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

Anemia--macrocytic, Microcytic, Normacytic?


mimommy

Recommended Posts

mimommy Contributor

Does anyone know what it means to have a low RDW (red cell distribution width) and normal MCV? I know these two tests are usually done in conjunction to diagnose anemia, but I read that in certain situations it can indicate villis atrophy. What about b-12 and folic acid--can just a low RDW affect them? Does anyone out there with anemia have blood counts like this?


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



Celiac.com Sponsor (A8-M):



TrillumHunter Enthusiast

Microcytic anemia would be most likely and this would indicate iron anemia. My hemotologist said the MCV is a good indicator of stored iron. So, you may have an issue with using both your dietary and stored iron because of damaged villi. Are you newly diagnosed? If so, it's best to give yourself some time to heal and then reassess your blood work. I'm one of the lucky :rolleyes: who, despite a strict gluten-free diet and healing, still cannot absorb iron.The dr calls it anemia of chronic autoimmune disease. Now I get to have iron infusions!!Yeah! But this is only after trying for two years to correct it through diet and supplements. Lots of us have anemia issues, both iron and B12.

Hope that helps. You aren't alone!

trents Grand Master

I think low RDW (red cell distribution width) is good. It indicates little variance in the diameter of the red blood cells, i.e. few poorly formed ones.

Normal MCV is also good. Just looking at those two indcators, I would not think you have low iron stores. What about your hemaglobin and hematocrit levels? Blood cells parameters don't affect folic acid and B12 levels. It is the other way around. And by the way, if you are taking a folic acid supplement it will mask B12 deciency, a serious problem that causes acute anemia. You need to be off of folic acid for a period if you suspect B12 deficiency and are getting tested for it. If this is the case, talk to your doctor to see how long.

mimommy Contributor

Thank you for responding. I guess I need to clarify--I have not been diagnosed with celiac, although I was tested recently. I am here for my daughter, who was diagnosed celiac earlier this year. However, the anemia question was for me. I have been experiencing many celiac symptoms, the worst of which is the inflammation/joint pain. My husband and I were both just tested for celiac, results negative. I recently saw an orthopedist for joint pain and he tested me for rheumatoid--also negative. I called around to have copies of all my blood work sent to me and came across this:

January, 2008 saw internist for joint pain ESR/CRP only showed

RDW 11.2 on an 11.6-14.8 range Low

MCV 96.4 on an 80-97 range High normal?

December, 2008 saw Ortho who ran CBC tests which only showed

RDW 10.9 on an 11.6-14.8 range still Low

MCV 94.8 on an 80-100 range normal?

I did some online reading and found a lot of info about macrocytic anemia and the b-12/folic acid connection. I also found an article suggesting that a low RDW and high normal MCV can indicate flattening of the villi.

So, my questions are--is 'normacytic anemia' actually anemia? If my ttg and IgA are normal, why am I having so many symptoms--D, C, nausea, dizziness, joint pain, visual disturbances, soy sensitivity, etc, etc, ad nauseum? Regarding dizzy spells, dry mouth and nose, fatigue, irregular periods--aren't these all symptoms of anemia? Finally, doesn't it seem odd that neither doctor ever mentioned the low RDW to me or found it to be a cause for further investigation?

This is a lot, I know, but I have been desperatley searching for an answer. Any advice from the forum would be very welcome.

ravenwoodglass Mentor
Thank you for responding. I guess I need to clarify--I have not been diagnosed with celiac, although I was tested recently. I am here for my daughter, who was diagnosed celiac earlier this year. However, the anemia question was for me. I have been experiencing many celiac symptoms, the worst of which is the inflammation/joint pain. My husband and I were both just tested for celiac, results negative. I recently saw an orthopedist for joint pain and he tested me for rheumatoid--also negative. I called around to have copies of all my blood work sent to me and came across this:

January, 2008 saw internist for joint pain ESR/CRP only showed

RDW 11.2 on an 11.6-14.8 range Low

MCV 96.4 on an 80-97 range High normal?

December, 2008 saw Ortho who ran CBC tests which only showed

RDW 10.9 on an 11.6-14.8 range still Low

MCV 94.8 on an 80-100 range normal?

I did some online reading and found a lot of info about macrocytic anemia and the b-12/folic acid connection. I also found an article suggesting that a low RDW and high normal MCV can indicate flattening of the villi.

So, my questions are--is 'normacytic anemia' actually anemia? If my ttg and IgA are normal, why am I having so many symptoms--D, C, nausea, dizziness, joint pain, visual disturbances, soy sensitivity, etc, etc, ad nauseum? Regarding dizzy spells, dry mouth and nose, fatigue, irregular periods--aren't these all symptoms of anemia? Finally, doesn't it seem odd that neither doctor ever mentioned the low RDW to me or found it to be a cause for further investigation?

