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

Low Iga Serum? And Lab Results For Other Tests


EmmaFrost

Recommended Posts

EmmaFrost Newbie

I have been on a gluten-free diet for a couple months. I am desperate to feel better so I decided the best way to determine if I had an issue with Gluten was to not eat it and see if I feel better. I will admit that I am losing faith in the Drs. I am currently taking B12 injections for B12 deficiency as well as Vitamin D for Vitamin D deficiency. I have been in and out of the Dr's for back pain and hip pain for over 20 years. I am now 43 and I've had horrible lower back pain and hip pain which has gotten progressively worse over time and I have MRI's which show degenerative disc disease. I had surgery last year for a moderately herniated disc in lower back and since the surgery I actually feel worse. It was during the recovery period when I found out that I was deficient in B12 and Vitamin D. I was also diagnosed with iron deficieny many times. I have alot of symptoms that I think may be indicative of Gluten intolerance or Gluten allergies and I was not aware of what exactly Celiacs disease was until I went to see a GI Dr. recently who ran a couple blood tests on me and then I started researching exactly what Celiacs was. Debilitating fatigue, joint pain, mostly my spine and hip, neuropathy hands and feet, foggy brain, infertility for many years, cysts and ovarian tumors, skin rash that no one seems to be able to diagnose why I get it or what exactly it is..b12 seemed to help with neuropathy. The skin rash I get a few times a years looks very similar to DH pictures I've seen. I get itchy bumps that eventually scab over and then leave scars. In any event, I don't think the GI Dr. ran all of the tests needed so I went to my family Dr. and he ran some additional tests and now I am attempting to intepret because they are telling me that it is negative for Gluten intolerance/allergy. I would just like some additional assurance and I know that no one here is a Dr. Can someone please tell me if I should pursue this further by the following results?:

For the first test I was gluten-free for a few weeks:

03/30/10

Tissue Transglutaminase AB IGA <3 u/mL (<5)

Reference range <5 U/mL Negative

IGA, Serum 71 mg/dL*

Reference range (81-463)

Tissue Transglutaminase AB IGG <3 U/mL

Reference range <7 U/mL Negative

I was also gluten-free for this test:

Gliadin AB IGG 5

Normal Range <11

Gliadin AB IGA <3

Normal Range <11

IGA Serum 83 mg/dL Normal Range 81-463

IGG Serum 907 mg/dL Normal Range 694-1618

IGM Serum 257 mg/dL Normal Range 48-271

IGE Serum 21 kU/L Normal Range 0-114

IGD Serum 15 mg/L Normal Range <179

IGG 1 517 mg/dL Normal Range 382-929

IGG 2 223 mg/dL(abn:L) Normal Range 241-700

IGG 3 77 mg/dL Normal Range 22-178

IGG 4 8.9 mg/dL Normal Range 4.0-86.0

IGG Total 870 mg/dL Normal Range 723-1685

He also ran a full blood panel and the only thing off which has showed consistently off in my blood tests is MCH which is 34.5 and range is 27-33. My Red Blood Cell Count is 3.84 Million/uL Normal Range is 3.8-10.8. MCV is 100 fL and Normal is 80-100.

Thanks in advance for anyone who has a chance to look it over. Not sure any of the blood panel work is relevant. Since I've been taking the B12 injectible and D my levels are now within the normal range on the labwork. B12 is above higher range now and Vitamin D is 40 with normal range of 20-100.


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



Celiac.com Sponsor (A8-M):



mushroom Proficient

Hi, and welcome to the forum.

Has none of your doctors told you that you need to be consuming gluten for a valid celiac blood test??? Tests run when you are gluten free have no meaning because in order to make the antibodies which the tests measure, you must be consuming the gluten which triggers antibody production. No gluten = no antibodies.

That being said, there is one test result of interest, the first total serum IGA, a test run as a control, was abnormally low. This in and of itself can also invalidate the testing, because if you are a low antibody producer the other results are unreliable. So on both counts you cannot trust these results.

