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

What Is Likelihood Of Getting Positive Endoscopy If Blood Labs Were Negative?


JChi

Recommended Posts

JChi Newbie

Hi, I had a full panel for celiac testing done last week which came back negative (although dgp igg/iga was not tested.)  I have a colonoscopy and endoscopy scheduled for next week.  Are there people who have had neg blood but positive endoscopy?  It seems like I mostly see posts for the other way around.

 

I have been eating "very low" gluten diet for about 2 years and back to full gluten for the past 6 weeks.  I didn't feel too bad for the first 3 weeks or so but recently, I've had stomach cramps/pain everyday, frequent diarrhea, pain in hips, legs and low back (right side).  I'm hoping 7 weeks eating gluten will be long enough for my doc to see if there is any damage.  I've read I should ask him to take 6 - 8 samples, even in areas that might look ok.  Is this accurate?  Any other tips or advise from those who have been through this would be greatly appreciated.  Thanks


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

Open Original Shared Link

Is it possible to have a negative blood test, but a positive biopsy?

While rare, it is possible to have a negative blood test and still have celiac disease. tTG sensitivity is approximately 98%, which means that 2% of all celiacs may have a normal tTG level. Sometimes tTG antibodies are not produced enough to show up in the blood stream and can only be detected in the intestinal mucosa by special means.

IgA deficiency is a reason why you might have a negative blood test, but a positive biopsy.

Further medical evaluation is important for anyone still experiencing symptoms in order to establish the diagnosis or to rule out celiac disease as a part of establishing another diagnosis. In some cases, celiac disease is the wrong diagnosis as such conditions as Crohn’s Disease and food protein allergy Open Original Shared Link.

JChi Newbie

Thanks for your response kareng. I should have mentioned above that my Total Iga was normal.

IrishHeart Veteran

Being "very low gluten" for 2 years could explain a lot.

 

Yes, there are people who have had negative blood panels with positive biopsies.

 

They mention " latent or partially treated" celiac as the reason. Also, people with gluten ataxia or dermatitis herpitiformis may have negative blood work but positive biopsies. Dr. Green's book mentions this, I believe.(And one "real" example among us--- I think Bubba's Mom--a member on here-- had this happen.)

 

Make sure the  doc biopsies from different areas of the small intestine and does enough samples while down there.

Good luck. Keep us posted.

Bubba's Mom Enthusiast

 

 

I had negative bloodwork, (they say 20-30% of us do) but severe villi flattening when scoped.  I was told I had Celiac, and to not eat gluten.  I went gluten-free and had some almost immediate relief of symptoms (GERD, bloating,nausea), but then realized I was getting bad reactions from soy too, then dairy, and other foods.  So, to make sure my DX was correct, I was given the gene test.  I had a DQ2.2, which was "equivical", meaning they couldn't rule it in or out.

 

I went to the Mayo Clinic for further testing and Dr. Murray there said I could be Celiac, or just severly gluten intollerant.  He did a SIBO test and found I not only had high hydrogen, but methane too.  He said that's indicative of SIBO, and he felt I probably had a severe case of it.  He said SIBO can mimic Celiac, in that it destroys villi and makes the gut "leaky" causing particles to pass into the blood stream that shouldn't be there, which our bodies react to.  He said the "bad" bacteria can give off toxins as well, giving various symptoms. We tried several different antibiotics, with no change in symptoms.  He said we'd use "good" bacteria to fight off the bad. 

 I wasn't digesting food very well on my own, so he prescribed pancreatic enzymes and a low dose steroid that's commonly used for Chrohn's disease to quiet down my immune system.  He also said to take probiotics every day, which I have done.

 

I'm going back to Mayo the week of May 6 for another scope and a lot of blood work, and a repeat of the SIBO test.  I have been off the steroids and digestive enzymes since Nov. I am still "losing" foods due to bad reactions.  Most recently eggs, and peas.  They are not true food allergies, but intollerances. 

Sooo..now I'm intollerant of gluten, soy, dairy, peanuts, MSG, corn flour, yeast,peas, navy beans.  i've seen several Dr.s and they all say the same thing..."I'm an interesting case". :blink:

 

I have found that I do best on a Paleo diet.  I occasionally eat rice, but no other grains.  I use tapioca starch for thickening sauces, and don't eat breads or baked goods of any kind.  The Paleo diet is a growing trend.  There's a reason for that.  Our food has become "poisoned" with chemicals, artificial sugars, and GMO corn and soy.  Many people find that they feel a lot better eating a diet that is close to what our ancestors ate.  It's what are bodies are designed to eat.

 

I hope I haven't confused you with my answer to this question?  The point is...if you are having symptoms, there's a reason for it.  It's not "all in your head", as some of us have been told.  You can have Celiac with a negative blood test, you can have Celiac like symptoms with a severe bacterial overgrowth,  You may be gluten intollerant (there's no good test for this aside from avoidance and then reintroduction to see if there's a reaction at this time),  your body may be reacting to GMO foods, or the chemicals and dyes in foods, or other food intolerances.

