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

Genetic Question...


Lizzylulu

Recommended Posts

Lizzylulu Newbie

Over a year ago I was diganosed with Celiacs disease followed by my middle child being diganosed not to long after this. I have two other children, one is symptmatic and the other is gluten-free because she was a baby when I was diganosed and she has just always eaten what her sister & I eat. I recently discovered that because I am DQ2 DQ8 thta i will pass on one of these genes to all of my children. Futhermore I discover because my middle child who is DQ2 Homomzygous (she has two DQ2 genes) that it is more than possible she recieved one from myself and one from her father, Which puts all our children at greater risk.

Does anyone have anymore information on this?


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



Celiac.com Sponsor (A8-M):



heidi g. Contributor

I know that people can have the genes for celiac but not have an active case of it. For example: the celiac gene has been passed down in my family for generations. But no one has an active case for like hundreds of years (unless they hid the symptoms and never told anybody) but when something traumatic happened to me it was "triggered" and now i am the only one in my family who has it. That is really all the knowledge i have on it. Hope it somewhat helps.

heidi g. Contributor

Also, celiac disease is hereditary so most likely all your children have the genes. It doesn't mean their all going to have it though.

Lisa Mentor

Here is some information that you might find has value to your situation:

Open Original Shared Link

cyberprof Enthusiast

Over a year ago I was diganosed with Celiacs disease followed by my middle child being diganosed not to long after this. I have two other children, one is symptmatic and the other is gluten-free because she was a baby when I was diganosed and she has just always eaten what her sister & I eat. I recently discovered that because I am DQ2 DQ8 thta i will pass on one of these genes to all of my children. Futhermore I discover because my middle child who is DQ2 Homomzygous (she has two DQ2 genes) that it is more than possible she recieved one from myself and one from her father, Which puts all our children at greater risk.

Does anyone have anymore information on this?

OK, as you noted, each person has two chances to have a celiac gene.

This is what we know:

You - DQ2/DQ8

Middle Daughter - DQ2/DQ2

cassP Contributor

all great info above!

from my understanding, and what ive learned on here-> DQ2s and DQ8s are the stereotypical Celiac genes (predisposing u, tho u dont have to get it)... but that ALL the DQ genes also make it possible to trigger Celiac. people overseas have been dx with Celiac withOUT having either the 2 or the 8. and that having 2 of the same DQ genes tends to make u more vulnerable to triggering Celiac

researchmomma Contributor

all great info above!

from my understanding, and what ive learned on here-> DQ2s and DQ8s are the stereotypical Celiac genes (predisposing u, tho u dont have to get it)... but that ALL the DQ genes also make it possible to trigger Celiac. people overseas have been dx with Celiac withOUT having either the 2 or the 8. and that having 2 of the same DQ genes tends to make u more vulnerable to triggering Celiac

People in the US also have been diagnosed without genes. In a study at UC Irvine they have 800 biopsy confirmed Celiacs and 5% do not have the genes. I emailed back and forth with the sub-investigator on the study and she confirmed this.


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



Celiac.com Sponsor (A8-M):



cyberprof Enthusiast

People in the US also have been diagnosed without genes. In a study at UC Irvine they have 800 biopsy confirmed Celiacs and 5% do not have the genes. I emailed back and forth with the sub-investigator on the study and she confirmed this.

Yes, our own Ravenwoodglass is one of those.

It's a moot point for the OP, Lizzy, because she, her kids' dad and her kids all have at least one celiac gene, predisposing them to celiac (but not making celiac a certainty).

cassP Contributor

researchmomma- very interesting!! i hope the rest of the medical community catches up with that study

and i THINK Ravenwoodglass is overseas, no???

cyberprof Enthusiast

researchmomma- very interesting!! i hope the rest of the medical community catches up with that study

and i THINK Ravenwoodglass is overseas, no???

No, I'm pretty sure Raven lives in the US.

Avalon451 Apprentice

After reading this I got to wondering about our family. As many of you know, DD16 was definitely positive, by blood, plus skin and endo biopsies. The younger two had positive blood tests (we didn't have them biopsied). I had only one faint "possible positive" on the blood test, but lots of symptoms, so the GI did an endo which has just come back negative.

So I'm wondering if both hubby and I have the genes, one or both of them-- or did DD16 just get the full matched set and therefore triggered? And I wonder if my younger two also have the full set? Are they more liable to get the whole range of complications down the line?

So I emailed my PCP and asked if hubby and I could get the gene test. He replied (kind of abruptly, for him, usually he's very accommodating) that he is not even able to order that test, but the GI doc might. and that he doesn't see that it would be of any use except to satisfy curiosity. Ouch. I just want to know if my younger two kids are more or less likely to be very affected with complications. I was going to ask their pediatrician to order the gene test after hubby and I had ours.

I think I will take it up with the pediatric GI doc at Children's Hospital. He'll understand our concerns better, I think.

Roda Rising Star

People in the US also have been diagnosed without genes. In a study at UC Irvine they have 800 biopsy confirmed Celiacs and 5% do not have the genes. I emailed back and forth with the sub-investigator on the study and she confirmed this.

I'm diagnosed with blood work and biopsy only. I've never had the genetic test so I have no idea what genes I have. I am curious though. If I was to get it done I want to know if I can get the test without going through my doctor? I don't need them second guessing my diagnosis, if I happen to not have the DQ2 or DQ8. I've been thinking about it for my youngest son. If he has either of those genes then I could cinch his diagnosis for sure.

Skylark Collaborator

So I'm wondering if both hubby and I have the genes, one or both of them-- or did DD16 just get the full matched set and therefore triggered? And I wonder if my younger two also have the full set? Are they more liable to get the whole range of complications down the line?

