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

Background Heritage Question


CMCM

Recommended Posts

CMCM Rising Star

After reading all my celiac realted books, they keep stressing that celiac disease has a higher prevalence in people with Northern European/Irish/Italian heritage. I'm curious about that....what are your backgrounds on both parents' sides?

I'll start....for me, Swedish on my Dad's side, and on my mom's side Germanic/Russian/English. So I definitely fit that profile.

How about the rest of you?


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



Celiac.com Sponsor (A8-M):



Bonnie Explorer

I was born in Scotland and my heritage is all Scottish!!

Yvonne

taweavmo3 Enthusiast

Part Irish from my mother's side, and Greek from my father's side. I'm not sure where the celiac genes came from.....my mom's entire family has intestinal issues, but my father's family on the maternal side all had stunted growth and late maturity. His mother was only 4'10. So maybe both, who knows. I would love to have them all gene tested, but I don't think I can get everyone to cooperate! All of my kids (only one actually tested +) have gluten reactions and are now gluten free. My brother, me and I believe my late sister (if she was still here to be tested, she was bipolar, and only 4'9 at maturity) have celiac as well. Only my other older sister seems symptom free. So it's very pervasive in my family, which I think is really interesting.

RoseNNJ Apprentice

100 percent Italian :D

hungryforlife Apprentice

My Mom's Side

GM (Scotch-Irish) Grandfather:(English- ancestor was John Wesley)

Dad's side:

Don't know? His last name was Ellis so I assume English.

jerseyangel Proficient

Italian--both sides :D

penguin Community Regular

sweedamickacanuckaho

Sweedish (dad)

Irish (mom)

French-Canadian (dad)

Native American (mom)

Blindingly pale, easily burned, redhead personality :D

Do I fit the profile, or what :P


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



Celiac.com Sponsor (A8-M):



Rachel--24 Collaborator

Moms side....Italian/Spanish

Dad's side....Mexican (I dont know if there's anything mixed in with that)

It had to come from my mom. <_<

mrsnj91 Explorer

Wow this is interesting!

We are having my DD tested for this so I will give you HER parents background ;) .....

Me-Irish, Spanish and American Indian

Daddy's-English and Polish

Just from the few responses....your books seem right! I will have to show my husband this as we were just talking about this over the weekend!

Added: I was looking over the responses again and noticed that some said only one side that fit that discripition. I heard a ped. GI speak this weekend and she said that BOTH parents have to carry the gene. Not necessarily have Celiac but carry the gene(s). Interesting how some on here have one parent that doesn't fit the 'mold'. Just some food for thought! I just found this post interesting.

CMCM Rising Star

Since the theory is that those areas most recently exposed to gluten/wheat would have the HIGHEST rates of celiac disease, and those areas which have eaten gluten the longest have the lowest rates (because natural selection over several thousand years has been eliminating the celiacs!!!), I would expect the very highest rates to be in Native Americans!!! There was a woman here back in January who was Native American, but I haven't seen her around for awhile. I wonder how many others are celiac and don't know it?

Another interesting thing....the original cultivated wheat did not have nearly as much gluten as the wheat does today. Because of the desirable qualities of wheat in cooking (lightness and puffiness in baking), wheat has actually been developed to have a much higher gluten content that the original wheat did, so I guess people are more affected now.

Anyhow, this is all intereting....

francelajoie Explorer

Both parents are French Canadians

mrsnj91 Explorer

The GI said that North Europian decent where at higher risk. But if you go by your theory with the American Indian then I gave a double whammy there! LOL! My guess is that American Indians had more of a corn intake as their base for grain?

Interesting on the grains evolving. I can see that.

Ursa Major Collaborator

100% German

DingoGirl Enthusiast

One-quarter Norwegian and the rest, Scottish, Irish, English.

I think there was another thread juts like this running the last few days, also inspired by that book (I'm waiting for my copy!). Seemed to me that it had gotten to be several pages....check it out!

Rachel--24 Collaborator
Added: I was looking over the responses again and noticed that some said only one side that fit that discripition. I heard a ped. GI speak this weekend and she said that BOTH parents have to carry the gene. Not necessarily have Celiac but carry the gene(s). Interesting how some on here have one parent that doesn't fit the 'mold'. Just some food for thought! I just found this post interesting.

Someone can correct me if I'm wrong but as far as I know both parents do not need to have a celiac gene in order for the child to aquire a gene. You only need one Celiac gene to develop the disease and you can get that from either parent.

CMCM Rising Star
Someone can correct me if I'm wrong but as far as I know both parents do not need to have a celiac gene in order for the child to aquire a gene. You only need one Celiac gene to develop the disease and you can get that from either parent.

I asked that of Dr. Fine when I got my test results, and he confirmed that you only actually need one celiac gene to have a predisposition. You get one gene from each parent, so you could get one celiac gene, plus a second gene from the other parent that was some non-gluten related gene, so you either could get celiac or you might not, 50% chance I guess.

gfmelissa Apprentice

My parents are portuguese and the other is english/german.

