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

Blood Test Negative, But Could It Be Celiac?


kbenj1

Recommended Posts

kbenj1 Newbie

Hi, I am new to the gluten free diet. I tested negative for celiac in a blood test, but all of my symptoms disappeared once I went gluten free. Last night I ate a publix rotisserie chicken, and within an hour I hade aphthos ulcers on my throat, I was nauseous, my stomach was cramping, and I was gassy. My doctor thinks that the chicken was bad, but I think it was the gluten. It's been 24 hours, and I'm still not right. Could I have celiac?


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



Celiac.com Sponsor (A8-M):



Ninja Contributor

Hi kbenj1,

My diagnosis was tumultuous, just like many others' here. What I've learned (which may or may not be a popular opinion) is that it could always be Celiac. The tests are fallible - some have a 30% false neg. rate. Even with genetic testing, there's just so little known about the cause and necessary contributing factors that it's hard to make diagnosis fool-proof! It could be that the chicken was bad or it could be the gluten. Did anyone else have the chicken? Did they get sick?

I suggest that you request copies of all of the Celiac lab work. Many times doctors do not order the full Celiac panel, opting to just test TTG and total IgA. That would be the first thing to do. Does your family have a history of autoimmune diseases? Fertility issues? Vitamin deficiencies? All of the above? (:P)

Laura

Madagascar Rookie

if you've already gone gluten-free, getting tested again might not show if you do have gluten intolerance. Perhaps, as Laura said, you'll have more information if you see copies of your actual test results. my daughter (20) was tested last january and everything came back negative. we breathed a sigh of relief and celebrated. but her symptoms kept getting worse - she kept developing more food allergies, feeling worse, having more anxiety, and by november, i actually thought she was developing schizophrenia.

she went gluten & dairy free and within 4 days we were saying it was the gluten. it's now been a couple of months and she's a world better in every way. i got tested and mine came back positive, and i have the genes.

my point is that the tests aren't very reliable. what is reliable is if you go gluten-free for a 6 week trial and find that you are better. the reason people go gluten & dairy free is because the milk protein, casein, in some people's bodies, can 'look' like gluten and the body can react to it. i didn't go dairy free because i'm stubborn, i guess, but i'm doing fine.

rotisserie chicken does have gluten added to it by some stores. i don't know if all do, but i saw it listed on one i looked at. you could contact the store and see if anyone else reported getting ill. if no one else that ate it with you got sick as well, i'd think it was not food poisoning.

kbenj1 Newbie

Thanks so much for your replies. My husband and daughter ate the chicken and were fine. The one I ate was the barbecue flavor, and it definitely has gluten. There are autoimmune issues in my family-my mother has 7 different ones, and I'm wondering if she has celiac but doesn't know it. My daughter has stomach problems and eczema, and I'm wondering if she might have an allergy as well. The tests I had done were the IgG IgA. Are there others tests I should do? I know having gone gluten free will alter any biopsies I may need, but I am desperate for relief!

mushroom Proficient

You may or may not have celiac, but it does sound like you might be gluten intolerant. There are several other tests which make up the celiac panel, which consists of the following:

Anti-Gliadin (AGA) IgA

Anti-Gliadin (AGA) IgG

Anti-Endomysial (EMA) IgA

Anti-Tissue Transglutaminase (tTG) IgA

Deamidated Gliadin Peptide (DGP) IgA and IgG

Total Serum IgA

As you can see, none of them is labelled IgG IgA (maybe it was AGA IgA?) They normally run the IgA versions of tests unless total serum IgA is insufficient. My personal opinion is that the DGP is the most likely to give an accurate result, although if any of the tests is positive it should be explored further. I don't know how long you have been eating gluten free? If longer than two weeks you would need to resume eating gluten for a while.

kbenj1 Newbie

My blood work only lists IgG and IgA. It doesn't break those tests down the way you did. I will ask my doctor about it. I have been gluten free for 16 days now, and have felt better than I have in years. But my symptoms have started to recur after eating the publix chicken(see above post). Not sure if it is gluten or something else. It's been over 48 hours and I'm still not feeling well. Had an ultra sound of my abdomen today to rule out other problems. I see my dr next week, so hopefully I will get some answers.

