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Celiac Test Done: High IGA and IGM Levels: Is This Precursor to ...
Last year I went to a Doctor for Low Testosterone. Only because I thought I had low testosterone. I told him that I was not feeling on top of my game and that my dad had celiac.
Well he order a complete panel of like everything. The lab bill was like 1500.00 dollars. Covered by insurance thankfully.
Everything turned out fine and I did not have low testosterone.
Except I had an elevated IGA levels. He was perplexed by this and had me see a Hematologist immediately.
I did not know these Doctors usually work at the Cancer centers so when I called I kind of freaked out and started to think I had cancer.
In any rate the Hematologist looked at me after seeing my results and just look at me like I was dumb and why am I not all enjoying my life and why are you acting like all Hypochondriac like. I was kind of offended but I did not say anything.
So far I have had like 5 complete blood work tests done. I did not feel comfortable with this Doctor entirely so I went back to my primary doctor which I have two of them and they both ran complete tests.
All test come back fine except that I have elevated IGA mainly and a little elevated IGM.
I even went to an allergist certified doctor which told me that clinically that elevated IGA means nothing.
My primary doctor says that is what just makes you, you. That these results are based on a bell curve and that sometimes people are outliers. Is this true in my case?
Questions:
What does elevated IGA mean exactly?
What does elevated IGM mean exactly?
What does “An apparent polyclonal gammopathy: IgA and IgM. Kappa and lambda
typing appear increased.” mean exactly?
What does “The SPE pattern appears essentially unremarkable. Evidence of
monoclonal protein is not apparent.” mean exactly?
Is this anything I should worry about or do I just simply ignore this and move on with my life?
Does this have anything to with allergies or chronic sinusitis possibly? Because I have read up on this and have found that it might be do to that and I do have bad sinuses.
If everything is fine now, can everything stay fine or does this mean I can develop “Multiple Myeloma” or some form of “cancer” in the future based on these results? I mean I know everyone has a chance of getting cancer I am just wondering if I have an increased chance or something based on these results.
I am asking this because it just doesn’t seem like any of my Doctors either are not really concerned by this or just don’t really know what to make of it. I wish they could just tell me exactly what it is and what I should either prepare for or not prepare for.
I have seen the following Doctors:
Two primary doctors
One hematologist
Allergist
Endocrinologist
And have also had an ultra sound and a CT scan of my pelvis and stomach because I believe I have IBS instead of Celiac Disease like my Father.
So please let me know what I should do or what I should know.
Results:
2014 – March
Immunoglobulin A, Qn, Serum 710 High mg/dL 91 − 414 01
Endomysial Antibody IgA Negative Negative 01
2014 – April
Beta Globulin 1.4 High g/dL 0.6 − 1.3 01
Immunoglobulin A, Qn, Serum 721 High mg/dL 91 − 414 01
Immunoglobulin M, Qn, Serum 271 High mg/dL 40 − 230 01
THE SPE PATTERN APPEARS ESSENTIALLY UNREMARKABLE.EVIDENCE OF MONOCLONAL PROTEIN IS NOT APPARENT.
2014 – October
Beta Globulin 1.4 High g/dL 0.6 - 1.3 01
Immunoglobulin A, Qn, Serum 753 High mg/dL 91 - 414 01
Immunoglobulin M, Qn, Serum 270 High mg/dL 40 - 230 01
P E Interpretation, S 01 The SPE pattern appears essentially unremarkable. Evidence of
monoclonal protein is not apparent.
I have the two from my primary doctor but they just say elevated IGA and they are not worried about it.
All of these blood tests have much more information and tests on them but they are all normal so I didn’t bother putting them up here.
I am just wondering is my Doctors not telling me something because they do not want to get me down or depressed. By telling me that this can turn into something or is it truly something not to worry about?
I have seen many Doctors. Do any of you know of anyone else that I can go to that can truly tell me what these results mean?
Also can you explain to me where I can post these results to where I can get some answers and also do you know anything about these results?
