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

Negative Biopsy But Chronic Inflammation


susanm

Recommended Posts

susanm Apprentice

I know I don't react well to gluten. My antigliadins were high. My biopsy was negative, though it showed chronic inflammation. What does this mean?

I had a 2 bites of cake the other day and got crampy. Why wouldn't the biopsy show something? He said he took the biopsy from a few areas.


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



Celiac.com Sponsor (A8-M):



ShayFL Enthusiast

A "few" areas could mean 2. Six or more is better. Maybe you are at the beginning stage with only inflammation. This is good that you caught it early. You should request genetic testing. If you have the Celiac genes and with POS blood and inflammation, you can either stop eating gluten and get well. OR keep eating it until you get sick enough to show damage to your villi. Believe it or not, this is exactly what most doctors will have you do. They will tell you that you are fine and to keep eating gluten. Then years later.....you get dx properly.

happygirl Collaborator

Couple things:

You may not have Celiac, but a non Celiac gluten problem. Open Original Shared Link

You may have Celiac, but the biopsy didn't pick up on it. Open Original Shared Link

Open Original Shared Link

You may have something else that is causing the inflammation, and have a separate gluten issue.

Lots of options, unfortunately.

If your goal is to determine if gluten is causing your overt symptoms, than a gluten free diet 'trial' may be worth it.

susanm Apprentice

Hi happygirl, I couldn't see the link you sent me, but I did some of my own research. I probably have non-celiac gluten sensitivity (NCGS).

I just needed some justification to continue my gluten-free diet and feeling much healthier with it. I know I don't really have to justify it to anyone but myself, but it is a major lifestyle change. I mean, why would I have chronic inflammation? I don't have heartburn or H. pylori or Giardia. What I do know is that I feel really lousy when I have pasta or bread, so I'll just go with that. Also, my friend said that my complexion seemed a lot better.

Thanks

nora-n Rookie

I think you might be celiac, but that the method of diagnosis is close to medieval.

LIke in the old days, they would not diagnose you with flattened villi, only total villous atrophy would do.

Now they are moving more towards the inflammation thing, that you are celiac when there are more than let's say 20 leucocytes per 100 cells or something like that. Check all the blog notes Dr. Lewey has written on that: www.thefooddoc.com .

Some places can diagnose you with inflammation. aldo google the marsh scale.

nora

happygirl Collaborator
Hi happygirl, I couldn't see the link you sent me, but I did some of my own research. I probably have non-celiac gluten sensitivity (NCGS).

Which of the three links were you having trouble accessing?

TracyB Apprentice
I know I don't react well to gluten. My antigliadins were high. My biopsy was negative, though it showed chronic inflammation. What does this mean?

I had a 2 bites of cake the other day and got crampy. Why wouldn't the biopsy show something? He said he took the biopsy from a few areas.

Hi - I saw something (I think last night) on the tv show called The Doctors. They were demonstrating the pill camera that a patient can swallow - anyway, there was a woman on that had been very ill for 7 years - down to 70 lbs. at her worst - she was finally diagnosed with Crohns Disease - but from the pictures (showed a healthy intestine vs her intestine) there was such an obvious difference. However, I believe they did use the terminology "chronic Inflammation". Apparently, she was hard to diagnose because the scope that is used can sometimes not reach the area they need to view - thus the little pill camera they used to diagnose her.

Just a thought - I think with Crohns there is a lot of pain as a major symptom.

TracyB


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



Celiac.com Sponsor (A8-M):



susanm Apprentice
Which of the three links were you having trouble accessing?

I'm having trouble viewing the first link you provided. Ohh, there's so much to think about. The more I read, the more confused I am. I'll just stick with gluten-free to be safe.

happygirl Collaborator

here's the text:

Open Original Shared Link

Celiac Disease vs. Gluten Sensitivity

By Tricia Thompson, MS, RD, the gluten free dietitian

"When I first started working in this field, the term gluten sensitivity was used interchangeably with the term celiac disease they basically meant the same thing.

Times have changed. We are now learning that there is a group of people who do not have celiac disease and do not have an allergy to wheat but nonetheless can not tolerate gluten. This condition is being called gluten sensitivity.

Very little research has been conducted on gluten sensitivity. However, a study abstract on this condition was recently presented at a medical conference known as Digestive Disease Week. One of the study authors was Alessio Fasano, M.D., Medical Director of The University of Maryland Center for Celiac Research.

Dr. Fasano was gracious enough to answer some questions about gluten sensitivity.

The term non-celiac gluten sensitivity is being used with more frequency. Can you please define what it is and how it differs from celiac disease?

Gluten sensitivity is a non-allergic, non-autoimmune reaction to gluten that can cause symptoms similar to those experienced by people with celiac disease.

In your medical practice, how do you determine if a patient has non-celiac gluten sensitivity?

Because gluten sensitivity is not a food allergy (like wheat allergy), or an autoimmune process secondary to exposure to gluten (like celiac disease), the diagnosis is based on exclusion criteria. In other words, people that experience symptoms that are suspected as being related to gluten exposure will be tested for wheat allergy and celiac disease. If they are negative for both, gluten sensitivity is considered. The diagnosis will be confirmed if symptoms resolve following the embracement of a gluten free diet.

An abstract was presented at Digestive Disease Week that you co-authored entitled, "Role of the innate immune system in the pathogenesis of gluten sensitivity: Preliminary study." The abstract suggests that celiac disease and gluten sensitivity may be two separate diseases. Can you please explain?

As mentioned above, celiac disease is a true autoimmune disease (like type 1 diabetes and multiple sclerosis) in which both innate and adaptive immunity are involved. Conversely, gluten sensitivity is a non-autoimmune reaction to gluten in which only the innate immune system is involved.