This is a lot, I know, but I have been desperatley searching for an answer. Any advice from the forum would be very welcome.

I can't answer about the original question but am wondering if you are giving the diet a good try? With a DD firmly diagnosed and all your symptoms I would question whether your test was a false negative.

mimommy Contributor

Thanks, Raven--you are always so kind and caring in all your repsonses. People need that kind of compassion in this world--the forum is lucky to have you as a member!

Yes, I am giving the gluten-free diet a good try. Two weeks and counting, although accidentally had some gluten last Saturday at a family gathering--geez, they slip that stuff into everything, even cole slaw!

Haven't really noticed any difference, but am going completely gluten-free in whole household for daughter's sake. Too many cc's lately.

I found it's harder to make an adult diet gluten-free than a child's, as for the difference in palate. Having to learn to cook again.

Also, all other tests were normal--hgb, hct, wbc, rbc. I have had anemia several times in my life, and have had low b-12 bad enough that my head would shake and I would hum in my sleep (had a tendency toward starvation more than once--when the going gets tough I stop eating and gain a lot of weight.)

Anyway, thanks for your answers. I feel like I keep saying, "But..it HURTS. How can nothing be wrong?" The dizziness is so bad just scrolling on the computer makes me spin :(

ravenwoodglass Mentor
Thanks, Raven--you are always so kind and caring in all your repsonses. People need that kind of compassion in this world--the forum is lucky to have you as a member!

Yes, I am giving the gluten-free diet a good try. Two weeks and counting, although accidentally had some gluten last Saturday at a family gathering--geez, they slip that stuff into everything, even cole slaw!

Haven't really noticed any difference, but am going completely gluten-free in whole household for daughter's sake. Too many cc's lately.

I found it's harder to make an adult diet gluten-free than a child's, as for the difference in palate. Having to learn to cook again.

Also, all other tests were normal--hgb, hct, wbc, rbc. I have had anemia several times in my life, and have had low b-12 bad enough that my head would shake and I would hum in my sleep (had a tendency toward starvation more than once--when the going gets tough I stop eating and gain a lot of weight.)

Anyway, thanks for your answers. I feel like I keep saying, "But..it HURTS. How can nothing be wrong?" The dizziness is so bad just scrolling on the computer makes me spin :(

I am glad to hear you are sticking with it. It is hard at first but it will become easier with time. I am glad your other tests were good. I can certainly identify with that last paragraph! It sounds like you may have some strong neuro issues going on and unfortunately many of us tend to be on the supersenstive side. It would be a good idea at first to avoid the gluten grain vinegars and alcohols, wait until your feeling good then challenge them and see if you tolerate them. Be as strict as you possibly can in the beginning, it will help you heal quicker and the nerves can take awhile so you want to make that process as quick as you can. You may also want to make sure you take some sublingual B12 for a while it helps the nerves fire the way they should and may help with the 'spinning'.

Thank you also for your kind words, they mean a lot to me. You really brightened my day. :)


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



Celiac.com Sponsor (A8-M):



thleensd Enthusiast
Does anyone know what it means to have a low RDW (red cell distribution width) and normal MCV? I know these two tests are usually done in conjunction to diagnose anemia, but I read that in certain situations it can indicate villis atrophy. What about b-12 and folic acid--can just a low RDW affect them? Does anyone out there with anemia have blood counts like this?

Your RDW isn't all that low...it's really pretty close to range. Keep in mind that different labs set different "normal" standards, too. Some define "low" as below 10.2.

However, you should insist that your doc follows up to be sure. I'd be more concerned with the low RBC count.

If your low RBC count is caused by iron deficiency, your doc needs to do iron studies (serum, ferretin, TIBC). They should also "routinely" check for B12...but, you may have to ask. I had to be very insistent with my doc to follow up on blood tests, but I'm glad I did. (then I found a new doc!!) =)