Thank you for your time and I greatly appreciate your feedback.
Well he order a complete panel of like everything. The lab bill was like 1500.00 dollars. Covered by insurance thankfully.
Everything turned out fine and I did not have low testosterone.
Except I had an elevated IGA levels. He was perplexed by this and had me see a Hematologist immediately.
I did not know these Doctors usually work at the Cancer centers so when I called I kind of freaked out and started to think I had cancer.
In any rate the Hematologist looked at me after seeing my results and just look at me like I was dumb and why am I not all enjoying my life and why are you acting like all Hypochondriac like. I was kind of offended but I did not say anything.
So far I have had like 5 complete blood work tests done. I did not feel comfortable with this Doctor entirely so I went back to my primary doctor which I have two of them and they both ran complete tests.
All test come back fine except that I have elevated IGA mainly and a little elevated IGM.
I even went to an allergist certified doctor which told me that clinically that elevated IGA means nothing.
My primary doctor says that is what just makes you, you. That these results are based on a bell curve and that sometimes people are outliers. Is this true in my case?
Questions:
What does elevated IGA mean exactly?
What does elevated IGM mean exactly?
What does “An apparent polyclonal gammopathy: IgA and IgM. Kappa and lambda
typing appear increased.” mean exactly?
What does “The SPE pattern appears essentially unremarkable. Evidence of
monoclonal protein is not apparent.” mean exactly?
Is this anything I should worry about or do I just simply ignore this and move on with my life?
Does this have anything to with allergies or chronic sinusitis possibly? Because I have read up on this and have found that it might be do to that and I do have bad sinuses.
If everything is fine now, can everything stay fine or does this mean I can develop “Multiple Myeloma” or some form of “cancer” in the future based on these results? I mean I know everyone has a chance of getting cancer I am just wondering if I have an increased chance or something based on these results.
I am asking this because it just doesn’t seem like any of my Doctors either are not really concerned by this or just don’t really know what to make of it. I wish they could just tell me exactly what it is and what I should either prepare for or not prepare for.
I have seen the following Doctors:
Two primary doctors
One hematologist
Allergist
Endocrinologist
And have also had an ultra sound and a CT scan of my pelvis and stomach because I believe I have IBS instead of Celiac Disease like my Father.
So please let me know what I should do or what I should know.
Results:
2014 – March
Immunoglobulin A, Qn, Serum 710 High mg/dL 91 − 414 01
Endomysial Antibody IgA Negative Negative 01
2014 – April
Beta Globulin 1.4 High g/dL 0.6 − 1.3 01
Immunoglobulin A, Qn, Serum 721 High mg/dL 91 − 414 01
Immunoglobulin M, Qn, Serum 271 High mg/dL 40 − 230 01
THE SPE PATTERN APPEARS ESSENTIALLY UNREMARKABLE.EVIDENCE OF MONOCLONAL PROTEIN IS NOT APPARENT.
2014 – October
Beta Globulin 1.4 High g/dL 0.6 - 1.3 01
Immunoglobulin A, Qn, Serum 753 High mg/dL 91 - 414 01
Immunoglobulin M, Qn, Serum 270 High mg/dL 40 - 230 01
P E Interpretation, S 01 The SPE pattern appears essentially unremarkable. Evidence of
monoclonal protein is not apparent.
I have the two from my primary doctor but they just say elevated IGA and they are not worried about it.
All of these blood tests have much more information and tests on them but they are all normal so I didn’t bother putting them up here.
I am just wondering is my Doctors not telling me something because they do not want to get me down or depressed. By telling me that this can turn into something or is it truly something not to worry about?
I have seen many Doctors. Do any of you know of anyone else that I can go to that can truly tell me what these results mean?
Also can you explain to me where I can post these results to where I can get some answers and also do you know anything about these results?
Thank you for your time and I greatly appreciate your feedback.
