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

How confident should I be with these results?


orion

Recommended Posts

orion Newbie
(edited)

Hi folks,

I went in to see a gastroenterologist in the beginning of December due to ongoing reflux and digestive issues that cropped up a month or so prior. I was put on omeprazole and carafate and scheduled for an upper endoscopy and colonoscopy in January. There were no visible issues found during that procedure, but they also biopsied my stomach, small intestine and colon. Stomach and colon were normal but the small intestine had "increased itraepithelial lymphocytes, and villous blunting" with a note of "histology could be seen in the setting of sprue." 

Based on that finding, my doctor said suggested it could be celiac disease and ordered additional labs. I had a celiac disease panel and HLA dna testing done and I just got those results back yesterday. The blood panel included Endomysial Antibody IgA, t-Transglutaminase (tTG) IgA, and Immunoglobulin A, Qn, Serum.  The Endomysial Antibody IgA was negative, the t-Transglutaminase (tTG) IgA was "weak positive" 4 (reference ranges were 0-3 negative, 4-10 weak positive, >10 positive), and Immunoglobulin A, Qn, Serum was 217 (reference range 90-386 is normal). 

The HLA test showed I was positive for HLA-DQ2 (DQA1*02:AC,05:BPGVU positive, one copy | DQB1*02:CHJSJ,03:BZUXK positive, one copy). Since my parents have both done 23andme tests, I know that my mother doesn't have any celiac genes, but my father has an HLA-DQB1 variant, and apparently my great uncle on his side has Celiac disease. Of course no one told me any of this until my own tests came up, lol.

My doctor told me that while it would have been a home run if my labs were higher, my results were enough to diagnose me with Celiac disease and for me to go ahead and start a gluten-free diet. I'll have follow-up appointments at 3 and 6 months, with a repeat biopsy around a year out. I'm also supposed to be setting up an appointment with a nutritionist/dietitian. 

I'm very new to all of this, so I just wanted to get a feel for if my results are just borderline and could be something else or if I can be reasonably confident in the diagnosis.

Thanks!

- Jake

 

Edited by orion

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



Celiac.com Sponsor (A8-M):



Scott Adams Grand Master

We can't officially diagnose you from this info, but certainly the villi damage along with positive tests, even weak positive blood test results, together are probably a good sign that you're on the right track by going gluten-free. If your digestive issues resolve on the diet it would be a slam dunk, but you need to be certain that your diet is 100% gluten-free, which isn't as simple as it sounds.

Fenrir Community Regular

As Scot says we can't diagnose you but 98% of people that are positive (weak or strong doesn't matter)for TTG IgA are celiacs. 

The quote you posted from the pathology report (I used work with pathologists as a lab tech) would indicate you have Celiac Disease (that's what they mean by sprue). 

IMO, and I'm no doctor, is that you have a very solid diagnosis of celiac disease. You have positive blood tests and a pathology report suggesting celiac disease. 

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now
  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,242
    • Most Online (within 30 mins)
      7,748

    rickak
    Newest Member
    rickak
    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

    • knitty kitty
      Welcome to the forum, @McKinleyWY, For a genetic test, you don't have to eat gluten, but this will only show if you have the genes necessary for the development of Celiac disease.  It will not show if you have active Celiac disease.   Eating gluten stimulates the production of antibodies against gluten which mistakenly attack our own bodies.  The antibodies are produced in the small intestines.  Three grams of gluten are enough to make you feel sick and ramp up anti-gluten antibody production and inflammation for two years afterwards.  However, TEN grams of gluten or more per day for two weeks is required to stimulate anti-gluten antibodies' production enough so that the anti-gluten antibodies move out of the intestines and into the bloodstream where they can be measured in blood tests.  This level of anti-gluten antibodies also causes measurable damage to the lining of the intestines as seen on biopsy samples taken during an endoscopy (the "gold standard" of Celiac diagnosis).   Since you have been experimenting with whole wheat bread in the past year or so, possibly getting cross contaminated in a mixed household, and your immune system is still so sensitized to gluten consumption, you may want to go ahead with the gluten challenge.   It can take two years absolutely gluten free for the immune system to quit reacting to gluten exposure.   Avoiding gluten most if the time, but then experimenting with whole wheat bread is a great way to keep your body in a state of inflammation and illness.  A diagnosis would help you stop playing Russian roulette with your and your children's health.      
    • trents
      Welcome to the celiac.com community, @McKinleyWY! There currently is no testing for celiac disease that does not require you to have been consuming generous amounts of gluten (at least 10g daily, about the amount in 4-6 slices of wheat bread) for at least two weeks and, to be certain of accurate testing, longer than that. This applies to both phases of testing, the blood antibody tests and the endoscopy with biopsy.  There is the option of genetic testing to see if you have one or both of the two genes known to provide the potential to develop celiac disease. It is not really a diagnostic measure, however, as 30-40% of the general population has one or both of these genes whereas only about 1% of the general population actually develops celiac disease. But genetic testing is valuable as a rule out measure. If you don't have either of the genes, it is highly unlikely that you can have celiac disease. Having said all that, even if you don't have celiac disease you can have NCGS (Non Celiac Gluten Sensitivity) which shares many of the same symptoms as celiac disease but does not involve and autoimmune reaction that damages the lining of the small bowel as does celiac disease. Both conditions call for the complete elimination of gluten from the diet. I hope this brings some clarity to your questions.
    • McKinleyWY
      Hello all, I was diagnosed at the age of 2 as being allergic to yeast.  All my life I have avoided bread and most products containing enriched flour as they  contain yeast (when making the man made vitamins to add back in to the flour).  Within the last year or so, we discovered that even whole wheat products bother me but strangely enough I can eat gluten free bread with yeast and have no reactions.  Obviously, we have come to believe the issue is gluten not yeast.  Times continues to reinforce this as we are transitioning to a gluten free home and family.  I become quite ill when I consume even the smallest amount of gluten. How will my not having consumed breads/yeast/gluten for the better part of decades impact a biopsy or blood work?  I would love to know if it is a gluten intolerance or a genetic issue for family members but unsure of the results given my history of limited gluten intake.   I appreciate the input from those who have gone before me in experience and knowledge. Thank you all!
    • trents
      I know what you mean. When I get glutened I have severe gut cramps and throw up for 2-3 hr. and then have diarrhea for another several hours. Avoid eating out if at all possible. It is the number one source of gluten contamination for us celiacs. When you are forced to eat out at a new restaurant that you are not sure is safe, try to order things that you can be sure will not get cross contaminated like a boiled egg, baked potatos, steamed vegies, fresh fruit. Yes, I know that doesn't sound as appetizing as pizza or a burger and fries but your health is at stake. I also realize that as a 14 year old you don't have a lot of control over where you eat out because you are tagging along with others or adults are paying for it. Do you have support from your parents concerning your need to eat gluten free? Do you believe they have a good understanding of the many places gluten can show up in the food supply?
    • Peace lily
      Okay went online to check green mountain k cups .It was said that the regular coffees are fine but they couldn’t guarantee cross contamination.with the flavors. im trying to figure out since I eliminated the suyrup so far so good. I’m hoping. thanks it feels good to listen to other people there views.
×
×
  • 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.