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 Celiac.com!
    eNewsletter
    Donate

When To Introduce Gluten To Babies


cfriedman

Recommended Posts

cfriedman Newbie

Hello,

I was just diagnosed with Celiac Disease 4 months after my son was born. My sister also has been diagnosed. I am concerned about my son having Celiac Disease. He is only 6 months old now and I am not sure when I should try and introduce gluten to him. There was a recent study that came out in May 2005 that indicated that those children at greater rist for celiac disease may have a decreased chance of getting the disease if introduced to gluten between 4 and 7 months. I wanted to see if anyone else has had to make the decision about introducing gluten to their child between 4 and 7 months or waiting until they are older.

Jack's mom

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



shan1523 Rookie

Im not an expert by any means, and am still new to all of this as far as background info, but I know that I gave my son gluten at 5 months (we did rice cereal at 4.5 months then started baby oatmeal at 5 months then baby barley cereal at 5.5 months) and my son showed signs immediately. THere are no celiacs in my familly that we are aware of (lots of crohns, colitis, and IBS all throughout though so I wonder if some missed the diagnosis)

My point...I gave it to my son in that window without any known risks, and well he showed and shows signs big time.

just thought Id add my experiance

Shannon

Link to comment
Share on other sites
MySuicidalTurtle Enthusiast

I showed signs of Celiac Disease as a newborn and so did my brother. You can't really know yet how he will react. Maybe he doesn't even have Celiacs, maybe he won't show symptoms until he is very old, or maybe he will be like my brother and I and be sick from the start. Just do what you think he is ready for.

Link to comment
Share on other sites
rgeelan Apprentice

My son was introduced at 3 months and was diagnosed with celiac disease at 3 years. My daughter wasn't introduced till 5 months and hasn't been diagnosed yet (but I may test her again now that she is over 2 years) I plan on waiting till about 5 months to introduce gluten to our youngest just to give her a better chance. My theory is why push my luck. Even if it just decreases her chance a little it's better than nothing!

Link to comment
Share on other sites
Merika Contributor

The *new* AAP (American Academy of Pediatrics) recommendations are to breastfeed EXCLUSIVELY until age 6 months. So that would mean no gluten under age six months. Studies also show the longer you breastfeed, the less likelihood your child will contract celiac (diminish NOT eliminate risk).

As for the studies that show the 4-6 month "window", I think there probably is some truth to the timing of when to introduce grains HOWEVER, given that the availability of babies to study who were NOT introduced to wheat until older is so small (and not really a large enough research group) just says to me to wait to introduce gluten, and not do it when babies are 0-3 months. I believe this one-time study (recent, and I am looking forward to others that investigate this further) was in Britain which I am under the impression has even less breastfeeding and more early-foods feeding than in the US.

Merika

Link to comment
Share on other sites
celiackara Newbie

I have a seven 1/2 month old daughter. I was diagnosed several years ago, and was gluten-free my whole pregnancy. I quizzed every pediatrician I could get my hands on in the hospital and in our pediatric group and they all said to wait until she was at least two years old to introduce gluten. They felt that two years (or three if I felt like it) was a good age to challenge her, since she would have gone through most of her growing by that point. Several of them also pointed out that it would be a healthier diet too.

I also read a La Leche League article about breastfeeding and celiac disease. They quoted a study that said that breastfeeding up to two years seemed to significantly reduce the incidence of celiac disease in babies. The pediatricians I talked to also recommended breastfeeding instead of formula; they were worried about gluten contamination in formula.

What the peds stressed most was that being a child of a celiac parent is not an automatic sentence, and that these are just precautions.

ktm

Link to comment
Share on other sites
MySuicidalTurtle Enthusiast

If you are breastfeeding and eating gluten it will pass on to your child. So, that doesn't help with not feeding them gluten. Plus, Celiac Disease isn't something one can contract. It is a genetic auto-immuine disorder.

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



lovegrov Collaborator

There is no reason to screen babies for Celiac Disease. Babies must

have been ingesting gluten into their systems for six to nine months

before an autoimmune response can develop.

