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

What Could A Pos Blood Test, But Neg Biopsy Be?


GEF

Recommended Posts

GEF Explorer

About a year ago, I was referred to a GI specialist due to IBS symptoms. I am quite sensitive to lactose but was being pro-active about my health and wanted to make sure there was nothing else wrong. The doctor routinely ran some blood tests and it came back as high in gliadin antibodies. (I'll have to check which test it was). Shortly thereafter I had an endoscopy to confirm the celiac diagnosis, but no abnormalities were found and the doctor said I wasn't celiac. My question is this though, what could the high blood test be if I have the symptoms, but no villious atrophy? Anyone know or have this same issue?

Thank you!

GEF


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



Celiac.com Sponsor (A8-M):



Tasha2004 Contributor

I have high Gliadin IgA not IgG.

I didnt want a biopsy, since I figured nothing was going to be there anyway. My Ttg was also totally negative, but that is the one test they have decided to run every few years to make sure I dont have full blown Celiac. Right now the most information I can gather is that it could be developing.

Maybe someone with more experience has more to share.

Guest jhmom

Hi GEF, welcome :)

There are several people here that have had positive blood test results and negative biopsy or vice versa. Heck... some of us had both negative test results and biopsy and still have Celiac/gluten sensitivity. Hang in there and I hope you get some answers soon!

Maybe someone will be along soon with more experience on the Celiac blood tests.

GEF Explorer

Thank you for your support. I have read so many of the posts and it does appear that many are in the same situations.. and many without the support of their doctor. I threw out gluten intolerant & celiac diagnosis when my doctor threw it out after the biopsy was normal. Looking back, I find myself disappointed that he didn't recommend gluten-free, especially when I hear how much damage can occur to your body if you are intolerant or celiac. He gave me the IBS diagnosis, which I can't seem to come to terms with. I was reading on EnteroLab's (enterolab.com) site that even someone with gluten intolerance can suffer malabsorption and all the celiac symptoms. I'm considering another dr's appointment to check for the level of malabsorption. I'm a frequent sufferer of "cloud-head", have many intestinal symptoms (diar, bloating, lactose intol), have clouds in my fingernails, poor teeth enamel, am borderline underweight. I would have to say the thing that bothers me the most is the "cloud-head" (there's nothing like feeling like that when you're paid to work well and productively) and if a gluten-free diet would cure that alone, it would be 100% worth it for me. I'm 28 and had GI symptoms for at least 13 years. Fiance is in total support of trying the diet and I'm finally to the point (after a year) where I can accept this.

(positive gliadin test, normal biopsy, IBS diagnosis)

GEF

j9n Contributor

I am in the same boat althought now they say "borderline celiac" whatever that means. I started to think about it and came to the realization that practically nothing healthy is made from wheat and there are better sources of fiber. Its all just "filler" food and if staying away makes me feel better than I am all for it.

Guest jhmom

You are welcome; this is a great place for support!

I too suffered for over a year and was given the famous IBS diagnosis; it should be called the IDK syndrome (I don't know) lol. I knew after losing 40lbs in 2 months that there was something more to it than the doctors could find. I went through all the conventional testing, emptying scan, colonoscopy, upper GI w/ follow through, endoscopy and CT scan. All of these came back normal with the exception of the endoscopy, which showed "patchy inflammation", but it wasn't enough to make a dx.

I finally decided to get tested through Enterolab and the $200.00 I spent for the tests was WELL worth it. I tested positive for gluten sensitivity and malabsorption due to intestinal damage. I immediately started the gluten-free diet and could tell a difference within a couple of days.

It is great that your fianc

GEF Explorer

I called a new GI this morning and got an appointment...this morning. Can you believe that? The new doctor was actually very kind and listened compassionately to my plight. I did find out that the test I took last year that was positive was IGG. It was 33, with normal levels below 20. Lucky me has lupus in the family so I have to get more bloodwork and a colonoscopy done :blink: Anyway, since the igg test above is about a year'ish old, the doctor ordered some new ones just in case. I really do wish I'd get better with something as simple (I know it's not simple) as a diet.... I'd just prefer that over meds! But, I'll let you know. Anyway, I'm just like everyone one of you that just won't be satisfied until they've exhausted being proactive about their health. When you know something's wrong, you know it's wrong.

