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

How Long Is Gluten Detectable In Your Skin Or Blood After You Go gluten-free?


crazyitch

Recommended Posts

crazyitch Newbie

I just have a quick question for anybody here who may have an answer or some information.  I am wondering how long it takes of being gluten free for the gluten not to show up in skin/blood tests done by a dermatologist?  I have read much in here about gluten challenges and they say you have to be on gluten for minimum 2 months for it to be detected in testing but I haven't seen anything about how long you need to be gluten free in order for the result to be negative.  I ask because I have been gluten free for almost 3 weeks (I may have had some contamination as I haven't seen much improvement yet) but I am wondering if I will already show negative if he decides to do testing?  My appointment is in 6 days. Thanks in advance for any information on this......

 

Elaine


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

I know it can takes weeks or months to get antibodies down. But, if you don't have a lot of antibodies, a few weeks gluten-free can make a difference. For the skin biopsy, you need a fresh lesion. Not sure if you are still getting them gluten-free?

Open Original Shared Link

I stopped eating gluten right before my blood screening. Will that impact my results?

To get the most accurate screening results, we recommend 12 weeks of daily gluten intake prior to blood testing. If you’ve followed a gluten-containing diet, as recommended, but went gluten-free a few days prior to your screening, it’s likely that you’ll still see accurate results from your tests.

Open Original Shared Link

How much gluten should be consumed prior to being screened for celiac disease?

It’s best to continue a normal, gluten-containing diet before being screened and diagnosed. If a gluten-free diet has been followed for more than a few weeks, then we recommend eating at least 1 serving of gluten (1/2 slice of bread or a cracker, for example) every day for 12 weeks prior to a blood test and 2 weeks prior to a biopsy. This is often referred to as a “gluten challenge” and should be done under the care of a medical professional.

GottaSki Mentor

If there are active DH lesions, the antibodies can stay in the skin for quite some time.

 

For blood/antibody testing -- it depends.  Generally you will see numbers decrease substantially by 3 or 6 months and be very low by the one year check.

 

There is no reason to re-test blood/antibodies at 3 weeks.  The earliest is 3 months -- many doctors wait until 6 months.

crazyitch Newbie

Thank you for the information.  I am not even sure I have DH, I have had a nasty rash for almost 6 months that sent me to the internet doing my own research which is how I ended up here.  I've had 7 dr's appts and  4 different diagnosis' (3 of the appts only netted me baffled looks from the gps and prescriptions for cream and antihistamines).  I have started a gluten free diet to see if it get any result from it.  I know that it takes quite a while see an improvement so I don't expect much yet.  I just wondered if I would still have gluten in my system.  I will explain it all to the dermatologist and I am sure he will know whether to bother testing or if it is going to be a waste of time

 

Thanks again!

Elaine

powerofpositivethinking Community Regular

ive been super strict about my diet, but I finally entered the weak postive range on my blood tests after about 9 months.  I honestly thought I would be in the negative range because I have hardly eaten out, am very careful about CC and all my personal care products are gluten-free.  Everything is moving in the right direction, so that's the positive :) Hope your appointment goes well!

squirmingitch Veteran

Elaine, I think you're talking about the skin biopsy right? I don't have an exact answer on just how long the skin biopsy can pick up the antibodies but it's not long. Testing is not as sensitive as our skin is sensitive. But here's an answer for you from the U of Chicago Celiac Disease Center re: skin biopsy for dh:

Open Original Shared Link

 

It says:

I’m scheduled to have a skin biopsy to screen for celiac disease, should I maintain a gluten-containing diet similar to those who are being screened via blood or intestinal biopsy?
Yes.
cahill Collaborator

 If you are going to have  any testing for celiacs Do not stop eating gluten until your testing is complete .

 

 

  That said ...

 

 

I had active DH lesions well into my second year gluten free.The fact that I was undiagnosed for an extremely long time and am super sensitive are major factors that contributed to this I am sure .


