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

Should I push for an Endoscopy? Negative Blood Test...


meg-c

Recommended Posts

meg-c Explorer

Hi, everyone. I haven't been diagnosed with Celiac disease, so I hope it's okay for me to post here.

I'm a 21-year-old female who has been struggling with some chronic symptoms for about a year now.

Out of nowhere, I started losing weight. To date, I've lost upwards of 70 pounds. I was very much overweight beforehand, and I'm now hovering at a healthy weight. The weight has seemed to plateau somewhat recently, though. I was overweight my entire life, losing weight was never easy for me... even as an athlete. I'm now very sedentary. Along with the weight loss, I'm always super tired, I've lost lots of weight, have crazy dry skin/rash between my fingers, etc. I have occasion GI problems (intermittent diarrhea and constipation), sometimes floating stools. However, the never really cause me a huge inconvenience, just a difference I've noticed in my own habits. I also do not have any worthwhile stomach pain, cramps, or vomiting.

I've never had any of my vitamin/minerals checked, but I do know that I am anemic. I have a very low ferritin (11 on last check, but that was a long time ago) along with a low hemoglobin, hematocrit, etc. I've been treating with an oral multivitamin with iron and I'm due to have levels rechecked soon.

I had a blood test for Celiac disease preformed a long time ago. It checked both my tTG IgA and total IgA -- both were within range. I was eating gluten at the time (and I still am, no plans to stop unless I receive a proper diagnosis).

It may also be worth noting that both my parents have autoimmune diseases. My father had T1 diabetes and my mother had transient Graves' disease. I know that autoimmune diseases can be more likely to run in families.

Anyways. Should I push my doctor for a scope to rule out Celiac disease once and for all? Should I only request a scope if my anemia hasn't improved on iron?

Any thoughts, suggestions, recommendations, or similar experiences would be greatly appreciated.

Thank you!


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



Celiac.com Sponsor (A8-M):



Pegleg84 Collaborator

Hi Meg,

I was in a somewhat similar situation before I went gluten free: lost a bunch of weight very quickly (I was not overweight, so looking 10+lb in a month was alarming), felt like crud after eating anything, really bad anxiety, low vitamin levels/iron anemia, etc etc. I had blood tests done a couple times (once after my mom was diagnosed with Celiac, and later when my symptoms popped up) which were both negative (not sure if they ran the full panel, though). However, that didn't stop me from being pretty sure I had Celiac. The disease runs on both sides of my family (not sure if my dad had it, but a couple of his siblings do), and my sister also had negative blood tests but an endoscopy showed positive for villi damage. i got sick of being sick all the time and didn't want to wait for however long it would take to get an endoscopy done in a small city (and just before moving) so went gluten-free and never turned back. Given the improvement in my symptoms, I have always considered myself to have Celiac and no one can tell me otherwise. No way would I do a gluten challenge and ruin my health just to have a confirmed diagnosis.

All that to say: YES! You should push for an endoscopy. First, talk to your doctor about your symptoms and get the full blood panel redone (lots of posts here with the full rundown of what you should ask for). Tell them that there are AI disorders on both sides of your family (two positives make a negative? Still not sure how that works but probably what happened in me&my sister's case) and want to confirm with an endoscopy regardless of the blood results. Keep enjoying your glutens until then.
You should also get your vitamin/mineral levels checked, because low levels + the sudden weight loss, fatigue, etc definitely sounds like a malabsorption issue. Also, it'll let you know how much to supplement (and if you are Celiac, you'll need extra supplementation for quite a while to bring them back to normal)

So, go see your doctor armed with all the info you can get, and good luck!

Victoria1234 Experienced

Personally I would do the blood test first. It's far cheaper and easier. You need to have the full celiac panel done... I'm sure someone else will pipe in exactly what that is. Even though you had part of the blood panel done years ago doesn't mean your results will be the same. And a complete panel will tell you the complete picture.

TexasJen Collaborator

I think you have 3 questions:

1. Why am I losing weight?

2. What is the cause of the anemia?

3. Do I have celiac?

Since your symptoms are new and there is a high suspicion for celiac, you should have a repeated blood test for celiac with the full panel. Anti - TTG - IgA and IgG, deaminated gliadin - IgA and IgG, endomysial antibodies. (You don't need to repeat the IgA test because you know you are not IgA deficient)

But, normally, unless you have extremely heavy periods, you would also have a scope to evaluate the anemia - usually including a colonoscopy. 