Igg 33, everything else negative... who knows????

Gretchen


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



Celiac.com Sponsor (A8-M):



burdee Enthusiast

This may be hearsay, but my local celiac support group has discussed this topic (positive blood test, negative biopsy) a LOT. I also discussed rationale for doing blood tests and biopsies with my naturopath when I first suspected I had celiac. Here's what I understand about the blood test/biopsy disagreement phenomena:

The blood test indicates gliadin antibodies, but the biopsy shows damaged small intestinal tissue or flattened villi. Unless the patient has 100% of their small intestine damaged from longterm celiac, it's very possible that the biopsy tube can MISS the damaged area. Then it takes chunks of healthy tissue, rather than damaged tissue. So biopsies can be pretty hit and miss, unless a large percentage of the small intestine is damaged from long undiagnosed celiac disease. If you read Dr. Fine's speech under the Enterolab topic on this board (or just go to the Enterolab site), he also discusses the problems with biopsies.

I hope that helps. BTW I did the Enterolab tests for my diagnosis, after my naturopath explained how hit & miss the 'old' standard biopsies can be. :D

BURDEE

Tasha2004 Contributor

Burdee: Thanks for that explantion. What I dont get, most people with celiac disease have high IgG. Many have low IgA.

I have IgA only, and I have not found much literature at all to tell me what that really means. Dr. Fine said Gluten sensitivity only........

j9n Contributor

That is pretty interesting. I have lupus in my family as well and my GI didn't look twice at it. Also diabetes. I am curious as to what your new doctor says.

GEF Explorer

From what I've heard, having lupus in the family can mean your risks of celiac disease are also there as well. It's something about those auto-immune diseases that stick close together. The doctor requested some auto-nuclear test to pick up lupus today, so maybe that'll give some answers. Since the family history is there, it's worth checking out. Although the colonoscopy doesn't sound so pleasant, I'm wondering what it will show (I won't have that until 7/16). I have never had any GI issues associated with my stomach... just mid to lower intestinal. That positive IGG certainly makes me wonder. I just want to feel better though, I don't care what they have to test. Know what I mean?? And by golly, I won't stop until I get some answers... a trait that most of you here have... tenacity ;)

Gretchen

Guest jhmom

I'm also being tested for Lupus too, I show many signs of the disease. There has to be a link between these two diseases'.

GEF Explorer

Stacie,

I'd be interested to hear what your doc finds... I'll keep you posted from my end. I'm assuming I'll know something by early next week.

Gretchen

Guest jhmom

Gretchen,

I will let you know when/if I am diagnosed and yes please do keep me posted on your results as well.

All this started for me in January 04 and I've heard sometimes it can take months even years to be diagnosed. When I started feeling bad with the fatigue and other things I researched it on the Internet and it all pointed to Lupus, I went to my doc and explained my fatigue to him and he ran the ANA and it was POSITIVE! I was sort of scared and excited at the same time (if that makes ANY sense) ;) . You see with all this Celiac stuff all my test came back negative but I knew something was wrong and then these new things started happening and at least with the positive labs the doctors knew what path to take and in what direction to look at.

Anyway, let me know what your test show.

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. - suek54 replied to suek54's topic in Dermatitis Herpetiformis
      7

      Awaiting dermatitis herpetiformis confirmation following biopsy

    2. - knitty kitty replied to suek54's topic in Dermatitis Herpetiformis
      7

      Awaiting dermatitis herpetiformis confirmation following biopsy

    3. - suek54 replied to suek54's topic in Dermatitis Herpetiformis
      7

      Awaiting dermatitis herpetiformis confirmation following biopsy

    4. - trents replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      how much gluten do I need to eat before blood tests?