I am wondering more about that GI you heard speak that said both parents have to be carriers of the gene? did they mention what the theory is on that? If not thats cool, just wondering.

danikali Enthusiast

I don't fit the profile. I'm mostly Polish and a little bit German. Unless somewhere down the line there is something else that I don't know about. But how could you not know?

CMCM Rising Star
My parents are portuguese and the other is english/german.

I am wondering more about that GI you heard speak that said both parents have to be carriers of the gene? did they mention what the theory is on that? If not thats cool, just wondering.

No no no....I specifically asked Dr. Fine about this once...both parents do not have to give you a gene. You need only ONE gene to have problems. If you have TWO genes (one from each parent) your likelihood of having problems is far greater, however. And there are some people with no identified genes that have celiac disease, so there are obviously some genes that are related to this which have not yet been identified. I think it's about 1% with that scenario.

Smunkeemom Enthusiast

wow. it's difficult to answer. It's my girls who have celiac, and other people in my family. My mother is Irish/Scotish, and that's the side the celiac is on, so I suppose that's the answer.

luvs2eat Collaborator

Both parents are Scottish/Irish.

Angelina Newbie
After reading all my celiac realted books, they keep stressing that celiac disease has a higher prevalence in people with Northern European/Irish/Italian heritage. I'm curious about that....what are your backgrounds on both parents' sides?

I'll start....for me, Swedish on my Dad's side, and on my mom's side Germanic/Russian/English. So I definitely fit that profile.

How about the rest of you?

1/2 Irish from my father (who i dont know)

Scottish, Native American.. Mother side

I know who I got my genes from! grrr

nikki-uk Enthusiast
No no no....I specifically asked Dr. Fine about this once...both parents do not have to give you a gene. You need only ONE gene to have problems. If you have TWO genes (one from each parent) your likelihood of having problems is far greater, however. And there are some people with no identified genes that have celiac disease, so there are obviously some genes that are related to this which have not yet been identified. I think it's about 1% with that scenario.

I was trying to explain this to my 16 yr old son (who has symptoms and we want to get tested)

He wanted to know the chances of him having celiac disease.(His Dad has biopsy proven celiac disease-no gene test though)

I (tried) to explain to him that assuming his Dad has one of the two HLA markers that predispose you to celiac disease,he may have passed that gene onto him(but not necessarily so).

And even if he has passed the gene onto him,there has to be a 'trigger' for celiac disease to occur(illness, huge stress etc.)

And of course I (his Mum) may carry the gene too,(I don't have celiac disease).

In which case he would have 2 genes for celiac disease,or 1 or none.

Did everyone follow that? :blink::lol:

CMCM Rising Star
I was trying to explain this to my 16 yr old son (who has symptoms and we want to get tested)

He wanted to know the chances of him having celiac disease.(His Dad has biopsy proven celiac disease-no gene test though)

I (tried) to explain to him that assuming his Dad has one of the two HLA markers that predispose you to celiac disease,he may have passed that gene onto him(but not necessarily so).

And even if he has passed the gene onto him,there has to be a 'trigger' for celiac disease to occur(illness, huge stress etc.)

And of course I (his Mum) may carry the gene too,(I don't have celiac disease).

In which case he would have 2 genes for celiac disease,or 1 or none.

Did everyone follow that? :blink::lol:

It makes perfect sense to me. Awareness is the key....but knowing the genes from both parents is great because then you really have a firmer idea. Obviously if you have been diagnosed celiac you have at least ONE gene, but if like me, you find out you have TWO genes, then you know for sure your kids have at least one problem gene. For me, the wild card is my husband....being Irish & Norwegian he just might have one, but we don't know. I guess getting one celiac/gluten gene from each parent might mean your likelihood of eventual problems is greater than with just one. Since I have two, I therefore know my two kids have one or the other of my genes, therefore they have the predisposition at the very least and should be watching for it throughout their lives. Lacking any sort of real symptoms now, they certainly don't want to change their diets or even think about it much, but down the road if something triggers symptoms, at least they know where to start looking.....whereas I was kind of oblivious to the idea for most of my life! :D

Guest mvaught

Irish

French

Native American

German

Welch

luck of the Irish?