The effect of timing of gluten ingestion has been studied at the

University of Colorado. This new study, published in the Journal of the

American Medical Association, suggests that children are less likely to

develop Celiac Disease if they were introduced to gluten-containing

cereals between 4-6 months of age. Children exposed to gluten in the first 3

months had a 5-fold increased risk when compared to the 4-6-month group. The

follow-up on the patients was only 4.8 years.

Dr. Guandalini also said that a small amount of gliadin protein does

pass through breast milk. However, this condition may be okay; it may

induce some tolerance. Breast feeding seems to be protective for Celiac

Disease.

Above is the short version of the latest research, copied from a post at the St. John's site.

richard

Link to comment
Share on other sites
lbsteenwyk Explorer

I agree with Merika, you should breast feed as long as possible. It's the one factor you can control to decrease your child's risk of developing celiac disease. My daughter was introduced to gluten during the recommended "window" of 4-6 months and she still developed celiac disease, but didn't have symptoms until about 20-22 months. She was breastfed for 1 year. I also introduced my son to gluten between 4-6 months, but he's received much less of it simply due to the fact that we have fewer of these foods in the house now. He has had no symptoms of celiac disease at this point. I think it's basically a crap shoot. The two factors in your control are breastfeeding and gluten introduction; there are probably other factors that research has not yet uncovered.

Link to comment
Share on other sites
Merika Contributor
This new study, published in the Journal of the

American Medical Association, suggests that children are less likely to

develop Celiac Disease if they were introduced to gluten-containing

cereals between 4-6 months of age.  Children exposed to gluten in the first 3

months had a 5-fold increased risk when compared to the 4-6-month group.  The

follow-up on the patients was only 4.8 years. 

   

richard

<{POST_SNAPBACK}>

Thanks! See what bothers me is the implication that it's best to introduce gluten between 4-6 months, when really all the study shows is that it's preferable than introducing it at 0-3 months of age. I don't think they really had enough babies/kids in older groups. Maybe, as ktm posted, a better time to introduce it is after age 2. The thing is *we just don't know yet* what the best age to introduce it is. But earlier does not seem to be better.

Merika

Link to comment
Share on other sites
cfriedman Newbie

Thank you all for your feedback! I meet with my son's ped. tomorrow. I am going to ask her again her thoughts. Then my husband and I will have to decide what we are comfortable with. I wish they knew more about this and had more studies to go by. I really hate to think that there could be a "window of opportunity" and what if I miss it.

Link to comment
Share on other sites

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,069
    • Most Online (within 30 mins)
      7,748