The weight loss could be all related but if the above tests are normal - no celiac, no IBD, ulcers, etc then you would get more tests to look into the cause of the weight loss.

meg-c Explorer
1 hour ago, Pegleg84 said:

Hi Meg,

I was in a somewhat similar situation before I went gluten free: lost a bunch of weight very quickly (I was not overweight, so looking 10+lb in a month was alarming), felt like crud after eating anything, really bad anxiety, low vitamin levels/iron anemia, etc etc. I had blood tests done a couple times (once after my mom was diagnosed with Celiac, and later when my symptoms popped up) which were both negative (not sure if they ran the full panel, though). However, that didn't stop me from being pretty sure I had Celiac. The disease runs on both sides of my family (not sure if my dad had it, but a couple of his siblings do), and my sister also had negative blood tests but an endoscopy showed positive for villi damage. i got sick of being sick all the time and didn't want to wait for however long it would take to get an endoscopy done in a small city (and just before moving) so went gluten-free and never turned back. Given the improvement in my symptoms, I have always considered myself to have Celiac and no one can tell me otherwise. No way would I do a gluten challenge and ruin my health just to have a confirmed diagnosis.

All that to say: YES! You should push for an endoscopy. First, talk to your doctor about your symptoms and get the full blood panel redone (lots of posts here with the full rundown of what you should ask for). Tell them that there are AI disorders on both sides of your family (two positives make a negative? Still not sure how that works but probably what happened in me&my sister's case) and want to confirm with an endoscopy regardless of the blood results. Keep enjoying your glutens until then.
You should also get your vitamin/mineral levels checked, because low levels + the sudden weight loss, fatigue, etc definitely sounds like a malabsorption issue. Also, it'll let you know how much to supplement (and if you are Celiac, you'll need extra supplementation for quite a while to bring them back to normal)

So, go see your doctor armed with all the info you can get, and good luck!

Thank you so much for this reply, I'm happy to hear that you're doing so much better now. 

I definitely agree that it sounds like some kind of malabsorption problem -- I will probably send a note to one of my doctors asking if he can add it to the list of blood work I am due to have in a few weeks. No harm in asking. 

meg-c Explorer
1 hour ago, TexasJen said:

I think you have 3 questions:

1. Why am I losing weight?

2. What is the cause of the anemia?

3. Do I have celiac?

Since your symptoms are new and there is a high suspicion for celiac, you should have a repeated blood test for celiac with the full panel. Anti - TTG - IgA and IgG, deaminated gliadin - IgA and IgG, endomysial antibodies. (You don't need to repeat the IgA test because you know you are not IgA deficient)

But, normally, unless you have extremely heavy periods, you would also have a scope to evaluate the anemia - usually including a colonoscopy. 

The weight loss could be all related but if the above tests are normal - no celiac, no IBD, ulcers, etc then you would get more tests to look into the cause of the weight loss.

Yeah, you're right. 

The weight loss has thankfully been fairly stable the past couple of months, especially now that I am at a healthy weight. It's often hard to get the doctors to be receptive, as they were almost "happy" I was losing weight, you know? I was 230 pounds, I now hover somewhere around 155-160 pounds (at 5'10"). 

I wouldn't consider my periods to be especially heavy, although doctors are quick to blame that i a young female patient. I had my ferritin checked awhile ago, and it was 11 -- no action was taken as it was just within normal range and my CBC was normal. I had a repeat CBC months later and my hemoglobin, hematocrit, along with others fell outside of range. I did ask my PCP if my numbers weren't improved with three months of supplementation if we'd further investigate GI causes. Shs agreed to that. I am due to have a repeat CBC and full iron panel in the next few weeks. 

