Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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 Do I Interpret The Results?


JoanneHoward

Recommended Posts

JoanneHoward Newbie

My daughter is 4 soon to be 5. My mothear is a celiac and we have had issues with my daughter for 6weeks old. Todate she have not been diagnosed a celiac. My mother is newly diagnosed in the last 3 years. we just had dblood work done on my daught and these are the results IgG 30, IgA 3, and tissue transglutaminase 14. The results say that it is unlikely she is a celiac. i don't understand where the high IgG comes form if she isn't gluten sensitive??? Her symptoms have not been typical. Cronic constipation form the time she was introduced to formula at 6 weeks the pediatric gastroenterologist we saw asid that she was haveing bowel movements that were so large it would be like us passing a 3" diameter movement. she would be torn and bleeding after she went. this is still and issue 4 years later and she hates going to the bathroom. the only time we say the stool soften was when we removed gluten for a week. as soon as we reintroduced it the painful movements returned. what do I do? Gluten doesnt make her ill and it doesn't stunt her growth or inhibit her development but i believe the has to be some sort of sensitivity ther or we would not have seen the easier bowel movements. i don't know waht to do sincle they have ruled out celiac!!!!!

Help please, Joanne in Peterborough Ontario


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



Celiac.com Sponsor (A8-M):



celiac3270 Collaborator

Normal Bloodtest Results

Antigliadin IgA -- Less than 18

Antigliadin IgG -- Less than 24

EMA -- Reads positive or negative

tTg IgA -- Less than 13

tTg IgG -- Less than 30

Also, certain tests are more accurate than others--in terms of: if a certain test is positive, it means that you likely have it, where as another test, which isn't as accurate doesn't carry much weight.

One thing you should suggest to the doctor is that your daughter might be IgA deficient. 1 in 200 are, and that could make her IgA look normal (as it does). Additionally, many have a naturally high IgA and don't have celiac, so a low IgA seems strange. Talk to your doctor about that. For the IgG, which your daughter tested positive in, that positive reading gives her somewhere between a 20% and 95% chance of having celiac disease. I don't know about the tTG....

If the dr. does not take you seriously and you want to be sure she doesn't have celiac, you can do an endoscopy. It's pretty likely since celiac disease is genetic and it often skips generations.

Also, if you find out it's not celiac, check into other things. A high IgG level can indicate other things: Crohn's disease, parasitic infections, colitis, allergic gastroenteropathy, and lymphoma....according to a book I checked about this. This is in the event of a low IgA...such as in this case.

Good luck :)

Guest elysealec

Hi. My daughter (8) and I both have celiac disease. I was diagnosed last spring and I only had my three children tested for that reason. My daughter had not shown any symptoms other than anxiety. In fact, she was over 9 lbs when born and has consistently been in the 95th percentile since. Her blood levels were higher than your daughters' and I was advised by her pediatrician to just keep an eye on it because her growth was exceptional and she did not show any classic symptoms. I went further and spoke with Dr. Ivor Hill at Wakeforest University and he explained that celiac disease manifests in many different ways and anxiety was one of them. She had a biopsy done in October and was not only positive but had considerable damage to her intestines. After two weeks of gluten-free, it was like her whole personality changed. The anxiety disappeared. I strongly advise to go further and find a pediatric gastroenterologist who has knowledge of celiac disease. Good luck.

Vicki

Boojca Apprentice

Do you know what the "normal" ranges are for the blood tests you had run? The reason I ask is that every lab has it's own norms. For instance, in our test for TTG anything over 30 was positive for celiac disease. But I've heard two other labs norms being 20 and 10, so that is important to know.

Bridget

JoanneHoward Newbie

thank you so much for the speedy and informative responses! you have given me other avenues i hadn't considered. Bridget asked about the range they used in the tests preformed. The testing site was McMaster university in Hamilton ontario and they are one of the top research hospitals in the area. less than 20 was negative, greater than 25 was positive and 20-25 was borderline. they have typed on the form that " The enzyme tissue transglutaminase has been identified as the major if not sole autoantigen detedted in the IFA Endomycial Antibody assays. Interpretation: Negative IgA antibodies rule out active celiac disease in virtually all cases and dermatitis herpetiformis in approximately 80% of cases. Elevated IgG gladin andtibodies indicate that DH cannot be ruled out. Although the specifity of the antibody is limited."

Does this mean anything to any one?

celiac3270 Collaborator

Well, if you have DH, you must have celiac...they go hand-in-hand--you can have celiac and not dh, but you can't have dh without celiac. So that seems strange...anyway...did you mention the possibility of IgA deficiency? Because the IgG is positive....

scaredparent Apprentice

My son is 20 months old and all of his test came back negitive but we had positive dietary change. I say if it makes them better do it. Put him on the diet hope for the best.


