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Reuters Has Article Saying Dermatologists Claim Dh Celiac Remission


Takala

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Takala Enthusiast

There have been all sorts of goofy, inaccurate gluten intolerant and celiac articles in the main stream glutenoid media this past year, but this one takes the rice cake.

According to a Dr Stephen Katz at the NIH, National Institutes of Health, he is claiming (!!!) that a small percentage of patients with DH go into remission after treatment with dapsone and can go back to eating a normal diet instead of a gluten free one, as long as they don't have intestinal symptoms.

Open Original Shared Link

Reuters Health

Painful "gluten rashes" might not be forever

by Alison McCook 11/19/2010

(Reuters Health) - A small percentage of people with a painful, blistering skin disease may eventually go into remission, saving them from medication and a strict diet, a new study reports.

"A 'lifelong' disease may not be lifelong," study author Dr. Stephen Katz at the National Institutes of Health told Reuters Health.

But the new study found that, among 86 people with dermatitis herpetiformis, 10 never saw their symptoms return after stopping medication and resuming a normal diet.

So even though people with celiac disease are supposed to stay gluten-free indefinitely, for those with dermatitis herpetiformis who don't have intestinal symptoms, it makes sense to stop the diet and see if they feel okay, Katz said.

"I always tell them to cheat a little bit, see if they need the diet," he said. "Because if some patients don't need the medicine, they may no longer need the diet."

In the current study, published in the Archives of Dermatology, one-third of dermatitis herpetiformis patients had once had symptoms of celiac disease - but they were just as likely to go into remission as those with no celiac symptoms.

Unfortunately, there were no obvious differences between the patients who went into remission and those who didn't, Katz noted. "We couldn't make sense of it."

Dr. John Zone, chair of the department of dermatology at the University of Utah, who reviewed the findings for Reuters Health, said the remission rate of 12 percent matches what he's seen in his practice. "I agree with the percentage of people who have spontaneous remission."

There is concern, he added, that people who don't stick with the diet may have a higher risk of lymphoma and other complications. Consequently, Zone suggested that patients with dermatitis herpetiformis who decide to stop the diet have their blood tested occasionally to look for celiac antibodies, even if their skin symptoms never return.

Luckily, a small percentage of them will be able to enjoy a normal diet and a life without dermatitis herpetiformis medication, Zone said -- which is a very good thing.

The only people I have ever heard of who had a remission from gluten intolerant or celiac symptoms were those who were successfully treated for Lyme disease.

Am I missing something here ?

Isn't it once a celiac or gluten intolerant, always a celiac or gluten intolerant ? Aren't most symptoms so vague the majority of us get no diagnosis or the wrong one anyway ?

Should doctors be telling celiacs to go ahead and cheat and see how they feel ? That 10 out of 86 patients who supposedly stopped the diet and never saw the symptoms return would be 11% of celiacs with DH. How long was the followup period and were all of them tracked for decades ? The study went from 1972 to 2010, thirty eight years. Older patients were more likely to stop displaying symptoms than younger ones.

This story was also reported in the Nov 15th Archives of Dermatology. Open Original Shared Link

The long-term primary outcome was defined as absence of skin lesions and symptoms of DH for more than 2 years while not taking sulfones (dapsone or sulfoxone), sulfapyridine, anti


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lovegrov Collaborator

While it sounds weird, my own father took dapsone for something like 20 years. He forgot to take it for a couple of days and when nothing happened, he just quit taking it. No DH for more than 5 years and no celiac-like symptoms (he didn't know about celiac and hadn't been tested). The DH finally returned and after I was diagnosed he also tested positive. But for those 5 years I would say that he was basically in sort of a remission.

richard

cassP Contributor

you could be asymptomatic and still have autoimmune destruction going on in your small intestine... most Celiacs dont have any gut symptoms..

ive had every classic symptom + neurological, mental, and skin symptoms for over 25 years... with ebbs & flows.. but i didnt get DH till i was 38 years old.

most of my issues are completely gone... my DH is fading and doesnt itch anymore.. does that mean that i can start eating gluten again???? :lol:

YoloGx Rookie

My mother got dh when she was 4 years old. She was treated for sprue until she was 18 or 20. After that she went back to eating gluten. It was thought that she "grew out of it." What no one notices was that she had other probably related symptoms to gluten intolerance. Increased anxiety, panic attacks. Frozen shoulder and frequent tendonitus. Frequent migraines. Dry eyes and glaucoma. Tendency to get colds and flu. In her old age however the DH came back--at age 91 or 92. At first we thought it was some kind of bug biting her... She is now 95.

