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

Why Endoscopy If Blood Tests Show Celiacs?


gfny

Recommended Posts

gfny Newbie

If my blood tests came back very high (the one that is supposed to be 10 was over 100, and the one that is supposed to be around 5 was 67), and my doctor has told me that I have celiacs, then why do I have to get the endoscopy?

Also, can I do this all on my own? Or do I need to find a nutritionist even if my insurance won't cover it?

Thanks for the help!

Katie


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



Celiac.com Sponsor (A8-M):



Tim-n-VA Contributor

I have read on another Celiac oriented website that other auto-immune diseases can cause a false positive. The endoscopy is s check against that. I can't provide any information as to how common/likely that is.

Rikki Tikki Explorer

Katie:

If I had it to do again knowing what I know now I would go with the blood test, stay gluten free and then have the blood drawn again in a couple of months and the numbers should go down to normal. If they don't have the doctor look for something else, if you feel better and the numbers are normal it would confirm in my own mind that it is celiac.

I think there is so much information out there now you can probably find out what is gluten free on your own, at least I didn't find that a nutirtionist was that helpful, she didn't know that much about it. This site will help you a lot.

buffettbride Enthusiast

Another reason to have the biopsy is that a positive biopsy result can also make you eligible for some medical studies, etc.

However, for your own peace of mind, with the blood test and trying the diet w/ a positive response, meaning an improvement of symptoms, would be diagnosis for me enough. I agree with the previous poster who said following up to see if your blood tests change after a period of months on the gluten-free diet. (My daughter went from the 100's range to the normal range with just 3 months being gluten-free).

If your insurance doesn't cover a nutritionist, many of which are not entirely knowledgeable about Celiac Disease, you can probably achieve the same guidance from a site like this and many books that are available about the disease.

I have learned more from this web site than any other resource.

Darn210 Enthusiast

If the insurance won't pay for the nutritionist, I would skip it. By the time I was able to get in, I already knew just about everything she told me. I think she answered two questions for me and I could have posted them here and would have gotten the same answer.

My daughter's GI said that he thinks the endoscopy will probably be phased out over the next ten years or so. The old blood test (I think it was just the IgA) had a lot of false positives so then they felt the need to scope. The new test (Ttg) is much more reliable. He thinks that once the data proves it out, the scoping will be eliminated but that won't be for awhile yet.

WW340 Rookie

My GI diagnosed me based on my sky high numbers, but he did the endoscopy and colonoscopy to make sure there was nothing else going on.

I had been sick for a long time and he thinks my celiac disease has been active all my life, so he wanted to make sure there were no serious complications developing.

If your GI is only doing it for confirmation of the diagnosis then you might not need it, but he might be checking for other things as well depending on your symptoms and your age.

I saw a nutritionist and thought that was totally worthless for me. I had already read a lot about the diet by the time I saw her and she was giving out some old and incorrect information.

Furthermore, she was unable to answer the only question I had, so it was a waste for me.

Guest j_mommy

I had an endoscopy as well. They use it as a gold standard for testing celiac....it's also good to check to see if anything else is happening.

I have never seen a nutritionist. My 6 month blood work was down to normal levels so I'm doing something right. I would wait, do checking and learning on your own. If you are having problems then go to see someone...preferably one knowledgable with celiac.


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



Celiac.com Sponsor (A8-M):



Gemini Experienced
If my blood tests came back very high (the one that is supposed to be 10 was over 100, and the one that is supposed to be around 5 was 67), and my doctor has told me that I have celiacs, then why do I have to get the endoscopy?

Also, can I do this all on my own? Or do I need to find a nutritionist even if my insurance won't cover it?

Thanks for the help!

Katie

I was in the same boat as yourself....I failed 4 out of 5 of the blood tests done and my numbers were ridiculously high.

I may have considered an endoscopy but at that point, I was so sick I was losing a pound per day and the stupid doctors needed "time" to set up an endoscopy! By the time they got around to it, I would have had to be hospitalized from dehydration and low body weight.....no thanks! I immediately went gluten-free and 3 days later, my most severe symptoms started to subside all on their own. I had my answer.

