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 Our Content
    eNewsletter
    Donate

Is Zonulin a Marker for Niacin Issues in People with Leaky Gut Syndrome, NCGS and/or Celiac disease?


Posterboy

Recommended Posts

Posterboy Mentor

To All,

I came across this Old Live Journal blog a few years ago doing research on Zonulin and/or Niacin to see if I could find a "Metabolic link" to Pellagra in Celiac disease and I never had a good opportunity or chance to use it......but thought it was research worth discussing so I thought I would start a thread about it to see what others thought about it?

https://alobar.livejournal.com/2930798.html#%2F2930798.html

Could Zonulin be the body's way to tell the body it needs more Niacin?

This researcher seems to think so and the research seems to indicate.....and I tend to agree with it/them what do others think about this?

quoting from the blog post...

"For a number of years I have mentioned some articles talking about gluten and corn protein having the effect of opening up the permeability

of the intestines WHEN (and only when) the animals were niacin deficient at the time of exposure."

And also a little lower in the blog post see this quote...

"Jon Pangborn and I have had conversations about a shift that may have occurred since he began looking at plasma amino acid profiles years ago and saw many with elevated tryptophan. I don't see elevated tryptophan that much, but I do see a lot of reports (20%) that don't have a figure for tryptophan. I think this is because it was not detected, although I WISH the labs were clearer about SAYING that instead of just leaving it blank. One reason for my suspicion that the blank field means "not detected" is that I've seen repeat tests from some children, and on other tests, they had measurable tryptophan but it was very, very

low. Regardless, tryptophan was above the mean in only about 15% of my database, and below the mean in 81% of the ones where there was a number there. That is nothing like a normal distribution! So, maybe there is something about having low niacin that suddenly makes peptides from gluten (and to some extent corn zein) become signalling molecules, and the raised level of zonulin may just be a "reasonable" response to that signal. In other words, this (Zonulin) might be a "Plan B for niacin" signal. You will see, in the first article below, they did find low plasma tryptophan in people with celiac disease and an altered low neutral amino acid to tryptophan ratio."

He was remarking about this study in Celiac children...

Entitled "Plasma precursor amino acids of central nervous system monoamines in children with coeliac disease.....American spelling Celiac disease.

https://pubmed.ncbi.nlm.nih.gov/1773952/#:~:text=A significantly lower ratio of plasma tryptophan to,children and was more pronounced in untreated children.

Here is the full abstract for anyone who wants to read it.

Abstract

"Some children with coeliac disease show behavioural disorders such as depression and other signs which have been correlated with reduced central monoamine metabolism. We have therefore investigated the brain availability of the monoamine precursors tryptophan and tyrosine in 15 untreated children with coeliac disease and 12 treated children with coeliac disease as well as in 12 control children. Significantly decreased plasma concentrations of tryptophan were found in untreated children (mean (SD) 13 (4) mumols/l, p less than 0.001) compared with treated children (31 (13) mumols/l), and in both groups of coeliac children when compared with control children (81 (22) mumols/l). A significantly lower ratio of plasma tryptophan to large neutral amino acids (tyrosine, valine, isoleucine, leucine, and phenylalanine) was also observed, which could indicate impaired brain availability of tryptophan in coeliac children and was more pronounced in untreated children. The impaired availability of tryptophan could produce decreased central serotonin synthesis and in turn behaviour disorders in children with coeliac disease."

I would be interested what people think.....is impaired tryptophan metabolism in children with celiac disease proof enough for you to convenience you that at least at  a "Metabolic" level Pellagra is occurring in Celiac disease going undiagnosed?

This same metabolic maker of impaired tryptophan metabolism has also been found in adult Celiac's as well!

I hope this is helpful but it is not medical advice.

Posterboy,


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



Celiac.com Sponsor (A8-M):



Scott Adams Grand Master

It's an interesting connection, and points to niacin deficiency as a possible trigger for leaky gut, and perhaps even celiac disease in those who are genetically susceptible. 

  • 8 months later...
Dtoc Apprentice
On 7/8/2022 at 6:44 PM, Posterboy said:

To All,

I came across this Old Live Journal blog a few years ago doing research on Zonulin and/or Niacin to see if I could find a "Metabolic link" to Pellagra in Celiac disease and I never had a good opportunity or chance to use it......but thought it was research worth discussing so I thought I would start a thread about it to see what others thought about it?

https://alobar.livejournal.com/2930798.html#%2F2930798.html

Could Zonulin be the body's way to tell the body it needs more Niacin?

This researcher seems to think so and the research seems to indicate.....and I tend to agree with it/them what do others think about this?

quoting from the blog post...

"For a number of years I have mentioned some articles talking about gluten and corn protein having the effect of opening up the permeability

of the intestines WHEN (and only when) the animals were niacin deficient at the time of exposure."

And also a little lower in the blog post see this quote...

"Jon Pangborn and I have had conversations about a shift that may have occurred since he began looking at plasma amino acid profiles years ago and saw many with elevated tryptophan. I don't see elevated tryptophan that much, but I do see a lot of reports (20%) that don't have a figure for tryptophan. I think this is because it was not detected, although I WISH the labs were clearer about SAYING that instead of just leaving it blank. One reason for my suspicion that the blank field means "not detected" is that I've seen repeat tests from some children, and on other tests, they had measurable tryptophan but it was very, very

low. Regardless, tryptophan was above the mean in only about 15% of my database, and below the mean in 81% of the ones where there was a number there. That is nothing like a normal distribution! So, maybe there is something about having low niacin that suddenly makes peptides from gluten (and to some extent corn zein) become signalling molecules, and the raised level of zonulin may just be a "reasonable" response to that signal. In other words, this (Zonulin) might be a "Plan B for niacin" signal. You will see, in the first article below, they did find low plasma tryptophan in people with celiac disease and an altered low neutral amino acid to tryptophan ratio."

