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

Wheat Starch


chrissy

Recommended Posts

chrissy Collaborator

after someone on here asked about finding tritamyl flour, i did a little research on wheat starch. i found some articles on celiac.com that say studies have been done that show wheat starch does not harm a celiac. some of the info on wheat starch comes from other countries, who are supposed to be ahead of the USA in celiac research, and they are allowing the use of wheat starch in a celiac's diet. why are we different here in the USA?

i know i have seen many people say the USA is behind in celiac research, but i also see people who would never dream of including wheat starch in their diet-----maybe these are not the same people sayaing this?

is there anyone that has consumed products with wheat starch and then had follow up blood work done?


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor
after someone on here asked about finding tritamyl flour, i did a little research on wheat starch. i found some articles on celiac.com that say studies have been done that show wheat starch does not harm a celiac. some of the info on wheat starch comes from other countries, who are supposed to be ahead of the USA in celiac research, and they are allowing the use of wheat starch in a celiac's diet. why are we different here in the USA?

i know i have seen many people say the USA is behind in celiac research, but i also see people who would never dream of including wheat starch in their diet-----maybe these are not the same people sayaing this?

is there anyone that has consumed products with wheat starch and then had follow up blood work done?

I would not touch wheat starch with someone else's hand but with that being said I believe, and this is only my opinion folks, that in the US it takes so very long to diagnose us while they hand us pills and tell us we need therapy that we in the US end up being much more sensitive than folks in countries where they routinely screen or where diagnosis takes an average of 2 to 3 weeks rather than 10 to 15 years.

pamelaD Apprentice

Technically the wheat protein (giladin- what we react to) can be separated from the wheat starch. I am sure it is a similar process to making corn starch (separating the starch component from the protien, fat) and tapioca starch, etc...

My concern would be the same in any manufacturing process - cross contamination. We don't care if corn or tapioca starch might be contaminated with trace amounts of corn or tapioca protiens because we do not react to them.

So I would demand gluten testing or some sort of assurance from the manufacturer before I would try it.

Pam

aikiducky Apprentice

Also not all wheat starch is made equal. The wheat starch that is used in SOME gluten-free products here in Europe is specifically made to contain gluten only under a certain norm. NOT all european products containing wheat starch are in this category, just the ones that use the wheat starch that is "pure" enough. Even so, not all european celiacs (including me) eat wheat starch, and if people don't improve on a gluten-free diet containing wheat starch they are adviced not to eat it anymore. Oh, and people are usually warned not to eat "too many" wheat starch containing products in one day. Where you draw the line though is what I always wonder...

Personally I think it's a bit crazy to try and continue eating wheat in any shape or form but apparently lots of people over here do keep eating wheat starch products, and I assume at least some of them are being monitored by a doctor, too, to see that their antibodies don't go up... :D

Pauliina

Ursa Major Collaborator

I myself wouldn't eat wheat starch. Even though they are ahead in Europe on testing and diagnosing people with celiac disease, I think they are behind in that with them being gluten-free doesn't mean being 100% gluten-free, because of their codex alimentarius, allowing products being labelled gluten-free that still contain small amounts of gluten.

Many professionals also think that wheat germ oil doesn't contain gluten and won't be harmful. But I've found that I react badly to it.

So, I guess it's everybody's own decision what they want to believe, and if they want to risk it.

jerseyangel Proficient

I know I reacted to wheat starch--and I didn't even eat it!

It was an ingredient in some hair gel I was using before I knew better--I tend to bite my fingernails when I'm anxious, and I glutened myself that way. The mystery afternoon gluten episodes ended once I tossed the hair gel.

KaitiUSA Enthusiast

Stay completely away from it.


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



Celiac.com Sponsor (A8-M):



Ruth52 Newbie

I stay clear of products that contain wheat starch. I know that i reacted to marshmellows and the only ingredient on the packet that was suspicious was the wheat starch.

gfp Enthusiast

Lets put this straight.....

Firstly wheat starch is usually produced by washing the grain in water.