If your doctor did an EMA blood test on you and that showed positive, you have celiac disease. It's specific to celiac disease only. I probably would advise going gluten-free based on blood work and if your symptoms do not improve within a week, you may have to reconsider the scope to see if there are any other problems. It really is personal choice and you have to do what makes you comfortable.

gfny Newbie

Thanks everyone! This is such a wonderful site! I'm going to go ahead and have the endoscopy and skip the nutritionist for now! I'm trying to start the gluten free diet and hopefully it will get easier in time...right? You all are wonderful!

--Katie

P.S. My mom and my sister are both joining me on this gluten-free diet as they both have some of the Dermatitis Herpetiformis symptoms...gotta love family :D

Offthegrid Explorer

I didn't have an endoscopy (blood test and very positive dietary response), so I'm sure someone else on here will come along with an answer, but I don't believe you're supposed to go gluten-free before the test, especially if you will have to wait a while.

Fiddle-Faddle Community Regular

Sounds like an absolute given that either gluten intolerance or celiac is a family problem for you!

Which means that the GI doc will be very happy--he'll make lots of money doing endoscopies on all of you to confirm what the bloodwork already tells him--you shouldn't eat gluten.

The bloodwork is more accurate than the endoscopy; you have 22 feet of intestine, and they only take a few 1/4"- 1/2" samples. Let's say a total of 6 samples--that's a total of 3 inches at most out of 262 total inches of intestines. Remember that villi damage is often patchy, and it becomes clear that the odds of hitting an affected spot are not great. So a negative biopsy doesn't mean that your villi are in good shape. It just means that they didn't happent o hit an affected area, and you still don't know if there ARE any affected areas, or how many if there are.

Not to say that there is no value whatsoever in an endoscopy; I am just saying that if gluten is the one and only problem, then you don't need an expensive invasive endoscopy along with the risks of twilight anesthesia. You just need to go off gluten.

Tim-n-VA Contributor
.... you have 22 feet of intestine, and they only take a few 1/4"- 1/2" samples. Let's say a total of 6 samples--that's a total of 3 inches at most out of 262 total inches of intestines. Remember that villi damage is often patchy, and it becomes clear that the odds of hitting an affected spot are not great. So a negative biopsy doesn't mean that your villi are in good shape. It just means that they didn't happent o hit an affected area, and you still don't know if there ARE any affected areas, or how many if there are...

This is just not a realistic picture of what happens. The endoscopy is done by looking with a small camera at the small intestines and taking a biopsy on sites that appears to be damaged. This greatly increases the odds of finding damage if it exists versus the random sample alluded to in the quoted portion.

Fiddle-Faddle Community Regular

From a talk by Dr. Kenneth Fine:

"Small Bowel Biopsies

Samples of tissue lining the upper small intestine are taken with an instrument inserted through the throat and stomach. The tissue is examined for damage under a microscope. This test been a standard but it also has some reputation for not finding any damage in some patients that nevertheless have better health on a gluten fee diet. Sometimes the small bowel damage is patchy and is missed by the biopsy. Sometimes damage is too small to easily find under a microscope. Sometimes reactions happen elsewhere in the body without visibly affecting the upper small intestine.

Small bowel biopsies can be useful in seeing if the intestines have been very badly injured, but they cannot be relied upon for a confident proof that a patient has no reaction to gluten."

finally diagnosed Apprentice
If my blood tests came back very high (the one that is supposed to be 10 was over 100, and the one that is supposed to be around 5 was 67), and my doctor has told me that I have celiacs, then why do I have to get the endoscopy?

Also, can I do this all on my own? Or do I need to find a nutritionist even if my insurance won't cover it?

Thanks for the help!

