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

Celiac And Gluten Intolerance Within Families


Guest Kathy Ann

Recommended Posts

Guest Kathy Ann

I keep reading that within immediate families something like only 10 percent are likely to have celiac or gluten intolerance if a parent has it, for instance. At that rate, since I am celiac and have 8 children, only 1 of them statistically would have it.

Yet, as I'm reading a lot of the bios and signatures on this board, it sure looks like MOST of the children of celiacs and gluten intolerants seem to have some form of it. I'm also amazed at how many husbands and wives BOTH have gluten issues, which has nothing to do with being blood related. Just curious about your opinions and observations. :)


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



Celiac.com Sponsor (A8-M):



2Boys4Me Enthusiast

In our family my one son has celiac. My husband, older son, my Mom and I were tested and none of us have it. No one on my husband's side of the family has been tested, and neither my dad, brother, nor sister were tested either. Presumably if my husband or I had it, then our siblings would get tested.

AndreaB Contributor

Kathy Ann,

We were tested through enterolab and myself and two oldest children tested postive. My husband has 2 celiac genes though. My infant son is who led us down this trail due to his eczema outbreak around 2 months of age. He is completely clear since going gluten free. I feed him oatmeal cereal at 8 months and he was crabby the whole week so I suspect he will be intolerant also.

celiacgirls Apprentice

It seems higher than 10% to me. I think I read on Enterolab's site that 80% of the relatives will test positive after one does.

In my family, my 2 children and I are all gluten intolerant per Enterolab. My husband only did the gene test and he has 1 celiac gene and 1 gluten intolerant gene. I have one of each also. I don't know about the kids.

My mother had the endoscopy to look for celiac and it was negative. She had been gluten free for some time before that but started eating some gluten for the test. She has had a positive dietary response so is gluten free. Her mother had biopsy-proven celiac.

One sister and her two children tested positive by Enterolab. My brother was positive. My other sister did not test herself but her two children are positive. We know one brother-in-law has either 2 celiac genes or one gluten intolerant gene and one celiac gene.

Not all of them are actually on the diet yet but it is impressive to me that they were all tested.

hannahsue01 Enthusiast

Our daughters GI claims that even if I and her sister have celiacs that she would only have 3% chance of having it. I personally think that is BULL ****!!!!!!!!!! It seems Everbody so far in our family in the same blood line has the disease from there great grandmother on down the line. Grandparents.....great grandparents.....aunts......great aunts......second cousins........sisters......and there is evidence way down the line of the disease in our family. Besides our baby it seems that everyone in the blood line has it......seems a little fishy to me.

prinsessa Contributor

The only ones to be tested in my family are me and my kids. Both mine and my son's blood test came back negative. I decided to test the kids through Enterolab and they both came back gluten intolerant. I didn't test myself because I already know I have gluten intolerance through dietary changes. I would like my husband to be tested for intolerances because he has constant digestive problems. He says he doesn't and won't get tested. I know for sure he has digestive problems because we have lived together for years. You can't hide things like that from your spouse ;)

My mom and brother won't get tested either even though my mom has complained of digestive problems. And she said my grandmother had chronic diarrhea.

happygirl Collaborator

hannahsue,

Obviously there is much more at play than just genetics, otherwise why would some families have "lots" of Celiacs and others have none. And, statistics refer to a general population, not individual families.

Leading Celiac experts recommend that all first degree relatives of Celiacs are tested. In terms of the latest research, Dr Fasano's study reports that: (taken from an abstract on celiac.com)

According to a recently published large-scale multi-year and multi-center study, 1 in 133, or a total of 2,131,019 Americans have celiac disease. Alessio Fasano, MD, et. al., and colleagues screened 13,145 subjects using serum antigliadin antibodies and anti–endomysial antibodies (EMA). Those who had positive EMA results were screened again for human tissue transglutaminase IgA antibodies and celiac disease-associated human leukocyte antigen DQ2/DQ8 haplotypes, and when possible, intestinal biopsies were also given. Additionally, for those with biopsy-proven celiac disease, 4,508 first-degree relatives and 1,275 second-degree relatives were also screened for the disease. A total of 3,236 symptomatic patients and 4,126 not-at-risk individuals were screened.

The study determined the following:

Group Prevalence

First degree relatives 1 in 22

Second-degree relatives 1 in 39

Symptomatic patients 1 in 56

Not-at-risk individuals (overall prevalence) 1 in 133

These results are much higher than previous studies have found, and they indicate that celiac disease is perhaps the most common genetic disorder in the United States, as well as one of the most poorly diagnosed diseases.

(end of abstract)

However, this study does not take into account "mere" gluten intolerance (vs. Celiac) or those who have Celiac but don't come up positive on traditional testing. Its really interesting to me...why are there some families like yours (Full of Celiacs!) and others (even through testing) have only one....