In an article you wrote about Digestive Disease Week for Medscape Gastroenterology you state that gluten sensitivity "may be related to activation of the innate immune system without the involvement of the adaptive immune system." Can you please explain further, including what is meant by innate immune system and adaptive immune system?

The innate immune system is the most ancestral form of defense we have against "invaders," while the adaptive immune system is a more recent branch of our immune system. Once our body comes in contact with a substance from the environment that may represent a signal of danger, the innate immune system reacts immediately to try to eliminate the "attacker."

At the same time, the adaptive immune system will intervene with a more sophisticated, long process, during which the attacker is studied, its conformation evaluated, and a "customized response" to that particular molecule is engineered (i.e. specific antibodies). Further, the adaptive immune system will save this information as immune response memory, so that at the next encounter there is no need to re-do the job.

In autoimmune diseases, like celiac disease, there is a coordinate response between innate and adaptive immune system, a response that ends up in the wrong direction (i.e.; attacking its own body rather than the "invader"). In gluten sensitivity, there is only an innate immune response, since the adaptive immune system seems not involved.

Thank you Dr. Fasano!

It is important to remember that regardless of whether you have celiac disease or non-celiac gluten sensitivity the treatment is the same a strict gluten-free diet."

susanm Apprentice

Thank you for printing that for me. I think my adaptive immune system is at work because I also have hypothyroidism and Addison's disease, two autoimmune diseases. I know what he's talking about. Hayfever is probably an innate immune response. However, with my autoimmune diseases, the chronic inflammatory changes, and high antigliadin response on blood test (although I guess that could be innate too, I don't know), I would think that would be more celiac.

I'm not sure I'll ever really know. I'll just go gluten-free and maybe one day they will have enough research to really understand this thing.

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. - asaT replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      48

      Supplements for those Diagnosed with Celiac Disease

    2. - asaT replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      48

      Supplements for those Diagnosed with Celiac Disease

    3. - nanny marley replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      20

      Insomnia help

    4. - David Blake commented on Scott Adams's article in Product Labeling Regulations
      1

      FDA Moves to Improve Gluten Labeling—What It Means for People With Celiac Disease

    5. - nanny marley replied to wellthatsfun's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      4

      nothing has changed

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

    • Total Members
      133,343
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • asaT
      plant sources of calcium, such as spinach, have calcium bound to oxalates, which is not good. best source of calcium is unfortunately dairy, do you tolerate dairy? fermented dairy like kefir is good and or a little hard cheese. i do eat dairy, i can only take so much dietary restriction and gluten is hard enough! but i guess some people do have bad reactions to it, so different for everyone.  
    • asaT
      i take b12, folate, b2, b6, glycine, Nac, zinc, vk2 mk4, magnesium, coq10, pqq, tmg, creatine, omega 3, molybdnem (sp) and just started vit d. quite a list i know.  I have high homocysteine (last checked it was 19, but is always high and i finally decided to do something about it) and very low vitamin d, 10. have been opposed to this supp in the past, but going to try it at 5k units a day. having a pth test on friday, which is suspect will be high. my homocysteine has come down to around 9 with 3 weeks of these supplements and expect it to go down further. i also started on estrogen/progesterone. I have osteoporosis too, so that is why the hormones.  anyway, i think all celiacs should have homocysteine checked and treated if needed (easy enough with b vit, tmg). homocysteine very bad thing to be high for a whole host of reasons. all the bad ones, heart attack , stroke, alzi, cancer..... one of the most annoying things about celiacs (and there are so many!) is the weight gain. i guess i stayed thin all those years being undiagnosed because i was under absorbing everything including calories. going gluten-free and the weight gain has been terrible, 30#, but i'm sure a lot more went into that (hip replacement - and years of hip pain leading to inactivity when i was previously very active, probably all related to celiacs, menopause) yada yada. i seemed to lose appetite control, like there was low glp, or leptin or whatever all those hormones are that tell you that you are full and to stop eating. my appetite is immense and i'm never full. i guess decades or more ( i think i have had celiacs since at least my teens - was hospitalized for abdominal pain and diarrhea for which spastic colon was eventually diagnosed and had many episodes of diarrhea/abdominal pain through my 20's. but that symptom seemed to go away and i related it to dairy much more so than gluten. Also my growth was stunted, i'm the only shorty in my family. anyway, decades of malabsorption and maldigestion led to constant hunger, at least thats my theory. then when i started absorbing normally, wham!! FAT!!!    
    • nanny marley
      Great advise there I agree with the aniexty part, and the aura migraine has I suffer both, I've also read some great books that have helped I'm going too look the one you mentioned up too thankyou for that, I find a camomile tea just a small one and a gentle wind down before bed has helped me too, I suffer from restless leg syndrome and nerve pain hence I don't always sleep well at the best of times , racing mind catches up I have decorated my whole house in one night in my mind before 🤣 diet changes mindset really help , although I have to say it never just disappears, I find once I came to terms with who I am I managed a lot better  , a misconception is for many to change , that means to heal but that's not always the case , understanding and finding your coping mechanisms are vital tools , it's more productive to find that because there is no failure then no pressure to become something else , it's ok to be sad it's ok to not sleep , it's ok to worry , just try to see it has a journey not a task 🤗
    • nanny marley
      I agree there I've tryed this myself to prove I can't eat gluten or lactose and it sets me back for about a month till I have to go back to being very strict to settle again 
    • trents
      You may also need to supplement with B12 as this vitamin is also involved in iron assimilation and is often deficient in long-term undiagnosed celiac disease.
×
×
  • 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.