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

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.

  • 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. - knitty kitty replied to Jane02's topic in Gluten-Free Foods, Products, Shopping & Medications
      9

      Desperately need a vitamin D supplement. I've reacted to most brands I've tried.

    2. - Jane02 replied to Jane02's topic in Gluten-Free Foods, Products, Shopping & Medications
      9

      Desperately need a vitamin D supplement. I've reacted to most brands I've tried.

    3. - knitty kitty replied to Jane02's topic in Gluten-Free Foods, Products, Shopping & Medications
      9

      Desperately need a vitamin D supplement. I've reacted to most brands I've tried.

    4. 0

      Penobscot Bay, Maine: Nurturing Gluten-Free Wellness Retreat with expert celiac dietitian, Melinda Dennis

    5. - Scott Adams replied to Jane02's topic in Gluten-Free Foods, Products, Shopping & Medications
      9

      Desperately need a vitamin D supplement. I've reacted to most brands I've tried.

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

    • Total Members
      133,331
    • Most Online (within 30 mins)
      7,748

    Kristy2026
    Newest Member
    Kristy2026
    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)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • knitty kitty
      @Jane02, I hear you about the kale and collard greens.  I don't do dairy and must eat green leafies, too, to get sufficient calcium.  I must be very careful because some calcium supplements are made from ground up crustacean shells.  When I was deficient in Vitamin D, I took high doses of Vitamin D to correct the deficiency quickly.  This is safe and nontoxic.  Vitamin D level should be above 70 nmol/L.  Lifeguards and indigenous Pacific Islanders typically have levels between 80-100 nmol/L.   Levels lower than this are based on amount needed to prevent disease like rickets and osteomalacia. We need more thiamine when we're physically ill, emotionally and mentally stressed, and if we exercise like an athlete or laborer.  We need more thiamine if we eat a diet high in simple carbohydrates.  For every 500 kcal of carbohydrates, we need 500-1000 mg more of thiamine to process the carbs into energy.  If there's insufficient thiamine the carbs get stored as fat.  Again, recommended levels set for thiamine are based on minimum amounts needed to prevent disease.  This is often not adequate for optimum health, nor sufficient for people with absorption problems such as Celiac disease.  Gluten free processed foods are not enriched with vitamins like their gluten containing counterparts.  Adding a B Complex and additional thiamine improves health for Celiacs.  Thiamine is safe and nontoxic even in high doses.  Thiamine helps the mitochondria in cells to function.  Thiamine interacts with each of the other B vitamins.  They are all water soluble and easily excreted if not needed. Interesting Reading: Clinical trial: B vitamins improve health in patients with coeliac disease living on a gluten-free diet https://pubmed.ncbi.nlm.nih.gov/19154566/ Safety and effectiveness of vitamin D mega-dose: A systematic review https://pubmed.ncbi.nlm.nih.gov/34857184/ High dose dietary vitamin D allocates surplus calories to muscle and growth instead of fat via modulation of myostatin and leptin signaling https://pubmed.ncbi.nlm.nih.gov/38766160/ Safety of High-Dose Vitamin D Supplementation: Secondary Analysis of a Randomized Controlled Trial https://pubmed.ncbi.nlm.nih.gov/31746327/ Vitamins and Celiac Disease: Beyond Vitamin D https://pmc.ncbi.nlm.nih.gov/articles/PMC11857425/ Investigating the therapeutic potential of tryptophan and vitamin A in modulating immune responses in celiac disease: an experimental study https://pubmed.ncbi.nlm.nih.gov/40178602/ Investigating the Impact of Vitamin A and Amino Acids on Immune Responses in Celiac Disease Patients https://pmc.ncbi.nlm.nih.gov/articles/PMC10814138/
    • Jane02
      Thank you so much @knitty kitty for this insightful information! I would have never considered fractionated coconut oil to be a potential source of GI upset. I will consider all the info you shared. Very interesting about the Thiamine deficiency.  I've tracked daily averages of my intake in a nutrition software. The only nutrient I can't consistently meet from my diet is vitamin D. Calcium is a hit and miss as I rely on vegetables, dark leafy greens as a major source, for my calcium intake. I'm able to meet it when I either eat or juice a bundle of kale or collard greens daily haha. My thiamine intake is roughly 120% of my needs, although I do recognize that I may not be absorbing all of these nutrients consistently with intermittent unintentional exposures to gluten.  My vitamin A intake is roughly 900% (~6400 mcg/d) of my needs as I eat a lot of sweet potato, although since it's plant-derived vitamin A (beta-carotene) apparently it's not likely to cause toxicity.  Thanks again! 
    • knitty kitty
      Hello, @Jane02,  I take Naturewise D 3.  It contains olive oil.   Some Vitamin D supplements, like D Drops, are made with fractionated coconut oil which can cause digestive upsets.  Fractionated coconut oil is not the same as coconut oil used for cooking.  Fractionated coconut oil has been treated for longer shelf life, so it won't go bad in the jar, and thus may be irritating to the digestive system. I avoid supplements made with soy because many people with Celiac Disease also react to soy.  Mixed tocopherols, an ingredient in Thornes Vitamin D, may be sourced from soy oil.  Kirkland's has soy on its ingredient list. I avoid things that might contain or be exposed to crustaceans, like Metagenics says on its label.  I have a crustacean/shellfish/fish allergy.  I like Life Extension Bioactive Complete B Complex.  I take additional Thiamine B 1 in the form Benfotiamine which helps the intestines heal, Life Extension MegaBenfotiamine. Thiamine is needed to activate Vitamin D.   Low thiamine can make one feel like they are getting glutened after a meal containing lots of simple carbohydrates like white rice, or processed gluten free foods like cookies and pasta.   It's rare to have a single vitamin deficiency.  The water soluble B Complex vitamins should be supplemented together with additional Thiamine in the form Benfotiamine and Thiamine TTFD (tetrahydrofurfuryl disulfide) to correct subclinical deficiencies that don't show up on blood tests.  These are subclinical deficiencies within organs and tissues.  Blood is a transportation system.  The body will deplete tissues and organs in order to keep a supply of thiamine in the bloodstream going to the brain and heart.   If you're low in Vitamin D, you may well be low in other fat soluble vitamins like Vitamin A and Vitamin K. Have you seen a dietician?
    • Scott Adams
      I do not know this, but since they are labelled gluten-free, and are not really a product that could easily be contaminated when making them (there would be not flour in the air of such a facility, for example), I don't really see contamination as something to be concerned about for this type of product. 
    • trents
×
×
  • 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.