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

Connection With Heart Disease And Cd?

VydorScope

By VydorScope
in Related Issues & Disorders

Recommended Posts

VydorScope Proficient
VydorScope
Posted

I am to young for this, not even hit middle age yet, but couple years ago I was diagnosed with heart condition. Its likly it been there most of my life, but unknown till a radom EKG was run on me with realtion to a differnet matter. I have what is known as a Left Bundle Branch Block. This means the nerve on the left side of my heart, the one responisble for beating the heart, is completely dead. The design of the heart has a way to compenstate for this by sending the beat signel down the right side nerve and having it jump to the left side via the muscles. If not for this design I would be dead. How ever, this "backup" method is not as effecitent as the normal way, so my heart pumps slightly out of beat, and somewhat signifigantly less blood then it should. My Cardio-doc says I may need a pacemaker down the road a bit. There is no known cuase for it in me that they could find at the time.

So I was wondering, is there a known celiac disease connection?

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

Celiac.com Sponsor (A8-M):


nettiebeads Apprentice
nettiebeads
Posted
I am to young for this, not even hit middle age yet, but couple years ago I was diagnosed with heart condition. Its likly it been there most of my life, but unknown till a radom EKG was run on me with realtion to a differnet matter. I have what is known as a Left Bundle Branch Block. This means the nerve on the left side of my heart, the one responisble for beating the heart, is completely dead. The design of the heart has a way to compenstate for this by sending the beat signel down the right side nerve and having it jump to the left side via the muscles. If not for this design I would be dead. How ever, this "backup" method is not as effecitent as the normal way, so my heart pumps slightly out of beat, and somewhat signifigantly less blood then it should. My Cardio-doc says I may need a pacemaker down the road a bit. There is no known cuase for it in me that they could find at the time.

So I was wondering, is there a known celiac disease connection?

<{POST_SNAPBACK}>

It's not an inherited condition? Were you born with it or did it develop later in life?

VydorScope Proficient
VydorScope
Posted
  • Author
It's not an inherited condition?  Were you born with it or did it develop later in life?

<{POST_SNAPBACK}>

No one else in my family has it. And as far as we know I was born with a healthy heart. BUT heres the thing it only shows up in a EKG, or other heart scan (MUGA, Echocardiogram, etc). My first EKG at a docs offics was when it was discovered, so no way to know when it set in. I was 27 or 28 at the time.

nettiebeads Apprentice
nettiebeads
Posted
No one else in my family has it. And as far as we know I was born with a healthy heart. BUT heres the thing it only shows up in a EKG, or other heart scan (MUGA, Echocardiogram, etc). My first EKG at a docs offics was when it was discovered, so no way to know when it set in. I was 27 or 28 at the time.

<{POST_SNAPBACK}>

All of my reading re: celiac disease links celiac disease with other digestive issues and hormonal (like thyroid and now pcos). I kinda doubt that there's a link, but then again, the more research done with regards to celiac disease and its effects the more pervasive it seems. But I'm leaning more towards another abnormality causing it. My mother has mytral valve prolapse, no one else in her generation or preceding generations have heart problems, but now it was discovered recently in my brother at age 44. And it's known that this kind of heart problem is inherited.

bmorrow Rookie
bmorrow
Posted

I also have mitral valve prolapse. This was not discovered until three years after the Celiac symptons started. I don't know of anyone in my family having this heart condition. I wonder if Celiac can affect the heart?

debbiewil Rookie
debbiewil
Posted

Well, there isn't a lot of research on celiac disease and heart disease, but there is some, and most of it seems to show higher rates of heart disease among celiac disease patients.

https://www.celiac.com/st_prod.html?p_prodi...-50105572217.03

Debbie

melisadki Explorer
melisadki
Posted

My husband had a five way bypass at 34 so I am so glad he decided to go gluten-free with me. I dont know if celiac caused this as he doesnt want to get tested he says its a waste of money.. :angry: but he is going gluten-free.

Interesting topic? <_<

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

Celiac.com Sponsor (A8-M):


Archived

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

Go to topic listing
  • Celiac.com Sponsor (A19):


  • Member Statistics

    • Total Members
      129,722
    • Most Online (within 30 mins)
      7,748
    Damir21
    Newest Member
    Damir21
    Joined
  • Celiac.com Sponsor (A20):

  • Forum Statistics

    • Total Topics
      121.2k
    • Total Posts
      1m
  • Celiac.com Sponsor (A22):



  • Celiac.com Sponsor (A21):


  • Upcoming Events

  • Posts

    • Idnam
      Ectopic heartbeats - any relation to digestive issues?

      By Idnam · Posted

      They do work for me. I am feeling much better now that I am watching my histamine intake and only take the DAO once  a day.   I had acid reflux for 12 years and was prescribed PPI's.  which I refused to take. Ranitidine was prescribed as an option that I did use only as and when I had chest pain. They were prescribed for me to reduce the acid in my body.
    • Yaya
      Does anyone here also have Afib

      By Yaya · Posted

      This is difficult for me to deal with.  B complex is what stands between me and migraines.  Whenever I stop B for just a few days, I get a migraine.  All my adult life I would get a violent migraine for 3 days like clockwork until a doctor told me to try B complex and it worked.  The only time I get a migraine is when I've run out of B.  This has worked for me for over 15 years.  I am soon to be 79.   My cardiologist has me stop all vitamins for about 3 days and I always have a migraine when I go in for the bloodwork.   D level is nearly at optimal.  I don't take A, I get enough from food.   What a dilemma!
    • Scott Adams
      What apps or tech tools help you manage celiac disease?

      By Scott Adams · Posted

      I think the best approach is to lean how to read product labels, especially the allergen warnings, and these lists might be helpful:      
    • Scott Adams
      Any bad experience with King Arthur Gluten-free bread flour

      By Scott Adams · Posted

      It looks like you are referring to this product: https://shop.kingarthurbaking.com/items/gluten-free-bread-flour Their site says: "Made with gluten-free wheat starch to give baked goods incredible taste and texture, it’s ideal for classic yeasted recipes like artisan boules, bagels, cinnamon rolls, and burger buns", and it is true that Codex quality wheat starch is gluten-free, and does make better baked goods. However, it also contains very low levels of gluten (under 20ppm), and some celiacs do react to this level, so if you are super sensitive it's best to avoid it. They also make this very similar product, which doesn't include any wheat ingredient, and is certified gluten-free: https://shop.kingarthurbaking.com/items/gluten-free-bread-flour Although labeling products in the USA as "gluten-free" that contain such wheat starch is relatively new, it has been offered in Europe for decades. You can read more about studies on it here: https://www.celiac.com/celiac-disease/miscellaneous-information-on-celiac-disease/gluten-free-diet-celiac-disease-amp-codex-alimentarius-wheat-starch/
    • DebJ14
      Does anyone here also have Afib

      By DebJ14 · Posted

      Our Functional Medicine doctor has always ordered the Spectracell Test for Micronutrient Deficiencies.  It tests the intracellular levels of the nutrients, not blood levels.  When high dose, targeted supplementation did not resolve the deficiencies after retesting at 6 months and then a year, he ordered genetic tests.  I have a genetic inability to process Vitamin D, B12 and antioxidants, so I am on high doses of those for life.  The rest of the initial deficiencies resolved within 6 months to a year and a good multi vitamin is sufficient to address those.  My husband has historically had high homocysteine levels and his low folate, B 12 and B6  levels are because of his MTHFR gene mutation.  Always good to get to the root cause!
×
×
  • Create New...