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

Neurological Symptoms And Brain Abnormalities


Pegleg84

Recommended Posts

Pegleg84 Collaborator

Hi all

So I took a peek at the summary of this research in the newsletter this morning, on a study showing several Celiac disease patients with significant brain abnormalities, especially with people who have issues with headaches, dizziness, and other neurological issues:

https://www.celiac.com/articles/23041/1/Brain-Abnormalities-in-Patients-with-Celiac-Disease-and-Neurological-Issues/Page1.html

I found this really interesting, and some proof that there's definitely brain stuff going on with Celiac. Last year I went through rounds of test to figure out what was causing my dizziness, thinking it was an inner ear problem. Now that I've cut out milk, a lot of salt, and soy it's gotten 10 times better, but still interesting to see there could be a link to actual abnormalities in the brain.

Most people wouldn't have had an MRI without good reason, but last year I had two - one to check out my inner ear, which turned up nothing, and another to screen for aneurism, as my father died of one when he was only 35.

It turned up something: a (according to the neurologist) very tiny aneurism that probably won't get any bigger and isn't likely to cause problems. I haven't yet gone back to get it rescanned with contrast and have a better assessment, but it does make me wonder if that kind of abnormality could be Celiac related?

As far as I know, there weren't any other oddities with my brain, but you know doctors, they look for what they're supposed to and often ignore the rest.

We don't know if my father had Celiac, but it runs on his side of the family as well as on my mothers, so you never know.

I was just wondering if anyone else knows of any other research on brain abnormalities and Celiac, or knows they have similar issues as well.

Its an interesting possible link, and a sign that Celiac disease affects much much more than we thought.

Cheers

Peg


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



Celiac.com Sponsor (A8-M):



NorthernElf Enthusiast

I am looking forward to more research being done on this. I believe the study had a small sample group of around 30 some people.

Last April a rheumy sent me for an MRI of my head & neck as I was having a lot of joint issues and he didn't like my reflexes. My bloodwork did not show any arthritic conditions. My scan picked up some white matter issues that *could* be indicative of MS. I was quickly sent to a neruologist who all but ruled it out. I have no true MS symptoms (he did a lot of physical tests on me) - he said such scans can be over reported. It was scary. I will have another scan in a year but he thinks I don't have MS.

That article made me feel a bit better - one because of that scan and two because I am undiagnosed celiac. I could hire myself out as a gluten detector as I am pretty sensitive ! However, my original doc didnt' think I could have it and did not test me properly. I had a negative blood test and it took a few months to get my endoscope, at which time I quit eating gluten (didn't now I shouldn't)....and then she only ordered it to check for relux issues. I was very upset when I asked the doc who did it after if he saw signs of celiac and he said he hadn't been told to look for any !

Anyway, brain changes are still pretty unsettling even if it could prove to my new doc I really am celiac and not following some fad diet. I do think he believes me but if they don't have a test that says it they seem reluctant to use the word celiac.

ravenwoodglass Mentor

My scan picked up some white matter issues that *could* be indicative of MS. I was quickly sent to a neruologist who all but ruled it out. I have no true MS symptoms (he did a lot of physical tests on me) - he said such scans can be over reported. It was scary. I will have another scan in a year but he thinks I don't have MS.

Those lesions you speak of are called UBO's or Unidentified Bright Objects. They are found in folks that have gluten ataxia. Many neuros are clueless about them. Folks that have neuro issues from gluten often need to be very strict with the diet. The neuro issues can also show up long before the usual gut symptoms strike. I had neuro problems and DH from childhood but the gut stuff didn't get to the point of being a problem until my 30's.

Takala Enthusiast

Read here:

Open Original Shared Link Gluten sensitivity as a neurological illness, Hadjivassiliou, Journal of Neurology, Neurosurgery, Psychiatry

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,896
    • Most Online (within 30 mins)
      7,748

    debbiebryant12
    Newest Member
    debbiebryant12
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Gigi2025
      No, I've not been diagnosed as celiac.  Despite Entero Labs being relocated to Switzerland/Greece, I'll be doing another test. After eating wheat products in Greece for 4 weeks, there wasn't any reaction.  However, avoiding it here in the states.   Thanks everyone for your responses.  
    • Rejoicephd
      Thank you @JulieRe so much for sharing this extra information. I'm so glad to hear you're feeling better and I hope it keeps moving in that direction. I feel I'm having so many lightbulb moments on this forum just interacting with others who have this condition. I also was diagnosed with gastric reflux maybe about 10 years ago. I was prescribed ranitidine for it several years back, which was working to reduce my gastric reflux symptoms but then the FDA took ranitidine off the shelves so I stopped taking it. I had a lot of ups and downs healthwise in and around that time (I suddenly gained 20 pounds, blood pressure went up, depression got worse, and I was diagnosed with OSA). At the time I attributed my change in symptoms to me taking on a new stressful job and didn't think much else about it. They did give me a replacement gastric reflux drug since ranitidine was off the shelves, but when I went on the CPAP for my OSA, the CPAP seemed to correct the gastric reflux problem so I haven't been on any gastric reflux drug treatment for years although I still do have to use a CPAP for my OSA. Anyway that's a long story but just to say… I always feel like I've had a sensitive stomach and had migraines my whole life (which I'm now attributing to having celiac and not knowing it) but I feel my health took a turn for much worse around 2019-2020 (and this decline started before I caught covid for the first time). So I am now wondering based on what you said, if that ranitidine i took could have contributed to the yeast overgrowth, and that the problem has just been worsening ever since. I have distinctly felt that I am dealing with something more than just stress and battling a more fundamental disease process here. I've basically been in and out of different doctor specialties for the past 5 years trying to figure out what's wrong with me. Finally being diagnosed with celiac one year ago, I thought I finally had THE answer but now as I'm still sick, I think it's one of a few answers and that maybe yeast overgrowth is another answer. For me as well, my vitamin deficiencies have persisted even after I went gluten-free (and my TTG antibody levels came down to measurably below the detectable limit on my last blood test). So this issue of not absorbing vitamins well is also something our cases have in common. I'm now working with a nutritionist and taking lots of vitamins and supplements to try and remedy that issue. I hope that you continue to see improvements in working with your naturopath on this. Keep us posted!
    • ElenaM
      Hello everyone. I am Elena and am 38 years old. I suspect I have a gluten intolerance even if my celiac panel is ok. I have the following symptoms : facial flushing, Red dots not bumps în face, bloating abdominal distension, hair loss, depression anxiety even with meds and even bipolar. Fatigue extreme to the point of not being able to work. All of these after I eat gluten. Could I have non celiac gluten sensitivity? Thanks anyone else with these symptoms?
    • JulieRe
      Hi Everyone,  I do appreciate your replies to my original post.   Here is where I am now in this journey.  I am currently seeing a Naturopath.  One thing I did not post before is that I take Esomeprazole for GERD.  My Naturopath believes that the decrease in the gastric acid has allowed the yeast to grow.    She has put me on some digestive enzymes.  She also put me on Zinc, Selenium, B 12, as she felt that I was not absorbing my vitamins. I am about 5 weeks into this treatment, and I am feeling better. I did not have any trouble taking the Fluconazole.  
    • Ceekay
      I'm sure it's chemically perfect. Most of them taste lousy!        
×
×
  • 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.