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

Help...what Do These Results Mean?


Cin

Recommended Posts

Cin Rookie

Hi,

I am new here, I do not have celiac symptoms....yet. I was tested because my mom, brother and his 2 children have been diagnosed with celiacs. I am wondering if someone could help me with these results. I as a rule do not eat bread or pasta or much with gluten as a personal preference for weight loss but 4 days prior to the testing I did eat bread (white) and macaroni-(incidentally I did have "gas" and bloating those days.)

I also fasted that morning for my cholesterol. I don't know if this makes a difference.

My doctor said the testing was inconclusive and it would not hurt me to eat gluten free but ya know.....if I want to eat bread, I want to eat bread lol. In other words I don't mind going gluten free if I have to but I kinda just want to know if I will be "damaging" myself if I go off.

Here are the results.

Gliadin Igg antibody 1.8 reference rang <25.0

Gliadin IGa antibody 43.5 reference range < 25

Endomysial ABS,S negative

What do you experts think??????

Thanks

Cindy


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



Celiac.com Sponsor (A8-M):



Guest nini

well first of all you didn't have the complete panel of tests for Celiac done, but what you did have does show one elevated number...

I've lost over 100 pounds in three years by being gluten free, if you have noticed that you lose weight on a low gluten diet, that sends up a red flag for me right there that you at the very least have a problem with gluten. With your mom and brother and his kids being Celiac, you also have a predisposition. If you notice gas and bloating with eating gluten, that too is a signal...

If indeed you do have Celiac, which I suspect you do, you will need to be 100% gluten free, no cheating ever, there are some decent gluten-free breads that can satisfy they need for that bread fix... Chebe bread is one and Kinnikinick has a ton of products, also Whole Foods Gluten Free bakehouse. Anyway.

In my opinion, positive dietary response is your best indicator of if you have this or not, so I would suggest trying the diet for a good 6 months and keeping a food log and noting any symptoms or cessation of symptoms. After that time period if you want to challenge the diet, you can, also keeping a log of any symptoms. You may find after six months, that you don't want to put gluten back in your system. There is also a learning curve with the diet and it may take you that long to figure out where a lot of the hidden glutens are hiding.

Since you say you are already on a low gluten diet, I think that would have messed with your blood test results, and if you were to have a biopsy, that too could be falsely negative.

So, listen to your body, try the diet and see if you notice a difference.

Cin Rookie
well first of all you didn't have the complete panel of tests for Celiac done, but what you did have does show one elevated number...

I've lost over 100 pounds in three years by being gluten free, if you have noticed that you lose weight on a low gluten diet, that sends up a red flag for me right there that you at the very least have a problem with gluten. With your mom and brother and his kids being Celiac, you also have a predisposition. If you notice gas and bloating with eating gluten, that too is a signal...

If indeed you do have Celiac, which I suspect you do, you will need to be 100% gluten free, no cheating ever, there are some decent gluten-free breads that can satisfy they need for that bread fix... Chebe bread is one and Kinnikinick has a ton of products, also Whole Foods Gluten Free bakehouse. Anyway.

In my opinion, positive dietary response is your best indicator of if you have this or not, so I would suggest trying the diet for a good 6 months and keeping a food log and noting any symptoms or cessation of symptoms. After that time period if you want to challenge the diet, you can, also keeping a log of any symptoms. You may find after six months, that you don't want to put gluten back in your system. There is also a learning curve with the diet and it may take you that long to figure out where a lot of the hidden glutens are hiding.

Since you say you are already on a low gluten diet, I think that would have messed with your blood test results, and if you were to have a biopsy, that too could be falsely negative.

So, listen to your body, try the diet and see if you notice a difference.

okay, you say I didnt have all the tests done......what are all the tests you recommend?

Do you recommend going to see a gastroenterologist as this was just my PCP?

Thanks for the input.....

Cindy

Guest nini

Anti-Gliadin (AGA) IgA

Anti-Gliadin (AGA) IgG

Anti-Endomysial (EMA) IgA

Anti-Tissue Transglutaminase (tTG) IgA

Total Serum IgA

This is the complete panel...