Katie

I would have the endoscopy for the fact that, they will see how much damage you have, check for other damage as well to your small intestine and esophagus. I had my endoscopy done and found out that i had done damange to the bottom of my esophagus right into my intestine. I had patches that showed healing vili as well as damaged vili. When I have my follow up scope, they are hoping that the intestine is on its way of healing. They use this as a base, (kidna like a mammogram)its not fun, but on the flip side, there is no prep like the colonoscopy :). Your insurance company should cover the nutrition visit because you have a diganosis. But you really need to find someone who knows what celiac is. Good luck in what you decide. Lorrie

Tim-n-VA Contributor
Small bowel biopsies can be useful in seeing if the intestines have been very badly injured, but they cannot be relied upon for a confident proof that a patient has no reaction to gluten."

There is no doubt that any medical test can yield false results and/or miss the problem. My issue was with you taking non-quantified phrases like "sometimes" and "usually not great" and throwing out numbers of inches to present a distorted view.

Of course a bioposy isn't proof that a patient wil have no reaction to gluten because it only tests for one type of reaction (classic celiac auto-immune villi damage) and doesn't test for classic allergy or other intolerances.

It comes down to what you want and need to know. If you just want to feel better, a dietary response without any other test is sufficient. But since many diseases occur in clusters, there are reasons to know exactly what is going in the body to cause the reaction to gluten. It isn't just to make money for a doctor.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - cristiana replied to KathyR37's topic in Coping with Celiac Disease
      4

      New here

    2. - trents replied to KathyR37's topic in Coping with Celiac Disease
      4

      New here

    3. - Theresa2407 replied to Theresa2407's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Probiotics

    4. - KathyR37 replied to KathyR37's topic in Coping with Celiac Disease
      4

      New here

    5. - Scott Adams replied to KathyR37's topic in Coping with Celiac Disease
      4

      New here


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,814
    • Most Online (within 30 mins)
      7,748

    ColbyBowlin
    Newest Member
    ColbyBowlin
    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

    • cristiana
      Hi @KathyR37 and a very warm welcome here.  I am so very sorry that you are going through all of this. I just wanted to check, have you ever been tested for any other gastrointestinal conditions? Cristiana  
    • trents
      @KathyR37, I would suspect that in addition to gluten intolerance, you have other food intolerances/sensitivities. This is very common in the celiac community. The most common offenders are oats, dairy, soy, corn and eggs with dairy and oats being the big two. Have you considered this? Have you tried keeping a food diary to detect patterns?
    • Theresa2407
      thank you for your advice.   I have always taken them and I use Stonehedge because they are in a glass bottle, but don't have to be refrigerated.  I also like they are 3rd party tested and state gluten free. But you never know if something better has come alone over the years.
    • KathyR37
      Thank you for your response. I have already learned about the info you sent but i appreciate your effort. I am the only one in my family cursed by this disease. I have to cook for them too. I make sure that my utensils are free of gluten and clean after using them for other food. I use non-porous pots and pans and  gloves when cooking for them. One huge problem I have is a gag reflex out of this world and if something doesn't taste good it is not going down. Most commercially made breads and such taste like old cardboard.Pastas are about the same. I did find one flour that I like and use it regularly, but it is so expensive! All gluten free food is way more expensive. I only eat twice a day because I cannot afford to buy all that. We live on a very low income so my food purchases are quite limited.
    • Scott Adams
      What you've described—the severe weight loss, the cycle of medications making things worse, and the profound fear of eating before leaving the house—is a heavy burden to carry for 15 years. It is absolutely not your fault. While everyone's journey with celiac is different, the struggles with the learning curve, social isolation, and dietary grief are feelings many in the community know all too well. Your question about whether you should just eat what you want and manage the symptoms is a heartbreaking one, born from years of frustration. It's crucial to know that the diarrhea is a sign of ongoing damage to your small intestine from gluten, and simply managing the symptom with Imodium doesn't stop that internal harm or the risk of other complications. The fact that you are still getting sick within an hour of eating, even while trying to be gluten-free, is a huge red flag that something isn't right. This could be due to cross-contamination in your kitchen (e.g., using a shared toaster, colander, or condiment jars), hidden gluten in foods, or the possibility of another concurrent condition like refractory celiac disease. Don't give up!  This article has some detailed information on how to be 100% gluten-free, so it may be helpful (be sure to also read the comments section.):    
×
×
  • 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.