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



Celiac.com Sponsor (A8-M):



kmag Rookie

I just saw a dermatologist at Women's College Hospital in Toronto three weeks ago and was assured that the antibodies would still be in my skin after three years gluten free.  I had the biopsy done for DH and will get the results on Feb 27.  She was absolutely certain that they stay in your skin for a very long time.  I also read a research article recently that said the average clearing time was close to 12 years.  

cahill Collaborator

I just saw a dermatologist at Women's College Hospital in Toronto three weeks ago and was assured that the antibodies would still be in my skin after three years gluten free.  I had the biopsy done for DH and will get the results on Feb 27.  She was absolutely certain that they stay in your skin for a very long time.  I also read a research article recently that said the average clearing time was close to 12 years.  

Was this article on-line,,, if so could you give me the link I would love to read it . :)

squirmingitch Veteran

I just saw a dermatologist at Women's College Hospital in Toronto three weeks ago and was assured that the antibodies would still be in my skin after three years gluten free.  I had the biopsy done for DH and will get the results on Feb 27.  She was absolutely certain that they stay in your skin for a very long time.  I also read a research article recently that said the average clearing time was close to 12 years.  

I also would love to read this research article.

crazyitch Newbie

Hi Squirming, I am talking about a skin biopsy and maybe blood tests if they do them. I am not sure if I have new lesions, the rash is spreading on my arms and legs and I seem to get the sores from scratching. I dont even know if the itch would break out into sores if I didnt scratch them. Once I have the scabs they get scratched and rescratched because they are so damn itchy. This whole rash is so confusing. It fits many of the DH characteristics but it is definitely not blisters so I am not even sure of what it is. I would rather have a definite answer as to what it is than be left with a another baffled dr and 'stab in the dark' 'spin the bottle' diagnosis. Not knowing leaves me guessing at how to tackle it.

I would also like to read the article mentioned in the previous posts. I am trying to gain as much knowledge and info as I can.

Such a frustrating ailment....grrrrrrrrr

squirmingitch Veteran

I understand Elaine. Please do not get hung up on the blisters part ~~~ that's the same thing derms do & why it's so frustrating. DH doesn't always present as blisters. Um, what you're describing with itchiness speaks for itself ~~~ you can't leave it alone long enough to find out if it will erupt ~~~ I'm betting it would if you could not touch it but you can't & I understand that. I understand you want a solid dx. I know you're frustrated beyond belief. How many different incorrect dx's have you had????? And how many different treatments???? So you know it isn't any of those things.

So go to the derm & if he/she says they will biopsy for dh then go home & eat gluten for 2 months & go back to the derm & get a biopsy. The biopsy is stained with a fluorescent dye & the lab tech looks through a microscope looking for a specific pattern. The lab tech has to know what they're doing & what they're looking for so the doc has to be specific on the orders. This is not something where a piece of litmus paper is stuck in some fluid & it comes out positive or negative. This is subject to human error in interpretation. 

squirmingitch Veteran

I edited my post above so if you had read it, then please read it again.

 

And if the derm takes a biopsy now, then when it comes back negative you will still not have your answer b/c you won't know if it's a false negative or not. And if the derm does a biopsy now & it comes back negative WILL THE DERM AGREE TO DO ANOTHER BIOPSY AFTER YOU HAVE EATEN GLUTEN FOR 2 MONTHS???????

And if you eat gluten for 2 months & then get a dh biopsy ~~~ it would be better to get 2 biopsies & have them sent to different labs so you have 2 techs reading them.

And if you eat gluten for 2 months & you get a celiac blood panel then I hope you are not one of the 60% of us who test false negative on the blood panel.

 

These are the choices. None of us like them. They flat out suck! Every single person on here who does not have one, wishes they had a solid dx. Well, almost everyone. My hubs does not care about a dx by a doc b/c my hubs knows what he has. There may be others who feel the same.

 

And I am again going to give you this link & ask that you read the descriptions of dh that Henry Weightman Stelwagon wrote. 

