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

Citric Acid


Karina

Recommended Posts

Karina Explorer

This is in a lot of things, so it is important to know. Has anyone heard this is NOT always gluten-free? Someone told me today that they have a friend who cannot have citric acid as it is sometimes from a gluten-containing source. This was news to me. Anyone heard about this?

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



celiac3270 Collaborator

Citric acid is always fine.....

Maybe since this wasn't the actual celiac, but a friend, it was a different ingredient? If you check the ingredient list, too, citric acid won't be there. It's fine.

Link to comment
Share on other sites
KaitiUSA Enthusiast

If you have trouble with citric acid it do not think it would not be a celiac issue because as celiac3270 said citric acid is fine. I've never heard of it being a problem in the US...outside of the US I'm not sure.Hope this helps you out a bit :D

Link to comment
Share on other sites
tarnalberry Community Regular

I've never heard of citric acid being a problem due to gluten.

It can sometimes be a problem for those who are CORN sensitive, because it can often be derived from corn.

Link to comment
Share on other sites
seeking-wholeness Explorer

I think outside the US citric acid is often derived from wheat (since corn is pretty much an American crop), so if the food was imported there might be a problem. I keep having problems with artichoke hearts imported from Spain--but I can't find any that are packed in the US to compare them with!

--Sarah

Link to comment
Share on other sites
flagbabyds Collaborator

I have never heard of it in the US being a problem, I wouldn't know outside the US of course...

Link to comment
Share on other sites
girlygirl Newbie

As a matter of fact citric acid is a problem. Citric acid many times contains MSG which is off limits to many celiacs. MSGmyth.com and truthinlabeling.org are excellent sites that will give you a wealth of information on how msg is hidden in your foods. I recently had a rash that would not go away (good old comming back DH), I was very perplexed as to how I getting gluten since my diet has very little room for improvemnt. I found that citric acid was in my vitamins and calcium supplements. I found that the butter I porchased from Whole Foods (thier own brand) contained annatto. I also found out the the TAZO Zen tea I was drinking was not considered gluten free after calling the manufacturer to question what the spices on the label were all about. So unfortunately it gets very tricky these days!! :o

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



lovegrov Collaborator

Once again, MSG is NOT off-limits to people with celiac. This is just flat-out wrong.

richard

Link to comment
Share on other sites
KaitiUSA Enthusiast

Yes Richard again is correct. MSG is NOT off limits to celiacs. And I have never known citric acid to be a problem in the US.

Link to comment
Share on other sites
2new2celiacs Newbie

I would be very surprised if citric acid was truly harmful to celiacs. :huh: I am a Mountain Dew fanatic and it so happens to contain citric acid. Although, I know it is one of the worst sodas out there for my body's sake :( , I have never had any reaction what so ever. Also, my dietician made it very clear that this was indeed safe for me to consume.

Link to comment
Share on other sites
KaitiUSA Enthusiast

Citric acid is fine in the US and I have never had a reaction to anything with citric acid in it.

2new2celiacs-I'm a mountain dew fanatic too and I never had a reaction either and I am pretty sensitive now

MSG is fine in the US as well.

http://www.enabling.org/ia/celiac/sn/spnk9804.html

Here is a link that has a section near the bottom about MSG.

Link to comment
Share on other sites
Guest gillian502

I also wanted to mention that as far as I know, Annato is also fine. I know there has been some dispute over annato in the past, but as far as I know it is now known to be ok. Am I wrong on this?

Link to comment
Share on other sites
lovegrov Collaborator

Annatto is gluten-free. No question.

richard

Link to comment
Share on other sites
girlygirl Newbie

On celiac.com it is stated "Soy and Msg are examples of products that many celiacs have trouble with". I have been reading over and over again that MSG is a problem. Not only is it a problem for celiacs but it is a problem for many people. MSG is not in any way shape or form healthy. Just because something is gluten free doesn't mean that it is always healthy i.e. soda, ice cream,cake, cookies, candy bars, potato chips, etc....

On allergiesabout.com:

On celiac/gluten intolerance;

"Other key words to watch for are farina, flour, caramel coloring, enriched flour, cereal, malt flavoring and extracts, MSG, modified food starch, emulisfiers, stabilizers, distilled vinegar, semolina, durum and tritcale".