Good luck.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,337
    • Most Online (within 30 mins)
      7,748

    jojocle
    Newest Member
    jojocle
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      70.8k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • cristiana
      I'd like to second supplementation.  Around the time of my diagnosis and for a good while afterwards I had twitching muscles, including my face, as well as pins and needles and numbness.  We do have tremors in my family anyway, regardless of being coeliac, so I can't really comment on that. If you can find out where you are with your iron levels and B12, that's a good start.  I am not sure where you are posting from but in the UK normal lab results for B12 are quite a bit lower than in other countries, so you might find if you are borderline you will get some improvement by continuing to supplement that.   I found taking magnesium also incredibly helpful against facial twitches. I don't know about you, but all these symptoms increased my anxiety levels as I was worried about them.  That only served to make the symptoms worse.  So it might be worth looking into addressing any underlying anxiety issues.   I still notice that if I'm nervous, or worried, my blood sugar levels are down, some of the symptoms comes back temporarily.  It's like there is still a bit of a weakness there.
    • knitty kitty
      Hello, @Itsabit, Your journey sounds very similar to mine.   I'm very concerned about your diet since you say you don't eat a lot of meat, which is the main source of B vitamins.  Nutritional deficiencies go along with Celiac Disease.  Blood tests are not accurate measurements of deficiency states.  The body robs stored vitamins from organs to circulate in the bloodstream to supply the brain and heart.  You can have deficiency symptoms before blood levels change. I have a hypersensitivity to sulfites, so much so that I had to switch my toothpaste to one that doesn't contain Sodium Lauryl Sulfate.  SLS can cause oral irritation as a side effect, too.   My mouth would burn and I avoided certain foods.  Dapsone contains sulfites, as do antibiotics.  Treatment with sulfites can precipitate a Thiamine deficiency disorder because sulfites cut thiamine in two making it useless. https://pubmed.ncbi.nlm.nih.gov/35506963/ https://pmc.ncbi.nlm.nih.gov/articles/PMC10506142/ I have an allergy to nickel, also.  Zinc helps keep other metals in balance in the body.  Zinc is also terribly important to skin health and oral health. https://pubmed.ncbi.nlm.nih.gov/8445075/ https://pmc.ncbi.nlm.nih.gov/articles/PMC11274920/ https://pubmed.ncbi.nlm.nih.gov/1977254/ Thiamine (Vitamin B 1) deficiency disorder symptoms and altered thiamine metabolism can occur after radiation or chemo.   Thiamine and Niacin B 3 are important in nerve conduction.  When I was very malnourished, I had paresthesia that made me feel itchy all over, and made my dermatitis herpetiformis extremely unbearable.  The form of Niacin that causes flushing, Nicotinic Acid (not the same as nicotine in cigarettes) is beneficial because the flushing helps open the small capillaries in the skin which allows the antibodies to be cleared and disposed.  Pellagra can occur in Celiac Disease.   I had it, and my doctor didn't properly diagnose it, either.   I had a rash around my neck, Casal's Necklace, along with a blistering rash on my arms and any skin exposed to the sun.   https://pubmed.ncbi.nlm.nih.gov/8445075/ https://cgp.iiarjournals.org/content/10/4/169 https://pmc.ncbi.nlm.nih.gov/articles/PMC11722086/ https://pmc.ncbi.nlm.nih.gov/articles/PMC6780714/ https://pmc.ncbi.nlm.nih.gov/articles/PMC10229844/ https://pubmed.ncbi.nlm.nih.gov/1977254/ You should be checked for more than just B12 deficiency.  The eight B vitamins work together, and we need more of them when we're trying to heal.  They are water soluble, so the body can easily excrete them if not needed. Have you had your Vitamin D level checked?  Vitamin D regulates the immune system and lowers inflammation.   I hope you can find some benefit from my experiences.  Keep us posted on your progress.  
    • knitty kitty
      Hello, @Jack Common, I know how frustrating health mysteries can be. Perhaps you're having a reaction to the medication you were given for the giardiasis you mentioned in another post. The giardiasis infection would account for the high Igg results.  Have you been reinfected? The site I've linked below has lots of information about the long term consequences of being treated with a medication frequently prescribed for giardiasis infection.   https://hormonesmatter.com/metronidazole-toxicity-doctor-denial/ https://hormonesmatter.com/?s=metronidazole https://pmc.ncbi.nlm.nih.gov/articles/PMC3870550/ Please let us know if your symptoms may be due to this reaction to the prescription for giardiasis. Best wishes.
    • knitty kitty
      Hello, @Jack Common, I know how frustrating health mysteries can be. Perhaps you're having a reaction to the medication you were given for the giardiasis. The giardiasis infection would account for the high Igg results.  Have you been reinfected? The site I've linked below has lots of information about the long term consequences of being treated with a medication frequently prescribed for giardiasis infection.   https://hormonesmatter.com/metronidazole-toxicity-doctor-denial/ https://hormonesmatter.com/?s=metronidazole https://pmc.ncbi.nlm.nih.gov/articles/PMC3870550/ Please let us know if your symptoms may be due to this reaction to the prescription for giardiasis. Best wishes.
    • Itsabit
×
×
  • Create New...