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

Help With My Test Results Please.


nettinpete

Recommended Posts

nettinpete Newbie

Hi all,

 

I have had my blood test results back from my doctor and would like an opinion on if you think I would have a high chance of having celiac disease. He has suggested to me it looks like I would be but has sent me for further blood tests. He then has said I need to cut out gluten for one month and be retested. I have had these tests performed as I have terrible bloating and pain after eating also loose stools.  

 

My results are

 

Deamidated Gliadin IgG  <25U/mL

Tissue Transglutaminase IgA 94

 

Endomysial IgA says Weakly Positive.

 

Can someone please give me feedback on what these would mean as the doctor I seen was certainly not informative or helpful or easy to understand at all.

 

There was also an allergy testing performed which came back a result of 10.10 (high) for Grass Mix. Not sure if this has anything to do or related to Cealiac disease. Just curious as I'm thinking wheat is a type of grass....not sure.

 

Cheers,

Annette

 


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

Those look very positive in the ranges I have seen. What were the reference ranges? For example, "TTG IGA normal <10 ."They can be different from different labs.

nettinpete Newbie

Those look very positive in the ranges I have seen. What were the reference ranges? For example, "TTG IGA normal <10 ."They can be different from different labs.

The reference ranges are

Deamidated Gliadin IgG Normal <25, Low (25-50), Mod (51-80), Strong (>80)

Tissue Transglutaminase IgA Normal <20, Low (20-50), Mod (51-80), Strong (>80)

 

Hope this helps.

kareng Grand Master

The reference ranges are

Deamidated Gliadin IgG Normal <25, Low (25-50), Mod (51-80), Strong (>80)

Tissue Transglutaminase IgA Normal <20, Low (20-50), Mod (51-80), Strong (>80)

 

Hope this helps.

Welcome to the club!

Open Original Shared Link

"Is tTG elevated in persons with non-celiac gluten sensitivity?

Non-celiac gluten sensitivity does not cause any elevation of tTG antibodies in the blood stream."

kareng Grand Master

Also, if you are going to have an endoscopy, you shouldn't stop eating gluten. And 1 month off gluten might not be enough time to see a significant drop in the numbers. People seem to keep making antibodies for a few weeks after they stop eating gluten. And a big reason they don't drop to 0 is that a month may not be enougt time for you to get all the gluten out of your life. There is a bit of a learning curve.

The Celiac Center suggests you wait 3-6 months for your first follow-up blood test.

Open Original Shared Link

cyclinglady Grand Master

The next step is usually an endoscopy to obtain intestinal biopsies. The rule is that you should be eating gluten until all testing is complete. You should not need another blood test so soon. Sounds like your doctor is not knowledgeable. You may need to have another six months later to see if you are diet compliant.

Here is a link regarding celiac testing from the University of Chicago, a leader in celiac research:

Open Original Shared Link

nettinpete Newbie

Well thankyou all for your help. The links were great KarenG. I feel I now understand a bit more. This is all new to me and a bit overwhelming at the moment.

 

The next lot of blood tests the doctor has ordered me to get are :

 

Coeliac Serology HLA-DQ2/DQ 8 Endomyseal antibody. After reading one of the links it sounds like one test is for a gene test?

 

There was one more test that I did as part of my first round of blood tests but the results weren't back for that test yet. Not sure what that test was, but it had to be sent somewhere else for testing which takes longer.

 

So my readings in my above results are these alarmingly high or normal for Celiac Disease? Would you say I have celiac disease or should I not be alarmed till after I have an endoscopy?

 

And obviously my doctor isn't knowledgeable cyclinglady....looks like I will need to find a better doctor or at least hopefully when I get the next lot of results back they will refer me to a specialist who will hopefully be able to help me out more.


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



Celiac.com Sponsor (A8-M):



RMJ Mentor

Grass mix probably means perennial ryegrass, Kentucky bluegrass, Bermuda grass, and other lawn grasses. Allergies to grasses are pretty specific so I don't think wheat would cross react.

kareng Grand Master

Grass mix probably means perennial ryegrass, Kentucky bluegrass, Bermuda grass, and other lawn grasses. Allergies to grasses are pretty specific so I don't think wheat would cross react.

