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

Total Serum Iga And Iga Deficiency......


wolfie

Recommended Posts

wolfie Enthusiast

Long story short.....my nutritionist suggested I get tested for Celiac and rule it out (I had been diagnosed with IBS and was trying to recover from an eating disorder). My PCP ordered the tests (I had no idea what the tests involved at this point in time ~ Dec 2005). The results came out IgG was positive at 55 (should be under 20). Anti-gliadin IgA was 5 (normal) and TtG was 2 (normal). PCP advised gluten-free diet and said I could see a GI specialist if I wanted. I went gluten-free and did end up seeing a GI after that. GI wanted to do endoscopy, but I had such a positive dietary response, she was okay with my just continuing the gluten-free diet unless I stopped feeling well or new symptoms arose. Fast forward to June....I finally convinced my kids Ped to test my son (10) and his TtG came back highly positive at 222 (supposed to be under 100). He is awaiting a GI appt on 8/15, still on gluten..LOL. So now I wonder......Is it possible the reason my tests came back the way they did is because I have an IgA deficiency? Can they test that now that I am off gluten? Not that it matters, but it may explain why the tests "looked" normal. Another factor....I had been on South Beach (lower carbs) for almost a year before I was tested, so that could have effected the test, too. One of the reasons I am curious, too, I want my dr to re-test either at 6 months or 1 yr gluten-free to make sure that all the tests are normal and wanted to know that if I do have that deficiency, whether or not the gluten-free diet will make a difference or whether that number will still how a deficiency if there is one. Sorry if that is confusing......I tried to make it as clear as possible.

Thanks for all thoughts. :)


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



Celiac.com Sponsor (A8-M):



chrissy Collaborator

i'm a little confused as to what you are asking. are you wondering about your anti-gliadin and TTg levels being in the normal range? what IgG levels came back high?(endomysial, TTg, etc.?) my son is IgA deficient also. on his original TTg test he came back with a .1-----the rest of us (normal IgA) came back with values such as: .6, .7, etc.----except the kids with celiac, of course---they were higher. we did testing through promethius on him, which showed he as the DQ2 gene, but showed no active disease. he also says the test is inconclusive (i'm a tad confused here?) he told us that ian needs to be tested yearly. i'm sure none of this helped.......but this is our experience with IgA deficiency.

TCA Contributor

We did gene testing through proemehteus, but the other tests were through a local lab and IgA deficiency wasn't tested. Prometheus sent us a nice little packet by calling 1-888-423-5227 if you want one. I have the same question you have (I understood, believe it or not, :P ). Does a gluten-free diet improve IgA deficiency?

wolfie Enthusiast

The IgG was Anti-gliadin...sorry!!

Yes, does a gluten-free diet improve the IgA deficiency or would that remain.

chrissy Collaborator

i don't think a gluten free diet will change the total IgA serum levels. our ped gi tested the total IgA serum levels when he did the first TTg levels on our family, i assume so that he would know what tests to run in the future.

if i understand things right, TTg shows how much damage there is, and anti-gliadin levels can be raised in other conditions besides celiac. ( i think crohns might raise it)

how are you doing in your recovery from your eating disorder----i'm really hoping you're going to tell me something positive!!!

loraleena Contributor

Not that this is what you are asking, but I am amazed at how many of us have or have had eating disorders. I wouldn't be surprised if this was a triggering factor for me.

wolfie Enthusiast
i don't think a gluten free diet will change the total IgA serum levels. our ped gi tested the total IgA serum levels when he did the first TTg levels on our family, i assume so that he would know what tests to run in the future.

if i understand things right, TTg shows how much damage there is, and anti-gliadin levels can be raised in other conditions besides celiac. ( i think crohns might raise it)

how are you doing in your recovery from your eating disorder----i'm really hoping you're going to tell me something positive!!!

I am doing very well in my recovery, thanks for asking. I am 33 now, but started with anorexia at 15 (got down to 95 lbs at 5'7" tall). I was recovered the first time by 17, but never had counseling and was never told that I could relapse. Last year at 32 and 2 kids later, I found myself back in my old habits.....obsessing about my weight (more specifically the # involved....OCD) and restricting foods (calories/carbs). I wasn't even overweight at the time (5'7" and 128 lbs), just had a lot of anxiety and OCD issues. I told my dr at my yearly (down to 118) in Oct and she put me on Lexapro and referred me to a counselor and nutritionist (the one who caught my Celiac/gluten intolerance). I was honestly trying to get better at that point, but so many foods bothered me that I think subconciously I wasn't eating anymore b/c it hurt. Now, almost 6 months into the gluten-free diet I am up 10 pounds and feel better than I have in years. I am hoping to get off the Lexapro in the next 6 months, as I hope the anxiety is much improved since removing gluten from my diet.

Sorry that got so long!!!