    5. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      how much gluten do I need to eat before blood tests?

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,258
    • Most Online (within 30 mins)
      7,748

    Tdodge
    Newest Member
    Tdodge
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • suek54
      Wow KK, thank you so much for all your attached info. I had a very quick scan but will read more in depth later.  The one concerning corticosteroid use is very interesting. That would relate to secondary adrenal insufficiency I think , ie AI caused by steroids such as taken long term for eg asthma. I have primary autoimmune AI, my adrenals are atrophied, no chance if recovery there. But I am in touch with some secondaries, so something to bear in mind. .  Niacin B3 Very interesting too. Must have a good read about that.  Im sure lots of questions will arise as I progress with dermatitis herpetiformis. In the mean time, thanks for your help.
    • knitty kitty
      Welcome to the forum, @suek54, I have Dermatitis Herpetiformis, too.  I found taking Niacin B3 very helpful in clearing my skin from blisters as well as improving the itchies-without-rash (peripheral neuropathy).  Niacin has been used since the 1950's to improve dermatitis herpetiformis.   I try to balance my iodine intake (which will cause flairs) with Selenium which improves thyroid function.   Interesting Reading: Dermatitis herpetiformis effectively treated with heparin, tetracycline and nicotinamide https://pubmed.ncbi.nlm.nih.gov/10844495/   Experience with selenium used to recover adrenocortical function in patients taking glucocorticosteroids long https://pubmed.ncbi.nlm.nih.gov/24437222/   Two Cases of Dermatitis Herpetiformis Successfully Treated with Tetracycline and Niacinamide https://pubmed.ncbi.nlm.nih.gov/30390734/   Steroid-Resistant Rash With Neuropsychiatric Deterioration and Weight Loss: A Modern-Day Case of Pellagra https://pmc.ncbi.nlm.nih.gov/articles/PMC12532421/#:~:text=Figure 2.,(right panel) upper limbs.&text=The distribution of the rash,patient's substantial response to treatment.   Nicotinic acid therapy of dermatitis herpetiformis (1950) https://pubmed.ncbi.nlm.nih.gov/15412276/
    • suek54
      Thank you all for your advice and the dermatitis herpetiformis article. The latter made me realise I had stopped taking my antihistamine, which I will restart today. The Dapsone has cleared the rash entirely but I still get quite a bit itching, absolutely nothing to see though. I know its notoriously hard to clear and its still relatively early days for me.  The iodine issue is very interesting. I do eat quite a bit of salt because I have Addison's disease and sodium retention is an issue. I also have autoimmune hypothyroidism, not sure how a low iodine diet would play into that? Because of my Addison's I am totally steroid dependent, I take steroids 4 x daily and cannot mount any defence against inflammation. I need to increase my meds for that. Now that I know what is wrong I can do just that if Im having a bad day. Life is very sweet, just so damn complicated sometimes! Hey ho, onwards. Thank you again for your advice.  
    • trents
      So, essentially all of the nutrition in the food we eat is absorbed through the villous lining of the small bowel. This is the section of the intestinal track that is damaged by celiac disease. This villous lining is composed of billions of finger-like projections that create a huge amount of surface area for absorbing nutrients. For the celiac person, when gluten is consumed, it triggers an autoimmune reaction in this area which, of course, generates inflammation. The antibodies connected with this inflammation is what the celiac blood tests are designed to detect but this inflammation, over time, wears down the finger-like projections of the villous lining. Of course, when this proceeds for an extended period of time, greatly reduces the absorption efficiency of the villous lining and often results in many and various nutrient deficiency-related health issues. Classic examples would be osteoporosis and iron deficiency. But there are many more. Low D3 levels is a well-known celiac-caused nutritional deficiency. So is low B12. All the B vitamins in fact. Magnesium, zinc, etc.  Celiac disease can also cause liver inflammation. You mention elevated ALP levels. Elevated liver enzymes over a period of 13 years was what led to my celiac diagnosis. Within three months of going gluten free my liver enzymes normalized. I had elevated AST and ALT. The development of sensitivities to other food proteins is very common in the celiac population. Most common cross reactive foods are dairy and oats but eggs, soy and corn are also relatively common offenders. Lactose intolerance is also common in the celiac population because of damage to the SB lining.  Eggs when they are scrambled or fried give me a gut ache. But when I poach them, they do not. The steam and heat of poaching causes a hydrolysis process that alters the protein in the egg. They don't bother me in baked goods either so I assume the same process is at work. I bought a plastic poacher on Amazon to make poaching very easy. All this to say that many of the issues you describe could be caused by celiac disease. 
