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

Need Help From Those With Experience, Blood Test?


arian

Recommended Posts

arian Apprentice

I just got my blood test back from the allergist, and he said my body is making antibodies against gluten. The thing is, I just wanted to confirm through him, what I already knew ( I knew before the appointment that I was gluten intolerant from my own elimation diet ) Anyway, heres my question. I haven't eaten ANY gluten in over 2 months, but it's still showing up on the blood test. Does this mean I'm possibly celiac or highly intolerant? For ex. if i was eating gluten everyday for six weeks before the test, would the antibody number be extremely high? thank you!


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



Celiac.com Sponsor (A8-M):



T.H. Community Regular

If you have antibodies, my understanding is that this is Celiac Disease; gluten intolerance doesn't involve the antibodies. Not as I understand it, anyway. I believe it is an entirely different physiological reaction than Celiac Disease.

Gluten contamination might be the explanation for the still high numbers, in that case, or if you were severely damaged and had extremely high antibodies, they might not have dropped enough yet. I think the former is more likely, though.

arian Apprentice

If you have antibodies, my understanding is that this is Celiac Disease; gluten intolerance doesn't involve the antibodies. Not as I understand it, anyway. I believe it is an entirely different physiological reaction than Celiac Disease.

Gluten contamination might be the explanation for the still high numbers, in that case, or if you were severely damaged and had extremely high antibodies, they might not have dropped enough yet. I think the former is more likely, though.

Thank you so much, thats what I thought :( the answer to 6 years of problems I think has been discovered, YAY:D I've been dealing with so many problems for so long, and not knowing the answer to what was causing all of it. I think I do now :)

IrishHeart Veteran

What blood tests did he do? Just curious.

and...yes, as TH says, if your antibodies are high, you've got a gluten problem.

Lisa Mentor

Anyway, heres my question. I haven't eaten ANY gluten in over 2 months, but it's still showing up on the blood test. Does this mean I'm possibly celiac or highly intolerant? For ex. if i was eating gluten everyday for six weeks before the test, would the antibody number be extremely high? thank you!

I think you're asking that if you ate a full gluten diet, prior to your testing, would your results be more positive? Maybe, maybe not. But, that's not too important. Positive is Positive. :)

Can you post the type of blood test your allergist recommended and your full results? You have mentioned that you feel better off gluten, that's a piece of the puzzle.

It's also possible, that although you are certain you were 100% gluten free, that you may not have been. Gluten is very tricky and it hides well. Lotions, shampoos, lipsticks/balm, some meds, shared toasters and dining out can be a real challenge...etc. The learning curve is steep.

arian Apprentice

What blood tests did he do? Just curious.

and...yes, as TH says, if your antibodies are high, you've got a gluten problem.

Ok so I asked, and my Ige was no number, but my Igg had a number -.- is that even a celiac test, I thought Iga was celiac test? Man im so bummmed, my allergist is NO help !!! someone help:(

IrishHeart Veteran

The antigliadin antibodies IgG and IgA recognize a small piece of the gluten protein called gliadin. These antibodies became available during the late 1970′s and were the first step towards recognizing celiac disease as an autoimmune disorder.

Antigliadin IgG has good sensitivity, while antigliadin IgA has good specificity, and therefore their combined use provided the first reliable screening test for CELIAC DISEASE.

Unfortunately, many normal individuals without CELIAC DISEASE will have an elevated antigliadin IgG, causing much confusion among physicians. The antigliadin IgG is useful in screening individuals who are IgA deficient, as the other antibodies used for routine screening are usually of the IgA class. It is thought that 0.2-0.4% of the general population has selective IgA deficiency, while 2 to 3% or more of celiacs are IgA deficient.

If a patient’s celiac panel is only positive for antigliadin IgG, this is not highly suggestive for CELIAC DISEASE if the patient has a normal total IgA level, corrected for age.

Younger children make less IgA than older children and adults.

A markedly elevated antigliadin IgG, such as greater than three to four times the upper limit of normal for that lab, is highly suggestive of a condition where the gut is leakier to gluten.

This can happen in food allergies, cystic fibrosis, parasitic infections, Crohn’s disease, and other types of autoimmune GI diseases. These antibodies may also be slightly elevated in individuals with no obvious disease.

that information is here:

Open Original Shared Link

Given this information, I would not assume I had Celiac Disease until I had a celiac panel run. The allergist did not run the IgA.....and according to this information, people can have elevated antigliadin IgG and have another condition-- as listed above. Or it could be nothing at all.

IMHO, you may wish to see a gastrointestinal doctor and bring these test results to him/her.? Something is going on and the allergist may not be able to help much further.

You have some information from this IgG test, yes, but I am not really sure if that is enough to say it's celiac disease or not.

Maybe someone else knows more and will chime in here.


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
      131,961
    • Most Online (within 30 mins)
      7,748

    Noa
    Newest Member
    Noa
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.