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

Blood Test Question - Are There Different Reference Limits For Gluten Intolerance Versus Celiac?


Tim86

Recommended Posts

Tim86 Apprentice

I recently received my results from blood testing for Celiac. They are calling the results "negative for Celiac", since everything is within their reference limits. Are the limits different for gluten intolerance? For example, on the IgA, let's imagine there were a limit of 200 to indicate intolerance, but you have to be over 400 to call it Celiac. If that were true, I would be positive for gluten intolerance (I had a 247). Just wondering...because it seems that gluten intolerance is simply a milder version of Celiac.

My results:

Tiss Transglutamin IgA - 1 U/mL (0-3 reference)

Tiss Transglutamin IgG - 1 U/mL (0-3 reference)

Anti-Gliadin IgG Ab - 2.4 U/mL (0-10 reference)

Anti-Gliadin IgA Ab - 3.3 U/mL (0-10 reference)

Endomysial IgA Ab - Negative

IgA - 247 MG/DL (70-400 reference)


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



Celiac.com Sponsor (A8-M):



Korwyn Explorer
I recently received my results from blood testing for Celiac. They are calling the results "negative for Celiac", since everything is within their reference limits. Are the limits different for gluten intolerance? For example, on the IgA, let's imagine there were a limit of 200 to indicate intolerance, but you have to be over 400 to call it Celiac. If that were true, I would be positive for gluten intolerance (I had a 247). Just wondering...because it seems that gluten intolerance is simply a milder version of Celiac.

My results:

Tiss Transglutamin IgA - 1 U/mL (0-3 reference)

Tiss Transglutamin IgG - 1 U/mL (0-3 reference)

Anti-Gliadin IgG Ab - 2.4 U/mL (0-10 reference)

Anti-Gliadin IgA Ab - 3.3 U/mL (0-10 reference)

Endomysial IgA Ab - Negative

IgA - 247 MG/DL (70-400 reference)

Gluten intolerance is not just a milder version of Celiac. Celiac is a auto-immune disease triggered secondary to a pathological response to the gluten protein. Simple gluten intolerance will not cause auto-immune disorder. However that said, GI can be a sickening as celiac disease and can lead to a host of other issues such as leaky gut, which can cause a huge number of secondary or tertiary related conditions, not the least of which are nutrient deficiencies.

nora-n Rookie

This IgA test here is not a celiac test per se, it is to check if you are IgA deficient. 10% are IgA deficient and in that case, the IgA version of the tests here (ttg IgA, Antigliadin IgA) are not valid since the total Ig is low.

Yours is normal I think.

Note that your tests have a number, they are not 0, maybe that means something.

Those tests are calibrated so they do not turn positive until there is a lot of gut damage. Usually it is hard or impossible to detect early celiac. Scientists have tested relatives of celiacs over a period of years, and first the antigliadin IgG tests turned positive, then the others. (that is shy doctors regard those tests for unreliable, because they can tur out positive even though the biopsy is still negative)

Tim86 Apprentice
Gluten intolerance is not just a milder version of Celiac. Celiac is a auto-immune disease triggered secondary to a pathological response to the gluten protein. Simple gluten intolerance will not cause auto-immune disorder.

If they are not the same thing, then does gluten intolerance require the same "all or nothing" approach to a gluten-free diet as Celiac? For example, if you unknowingly consume a small amount of gluten, is it not as big of a deal if you are gluten intolerant, compared to if you had Celiac?

elle's mom Contributor

Good question Tim86, I am wondering the same thing. If a "gluten-intolerant" person cannot be detected by antibodies or endoscopy, even though they have symptoms, wouldn't it stand to reason that simply lowering the gluten intake enough to alleviate symptoms would be OK, since there isn't an actual autoimmune component harming their intestines? Does anyone know the answer to this?

ang1e0251 Contributor

I don't think there is a consensus on this question. I understood it to be the way you described when I started out but since then I have read so many opposing medical opinions that I don't know who is right. I tend to think, just my personal opinion, the GI is the starting point to further damage that can at the correct point of intestinal damage be labeled as celiac disease. And how do we know which tests are accurate or not, or interpreted correctly or not. It seems like kind of a crap shoot to me.

