Epstein Barr Nuclear AG AB IGG result of over 600
Hello, I am searching for information and also input because of my hideously high lab results for EBNA Nuclear AB IGG. My result was given as over 600. The range is less than 18 is negative. Over 22 is positive. To restate, my lab result is over 600.
I am 52. I did have mono at age 11. For at least four years I have complained on numerous times to my PCP of fatigue. We suspected thyroid but that has been treated and I still have suffered from bouts of fatigue, feeling like I was coming down with a bug, dizziness, etc for 3 or 4 days out of just about every month for the last eighteen months. I finally saw a naturopath who tested me for EBV.
I love my Naturopath, but I am wondering if I should be seeing a specialist because of this high lab result.
I am on a treatment plan of antiviral supplements, and immune supporting vitamins and supplements which she said will probably need to be taken for at least three months.
Has anyone else had numbers this high? I am having trouble finding much information on reactivated EBV.
Thank you!
Lisa
Interested in more discussions like this? Go to the Infectious Diseases Support Group.
Hello, Yes, I have Celiac Disease and Grave’s disease. My EPV was triggered after having COVID. It had been dormant for 12 years. Hope this helps answer your question. Tricia
Thx so much for your reply. I’m very sorry to hear COVID reactivated EBV. Hoping your COVID was mild and you’re feeling better now.
- what was your COVID experience like?
- How did you discover EBV Re activation?
- how are you doing post COVID?
- any long COVID symptoms?
- Did you experience any EBV symptoms?
“Drbeen Medical Lectures” EBV YouTubes includes one about EBV reactivation … his other EBV YouTube’s are very helpful in understanding EBV too.
Epstein-Barr Virus Reactivation
Discovered some interesting info re the role EBV may play in autoimmune diseases and cancer in the Q&A section at bottom of EBV article below
https://ada.com/conditions/epstein-barr-virus/
Welcome links to any info you have discovered + find helpful too.
Hi!
Thank you so much for your post. I so understand and empathize with all you’re going through.
When I initially experienced fatigue in 2011, I was tested and diagnosed with Hashimoto’s Thyroiditis.
I have since learned …
1) “ Hashimoto's thyroiditis, also known as chronic lymphocytic thyroiditis, is the most common cause of hypothyroidism in the United States. It is an autoimmune disorder involving chronic inflammation of the thyroid. This condition tends to run in families.”
https://www.google.com/url?sa=t&rct=j&q=&esrc=s&source=web&cd=&ved=2ahUKEwjj4eiansj8AhUlJkQIHVkeArQQFnoECA4QAw&url=https%3A%2F%2Fwww.thyroid.org%2Fhashimotos-thyroiditis%2F&usg=AOvVaw3L83rd3jzQFsvk-n17_Dxz
2) “Having another autoimmune disease — such as rheumatoid arthritis, type 1 diabetes or lupus — increases your risk of developing Hashimoto's disease.”
https://www.mayoclinic.org/diseases-conditions/hashimotos-disease/symptoms-causes/syc-20351855
3) “high anti-EBNA-1 antibody levels may reflect a deficient control of the EBV infection, increasing the tendency toward autoimmunity.”
https://www.frontiersin.org/articles/10.3389/fneur.2019.01368/full
4) “Rheumatologists diagnose, treat and manage a broad range of conditions, including … Autoimmune diseases that happen when your immune system attacks healthy tissue.”
https://my.clevelandclinic.org/health/articles/22335-rheumatologist
I have also discovered “Drbeen Medical Lectures” EBV YouTube’s … which I’m finding very insightful + helpful. Dr Been makes learning about EBV easy + enjoyable.
Epstein-Barr Virus (EBV) Serology
Epstein-Barr Virus Reactivation
Epstein-Barr Virus (EBV) - Long Covid
Evidence of Epstein-Barr Virus Reactivation in Long Covid Patients
I will greatly appreciate + look forward to updates + links to information about anything you learn.
Thank you for the helpful info. I am unsure which doctor's to even go to these days with my post covid issues. Almost all of them seem like a deer in headlights when you tell them your issues, and even show them your >600 EBV values post covid. I was competitive tennis player 2 hour a night prior to covid in 2021, and now have more muscle pains than ever before, and even lymph issue when trying to even exercise a little more on the tennis court. It is disheartening to know no doctor's seem to know what is going on with all this funding that has been given out. I have read that high EBV post covid and cause ME/Chronic Fatigue, as well as Hodgkins Lymphoma. Kind of worried about this, and wondering can anyone suggest the correct doctor's to see to rule out this stuff? I told my PCP my lymphs in neck hurt, muscle pain, etc. and basically gave me prednisone. I just want to find the correct type of doctor that will do the correct tests if anyone has suggestions? I see mention of rheumatologists, etc. but I have been there and they said I have mixed connective tissue disorder post covid, but that does not explain lymph issues now. Any suggestions would be appreciated.