Do I recommend going to a GI? No. I think that the dietary response is the most valid diagnostic tool and you do not need a Dr. for that. What can a GI do for you? Well, they COULD run the full panel of tests and do a biopsy and IF they are positive they could confirm the dx of Celiac, But, since so many Dr.s know so very little about Celiac and are reluctant to dx it if results are borderline or only showing early signs of damage. Very few Dr.s are willing to dx. celiac based on they believe that the ONLY way to dx this is by biopsy. Problem with this is that in early stages damage can be very sporadic and easily missed by biopsy. And they do not take near enough samples most of the time for a valid test.

Some people feel more comfortable getting a Dr. dx. but you have to keep in mind that Dr.s are human, they are usually under pressure by Pharmaceutical companies to prescribe drugs (even getting kickbacks) and are under pressure by Insurance companies to keep visits short so they can see more patients so you don't get quality of care. I've lost faith in the medical community and I think we need to get back to listening to our bodies. And if our bodies tell us that gluten is a problem, by all means, eliminated it from your diet. Don't just take drugs to treat the symptoms. This will only make it worse.

Did I have a Dr. dx.? Yes, but it was only confirmation of what I already knew in my heart. I had tried the gluten-free diet before and it had worked, but I had let another Dr. talk me out of it because he said it was all in my head. If I had listened to my body the first time, I could have saved myself from 4 more years of ill health. By the time I got my dx. my blood work was so highly positive that I did not need the biopsy to confirm the dx.

Guest Robbin

I am pretty new at this--nini is an expert--but I would add that even if you didn't have any gastro symptoms, you could be getting neurological damage, and THAT is something to take extremely serious. If you want to get easier answers, aside fromthe diet, I suggest maybe trying enterolab. Even just getting the gene test, at the least. I am awaiting my results in a week or so and it couldn't have been easier. Far easier than putting up with the run-around at the drs. You don't have to listen to a so-called-expert to know what YOUR body already tells you, though. Take care. :)

  • 4 weeks later...
ladyx Newbie
Hi,

I am new here, I do not have celiac symptoms....yet. I was tested because my mom, brother and his 2 children have been diagnosed with celiacs. I am wondering if someone could help me with these results. I as a rule do not eat bread or pasta or much with gluten as a personal preference for weight loss but 4 days prior to the testing I did eat bread (white) and macaroni-(incidentally I did have "gas" and bloating those days.)

I also fasted that morning for my cholesterol. I don't know if this makes a difference.

My doctor said the testing was inconclusive and it would not hurt me to eat gluten free but ya know.....if I want to eat bread, I want to eat bread lol. In other words I don't mind going gluten free if I have to but I kinda just want to know if I will be "damaging" myself if I go off.

Here are the results.

Gliadin Igg antibody 1.8 reference rang <25.0

Gliadin IGa antibody 43.5 reference range < 25

Endomysial ABS,S negative

What do you experts think??????

Thanks

Cindy

Not an expert but I would want to know for sure too. wouldn't want to give up bread if I didn't have to. It's all about finding the right doctor...I had seen several GI's and all my kids had seen one since they were little and we weren't diagnosed...when my son went to see his new pediatric GI people called him the celiac doctor...they said if you had it he would find it. So ask around find people that have celiac diease and ask if they know a good doctor who will work hard to find out for sure... I am not sure you can be 100% sure but get a full test done by a good lab. Call your local GI's and ask if they have support groups for celiac paitents and then ask if you could find out when they met so you can go...you might find some good stories to help you. Hope this helps!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,685
    • Most Online (within 30 mins)
      7,748

