Is ANA titer of 1:320 insignificant?? - Immune Disorders Message Board

lynn41 · 04-20-2008, 07:04 PM

I understand that there are many parts to making a diagnosis of Lupus or other auto-immune disorders. My ANA titer in December was very weak at 1:40 with speckled pattern to now being 1:320. I also have had joint pain, rash on upper torso and fatigue for 17 months. I saw a new rheumatologist recently who dismissed the ANA titer of 1:320 as insignificant and said since the rash wasn't the typical rash on the face, he had no explanation. He said since the other "Lupus specific tests were negative" that I "probably have fibromyalgia" and dismissed me with no f/up.

Meanwhile, I still feel horrible. I have no idea what to do now. Is the ANA titer at 1:320 insignificant in this situation? Should I just accept a diagnosis of fibromylgia in light of the rashes that go along with the joint pain and fatigue?

Thanks for any replies.

Wallis86 · 04-20-2008, 09:09 PM

Have they tested you for any other autoimmune conditions? Some healthy people have raised ANAs but I wouldn't dismiss such a high ANA. As you probably know, normal is less than 1:40. Lots of autoimmune conditions can raise your ANA, and often specific patterns are limited to certain kinds of conditions. I'm fairly certain it is not common to have lupus with a speckled pattern. What other "lupus tests" were run by your doctor? Have you been diagnosed with any other illnesses, even infections? My general feeling on fibromyalgia, which I've been diagnosed with since I was 11 (10 years ago), is that it is a symptom, not a diagnosis. Fibro essentially means "body pain", which doesn't help explain why you are experiencing those symptoms. I'm currently in a similar situation, awaiting some more diagnostics. I have a whole slew of autoimmune conditions, but for the first time in 10 years I have a positive ANA of 1:80 homogenous, neurological issues (spasticity in my legs, clonus, hyperreflexia), joint pain (I have enteropathic arthritis, but I'm on tons of biologic meds), muscle pain, heart fluttering... I'm waiting on the lupus specific tests and MRI results. Hope you figure things out.

lynn41 · 04-21-2008, 10:04 AM

All I got was a letter from the rheumy indicating the following:

ANA test again positive at 1:320
Double stranded DNA for lupus - negative
Rheumatoid - negative
CBC - normal
ESR / CRP: normal
SM, RNP, SSA and SSB - negative
CCP negative.

It just seems odd to me that the he would consider the ANA jump to 1:320 as insignificant. Then again - I'm new to all this and I have read the articles about false positives and the fact that the ANA by itself is not significant in making a diagnosis. It's not just the ANA though - it's the pain, fatigue, rashes, etc. that are wearing me out!

Thanks for your reply!

Kimmioh · 04-24-2008, 11:25 PM

Quote:

Originally Posted by lynn41

All I got was a letter from the rheumy indicating the following:

ANA test again positive at 1:320
Double stranded DNA for lupus - negative
Rheumatoid - negative
CBC - normal
ESR / CRP: normal
SM, RNP, SSA and SSB - negative
CCP negative.

It just seems odd to me that the he would consider the ANA jump to 1:320 as insignificant. Then again - I'm new to all this and I have read the articles about false positives and the fact that the ANA by itself is not significant in making a diagnosis. It's not just the ANA though - it's the pain, fatigue, rashes, etc. that are wearing me out!

Thanks for your reply!

Mine was positive aith the resulrt of 1:2560, and a positive Rf at 600, Pstv anti ro and anti la, ngtv everything else. My Hair and lashes are falling out everywhere allready, and it's only been two months. What is to be done to pre THanks. A concerned frient.vent hair loss?

tinker1948 · 04-26-2008, 04:53 PM

I would not dismiss it as just fibromyalgia. I have fibromyalgia for nearly 25 years now.I was diagnosed with lupus 12 years ago but now new rhuemy not sure. Says speckled pattern leaning to wards scleredoma and or UDCTD. I also have RA and raynauds but feel left in a lurch as to what I really have.I am on plaquinal.