Unfortunately, your test results have not provided you with any information about how you respond to gluten. :( At this point I don't even know what to suggest. How has the gluten free diet worked for you, symptom wise? And are you sure you have eliminated ALL the gluten, because it is a master of disguise thanks to the food processors and their labelling??

It must be frustrating after all these years to be not farther ahead. Have you had a bone density scan?

I am hoping others will have some more ideas for you.

P.S. If you still have any active DH-type lesions, you could have a biopsy done of the skin adjacent to the lesion, looking for antibodies. Or you could perhaps resume gluten until one appeared that you could have biopsied. Your lesions certainly sound like they could be DH is they leave a scar.

frieze Community Regular

the IgA is certainly suspect....the MCV is still on the high side, i would try methylcobalamin by mouth on top of the shots....the D could be higher also....normal lab values are often skewed low....off topic, but you might want to check out the relationship between low IgG2 and influenza A, at least the swine flu of last year....good luck

mushroom Proficient

the IgA is certainly suspect....the MCV is still on the high side, i would try methylcobalamin by mouth on top of the shots....the D could be higher also....normal lab values are often skewed low....off topic, but you might want to check out the relationship between low IgG2 and influenza A, at least the swine flu of last year....good luck

I agree with frieze - MCV is often overlooked by doctors if it is just slightly high. Mine went back to normal with B12 and folate. And you need to be mid-range on D to really feel good. The sublingual B12 is a good idea, and although I can't see your post right now, you probably need to up your D. Try taking the folate too, or a good strong B complex.

EmmaFrost Newbie

I agree with frieze - MCV is often overlooked by doctors if it is just slightly high. Mine went back to normal with B12 and folate. And you need to be mid-range on D to really feel good. The sublingual B12 is a good idea, and although I can't see your post right now, you probably need to up your D. Try taking the folate too, or a good strong B complex.

Thanks soo much for your replies! I've felt slightly better on the gluten-free diet, but I suspect I've unintentionally ate it because as you said it's in everything. I've not been feeling well for years, so perhaps it will take that long to feel better of the Gluten. As for the low IGA serum blood test, I do not understand why the Dr(s) wouldn't see the IGA serum value as a red flg if that is the control. So your saying that besides my not eating gluten then, my IGA serum level in and of itself even if I was not on gluten-free diet can cause a false negative? When the GI Dr. intially mentioned testing for Celiacs, my first thought was I don't have diarreah so it was waste of time. This was before I knew it was not the only symptom and not necessararily always a symptom since as of late I have the opposite issue. While I do not want it to be Celiacs, at this point I want an answer. While eating gluten-free is tough and I commend everyone who can adhere to such a diet with all the gluten in diguise, it's everywhere in everything, changing my diet is small price to pay if that will make me feel better. I'm leaning towards the DNA/Genetics test. While I know that a positve result only means predisposition at least with a negative I will know for sure I don't have it right?

While I also hear the "Gold" standard for diagnosing Celiacs disease is the biopsies, at this point I am not willing to put myself through any sort of procedure that requires anesthisia or going under the knife again anytime soon because I just don't feel healthy enough and it doesn't seem like it's 100% accurate in every case. I've had quite a hard time recovering from the back surgery which I had LAST APRIL 2009 (microdisectomy). I was required to go to Physical Therapy both before and after and I felt soo tired and weak I had a difficult time just making it to the appointments, let alone getting on a treadmill and doing pushup and situps and yoga exercises. In 2006 I had a C-Section and had a son, rough recovery as well and the fertility treatments which resulted in the pregnancy were stressful and exhausting, but he is the best thing that ever happened to me so well worth it :) I had nauseau and puked my entire pregnancy and was miserable, ironic my staple food was crackers/bread, bread & wheat thins my all time favorite. Prior to that in 2004 I went in for a diagnostic laparascopy, about the 6th laparascopic surgery over the years after being plagued with ovarian cysts, tubal pregnancies and fertility issues. I woke up to find out they had to do a laparatomy and remove one of my ovaries due to a tumor that had enveloped the ovary. I had a super tough time recovering from that surgery . I had other invasive procedures when they were looking at my tubes and uterus, they never found anything to explain the ectopic pregnancies. I suspect I had other early losses. In the end I probably wouldn't haven't minded all the invasive procedures if I had felt healthier and if they actually found something, a reason or firm diagnosis.

