Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Iga At 203.74 Am I Celiac?


cindybea

Recommended Posts

cindybea Newbie

Doctors spend 15 minutes with you. That is the time you get. I am consulting you ... whoever is out there... (I have never blogged before) because I am overwhelmed and do not know what to do next.  I suffered from stomach pain during my early childhood. Finally, I had my appendix removed when I was 14 (1979). I am a school librarian, mother of 3, and fairly active but nearly always in pain. Just sold our motorcycle because of so much hip and joint pain. My doctor, 4 years ago, put me on Lyrica. I took it for a month and dumped it in the garbage and lived with the neuropathy, joint pain, and "fibromyalgia" my doctor diagnosed me with.  I am very active and work with K - 5th grade students. In December 2013 I read Wheat Belly and decided to go off gluten. I am Italian and this was a very difficult thing to do. I felt a lot  better but did not really go off. I just read Grain Brain (Brother had Schizophrenia / Dad suffering from Dementia) by Perlmutter and decided to switch doctors and ask for a celiac panel test. My IGA came out at 203.74. The test information said anything over 30 was bad. My doctor casually mentioned that I should stay away from gluten. I pretty much was off of it since December 2013. I had the test 2 weeks ago. I am overwhelmed. She did not diagnose me as having Celiac disease. I feel like I have it. There are so many people who do not believe it could be that and suggest gluten containing products to me. Since Monday (when I received the numbers I have been researching and will stay off all of it) but I guess I am simply asking for your input. Should I look further and get a biopsy? Should I take the number and just stay off gluten and who cares what family and friends are thinking? Sorry I sound so illogical.  I am not that type of person but I am overwhelmed at this point in time.

Thanks to anyone who is out there who has been through this or can assist. 

Cindy Bea


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



Celiac.com Sponsor (A8-M):



nvsmom Community Regular

Welcome to the board! Glad you found us. :)

 

Do you know exactly which test you had done?  The IgA (immunoglobulin A often called total serum IgA) is not actually a celiac test but a measure of you immune response in the mucosal linings of the body (intestines, mouth, etc).  Some doctors (incorrectly) shorten some of the celiac disease test names that are based on IgA, so it can get confusing.

 

These are the actual celiac disease tests:

  • tTG IgA and tTG IgA (tTG = anti-tissue transglutaminase) - the most common celiac disease tests
  • DGP IgA and DGP IgG (anti-deaminated gliadin peptides) - a new test which is good at detecting earlier celiac disease
  • EMA IgA (anti-endomysial)  -  similar to the tTG IgA but tends to be positive in more advanced cases
  • total serum IgA - a control test to ensure that the patient makes enough IgA for the IgA based celiac disease tests (tTG IgA, etc) to be accurate; 5% of celiacs are deficient in IgA but it generally does not impact one's health
  • AGA IgA and AGA IgG (anti-gliadin antibodies) - older and less reliable tests
  • Endoscopic biopsy (6+ samples taken)

For accurate tests, you must be consuming gluten (1-2 slices of bread per day or the equivalent) in the 8-12 weeks prior to testing; the biopsy only requires 2-4 weeks on gluten. A celiac who is gluten-free for a time (weeks to months) will eventually have falsely negative tests.

 

My guess, and it's only a guess, is that the doctor either ran the tTG IgA or AGA IgA, and it was positive so you are most likely a celiac OR he just ran the (total serum) IgA and mistakenly thinks it is a celiac test.

 

Can you clarify which tests were run?  It's confusing, isn't it.  Hang in there.

SMRI Collaborator

I would find a Celiac center or a GI that specializes in Celiac disease.  They will have the resources to help you and properly diagnose you.  There is a board here to search for doctors or ask for help, but if you are near a major metro area, chances are there is a Celiac clinic near you.   I use the analogy that sure, your dermatologist is a doctor and can probably deliver your baby, but going to an Ob/Gyn is better.  I see a lot of people here go to their GP dr for Celiac testing, and while there is nothing wrong with starting there, a Celiac specialist will be more up on the latest news and have more resources for you.

cindybea Newbie

Dear Nvsmom and Smri,

Thank you so much for replying. I learned from your posts and I appreciate it. I believe my next step is to find a specialist ... very good advice. 

I did see my General Practitioner. She said she did a "Celiac Panel blood test". The report says:

 

Gliadin IGG : 9.35       < 15 normal

 

Gliadin IGA 203.74      <15 normal

 

Endomysial IgA AB   Negative

 

Antireticulin AB IgA   Negative

 

Reference Lab: Quest Diagnostics Wood Dale IL, 

 

CCp AntiBody IgG:  1.50     <4.0 normal

 

"Results obtained from this date forward were obtained with the Immulite 2000. Results from other manufacturers assay methods may not be used interchangeably."

