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 Bilirubin Count Warning Sign Of Celiac? (gilbert's Syndrome)


Pegleg84

Recommended Posts

Pegleg84 Collaborator

Hello all,

well, I've tried to stop stressing about the possibility of having celiac for a bit, but I just got my most recent blood test results back and my liver bilirubin count is still high. Normals are 2-18, but mine is currently 29. There is no real danger caused by this elevation of bilirubin, but could it possibly a sign or symptom of celiac disease? The reason why I suspect this is because my mother, who was diagnosed with celiac over a year ago, had elevated bilirubin counts since she was my age (early 20's). Our doctor has always said that it was a mild form of a rare condition called Gilbert's sydrome (which when severe can cause jaundice), which is hereditary. Anyway, now that she is on an gluten free diet, my mother's bilirubin counts have gone down more or less to normal, suggesting a link to celiac disease.

now, of course we have mentioned this possibility to our doctor and he thinks it's coincidence (though he's not overly informed about celiac), but it is yet another sign that I could be the next on the list of family members with celiac.

If anyone has any information about this possible link, I would love to know.

For those who are bound to ask. Both my mother and my only sister both have the disease. It's on both my mother and father's side of the family, I have so far tested negative in 2 successive IgA,IgG blood tests, but am nevertheless suffering increasing gastrointestrinal problems, including stomach pains, bloating, hemrhoids (fun fun), and all kinds of other possibly related stuff.

as always, any help and information is greatly appreciated.


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



Celiac.com Sponsor (A8-M):



mimommy Contributor
Hello all,

well, I've tried to stop stressing about the possibility of having celiac for a bit, but I just got my most recent blood test results back and my liver bilirubin count is still high. Normals are 2-18, but mine is currently 29. There is no real danger caused by this elevation of bilirubin, but could it possibly a sign or symptom of celiac disease? The reason why I suspect this is because my mother, who was diagnosed with celiac over a year ago, had elevated bilirubin counts since she was my age (early 20's). Our doctor has always said that it was a mild form of a rare condition called Gilbert's sydrome (which when severe can cause jaundice), which is hereditary. Anyway, now that she is on an gluten free diet, my mother's bilirubin counts have gone down more or less to normal, suggesting a link to celiac disease.

now, of course we have mentioned this possibility to our doctor and he thinks it's coincidence (though he's not overly informed about celiac), but it is yet another sign that I could be the next on the list of family members with celiac.

If anyone has any information about this possible link, I would love to know.

For those who are bound to ask. Both my mother and my only sister both have the disease. It's on both my mother and father's side of the family, I have so far tested negative in 2 successive IgA,IgG blood tests, but am nevertheless suffering increasing gastrointestrinal problems, including stomach pains, bloating, hemrhoids (fun fun), and all kinds of other possibly related stuff.

as always, any help and information is greatly appreciated.

Hello. I just wanted to say that my 8 year old daughter's liver enzymes were drastically elevated prior to diagnosis (total bilirubin 1.1 w/ o.o-o.7 range, ALT 715 w/ 24-49 range, AST 303 w/ 15-37 range). My child was negative for all hepatitis screenings. All numbers have returned to normal with gluten free diet. Below is a link to read over suggesting the celiac/liver disease connection--scroll down to the pdf page for hepatitis. I call celiac the "Equal Opportunity Destroyer".

Open Original Shared Link

Gen Rookie
Hello all,

well, I've tried to stop stressing about the possibility of having celiac for a bit, but I just got my most recent blood test results back and my liver bilirubin count is still high. Normals are 2-18, but mine is currently 29. There is no real danger caused by this elevation of bilirubin, but could it possibly a sign or symptom of celiac disease? The reason why I suspect this is because my mother, who was diagnosed with celiac over a year ago, had elevated bilirubin counts since she was my age (early 20's). Our doctor has always said that it was a mild form of a rare condition called Gilbert's sydrome (which when severe can cause jaundice), which is hereditary. Anyway, now that she is on an gluten free diet, my mother's bilirubin counts have gone down more or less to normal, suggesting a link to celiac disease.

now, of course we have mentioned this possibility to our doctor and he thinks it's coincidence (though he's not overly informed about celiac), but it is yet another sign that I could be the next on the list of family members with celiac.

If anyone has any information about this possible link, I would love to know.

For those who are bound to ask. Both my mother and my only sister both have the disease. It's on both my mother and father's side of the family, I have so far tested negative in 2 successive IgA,IgG blood tests, but am nevertheless suffering increasing gastrointestrinal problems, including stomach pains, bloating, hemrhoids (fun fun), and all kinds of other possibly related stuff.

as always, any help and information is greatly appreciated.

I am still getting used to this whole glutten thing so I can't advise you too much on that. That being said elavated billirubin levels can be a problem. Having been through that with my mother. There is a little known probable autoimune disease called Primary Billalilary Chirrosis (PBC). It too is like celiacs in that it is often undiagnosed or misdiagosed for years. It took my mom about 15 years to get a definative diagosis. There also appears to be a link between celiac's and even thyroid disease. Oh and one of the symtoms is incessant itching. You need to see a hepatoligist who knows something about this disease to rule it out.

Please don't let the word cirrosis scare you is isn't caused by drinking or exteral factors. It's an autoimune response to something unknown.

Good luck.

eringopaint Newbie

I have had a high bilirubin count for years, and doctors always ignored it since it wasn't dangerously high. I am due for blood test soon to see if my vitamin D level has returned to normal (it was very low) so I am anxious to see what the bilirubin will look like now that I am gluten-free.

I went gluten free last April but it took about 3 months to start to see real positive changes... it is well worth the effort. really. I pretty much blame all my medical problems on celiac - as I was undiagnosed for 30 yrs and now am seeing so many problems disappear.