You will see that not all dh presents as water filled blisters.

https://www.celiac.com/forums/topic/84513-descriptions-of-dh-types/

squirmingitch Veteran

Elaine, I hope you got some kind of answers today. At least something that will help you settle this in your mind & a derm who is knowledgeable. 

crazyitch Newbie

Hi I am back and no definite answers, The dermatologist says she thinks it  looks eczematic.  I had pictures of my tummy and back to show her from when I stopped the prednisone (it was really bad then) just to show her what the flare up looked like. I told her I had seen similar rashes that were caused from gluten sensitivity and was trying the gluten free diet  to see if I saw any improvement.  She said exactly what you thought she would say, that it wasn't on my knees or my scalp etc so it probably wasn't DH. She wanted to know if the lesions come as a result of my scratching or if they are there whether I scratch or not. I said my skin itches and burns with nothing apparent and then I scratch and voila a bleeding sore.  Then that sore takes forever to heal because it continues to itch and be scratched.  She doesn't have an answer as to what it is but said that it appears that my scratching is making it flare more and seems to think that if she can stop the itch that it should clear up. She prescribed more cortisone cream with more antihistamines and seems to feel if I put it on more often that it should work.  She also put me on a diet of lamb, rice, pears, and water....yep that is all I can eat for 2 weeks....no salt, spices, sugar, caffeine, gluten, dairy soy, etc etc.  She only decided on that treatment after I told her I had cut out the gluten, felt like she was 'one upping' my gluten free thing lol.  I have to go back in two weeks and she is going to assess the rash. If it isn't better she said she may try a skin biopsy but says there is nothing really to biopsy.  I am beyond frustrated at this point.  I am not sure what the point of restricting my diet to that degree is all about, she did not elaborate on that.  So I guess all I can say at this point is stay tuned! :unsure:
 
On another note, after the appointment I was at the grocery store (buying the most expensive meat on the planet...yes you guessed it baaaaaaaaaa) and I happened to start talking to a lady who was working there doing food demo's  I told her I couldn't have what she was offering as I was on a restricted diet.  After much Yada yada yada-ing....(she told me her tale of food woes) she suggested a naturopath.  Just wondering if anyone has any thoughts on going that route?  She said the naturopath did blood panels that specifically screen for food sensitivities and deficiencies and after she stopped eating the things the naturopath identified as bad for her, her skin cleared and her migraines stopped. Any thoughts or experience on this would be appreciated.  I live in Canada and our health is universal but doesn't cover naturopaths.  The blood tests are several hundred dollars not sure if that's a good idea or not.  Anyway I am no further ahead at this point except for being out of pocket for lamb chops and betamethasone :unsure:....I will climb back onto my hamster wheel and wait for a response........
 
E

squirmingitch Veteran

I'm so sorry Elaine. :( I had hoped you would get lucky with a derm who knows what's what & at least get some kind of answer or hope of one.

And how many times have people been on this forum who have been to the derm & the derm says they made the rash/lesions come by scratching? I don't even want to count.

The diet she has you on is ensuring nothing you're eating is aggravating your skin. And if it & the creams she gave you work then she will feel all superior & I told you so-ish while conveniently "forgetting" that you've been gluten free & low iodine for an 2 additional weeks. HA! So she has you on a gluten free diet without having to admit she's got you on a gluten free diet. 

 

I can't answer as to a naturopath. I have never been to one. Pricklypear has & maybe she will have some advice for you.

crazyitch Newbie

Has Prickly posted about her experience with the naturopath?  I am just wondering how I would find those posts.....I am not too savvy on finding specific info on this forum. 

 

My husband thinks the naturopath with the blood panels specifically targeting food sensitivity is the route to go so we may try that. 

 

I am curious as to what the derm will say when  I show up in a week and a half and still have the rash......if it is gone by then I will eat my  hat and my husbands too (as long as they are gluten free B)).  On the upside I have lost 6 lbs on this diet.....if I can calm the rash I may yet have hope for a bikini this summer!!!

squirmingitch Veteran

Well, your photo surely does not reflect that you have a need to loose weight & I love that happy, bright smile.  However, celiacs come in all shapes & sizes & is yet another source of frustration for us with the doctors as most of them think you have to be emaciated to be a celiac. You won't be the first to loose weight on the diet! Malabsorption can cause us to be skinny or plump.