 

.....From my written report (Gliadin Iga) is what is listed....since it is not written  tTG Iga or DGP IGA can I assume that it is an AGA IGA number? 

 

I should see a specialist to explain but I don't want to start eating gluten again. My, that would kill me. I have been off since December (with a few cheating because I did not know what I was dealing with). Seeing my IGA (which ever one that means) at 203 and knowing that anything over 15 is not normal....I'm scared and now view gluten as a poison.

 

I can't help but think what are all those antigens doing in my body now and I do not want to create more by eating gluten every day in order to have another test.

 

I probably should see a specialist so they can educate me. It is confusing. I have been reading for days. Maybe I can call the lab and have them further explain the tests as well.  

 

Thank you ... truly... for being kind and educating me. I appreciate all the knowledge you can bestow. 

 

Cindy

SMRI Collaborator

Others will know better than I but an Glidan IgA of over 200 being Gluten free for over 6 months seems suspect, especially with everything else being in the normal range.  I would get with a Celiac dr as soon as you can and see what is really going on.

cindybea Newbie

Thank you again for your help. I just made an appointment with a GI doctor who specializes in Celiac. I have the appointment July 31st. I feel like I am on a not so fun journey. 

Cindy Bea

nvsmom Community Regular

You could always try the other tests (tTG IgA, tTG IgG, DGP IgA and DGP IgG) now.  It is possible that your body still has high enough auto-antibody levels after 6 months of eating gluten-light - it sounds like you were not quite gluten-free which requires zero gluten. Sometimes a little gluten is enough for those tests, and sometimes the auto-antibodies are made for a long time.  You might get answers if you test now.

 

I agree that the test you were positive on was probably the AGA IgA.  They ran an older panel on you, the anti- reticulin IgA is an older test that is very rarely used anymore. The AGA IgA usually indicates a gluten sensitivity if it is positive. Some doctors believe that a positive AGA test can indicate non-celiac gluten sensitivity (NCGS) as well as celiac disease, but in my mind there isn't much difference between them except that celiac disease also damages the intestines and is better known than NCGS - they have the same symptoms. I believe the AGA IgA is about 80-95% specific to celiac disease as seen on this report (pages 10-12): Open Original Shared Link

 

See a GI specialist if you can.  He might want to do an endoscopic biopsy which requires only an 2-4 week gluten challenge. That would also tell you whether the positive AGA IgA is caused by celiac disease or NCGS... probably - the test is only 80% accurate.

 

Feel free to go gluten-free now though. Just be aware of nutritional deficiencies that can appear like low Cu, Fe, Mg, K, Ca, D, B12, A, ferritin, zinc. Also be aware that hypothyroidism is found in 10-15% of celiacs so know those symptoms and maybe get tested for it (TSH, free T4 and free T3, TPO Ab). 

 

Best wishes.  :)


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



Celiac.com Sponsor (A8-M):



Gemini Experienced

Cindy.........The test you were positive on is the AGA IgA, which shows you are reacting to gluten, big time. The rest of your testing appears normal but the bottom line is that you are strongly reacting to gluten.  You could either have the testing done again with the tests that nvsmom has so expertly suggested or push for a biopsy, if an official diagnosis is what you want.  Your IgA test could have been much, much higher before you went gluten free/gluten lite.  I am not sure how strict you were with your diet. You know you need to be ingesting gluten for more testing but the fact it still was that high after being gluten-free for awhile speaks volumes.  You either were gluten lite or you were gluten free and your numbers were much higher and have come down to the 200+ number, which would not be unusual with numbers that high.  It can take a couple of years for blood work to normalize.

 

You need to be gluten free but whether you want to be further aggravated with doctors or just go gluten free and not look back is up to you.  I wish you luck!

cindybea Newbie

Thank you all. You have provided me with very useful information. Life is busy and active so I greatly appreciate you taking the time to help me. I will keep you posted. For now I will continue eating healthy as I am without gluten and share everything with my doctor July 31st. In the meantime I will keep reading and educating myself. I know I feel much better not eating gluten. One step at a time. It sure is comforting knowing you are here. Also...thank you for the vitamin/mineral information. I will take a supplement and share that also with doctor. 

