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

Elevated Liver Enzymes


tabdegner

Recommended Posts

tabdegner Apprentice

I'm concerned about DH having celiac.

For years and years he has had very very elevated tranaminaise enzymes in his liver. He's had every test done in the book on his liver and no one can find anything wrong with him. The only thing one doctor found was that the enzymes were related to a very high level of "autoimmune antibodies" or something like that he had in his blood. Basically he said he had a very high risk of getting some form of autoimmune disease sometime in his life. (Not surprising, his family is an autoimmune disease factory.)

Fast forward to this week -- his doctor is trying to find out why he has such severe RLS and finds he has a huge ferritin (iron stores) deficiancy. (Which I know can be due to celiac). So now he's on HUGE doses of iron pills.

So I'm reading up on stuff and found quite a few studies online that linked unexplained elevated liver enzymes to silent adult celiac. I had never heard of this before. But it would explain a lot with his iron levels, "brain fog", liver enzymes, and a gallbladder that is only functioning at 25% (no gallstones).

Has anyone else had these elevated enzymes? DH has a strong history of autoimmune diseases in his family, but no celiac. Would a doctor call him crazy for asking for the blood tests based on our "own" research online?

Thanks for your input.


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



Celiac.com Sponsor (A8-M):



trents Grand Master

I'm one of those who had mildly elevated liver enzymes for years and my family doc could not offer an explanation. He did all the hepatitis tests and other tests and they were all negative. I finally went to a gastroenterologist because of the liver enzymes and he tested me right away for celiac disease and, of course, it was positive. Since going gluten-free, my liver enzymes have returned to normal but my albumin and total protein have continued to be moderately depressed. I'm guessing there was some liver damage done by all those years of low grade inflamation. Keep in mind, I had very minimal GI distress so I would never have gotten the celiac disease dx if it were only for that. I was one of those "silent" adult onset celiacs. It was the elevated liver enzyme problem that brought the Celiac dx. Here is a startling fact: at least 18% of Celiacs have elevated liver enzymes; some estimates place it at much higher. Please see the following link:

https://www.celiac.com/st_prod.html?p_prodid=1323

ravenwoodglass Mentor
I'm concerned about DH having celiac.

For years and years he has had very very elevated tranaminaise enzymes in his liver. He's had every test done in the book on his liver and no one can find anything wrong with him. The only thing one doctor found was that the enzymes were related to a very high level of "autoimmune antibodies" or something like that he had in his blood. Basically he said he had a very high risk of getting some form of autoimmune disease sometime in his life. (Not surprising, his family is an autoimmune disease factory.)

Fast forward to this week -- his doctor is trying to find out why he has such severe RLS and finds he has a huge ferritin (iron stores) deficiancy. (Which I know can be due to celiac). So now he's on HUGE doses of iron pills.

So I'm reading up on stuff and found quite a few studies online that linked unexplained elevated liver enzymes to silent adult celiac. I had never heard of this before. But it would explain a lot with his iron levels, "brain fog", liver enzymes, and a gallbladder that is only functioning at 25% (no gallstones).

Has anyone else had these elevated enzymes? DH has a strong history of autoimmune diseases in his family, but no celiac. Would a doctor call him crazy for asking for the blood tests based on our "own" research online?

Thanks for your input.

Boy he sure does not sound like a silent celiac, he may not have constant D but he is not symptomsless. Who cares if his doctor thinks he is crazy he should not ask for the test he should demand it. There is no reason for his doctor not to at least blood test. If he should refuse or you want to go another route you can use Enterolab for stool and gene testing. Many have found them to be very helpful. You could also try eliminating gluten from the diet, you have to be strict about it, and after a couple months he could do a gluten challenge and see if his symptoms return or become worse. Another valid way of diagnosis. Oh and like many others I had my liver numbers return to normal after diagnosis and also had a few autoimmune disorders go into complete remission.

tabdegner Apprentice

Thanks for the replies. You're right, he's definitely not a "silent" celiac or whatever he has. I think he definitely needs to be tested. He's had so many problems the last year. Now he's on antidepressents (which he wants to get off of) due to the "brain fog" and being tired (and tons of stress at his old job), and a pretty high dose of Requip (for RLS), which is not working well. It would be nice if he could get off of all the meds and just be gluten free. We're waiting to hear (hopefully today) if he gets this new job he interviewed for, which would lead to better insurance. But if not, he still needs to be tested. I think he's going to make an appointment w/his primary doctor today. The sleep doctor just said take the iron pills for 1-2 months and then get it retested. But, come on, even if the pills bring his levels up, there's got to be some other issue going on to have iron stores be THAT low.