Although my RN sister is in denial about the whole thing, its clear to me (from observation) that when my mother eats gluten she gets lesions afterwards and is more confused mentally.

She also recalled to me about three years ago that she was tested some 20 years previous at Kaiser and still came out positive for celiac...this was when she was having symptoms of "occult diabetes"...

  • 2 years later...
lil'chefy Apprentice

I have "had" celiac, via DH diagnosis for 23 years. I have taken Dapsone for 20 years (100mg.). I stopped the Dapsone maybe 1-2 years ago. I was on a gluten free diet for about a year of that time (strict), after going off of the dapsone. I am eating a clean regular gluten included diet right now, but considering going gluten free again. To date, I have not had a DH breakout in many years. I had a skin biopsy confirming DH done 3 or 4 times. Right now, I am struggling with the idea of going gluten-free again. I hate eating food that is in no way comparable. There relly is nothing as delicious a a steaming loaf of homemade gluten derived bread, ya know? The fact that I have not broken out makes it very difficult for me to go on such a strict regimin. Now I will move on to my current symptoms, and maybe someone could help me understand why I am not breaking out, or what the relationship is for me. First, you should know, I have had the celiac panel--- It says I don't have celiac disease. I have had a blood test done for food allergies---It says I don't have any, accept for sesame, which I eat all the time, and have never had a reaction to. I have had an endoscopy done, no sign of celiac disease there either.

Now I will list the health problems that I have been struggling with for a couple to a few years now. First off, I have stopped making ALL hormones, at 36 years old:-(. I am currently on bioidentical hormone therapy, but so far, that has yet to help me feel better. I have had saliva testing done and blood work done for my hormones. Both show that I am not even in menapause, I am not making any HORMONES. I have extreme adrenal fatigue. I have always had ADHD symptoms. I have pervasive, relatively new joint pain. Literally all of the sudden, my skin is ridiculously dry, and my skin is aging VERY rapidly. I am having massive female problems, but still mensing. I have been passing out, only twice, but still, I have a 5 year old and a 3 year old! Tests show that I am flirting with hypothyroidism, I test on the low side of normal. I have been having severe anxiety/ mood swings for a few years. I CANNOT lose weight, no matter what I do. I count calories, and run for exercise. I don't lose any weight, I just make my bones hurt and make my exhaustion profound. My feet hurt so badly, that I don't feel like I can walk correctly sometimes. I am in school and I nod off sometimes! That is so not like me. My blood pressure is so low, sometimes at the doctor's office, they don't want me to drive home. I take immaculate care of my teeth and my mouth, but to no avail (they are decaying at a rapid speed, and my gums are so sore). I should also mention that I got crazy, they won't stop nose bleeds when I was little, but was always only on the brink of being anemic. All these reasons and many others are why I decided to go gluten free once and for all November of last year. And so I did....... I got absolutely NO relief from any symptoms what so ever. It was very depressing for me. I thought I had finally nailed it...that silver bullet that so many doctors miss. They have run a lupus panel. I don't have that. I am SO tired of feeling like crap. If anyone has any info for me, it would be invaluable for me. I have an appointment with an endocrinologist later this month, but I am pretty pessimistic about the outcome.