    angie78
    Newest Member
    angie78
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Fluka66
      Thank you again for your reply and comments which I have read carefully as I appreciate any input at this stage. I'm tending to listen to what my body wants me to do, having been in agony for many years any respite has been welcome and avoiding all wheat and lactose has thankfully brought this.  When in pain before I was seen by a number of gynacologists as I had 22 fibroids and had an operation 13 years ago to shrink them . However the pain remained and intensified to the point over the years where I began passing out. I was in and out of a&e during covid when waiting rooms where empty. My present diet is the only thing that's given me any hope for the future. As I say I had never heard of celiac disease before starting so I guess had this not come up in a conversation I would just have carried on. It was the swollen lymph node that sent me to a boots pharmacist who immediately sent me to a&e where a Dr asked questions prescribed antibiotics and then back to my GP. I'm now waiting for my hospital appointment . Hope this answers your question. I found out more about the disease because I googled something I wouldn't normally do, it did shed light on the disease but I also read some things that this disease can do. On good days I actually hope I haven't got this but on further investigation my mother's side of the family all Celtic have had various problems 're stomach pain my poor grandmother cried in pain as did her sister whilst two of her brother's survived WW2 but died from ulcers put down to stress of fighting.  Wishing you well with your recovery.  Many thanks  
    • knitty kitty
      Welcome to the forum, @Nacina, What supplements is your son taking?
    • knitty kitty
      @BluegrassCeliac, I'm agreeing.  It's a good thing taking magnesium. And B vitamins. Magnesium and Thiamine work together.  If you supplement the B vitamins which include Thiamine, but don't have sufficient magnesium, Thiamine won't work well.  If you take Magnesium, but not Thiamine, magnesium won't work as well by itself. Hydrochlorothiazide HCTZ is a sulfonamide drug, a sulfa drug.  So are proton pump inhibitors PPIs, and SSRIs. High dose Thiamine is used to resolve cytokine storms.  High dose Thiamine was used in patients having cytokine storms in Covid infections.  Magnesium supplementation also improves cytokine storms, and was also used during Covid. How's your Vitamin D? References: Thiamine and magnesium deficiencies: keys to disease https://pubmed.ncbi.nlm.nih.gov/25542071/ Hiding in Plain Sight: Modern Thiamine Deficiency https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533683/ The Effect of a High-Dose Vitamin B Multivitamin Supplement on the Relationship between Brain Metabolism and Blood Biomarkers of Oxidative Stress: A Randomized Control Trial https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316433/ High‐dose Vitamin B6 supplementation reduces anxiety and strengthens visual surround suppression https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9787829/ Repurposing Treatment of Wernicke-Korsakoff Syndrome for Th-17 Cell Immune Storm Syndrome and Neurological Symptoms in COVID-19: Thiamine Efficacy and Safety, In-Vitro Evidence and Pharmacokinetic Profile https://pubmed.ncbi.nlm.nih.gov/33737877/ Higher Intake of Dietary Magnesium Is Inversely Associated With COVID-19 Severity and Symptoms in Hospitalized Patients: A Cross-Sectional Study https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9132593/ Magnesium and Vitamin D Deficiency as a Potential Cause of Immune Dysfunction, Cytokine Storm and Disseminated Intravascular Coagulation in covid-19 patients https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7861592/ Sulfonamide Hypersensitivity https://pubmed.ncbi.nlm.nih.gov/31495421/
    • BluegrassCeliac
      Hi,   Not saying Thiamine (B1) couldn't be an issue as well, but Mg was definitely the cause of my problems. It's the only thing that worked. I supplemented with B vitamins, but that didn't change anything, in fact they made me sick. Mg stopped all my muscle pain (HCTZ) within a few months and fixed all the intestinal problems HCTZ caused as well. Mom has an allergy to some sulfa drugs (IgG Celiac too), but I don't think I've ever taken them. Mg boosted my energy as well. It solved a lot of problems. I take 1000mg MgO a day with no problems. I boost absorption with Vitamin D. Some people can't take MgO,  like mom, she takes Mg Glycinate. It's one of those things that someone has try and find the right form for themselves. Everyone's different. Mg deficiency can cause anxiety and is a treatment for it. A pharmacist gave me a list of drugs years ago that cause Mg deficiency: PPIs, H2 bockers, HCTZ, some beta blockers (metoprolol which I've taken -- horrible side effects), some anti-anxiety meds too were on it. I posted because I saw he was an IgG celiac. He's the first one I've seen in 20 years, other than my family. We're rare. All the celiacs I've met are IgA. Finding healthcare is a nightmare. Just trying to help. B  
    • Scott Adams
      It sounds like you've been through a lot with your son's health journey, and it's understandable that you're seeking answers and solutions. Given the complexity of his symptoms and medical history, it might be beneficial to explore a few avenues: Encourage your son to keep a detailed journal of his symptoms, including when they occur, their severity, any triggers or patterns, and how they impact his daily life. This information can be valuable during medical consultations and may help identify correlations or trends. Consider seeking opinions from specialized medical centers or academic hospitals that have multidisciplinary teams specializing in gastrointestinal disorders, especially those related to Celiac disease and Eosinophilic Esophagitis (EOE). These centers often have experts who deal with complex cases and can offer a comprehensive evaluation. Since you've already explored alternative medicine with a nutrition response doctor and a gut detox diet, you may want to consider consulting a functional medicine practitioner. They take a holistic approach to health, looking at underlying causes and imbalances that may contribute to symptoms. Given his low vitamin D levels and other nutritional markers, a thorough nutritional assessment by a registered dietitian or nutritionist specializing in gastrointestinal health could provide insights into any deficiencies or dietary adjustments that might help alleviate symptoms. In addition to routine tests, consider asking about more specialized tests that may not be part of standard screenings. These could include comprehensive stool analyses, food intolerance testing, allergy panels, or advanced imaging studies to assess gut health.
×
×
  • Create New...