other possibilities if the tTG doesn't come down soon.

 

I have a question about the lab reference range thing in general, but I'll post it in another thread. The way the reference ranges are calculated actually does seem to matter quite a lot in terms of how quickly I'd expect the numbers to fall.

Cara in Boston Enthusiast

My son was still positive after 6 months (diagnosed at age 5) and the doctor said "as long as it is going down, we are successful."  He was negative at his one year test and has been since.  I wouldn't worry too much about it.  It WOULD NOT be going down if she was still eating gluten.

 

My blood test were negative after just a few weeks being gluten free.   It is different for everyone.

greenbeanie Enthusiast

I am feeling much better about her results now that I realize (from info on another thread) that her tTG level actually was very high at diagnosis, especially for a young child. I'd been seeing that some people had numbers over 100, so I'd thought that in comparison 65 wasn't all that high, which led me to expect it to come down to normal more quickly.

 

However, since our lab has a reference range of 4 and up as positive, her initial level was actually more than 16x normal at diagnosis! From that perspective, coming all the way down to just over 2x normal seems like great progress for six months. 


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



nvsmom Community Regular

That is a great improvement.  :)

GwenO Apprentice

We are at almost two years.  My daughter's have gone down steadily but still nowhere near where I thought.  Our doc says the same:  the numbers have gone down steadily so it's all good.  Frustrating though because we are very careful.

Archived

This topic is now archived and is closed to further replies.

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - lil-oly replied to Jmartes71's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Gluten tester

    2. - knitty kitty replied to JudyLou's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      11

      Seeking advice on potential gluten challenge

    3. - JudyLou replied to JudyLou's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      11

      Seeking advice on potential gluten challenge

    4. - knitty kitty replied to JudyLou's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      11

      Seeking advice on potential gluten challenge

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,155
    • Most Online (within 30 mins)
      7,748

    Beccad611
    Newest Member
    Beccad611
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • lil-oly
      Hey there, have you been tested for allergies? You may not only have celiac disease but be allergic. I have celiac disease and am allergic to Barley, wheat and rye. 
    • JudyLou
    • knitty kitty
      I have osteopenia and have cracked three vertebrae.  Niacin is connected to osteoporosis! Do talk to your nutritionist and doctor about supplementing with B vitamins.  Blood tests don't reveal the amount of vitamins stored inside cells.  The blood is a transportation system and can reflect vitamins absorbed from food eaten in the previous twenty-four to forty-eight hours.  Those "normal limits" are based on minimum amounts required to prevent disease, not levels for optimal health.   Keep us posted on your progress.   B Vitamins: Functions and Uses in Medicine https://pmc.ncbi.nlm.nih.gov/articles/PMC9662251/ Association of dietary niacin intake with osteoporosis in the postmenopausal women in the US: NHANES 2007–2018 https://pmc.ncbi.nlm.nih.gov/articles/PMC11835798/ Clinical trial: B vitamins improve health in patients with coeliac disease living on a gluten-free diet https://pubmed.ncbi.nlm.nih.gov/19154566/   Nutritional Imbalances in Adult Celiac Patients Following a Gluten-Free Diet https://pmc.ncbi.nlm.nih.gov/articles/PMC8398893/ Nutritional Consequences of Celiac Disease and Gluten-Free Diet https://www.mdpi.com/2036-7422/15/4/61 Simplifying the B Complex: How Vitamins B6 and B9 Modulate One Carbon Metabolism in Cancer and Beyond https://pmc.ncbi.nlm.nih.gov/articles/PMC9609401/
    • JudyLou
      Thank you so much for the clarification! Yes to these questions: Have you consulted dietician?  Have you been checked for nutritional deficiencies?  Osteoporosis? Thyroid? Anemia?  Do you take any supplements, or vitamins? I’m within healthy range for nutritional tests, thyroid and am not anemic. I do have osteopenia. I don’t take any medications, and the dietician was actually a nutritionist (not sure if that is the same thing) recommended by my physician at the time to better understand gluten free eating.    I almost wish the gluten exposure had triggered something, so at least I’d know what’s going on. So confusing!    Many thanks! 
    • knitty kitty
      @JudyLou,  I have dermatitis herpetiformis, too!  And...big drum roll... Niacin improves dermatitis herpetiformis!   Niacin is very important to skin health and intestinal health.   You're correct.  dermatitis herpetiformis usually occurs on extensor muscles, but dermatitis herpetiformis is also pressure sensitive, so blisters can form where clothing puts pressure on the skin. Elastic waist bands, bulky seams on clothing, watch bands, hats.  Rolled up sleeves or my purse hanging on my arm would make me break out on the insides of my elbows.  I have had a blister on my finger where my pen rested as I write.  Foods high in Iodine can cause an outbreak and exacerbate dermatitis herpetiformis. You've been on the gluten free diet for a long time.  Our gluten free diet can be low in vitamins and minerals, especially if processed gluten free foods are consumed.  Those aren't fortified with vitamins like gluten containing products are.  Have you consulted dietician?  Have you been checked for nutritional deficiencies?  Osteoporosis? Thyroid? Anemia?  Do you take any supplements, medicine, or vitamins? Niacin deficiency is connected to anemia.  Anemia can cause false negatives on tTg IgA tests.  A person can be on that borderline where symptoms wax and wane for years, surviving, but not thriving.  We have a higher metabolic need for more nutrients when we're sick or emotionally stressed which can deplete the small amount of vitamins we can store in our bodies and symptoms reappear.   Exposure to gluten (and casein in those sensitive to it) can cause an increased immune response and inflammation for months afterwards. The immune cells that make tTg IgA antibodies which are triggered today are going to live for about two years. During that time, inflammation is heightened.  Those immune cells only replicate when triggered.  If those immune cells don't get triggered again for about two years, they die without leaving any descendents programmed to trigger on gluten and casein.  The immune system forgets gluten and casein need to be attacked.  The Celiac genes turn off.  This is remission.    Some people in remission report being able to consume gluten again without consequence.   However, another triggering event can turn the Celiac genes on again.   Celiac genes are turned on by a triggering event (physical or emotional stress).  There's some evidence that thiamine insufficiency contributes to the turning on of autoimmune genes.  There is an increased biological need for thiamine when we are physically or emotionally stressed.  Thiamine cannot be stored for more than twenty-one days and may be depleted in as little as three during physical and emotional stresses. Mitochondria without sufficient thiamine become damaged and don't function properly.  This gets relayed to the genes and autoimmune disease genes turn on.  Thiamine and other B vitamins, minerals, and other nutrients are needed to replace the dysfunctional mitochondria and repair the damage to the body.   I recommend getting checked for vitamin and mineral deficiencies.  More than just Vitamin D and B12.  A gluten challenge would definitely be a stressor capable of precipitating further vitamin deficiencies and health consequences.   Best wishes!    
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.