An allergy test has nothing to do with Celiac disease. Celiac is not an allergy to grasses or wheat.

cyclinglady Grand Master

Karen did welcome you to the club....but we are not doctors here. Just folks who have been there and done that!

Genetic testing in my opinion is not important at this point. Get in to see a GI doctor and one that has had celiac patients! Once all testing is complete, then you can go gluten free.

We are here to help! No need to be alarmed. The good news is that you should feel better soon!

Most celiacs do have issues with dairy. So, in the meantime ditch it for now. Once healed you most likely can start eating ice cream again. And giving up dairy will not affect celiac testing. You could have other food intolerances, but dairy is a good start.

nettinpete Newbie

Thankyou everyone for your helpful posts. I shall now try and find a reputable doctor or specialist for after my results come back to be referred to. And yes it will be good to hopefully some day start feeling better again. I always have been lactose intolerant so limit my dairy already....just "need" my milk for my coffee...can't quite give that away completely.

ravenwoodglass Mentor

I hope you finish testing soon so you can get gluten-free and start feeling better. some of us do find we are able to tolerate dairy after we heal a bit so someday you may be able to eat some gluten-free cheesecake with that cup of coffee.

One more quick note. You mention your doctor doing gene testing on you. If by any chance you turn out not to have one of those 2 genes don't let that negate your positive blood work. There are rare instances when someone will have celiac but not have one of the two most common celiac associated genes. 

SMRI Collaborator

I hope you finish testing soon so you can get gluten-free and start feeling better. some of us do find we are able to tolerate dairy after we heal a bit so someday you may be able to eat some gluten-free cheesecake with that cup of coffee.

One more quick note. You mention your doctor doing gene testing on you. If by any chance you turn out not to have one of those 2 genes don't let that negate your positive blood work. There are rare instances when someone will have celiac but not have one of the two most common celiac associated genes.

 

You've said this before but simple biology says that what you are saying is not possible.  

ravenwoodglass Mentor

You've said this before but simple biology says that what you are saying is not possible.  

More is being found out about genetics every day. My gene DQ 9 has now been shown to be also associated with celiac. A quick search of peer reviewed sites will show this. 

SMRI Collaborator

More is being found out about genetics every day. My gene DQ 9 has now been shown to be also associated with celiac. A quick search of peer reviewed sites will show this. 

 

It's possible that other genes are associated with Celiac I guess, but there has to be some genetic component or it's not Celiac.

notme Experienced

Thankyou everyone for your helpful posts. I shall now try and find a reputable doctor or specialist for after my results come back to be referred to. And yes it will be good to hopefully some day start feeling better again. I always have been lactose intolerant so limit my dairy already....just "need" my milk for my coffee...can't quite give that away completely.

if you have access to lactose free milk ( i use lactaid brand) it's pretty good for your coffee (or, in my instance, tea :)  )  i still use it even though i can have dairy now.  

nvsmom Community Regular

It's possible that other genes are associated with Celiac I guess, but there has to be some genetic component or it's not Celiac.

There probably are other genetic components that cause celiac disease. We have only known about the DQ2 and DQ8 for a few years now, and doctors agree that approximately 3% of celiacs do not have either of those genes.... It happens. It will be interesting what other links they discover in the next few years.

Welcome to the board, nettinpete. It looks like you belong with us. You have the same positive tests that I had. Hope you are well soon.

SMRI Collaborator

There probably are other genetic components that cause celiac disease. We have only known about the DQ2 and DQ8 for a few years now, and doctors agree that approximately 3% of celiacs do not have either of those genes.... It happens. It will be interesting what other links they discover in the next few years.

Welcome to the board, nettinpete. It looks like you belong with us. You have the same positive tests that I had. Hope you are well soon.