He was remarking about this study in Celiac children...

Entitled "Plasma precursor amino acids of central nervous system monoamines in children with coeliac disease.....American spelling Celiac disease.

https://pubmed.ncbi.nlm.nih.gov/1773952/#:~:text=A significantly lower ratio of plasma tryptophan to,children and was more pronounced in untreated children.

Here is the full abstract for anyone who wants to read it.

Abstract

"Some children with coeliac disease show behavioural disorders such as depression and other signs which have been correlated with reduced central monoamine metabolism. We have therefore investigated the brain availability of the monoamine precursors tryptophan and tyrosine in 15 untreated children with coeliac disease and 12 treated children with coeliac disease as well as in 12 control children. Significantly decreased plasma concentrations of tryptophan were found in untreated children (mean (SD) 13 (4) mumols/l, p less than 0.001) compared with treated children (31 (13) mumols/l), and in both groups of coeliac children when compared with control children (81 (22) mumols/l). A significantly lower ratio of plasma tryptophan to large neutral amino acids (tyrosine, valine, isoleucine, leucine, and phenylalanine) was also observed, which could indicate impaired brain availability of tryptophan in coeliac children and was more pronounced in untreated children. The impaired availability of tryptophan could produce decreased central serotonin synthesis and in turn behaviour disorders in children with coeliac disease."

I would be interested what people think.....is impaired tryptophan metabolism in children with celiac disease proof enough for you to convenience you that at least at  a "Metabolic" level Pellagra is occurring in Celiac disease going undiagnosed?

This same metabolic maker of impaired tryptophan metabolism has also been found in adult Celiac's as well!

I hope this is helpful but it is not medical advice.

Posterboy,

this is so enlightening, thank you!! I was fearful of niacin, yet once I overcame that fear, the results were/are amazing! I feel so much 'lighter' not only in my gut, but my mind and overall well being also. I wish someone had recommended this when I was kid 60 yrs ago, lol!

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

  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      126,112
    • Most Online (within 30 mins)
      7,748

    cam4180
    Newest Member
    cam4180
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.9k
    • Total Posts
      69.2k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • StaciField
      There’s a Cosco in Auckland in New Zealand. It’s a bit away from where I live but it’s worth the travel for me. Very appreciative of your advice.
    • Wheatwacked
      It seems you have proven that you cannot eat gluten.  You've done what your doctors have not been able to do in 40 years. That's your low vitamin D, a common symptom with Celiac Disease.  Zinc is also a common defiency.  Its an antiviral.  that's why zinc gluconate lozenges work against airborne viruses.  Vitamin D and the Immune System+ Toe cramps, I find 250 mg of Thiamine helps.   When I started GFD I counted 19 symptoms going back to childhood that improved with Gluten Free Diet and vitamin D. I still take 10,000 IU a day to maintain 80 ng/ml and get it tested 4 times a year. Highest was 93 ng/ml and that was at end of summer.  Any excess is stored in fat or excreted through bile.   The western diet is deficient in many nutrients including choline and iodine.  Thats why processed foods are fortified.  Celiac Disease causes malabsorption of vitamins and minerals from the small intestine damage.  GFD stops the damage, but you will still have symptoms of deficiency until you get your vitamins repleted to normal.  Try to reduce your omega 6:3 ratio.  The Standard American Diet is 14:1 or greater.  Healthy is 3:1.  Wheat flour is 22:1.  Potatoes are 3:1 while sweet potatoes are 14:1.  So those sweet potatos that everyone says is better than Russet: they are increasing your inflammation levels.   
    • Scott Adams
      My mother also has celiac disease, and one of her symptoms for many years before her diagnosis was TMJ. I believe it took her many years on a gluten-free diet before this issue went away.
    • Jeff Platt
      Ear pain and ringing your entire life may or may not be TMJ related but could be something else. A good TMJ exam would be helpful to rule that out as a potential cause from a dentist who treats that. I have teens as well as adults of all ages who suffer from TMJ issues so it’s not a certain age when it shows up.   
    • cristiana
      Not sure if related to coeliac disease but my ear ringing  has stepped up a notch since diagnosis.  Even since a child silence really hurts my ears - there is always a really loud noise if there is no other noise in a quiet room - but my brain has learned to filter it out.  Since diagnosis in my forties I also get a metallic ringing in my ears, sometimes just one, sometimes both.  But it comes and goes.   My sister also suffers now, we are both in our fifties, but she is not a coeliac, so for all I know it could just be an age thing.  I do get occasional stabbing pain in my ears but that has been all my life, and I do appear to be vulnerable to outer ear infections too.  So not a particularly helpful reply here, but I suppose what I am trying to say is it might be related but then again it could just be one of those things.   I think in the UK where I live doctors like you to report if you get tinnitus in just the one ear.  I reported mine but no cause was found.  Most of the time it is nothing but sometimes it can have a cause that can be treated, so perhaps worth reporting to your GP.  
×
×
  • Create New...