If I suspected I was GI, I think I would try to be concientous about the diet. Just because dr's might now say you aren't sustaining other damage, doesn't mean I believe that. After all you are experiencing strong symptoms and how can that be if there is no kind of inflammation or damage. And it wasn't that long ago that Dr's said children could be healed from celiac disease and go back to eating gluten. Many have been harmed by that advice.

jamied Newbie

i just received fibromyalgia diagnosis few months ago after 10yrs of off/on problems.

it was severe enough around Good Friday that I ultimately could not climb the stairs in my house, my bf had to carry me!!??

since the diagnosis i been doing ALOT of reading...

was my ingestion of gluten causing my inflammatory markers to be high from last October to May??

i have stopped eating 99% of all gluten (except that lil bit that gets thru the ingredient detection radar, lol)

and have had REMARKABLE results to date.

so, will i benefit frm genetic testing??

i am UNWILLING to begin consuming gluten again.

side note: i used to vomit on a daily basis for no apparent reason at all....since childhood,

after 32yrs of getting sick, i have not been nausea or vomited since going gluten-free.

crazy!!!!!!!!!!!!!!!

ive had brain scans, mri, cat scans, nuclear testing etc....im thinking this is what was making me sick!


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



Celiac.com Sponsor (A8-M):



JennyC Enthusiast
Note that your tests have a number, they are not 0, maybe that means something.

Those tests are calibrated so they do not turn positive until there is a lot of gut damage. Usually it is hard or impossible to detect early celiac. Scientists have tested relatives of celiacs over a period of years, and first the antigliadin IgG tests turned positive, then the others. (that is shy doctors regard those tests for unreliable, because they can tur out positive even though the biopsy is still negative)

Only numbers above the reference range are indicative of celiac disease. The values seen within the reference ranges can frequently be seen in the healthy population, and it also gives a little "wiggle room" for slight error that may be inherent in the test or differences between technologists in their reporting.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,189
    • Most Online (within 30 mins)
      7,748

    Eric bell
    Newest Member
    Eric bell
    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