 

My advice...get the scope, get the gene test (they are now finding that there are other genes involved besides DQ2 and DQ8, but it might help get a DX), go gluten-free and eat a whole foods diet consisting of plenty of veggies (organic when available), nuts and seeds, healthy fats like coconut oli (which feeds your brain, raises good cholesterol, and kills bad bacteria), grass fed/free range meats, eggs and fruits.  Shop the outer perameter of the grocery store and don't eat processed foods.  Take probiotics. Have your vitamin/mineral levels tested and take soy free supplements fior anything you are low on. Additionally, take krill oil or soy free fish oil, and limit sugars.

 

Keep a log of what you eat.  A little notebook is fine.  List what you eat and note any symptoms you have. If you have other intollerances going on, this is the best way to find them.

My best wishes to you in finding the answrs you need to help you get your good health back.  Remember too, no matter what is giving you symptoms, it will take time for your body to heal once you remove the offending irritant.

IrishHeart Veteran

Thanks for telling the OP your story, Bubba. ;) It sheds more light on the topic.

JChi Newbie

Thank you for the advice Bubba's Mom. I did have the gene test and I am DQ 2 and 8. I am hoping to get some answers from the endoscopy but even if the result is negative, my doc still wants me to try 100% gluten, dairy and sugar free for at least 2 months to see if that makes a difference. And yes, I have been reading a lot about Paleo and it seems like a good way to eat, just worried that it would require making ALL my own food and how to find the time to do that with 2 kids.


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



Celiac.com Sponsor (A8-M):



notme Experienced

hi jchi - i also had negative blood test for celiac put positive endoscopy.  i had already been gluten free for (i think) a month at the advice of my gp doc.  feeling so much better being gluten free really pushed me into going for the testing/scope.  my GI tested for so many things as well, for crohns, thyroid, etc. - to narrow it down.  but when i had my scope and was coming out of the anesthesia, she out and out told me she could actually *see* the damage.  i kind of went "whoa" - no wonder i felt like i could die.  

 

that being said:  anyone who knows me can tell the difference changing my diet has made.  whether i had gotten a definite diagnosis or not i would have continued with the diet.  it's really the only thing that ever worked, out of all the years of pills and misery, something as simple as changing my diet has made me so much better!  i tell my husband, i feel like an onion, peeling away symptoms like layers of skins (ok that's gross, but hopefully you know what i mean :)  

JChi Newbie

Thanks for sharing your experience Notme. My test is in 2 days and I am so ready to get back to gluten-free eating. My stomach cramps have been getting worse.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,163
    • Most Online (within 30 mins)
      7,748

    Estee
    Newest Member
    Estee
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)


  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • DAR girl
      Looking for help sourcing gluten-free products that do not contain potato or corn derived ingredients. I have other autoimmune conditions (Psoriatic Arthritis and Sjogrens) so I’m looking for prepared foods as I have fatigue and cannot devote a lot of time to baking my own treats. 
    • Scott Adams
      I am so sorry you're going through this. It's completely understandable to feel frustrated, stressed, and disregarded after such a long and difficult health journey. It's exhausting to constantly advocate for yourself, especially when you're dealing with so many symptoms and positive diagnoses like SIBO, while still feeling unwell. The fact that you have been diligently following the diet without relief is a clear sign that something else is going on, and your doctors should be investigating other causes or complications, not dismissing your very real suffering. 
    • Oldturdle
      It is just so sad that health care in the United States has come to this.  Health insurance should be available to everyone, not just the healthy or the rich.  My heart goes out to you.  I would not hesitate to have the test and pay for it myself.  My big concern would be how you could keep the results truly private.  I am sure that ultimately, you could not.  A.I. is getting more and more pervasive, and all data is available somewhere.  I don't know if you could give a fake name, or pay for your test with cash.  I certainly would not disclose any positive results on a private insurance application.  As I understand it, for an official diagnosis, an MD needs to review your labs and make the call.  If you end up in the ER, or some other situation, just request a gluten free diet, and say it is because you feel better when you don't eat gluten.      Hang in there, though.  Medicare is not that far away for you, and it will remove a lot of stress from your health care concerns.  You will even be able to "come out of the closet" about being Celiac!
    • plumbago
      Yes, I've posted a few times about two companies: Request a Test and Ulta Labs. Also, pretty much we can all request any test we want (with the possible exception of the N protein Covid test and I'm sure a couple of others) with Lab Corp (or Pixel by Lab Corp) and Quest. I much prefer Lab Corp for their professionalism, ease of service and having it together administratively, at least in DC. And just so you know, Request a Test uses Lab Corp and Quest anyway, while Ulta Labs uses only Quest. Ulta Labs is cheaper than Request a Test, but I am tired of dealing with Quest, so I don't use them so much.
    • Scott Adams
      PS - I think you meant this site, but I don't believe it has been updated in years: http://glutenfreedrugs.com/ so it is best to use: You can search this site for prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
×
×
  • Create New...