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

My Blood Tests Were Very Positive But My Biopsy Was Negative


becca42

Recommended Posts

becca42 Newbie

Hi, I am new. I am confused. I had the celiac screening test in back in March. All 3 tests came back positive; tTG ab, IgA = 48.3, Gliadin Peptide Ab, IgG = 50.6, Gliadin Peptide Ab, IgA = 121.0 (for all the tests >25 means positive0. My doctor said there was greater that 90% chance I have celiacs.

I had the endoscopy in April and the results came back negative for celiacs. I did NOT stop gluten before the biopsy.

The gastroenterologist sent me the results, but did not explain anything to me. They said there was no need for follow up and to continue with the gluten free diet. I went to my regular Doctor, he was surprised and couldn't explain it either.

How could my numbers be so high without having celiacs? Am I allergic to gluten or do I have gluten sensitivity? What is the difference?

I would appreciate any advice. Thank you


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

Possible the biopsies missed the bad spots. if 25% of your small intestine is " bad" you would feel awful. Every biopsy he takes has a 1 in 4 chance of getting a bad spot. If he did 2 biopsies, he probably missed it.

Get a copy of the procedure report, blood tests and pathology ( biopsy) report. Read them yourself. Sometimes docs don't know what they are reading. Also, perhaps your regular doc should call the GI and get some info?

IrishHeart Veteran

A positive blood test is positive for celiac.

As Karen says, the biopsy could be wrong or you just have patchy erosion at this point and he missed it.

Your doctor is partly correct--you should be gluten free, but there is always a need for follow up care.

You need lab work to make sure you do not have any vitamin deficiencies for starters.

What the hell is wrong with your GI doctor? :rolleyes: You don't just dismiss a patient with that insufficient info.

Start reading about Celiac yourself so you can know what you are dealing with.

For starters, it is not a "gluten allergy", hon----it's an autoimmune disease. Not an allergy.

Try to find a doctor who knows what the hell he is talking about.

call the local celiac support group and see which MD is on their advisory board. They can help you find a good celiac-savvy doc.

Start reading about celiac here

Open Original Shared Link

and search celiac.com for more help.

I'll start you off:

Cara in Boston Enthusiast

I too had positive blood tests and negative biopsy. I had tons of symptoms (for 5 years) and all seem to go away on the gluten free diet. I was "technically" diagnosed with gluten intolerance.

Don't let your negative biopsy be "permission" to cheat on the diet. You very likely have celiac disease, it just wasn't found (maybe damage missed, maybe not enough damage yet, who knows?)

Also, everyone in your family should be tested (regardless of symptoms) as it is inherited. (Again, don't dismiss this important step just because your biopsy was negative.) My 7 year old son was diagnosed with celiac disease (biopsy) and had very few (almost none) symptoms.

Cara

Skylark Collaborator

You are what celiac experts call latent celiac. You are somewhere in the process of developing full-blown celiac disease and the only way to reverse it is the diet.

People with positive bloodwork on highly specific tests (your combo of TTG IgA and gliadin peptide IgG is highly specific) who elected to keep eating were followed in a study and most went on to develop positive biopsies during the study. There was also a study where blood+/biopsy- people were found to have the same metabolic markers as blood+/biopsy+ celiacs, showing that once you are blood+, your metabolism is messed up even without the positive biopsy.

As other folks have pointed out, damage can be patchy and many doctors simply do not take enough biopsies to have a good chance of hitting a spot with damage.

If I were you, I'd consider myself celiac, go gluten free, and be really grateful that at least the bloodwork was positive. People with latent celiac almost always feel better gluten-free. Get your doctor to rerun your celiac panel in six months. The antibodies should be dropping if not gone from the gluten-free diet, which is more proof of celiac disease.

1974girl Enthusiast

My daughters was only in the duadenal bulb. All other biopsies showed normal. I wonder how many biopsies were taken and from where.

nora-n Rookie

maybe they by mistake switched the biopsy samples.....because some of these blood tests are very specific for celiac.


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



Celiac.com Sponsor (A8-M):



MitziG Enthusiast

If you had only 1 of those tests be strongly positive, it is pretty much guaranteed you have celiac. To have all of them be so means there is no question whatsoever. Just doesn't happen.