Madagascar Rookie

the only part of my tests that came back definitive was the TTG - Tissue Transglutanimase IGA. Labs measure things differently, but I had mine sent to Prometheus Labs and the local lab accidentally sent it to their usual PeaceHealth Labs. So i ended up with results from 2 different labs, interpreted differently, from the exact same blood sample.

The tests these 2 labs ran were

Immunoglobulin A (IgA)

Endomysial Antibody, IgA

Gliadin IgG

Gliadin IgA

Tissue Transglutaminase IGA

The celiac specialist my family is working with said that a study was done where blood samples from people with known celiac disease were sent to various labs and there was only a 30% accuracy rate in the results. Meaning that they missed 2/3 of the diagnoses.

The fact sheets on this page from the University of Chicago's Celiac Center are full of great information: Open Original Shared Link

and this e-book (lower right corner of page) is equally helpful: Open Original Shared Link

Celiac disease is genetic. When my daughter went gluten-free, I spent the next 3 days researching online and by the time i was done i knew without a doubt that I also had it, my brother and mother as well. I opened a facebook conversation with 8 of my cousins on my mom's side to ask them about health problems - and the answers just confirmed for me that was the genetic link. Getting the test was just a formality.

There's really no advantage to having a diagnosis in the US, unless you want one. If you thrive being gluten-free and are sick when you eat it, that's really all you need to know. i did get the genetic test, which Prometheus Labs will do. However, while I have the gene, by its location the Prometheus Labs report says that i have a low chance of having celiac - 2 out of their scale of 8. And yet, I have it. the Celiac Specialist here said that if you have the gene, you have it.

What you're describing with your mom and your daughter sounds like you're all in the same boat.


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



Celiac.com Sponsor (A8-M):



kbenj1 Newbie

Thank you so much for the information!

Madagascar Rookie

good luck!

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. - trents replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      IBS-D vs Celiac

    2. - trents replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      how much gluten do I need to eat before blood tests?

    3. - SilkieFairy posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      IBS-D vs Celiac

    4. - catnapt posted a topic in Related Issues & Disorders
      0

      anyone here diagnosed with a PARAthyroid disorder? (NOT the thyroid) the calcium controlling glands

    5. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      how much gluten do I need to eat before blood tests?

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,322
    • Most Online (within 30 mins)
      7,748

