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

Recently Tested For Celiac - Questions & Confused


newjoy82

Recommended Posts

newjoy82 Rookie

Hello,

I recently had blood work done and I'm a bit confused by the results and was hoping to see if anyone could help figure it out... I tested weak positive on TGG IgG but negative on everything else. My doctor says I need to go on a gluten free diet and I have celiac disease. Additionally, I had some blood work done at my allergy doctor a few weeks prior to this and have low IgA (IgA deficiency)...my level was 55 and it was supposed to be between 90 something and 400 something. I'm a little confused by the terminology. I read a couple articles that said having IgA deficiency can cause some of your celiac test results to be lower than they are or have a false negative. The doctor said people typically either are really low or really high, but don't usually result with a weak positive.

 

"While it is rare, it is possible for patients to have a negative antibody test results and still have celiac disease. IgA deficiency is one example where this could occur. Further medical evaluation is important for anyone who is still experiencing symptoms, to establish the diagnosis or to rule out celiac disease as a part of establishing another diagnosis."  Open Original Shared Link

 

In addition to this I was diagnosed with Fibromyalgia at 16 years old (almost 32 now). I went to the doctor because I have not been treated for FMS for years and wanted to verify the diagnoses was correct as I've still had symptoms for many years. Out of the blood work that has been done I had low vitamin D and the weak positive on the IgG (plus the low IgA results).

 

Is it normal to have only one positive out of the results? Any FMS - celiac connection?

 

My typical symptoms - stomach issues, muscle/joint pain, headaches (migraines or in both eyes), tired...all the time, sleep issues, muscle cramps, etc.

 

The doctor has not mentioned any further testing, but recommended following a gluten free diet.

 

My results:

 

GLIADIN AB, DEAMID. IgG   1.9 U/ML
NEGATIVE U/ML <20

 

GLIADIN AB, DEAMID. IgA  1.7 U/ML
NEGATIVE U/ML <20

 

TTG IgG [H] 6.2 U/ML
WEAK POSITIVE U/ML 6-9

 

TTG IgA 0.6 U/ML
NEGATIVE U/ML <4


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

Yes, you can have just positive out of the all the tests. That is why it is imperative to have all the celiac tests done. Even with the IGA deficiency, you still tested positive.

Many people here on this forum have Fibro as well. I have celiac disease and my Mom has Fibro. There could be a relationship.

bartfull Rising Star

Congratulations! Your doctor has given you a diagnosis. SO many here have struggled with doctors who either refuse to test them, perform the tests wrong, or read the tests wrong. Your doctor sounds like a good one! While to many folks a diagnosis isn't important, for some folks it is. It gives them the extra willpower to stick to the diet. Others need that piece of paper for school or work to take them seriously. And if you are ever hospitalized, that piece of paper can make the difference between getting a gluten-free meal or having to live on jello while you're there.

 

Now what you need to do is go to the coping section here and read the Newbie 101 thread. Make sure you click on all of the links provided in the different posts there. It'll give you a real education about celiac disease and how to do the diet right. Then come back and ask as many questions as come to mind.

newjoy82 Rookie

Thank you Cycling Lady...that information is very helpful. 

 

Thank you Bartfull...I am happy to have the diagnosis, but also want to understand what it means and the test results and how it relates to the other issues I mentioned. Thank you for the information regarding the newbie forum I will definitely check it out.

cyclinglady Grand Master

You might find relief from your Fibro symptoms after you have been gluten free for a few months to a year or longer (takes lots of time to heal your intestinal tract). As mentioned in " Newbie 101", you might have additional intolerances, again resulting from intestinal damage. It is strongly encourage to give up all dairy for a while and keep a food journal to help identify other intolerances.

https://www.celiac.com/forums/topic/91878-newbie-info-101/

I also had only one of the celiac disease blood tests come back positive. I went on for a biopsy for many reasons: 1) I was already there for a routine colonoscopy, 2) I was severely anemic, and 3) I could not imagine that both my husband (who has been gluten free for 13 years) and I would both have issues with gluten....I mean what are the odds?

I wish you well!

GottaSki Mentor

The celiac antibody tests are IgA and IgG based. With deficient total serum IgA, the IgA based celiac antibody tests are not valid and make the IgG tests that much more important.

Another important item you mention was deficient Vitamin D...celiac disease prevents proper absorption of many nutrients.

It takes a doctor that understands the combination of symptoms, nutritional deficiencies and proper celiac antibody testing to diagnose celiac disease in many cases.

I agree with the diagnosis, but highly suggest further nutrient testing as many need to supplement until the digestive system has a chance to heal and begin to properly absorb nutrients.

All that said...if you are not comfortable with the diagnosis, I suggest you seek out a gastroenterologist with celiac experience to discuss the possibility of further testing.

Undiagnosed celiac disease can cause all of the symptoms known as Fibromyalgia....as others have mentioned, it can take time for these symptoms to improve.

The complete removal of gluten is not an easy transition, but once you are past the learning curve it becomes much easier to live gluten-free.. Do read the newbie thread others have linked to.

If you are thinking of consulting with Gastro...do not remove gluten until you do. Further testing (endoscopy with small intestine biopsy) requires continued gluten consumption until the endo has been completed.

Welcome to the best club you never wanted to join :)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,692
    • Most Online (within 30 mins)
      7,748

    Linda M Rush
    Newest Member
    Linda M Rush
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)

    • There are no registered users currently online

  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • 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
    • Rejoicephd
      That and my nutritionist also said that drinking cider is one of the worst drink choices for me, given that I have candida overgrowth.  She said the combination of the alcohol and sugar would be very likely to worsen my candida problem.  She suggested that if I drink, I go for clear vodka, either neat or with a splash of cranberry.   So in summary, I am giving ciders a rest.  Whether it's a gluten risk or sugars and yeast overgrowth, its just not worth it.
×
×
  • 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.