It seems like many celiacs are asking about some of these ingredients that I have responded to because they may have already had a reaction or suspected something about the additive. I know that NOT everyone will experience a reaction but to just plain say that MSG is not a problem for celiacs at all is not the case.

Link to comment
Share on other sites
KaitiUSA Enthusiast

Wheat and gluten can be hidden under alot of things yes . MSG most of the time in the US is derived from corn and is therefore NOT off limits to celiacs.

MSG is bad for you altogether it is not healthy. It's not good for anyone but many celiacs are in fact fine with it because it is derived from corn. It can be derived from wheat and that is mostly seen outside of the US.

Soy is also fine for Celiacs unless you are allergic to soy.

Some people very well may have a problem with MSG but not all of celiacs do...as far as I know a majority actually don't have a reaction.

As for citric acid..this article has a bunch of ingredients..citric acid being listed as gluten free.

http://www.glutenfreeliving.com/ingredients.htm

Link to comment
Share on other sites
lovegrov Collaborator

From my experience most people with celiac have no problem with MSG. Some do.

There's absolutely nothing wrong with suggesting that somebody who is having a problem might want to cut out MSG and then explain why. But your first posts clearly said ALL people with celiac needed to avoid MSG ALL the time, as if MSG had gluten or made all celiacs sick. And this simply is not true. We have enough problems with our diet without adding false alarms. Soy does indeed bother some people, but most ewith celiac have no trouble at all with it.

"On allergiesabout.com:

On celiac/gluten intolerance;

"Other key words to watch for are farina, flour, caramel coloring, enriched flour, cereal, malt flavoring and extracts, MSG, modified food starch, emulisfiers, stabilizers, distilled vinegar, semolina, durum and tritcale".

If this is the kind of information this site is distributing, I wouldn't trust it. We've know now for more than three years that distilled vinegar is not a problem. Caramel coloring in the U.S. is not a problem and it probably isn't anywhere else. Emulsifiers and stabilizers also shouldn't be a problem.

richard

Link to comment
Share on other sites
tom Contributor

Certainly the msg and annatto comments may have been overstated, tho girlygirl's " . . . .MSG which is off limits to many celiacs" REALLY only says "many celiacs", not all.

While i don't know how many is many, i DO know that i'm one celiac w/ a problem w/ annatto coloring and/or annatto. I've read plain annatto may be fine while 'annatto coloring' isn't and i haven't tested myself for that. Annatto Coloring gives me symptoms almost as bad as gluten.

FYI: i am NOT claiming that these have gluten. Just that it's not uncommon for celiacs to have problems w/ them.

Link to comment
Share on other sites
lovegrov Collaborator

You are right that on this thread girlygirl said "some" celiacs. But she posted the same info on about four threads and on some of those she said things like msg is a "big NONO" for celiacs (not "some" celiacs") and "it is not safe for celiacs to eat." Her posts made it sound like MSG is chock full of gluten. It's not.

As I pointed out to her, there's absolutely nothing wrong with telling people about her experience with MSG and suggesting that they might want to see whether they are also sensitive to it. There's nothing wrong with her campaigning against MSG as not being good for people in general. But I think you need to be perfectly clear this is separate from the gluten issue. She did not and I was trying to clear it up. Apparently I offended her in the process. For that I'm sorry.

richard

Link to comment
Share on other sites
mommida Enthusiast

It's just another issue about grammar then?

I personally have noticed problems with msg and annatto.

Maybe the best way to give advice about those ingredients would be...

They are listed as gluten free in the u.s.,

if you are unsure, check with the manufacturer

keep a food diary, if you notice a particular ingredient causes problems, research into that ingredient, and DON"T EAT IT!

There are products out on the market that people (Celiac or not) should reasearch further. Artificial sweeteners, msg, carrageenan, and others have had negative reports.

Laura

Link to comment
Share on other sites
lovegrov Collaborator

Post removed by author

Link to comment
Share on other sites
mommida Enthusiast

All right then not a grammer issue, but not worded the way you feel comfortable with. (That is my best attempt at staying politically correct.) Some or all? Big difference. How many is many? "As if" or like?

