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

High Inflammation Markers


ysali

Recommended Posts

ysali Rookie

Hello all,

I was diagnosed with celiac a few months ago and have been on a strict gluten free diet since then. One of my initial symptoms that led to testing was elevated inflammatory markers discovered during blood tests. 

My three month follow up was last week and I had just gone through a really bad reaction after some unfortunate cross-contamination from froyo (102.7 fever and severe diarrhea) which concerned my doctor so she ordered some more blood tests and allergy panels. She is now ordering a stool test because the inflammation markers are still extremely high and they have been unable to find a cause and the receptionist told me that if they found nothing in the stool I'd have to go see a rheumatologist. The blood work also showed celiac markers which I assume was due to the cross contamination so I was reminded to follow a strictly gluten free diet. 

Has anyone else dealt with elevated inflammation markers or could it possibly be the gluten ingestion that's causing inflammation? 

I of course am freaking out and probably will be until these results come in - unless of course I have to see a rheumatologist.

Thanks! 


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



Celiac.com Sponsor (A8-M):



Ennis-TX Grand Master

I have been on a strict gluten free diet for over 3 years, I still had severe inflammation markers and inflamed intestines on my last check up. Seems I also had Ulcerative Colitis, which was reacting to other foods which was diagnosed at that time.  Not had it checked since my new ketogenic diet and some meds they got me on to get it back down.   The fever might be a allergic reaction to something? I never got a fever with gluten exposure, but I always run a 99-103F fever with corn which I am highly allergic to. I also get bleeding, and blood blisters in my digestive tract when exposed to corn, I would imagine it causes extensive inflammation.  Wish you luck in finding out the cause in your case.

ysali Rookie
5 hours ago, Ennis_TX said:

I have been on a strict gluten free diet for over 3 years, I still had severe inflammation markers and inflamed intestines on my last check up. Seems I also had Ulcerative Colitis, which was reacting to other foods which was diagnosed at that time.  Not had it checked since my new ketogenic diet and some meds they got me on to get it back down.   The fever might be a allergic reaction to something? I never got a fever with gluten exposure, but I always run a 99-103F fever with corn which I am highly allergic to. I also get bleeding, and blood blisters in my digestive tract when exposed to corn, I would imagine it causes extensive inflammation.  Wish you luck in finding out the cause in your case.

I know I'm probably over-reacting because I'm an obsessive googler which I know does more harm than good since it just makes me even more worried but it's a habit I can't seem to break.

The fever was one of the red flags that caused me to go to the GI in the first place. I'd be in the bathroom for 2-3 hours a few nights out of the week and it would end with me curled in bed with 101+ fever. I read somewhere that it's your body responding to the gluten you've ingested but who knows. My doctor did rule out Familial Mediterranean Fever just to be sure it wasn't coming from that and my colonoscopy came back clear so she ruled out UC, Crohns, and other things related to that. 

The fact that I got two sick two nights in a row after eating the fro-yo and then a gluten-free cheesecake I made worried her so she did some food allergy panels that all came back normal. I am lactose intolerant but taking a lactose pill or two handles that pretty well.

Something tells me that I'm consistently ingesting gluten due to shared kitchen space so I'm working on finding a solution to that which has proven to be difficult. I'm honestly hoping that this is what's causing the elevated markers because my family has a history of lupus, rheumatoid arthritis, UC, IBS, and lymphoma. 

MelMel Newbie

From some other posts I've read, Iodine in food is also a culprit.

 

Ennis-TX Grand Master
1 hour ago, ysali said:

I know I'm probably over-reacting because I'm an obsessive googler which I know does more harm than good since it just makes me even more worried but it's a habit I can't seem to break.

The fever was one of the red flags that caused me to go to the GI in the first place. I'd be in the bathroom for 2-3 hours a few nights out of the week and it would end with me curled in bed with 101+ fever. I read somewhere that it's your body responding to the gluten you've ingested but who knows. My doctor did rule out Familial Mediterranean Fever just to be sure it wasn't coming from that and my colonoscopy came back clear so she ruled out UC, Crohns, and other things related to that. 

