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

What's The Difference?


7-cody

Recommended Posts

Jestgar Rising Star

Tissue transglutaminase. A specific protein found in the gut.

Immunoglobin G. A generic name for a type of antibodies. They can be against almost anything (which means they recognize ) but each individual molecule is specific for it's individual thing.

Think of them like little kids in a shopping cart being pushed through a store. Every kid reaches out and grabs his/her favorite thing. Some of them grab the same thing as a different kid, but kid A always grabs Fruit Loops for example. anti-gliadin IgG always grabs gliadin.


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



Celiac.com Sponsor (A8-M):



  • Replies 78
  • Created
  • Last Reply
JennyC Enthusiast
dumb question here--what is the difference between tTG and IgG?

There's no such thing as a dumb question--especially not regarding this complicated stuff! IgG is an immunoglobulin or antibody. We have numerous types in our body such as IgA, IgM, IgE and IgG. They are meant to protect us from infection but also give rise to allergies. tTG is an enzyme. I think it is called tissue transglutaminase. I don't know the normal function off of the top of my head, but in celiac disease it alters the gluten molecule and it is one of the steps that takes place when celiac patients react to gluten.

Happygirl, thanks for posting that link. It's very interesting.

Guest Doll

Great posts and discussion on this thread! I just wanted to add that it is not uncommon to have antibodies against a specific target and not yet have clinical detectable disease. Examples of this are found in people who have antibodies to their thyroid gland, adrenal glands (Addison's Disease), or pancreas (Type 1 diabetes). Antibody screening is used to single out those who may be developing any of the above autoimmune diseases or is at high risk to develop them at a later date.

Perhaps we can assume that latent Celiac Disease (pos. antibodies, neg. biopsy) falls into the same category, assuming the negative biopsy is correct.

Another explanation I explained earlier, people with autoimmune diseases likely all share a leaky gut. Some genetics overlap, but you probably need additional genetics and seperate triggers for each autoimmune disease in addition to the shared genes and leaky gut.

So someone with autoimmune diseases or such in their family likely has a leaky gut and possibly will have some sort of response to gluten (ex. Anti-Gliadin antibodies) show up in bloodwork. But, they do not have the *additional* genetics needed for actual intestinal damage (Celiac Disease). I don't think anyone here can claim that gluten in and of itself can cause intestinal damage in those without the susceptible genes. People with a leaky gut will be having serious reactions, but not necessarily intestinal damage. People with a leaky gut and the genes for autoimmune diseases may benefit from the gluten-free diet, since it removes gluten as an immune system target. That doesn't mean gluten is the cause of these diseases, just that it is another foreign protein those with a leaky gut can react to, increasing inflammation. Inflammation is a state needed for autoimmune disease to develop, and it can be a symptom of autoimmunity as well (what I think).

Think of it this way...use another autoimmune disease, with the same type of pathology as Celiac. You are born with the genes for Type 1 diabetes. You cannot get the disease until something(s) in the environment "triggers" it. This is the understood model of autoimmunity.

Let's say the trigger is the coxsackie virus and then exposure to casein. Type 1 diabetes occurs in about 1 in 600 kids (give or take). The vast majority of kids can be exposed to the coxsackie virus and casein all day long, and they never get Type 1 diabetes. No matter what. Ever. Why? Because they were not born with the genes to develop it.

I think this was what Rachel-24 was saying, and I agree with her.

That said, those with the genes for autoimmunity in general would benefit from a gluten-free diet, even without intestinal damage. Why? Likely because they have a leaky gut and gluten may play a role in increasing "gut leakiness" and immune stimulation in those with a leaky gut. That said, those people will not get intestinal damage without the genes for actual Celiac though (from what I know).

If you seem to have a leaky gut from something else (mercury? Lyme? Bacterial overgrowth?) without any autoimmunity genes (including those for Celiac), then it would not make any sense to think that those people would get intestinal damage.

hathor Contributor

Oh, that clarifies things! (Though I disagree with their statement that 1% of the population is affected. That's all that's been diagnosed, but, as you say, it takes 11 years to get diagnosed, so the number of people affected must be substantially higher than 15!)

No, the 1% figure for celiacs is based on a study of blood donors (I believe it was) that were screened for celiac. There is no where NEAR that many people generally in this country who have actually been diagnosed. The figure I've always heard is that 97% are NOT diagnosed. One example:

"Roughly one out of every 133 Americans has celiac disease, but 97% remain undiagnosed. This means that almost three million Americans have celiac disease and only about 100,000 know they have it."

Open Original Shared Link

I've heard assorted figures for those who are gluten insensitive all over the ballpark, from 10% to 30% or more. I believe that Dr. Fine's research indicates a percentage meeting his diagnostic criteria near the upper end. I can't remember where I saw that though, so I can't tell you the number offhand. I've seen other estimates, but those folks don't say where their percentage comes from.

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. - Wheatwacked replied to GlutenFreeChef's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      12

      Blood Test for Celiac wheat type matters?