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



Celiac.com Sponsor (A8-M):



celiac3270 Collaborator

A good number here do not have an official diagnosis--either because they tried the diet, found it helped, and didn't want to go back to gluten to get tested, or because they got negative testing, tried the diet anyway, and found it worked for whatever reason...I agree that if it works, it doesn't matter what the tests show, but that's the way to eat.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,181
    • Most Online (within 30 mins)
      7,748

    Ruby B
    Newest Member
    Ruby B
    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

    • Jane878
      By the time I was 5 I had my first auto0immune disorder, Migraine headaches, with auras to blind me, and vomiting, sensitivity to light and sound. I was 5 years old, and my stepfather would have pizza night, milling his own flour, making thick cheesy gluten pizza, that I would eat and the next day, I would have serious migraines, and my mother & stepfather did nothing about my medical problems. When I was 17 in my first year at college, I was diagnosed with my 2nd known auto-immune disorder, Meniere's disease. I was a elite athlete, a swimmer, and soccer player. And once again my parents didn't think anything of understanding why I had a disorder only older people get. Now after my mother passed from Alzheimer's disease she also suffered with living with gluten. She had a rash for 30 years that nobody could diagnose. She was itchy for 45 years total. My brother had a encapsulated virus explodes in his spleen and when this happened his entire intestines were covered with adhesions, scar tissue and he almost lost his life. He has 5 daughters, and when I finally was diagnosed after being pregnant and my body went into a cytokine storm, I lost my chance to have children, I ended up having Hashimoto's disease, Degenerative Disc disease, and my body started to shut down during my first trimester. I am 6ft tall and got down to 119lbs. My husband and I went to a special immunologist in Terrace, California. They took 17 vials of blood as we flew there for a day and returned home that evening. In 3 weeks, we had the answer, I have Celiac disease. Once this was known, only my father and husband made efforts to change their way of feeding me. At the family cabin, my stepfather & mother were more worried that I would ruin Thanksgiving Dinner. It wasn't until one of my cousins was diagnosed with Celiac disease. They finally looked into getting Gluten Free flour and taking measures to limit "gluten" in meals. He did nothing but ask for me to pay for my own food and wi-fi when I came to the cabin to stay after our house burned down. When he informed my mother, they proceeding to get into a physical fight and she ended up with a black eye. The is just more trauma for me. Sam had no interest in telling the truth about what he wanted. He lied to my mother that he had asked my husband if I could pay for "food" when he asked Geoffrey if I had money to pay for my wi-fi. My mother hates when he spends so much time on the computer so he lied and said I could pay for my own food. I will remind you I weighed 119lbs at this time. (At 6ft) that is a very sick looking person. Neither parent was worried about my weight, they just fought about how cheap my stepfather was. As my mother was diagnosed with Alzheimer's disease in 2014. He had her sign over the will to a trust and added his children. He had no testimonial capacity at the time, so she signed without proper papers. Making this Trust null and void. When I gave my brother my childhood home, my mother stated I would be getting an equal part of inheritance to the house on Race. It currently worth 2.0 million $. I got nothing, and my stepfather has since disowned me b/c of my claim and he knows that my mother would never have left it uneven between my biological brother and myself. She sat me and my husband down, as we lived at the Race Street house and treated and took care of it as our own. My brother took over b/c he was going through a horrific divorce and needed a home so he could get a better custody deal with his soon to be ex-wife who was a Assist DA for Denver. She used the girls against him, and he & I were the primary caregivers. We, Judd and I spent the most time with them pre the divorce. Once Judd moved into the house, he threw all of my mother, grandmother and my family heirlooms out to the Goodwill. Nobody told my mother about this as she was going through cancer treatment and had Alzheimer's disease in her mother and her sister. My stepfather and biological brother took advantage of this matter, as I called a "family council" that my brother just never could make it to at the last moment. All of the furnishing, kitchen ware, everything was in the house my brother just moved into. He had had 2 weddings, I chose to elope b/c my stepfather ruined my brother's first wedding by talking about his relationship with my brother in front of my dad and his entire family, insulting him and having my grandfather leave the ceremony. It was a disaster. My stepfather just plays dumb and blames my father for the slight. I was the only child not to have a wedding. So, my mother and stepfather never had to pay for a thing. My mother had had an agreement with my father he'd pay for college and all medical issues with their kids, myself and Judd. So truly my mother never had to pay for anything big for me in her entire life. I am looking for anyone that has had a similar story, where they grew up in a household that had a baker that regularly milled flour and ate gluten. What happened to you? DId you suffer from different auto-immune diseases b/c of living with a baker using "gluten" Please let me know. I have been looking into legal ways to get my stepfather to give me what my mother had promised, and he erased. Thank you for listening to my story. Jane Donnelly  
    • trents
      Possibly gluten withdrawal. Lot's of info on the internet about it. Somewhat controversial but apparently gluten plugs into the same neuro sensors as opiates do and some people get a similar type withdrawal as they do when quitting opiates. Another issue is that gluten-free facsimile flours are not fortified with vitamins and minerals as is wheat flour (in the U.S. at least) so when the switch is made to gluten-free facsimile foods, especially if a lot of processed gluten-free foods are being used as substitutes, vitamin and mineral deficiencies can result. There is also the possibility that she has picked up a virus or some but that is totally unrelated to going gluten-free.
    • Sheila mellors
      I asked about the new fruit and nut one and the Dietician said yes I could eat it safely. Hooe this helps
    • Heatherisle
      Daughter has started gluten free diet this week as per gastroenterologists suggestion. However says she feels more tired and like she’s been hit by a train. I suggested it could be the change to gluten free or just stress from the endoscopy last week catching up with her. Just wondering if feeling more tired is a normal reaction at this stage. I suppose it’s possible some gluten might have been present without realising. Have tried to reassure her it’s not going to resolve symptoms overnight
    • DAR girl
      Looking for help sourcing gluten-free products that do not contain potato or corn derived ingredients. I have other autoimmune conditions (Psoriatic Arthritis and Sjogrens) so I’m looking for prepared foods as I have fatigue and cannot devote a lot of time to baking my own treats. 
×
×
  • Create New...