 

Links have been posted disputing this claim and those 3% have been found to have something, not Celiac....if Celiac is an autoimmune disease, which it is, there has to be some genetic component present, identified or not.

ravenwoodglass Mentor

Links have been posted disputing this claim and those 3% have been found to have something, not Celiac....if Celiac is an autoimmune disease, which it is, there has to be some genetic component present, identified or not.

No one is saying that celiac is not genetic. Just that not all the associated genes are commonly known. In my own family I have seen one person who was diagnosed with positive blood and biopsy and then years later had their genes tested and was told since they didn't have DQ2 or DQ8 that they couldn't have celiac. So now they are back on gluten and suffering the effects. That is what encouraged me to get my genes tested. I have DH and am a firmly GI diagnosed celiac and I don't have either of those two genes. I have a double DQ9. IMHO no one who has positive blood tests should quit or not start the diet just because the gene test is negative. 

beth01 Enthusiast

No one is saying that celiac is not genetic. Just that not all the associated genes are commonly known. In my own family I have seen one person who was diagnosed with positive blood and biopsy and then years later had their genes tested and was told since they didn't have DQ2 or DQ8 that they couldn't have celiac. So now they are back on gluten and suffering the effects. That is what encouraged me to get my genes tested. I have DH and am a firmly GI diagnosed celiac and I don't have either of those two genes. I have a double DQ9. IMHO no one who has positive blood tests should quit or not start the diet just because the gene test is negative.

Can't dispute that. I think there is a lot that will be discovered about celiac now that it's the forefront of every discussion out there known to man due to the "fad" of gluten free. Just look how many AI diseases there are that they can't isolate a linked gene from.

  • 2 weeks later...
MitziG Enthusiast

Your ttg is positive, dgp negative. Ttg is generally Celiac but can also elevate with other autoimmune disorders. If you get a positive EMA then you have celiac. Gene test is controversial at best- if you have the genes or makes it more likely you have celiac, that is all. Glad you are finding a more knowledgeable dr.

nettinpete Newbie

Your ttg is positive, dgp negative. Ttg is generally Celiac but can also elevate with other autoimmune disorders. If you get a positive EMA then you have celiac. Gene test is controversial at best- if you have the genes or makes it more likely you have celiac, that is all. Glad you are finding a more knowledgeable dr.

What is EMA? I've booked to get my next blood tests done next Saturday morning.

nvsmom Community Regular

What is EMA? I've booked to get my next blood tests done next Saturday morning.

 

EMA IgA is the anti endomysial antiboies immunoglobulin A test. It is very similar to the tTG IgA test but it tends to appear later as the disease progresses.  It is often negative in early celiac disease or in very young children.  The EMA IgA is very specific to celiac disease though, so if you get a positive test, it is as close to a sure thing as a diagnosis can get.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,696
    • Most Online (within 30 mins)
      7,748

    Kerrie C
    Newest Member
    Kerrie C
    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

