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

Medication-gluten Digesting Enzymes


Candy

Recommended Posts

Candy Contributor
:( Has anyone been able to get the pills that are supposed to digest gluten ? I know about it from an article on this celiac.com website that I read about a year ago. Some medical place in the state Maryland was the one that mentioned it , and I'm sure it exists , but no one seems to want us to have it, or else it would have been offered to us all. I think it was brand new when it was mentioned last year. Maybe they have to test it or something. I wouldn't use it all the time like people think -I would use it occasionally when I eat pizza,pretzels,doughnuts,and Christmas bread stuffing,which isn't every every day,more like every two months. AND I wouldn't have to worry abouting eroding my small intestine and such.

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



Celiac.com Sponsor (A8-M):



tom Contributor

I believe you're talking about AT-1001, from a company (Alba Therapeutics) started by a U of Md Dr.

It's in testing now.

I was surprised to find that they're measuring its effectiveness with a test for the extent of permeability in leaky-gut.

From what I've read, it's more a treatment for leaky-gut - both repair & prevention I believe - than something more directly related to celiac or gluten, tho I do think leaky-gut is directly related to celiac. Uh-oh, that doesn't make as much sense as I'd hoped it would.

Anyway, it may turn out to be a very helpful drug in recovery from celiac damage, but is probably at least a couple yrs away. I've seen mention of it as a potential "cure", but to me, that's highly misguided.

Silly Yak Pete Rookie

A pill to toterate gluten would be a miracle pill. I hope it would be more effective then the lactose enzyme pills that we lactose suffers have to take.

JennyC Enthusiast

I don't think that any pill that breaks down gluten is a practical solution to celiac disease. Celiac disease is not like lactose intolerance! If Lactaid does not digest 100% of lactose consumed the worst that will happen is stomach cramps and diarrhea. If the gluten digesting pill does not digest 100% of the gluten, then it will set off an autoimmune response in the body. I very much doubt that any drug company will guarantee you that any enzyme supplement is 100% effective. With all the complications that can arise when a person with celiac disease continues to eat gluten, there's no way I would ever consider giving it to my son, unless he accidentally ate some gluten. (We usually don't even know he's had gluten until the next day, so the pill would still be of little value.)

I just needed to vent! :rolleyes:

ravenwoodglass Mentor
A pill to toterate gluten would be a miracle pill. I hope it would be more effective then the lactose enzyme pills that we lactose suffers have to take.

You may be sensitive to casein and not to lactose, in which case the lactose enzyme pills are not going to help at all. You may need to eliminate casein and not lactose, not easy I know cause I am there right now. There are lots of replacements for cheese and stuff that are lactose free but even a lot of stuff that says dairy free has casien.

As to the enzyme pill, my health food store has a product called something like glutenese digestive enzymes. It states clearly on the bottle that it is not for celaic. I don't take them but my DH does. He eats breakfast out almost every day and while he is knowledgeable about CC issues he does not like to mention the need for seperate cooking etc and just orders his eggs off the grill. He was getting CC constantly which effects him more neurologically than GI wise. He does not take it to be able to eat gluten but he does seem to be much less 'twitchy' from CC lately. He is on his second bottle and normally has to be really pushed to even take a vitamin so he must be noticing some difference himself.

Gemini Experienced

Jenny.....couldn't agree with you more! I highly doubt a pill will ever come about for celiac disease because it would have to stop the autoimmune reaction and doctor's just haven't even come close to conquering that monster. Look at the treatment and vaccines for AIDS....they have made strides but the bottom line is the immune system can adapt to meds they try and they are never completely effective.

I sometimes cannot understand why, aside from the money aspect of it, people have such a hard time with going and staying gluten-free. There is just so much good food out there that can replace whatever you crave. I don't know about anyone else but even if there was a complete cure, the thought of eating fast food or a donut makes me want to barf. I was way too sick to ever want to eat that crappy food again! I can't even stand the smell of fast food.

  • 3 weeks later...
threeringfilly Apprentice

I know this is an older thread, but I thought I might add my 2 cents...

I used to work with a little girl who was autistic, and her parents had her on a gluten-free casein-free diet, and I could definately see the difference in her when she was completely gluten-casein-free as opposed to when she ate anything with gluten or casein.

Her mom would buy an enzyme from Open Original Shared Link that she would have before having any gluten or casein - such as when they ordered pizza and or went out to eat. She would keep as much gluten or casein out of her diet as possible, but these enzymes helped.

They didn't cure her, but I remember it helping.

I also found this site Open Original Shared Link

Which seemed to have some pretty interesting information about studies and stuff.

Then this site: Open Original Shared Link

Which described the enzymes and probiotics.

I remember writing down the name of the exact enzyme she used, it's just a matter of finding that little piece of paper...


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



Celiac.com Sponsor (A8-M):



Fiddle-Faddle Community Regular
:( Has anyone been able to get the pills that are supposed to digest gluten ? I know about it from an article on this celiac.com website that I read about a year ago. Some medical place in the state Maryland was the one that mentioned it , and I'm sure it exists , but no one seems to want us to have it, or else it would have been offered to us all. I think it was brand new when it was mentioned last year. Maybe they have to test it or something. I wouldn't use it all the time like people think -I would use it occasionally when I eat pizza,pretzels,doughnuts,and Christmas bread stuffing,which isn't every every day,more like every two months. AND I wouldn't have to worry abouting eroding my small intestine and such.

