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

Oat Anti-bodies?


guy220d

Recommended Posts

guy220d Rookie

I know about tests for gliadin and reticulin antibodies, but is there such a thing as a blood test for avenin? I was curious because I think I have my strongest reaction (headache, nausea, cramping) to eating oats.


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



Celiac.com Sponsor (A8-M):



VydorScope Proficient
I know about tests for gliadin and reticulin antibodies, but is there such a thing as a blood test for avenin? I was curious because I think I have my strongest reaction (headache, nausea, cramping) to eating oats.

None that I have heard of yet. Wish there was!

hungryforlife Apprentice
I know about tests for gliadin and reticulin antibodies, but is there such a thing as a blood test for avenin? I was curious because I think I have my strongest reaction (headache, nausea, cramping) to eating oats.

Hi Guy22od:

Oats are the only thing that I have a strong reaction too. I can eat bread products, (I have the subtle symptoms, ie. tiredness, brain fog, occasional body dumping etc.) But when I eat oats it is fast and immediate, it is as if I have just been poisoned. I ate oatmeas EVERY day for about three years, along with changing to whole wheat products and a whole "healthy diet." I continued to get sicker and sicker, neuropathy, stomach, blood sugar issues, etc. I was to the point that I could not get out of bed. After taking oats out of my diet and am starting to feel better. I am having my scope at the end of the month and CANNOT wait to go completely gluten free.

Good luck to you. (I often wondered if I am just not allergic to oats?)

Guest Robbin

Oats and barley were the big ones for me, but I noticed everything starting with oat problems. Even the Irish oatmeal gave me a severe reaction. I almost wonder if it is because of gluten AND oat fiber. Have either of you noticed barley giving the same immediate reaction as with oats?

jenvan Collaborator

No test yet. Some Celiacs do react to pure oats. However, it also could have been gluten contamination in your oats that caused the issue.

hungryforlife Apprentice

Hi Robbin, I barley and rye are not really a part of my diet so I cannot comment on them. I try to believe the cross contamination rational, but I can eat pure whole wheat flour, or things like shredded wheat and not have a reaction. But one bowl of oats and the whole stomach thing starts again and stays with me for days. At first I thought it was the fiber, but I take fiber everyday and have forever, so I thought it may be too much fiber so gave up the physillim (sp?) and oats would still make me ill. I put the fiber back in and gave up oats and my issue went away. I ate oatmeal one day a week ago after my Gastro appointment, thinking I would just add them back in until my scope at the end of the month. BAD IDEA! A VERY BAD IDEA. I am still suffering the affects.

So, I figure, it could be cross contamination in some, but some just really have a bad reaction to oats. I know without a doubt oats will not be a part of my gluten free life.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,901
    • Most Online (within 30 mins)
      7,748

    tessycork47
    Newest Member
    tessycork47
    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

    • 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.