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

Testing: When And How


siouxsie

Recommended Posts

siouxsie Rookie

At 28, I finally found out I have celiac. Now my worry is how to handle it with my children. I'm convinced both of them have it but neither show strong signs. I see symptoms but that is because I'm looking. Neither child is sickly, but for example, my 9 mos old son never, and I mean never, spits up unless he has something w/ gluten and my 6 yr old is frieghtenly pale, even for an Irish girl :P . Her moods are starting to get a bit unruly and she is just beginning to complain about belly aches. Why aren't there tests that can diagnose without having to wait for damage to happen first? Just tonight I saw in some posts, there's a genetic test. Is this common and I just didn't know about it or is it still a work in progress? I heard of genetic testing for neurological disease when I was pregnant (also just found out Huntington's is in my family) but no one ever mentioned genetic testing for celiac. I just feel so frustrated and I want definite answers, which seem impossible!! I just want to make the best decision for my children and I feel like I don't have enough information to made a wise decision. Thanks for any advice.

---Suzanne


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



Celiac.com Sponsor (A8-M):



Guest jhmom

Hi Suzanne:

I went the conventional route looking for a dx, I went through all sorts of tests and everything came back negative. I was sick of being sick and being told that I had IBS that I finally ordered a stool panel test from Open Original Shared Link . This way of testing is more sensitive than blood and a more accurate way of testing.

After I was dx my daughter and I both went gluten-free but then I decided to have her tested as well, her test came back positive too. I was happy that she did not have to endure all the tests that I did and that after going gluten-free she was like a new kid.

Good luck to you and your children! :D

lovegrov Collaborator

Your 9-month-old is too young to be tested accurately. Your daughter should be tested immediately. Personally I'd go the conventional route starting with a FULL celiac panel. Iga, total Iga, Igg, and Ttg.

To my mind, the gene test is only moderately useful. If you don't have the genes then you know you don't have and can't get celiac disease. But if you do have the genes that doesn't tell you whether you have it or not. Many people have the genes but don't have celiac disease.

richard

plantime Contributor

Spitting up, paleness, moodiness, and tummy aches are all mild symptoms of celiac. Since you have celiac, have your doctor order the gene panels for both kids. It is hereditary, and it will make a difference in their lives. Enterolab has a stool test that is non-invasive, and very accurate. Yes, it is expensive, but not as expensive as repeated trips to the doctor! Since you are seeing signs in your children, then it is wise to get them tested. Using Enterolab, you can also take them gluten free right away. The sooner you know and start treatment, the healthier they will remain!

dana-g Newbie

It is completely untrue that many people have the gene for celiac disease but don't have the disease!!! If you have the gene, you have the disease. You may not have damage to the villi in your intestine, but you have celiac disease! I respecfully refer you to EneroLab's website and Dr. Fine's online lecture in which he explains how EARLY INTERVENTION is the point of these genetic tests, before any damage or symptoms are apparent. There may be other diseases in which a gene's presence doesn't necessaily mean you will get the disease, but celiac disease isn't one of them. I repeat, if you have the gene, you must go gluten-free!

lovegrov Collaborator

Dr. Fine is at odds with other well-known experts on this point.

dana-g Newbie

Two separate board-certified pediatric gastroenterologists on staff of our local children's hospital as well as my own doctor recommended genetic testing for me and my family. Dr. Fine may be a controversial figure, but genetic testing is regularly relied on by the mainsteam medical community. And all three docs said a positive result means no gluten for life.


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



Celiac.com Sponsor (A8-M):



taneil Apprentice

For the above posts talking about Dr. Fine. This is what is says on Enterolab website about Genetic Testing. He does not say that you have celiac disease if you have the gene. But Gluten Sensitivity is stil possible...Read the highlighted part.

I have also read his lengthy essay on the subject and he does not state that you have celiac disease if you have the gene.