I've had so many labs and workups done regarding the weight loss, I'm starting to feel like a crazy person! Many of my doctor's want to blame a psychological condition (anxiety, depression, eating disorder, etc), 

 

Thank you for your reply!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,902
    • Most Online (within 30 mins)
      7,748

    Patty6133
    Newest Member
    Patty6133
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Xravith
      Yes, you are right. Indeed, I’ve been feeling anemic since the beginning of this week, and today I felt horrible during a lecture at the university, I was trembling a lot and felt all my body incredibly heavy, so I had to come back home. I’ll do a blood test tomorrow, but I’m just worried about the possibility of it coming back negative. I’ve been eating two cookies in the morning as my only source of gluten over the past two weeks—could that affect the final result?
    • trents
      Welcome to the forum, @Judy M! Yes, he definitely needs to continue eating gluten until the day of the endoscopy. Not sure why the GI doc advised otherwise but it was a bum steer.  Celiac disease has a genetic component but also an "epigenetic" component. Let me explain. There are two main genes that have been identified as providing the "potential" to develop "active" celiac disease. We know them as HLA-DQ 2.5 (aka, HLA-DQ 2) and HLA-DQ8. Without one or both of these genes it is highly unlikely that a person will develop celiac disease at some point in their life. About 40% of the general population carry one or both of these two genes but only about 1% of the population develops active celiac disease. Thus, possessing the genetic potential for celiac disease is far less than deterministic. Most who have the potential never develop the disease. In order for the potential to develop celiac disease to turn into active celiac disease, some triggering stress event or events must "turn on" the latent genes. This triggering stress event can be a viral infection, some other medical event, or even prolonged psychological/emotional trauma. This part of the equation is difficult to quantify but this is the epigenetic dimension of the disease. Epigenetics has to do with the influence that environmental factors and things not coded into the DNA itself have to do in "turning on" susceptible genes. And this is why celiac disease can develop at any stage of life. Celiac disease is an autoimmune condition (not a food allergy) that causes inflammation in the lining of the small bowel. The ingestion of gluten causes the body to attack the cells of this lining which, over time, damages and destroys them, impairing the body's ability to absorb nutrients since this is the part of the intestinal track responsible for nutrient absorption and also causing numerous other food sensitivities such as dairy/lactose intolerance. There is another gluten-related disorder known as NCGS (Non Celiac Gluten Sensitivity or just, "gluten sensitivity") that is not autoimmune in nature and which does not damage the small bowel lining. However, NCGS shares many of the same symptoms with celiac disease such as gas, bloating, and diarrhea. It is also much more common than celiac disease. There is no test for NCGS so, because they share common symptoms, celiac disease must first be ruled out through formal testing for celiac disease. This is where your husband is right now. It should also be said that some experts believe NCGS can transition into celiac disease. I hope this helps.
    • Judy M
      My husband has had lactose intolerance for his entire life (he's 68 yo).  So, he's used to gastro issues. But for the past year he's been experiencing bouts of diarrhea that last for hours.  He finally went to his gastroenterologist ... several blood tests ruled out other maladies, but his celiac results are suspect.  He is scheduled for an endoscopy and colonoscopy in 2 weeks.  He was told to eat "gluten free" until the tests!!!  I, and he know nothing about this "diet" much less how to navigate his in daily life!! The more I read, the more my head is spinning.  So I guess I have 2 questions.  First, I read on this website that prior to testing, eat gluten so as not to compromise the testing!  Is that true? His primary care doctor told him to eat gluten free prior to testing!  I'm so confused.  Second, I read that celiac disease is genetic or caused by other ways such as surgery.  No family history but Gall bladder removal 7 years ago, maybe?  But how in God's name does something like this crop up and now is so awful he can't go a day without worrying.  He still works in Manhattan and considers himself lucky if he gets there without incident!  Advice from those who know would be appreciated!!!!!!!!!!!!
    • Scott Adams
      You've done an excellent job of meticulously tracking the rash's unpredictable behavior, from its symmetrical spread and stubborn scabbing to the potential triggers you've identified, like the asthma medication and dietary changes. It's particularly telling that the rash seems to flare with wheat consumption, even though your initial blood test was negative—as you've noted, being off wheat before a test can sometimes lead to a false negative, and your description of the other symptoms—joint pain, brain fog, stomach issues—is very compelling. The symmetry of the rash is a crucial detail that often points toward an internal cause, such as an autoimmune response or a systemic reaction, rather than just an external irritant like a plant or mites. I hope your doctor tomorrow takes the time to listen carefully to all of this evidence you've gathered and works with you to find some real answers and effective relief. Don't be discouraged if the rash fluctuates; your detailed history is the most valuable tool you have for getting an accurate diagnosis.
    • Scott Adams
      In this case the beer is excellent, but for those who are super sensitive it is likely better to go the full gluten-free beer route. Lakefront Brewery (another sponsor!) has good gluten-free beer made without any gluten ingredients.
×
×
  • 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.