Starch is soluble and gluten and glutamine are not ..... except there is really no such thing as not.

So parts of the gluten are carried intot he product BUT since the gluten is "non-toxic" noone cares (except us)

The scientific way this is described is by partition coefficients....

That is say you have a product (gluten) it has at a certain temperature and pressure a partition coefficient between water and alcohol. So if you add a mix and the partition coeff is .9 water/alcohol then 10% of it will go into the alcohol.

If you then take the same refined product and do it again then again 10% of the 10% (=1%) will be left and a 3rd time only 0.1% ....

Commercially starch and proteins from gains are seperated using either:

1) alkalia reduction .... this is highly efficient but destroys the gluten making it unsellable as a byproduct.

2) The Martin process: pretty much as described

This process has been in use since the 1920s and is still in use today. It is based on

the principle of forming a dough (made by mixing flour with ~85% of its weight in

water) and then washing the starch out of the dough. This is better than the alkali

process as it prevents the protein from being damaged, allowing it to be recovered

and sold as a by-product. Another advantage is that it is a much cheaper process to

run, since it uses water instead of an alkali.

Washing creates a ‘milk’ which is processed in centrifuges to extract the starch,

further washing purifies the product and produces a ‘starch cake’ recoverable at

the output. In general 60% of the weight of flour will be recovered as high-grade

starch and a further 15% can be recovered as second-grade starch (by hydrocylone

concentration). High grade starch is defined by higher percentage of large granule

starch, lower liquid content, lower protein content and a lower content of

impurities, compared to the lower grade starch.

The protein (gluten) can be dried and sold for use as an additive to foodstuffs.

3/ The 'batter process'

This process has been in use since the 1920s and is still in use today. It is based on

the principle of forming a dough (made by mixing flour with ~85% of its weight in

water) and then washing the starch out of the dough. This is better than the alkali

process as it prevents the protein from being damaged, allowing it to be recovered

and sold as a by-product. Another advantage is that it is a much cheaper process to

run, since it uses water instead of an alkali.

Washing creates a ‘milk’ which is processed in centrifuges to extract the starch,

further washing purifies the product and produces a ‘starch cake’ recoverable at

the output. In general 60% of the weight of flour will be recovered as high-grade

starch and a further 15% can be recovered as second-grade starch (by hydrocylone

concentration). High grade starch is defined by higher percentage of large granule

starch, lower liquid content, lower protein content and a lower content of

impurities, compared to the lower grade starch.

The protein (gluten) can be dried and sold for use as an additive to foodstuffs.

4/ Alpha-Laval decantation

So you can wash wheat in water (basically what all these processes do) and end up with say 95% pure starch (this is normal wheat starch) BUT and now we hit the madness this is all wrapped up in a definition by the WHO's agriculture and food commision .... which is funded and run by ... the food industry.

Since the alkali process destroys gluten which can be sold its not much used!

Now according to this when they first defined gluten free they decided on a "practical" limit. This limit was determined not in any medical way BUT by the industry over what was cheapest.

Then the industry went away and did tests... they said food under 200ppm would be tested on celiacs and they went off and did tests to prove this did no damage.

If this was my job here is how i would prove it ....

I would take wheat starch that conforms with the CODEX <200ppm (actually though that includes the harmelss glutamine portion as well as the gliadin portion....)

I would then purify this so that it had only 1 ppb (billion) gliadin because 1ppb is still less than 200 ppm and so it cheats the test definition which I invented specifically to be cheated.

I would then run the tests and say that within statistical error CODEX wheat starch did no damage.

No need to publish that you actually used 1ppb not 200ppm you just keep saying <200ppm.

So this is cool right.... 1 ppb means that the chance of any one celaic receiving this molecule is really small....and you can still say it was wheat starch according to CODEX and contained <200ppm....

You can even do studies and add 198 ppm glutamine and say its was 200 ppm total nitrogen dry matter (the definition)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,964
    • Most Online (within 30 mins)
      7,748

    Cbear
    Newest Member
    Cbear
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.