Yes, thyroid disease is linked to celiac - have that too.

good luck.

erin

  • 3 weeks later...
pmn Newbie

If any of you find out your results and any possible connexion between the two I would really like to know! I've been experiencing a slew of Coeliac-like symptoms for a couple of years now with no other explanation, and I have also been diagnosed with Gilbert's (my last 2 rounds of blood work showed levels in the 40s and 50s). I had a requisition for IgA IgG blood tests in November, but unfortunately moved to the other side of the country before I could get it done, and haven't followed up with a doctor since moving.

  • 5 weeks later...
Voss Newbie

I have celiac and are intolerant to salicylates, histamine, etc.

I found this research yesterday in my own quest for answers as how this is all related.

While googling more I also found this topic, so I registered to post this:

Gilbert's syndrome is caused by approximately 70%-75% reduced glucuronidation activity of the enzyme Uridine-diphosphate-glucuronosyltransferase isoform 1A1 (UGT1A1).

Open Original Shared Link

Open Original Shared Link

Deficient UDP-glucuronosyltransferase detoxification enzyme activity in the small intestinal mucosa of patients with coeliac disease.

Department of Gastroenterology, Radboud University Medical Center Nijmegen, Nijmegen, the Netherlands

Background Small intestinal malignancies in humans are rare; however, patients with coeliac disease have a relatively high risk for such tumours. Intestinal UDP-glucuronosyltransferases are phase II drug metabolism enzymes also involved in the detoxification of ingested toxins and carcinogens. As many toxins and carcinogens are ingested via food, the human gastrointestinal tract not only has an important role in the uptake of essential nutrients, but also acts as a first barrier against such harmful constituents of the food. Therefore, the gastrointestinal mucosa contains high levels of detoxification enzymes such as cytochromes-P450, glutathione S-transferases and UDP-glucuronosyltransferases.

Aim To compare the UDP-glucuronosyltransferase detoxification capacity in small intestinal mucosa of patients with coeliac disease vs. that in normal controls.

Methods We assessed UDP-glucuronosyltransferase enzyme activities towards 4-methylumbelliferone in small intestinal biopsies of patients with coeliac disease (n = 22) and age- and sex-matched controls (n = 27).

Results Small intestinal UDP-glucuronosyltransferase enzyme activity in controls was significantly higher than in patients with coeliac disease: 0.55

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      130,851
    • Most Online (within 30 mins)
      7,748

    Suzanne Clarke
    Newest Member
    Suzanne Clarke
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Awol cast iron stomach
      I just wanted to share my support for you. Rant away. We all know that, and have experiences like that at some point. I am sorry for that very unpleasant, and emotionally isolating reminder of your medical condition. Which always is exacerbated by the hunger. I will admit many of my family friends, and coworkers found it easier to exclude me than to accommodate me. I also have to be very strict with cross contamination so in hindsight they did me a favor.  The sting however can often still be unearthed when I read experiences like yours.  I am sorry you had that occur. I hope you, and the coworkers can find the easy more accommodating experiences again after this unfortunate incident. Best wishes. 
    • Awol cast iron stomach
      "...hemorrhoids, constipation and diarrhea" . Heard of indeed. Experienced too. In hindsight, I can remember from age 2 having, and trying to convey my issues. I went 38 years misdiagnosed. So yes one can have these issues. I did have to go back on gluten for a gluten challenge. I failed that challenge and 6 days in they give me permission to stop, and I proceed with my scopes as scheduled. Post those 6 days I had gained 13 intolerances. I had to remove many foods, and reintroduce them back in. Nine years later I have two that remain gluten, and corn. I found it helpful to follow a whole foods diet. I also found autoimmune (AIP) protocol diet/recipes, and Paleo diet/recipes helpful. I still enjoy many of those homemade version recipes. I still continue to make my own salad dressings even if I can find a gluten-free store bought version. Fresh taste best to this palate now.  I did give up many grains I was off many and reverted to coconut flour and almond flour as work arounds .  I still remember the first time my gut experienced the reintroduction of quinoa. It wasn't sure if it wanted to flare or not. In 30 minutes it reported back ok this will pass. Many foods were removed post gluten challenge for me for 2 years and 4 months. At the 2 year 4 month mark is when my body said ok let's eat again, but don't ever feed me gluten again! I wish you the best.   
    • Scott Adams
      if you have already learned that Gluten is the cause of your symptoms, of course there is no need to add it back into your diet— your decision could save you a lot of needless suffering. One thing to consider is that if you do have celiac disease, your first- degree relatives may also need to get screened for it, because, like diabetes the disease is genetic, although many of its triggers seem to be environmental factors. You may want to consider getting a genetic test for celiac disease, so you can at least warn your relatives if it turns out that you do carry a celiac gene.
    • lookingforanswersone
      Thanks everyone. I've decided to do a gluten challenge (4 slices of bread a day for 3 months) and then do a full gluten panel of all the tests that can be done, just to rule it in or out for sure. I think otherwise psychologically it will keep bothering me 
    • Suze046
      Thanks Scott. Those articles are really interesting. I’m cutting out gluten for 6 weeks but honestly I’m not sure I even want to reintroduce it! I ate at a restaurant for the first time on Wednesday and then Thursday was really uncomfortable and had a few trips to the loo.. wonder if there was some cross contamination 🤷‍♀️ if that’s how my body reacts after not eating it for 3 weeks I’m not sure it’s worth reintroducing it and re testing for celiac! It might have been a coincidence I realise that I’m not going to feel better all of a sudden and my gut is probably still trying to heal. Thanks for your supportive message! 
×
×
  • Create New...