Best Answer
Hi astrongtower. This is the anxiety forum which is a separate topic from whether or not you have celiac disease. If you would like help interpreting your test results or have questions regarding whether or not you have celiac disease, our celiac disease community is the place to post for help. http://www.medhelp.org/forums/Celiac-Sprue-Disease/show/226 We wish you the best an are now closing this thread. If you wish to start a new thread to discuss your anxiety, please do so.
*** thread closed***
*** thread closed***
I apologize. I meant to also ask:
Do I have “polyclonal Gammopathy of Unknown Significance (MGUS)”? or is this even possible?
This is what my Blood Test says:
Immunofixation, Serum
01
Immunofixation Result, Serum
An apparent polyclonal gammopathy: IgA and IgM. Kappa and lambda typing appear increased.
Result:
P E Interpretation, S
01
The SPE pattern appears essentially unremarkable. Evidence of monoclonal protein is not apparent.
It doesn’t mention anything of “Monoclonal” just “Polyclonal”
That is why I was wondering if this possibly existed:
polyclonal Gammopathy of Unknown Significance (MGUS)
or when:
“The SPE pattern appears essentially unremarkable. Evidence of monoclonal protein is not apparent.”
Cancels all this out …
Do you understand what I am trying to say?
Do I have “polyclonal Gammopathy of Unknown Significance (MGUS)”? or is this even possible?
This is what my Blood Test says:
Immunofixation, Serum
01
Immunofixation Result, Serum
An apparent polyclonal gammopathy: IgA and IgM. Kappa and lambda typing appear increased.
Result:
P E Interpretation, S
01
The SPE pattern appears essentially unremarkable. Evidence of monoclonal protein is not apparent.
It doesn’t mention anything of “Monoclonal” just “Polyclonal”
That is why I was wondering if this possibly existed:
polyclonal Gammopathy of Unknown Significance (MGUS)
or when:
“The SPE pattern appears essentially unremarkable. Evidence of monoclonal protein is not apparent.”
Cancels all this out …
Do you understand what I am trying to say?
1 Comments
Hello Everyone!
I’m back and I’m still here. However, I have some questions.
My Doctor said I was on the borderline now. So I pressed him harder and asked him what did he mean and he said since I am on the max level of 20 on my Gliadin Peptide Ab, IgA that I should go Gluten Free now. As all of you know this is a big life changing thing. No more bread, pizza, sub way sandwiches, pasty, Italian food, etc. etc. The list goes on forever. I know I can make adjustments and I am prepared to, however I want to make sure I am reading all this correctly.
I am just still unsure if I will have celiac or have it now just the precursor, or do I just have an insensitivity to gluten. Keep it light but I can manage it.
I am little confused.
Do I go gluten free because I will get Celiac Disease if I don’t?
Questions…
1-Do I have Celiac Disease or not?
2-If I don’t, does it looking like I am getting it?
3-What should I do?
4-Can you be in between it? Meaning can I be sensitive to gluten but yet eat it a little bit in moderation?
5-If I went 1 year off gluten, repaired my bloodwork numbers, and had little bits of bread here and there with gluten would I be okay?
6-My dad had celiac or thinks that he does, he never officially did the biopsy, however, he had lying on the floor pain to where he wanted to kill himself. Now that he is gluten free he never has that pain again. I have never experienced anything close to this. Will I?
7-Am I missing anything else from these results, does high iga or Ab, iga mean anything else with no other symptoms?
Note:
I have ibs out bursts, low intestine problems for sure off and on. Headaches sometimes. I am thinking that if I go off gluten anyway I am probably going to feel 1000 percent better. So I am thinking about trying it anyway, however its not the end of the world and I could keep eating loads of gluten, if everything stayed the same. However, if this blood work looks like I am heading for a on the floor screaming in pain session later in life, I mine as well take care of it now.
All my other full comp labs came back normal besides my slightly high bad cholesterol.
PLEASE HELP ME BECAUSE I AM SO CONFUSED. ANYTHING YOU CAN DO WOULD BE GREATLY APPRECIATED. PLEASE SEE ALL MY RESULTS BELOW RELATING TO CELIAC.