    • Ginger38
      So I recently had allergy testing for IGE antibodies in response to foods. My test results came back positive to corn, white potatoes, egg whites. Tomatoes, almonds and peanuts to name a few.  I have had obvious reactions to a few of these - particularly tomatoes and corn- both GI issues. I don’t really understand all this allergy versus celiac stuff. If the food allergies are mild do I have to avoid these foods entirely? I don’t know what I will eat if I can’t  have corn based gluten free products 
    • Kris2093u4
      Geography makes a difference.  I'm in the West and Trader Joe's gluten-free bread tastes great and is a better price than most gluten-free breads sold elsewhere in my area.  
    • JForman
      We have four children (7-14 yo), and our 7 year old was diagnosed with NCGS (though all Celiac labs were positive, her scope at 4 years old was negative so docs in the US won't call it celiac). We have started her on a Gluten Free diet after 3 years of major digestive issues and ruling out just about everything under the sun. Our home and kitchen and myself are all gluten-free. But I have not asked my husband/her dad or her other siblings to go completely gluten-free with us. They are at home, but not out of the home. This has led to situations when we are eating out where she has to consistently see others eating things she can't have and she has begun to say "Well, I can't have <fill in the blank>...stupid gluten."  How have you supported your gluten-free kiddos in the mental health space of this journey, especially young ones like her. I know it's hard for me as an adult sometimes to miss out, so I can't imagine being 7 and dealing with it! Any tips or ideas to help with this? 
    • Jane878
      By the time I was 5 I had my first auto0immune disorder, Migraine headaches, with auras to blind me, and vomiting, sensitivity to light and sound. I was 5 years old, and my stepfather would have pizza night, milling his own flour, making thick cheesy gluten pizza, that I would eat and the next day, I would have serious migraines, and my mother & stepfather did nothing about my medical problems. When I was 17 in my first year at college, I was diagnosed with my 2nd known auto-immune disorder, Meniere's disease. I was a elite athlete, a swimmer, and soccer player. And once again my parents didn't think anything of understanding why I had a disorder only older people get. Now after my mother passed from Alzheimer's disease she also suffered with living with gluten. She had a rash for 30 years that nobody could diagnose. She was itchy for 45 years total. My brother had a encapsulated virus explodes in his spleen and when this happened his entire intestines were covered with adhesions, scar tissue and he almost lost his life. He has 5 daughters, and when I finally was diagnosed after being pregnant and my body went into a cytokine storm, I lost my chance to have children, I ended up having Hashimoto's disease, Degenerative Disc disease, and my body started to shut down during my first trimester. I am 6ft tall and got down to 119lbs. My husband and I went to a special immunologist in Terrace, California. They took 17 vials of blood as we flew there for a day and returned home that evening. In 3 weeks, we had the answer, I have Celiac disease. Once this was known, only my father and husband made efforts to change their way of feeding me. At the family cabin, my stepfather & mother were more worried that I would ruin Thanksgiving Dinner. It wasn't until one of my cousins was diagnosed with Celiac disease. They finally looked into getting Gluten Free flour and taking measures to limit "gluten" in meals. He did nothing but ask for me to pay for my own food and wi-fi when I came to the cabin to stay after our house burned down. When he informed my mother, they proceeding to get into a physical fight and she ended up with a black eye. The is just more trauma for me. Sam had no interest in telling the truth about what he wanted. He lied to my mother that he had asked my husband if I could pay for "food" when he asked Geoffrey if I had money to pay for my wi-fi. My mother hates when he spends so much time on the computer so he lied and said I could pay for my own food. I will remind you I weighed 119lbs at this time. (At 6ft) that is a very sick looking person. Neither parent was worried about my weight, they just fought about how cheap my stepfather was. As my mother was diagnosed with Alzheimer's disease in 2014. He had her sign over the will to a trust and added his children. He had no testimonial capacity at the time, so she signed without proper papers. Making this Trust null and void. When I gave my brother my childhood home, my mother stated I would be getting an equal part of inheritance to the house on Race. It currently worth 2.0 million $. I got nothing, and my stepfather has since disowned me b/c of my claim and he knows that my mother would never have left it uneven between my biological brother and myself. She sat me and my husband down, as we lived at the Race Street house and treated and took care of it as our own. My brother took over b/c he was going through a horrific divorce and needed a home so he could get a better custody deal with his soon to be ex-wife who was a Assist DA for Denver. She used the girls against him, and he & I were the primary caregivers. We, Judd and I spent the most time with them pre the divorce. Once Judd moved into the house, he threw all of my mother, grandmother and my family heirlooms out to the Goodwill. Nobody told my mother about this as she was going through cancer treatment and had Alzheimer's disease in her mother and her sister. My stepfather and biological brother took advantage of this matter, as I called a "family council" that my brother just never could make it to at the last moment. All of the furnishing, kitchen ware, everything was in the house my brother just moved into. He had had 2 weddings, I chose to elope b/c my stepfather ruined my brother's first wedding by talking about his relationship with my brother in front of my dad and his entire family, insulting him and having my grandfather leave the ceremony. It was a disaster. My stepfather just plays dumb and blames my father for the slight. I was the only child not to have a wedding. So, my mother and stepfather never had to pay for a thing. My mother had had an agreement with my father he'd pay for college and all medical issues with their kids, myself and Judd. So truly my mother never had to pay for anything big for me in her entire life. I am looking for anyone that has had a similar story, where they grew up in a household that had a baker that regularly milled flour and ate gluten. What happened to you? DId you suffer from different auto-immune diseases b/c of living with a baker using "gluten" Please let me know. I have been looking into legal ways to get my stepfather to give me what my mother had promised, and he erased. Thank you for listening to my story. Jane Donnelly  
    • trents
      Possibly gluten withdrawal. Lot's of info on the internet about it. Somewhat controversial but apparently gluten plugs into the same neuro sensors as opiates do and some people get a similar type withdrawal as they do when quitting opiates. Another issue is that gluten-free facsimile flours are not fortified with vitamins and minerals as is wheat flour (in the U.S. at least) so when the switch is made to gluten-free facsimile foods, especially if a lot of processed gluten-free foods are being used as substitutes, vitamin and mineral deficiencies can result. There is also the possibility that she has picked up a virus or some but that is totally unrelated to going gluten-free.
×
×
  • Create New...