As to your biopsy- a few possibilities:

You have latent celiac, as another poster mentioned

Your doctor took an insufficient number of biopsies

Your doctor did not happen to biopsy the correct spot (celiac is often patchy, hence the need for multiple biopsies)

The person who read the biopsies was inexperienced- there is a great deal of skill required to correctly interpret subtle damage- and the pathologist who did yours may not have had it

Or...the lab screwed up. Always a possibility for human error.

Regardless- you have celiac dear. Because it is an autoimmune disorder, it must be taken seriously. If you do not strictly adhere to a gluten free diet you WILL develop additional ai disorders (hashimotos, sjorens, lupus, multiple sclerosis, rheumatoid arthritis...etc...) you also will run an increased risk of intestinal lymphoma.

And you will feel like total crap.

The good news is- stick to the diet, don't cheat, and hopefully you will avoid all of that.

Also may be wise to get a dr with a brain

becca42 Newbie

Possible the biopsies missed the bad spots. if 25% of your small intestine is " bad" you would feel awful. Every biopsy he takes has a 1 in 4 chance of getting a bad spot. If he did 2 biopsies, he probably missed it.

Get a copy of the procedure report, blood tests and pathology ( biopsy) report. Read them yourself. Sometimes docs don't know what they are reading. Also, perhaps your regular doc should call the GI and get some info?

Thank you. I have an appointment to get the pathology report.

becca42 Newbie

A positive blood test is positive for celiac.

As Karen says, the biopsy could be wrong or you just have patchy erosion at this point and he missed it.

Your doctor is partly correct--you should be gluten free, but there is always a need for follow up care.

You need lab work to make sure you do not have any vitamin deficiencies for starters.

What the hell is wrong with your GI doctor? :rolleyes: You don't just dismiss a patient with that insufficient info.

Start reading about Celiac yourself so you can know what you are dealing with.

For starters, it is not a "gluten allergy", hon----it's an autoimmune disease. Not an allergy.

Try to find a doctor who knows what the hell he is talking about.

call the local celiac support group and see which MD is on their advisory board. They can help you find a good celiac-savvy doc.

Start reading about celiac here

Open Original Shared Link

and search celiac.com for more help.

I'll start you off:

Thank you

becca42 Newbie

Thanks everyone!

Malisa1 Newbie

Hi, I am new. I am confused. I had the celiac screening test in back in March. All 3 tests came back positive; tTG ab, IgA = 48.3, Gliadin Peptide Ab, IgG = 50.6, Gliadin Peptide Ab, IgA = 121.0 (for all the tests >25 means positive0. My doctor said there was greater that 90% chance I have celiacs.

I had the endoscopy in April and the results came back negative for celiacs. I did NOT stop gluten before the biopsy.

The gastroenterologist sent me the results, but did not explain anything to me. They said there was no need for follow up and to continue with the gluten free diet. I went to my regular Doctor, he was surprised and couldn't explain it either.

How could my numbers be so high without having celiacs? Am I allergic to gluten or do I have gluten sensitivity? What is the difference?

I would appreciate any advice. Thank you

From all of the research I have done, it is only Celiac Disease if the villi in your small intestine are damaged. A positive blood test would still mean you are gluten intolerant, though. I also learned that untreated gluten intolerance/sensitivity (gluten free diet) can result in full blown Celiac Disease (damage to the villi in your intestine). You must not be to the point yet where there is intestinal damage. Also, sometimes, there is only minor damage to the villi and the biopsy catches a still healthy part. Perhaps being very strict with a gluten free diet can prevent this damage. I hope this has explained why your biopsy came back negative and blood test positive. If this has been answered below, I apologize. Short on time.