ravenwoodglass Mentor

It can take longer than 3 months to heal when many other body systems are impacted. In the first part of your post you state you are on a regular gluten containing diet right now but you also state you have been gluten-free since Nov. Are you going back and forth between gluten-free and not gluten-free? If you are then it would be a good idea to get very strict with the diet and give it time. It isn't always the gut that is the most severely impacted in us. It takes a while for brain, joint and other celiac impacted systems to heal. In my own case it was a good six months to see some resolution in joint and muscle issues and brain impact.

lil'chefy Apprentice

It can take longer than 3 months to heal when many other body systems are impacted. In the first part of your post you state you are on a regular gluten containing diet right now but you also state you have been gluten-free since Nov. Are you going back and forth between gluten-free and not gluten-free? If you are then it would be a good idea to get very strict with the diet and give it time. It isn't always the gut that is the most severely impacted in us. It takes a while for brain, joint and other celiac impacted systems to heal. In my own case it was a good six months to see some resolution in joint and muscle issues and brain impact.

I was strict with the diet for 1 year and one month, then I just started feeling like I was being restricted for no reason. I was showing NO signs of feeling better.

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pricklypear1971 Community Regular

I was strict with the diet for 1 year and one month, then I just started feeling like I was being restricted for no reason. I was showing NO signs of feeling better.

I would suggest that your primary symptoms that you FEEL may be adrenal, thyroid, and hormonal. And since those aren't resolved (and are so severe) you may not feel the difference from going gluten-free.

You need a good ND or somesuch. Not a whack job, but one that has a MD and ND background that treats you to improve thyroid/hormone function/adrenals. After a year of gluten-free I personally hit a wall, and until my new ND explained quite thoroughly the hormone/adrenal/thyroid connection and I started doing what I needed to do: exercise, specific supplements, eating on a schedule , etc. (I had been strictly gluten-free so that was already done) I did not see improvement.

I'd bet you aren't "borderline" hypothyroid, either.

I reco an ND over an MD because ND's usually work with patients differently and listen to your symptoms and help you relieve symptoms; not just treat the labs. But you never know. Keep looking til you find a doctor that is a good fit.