Hope everyone keeps positive when there seems to not be much help out there. Long haulers are now our own self-care covid clinics 🙁
I am 62 and my entire life I have felt tired. I am also a very smart individual who could have successfully become a doctor, lawyer, engineer. Instead I chose to be a stay at home mom and work part-time. I attended college several different times. When I told my primary care physician about me feelings as an adult he treated me for depression. The medicine only made my more tired. I have a female doctor now and she is more understanding and doing all kinds of test. She did the complete Epstein Bar and 2 of my results were high.
EBV NUCLEAR IGG
UNIT/VOL EXTERNAL U/mL
Value 466.0
Standard Range 0.0 - 17.9 U/mL which means at some point I had mono. I was never ever diagnosed with it. The second test results were how I found this chat … EBV VIRAL CAPSID
IGG UNIT/OL
EXTERNAL
U/mL
Value >600.0
Standard Range 0.0 - 17.9 U/mL. My doctor referred me to a rheumatologist because my older sister has both rheumatoid arthritis and Sjogrens ( not sure on the spelling) disease. I also have very high results on C-Reactive Protein and Eosinophils which are markers for inflammation. The rheumatologist wanted me referred to an infectious disease person. My doctor is not running more test and we will go from there. My doctor said she may talk to another rheumatologist. My sisters RA doctor is associated with Cleveland Clinic. My sister is going to ask her doctor if she would look at all my labs and see what she thinks. If I learn anything I will make another comment. Good luck to everyone else. It is sort of a relief to know I am not the only person feeling like this.
My ebv igg was over 600. I have a terminally ill family member. Should I stay away or can I see him?
Hi Lisa,
I believe I have reactivated EBV due to getting Covid-19 last March, 2022. I have been tired and dizzy since then. I started to see a new primary care nurse practitioner last fall, 2022, and all the efforts up to now are my own...pushing and pushing, asking for blood tests that I have learned about from family members. First my brother who has had fatigue, pain, brain fog and now depression since he contracted Covid-19 in the very beginning of the US pandemic 2020. He was a critical care nurse at the time. Face to face with intubated patients dying of Covid. He asked me if I had tested for EBV and that two of the antibody tests were "sky high". I then asked for those tests. The first panel I did included EBV VCA-IGM, EBV VCA-IGG and EBV EBNA-IGG...I was 488.00 H for VCA-IGG and >600.00 H for EBNA-IGG...both signaling a "past infection". I am 60 and had mono at 16!
I then started talking to my cousin who has been diagnosed with CFS/ME for 35 years who knows more than anyone I know about her own disease and it's connection to EBV. She was treated by a groundbreaking doctor in the Lake Tahoe area (Dr. Dan Peterson). He is a leading expert in CFS/ME. He used the EBV Early Antigen (EA) D AB (IGG) antibody test as a marker for EBV viral load in the body. Meaning (as far as I can tell from my own research) that your body is actively fighting the virus. So I asked my NP for an order for that specific test. My results were (just two weeks ago) >150 H. My cousin said THAT IS VERY HIGH...you need treatment, NOW. I am trying to get referred to infectious disease doc and so far...can't get one taking new patients. Very frustrating!
So I am doing my own research and found Mayo Clinic Connect. Best community I have found so far! Also, I just found a treatment plan that member @jenchaney727 talks about in detail. I am commencing her suggestions as soon as I get all the supplements. Meanwhile, I saw another discussion thread on here that suggesteds L-lysine
which I have had on hand for years for cold sores. I started 1000mg 3x day two days ago. I don't want to get prematurely excited, but I feel better now than I have in a very long time!
So, to reiterate, many commenters on this thread may need to get a different antibody test than the EBNA-IGG and get the EBV EA-D IGG test. Most docs will NOT order this for you unless you insist and they won't understand the results either. But experts in the field of EBV and CFS/ME do. These docs are VERY HARD TO FIND. And what I think I have is REACTIVATED EBV due to Covid-19. This is the chronic form of EBV-NOT mono. Also, my first clue was Post Exertional Malaise (PEM) after exercise. That was also my brother's primary symptom and it is also a hallmark of CFS/ME.
I hope you and some of the other commenters on this discussion have already found more help!
Hi, I have had Long Covid fatigue and dizziness for over a year due to what I believe is an EBV reactivation. I started getting blood tests this past fall and had a positive ANA. I guess it is a weak/low positive 1:40. Not sure where that plays into my symptoms. I was also low vitamin D.
Hi,
Not sure if you've already found relief since this post but you may want to read/follow the discussion thread under "Treatment for chronic Epstein-Barr virus (EBV)". I found loads of info on there!
At what point do you get chronic EBV? I was diagnosed in early February after pushing for the test. She said people don’t get it twice. HA! This is round 3 for me. Anyway I have sore throat with white patches, brain fog and the crushing fatigue. I would love to hear your thoughts.