  • 2 years later...
florentine Newbie

Great info! Both my daughter and I had a positive blood test, but no biopsy yet. I was wondering what was the outcome if the biopsy would be negative.

kareng Grand Master

From all of the research I have done, it is only Celiac Disease if the villi in your small intestine are damaged. A positive blood test would still mean you are gluten intolerant, though. I also learned that untreated gluten intolerance/sensitivity (gluten free diet) can result in full blown Celiac Disease (damage to the villi in your intestine). You must not be to the point yet where there is intestinal damage. Also, sometimes, there is only minor damage to the villi and the biopsy catches a still healthy part. Perhaps being very strict with a gluten free diet can prevent this damage. I hope this has explained why your biopsy came back negative and blood test positive. If this has been answered below, I apologize. Short on time.

Great info! Both my daughter and I had a positive blood test, but no biopsy yet. I was wondering what was the outcome if the biopsy would be negative.

Just a heads up a this was posted 2 years ago. A positive Celiac blood test does not indicate non- Celiac gluten intolerance. There aren't any medically reliable blood tests for that. Most likely what happens is a doctor doesn't so enough biopsied to find the damage. Encourage your doctor to do at least 6 - more is better. Also, continue to eat gluten until you get your tests finished.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,216
    • Most Online (within 30 mins)
      7,748

    billiam3some
    Newest Member
    billiam3some
    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

    • Scott Adams
      Your story is a powerful and heartbreaking testament to the profound damage that can be caused by undiagnosed celiac disease and the profound pain of not being believed or supported by family. It is sadly a common narrative within the celiac community to have suffered for years, even decades, while autoimmune conditions stack up, all while being dismissed. To answer your core question: yes, living in a environment with significant, constant gluten exposure, especially from airborne flour in a home where milling and baking occurred, would have created a perpetual state of autoimmune activation for you, even beyond the direct ingestion. This chronic exposure is strongly linked to the development and exacerbation of the very autoimmune disorders you describe—Migraines, Meniere's, Hashimoto's, and more. Your body was under constant attack, and the lack of care and understanding from your family compound that trauma significantly. It is not your fault. Many in the community share similar stories of a cascade of illnesses finally explained by a celiac diagnosis, often coming too late to prevent irreversible damage. While I cannot speak to the legal aspects of your inheritance situation, your experience with the medical neglect and the lasting impact of your childhood environment is deeply valid and shared by others who understand this unique type of suffering. Thank you for having the courage to share your truth. Celiac.com has published a book on our site by Jean Duane PhD called Gluten-Centric Culture, which covers many of the social aspects of having celiac disease: This chapter in particular covers issues around eating with family and others - Gluten-Centric Culture: Chapter 5 - Grabbing A Bite Together:    
    • Scott Adams
      It's incredibly tough to watch a young child grapple with the frustration and sense of deprivation that comes with a restrictive diet, and your empathy for her is the first and most important step. At seven, children are deeply focused on fairness, and her feelings are completely valid. To support her mental health, shift the narrative from "missing out" to "empowered choice." Instead of "you can't have that," use language like "we choose these safe foods so your tummy feels happy and strong." Involve her directly in her own care; let her be the "Gluten-Free Detective" at the grocery store, picking out exciting new treats, or make her the head chef in baking a special dessert that everyone gets to enjoy. When eating out, empower her by having her call the restaurant ahead to ask about safe options (with your help), making her feel in control rather than a passive victim. Acknowledge her feelings—"It's okay to feel sad that you can't have the roll, I sometimes feel that way too"—and then immediately pivot to a positive action, like unwrapping the special brownie you brought just for her. This combination of validation, involvement, and reframing turns a limitation into a shared family challenge where she feels supported, capable, and loved.
    • Scott Adams
      I know that Shiloh Farms makes this product, but I don't think it is labeled gluten-free.
    • Scott Adams
      Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful:    
    • Scott Adams
      It's strange to see two very different results in what appears to be a single blood test--one is positive and one is negative for a celiac disease test. Are these results separated by time? This article might be helpful. It breaks down each type of test, and what a positive results means in terms of the probability that you might have celiac disease. One test that always needs to be done is the IgA Levels/Deficiency Test (often called "Total IGA") because some people are naturally IGA deficient, and if this is the case, then certain blood tests for celiac disease might be false-negative, and other types of tests need to be done to make an accurate diagnosis. The article includes the "Mayo Clinic Protocol," which is the best overall protocol for results to be ~98% accurate.    
×
×
  • Create New...