The incidence of celiac disease is rising in first-world countries, but not in poorer countries with similar genetics. Type 1 diabetes is rising too. The incidence of celiac genes has not changed in the general population, so there is something about our lifestyle that is triggering the autoimmunity.

You are too worried about specific alleles that may confer some risk for celiac but are very, very clearly not the whole story. Celiac runs in families; chances are both you and DH have some genes that permit triggering of celiac disease under the wrong circumstances. Your kids do too, and because of whatever is going on with our lifestyle, the disease triggered in them much earlier than it did in you. Women seem more susceptible so your DH may have the genes but never show issues with gluten.

ravenwoodglass Mentor

researchmomma- very interesting!! i hope the rest of the medical community catches up with that study

and i THINK Ravenwoodglass is overseas, no???

Nope US born and raised. Interestingly my genes are usually genes that are found in the Middle East or Asian population and considered celiac associated genes there...but my parents were German, Dutch (Dad) and Welsh, Irish and English (Mom).

There is still an awful lot to be learned about celiac associated genetics.

cassP Contributor

Nope US born and raised. Interestingly my genes are usually genes that are found in the Middle East or Asian population and considered celiac associated genes there...but my parents were German, Dutch (Dad) and Welsh, Irish and English (Mom).

There is still an awful lot to be learned about celiac associated genetics.

is it Mushroom then???? im so out of the loop.... i remember 1 of you regulars was in australia or NZ and i was so surprised... hhhmmm???

  • 4 weeks later...
Lizzylulu Newbie

Thank you everyone! We have decided to have gentic testing done on my Husband, that way we know what we could be dealing with. My daughter that is symtamatic has an appt next week at the childrens hospital GI. I hoping to have fatser results then the Ped GI who diagnosed my younger child. As far as the baby goes (she's gonna be 2 in july) we will wait to see what my husbands gentic results are. Thank you again for all the advice :-)

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - asaT replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      48

      Supplements for those Diagnosed with Celiac Disease

    2. - asaT replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      48

      Supplements for those Diagnosed with Celiac Disease

    3. - nanny marley replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      20

      Insomnia help

    4. - David Blake commented on Scott Adams's article in Product Labeling Regulations
      1

      FDA Moves to Improve Gluten Labeling—What It Means for People With Celiac Disease

    5. - nanny marley replied to wellthatsfun's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      4

      nothing has changed

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,343
    • Most Online (within 30 mins)
      7,748

    emoryprose
    Newest Member
    emoryprose
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • asaT
      plant sources of calcium, such as spinach, have calcium bound to oxalates, which is not good. best source of calcium is unfortunately dairy, do you tolerate dairy? fermented dairy like kefir is good and or a little hard cheese. i do eat dairy, i can only take so much dietary restriction and gluten is hard enough! but i guess some people do have bad reactions to it, so different for everyone.  
    • asaT
      i take b12, folate, b2, b6, glycine, Nac, zinc, vk2 mk4, magnesium, coq10, pqq, tmg, creatine, omega 3, molybdnem (sp) and just started vit d. quite a list i know.  I have high homocysteine (last checked it was 19, but is always high and i finally decided to do something about it) and very low vitamin d, 10. have been opposed to this supp in the past, but going to try it at 5k units a day. having a pth test on friday, which is suspect will be high. my homocysteine has come down to around 9 with 3 weeks of these supplements and expect it to go down further. i also started on estrogen/progesterone. I have osteoporosis too, so that is why the hormones.  anyway, i think all celiacs should have homocysteine checked and treated if needed (easy enough with b vit, tmg). homocysteine very bad thing to be high for a whole host of reasons. all the bad ones, heart attack , stroke, alzi, cancer..... one of the most annoying things about celiacs (and there are so many!) is the weight gain. i guess i stayed thin all those years being undiagnosed because i was under absorbing everything including calories. going gluten-free and the weight gain has been terrible, 30#, but i'm sure a lot more went into that (hip replacement - and years of hip pain leading to inactivity when i was previously very active, probably all related to celiacs, menopause) yada yada. i seemed to lose appetite control, like there was low glp, or leptin or whatever all those hormones are that tell you that you are full and to stop eating. my appetite is immense and i'm never full. i guess decades or more ( i think i have had celiacs since at least my teens - was hospitalized for abdominal pain and diarrhea for which spastic colon was eventually diagnosed and had many episodes of diarrhea/abdominal pain through my 20's. but that symptom seemed to go away and i related it to dairy much more so than gluten. Also my growth was stunted, i'm the only shorty in my family. anyway, decades of malabsorption and maldigestion led to constant hunger, at least thats my theory. then when i started absorbing normally, wham!! FAT!!!    
    • nanny marley
      Great advise there I agree with the aniexty part, and the aura migraine has I suffer both, I've also read some great books that have helped I'm going too look the one you mentioned up too thankyou for that, I find a camomile tea just a small one and a gentle wind down before bed has helped me too, I suffer from restless leg syndrome and nerve pain hence I don't always sleep well at the best of times , racing mind catches up I have decorated my whole house in one night in my mind before 🤣 diet changes mindset really help , although I have to say it never just disappears, I find once I came to terms with who I am I managed a lot better  , a misconception is for many to change , that means to heal but that's not always the case , understanding and finding your coping mechanisms are vital tools , it's more productive to find that because there is no failure then no pressure to become something else , it's ok to be sad it's ok to not sleep , it's ok to worry , just try to see it has a journey not a task 🤗
    • nanny marley
      I agree there I've tryed this myself to prove I can't eat gluten or lactose and it sets me back for about a month till I have to go back to being very strict to settle again 
    • trents
      You may also need to supplement with B12 as this vitamin is also involved in iron assimilation and is often deficient in long-term undiagnosed celiac disease.
×
×
  • 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.