    avery144
    Newest Member
    avery144
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • trents
      Under the circumstances, your decision to have the testing done on day 14 sounds very reasonable. But I think by now you know for certain that you either have celiac disease or NCGS and either way you absolutely need to eliminate gluten from your diet. I don't think you have to have an official diagnosis of celiac disease to leverage gluten free service in hospitals or institutional care and I'm guessing your physician would be willing to grant you a diagnosis of gluten sensitivity (NCGS) even if your celiac testing comes up negative. Also, you need to be aware that oats (even gluten free oats) is a common cross reactor in the celiac community. Oat protein (avenin) is similar to gluten. You might want to look at some other gluten free hot  breakfast cereal alternatives.
    • SilkieFairy
      After the birth of my daughter nearly 6 years ago, my stools changed. They became thin if they happened to be solid (which was rare) but most of the time it was Bristol #6 (very loose and 6-8x a day). I was on various medications and put it down to that. A few years later I went on this strict "fruit and meat" diet where I just ate meat, fruit, and squash vegetables. I noticed my stools were suddenly formed, if a bit narrow. I knew then that the diarrhea was probably food related not medication related. I tried following the fodmap diet but honestly it was just too complicated, I just lived with pooping 8x a day and wondering how I'd ever get and keep a job once my children were in school.  This past December I got my yearly bloodwork and my triglycerides were high. I looked into Dr. William Davis (wheat belly author) and he recommended going off wheat and other grains. This is the first time in my life I was reading labels to make sure there was no wheat. Within 2 weeks, not only were my stools formed and firm but I was only pooping twice a day, beautiful formed Bristol #4.  Dr. Davis allows some legumes, so I went ahead and added red lentils and beans. Nervous that the diarrhea would come back if I had IBS-D. Not only did it not come back, it just made my stools even bigger and beautiful. Still formed just with a lot more width and bulk. I've also been eating a lot of plant food like tofu, mushrooms, bell peppers, hummus etc which I thought was the cause of my diarrhea before and still, my stools are formed. In January I ran a genetics test because I knew you had to have the genes for celiac. The report came back with  DQ 2.2 plus other markers that I guess are necessary in order for it to be possible to have celiac. Apparently DQ 2.2 is the "rarer" kind but based on my report it's genetically possible for me to have celiac.  I know the next step is to bring gluten back so I can get testing but I am just not wanting to do that. After suffering with diarrhea for years I can't bring myself to do it right now. So that is where I am!   
    • catnapt
      learned I had a high PTH level in 2022 suspected to be due to low vit D  got my vit D level up a bit but still have high PTH   I am 70 yrs old (today in fact) I am looking for someone who also has hyperparathyroidism that might be caused by malabsorption    
    • catnapt
      I am on day 13 of eating gluten  and have decided to have the celiac panel done tomorrow instead of Wed. (and instead of extending it a few more weeks) because I am SO incredibly sick. I have almost no appetite and am not able to consume the required daily intake of calcium to try to keep up with the loss of calcium from the high parathyroid hormone and/or the renal calcium leak.    I have spent the past 15 years working hard to improve my health. I lost 50lbs, got off handfuls of medications, lowered my cholesterol to enviable levels, and in spite of having end stage osteoarthritis in both knees, with a good diet and keeping active I have NO pain in those joints- til now.  Almost all of my joints hurt now I feel like someone has repeatedly punched me all over my torso- even my ribs hurt- I have nausea, gas, bloating, headache, mood swings, irritability, horrid flatulence (afraid to leave the house or be in any enclosed spaces with other people- the smell would knock them off their feet) I was so sure that I wanted a firm diagnosis but now- I'm asking myself is THIS worth it? esp over the past 2 yrs I have been feeling better and better the more I adjusted my diet to exclude highly refined grains and processed foods. I didn't purposely avoid gluten, but it just happened that not eating gluten has made me feel better.   I don't know what I would have to gain by getting a definitive diagnosis. I think possibly the only advantage to a DX would be that I could insist on gluten-free foods in settings where I am unable to have access to foods of my choice (hospital, rehab, nursing home)  and maybe having a medical reason to see a dietician?   please let me know if it's reasonable to just go back to the way I was eating.  Actually I do plan to buy certified gluten-free oats as that is the only grain I consume (and really like) so there will be some minor tweaks I hope and pray that I heal quickly from any possible damage that may have been done from 13 days of eating gluten.    
    • Jmartes71
      So I've been dealing with chasing the name celiac because of my body actively dealing with health issues related to celiac though not eating. Diagnosed in 1994 before foods eliminated from diet. After 25 years with former pcp I googled celiac specialist and she wasn't because of what ive been through. I wanted my results to be sent to my pcp but nothing was sent.I have email copies.I did one zoom call with np with team member from celiac specialist in Nov 2025 and she asked me why I wanted to know why I wanted the celiac diagnosis so bad, I sad I don't, its my life and I need revalidaion because its affecting me.KB stated well it shows you are.I asked then why am I going through all this.I was labeled unruly. Its been a celiac circus and medical has caused anxiety and depression no fault to my own other than being born with bad genetics. How is it legal for medical professionals to gaslight patients that are with an ailment coming for help to be downplayed? KB put in my records that she personally spent 120min with me and I think the zoom call was discussing celiac 80 min ONE ZOOM call.SHE is responsible for not explaining to my pcp about celiac disease am I right?
×
×
  • 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.