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    • marion wheaton
      Thanks for responding. I researched further and Lindt Lindor chocolate balls do contain barely malt powder which contains gluten. I was surprised at all of the conflicting information I found when I checked online.
    • trents
      @BlessedinBoston, it is possible that in Canada the product in question is formulated differently than in the USA or at least processed in in a facility that precludes cross contamination. I assume from your user name that you are in the USA. And it is also possible that the product meets the FDA requirement of not more than 20ppm of gluten but you are a super sensitive celiac for whom that standard is insufficient. 
    • BlessedinBoston
      No,Lindt is not gluten free no matter what they say on their website. I found out the hard way when I was newly diagnosed in 2000. At that time the Lindt truffles were just becoming popular and were only sold in small specialty shops at the mall. You couldn't buy them in any stores like today and I was obsessed with them 😁. Took me a while to get around to checking them and was heartbroken when I saw they were absolutely not gluten free 😔. Felt the same when I realized Twizzlers weren't either. Took me a while to get my diet on order after being diagnosed. I was diagnosed with small bowel non Hodgkins lymphoma at the same time. So it was a very stressful time to say the least. Hope this helps 😁.
    • knitty kitty
      @Jmartes71, I understand your frustration and anger.  I've been in a similar situation where no doctor took me seriously, accused me of making things up, and eventually sent me home to suffer alone.   My doctors did not recognize nutritional deficiencies.  Doctors are trained in medical learning institutions that are funded by pharmaceutical companies.  They are taught which medications cover up which symptoms.  Doctors are required to take twenty  hours of nutritional education in seven years of medical training.  (They can earn nine hours in Nutrition by taking a three day weekend seminar.)  They are taught nutritional deficiencies are passe' and don't happen in our well fed Western society any more.  In Celiac Disease, the autoimmune response and inflammation affects the absorption of ALL the essential vitamins and minerals.  Correcting nutritional deficiencies caused by malabsorption is essential!  I begged my doctor to check my Vitamin D level, which he did only after making sure my insurance would cover it.  When my Vitamin D came back extremely low, my doctor was very surprised, but refused to test for further nutritional deficiencies because he "couldn't make money prescribing vitamins.". I believe it was beyond his knowledge, so he blamed me for making stuff up, and stormed out of the exam room.  I had studied Nutrition before earning a degree in Microbiology.  I switched because I was curious what vitamins from our food were doing in our bodies.  Vitamins are substances that our bodies cannot manufacture, so we must ingest them every day.  Without them, our bodies cannot manufacture life sustaining enzymes and we sicken and die.   At home alone, I could feel myself dying.  It's an unnerving feeling, to say the least, and, so, with nothing left to lose, I relied in my education in nutrition.  My symptoms of Thiamine deficiency were the worst, so I began taking high dose Thiamine.  I had health improvement within an hour.  It was magical.  I continued taking high dose thiamine with a B Complex, magnesium. and other essential nutrients.  The health improvements continued for months.  High doses of thiamine are required to correct a thiamine deficiency because thiamine affects every cell and mitochondria in our bodies.    A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function.  The cerebellum of the brain is most affected.  The cerebellum controls things we don't have to consciously have to think about, like digestion, balance, breathing, blood pressure, heart rate, hormone regulation, and many more.  Thiamine is absorbed from the digestive tract and sent to the most important organs like the brain and the heart.  This leaves the digestive tract depleted of Thiamine and symptoms of Gastrointestinal Beriberi, a thiamine deficiency localized in the digestive system, begin to appear.  Symptoms of Gastrointestinal Beriberi include anxiety, depression, chronic fatigue, headaches, Gerd, acid reflux, gas, slow stomach emptying, gastroparesis, bloating, diarrhea and/or constipation, incontinence, abdominal pain, IBS,  SIBO, POTS, high blood pressure, heart rate changes like tachycardia, difficulty swallowing, Barrett's Esophagus, peripheral neuropathy, and more. Doctors are only taught about thiamine deficiency in alcoholism and look for the classic triad of symptoms (changes in gait, mental function, and nystagmus) but fail to realize that gastrointestinal symptoms can precede these symptoms by months.  All three classic triad of symptoms only appear in fifteen percent of patients, with most patients being diagnosed with thiamine deficiency post mortem.  I had all three but swore I didn't drink, so I was dismissed as "crazy" and sent home to die basically.   Yes, I understand how frustrating no answers from doctors can be.  I took OTC Thiamine Hydrochloride, and later thiamine in the forms TTFD (tetrahydrofurfuryl disulfide) and Benfotiamine to correct my thiamine deficiency.  I also took magnesium, needed by thiamine to make those life sustaining enzymes.  Thiamine interacts with each of the other B vitamins, so the other B vitamins must be supplemented as well.  Thiamine is safe and nontoxic even in high doses.   A doctor can administer high dose thiamine by IV along with the other B vitamins.  Again, Thiamine is safe and nontoxic even in high doses.  Thiamine should be given if only to rule Gastrointestinal Beriberi out as a cause of your symptoms.  If no improvement, no harm is done. Share the following link with your doctors.  Section Three is especially informative.  They need to be expand their knowledge about Thiamine and nutrition in Celiac Disease.  Ask for an Erythrocyte Transketolace Activity test for thiamine deficiency.  This test is more reliable than a blood test. Thiamine, gastrointestinal beriberi and acetylcholine signaling.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/ Best wishes!
    • Jmartes71
      I have been diagnosed with celiac in 1994, in remission not eating wheat and other foods not to consume  my household eats wheat.I have diagnosed sibo, hernia ibs, high blood pressure, menopause, chronic fatigue just to name a few oh yes and Barrett's esophagus which i forgot, I currently have bumps in back of my throat, one Dr stated we all have bumps in the back of our throat.Im in pain.Standford specialist really dismissed me and now im really in limbo and trying to get properly cared for.I found a new gi and new pcp but its still a mess and medical is making it look like im a disability chaser when Im actively not well I look and feel horrible and its adding anxiety and depression more so.Im angery my condition is affecting me and its being down played 
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