History of results:
2011
HDL Cholesterol = 32 L
Should be >39
2013
IgA = 682 H / Should be 68 - 379
Endo = Negative
tTg Ab, IgA = 8.3 / Should be <20
Gliadin Peptide Ab, IgG = 9.2 / should be <20
Gliadin Peptide Ab, IgA = 10.0 / should be <20
tTG Ab, IgG = 6.5 / Should be <20
2014
IgA = 608 / Should be 68 - 379
Endo = Negative
tTg Ab, IgA = 11.9 / Should be <20
Gliadin Peptide Ab, IgG = 9.7 / should be <20
Gliadin Peptide Ab, IgA = 12.1 / should be <20
tTG Ab, IgG = 10.1 / Should be <20
2014 – Different Test
CCP Antibodies IgG/IgA = 12 / should be 0 – 19
2014 – Different Test
Immunoglobulin A, Qn, Serum = 710 / should be 91 – 414
2014 – Different Test
Immunoglobulin A, Qn, Serum = 721 / should be 91 – 414
Immunoglobulin M, Qn, Serum = 271 / should be 40 - 230
2014 – Different Test [Later in the year]
Immunoglobulin A, Qn, Serum = 753 / should be 91 – 441
Immunoglobulin M, Qn, Serum = 270 / should be 40 – 230
2017
Immunoglobulin A = 690 / should be 68 – 379
Endomysial Screen = Negative
tTG Ab, IgA = 2 / should be <4
Gliadin Peptide Ab, IgG = 2 / should be <20
Gliadin Peptide Ab, IgA = 20 / should be <20
tTG Ab, IgG = 1 / should be 40
I’m back and I’m still here. However, I have some questions.
My Doctor said I was on the borderline now. So I pressed him harder and asked him what did he mean and he said since I am on the max level of 20 on my Gliadin Peptide Ab, IgA that I should go Gluten Free now. As all of you know this is a big life changing thing. No more bread, pizza, sub way sandwiches, pasty, Italian food, etc. etc. The list goes on forever. I know I can make adjustments and I am prepared to, however I want to make sure I am reading all this correctly.
I am just still unsure if I will have celiac or have it now just the precursor, or do I just have an insensitivity to gluten. Keep it light but I can manage it.
I am little confused.
Do I go gluten free because I will get Celiac Disease if I don’t?
Questions…
1-Do I have Celiac Disease or not?
2-If I don’t, does it looking like I am getting it?
3-What should I do?
4-Can you be in between it? Meaning can I be sensitive to gluten but yet eat it a little bit in moderation?
5-If I went 1 year off gluten, repaired my bloodwork numbers, and had little bits of bread here and there with gluten would I be okay?
6-My dad had celiac or thinks that he does, he never officially did the biopsy, however, he had lying on the floor pain to where he wanted to kill himself. Now that he is gluten free he never has that pain again. I have never experienced anything close to this. Will I?
7-Am I missing anything else from these results, does high iga or Ab, iga mean anything else with no other symptoms?
Note:
I have ibs out bursts, low intestine problems for sure off and on. Headaches sometimes. I am thinking that if I go off gluten anyway I am probably going to feel 1000 percent better. So I am thinking about trying it anyway, however its not the end of the world and I could keep eating loads of gluten, if everything stayed the same. However, if this blood work looks like I am heading for a on the floor screaming in pain session later in life, I mine as well take care of it now.
All my other full comp labs came back normal besides my slightly high bad cholesterol.
PLEASE HELP ME BECAUSE I AM SO CONFUSED. ANYTHING YOU CAN DO WOULD BE GREATLY APPRECIATED. PLEASE SEE ALL MY RESULTS BELOW RELATING TO CELIAC.