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - knitty kitty replied to rei.b's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      14

      High DGP-A with normal IGA

    2. - captaincrab55 replied to lmemsm's topic in Gluten-Free Foods, Products, Shopping & Medications
      11

      Finding gluten free ingredients

    3. - rei.b replied to rei.b's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      14

      High DGP-A with normal IGA

    4. - knitty kitty replied to rei.b's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      14

      High DGP-A with normal IGA

    5. - rei.b replied to rei.b's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      14

      High DGP-A with normal IGA


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,130
    • Most Online (within 30 mins)
      7,748

    Tony White
    Newest Member
    Tony White
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • knitty kitty
      @rei.b,  I understand how frustrating starting a new way of eating can be.  I tried all sorts of gluten-free processed foods and just kept feeling worse.  My health didn't improve until I started the low histamine AIP diet.  It makes a big difference.   Gluten fits into opioid receptors in our bodies.  So, removing gluten can cause withdrawal symptoms and reveals the underlying discomfort.  SIBO can cause digestive symptoms.  SIBO can prevent vitamins from being absorbed by the intestines.  Thiamine insufficiency causes Gastrointestinal Beriberi (bloating, abdominal pain, nausea, diarrhea or constipation).  Thiamine is the B vitamin that runs out first because it can only be stored for two weeks.  We need more thiamine when we're sick or under emotional stress.  Gastric Beriberi is under recognised by doctors.  An Erythrocyte Transketolace Activity test is more accurate than a blood test for thiamine deficiency, but the best way to see if you're low in thiamine is to take it and look for health improvement.  Don't take Thiamine Mononitrate because the body can't utilize it well.  Try Benfotiamine.  Thiamine is water soluble, nontoxic and safe even at high doses.  I thought it was crazy, too, but simple vitamins and minerals are important.  The eight B vitamins work together, so a B Complex, Benfotiamine,  magnesium and Vitamin D really helped get my body to start healing, along with the AIP diet.  Once you heal, you add foods back in, so the AIP diet is worth doing for a few months. I do hope you'll consider the AIP diet and Benfotiamine.
    • captaincrab55
      Imemsm, Most of us have experienced discontinued, not currently available or products that suddenly become seasonal.   My biggest fear about relocating from Maryland to Florida 5 years ago, was being able to find gluten-free foods that fit my restricted diet.  I soon found out that the Win Dixie and Publix supper markets actually has 99% of their gluten-free foods tagged, next to the price.  The gluten-free tags opened up a  lot of foods that aren't actually marked gluten-free by the manufacture.  Now I only need to check for my other dietary restrictions.  Where my son lives in New Hartford, New York there's a Hannaford Supermarket that also has a gluten-free tag next to the price tag.  Hopefully you can locate a Supermarket within a reasonable travel distance that you can learn what foods to check out at a Supermarket close to you.  I have dermatitis herpetiformis too and I'm very sensitive to gluten and the three stores I named were very gluten-free friendly.  Good Luck 
    • rei.b
      Okay well the info about TTG-A actually makes a lot of sense and I wish the PA had explained that to me. But yes, I would assume I would have intestinal damage from eating a lot of gluten for 32 years while having all these symptoms. As far as avoiding gluten foods - I was definitely not doing that. Bread, pasta, quesadillas (with flour tortillas) and crackers are my 4 favorite foods and I ate at least one of those things multiple times a day e.g. breakfast with eggs and toast, a cheese quesadilla for lunch, and pasta for dinner, and crackers and cheese as a before bed snack. I'm not even kidding.  I'm not really big on sugar, so I don't really do sweets. I don't have any of those conditions.  I am not sure if I have the genes or not. When the geneticist did my genetic testing for EDS this year, I didn't think to ask for him to request the celiac genes so they didn't test for them, unfortunately.  I guess another expectation I had is  that if gluten was the issue, the gluten-free diet would make me feel better, and I'm 3 months in and that hasn't been the case. I am being very careful and reading every label because I didn't want to screw this up and have to do gluten-free for longer than necessary if I end up not having celiac. I'm literally checking everything, even tea and anything else prepacked like caramel dip. Honestly its making me anxious 😅
    • knitty kitty
      So you're saying that you think you should have severe intestinal damage since you've had the symptoms so long?   DGP IgG antibodies are produced in response to a partial gluten molecule.  This is different than what tissue transglutaminase antibodies are  produced in response to.   TTg IgA antibodies are produced in the intestines in response to gluten.  The tTg IgA antibodies attack our own cells because a structural component in our cell membranes resembles a part of gluten.  There's a correlation between the level of intestinal damage with the level of tTg antibodies produced.  You are not producing a high number of tTg IgA antibodies, so your level of tissue damage in your intestines is not very bad.  Be thankful.   There may be reasons why you are not producing a high quantity of tTg IgA antibodies.  Consuming ten grams or more of gluten a day for two weeks to two months before blood tests are done is required to get sufficient antibody production and damage to the intestines.  Some undiagnosed people tend to subconsciously avoid lots of gluten.  Cookies and cakes do not contain as much gluten as artisan breads and thick chewy pizza crust.  Anemia, diabetes and thiamine deficiency can affect IgA antibody production as well.   Do you carry genes for Celiac?  They frequently go along with EDS.
    • rei.b
      I was tested for celiac at the same time, so I wasn't taking naltrexone yet. I say that, because I don't. The endoscopy showed some mild inflammation but was inconclusive as to celiac disease. They took several biopsies and that's all that was shown. I was not given a Marsh score.
×
×
  • 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.