Cindy Beatrice

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,085
    • Most Online (within 30 mins)
      7,748

    NoriTori
    Newest Member
    NoriTori
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Jmartes71
      I am actively dealing with a ray of issues, my skin, eyes and digestive even though not eating wheat.Menopuase has activated so much right now, considering its getting worse with my health. I have learned so much thanks to this website.I wasn't properly told of my celiac disease which was confirmed by colonoscopy and endoscopy in 1994 the same year I gave birth to my first son, my tolerance level was horrible. After being diagnosed and staying away from wheat continued problems. My chiropractor at the time in 2007 had my blood work sent off and turns out I have more food allergies. I told my primary of my celiac disease in 2000 and continued to see that doctor up until May if this year 2025 considering my celiac disease was ignored, disregarded and what Im currently going through and been through. I assumed my celiac disease was " registered " at the time in 1994 just as pregnancy and other ailments are reported. I was shocked to learn that its not a mandated reportable disease not documented by the state from hospitals which I for one think it should be considering all the medical gaslighting im dealing with which is causing depression. Im told not worry about other, well I am and its NOT right.It needs to be documented so others don't suffer and go through this nightmare. Im seriously ready to go down to the mayors office and make some noise. Thoughts?
    • Wheatwacked
      With all the bloodwork, have they checked your vitamin D?  What is it?  Celiac Disease causes malabsorption, so vitamin deficiencies are common.  Doctors rarely mention this. B1 Gastrointestinal beriberi, a severe thiamine deficiency, is characterized by symptoms including anorexia (loss of appetite), abdominal discomfort and pain, nausea, and vomiting. Other potential symptoms like abdominal fullness, indigestion, and constipation can also occur. These gastrointestinal issues may resist standard treatments, signaling a need to consider thiamine deficiency.  It is commonly believed that thiamine deficiency is not an issue in the western cultures, so rarely address by doctors. Doses of thiamine above 100 mg several times a day will quickly show improvement.  Borderline deficiency will come and go depending on what your eat.  Carbs use it up faster, so for example if you eat a lot of carbs today, tomorrow you may have symptoms.  Thiamine (Benfothiamine is a synthetic fat soluable thiamine) is water soluable, we only store maybe a weeks worth, and there is no upper limit on how much you consume.  Excess is stored or peed away.   For them it isn't a oroblem.  LOL.  They just say some people are like that and see the next patient.  
    • sillyac58
      I used the cream for 4 days as prescribed 3 years ago. While I cannot be sure it triggered these problems, the timing is very suspicious. Yes, the oats are gluten free, and while I knew some celiacs have a problem with oats, I only just thought to eliminate them.  I just read about corn on this website, which I do eat plenty of. I do eat dairy, and would be so terrible sad to give it up, but..... Thank you for the diary suggestions. I'll start one today. Thanks for responding!
    • trents
      Welcome to the forum, @sillyac58! Are you still using this topical medication for this precancerous spot on your lip? If not, are you saying you used it for a limited time and believe it triggered additional ongoing immune system reactions with unpleasant symptoms? I'm not clear on this. Are the oats you use certified gluten free? You may know this already, but even if they are certified gluten free, the oat protein avenin is similar enough to gluten to cause reactions in some celiacs. The development of other food intolerances is also common in the celiac community. Common offenders in addition to oats are dairy, eggs corn and soy. Dairy and oats are the most common, however. You might do well to keep a food diary and check for patterns.
    • sillyac58
      I was diagnosed about 10 yrs ago with Celiac by presenting with dermatitis herpetiformis rash. I had no stomach or intestinal discomfort, but of course showed intestinal damage. The dermatitis herpetiformis eventually went away and I've been religiously gluten free ever since. About 3 years ago I was given a topical drug by a dermatologist for pre cancerous spot on my lip. The drug is called Imiquimod/Aldara, and works by stimulating your immune system. ? The package insert and many releable online sources warn to use caution using this drug if one has an auto immune disease, I hace since found out. One of the side effects is flu like symtoms, which I had at the 10 day mark as warned. But these symptoms have been recurring regularly ever since. Low grade nausea (no vomiting), extreme fatique (sleeping in daytime) and often a migraine headache on day one or two. The bouts last around 5 days or more, usually the nausea being the persistent symptom. My dermatologist, and another I went to for second opinion say this isn't a problem. I have been ill about a third of my life ever since. I have had extensive bloodwork, been to numerous specialists, but cannot figure out what is making me sick. I have become neurotic about gluten at home, using separate cutting boards, pans, sponges, dish towels, etc. I rarely eat out, and usually only because I am traveling. I have begun taking my own food to peoples homes for dinners etc. The only thing I haven't done, until now, is to eliminated oats, which I eat fairly regularly, and are known to sometimes be a trigger. And I have to say, in my defense, that it took me a very long time to suspect gluten because my only original symtom was rash/dermatitis herpetiformis. So I didn't associate the nausea/headache/fatique with gluten for a long time. Nor did any one of the many doctors I saw suspect it. I finally had a couple of dermatitis herpetiformis spots (and severe migraine) when traveling and probably eating cross contaminated food. I've never been on one of these sights but I am desperate. I'm praying it's as simple as eliminating oats. But I am angry that I was given this drug that I truly believe set this off to begin with. Anyone?
×
×
  • Create New...