What role does genetic testing play in the diagnosis of gluten sensitivity?Currently, tests are available to detect the genes that control the immune system's reaction to gluten. These genes are called human leukocyte antigens or HLA. There are several types of HLA genes within each person. It is a particular type called HLA-DQ that is most useful in the assessment of the probability that a person may be gluten sensitive. The reason gene testing assesses probability rather than disease itself is because some people have the genes for gluten sensitivity but have no detectable evidence of the immune reaction to gluten or have no symptoms. In such people, gluten sensitivity is still possible but the probability (or in other words the chances or the odds) is lower than in a person who may be having symptoms attributable to gluten or that has antibodies detected. HLA testing is most useful when there is diagnostic confusion about whether or not a person is gluten sensitive. Such confusion often stems from one of the following: atypical intestinal biopsy results, the presence of associated diseases (such as microscopic colitis) that may mask the expected improvement of symptoms when gluten is withdrawn from the diet, negative tests for gluten antibodies in the midst of suggestive symptoms or signs of gluten sensitivity or celiac sprue (see the paragraph below to understand the difference), or when there are no symptoms at all and the person or the doctor can hardly believe that gluten sensitivity is really present. Other situations that HLA testing is useful is when a person is already on a gluten-free diet, and for testing family members (particularly children) for the odds that they have or will develop gluten sensitivity.

Just thought I would clear up the misinformation. You can even e-mail him if you want and he will write back himself with the answer. Hope this helps.

taneil Apprentice

One more note...if you have the gene, but don't have celiac disease, gluten could trigger celiac disease at some point in your life. I found out about my gluten sensitivity because I developed symptoms of Hashimoto's. I am sure the gluten in my diet triggered the Hashimoto's because since going gluten-free my symptoms for Hashimoto's Hypothyroidism have gone down. I however am still waiting on my test results from Enterolabs. I e-mailed my celiac disease blood panel results to Dr. Fine and he said I don't have celiac disease but am Gluten Sensitive.

All this to say havimg the gene does not mean you have or ever will have celiac disease, but at the same time it could be triggered at some point. Thus going gluten-free is a good prevention because you may be asymtomatic with celiac disease but it may trigger an autoimmune response such as thyroid problems, diabetes, MS, arthitis etc. as I believe it did with myself and my Grandfather.

mat4mel Apprentice

How will your blood tests show if you are just gluten sensitive, or actually have celiac?

taneil Apprentice

Here were the results of my blood test:

Antigliadin Abs, IgA was Negative

Antigliadin Abs, IgG was 34 H Units

t-Transglutaminase (tTg) IgA was Negative

Reticulin IgA Ab was Negative

Reticulin IgG Ab was Negative

This was the reply Dr. Fine gave me when I e-mail the results to him:

Your positive antigliadin antibody is a sign of gluten sensitivity. Going gluten free will indeed prevent celiac disease and help your thyroid maybe to the point of returning to normal.

He also gave me this link Open Original Shared Link to his essay which is were he talks about early diagnosis. I ordered the stool and gene test because I want to know how much if any damage has been done to my intestines. The essay gets a little technical in places, but he is very good and explaining even the technical stuff in layman's terms. Hope this helps.

I also have two childern. One 7 months and one 2 1/2 that I am trying to figure out what I am going to do with them. I have actually put the two year old on the gluten-free diet and am going to be careful to make sure the 7 month old doesn't get any gluten for awhile at least. We have to figure out if insurance will pay for the Enterolab tests before I can get the 2 year old tested.

taneil Apprentice

I guess I forgot to answer your question specifically...

Blood tests can't always confirm gluten senstivity or celiac disease which is what Dr. Fine explains in the essay, that is why he recommends the stool test. But in my case the main blood test for celiac disease which is tTg was negative but one of the Antigliadin antibodies was positive. Thus not to the point of celiac disease but on the way there.

dana-g Newbie

Thank you for the info, Taneil...I guess my doctors were recommending that if the gene was present we go gluten-free and not tempt fate! Good luck with your test results...waiting is the worst part.

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Iam replied to Larzipan's topic in Related Issues & Disorders
      33

      Has anyone had terrible TMJ/ Jaw Pain from undiagnosed Celiac?

    2. - trents replied to Scatterbrain's topic in Sports and Fitness
      6

      Feel like I’m starting over

    3. - bobadigilatis replied to Larzipan's topic in Related Issues & Disorders
      33

      Has anyone had terrible TMJ/ Jaw Pain from undiagnosed Celiac?