 

No, I don't recall Prickly specifically posting about her experiences with the naturopath. My recollection is that she would mention this or that but not that she did a specific post on the subject.

 

How is your rash doing lately anyway? Any improvement yet?

 

I'll see if I can't scare up Prickly for you.

squirmingitch Veteran

Well, I have a little info. for you but not a whole lot. Prickly never used an ND for allergy or food sensitivity testing. The diet the derm put you on is an allergy free elimination diet & then you get to add foods back one by one to see if you react. I might add that you are back on topical steroids again so even if you had a bad flare, any dh biopsy would be a invalid.

 

As far as the ND & the food sensitivity testing.... there are people who believe & those who don't. Same thing for going to an allergist for allergy testing with the pin prick stuff.... it's up to you. I've seen lots of people go get tested & end up coming up with all kinds of things they are "allergic to" & then later they find out they aren't allergic to those things at all. I can tell you that testing will not tell you if it's gluten. Personally, I think that stuff is very flawed, just my 2 cents worth & that's why I've never been tempted to do it. But you have to make your own decision & do your homework. 

 

Keep us posted.

BlessedMommy Rising Star

So frustrating! It seems like all the options out there for diagnosis are flawed. I hope that you find the answers that you're seeking. I am one who will always probably remain undiagnosed because I would not survive eating gluten for 2 months. My skin rash was clearly linked to gluten though.

crazyitch Newbie

My rash is basically the same on my legs and arm, but it has flared on my tummy again and this after severely restricting my diet.  I have not started using the steroid cream as the pharmacy has to send out for a compound, it is betamethasone mixed with aveeno or something like that.  I am taking doxepin, an antihistamine that I think, takes the itch from an unbearable 10 down to a just tolerable 6.  I have times in the day where it seems to go nuts and others when it is quiet. I know the rash wont be clear next week, so I don't know what the derm will do then. 

 

I am not staying strictly to lamb rice and pears, I just don't have that discipline in me.  I have added in herbal tea, black coffee, yams, fava beans, brussel sprouts quinoa and I cook my rice in almond milk with green curry paste and kaffir lime leaves.  I need some flavour!!  I am not having gluten dairy or soy. I have limited my salt to almost nothing. I am using some spices but I have googled hypoallergenic diets and the only thing that is a no no is black coffee.....forgive me this small pleasure, I may be a headline if I don't have my morning java!!

 

I am with you Ruth, the diagnostic procedure for this disease is severely lacking, I am surprised that in this day and age we cant come up with something definite and consistent to test for it.  I am going to continue with the gluten free thing and see what happens.  How long did it take you to be able to definitely tell that gluten was the culprit?  I am still having bad days where it flares and once the scabs are there it becomes a vicious cycle of itch/scratch/scab/itch/scratch/scab.......

squirmingitch Veteran

Aveeno = oatmeal. Oatmeal = gluten. Why? Because oats grow alongside wheat, mature at the same time, are harvested at the same time on the same wheat laden equipment & processed on the same gluten laden equipment in the facility. All of this = cross contamination.

 

We can have oats BUT ONLY OATS THAT HAVE BEEN GROWN IN DEDICATED FIELDS FAR FROM WHEAT & harvested using clean equipment & processed using clean equipment.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

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

    volivier
    Newest Member
    volivier
    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