TestyTommy Rookie

Boy, does this thread bring back bad memories. I was sick for years and went from doctor to doctor who told me that there was nothing wrong with me. The only lab test that wasn't normal was elevated liver enzymes. Two doctors refused to test me for celiac because I didn't have D. They all wanted to put me on anti-depressants (which i did for a while, and it made me feel incredibly bad).

Don't wait for a blood test. Get DH off of gluten and see what happens. A gluten-free diet has no side-effects and actually makes most of us eat much healthier than we used to. Also, the celiac bloodtest gives LOTS of false negatives. The only real test for celiac is whether you get better when you go gluten free. Most people start feeling better in a few weeks, though it may take years to heal.

If he's got celiac disease, evey day he eats gluten is another day of life he loses.

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - trents replied to K6315's topic in Coping with Celiac Disease
      3

      Newly gluten free… withdrawal?

    2. - K6315 replied to K6315's topic in Coping with Celiac Disease
      3

      Newly gluten free… withdrawal?

    3. - Sandi20 replied to Sandi20's topic in Gluten-Free Foods, Products, Shopping & Medications
      9

      Gluten Free Daily Vitamins for Kids w/ Celiac

    4. - trents replied to K6315's topic in Coping with Celiac Disease
      3

      Newly gluten free… withdrawal?

    5. - K6315 posted a topic in Coping with Celiac Disease
      3

      Newly gluten free… withdrawal?


  • Celiac.com Sponsor (A19):



  • Member Statistics

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

    Jojo W.
    Newest Member
    Jojo W.
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.4k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      One small study found that 50% of celiacs react to the dairy protein "casein" like they do to gluten. It is also common for celiacs to be lactose (the sugar in milk) intolerant, though that often disappears in time as the villi heal. About 10% of celiacs react to the oat protein "avenin" like they do gluten.
    • K6315
      Thank you so much Trents (Scott?)! I have started working with a dietitian and did a deep research dive as soon as I got the diagnosis. I am aware of what you mentioned in the first two paragraphs, and was not aware of anything in the third, so I am grateful for that information, and will talk to the dietitian about that. I think I was most interested in the withdrawal process - it gives me hope that, although I have felt unwell recently, I just need to be patient (not a strong suit). I have printed the article you sent and will look at it more closely. Thanks again!
    • Sandi20
      I really like Thorne!  I've researched thier products.  Thank you so much.
    • trents
      Welcome to the forum, @K6315! Gluten withdrawal typically lasts for a period of a few weeks. But there is a real learning curve involved in actually attaining to a gluten free dietary state. Much more is involved than just cutting out major sources of gluten such as bread and pasta. It's all the places that gluten is hidden in the food supply that is difficult to ferret out, like soy sauce and canned tomato soup, canned chili and canned pork n' beans, some "lite" pancake syrups, potato salad, flavorings, etc., etc. Gluten-containing grain products are hidden through alternate terminology and found in places you would never expect.  There is also "cross contamination" where naturally gluten free foods come into contact with gluten-containing grains during farming, transportation, storage and manufacturing processes. Then there is the issue of "cross reactivity" whereby you may be having gluten-like reaction to food proteins whose structure is similar to gluten. Chief among these are dairy, oats (even gluten-free oats), soy, corn and eggs. I am including this article that you might find helpful:   
    • K6315
      Prior to being diagnosed, I had a gluten heavy diet. I stopped all gluten exactly a week ago and have continued to feel sick in the ways I did prior to going gluten free - primarily on and off nausea, brain fog, and fatigue. Wondering if this is normal and, if so, how long can I expect to feel this way?
×
×
  • Create New...