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

Severe Intolerance To Gliadin?


mmm1017

Recommended Posts

mmm1017 Rookie

I went to my neuro-endocrinologist today to discuss my saliva test. He was excited to explain the "why" of my thyroid issues, fibromyalgia, migraines, and slew of other issues. He said it was a severe intolerance to gliadin and I should avoid all grains like the plague. He said not to get confused with celiac disease, that it was only a subset. My saliva test read an SIgA level of 31. What does this mean? There is very little information on the internet about this. When I google gliadin, I come up with gluten. My doctor said that my body was not "allergic" to grains, it was more serious than that. Grains (corn included) were toxic to my body. Does any of this make sense? Where to go from here?


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



Celiac.com Sponsor (A8-M):



Sarah Alli Apprentice

I went to my neuro-endocrinologist today to discuss my saliva test. He was excited to explain the "why" of my thyroid issues, fibromyalgia, migraines, and slew of other issues. He said it was a severe intolerance to gliadin and I should avoid all grains like the plague. He said not to get confused with celiac disease, that it was only a subset. My saliva test read an SIgA level of 31. What does this mean? There is very little information on the internet about this. When I google gliadin, I come up with gluten. My doctor said that my body was not "allergic" to grains, it was more serious than that. Grains (corn included) were toxic to my body. Does any of this make sense? Where to go from here?

Well, I'm normally inclined to trust a doctor about matters like this, but my understanding was that gliadin is the actual substance that celiacs react to, not gluten. Gliadin is a component of "true" gluten found in triticae grains (wheat, barley, rye) and that is what differentiates that true gluten from proteins in corn, rice, etc that are sometimes called gluten but are not dangerous for a celiac.

That's my understanding. If you're ONLY reacting to gliadin that theoretically corn should not be a problem. That said, it does seem like there's more going on than just a gliadin intolerance- I think you need to go back to the doctor and really find out what is happening.

By the way, IgA is immunoglobulin A, it's an antibody that is involved in immune reactions and is often elevated in gluten intolerance and celiac. SIgA is probably saliva IgA- not sure about how that correlates to serum (blood) IgA levels but in your blood, an anti-gliadin IgA of 31 would be considered elevated.

Not sure if that's helpful. Talk to your doctor again, for sure.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,350
    • Most Online (within 30 mins)
      7,748

    Cypsue
    Newest Member
    Cypsue
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.1k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      You are welcome! We frequently get similar comments. Knowledge about celiac disease in the medical community at large is, unfortunately, still significantly lacking. Sometimes docs give what are obviously bum steers or just fail to give any steering at all and leave their patients just hanging out there on a limb. GI docs seem to have better knowledge but typically fail to be helpful when it comes to things like assisting their patients in grasping how to get started on gluten free eating. The other thing that, to me at least, seems to be coming to the forefront are the "tweener" cases where someone seems to be on the cusp of developing celiac disease but kind of crossing back and forth over that line. Their testing is inconsistent and inconclusive and their symptoms may come and go. We like to think in definite categorical terms but real life isn't always that way.
    • Rogol72
      Hey @Morgan Tiernan, Sounds just like my experience. I was diagnosed with dermatitis herpetiformis over 10 years ago. It appeared suddenly as a very itchy rash which looked like Eczema. When a steroid cream didn't clear it up, my Dermatologist (who had come across it before) suspected dermatitis herpetiformis and performed a skin biopsy which came back positive for dermatitis herpetiformis. The important thing is to get a definitive diagnosis of dermatitis herpetiformis. What you've described sounds like classic dermatitis herpetiformis though. Hopefully, your Dermatologist has come across dermatitis herpetiformis before and performs the skin biopsy correctly as trents mentioned. I've had the blisters on the knees, hips, forearms/elbows or anywhere that pressure is applied to the skin ... from clothing or otherwise. They itch like nothing on earth, and yes salt from sweat or soaps/shower gels will irritate a lot. I've been on Dapsone and it is very very effective at eliminating the dermatitis herpetiformis itch, and improved my quality of life in the early stages of getting on top of dermatitis herpetiformis while I adjusted to the gluten-free diet. But it does have various side effects as trents said. It can effect the red blood cells, lowering hemoglobin and can cause anemia, and requires regular blood monitoring whilst on it. You would need to consider it carefully with your Dermatologist if you do have dermatitis herpetiformis. Here's a very informative webinar from Coeliac Canada discussing everything dermatitis herpetiformis related.  https://www.youtube.com/watch?v=PAdmsNiyfOw I've also found this recent interview with a Dermatologist about dermatitis herpetiformis to be educational.  https://www.youtube.com/watch?v=rZnLeKutgUY Keep the chin up and keep advocating for yourself for a proper diagnosis. Though it sounds like you're on top of that already. Are you in the UK or Ireland? I'm curious because your surname is Irish. 
    • Philly224
      Thanks again everyone! Twenty mins on here way more helpful than both Dr's combined 😅
    • trents
    • trents
      I would go for four weeks to ensure a valid test, if you can tolerate it, that is.
×
×
  • Create New...