    • RDLiberty
      So, I've been using a gluten free labeled toothpaste since being diagnosed with celiac. No big deal, the toothpaste seems to work. Question is, I just realized it contains hydrated silica.  Now, I've heard that silicon dioxide can cause issues in some people with celiac (was that ever confirmed though?), so to be safe, I cut it out of my diet entirely. But, as I understand it, hydrated silica is related to silicon dioxide. Is that something to worry about, or is the hydrated form not known to cause issues like the silicon dioxide form?  I've never seen it in food, but nearly every toothpaste I look at contains hydrated silica?  Issue or not?  Any scientific research (Not opinion pieces, not health bloggers, you get my gist), but actual science, that says it's an issue? I have a hard time believing 99% of what I read on random internet searches.    Thanks so much, Renee. 
    • Gigi2025
      Since 2015 we've spent extensive time in Italy and I've been able to eat their wheat products without incident. Initially, I was practically starving thinking foods in Sicily were not gluten-free.  An Italian friend who had lived in the US for over 20 years said she had celiac/gluten-free friends from the US who could eat Italian wheat products without problems. Hesitantly, I tried little by little without issues.  A few years later at a market, I asked a bread vendor if they had gluten-free loaves. Turns out she had lived in LA, said groups believe it's not the gluten that's causing our bodies harm, but potassium bromate; these groups have been trying to ban it.  Bromines and other halogens wreaks havoc to our endocrine system and, more specifically, our thyroids and immune systems. When bromines are ingested/absorbed into the body, it displaces iodine causing other health issues. Potassium bromate is a powerful oxidizing agent (dough 'conditioner') that chemically changes flour to enhance elasticity, bleaches the dough, and ages the flour much faster than open air.   Shortly thereafter while visiting friends in California, one family said they had gone gluten-free and the difference was incredible. The reason they choose this path was due them (a biologist/chemist/agriculturist scientist) having to write a portion of a paper about a certain product for the company he worked. Another company's scientist was directed to write the other portion. All was confidential, they weren't allowed to know the other company/employee.  After the research, they learned gluten was being removed from wheat, sent elsewhere, returned in large congealed blocks resembling tofu, and then added to wheat products. Potassium bromate has been banned for use in Europe, China, and other countries, but not in the US. Then we have the issues of shelf preservatives and stabilizers. What are we eating?  Why? We spend long periods of time in Italy and all has been good.  We just returned from an extended time in Greece;  no issues there either.  There is a man there we learned about on a travel show about Greece who walks the hills, picking herbs, pods, etc.  He is a very learned scholar, taught at the university level in Melbourne. It took a few days to locate him, but were finally successful. He too, is concerned about the additives and preservatives in American food (many of his customers are Americans, haven't been in the best of health, and have become healthier after visiting him). He suggested taking a food product from the US and the same product in Europe, and compare the different ingredients. Then ask why these things are being allowed in the US by the 'watch dog' of our foods and drugs. It would be amuzing if it weren't tragic. I'm presently looking for flour from Europe that I can make my own bread and pasta as the gluten-free bread is now $7.99 a (small) loaf.  BTW, studies are showing that many gluten-free individuals are becoming diabetic. My guess is because the gluten-free products are high in carbs. This is only my experience and opinion garnished by my personal research.  I hope it helps.  
    • knitty kitty
      Symptoms that get worse if you don't supplement is a sign of malabsorption, possibly due to Celiac disease. Blood tests for nutritional deficiencies are not very accurate, and should be done when you have been off of supplements for eight to twelve weeks, otherwise the vitamin supplements you've taken will be measured.  The blood circulation system is a transportation system.  It transports the vitamins you've absorbed around the body, but blood tests don't give an accurate picture of the vitamin and mineral stores inside organs and tissues where they are actually used.  You can have "normal" blood levels but still have deficiencies.  This is because the brain demands stored nutrients be put into the blood stream to supply important organs, like the brain and heart, while other organs do without.   If you are taking Thiamine Mononitrate in your supplements, you are probably low in thiamine.  Thiamine Mononitrate is used in many supplements because it won't break down sitting on a shelf.  This also means Thiamine Mononitrate is difficult for the body to utilize.  Only thirty percent of Thiamine Mononitrate on the label is absorbed and even less is able to be utilized by the body.  A different form of Thiamine called Benfotiamine has been shown to promote intestinal healing.   Talk to your doctor about doing a genetic test to look for Celiac markers.   I'm concerned that if you do a gluten challenge (10 grams of gluten per day for a minimum off two weeks) in your weakened state, the nutritional deficiencies will become worse and possibly life threatening.  
    • ElisaAllergiesgluten
      Hello, good afternoon!   I apologize, I didn’t see a notification and I’m just reading this. Thank you so much for sharing your thoughts and the link. Yes you are absolutely right, even so trying to get a response from them has been extremely difficult. They don’t answer but I will your practice of “guilty until proven innocent.”   I like and have a sense of trust here in this website, everyone is honest and thoughts are raw. The mutual understanding is amazing!   thank you Scott!
    • Scott Adams
      I'd go with a vodka tonic, but that's just me😉
×
×
  • 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.