Let's just get to the point. We are here to share information. The words that are used to convey our thoughts need to be chosen carefully. Some of the posts are starting to have an edge to them.

Richard,

I think you took my post as a personal post to you. It was not. I read her(girlygirl) post, and thought it was just an added concern about MSG. Your post was very clear, you think people could get the wrong message from that post. You stated clearly, MSG is gluten free. Citric acid is gluten free.

This is my opinion...

I wanted to add, if there is an ingredient you react to, don't consume it. It doesn't have to have gluten in it for a person to have a reaction to it. That's why someone might be on this website looking for information. They are reacting to something that is gluten free and want to know why.

Laura

Link to comment
Share on other sites
Donna F Enthusiast

Edited to put in separate thread......

Link to comment
Share on other sites
lovegrov Collaborator

Laura,

My apologies for being testy and taking it personally. I read too fast and it was dumb of me. Yesterday was a bad day and I should have just quit posting. I've taken that post down.

richard

Link to comment
Share on other sites
mommida Enthusiast

It must have been a bad day, that is not like you.

Hope you are feeling better today.

Warmest wishes, (since it's freezing here in Mi.)

Laura

Link to comment
Share on other sites
  • 3 weeks later...
Lynne Billington Newbie

:unsure: Over on Celiacforums.com they're saying citric acid CAN be a problem. That it can be made from mold grown on bread. And there's a link over there that I went and read because my husband had a reaction this weekend from a store brand strawberry jam and that's the ONLY thing in it that could have done it.

This is getting way too confusing for me. My husband's reaction is mouth ulcers and he was doing so good and now for the last week, he just has this horribly painful mouth that we can't seem to get under control. I'm lost! :angry:

Link to comment
Share on other sites

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now
  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Nacina's topic in Related Issues & Disorders
      1

      14 year old with Celiac & EOE still suffering...

    2. - Nacina posted a topic in Related Issues & Disorders
      1

      14 year old with Celiac & EOE still suffering...

    3. - trents replied to Fluka66's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      5

      Waiting for urgent referral.

    4. - Fluka66 replied to Fluka66's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      5

      Waiting for urgent referral.

    5. - Moodiefoodie replied to Moodiefoodie's topic in Related Issues & Disorders
      9

      Joint swelling when ill even on gluten-free diet


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,064
    • Most Online (within 30 mins)
      7,748

    abrooks91
    Newest Member
    abrooks91
    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