    • catnapt
      thank you so much for your detailed and extremely helpful reply!! I can say with absolute certainty that the less gluten containing products I've eaten over the past several years, the better I've felt.   I wasn't avoiding gluten, I was avoiding refined grains (and most processed foods) as well as anything that made me feel bad when I ate it. It's the same reason I gave up dairy and eggs- they make me feel ill.  I do have a bit of a sugar addiction lol so a lot of times I wasn't sure if it was the refined grains that I was eating - or the sugar. So from time to time I might have a cookie or something but I've learned how to make wonderful cookies and golden brownies with BEANS!! and no refined sugar - I use date paste instead. Pizza made me so ill- but I thought it was probably the cheese. I gave up pizza and haven't missed it. the one time I tried a slice I felt so bad I knew I'd never touch it again. I stopped eating wheat pasta at least 3 yrs ago- just didn't feel well after eating it. I tried chick pea pasta and a few others and discovered I like the brown rice pasta. I still don't eat a lot of pasta but it's nice for a change when I want something easy. TBH over the years I've wondered sometimes if I might be gluten intolerant but really believed it was not possible for me to have celiac disease. NOW I need to know for sure- because I'm in the middle of a long process of trying to find out why I have a high parathyroid level (NOT the thyroid- but rather the 4 glands that control the calcium balance in your body) I have had a hard time getting my vit D level up, my serum calcium has run on the low side of normal for many years... and now I am losing calcium from my bones and excreting it in my urine (some sort of renal calcium leak) Also have a high ALP since 2014. And now rapidly worsening bone density.  I still do not have a firm diagnosis. Could be secondary HPT (but secondary to what? we need to know) It could be early primary HPT. I am spilling calcium in my urine but is that caused by the high parathyroid hormone or is it the reason my PTH is high>? there are multiple feedback loops for this condition.    so I will keep eating the bread and some wheat germ that does not seem to bother me too much (it hasn't got enough gluten to use just wheat germ)    but I'm curious- if you don't have a strong reaction to a product- like me and wheat germ- does that mean it's ok to eat or is it still causing harm even if you don't have any obvious symptoms? I guess what you are saying about silent celiac makes it likely that you can have no symptoms and still have the harm... but geez! you'd think they'd come up with a way to test for this that didn't require you to consume something that makes you sick! I worry about the complications I've been reading about- different kinds of cancers etc. also wondering- are there degrees of celiac disease?  is there any correlation between symptoms and the amnt of damage to your intestines? I also need a firm diagnosis because I have an identical twin sister ... so if I have celiac, she has it too- or at least the genetic make up for having it. I did have a VERY major stress to my body in 2014-2016 time frame .. lost 50lbs in a short period of time and had severe symptoms from acute protracted withdrawal off an SSRI drug (that I'd been given an unethically high dose of, by a dr who has since lost his license)  Going off the drug was a good thing and in many ways my health improved dramatically- just losing 50lbs was helpful but I also went  off almost a dozen different medications, totally changed my diet and have been doing pretty well except for the past 3-4 yrs when the symptoms related to the parathyroid issue cropped up. It is likely that I had low vit D for some time and that caused me a lot of symptoms. The endo now tells me that low vit D can be caused by celiac disease so I need to know for sure! thank you for all that great and useful information!!! 
×
×
  • 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.