The fact that I got two sick two nights in a row after eating the fro-yo and then a gluten-free cheesecake I made worried her so she did some food allergy panels that all came back normal. I am lactose intolerant but taking a lactose pill or two handles that pretty well.

Something tells me that I'm consistently ingesting gluten due to shared kitchen space so I'm working on finding a solution to that which has proven to be difficult. I'm honestly hoping that this is what's causing the elevated markers because my family has a history of lupus, rheumatoid arthritis, UC, IBS, and lymphoma. 

Tips here, get a fold out table for your own prep space/safe zone.  Or use freezer/butcher paper on your prep surface. Get dedicated cook ware, if your cheap or in budget, I suggest getting nordicware microwave cook ware for omlettes, eggs, steamer, etc. so you can cook in a microwave and get a cheap counter top one of your own. I would also say get one of these combo rice cooker/crockpot/preasurecooker combo applaiance, great for soups, stews, roast, rice, riscotto, etc. You can use crockpot liners to be extra careful. Keep all your own food on the top shelfs, or on a dedicated table/organzier.  I was drove nuts living in a shared house and got my own dedicated gluten-free living space. and allergen free. Would have killed me staying in previous environment.

knitty kitty Grand Master

Hello, 

I think the problem might be your dairy consumption, Ysali.  Celiac Disease results in damaged villi in the small intestine. The damaged villi can't absorb nutrients well, and they can't produce digestive enzymes that break down the sugars in milk. Taking lactose pills may help break down the milk sugars a little, but the protein in dairy products, casein, can elicit a reaction just as if you've eaten gluten.  You may want to consider going dairy free for several months in order to give your body time to heal.  You may be able to reintroduce dairy after you've healed more. 

Open Original Shared Link

 

Celiac Disease causes malabsorption which results in malnutrition.  Damaged intestines can't absorb nutrients.  One frequently deficient vitamins is Vitamin D.  

Vitamin D is extremely important in regulating inflammation in the body.  

Open Original Shared Link

Your doctor may prescribe D 2 (synthetic) if you're low, but D 3 is the most bioavailable form.  

Other vitamins that help with inflammation are discussed in this article.

Open Original Shared Link

B vitamins are very important.  They all work together, so if you're low on one, supplementing them all would ensure proper functionality of each.

Open Original Shared Link

 

I hope this helps us all on our journey towards health.

 

 

 

sdlane Rookie

By inflammation marker, do you mean the C-reactive protein CRP test?  Mine dropped from 17 to 10 when I went gluten-free.  Acute inflammation is 5.  I demanded a referral to an allergist because I'm super gluten-free strict, but I was still feeling terrible.  Turns out I'm allergic to almost everything but wheat.  Go figure.  A severe reaction to peanuts, oats and almonds is the worst!  I travel a lot for work and those are my usual go-to items when I'm not at home.  With all that being said, have you tested for allergies that might be increasing your systemic inflammation?


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



Celiac.com Sponsor (A8-M):



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 lizzie42's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      6

      Son's legs shaking

    2. - lizzie42 replied to lizzie42's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      6

      Son's legs shaking

    3. - knitty kitty replied to lizzie42's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      6

      Son's legs shaking

    4. - lizzie42 replied to lizzie42's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      6

      Son's legs shaking

    5. - Scott Adams replied to Russ H's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Anti-endomysial Antibody (EMA) Testing