    2. - trents replied to JudyLou's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Seeking advice on potential gluten challenge

    3. - JudyLou posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Seeking advice on potential gluten challenge

    4. - marzian commented on Scott Adams's article in Diagnosis, Testing & Treatment
      5

      A Future Beyond the Gluten-Free Diet? Scientists Test a New Cell Therapy for Celiac Disease (+Video)

    5. - Jmartes71 posted a topic in Related Issues & Disorders
      0

      Medications

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

    • Total Members
      133,145
    • Most Online (within 30 mins)
      7,748

    Marsu
    Newest Member
    Marsu
    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)

  • Upcoming Events

  • Posts

    • Wheatwacked
      no argument. Never take the pills sold for Nuclear events, except in a nuclear event when instructed to by authorities.  Some of these go up to 130 milligrams per pill. 5000 times the strength of the dietary supplement.  130 times the safe upper limit.  130 mg = 130,000 mcg. Dietary supplements like Lugol's Solution and Liquid Iodine are 50 micrograms per drop.  It takes 20 drops to reach the safe upper limit. In the US the Safe upper limit is 1100 mcg.  In Europe 600 mcg and in Japan 3000 mcg ( 3 mg).
    • trents
      Welcome to the celiac.com community, @JudyLou! There are a couple of things you might consider to help you in your decision that would not require you to do a gluten challenge. The first, that is if you have not had this test run already, is to request a "total IGA" test to be run. One of the reasons that celiac blood antibody tests can be negative, apart from not having celiac disease, that is, is because of IGA deficiency. If a person is IGA deficient, they will not respond accurately to the celiac disease blood antibody tests (such as the commonly run TTG-IGA). The total IGA test is designed to check for IGA deficiency. The total IGA test is not a celiac antibody test so I wouldn't think that a gluten challenge is necessary. The second is to have genetic testing done to determine if you have the genetic potential to develop celiac disease. About 30-40% of  the general population have the genetic potential but only about 1% actually develop celiac disease. So, genetic testing cannot be used to diagnose celiac disease but it can be used to rule it out. Those who don't have the genetic potential but still have reaction to gluten would not be diagnosed with celiac disease but with NCGS (Non Celiac Gluten Sensitivity).  Another possibility is that you do have celiac disease but are in remission. We do see this but often it doesn't last.
    • JudyLou
      Hi there, I’m debating whether to consider a gluten challenge and I’m hoping someone here can help with that decision (so far, none of the doctors have been helpful). I have a history of breaking out in a horrible, burning/itchy somewhat blistering rash about every 8 years. This started when I was in my early 30’s and at that point it started at the ankles and went about to my knees. Every time I had the rash it would cover more of my body, so my arms and part of my torso were impacted as well, and it was always symmetrical. First I was told it was an allergic reaction to a bug bite. Next I was told it was eczema (after a biopsy of the lesion - not the skin near the lesion) and given a steroid injection (didn’t help). I took myself off of gluten about 3 weeks before seeing an allergist, just to see if it would help (it didn’t in that time period). He thought the rash looked like dermatitis herpetiformis and told me to eat some bread the night before my blood tests, which I did, and the tests came back negative. I’ve since learned from this forum that I needed to be eating gluten daily for at least a month in order to get an accurate test result. I’m grateful to the allergist as he found that 5 mg of doxepin daily will eliminate the rash within about 10 days (previously it lasted for months whether I was eating gluten or not). I have been gluten free for about 25 years as a precaution and recommendation from my doctor, and the pattern of breaking out every 8 years or so remains the same except once I broke out after just one year (was not glutened as far as I know), and now it’s been over 9 years. What’s confusing to me, is that there have been 3 times in the past 2 years when I’ve accidentally eaten gluten, and I haven’t had any reaction at all. Once someone made pancakes (they said they were gluten-free, they were not) and I ate several. I need to decide whether to do a gluten challenge and get another blood test. If I do, are these tests really accurate? I’m also concerned that I could damage my gut in that process if I do have celiac disease. My brother and cousin both had lymphoma so that’s a concern regarding a challenge as well, though there is a lot of cancer in various forms in my family so there may be no gluten connection there. Sorry for the ramble, I’m just doubting the need to remain gluten free if I don’t have any reaction to eating it and haven’t had a positive test (other than testing positive for one of the genes, though it sounds like that’s pretty common). I’d appreciate any thoughts or advice! 
    • Jmartes71
      Hello, just popped in my head to ask this question about medications and celiac? I have always had refurse reaction to meds since I can remember  of what little meds my body is able to tolerate. I was taking gabapentin 300mg for a week,  in past I believe 150? Any ways it amps me up not able to sleep, though very tired.However I did notice it helped with my bloating sibo belly.I hate that my body is that sensitive and medical doesn't seem to take seriously. Im STILL healing with my skin, eye, and now ms or meningioma ( will know in April  which)and dealing with this limbo nightmare. I did write my name, address ect on the reclamation but im not tech savvy and not sure if went through properly. I called my city representative in Stanislaus County and asked if theres a physical paper i can sign for proclamation for celiac and she had no clue about what I was saying, so I just said I'll go back on website. 
    • Scott Adams
      I'm not saying that some celiacs won't need it, but it should be done under a doctor's supervision because it can cause lots of problems in some people.
×
×
  • 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.