    • 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.
    • Nacina
      Hello, I am a 45 year old mom, who was diagnosed at 29 with Celiac. My now 14 year old son was diagnosed just before his 4th birthday. Needless to say, we are old pros with the diet. He was experiencing some issues, overall health took a major plummet a year ago, and through a bit of work, was diagnosed with EOE. Tried diet alone, but his follow up endoscopy didn't show the improvements his DR. wanted to see, so I tried the medication. (Steroid). He became extremely backed up, and they had him taking Miralax daily. His health plummeted. He is a straight A honor's 8th grader who plays club soccer very competitively. His health continued to decline and at 13 had a colonoscopy and another upper gi. (He was still compacted even with the prep). I finally pulled him off all meds and mira lax, after reading much negative literature online, and put him on a gut detox diet and took him to a nutrition response dr. Finally things have improved. However...over a year later and he is having relapse stomach pain, debilitating stomach pain. Missing a day of school a week, to three this week. This is where we downward spiral with him. He says it doesn't feel the same as when he has gotten backed up before. He is eating prunes, taking his supplements, drinking water...all of the things. Yet, he is feeling horrible. Pain is abdomen, headache, lethargy, diarrhea . He is on a strict gluten dairy, egg free diet. He has adapted well in regards to diet. But I feel like we are missing something here. He is too active, too outgoing to be feeling sick all of the time. His Bilirubin is constantly high. His white blood count always runs slightly low. His vitamin D was very low last time he ran tests, (last month) when he was sick for a week. His celiac markers show negative, so it isn't that. His last endoscopy showed no Eosinaphils in his esophagus.  I have taken him to multiple Ped. Gastro specialists. They run tests, and we get zero answers. I meticulously go through labs, hoping to make some sense and maybe catch something. Any thoughts or ideas would greatly be appreciated. 
    • trents
      But if you have been off of wheat for a period of weeks/months leading up to the testing it will likely turn out to be negative for celiac disease, even if you actually have celiac disease. Given your symptoms when consuming gluten, we certainly understand your reluctance to undergo  the "gluten challenge" before testing but you need to understand that the testing may be a waste of time if you don't. What are you going to do if it is negative for celiac disease? Are you going to go back to merrily eating wheat/barley/rye products while living in pain and destroying your health? You will be in a conundrum. Do I or do I not? And you will likely have a difficult time being consistent with your diet. Celiac disease causes inflammation to the small bowel villous lining when gluten containing grains are consumed. This inflammation produces certain antibodies that can be detected in the blood after they reach a certain level, which takes weeks or months after the onset of the disease. If gluten is stopped or drastically reduced, the inflammation begins to decrease and so do the antibodies. Before long, their low levels are not detectable by testing and the antibody blood tests done for diagnosing celiac disease will be negative. Over time, this inflammation wears down the billions of microscopic, finger-like projections that make up the lining and form the nutrient absorbing layer of the small bowel where all the nutrition in our food is absorbed. As the villi bet worn down, vitamin and mineral deficiencies typically develop because absorption is compromised. An endoscopy with biopsy of the small bowel lining to microscopically examine this damage is usually the second stage of celiac disease diagnosis. However, when people cut out gluten or cut back on it significantly ahead of time before the biopsy is done, the villous lining has already experienced some healing and the microscopic examination may be negative or inconclusive. I'm not trying to tell you what to do I just want you to understand what the consequences of going gluten free ahead of testing are as far as test results go so that you will either not waste your time in having the tests done or will be prepared for negative test results and the impact that will have on your dietary decisions. And, who are these "consultants" you keep talking about and what are their qualifications? You are in the unenviable position that many who joint this forum have found themselves in. Namely, having begun a gluten free diet before getting a proper diagnosis but unwilling to enter into the gluten challenge for valid testing because of the severity of the symptoms it would cause them.
    • Fluka66
      Thank you very much for your reply. I hadn't heard of celiac disease but began to notice a pattern of pain. I've been on the floor more than once with agonising pain but this was always put down to another abdominal problem consequently I've been on a roundabout of backwards and forwards with another consultant for many years. I originally questioned this diagnosis but was assured it was the reason for my pain. Many years later the consultant gave up and I had a new GP. I started to cut out certain food types ,reading packets then really started to cut out wheat and went lactose free. After a month I reintroduced these in one meal and ended screaming in agony the tearing and bloating pain. With this info and a swollen lymph node in my neck I went back to the GP.  I have a referral now . I have also found out that acidic food is causing the terrible pain . My thoughts are this is irritating any ulcers. I'm hoping that after a decade the outlook isn't all bad. My blood test came back with a high marker but I didn't catch what it was. My GP and I have agreed that I won't go back on wheat just for the test due to the pain , my swollen lymph node and blood test results.  Trying to remain calm for the referral and perhaps needed to be more forceful all those years ago but I'm not assertive and consultants can be overwhelming. Many thanks for your reply . Wishing you all the best.
    • Moodiefoodie
      Wow! Fascinating info. Thanks so much! I really appreciate the guidance. @Spacepanther Over the years I have had rheumatologists do full lab work ups on me. They told me they had screened me for arthritis, lupus, and Lyme disease (all negative). In addition to joint pain and stiffness I had swelling in both knees that later moved to my elbow as well.  I also experience stiffness and pain in my neck and shoulders when it flares. I vomited fairly often growing up, but there wasn’t a real pattern to it and I didn’t know it wasn’t normal (thought people caught stomach viruses often).  I don’t usually have stomach symptoms immediately after eating gluten that I notice.  The only other joint condition I know of is fibromyalgia. Good luck! Hope you can get it figured out. I only assumed my joint symptoms were due to the celiac’s because it is under control for the most part on a gluten-free diet.  The rheumatologist also mentioned that some inflammatory/autoimmune diseases can be slow-moving and not detectable until they progress.
×
×
  • Create New...