History of results:
2011
HDL Cholesterol = 32 L
Should be >39
2013
IgA = 682 H / Should be 68 - 379
Endo = Negative
tTg Ab, IgA = 8.3 / Should be <20
Gliadin Peptide Ab, IgG = 9.2 / should be <20
Gliadin Peptide Ab, IgA = 10.0 / should be <20
tTG Ab, IgG = 6.5 / Should be <20
2014
IgA = 608 / Should be 68 - 379
Endo = Negative
tTg Ab, IgA = 11.9 / Should be <20
Gliadin Peptide Ab, IgG = 9.7 / should be <20
Gliadin Peptide Ab, IgA = 12.1 / should be <20
tTG Ab, IgG = 10.1 / Should be <20
2014 – Different Test
CCP Antibodies IgG/IgA = 12 / should be 0 – 19
2014 – Different Test
Immunoglobulin A, Qn, Serum = 710 / should be 91 – 414
2014 – Different Test
Immunoglobulin A, Qn, Serum = 721 / should be 91 – 414
Immunoglobulin M, Qn, Serum = 271 / should be 40 - 230
2014 – Different Test [Later in the year]
Immunoglobulin A, Qn, Serum = 753 / should be 91 – 441
Immunoglobulin M, Qn, Serum = 270 / should be 40 – 230
2017
Immunoglobulin A = 690 / should be 68 – 379
Endomysial Screen = Negative
tTG Ab, IgA = 2 / should be <4
Gliadin Peptide Ab, IgG = 2 / should be <20
Gliadin Peptide Ab, IgA = 20 / should be <20
tTG Ab, IgG = 1 / should be 40
Also …
Do you think I have this:
MGUS: Monoclonal Gammopahty of Unknown Significance (MGSU)
http://www.webmd.com/hw-popup/monoclonal-gammopathy-of-unknown-significance-mgus
Or has this been ruled out by my blood tests?
Or
Bacteria Sinusitis or some kind of infection or allergy that my body has been trying to fight off for over a year?
Here are a couple of links to where people having elevated IGA and the Doctors really have no idea what to make of it when no others symptoms are present.
http://www.aaaai.org/ask-the-expert/levated-IgA-with-no-explanation.aspx
http://www.aaaai.org/ask-the-expert/recurrent-respiratory-infection.aspx
Any other ideas or ways to go? I have a feeling when I see my Hematologist next week they are just going to say, looks like your results are fine, good luck be safe out there, will run a follow up next year.
That’s it with no explanation.
I just find it hard to believe that in 2014 that is the best we can do with Blood Tests.
Do you think I have this:
MGUS: Monoclonal Gammopahty of Unknown Significance (MGSU)
http://www.webmd.com/hw-popup/monoclonal-gammopathy-of-unknown-significance-mgus
Or has this been ruled out by my blood tests?
Or
Bacteria Sinusitis or some kind of infection or allergy that my body has been trying to fight off for over a year?
Here are a couple of links to where people having elevated IGA and the Doctors really have no idea what to make of it when no others symptoms are present.
http://www.aaaai.org/ask-the-expert/levated-IgA-with-no-explanation.aspx
http://www.aaaai.org/ask-the-expert/recurrent-respiratory-infection.aspx
Any other ideas or ways to go? I have a feeling when I see my Hematologist next week they are just going to say, looks like your results are fine, good luck be safe out there, will run a follow up next year.
That’s it with no explanation.
I just find it hard to believe that in 2014 that is the best we can do with Blood Tests.
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1.You have seen a fair number of docs who think there is no problem. You are worried that one may exist and have outlined a lot of questions that you want answered here, however you should get doc to answer them instead. Doc is trained in that area and you have seen a few of them, so my guess is they can't all be wrong. Perhaps getting doc to answer the questions will relax you.
2. The second thing I notice is you have a feeling there may be some conspiracy among the docs to hide info from you. I doubt that is the case considering the potential for lawsuits (that is just one reason I doubt the conspiracy to hide info exists, btw), and do not agree with your reasoning below.
"I am just wondering is my Doctors not telling me something because they do not want to get me down or depressed. By telling me that this can turn into something or is it truly something not to worry about? "