    • trents
      @Riley, on this forum we sometimes get reports from people with similar experiences as you. That is, their celiac disease seems to go into remission. Typically, that doesn't last. At age 18 you are at your physical-biological peek in life where your body is stronger than it will ever be and it is able to fight well against many threats and abuses. As Wheatwacked pointed out, absence of symptoms is not always a reliable indicator that no damage is being done to the body. I was one of those "silent" celiacs with no symptoms, or at least very minor symptoms, whose body was being slowly damaged for many years before the damage became pronounced enough to warrant investigation, leading to a diagnosis. By that time I had suffered significant bone demineralization and now I suffer with back and neck problems. Please, if you choose to continue consuming gluten, which I do not recommend, at least get tested regularly so that you won't get caught in the silent celiac trap down the road like I did. You really do not outgrow celiac disease. It is baked into the genes. Once the genes get triggered, as far as we know, they are turned on for good. Social rejection is something most celiacs struggle with. Being compliant with the gluten free diet places restrictions on what we can eat and where we can eat. Our friends usually try to work with us at first but then it gets to be a drag and we begin to get left out. We often lose some friends in the process but we also find out who really are our true friends. I think the hardest hits come at those times when friends spontaneously say, "Hey, let's go get some burgers and fries" and you know you can't safely do that. One way to cope in these situations is to have some ready made gluten-free meals packed in the fridge that you can take with you on the spot and still join them but eat safely. Most "real" friends will get used to this and so will you. Perhaps this little video will be helpful to you.  
    • Wheatwacked
      @Riley., Welcome to the forum.   It was once believed that Celiac Disease was only a childhood disease and it can be outgrown.  That was before 1951, before gluten was discovered to be cause of Celiac Disease, also called Infantilism.  Back then Cileac Disease was thought to be only a gastro intestinal disease, once you  "outgrew" the colicky phase, you were cured. You were so lucky to be diagnosed at 5 years old so your developing years were normal.  Gluten can affect multiple systems.  The nervous system, your intellegence. The muscules, skeleton. It can cause neurological issues like brain fog, anxiety, and peripheral neuropathy.  It can cause joint pain, muscle weakness, and skin rashes. Epilepsy is 1.8 times more prevalent in patients with celiac disease, compared to the general population. Because through malabsorption and food avoidances, it causes vitamin D and numerouus other essential nutrient deficiencies, it allows allergies, infections, poor growth, stuffy sinuses and eustacian tubes. There is even a catagory of celiac disease called "Silent Celiac".  Any symptoms are explained away as this, that or the other thing. Gluten is one of the most addictive substances we consume.  Activating the Opiod receptors in our cells, it can numb us to the damage that it, and other foods are causing.  It has become socially acceptable to eat foods that make us feel sick.  "There's a pill for that".   It is generally accepted that n fact you are weird if you don't. The hardest part is that if you don't eat gluten you will feel great and think why not.  But slowly it will effect you, you'll be diagnosed with real diseases that you don't have. You'll be more susseptable to other autoimmune diseases.  As you read through the posts here, notice how many are finally dianosed, after years of suffering at older ages.  Is it worth it? I think not. Perhaps this book will help:  Here is a list of possible symptoms:   
    • Riley.
      Hi! Im Riley, 18 years old and have been diagnosed for 13 years.. the testing started bc I stopped growing and didn’t gain any weight and was really small and thin for my age.  I got diagnosed when I was 5 and have been living gluten free since, in elementary and middle school it was hard for me and I kept contaminating myself bc I wanted to fit in with my friends so so badly. I ate gluten secretly at school and mostly regretted it 30 minutes later.  I’ve had symptoms like diarrhea, nausea, headaches, stomachaches, threw up a lot and was really emotional.  In 2022 I really started working on myself and tried to stay gluten free and if I did eat gluten I wouldn’t tell anyone and suffer in silence.  Last year in July I begged my mom to let me „cheat“ one day bc I just wanted to fit in… I ate a lot of different stuff, all the stuff I missed out on in my childhood like nuggets, pizza and all that.. I didn’t have symptoms that day and was doing really fine My mom and I wanted to test how far we can go and said we would test it for 12 weeks to get my blood taken after to see if I’m doing good or if symptoms start showing  As a now 18 year old girl who finally gained a normal weight and doesn’t get symptoms I’m to scared to get tested/my blood taken cuz I finally found comfort in food and it got so much easier for me and my family.  A year and 4 months later i still didn’t get any symptoms and have been eating gluten daily.  I’m scared to get tested/my blood taken cuz what if I’m actually not fine and have to go back to eating gluten free. Any tips to get over that fear and „suck it up“ cuz I know I could seriously damage my body… sorry if I seem like a idiot here… just don’t really know what to do :,)
    • 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!
×
×
  • 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.