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

    • Total Members
      132,870
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • knitty kitty
      Blood tests for thiamine are unreliable.  The nutrients from your food get absorbed into the bloodstream and travel around the body.  So, a steak dinner can falsely raise thiamine blood levels in the following days.  Besides, thiamine is utilized inside cells where stores of thiamine are impossible to measure. A better test to ask for is the Erythrocyte Transketolace Activity test.  But even that test has been questioned as to accuracy.  It is expensive and takes time to do.   Because of the discrepancies with thiamine tests and urgency with correcting thiamine deficiency, the World Health Organization recommends giving thiamine for several weeks and looking for health improvement.  Thiamine is water soluble, safe and nontoxic even in high doses.   Many doctors are not given sufficient education in nutrition and deficiency symptoms, and may not be familiar with how often they occur in Celiac disease.  B12 and Vitamin D can be stored for as long as a year in the liver, so not having deficiencies in these two vitamins is not a good indicator of the status of the other seven water soluble B vitamins.  It is possible to have deficiency symptoms BEFORE there's changes in the blood levels.   Ask your doctor about Benfotiamine, a form of thiamine that is better absorbed than Thiamine Mononitrate.  Thiamine Mononitrate is used in many vitamins because it is shelf-stable, a form of thiamine that won't break down sitting around on a store shelf.  This form is difficult for the body to turn into a usable form.  Only thirty percent is absorbed in the intestine, and less is actually used.   Thiamine interacts with all of the other B vitamins, so they should all be supplemented together.  Magnesium is needed to make life sustaining enzymes with thiamine, so a magnesium supplement should be added if magnesium levels are low.   Thiamine is water soluble, safe and nontoxic even in high doses.  There's no harm in trying.
    • lizzie42
      Neither of them were anemic 6 months after the Celiac diagnosis. His other vitamin levels (d, B12) were never low. My daughters levels were normal after the first 6 months. Is the thiamine test just called thiamine? 
    • knitty kitty
      Yes, I do think they need a Thiamine supplement at least. Especially since they eat red meat only occasionally. Most fruits and vegetables are not good sources of Thiamine.  Legumes (beans) do contain thiamine.  Fruits and veggies do have some of the other B vitamins, but thiamine B 1 and  Cobalamine B12 are mostly found in meats.  Meat, especially organ meats like liver, are the best sources of Thiamine, B12, and the six other B vitamins and important minerals like iron.   Thiamine has antibacterial and antiviral properties.  Thiamine is important to our immune systems.  We need more thiamine when we're physically ill or injured, when we're under stress emotionally, and when we exercise, especially outside in hot weather.  We need thiamine and other B vitamins like Niacin B 3 to keep our gastrointestinal tract healthy.  We can't store thiamine for very long.  We can get low in thiamine within three days.  Symptoms can appear suddenly when a high carbohydrate diet is consumed.  (Rice and beans are high in carbohydrates.)  A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function, so symptoms can wax and wane depending on what one eats.  The earliest symptoms like fatigue and anxiety are easily contributed to other things or life events and dismissed.   Correcting nutritional deficiencies needs to be done quickly, especially in children, so their growth isn't stunted.  Nutritional deficiencies can affect intelligence.  Vitamin D deficiency can cause short stature and poor bone formation.   Is your son taking anything for the anemia?  Is the anemia caused by B12 or iron deficiency?  
    • lizzie42
      Thank you! That's helpful. My kids eat very little processed food. Tons of fruit, vegetables, cheese, eggs and occasional red meat. We do a lot of rice and bean bowls, stir fry, etc.  Do you think with all the fruits and vegetables they need a vitamin supplement? I feel like their diet is pretty healthy and balanced with very limited processed food. The only processed food they eat regularly is a bowl of Cheerios here and there.  Could shaking legs be a symptom of just a one-time gluten exposure? I guess there's no way to know for sure if they're getting absolutely zero exposure because they do go to school a couple times a week. We do homeschool but my son does a shared school 2x a week and my daughter does a morning Pre-K 3 x a week.  At home our entire house is strictly gluten free and it is extremely rare for us to eat out. If we eat at someone else's house I usually just bring their food. When we have play dates we bring all the snacks, etc. I try to be really careful since they're still growing. They also, of course, catch kids viruses all the time so I  want to make sure I know whether they're just sick or they've had gluten. It can be pretty confusing when they're pretty young to even be explaining their symptoms! 
    • Scott Adams
      That is interesting, and it's the first time I heard about the umbilical cord beings used for that test. Thanks for sharing!
×
×
  • 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.