Candy, from what I've read, it seems as though that pill is supposed to avoid reactions to cross-contamination; it's not a license to eat poison, not even every two months!

Unfortunately for us, there are studies that show that even eating a crumb a month is enough to cause visible villi damage in celiacs. :( That means that every time you cheat, you are triggering your immune system to destroy part of your body.

You can MAKE gluten-free pizza, doughnuts, and Christmas bread stuffing EASILY, and if you use the right recipes, it really does taste as good as the gluteny stuff. And Kinninkinnick makes gluten-free pretzels that taste exactly like--pretzels, and I have to fight my gluten-eating husband for them. Come to think of it, Kinnikinnick also makes really good chocolate doughnuts, too. :)

debmidge Rising Star

From what I know and read about these new discovery, Zonulin, which is still in Human Clinicial Trials, is that it's going to work on the molecular level; it won't work like lactose pills. It's supposed to stop a "t" cell response (or something like that).

https://www.celiac.com/articles/64/1/Protei...ease/Page1.html

Open Original Shared Link

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. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    2. - tiffanygosci posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Aldi Pueblo Lindo Yellow Corn Tortillas

    3. - tiffanygosci replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    4. - trents replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    5. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,979
    • Most Online (within 30 mins)
      7,748

    Susan Upchurch
    Newest Member
    Susan Upchurch
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Mari
      There is much helpful 'truth' posted on this forum. Truths about Celiac Disease are based on scientific research and people's experience. Celiac disease is inherited. There are 2 main Celiac 'genes' but they are variations of one gene called HLa - DQ What is inherited when a person inherits one or both of the DQ2 or the DQ8 is a predisposition to develop celiac disease after exposure to a environmental trigger. These 2 versions of the DQ gene are useful in diagnosing  celiac disease but there are about 25 other genes that are known to influence celiac disease so this food intolerance is a multigenic autoimmune disease. So with so many genes involved and each person inheriting a different array of these other genes one person's symptoms may be different than another's symptoms.  so many of these other genes.  I don't think that much research on these other genes as yet. So first I wrote something that seem to tie together celiac disease and migraines.  Then you posted that you had migraines and since you went gluten free they only come back when you are glutened. Then Scott showed an article that reported no connection between migraines and celiac disease, Then Trents wrote that it was possible that celiacs had more migraines  and some believed there was a causal effect. You are each telling the truth as you know it or experienced it.   
    • tiffanygosci
      Another annoying thing about trying to figure this Celiac life out is reading all of the labels and considering every choice. I shop at Aldi every week and have been for years. I was just officially diagnosed Celiac a couple weeks ago this October after my endoscopy. I've been encouraged by my local Aldi in that they have a lot of gluten free products and clearly labeled foods. I usually buy Milagro corn tortillas because they are cheap and are certified. However, I bought a package of Aldi's Pueblo Lindo Yellow Corn Tortillas without looking too closely (I was assuming they were fine... assuming never gets us anywhere good lol) it doesn't list any wheat products and doesn't say it was processed in a facility with wheat. It has a label that it's lactose free (hello, what?? When has dairy ever been in a tortilla?) Just, ugh. If they can add that label then why can't they just say something is gluten free or not? I did eat some of the tortillas and didn't notice any symptoms but I'm just not sure if it's safe. So I'll probably have to let my family eat them and stick with Milagro. There is way too much uncertainty with this but I guess you just have to stick with the clearly labeled products? I am still learning!
    • tiffanygosci
      Thank you all for sharing your experiences! And I am very thankful for that Thanksgiving article, Scott! I will look into it more as I plan my little dinner to bring with on the Holiday I'm also glad a lot of research has been done for Celiac. There's still a lot to learn and discover. And everyone has different symptoms. For me, I get a bad headache right away after eating gluten. Reoccurring migraines and visual disturbances were actually what got my PCP to order a Celiac Panel. I'm glad he did! I feel like when the inflammation hits my body it targets my head, gut, and lower back. I'm still figuring things out but that's what I've noticed after eating gluten! I have been eating gluten-free for almost two months now and haven't had such severe symptoms. I ate a couple accidents along the way but I'm doing a lot better
    • trents
      @Mari, did you read that second article that Scott linked? It is the most recently date one. "Researchers comparing rates of headaches, including migraines, among celiac patients and a healthy control group showed that celiac subjects experienced higher rates of headaches than control subjects, with the greatest rates of migraines found in celiac women.  Additionally, celiacs had higher rates of migraine than control subjects, especially in women. In fact, four out of five women with celiac disease suffered from migraines, and without aura nearly three-quarters of the time."
    • Mari
      As far as I know and I have made severalonline searches, celiac disease disease has not been recognized as a cause of migraines or any eye problems. What I wrote must have been confusing.
×
×
  • 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.