    Janahawk
    Newest Member
    Janahawk
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.3k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Thanks for the additional information. I was thinking of asking you if your daughter was taking methylated vitamins since she has the MTHFR gene but you beat me to it. To answer the question you posed in your original post, as I explained, celiac disease does not damage the colon but the lining of the small bowel. If the damage is pronounced enough and the doc doing it is experienced, yes, the damage done to the lining of the small bowel can be spotted with the naked eye.
    • cameo674
      I could not locate the correct Gary Brecka video where he explains the methylation process and specifically states things about how people with the MTRR homozygous gene mutation are known to suffer from heartburn due to a weakened valve/sphincter where the esophagus and the stomach connect.  My brother had the youtube video sent to him from 10x health which is probably why I cannot locate it.     I will have read up on mast cell activation.  I do not know anything about it.  Tums is my preferred gerd treatment.  I always figured a little extra calcium could not hurt me.  
    • cameo674
      Trents: Due to a genetic mutation, my daughter has inherited from both parents she cannot process the Folic Acid provided in the fortified American grains.   An MD told her to avoid eating fortified grains.   My daughter makes the assumption that unless she makes the food item, that the baker used a fortified grain so she has been limiting her gluten intake since 2020.   Her Psychiatrist was who tested her for MTHFR gene issue because she suffers from depression and severe anxiety. The Psychatrist also instructed my daughter to supplement with a methylated version of folate once she knew my daughter was homozygous, because the methylated version bypasses the mutated gene step so her body can absorb it.  Low folate absorption impacts serotonin and dopamine production.  My husband and I also both have two other homozygous gene mutations that interfere with vitamin absorption: MTRR and VDR taq.  The first interferes with B-12 absorption which requires us to take a methylated B-12 vitamin and the second with Vitamin D absorption so we have to take higher doses to stay within normal levels.   My brother, who has the exact same gene mutations, went through 10x health genetic testing for vitamin supplements (paid by his employer) and received a huge report saying the same things about which types of supplements had to be taken.  Gary Brecka does videos on how these gene mutations impact the vitamin absorption pathways.       If my brother had not gotten his testing through work, he would never would have started his supplement journey.  His testing is what triggered my getting functional health testing that tested similar biomarkers to his.  Again the celiac testing was an add-on test that I did off the cuff.  
    • trents
      Welcome to the forum, @growlinhard1! If eliminating gluten from your diet makes significant improvement in your symptoms then there are two possibilities. Either you have celiac disease (aka, gluten intolerance) or NCGS (Non Celiac Gluten Sensitivity, aka, gluten sensitivity). The difference is that celiac disease is an autoimmune disorder that creates inflammation and, over time, damages the lining of the small bowel which inhibits nutrient absorption whereas NCGS does not damage the lining of the small bowel. They share many of the same symptoms. At the end of the day, the antidote for both is to abstain from foods that contain wheat, barley or rye, the three gluten-containing grains. Some countries supply stipends and healthcare benefits for those with an official celiac diagnosis. If you live in the USA that does not apply. The main reasons for seeking an official celiac diagnosis are psychological and social. Many people have a hard time not falling off the gluten free bandwagon without an official diagnosis. They find it easy to rationalize it all away as being temporary or due to something else. When you have an official diagnosis, you tend to take gluten-free eating more seriously. Socially, family and friends are more likely to respect and attempt to comply with your need to eat gluten free if you have an official diagnosis of celiac disease. Your physician is more likely to take you seriously as well if you have an official diagnosis because there are typically other health problems that are spinoffs which develop from celiac disease in time. One autoimmune disease invites others. There are no tests for NCGS. Celiac disease must first be ruled out. We do have specific tests for celiac disease. By the way, some experts believe that NCGS can transition into celiac disease. If your endoscopy/biopsy is only a month away, I would encourage you to stick it out and go back on gluten to get an official diagnosis. You still have time to get a valid test result if you start back on gluten now, 10g of gluten daily which is about the amount found in 4-6 slices of wheat bread.
    • BoiseNic
      I have the same problem. No matter what I eat, I seem to get a break out every 1 to 2 months. I do not do oats, citrus fruits, apples, onions and other foods also, as those cause reactions. The only time I have zero problems is when I fast. The only staple grain I have is quinoa, as that doesn't seem to cause me issues. I have linked mine to a microbiome imbalance. I am currently on month 3 of Skinesa. It's supposed to take 3 months before seeing results. I guess we'll see.
×
×
  • Create New...