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,307
    • Most Online (within 30 mins)
      7,748

    Hcon74
    Newest Member
    Hcon74
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Iam
      Yes.  I have had the tmj condition for 40 years. My only help was strictly following celiac and also eliminating soy.  Numerous dental visits and several professionally made bite plates  did very little to help with symptoms
    • trents
      Cristiana makes a good point and it's something I've pointed out at different times on the forum. Not all of our ailments as those with celiac disease are necessarily tied to it. Sometimes we need to look outside the celiac box and remember we are mortal humans just like those without celiac disease.
    • bobadigilatis
      Also suffer badly with gluten and TMJD, cutting out gluten has been a game changer, seems to be micro amounts, much less than 20ppm.  Anyone else have issues with other food stuffs? Soy (tofu) and/or milk maybe causing TMJD flare-ups, any suggestions or ideas? --- I'm beginning to think it maybe crops that are grown or cured with glyphosphate. Oats, wheat, barley, soy, lentils, peas, chickpeas, rice, and buckwheat, almonds, apples, cherries, apricots, grapes, avocados, spinach, and pistachios.   
    • cristiana
      Hi @Scatterbrain Thank you for your reply.   Some of these things could be weaknesses, also triggered by stress, which perhaps have come about as the result of long-term deficiencies which can take a long time to correct.   Some could be completely unrelated. If it is of help, I'll tell you some of the things that started in the first year or two, following my diagnosis - I pinned everything on coeliac disease, but it turns out I wasn't always right!  Dizziness, lightheaded - I was eventually diagnosed with cervical dizziness (worth googling, could be your issue too, also if you have neck pain?)  A few months after diagnosis I put my neck out slightly carrying my seven-year-old above my head, and never assigned any relevance to it as the pain at the time was severe but so short-lived that I'd forgotten the connection. Jaw pain - stress. Tinnitus - I think stress, but perhaps exacerbated by iron/vitamin deficiencies. Painful ribs and sacroiliac joints - no idea, bloating made the pain worse. It got really bad but then got better. Irregular heart rate - could be a coincidence but my sister (not a coeliac) and I both developed this temporarily after our second Astra Zeneca covid jabs.   Subsequent Pfizer jabs didn't affect us. Brain fog - a big thing for people with certain autoimmune issues but in my case I think possibly worse when my iron or B12 are low, but I have no proof of this. Insomnia - stress, menopause. So basically, it isn't always gluten.  It might be worth having your vitamins and mineral levels checked, and if you have deficiencies speak to your Dr about how better to address them?    
    • knitty kitty
      @NanceK, I do have Hypersensitivity Type Four reaction to Sulfa drugs, a sulfa allergy.  Benfotiamine and other forms of Thiamine do not bother me at all.  There's sulfur in all kinds of Thiamine, yet our bodies must have it as an essential nutrient to make life sustaining enzymes.  The sulfur in thiamine is in a ring which does not trigger sulfa allergy like sulfites in a chain found in pharmaceuticals.  Doctors are not given sufficient education in nutrition (nor chemistry in this case).  I studied Nutrition before earning a degree in Microbiology.  I wanted to know what vitamins were doing inside the body.   Thiamine is safe and nontoxic even in high doses.   Not feeling well after starting Benfotiamine is normal.  It's called the "thiamine paradox" and is equivalent to an engine backfiring if it's not been cranked up for a while.  Mine went away in about three days.  I took a B Complex, magnesium and added molybdenum for a few weeks. It's important to add a B Complex with all eight essential B vitamins. Supplementing just one B vitamin can cause lows in some of the others and result in feeling worse, too.  Celiac Disease causes malabsorption of all the B vitamins, not just thiamine.  You need all eight.  Thiamine forms including Benfotiamine interact with each of the other B vitamins in some way.  It's important to add a magnesium glycinate or chelate supplement as well.  Forms of Thiamine including Benfotiamine need magnesium to make those life sustaining enzymes.  (Don't use magnesium oxide.  It's not absorbed well.  It pulls water into the intestines and is used to relieve constipation.)   Molybdenum is a trace mineral that helps the body utilize forms of Thiamine.   Molybdenum supplements are available over the counter.  It's not unusual to be low in molybdenum if low in thiamine.   I do hope you will add the necessary supplements and try Benfotiamine again. Science-y Explanation of Thiamine Paradox: https://hormonesmatter.com/paradoxical-reactions-with-ttfd-the-glutathione-connection/#google_vignette
×
×
  • 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.