I have 4 sisters and a brother, no problems getting pregnant that I know of. My family is not a family that goes to the Dr.'s much but I know for sure at least 3 of my sisters have had B12, vitamin D and iron deficiency at one time or another, one at least with diverticulosis, maybe more. My brother has been sick for years, looks like he is wasting away, plagued with GI issues, hiatel hernia, ulcers and migraines (cluster headaches) and he has asthma. He is now estranged from our family, went through a horrible divorce and from what I understand has been in and out of the ER and hospital for the aforementioned health issues, seems he maybe having some mental health issues based on temper the last couple years. My mom and dad both have arthritis, mom had knee surgery and a knee replacement surgery, high blood pressure and has various allergies and hive reactions to alot of things, but never been tested as she does not like going to the Dr.'s. 2 of her sisters passed recently, one from breast cancer and leukemia the other suddenly from agressive pancreatic cancer, not sure about her brother that passed. Her mother died at 32, mengitis I THINK?? I'm sure there is more I don't know since there were 6 kids and they were raised in orphanage.

Sorry so long, ironic your comment about B12 and D since my Dr. thinks my levels are great now and told me to back off. I'm not inclined to do so since my clinical symptoms don't seem to match what he is saying at all. B12 helped with neuropathy so far, that's it.

I'm wondering if it would be a waste of my money to have the DNA test run for Celiacs. Not sure I can get Dr. to order since I'm sure he or insurance may require biopsy first, which as I said I just can't go through right now until I feel a bit healthier. As for bumps, I had a biopsy in 2003 and I called to see if they still had the lab results and they are somewhere in a box and I suspect they were not specifically looking for DH. I think I figured out that if they are DH what causes them for me, gluten and seafood (shrimp/lobster/crab) because I just started eating the seafood last 8 years and really only eat at the beach which is when I get bumps. From what I undertand, iodine is the catalyst along with gluten. Always thought it was the suntan lotion. $375 for the genetic test from kimball labs.

EmmaFrost Newbie

I agree with frieze - MCV is often overlooked by doctors if it is just slightly high. Mine went back to normal with B12 and folate. And you need to be mid-range on D to really feel good. The sublingual B12 is a good idea, and although I can't see your post right now, you probably need to up your D. Try taking the folate too, or a good strong B complex.

One more thing is I looked back over blood work from a few years back and MCV is always running on the high end. I had the B12 prescribed after low results and elevated methymalonic acide and Vitamin D was a whopping 15 at the time, 25-OH, D3 15 and 25-OH, D2 <4 was the breakdown. Now it's 10 and 30, total 40 for D so I guess that looks good to my Dr. considering where I started.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,857
    • Most Online (within 30 mins)
      7,748

    LowellFrancis
    Newest Member
    LowellFrancis
    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

    • Rogol72
      Some interesting articles regarding the use of Zinc Carnosine to help heal gastric ulcers, gastritis and intestinal permeability. I would consult a medical professional about it's use. https://www.nature.com/articles/ncpgasthep0778 https://www.rupahealth.com/post/clinical-applications-of-zinc-carnosine---evidence-review https://pmc.ncbi.nlm.nih.gov/articles/PMC7146259/ https://www.fallbrookmedicalcenter.com/zinc-l-carnosine-benefits-dosage-and-safety/
    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
×
×
  • 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.