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

Yet Another Request For Thoughts On Lab Results


Nich617

Recommended Posts

Nich617 Newbie

I was recently tested for celiac with the tissue transglutaminase igA test (result was negative at 4.9. Reference range was <20=negative) and total igA (result was 381...just slightly higher than reference range of 69-380). I was also given a CBC with automated differentials that came back normal except for MCHC result was low at 32.2 with a range of 33-37.

Prior to this testing I had been eating a gluten free diet for about 3-4 weeks that resulted in a reduction of my symptoms. I am aware that my results may not be accurate due to the lack of gluten. I would be happy to listen to anyone's thoughts about my results. I have an appt with a new GI doc in a few weeks because the other left me hanging and communication was severely lacking. I am debating asking for another test when I go as I started eating gluten again a few days ago.

Also does anyone know what a high igA test result indicates?

Thanks!


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



Celiac.com Sponsor (A8-M):



Ksee Rookie

igA is produced naturally in the intestines. If abnormal there is indication of inflammation specific to intestinal problems but would suggest, not necessarily diagnose a condition.

MCH  indicates the size and color of red blood cells reflecting the concentration of hemoglobin in a sample. With otherwise normal values MCH can occasionally fall outside a normal range without being significant.

When a lab value falls slightly outside of normal, particularly in the presence of nothing to support the suspicion of a problem the common response is to wait. There are many variables affecting results that show up in this way such as machiine errors, time between blood draw and processing and normal body cycles.

Don't ever be afraid to ask. Education is power. :)

nvsmom Community Regular

I think the IgA is just one aspect of an active immune system, i believe it concerns areas of the body that has mucus like the intestinal tract and lungs. There are other parts too like the IgG, IgE, and IgM. I do not know of any problems of it being high but I am not an expert.

A biopsy might be a good idea for you at this point. Damage is often present for a while after going gluten-free. Autoantibodies go negative before the damage disappears.

After being gluten-free for a month, I imagine that you might have to consume gluten for a few weeks to get auto antibody levels up again... But again, I am not an expert. If you do have to eat gluten for a few weeks, I hope it isn't too hard on you.

Best wishes and welcome to the board.

Edited to say, the pp posted as I was, so ditto.

Deaminated Marcus Apprentice

Eat lots of gluten - bread till you see the new gastro - doctor.

 

This is a sample Celiac panel that covers more bases:

 

Total IgA
Transglutaminase IgA      tTG-IgA
Deaminated Gliadin IgA   DGP-IgA
Deaminated Gliadin IgG   DGP-IgG

 

Lucky you, I hope my doctor can send me to another gastro-doctor.

It didn't go well with the one I saw today.

Nich617 Newbie

Thank you all for your input. I appreciate it. I have read conflicting information and while I know no one can tell me exactly what is going  on but I am trying to get somewhat of an understanding as the Gastroenterologist I saw did not explain anything to me about my results and in fact, I couldn't even get a call back from her to ask these questions. To say I am irritated is an understatement. I wanted to discuss the possibility of doing an endoscopy but I refuse to go back so hopefully things will go better with the next doc. Good luck to all of you and thanks again!

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. - knitty kitty replied to Sarah Grace's topic in Related Issues & Disorders
      25

      Headaches / Migraines and Hypoglycaemia

    2. - trents replied to Sarah Grace's topic in Related Issues & Disorders
      25

      Headaches / Migraines and Hypoglycaemia

    3. - Scott Adams replied to Russ H's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      KAN-101 Treatment for Coeliac Disease

    4. - Scott Adams replied to miguel54b's topic in Related Issues & Disorders
      1

      Body dysmorphia experience

    5. - Scott Adams replied to Colleen H's topic in Related Issues & Disorders
      2

      Heat intolerant... Yikes


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,151
    • Most Online (within 30 mins)
      7,748

    Travis25
    Newest Member
    Travis25
    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

    • knitty kitty
      Excessive dietary tyrosine can cause problems.  Everything in moderation.   Sulfites can also trigger migraines. Sulfites are found in fermented, pickled and aged foods, like cheese.  Sulfites cause a high histamine release.  High histamine levels are found in migraine.  Following a low histamine diet like the low histamine Autoimmune Protocol diet, a Paleo diet, helps immensely.    Sulfites and other migraine trigger foods can cause changes in the gut microbiome.  These bad bacteria can increase the incidence of migraines, increasing histamine and inflammation leading to increased gut permeability (leaky gut), SIBO, and higher systemic inflammation.   A Ketogenic diet can reduce the incidence of migraine.  A Paleo diet like the AIP diet, that restricts carbohydrates (like from starchy vegetables) becomes a ketogenic diet.  This diet also changes the microbiome, eliminating the bad bacteria and SIBO that cause an increase in histamine, inflammation and migraine.  Fewer bad bacteria reduces inflammation, lowers migraine frequency, and improves leaky gut. Since I started following the low histamine ketogenic AIP paleo diet, I rarely get migraine.  Yes, I do eat carbs occasionally now, rice or potato, but still no migraines.  Feed your body right, feed your intestinal bacteria right, you'll feel better.  Good intestinal bacteria actually make your mental health better, too.  I had to decide to change my diet drastically in order to feel better all the time, not just to satisfy my taste buds.  I chose to eat so I would feel better all the time.  I do like dark chocolate (a migraine trigger), but now I can indulge occasionally without a migraine after.   Microbiota alterations are related to migraine food triggers and inflammatory markers in chronic migraine patients with medication overuse headache https://pmc.ncbi.nlm.nih.gov/articles/PMC11546420/  
    • trents
      Then we would need to cut out all meat and fish as they are richer sources of tyrosine than nuts and cheese. Something else about certain tyrosine rich foods must be the actual culprit. 
    • Scott Adams
      I agree that KAN-101 looks promising, and hope the fast track is approved. From our article below: "KAN-101 shows promise as an immune tolerance therapy aiming to retrain the immune system, potentially allowing safe gluten exposure in the future, but more clinical data is needed to confirm long-term effects."  
    • Scott Adams
      Thank you so much for having the courage to share this incredibly vivid and personal experience; it's a powerful reminder of how physical ailments can disrupt our fundamental sense of self. What you're describing sounds less like a purely psychological body dysmorphia and more like a distinct neurological event, likely triggered by the immense physical stress and inflammation that uncontrolled celiac disease can inflict on the entire body, including the nervous system. It makes complete sense that the specific sensory input—the pressure points of your elbows on your knees—created a temporary, distorted body map in your brain, and the fact that it ceased once you adopted a gluten-free diet is a crucial detail. Your intuition to document this is absolutely right; it's not "crazy" but rather a significant anecdotal data point that underscores the mysterious and far-reaching ways gluten can affect individuals. Your theory about sensory triggers from the feet for others is also a thoughtful insight, and sharing this story could indeed be validating for others who have had similar, unexplainable sensory disturbances, helping them feel less alone in their journey.
    • Scott Adams
      The most common nutrient deficiencies associated with celiac disease that may lead to testing for the condition include iron, vitamin D, folate (vitamin B9), vitamin B12, calcium, zinc, and magnesium.  Unfortunately many doctors, including my own doctor at the time, don't do extensive follow up testing for a broad range of nutrient deficiencies, nor recommend that those just diagnosed with celiac disease take a broad spectrum vitamin/mineral supplement, which would greatly benefit most, if not all, newly diagnosed celiacs. Because of this it took me decades to overcome a few long-standing issues I had that were associated with gluten ataxia, for example numbness and tingling in my feet, and muscle knots--especially in my shoulders an neck. Only long term extensive supplementation has helped me to resolve these issues.      
×
×
  • 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.