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,899
    • Most Online (within 30 mins)
      7,748

    dcarter1682
    Newest Member
    dcarter1682
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • trents
      Welcome to the forum, @Judy M! Yes, he definitely needs to continue eating gluten until the day of the endoscopy. Not sure why the GI doc advised otherwise but it was a bum steer.  Celiac disease has a genetic component but also an "epigenetic" component. Let me explain. There are two main genes that have been identified as providing the "potential" to develop "active" celiac disease. We know them as HLA-DQ 2.5 (aka, HLA-DQ 2) and HLA-DQ8. Without one or both of these genes it is highly unlikely that a person will develop celiac disease at some point in their life. About 40% of the general population carry one or both of these two genes but only about 1% of the population develops active celiac disease. Thus, possessing the genetic potential for celiac disease is far less than deterministic. Most who have the potential never develop the disease. In order for the potential to develop celiac disease to turn into active celiac disease, some triggering stress event or events must "turn on" the latent genes. This triggering stress event can be a viral infection, some other medical event, or even prolonged psychological/emotional trauma. This part of the equation is difficult to quantify but this is the epigenetic dimension of the disease. Epigenetics has to do with the influence that environmental factors and things not coded into the DNA itself have to do in "turning on" susceptible genes. And this is why celiac disease can develop at any stage of life. Celiac disease is an autoimmune condition (not a food allergy) that causes inflammation in the lining of the small bowel. The ingestion of gluten causes the body to attack the cells of this lining which, over time, damages and destroys them, impairing the body's ability to absorb nutrients since this is the part of the intestinal track responsible for nutrient absorption and also causing numerous other food sensitivities such as dairy/lactose intolerance. There is another gluten-related disorder known as NCGS (Non Celiac Gluten Sensitivity or just, "gluten sensitivity") that is not autoimmune in nature and which does not damage the small bowel lining. However, NCGS shares many of the same symptoms with celiac disease such as gas, bloating, and diarrhea. It is also much more common than celiac disease. There is no test for NCGS so, because they share common symptoms, celiac disease must first be ruled out through formal testing for celiac disease. This is where your husband is right now. It should also be said that some experts believe NCGS can transition into celiac disease. I hope this helps.
    • Judy M
      My husband has had lactose intolerance for his entire life (he's 68 yo).  So, he's used to gastro issues. But for the past year he's been experiencing bouts of diarrhea that last for hours.  He finally went to his gastroenterologist ... several blood tests ruled out other maladies, but his celiac results are suspect.  He is scheduled for an endoscopy and colonoscopy in 2 weeks.  He was told to eat "gluten free" until the tests!!!  I, and he know nothing about this "diet" much less how to navigate his in daily life!! The more I read, the more my head is spinning.  So I guess I have 2 questions.  First, I read on this website that prior to testing, eat gluten so as not to compromise the testing!  Is that true? His primary care doctor told him to eat gluten free prior to testing!  I'm so confused.  Second, I read that celiac disease is genetic or caused by other ways such as surgery.  No family history but Gall bladder removal 7 years ago, maybe?  But how in God's name does something like this crop up and now is so awful he can't go a day without worrying.  He still works in Manhattan and considers himself lucky if he gets there without incident!  Advice from those who know would be appreciated!!!!!!!!!!!!
    • Scott Adams
      You've done an excellent job of meticulously tracking the rash's unpredictable behavior, from its symmetrical spread and stubborn scabbing to the potential triggers you've identified, like the asthma medication and dietary changes. It's particularly telling that the rash seems to flare with wheat consumption, even though your initial blood test was negative—as you've noted, being off wheat before a test can sometimes lead to a false negative, and your description of the other symptoms—joint pain, brain fog, stomach issues—is very compelling. The symmetry of the rash is a crucial detail that often points toward an internal cause, such as an autoimmune response or a systemic reaction, rather than just an external irritant like a plant or mites. I hope your doctor tomorrow takes the time to listen carefully to all of this evidence you've gathered and works with you to find some real answers and effective relief. Don't be discouraged if the rash fluctuates; your detailed history is the most valuable tool you have for getting an accurate diagnosis.
    • Scott Adams
      In this case the beer is excellent, but for those who are super sensitive it is likely better to go the full gluten-free beer route. Lakefront Brewery (another sponsor!) has good gluten-free beer made without any gluten ingredients.
    • trents
      Welcome to the forum, @catsrlife! Celiac disease can be diagnosed without committing to a full-blown "gluten challenge" if you get a skin biopsy done during an active outbreak of dermatitis herpetiformis, assuming that is what is causing the rash. There is no other known cause for dermatitis herpetiformis so it is definitive for celiac disease. You would need to find a dermatologist who is familiar with doing the biopsy correctly, however. The samples need to be taken next to the pustules, not on them . . . a mistake many dermatologists make when biopsying for dermatitis herpetiformis. 
×
×
  • 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.