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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

My guess is that for relatives to all be biopsy proven celiacs, the rate very well could be 10%. It seems that a large percentage of us here either didn't have the biopsy or the biopsy was negative, but we have positive dietary response, and some have positive Enterolab or blood tests. Technically, I would not fall into the category of celiac for their study as my biopsy was negative after being gluten free and only going on a six week gluten challenge.

eKatherine Apprentice
However, this study does not take into account "mere" gluten intolerance (vs. Celiac) or those who have Celiac but don't come up positive on traditional testing. Its really interesting to me...why are there some families like yours (Full of Celiacs!) and others (even through testing) have only one....

It also doesn't take into account the difference between clinical gluten intolerance and subclinical.

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. - knitty kitty replied to Jordan Carlson's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      Fruits & Veggies

    2. - knitty kitty replied to pothosqueen's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      15

      Positive biopsy

    3. - trents replied to pothosqueen's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      15

      Positive biopsy

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

    • Total Members
      133,012
    • Most Online (within 30 mins)
      7,748

    jsslynjnes25
    Newest Member
    jsslynjnes25
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • knitty kitty
      Hello, @Jordan Carlson, So glad you're feeling better.   Tecta is a proton pump inhibitor.  PPI's also interfere with the production of the intrinsic factor needed to absorb Vitamin B12.  Increasing the amount of B12 you supplement has helped overcome the lack of intrinsic factor needed to absorb B12. Proton pump inhibitors also reduce the production of digestive juices (stomach acids).  This results in foods not being digested thoroughly.  If foods are not digested sufficiently, the vitamins and other nutrients aren't released from the food, and the body cannot absorb them.  This sets up a vicious cycle. Acid reflux and Gerd are actually symptoms of producing too little stomach acid.  Insufficient stomach acid production is seen with Thiamine and Niacin deficiencies.  PPI's like Tecta also block the transporters that pull Thiamine into cells, preventing absorption of thiamine.  One of the symptoms of Thiamine deficiency is difficulty swallowing, gagging, problems with food texture, dysphagia. Other symptoms of Thiamine deficiency are symptoms of ADHD and anxiety.  Vyvanse also blocks thiamine transporters contributing further to Thiamine deficiency.  Pristiq has been shown to work better if thiamine is supplemented at the same time because thiamine is needed to make serotonin.  Doctors don't recognize anxiety and depression and adult onset ADHD symptoms as early symptoms of Thiamine deficiency. Stomach acid is needed to digest Vitamin C (ascorbic acid) in fruits and vegetables.  Ascorbic acid left undigested can cause intestinal upsets, anxiety, and heart palpitations.   Yes, a child can be born with nutritional deficiencies if the parents were deficient.  Parents who are thiamine deficient have offspring with fewer thiamine transporters on cell surfaces, making thiamine deficiency easier to develop in the children.  A person can struggle along for years with subclinical vitamin deficiencies.  Been here, done this.  Please consider supplementing with Thiamine in the form TTFD (tetrahydrofurfuryl disulfide) which helps immensely with dysphagia and neurological symptoms like anxiety, depression, and ADHD symptoms.  Benfotiamine helps with improving intestinal health.  A B Complex and NeuroMag (a magnesium supplement), and Vitamin D are needed also.
    • knitty kitty
      @pothosqueen, Welcome to the tribe! You'll want to get checked for nutritional deficiencies and start on supplementation of B vitamins, especially Thiamine Vitamin B 1.   There's some scientific evidence that the fat pad that buffers the aorta which disappears in SMA is caused by deficiency in Thiamine.   In Thiamine deficiency, the body burns its stored fat as a source of fuel.  That fat pad between the aorta and digestive system gets used as fuel, too. Ask for an Erythrocyte Transketolace Activity test to look for thiamine deficiency.  Correction of thiamine deficiency can help restore that fat pad.   Best wishes for your recovery!  
    • trents
      Wow! You're pretty young to have a diagnosis of SMA syndrome. But youth also has its advantages when it comes to healing, without a doubt. You might be surprised to find out how your health improves and how much better you feel once you eliminate gluten from your diet. Celiac disease is an autoimmune disorder that, when gluten is consumed, triggers an attack on the villous lining of the small bowel. This is the section of the intestines where all our nutrition is absorbed. It is made up of billions of tiny finger-like projections that create a tremendous surface area for absorbing nutrients. For the person with celiac disease, unchecked gluten consumption generates inflammation that wears down these fingers and, over time, greatly reduces the nutrient absorbing efficiency of the small bowel lining. This can generate a whole host of other nutrient deficiency related medical problems. We also now know that the autoimmune reaction to gluten is not necessarily limited to the lining of the small bowel such that celiac disease can damage other body systems and organs such as the liver and the joints and cause neurological problems.  It can take around two years for the villous lining to completely heal but most people start feeling better well before then. It's also important to realize that celiac disease can cause intolerance to some other foods whose protein structures are similar to gluten. Chief among them are dairy and oats but also eggs, corn and soy. Just keep that in mind.
    • pothosqueen
    • pothosqueen
      I was just diagnosed at 26 after accidental finding. Any simple tips for newbies? Things a non celiac would never think of? I already went through my prescriptions and identified some medications that have gluten. Is there a beginners guide? Celiac for dummies?
×
×
  • 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.