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Rheumatoid Arthritis May Increase Pain Sensitivity

By Jennifer Davis

5/8/09 A new study suggests that people with rheumatoid arthritis are more sensitive to pain than those without the condition.

Researchers at Johns Hopkins University in Baltimore, found that people who live with rheumatoid arthritis are more reactive to pain in two ways – as a group they’re more sensitive to painful stimulation and appear to feel pain more strongly. And in the presence of pain, the immune systems of people with rheumatoid arthritis seem to react more vigorously, mounting a powerful inflammatory response.

The study was published in the May 2009 issue of Arthritis Research and Therapy.

Pain is the most commonly reported and debilitating complaint of people who have rheumatoid arthritis. But scientists say that given the scope of the problem for patients, there has been a relatively small amount of research into the topic of pain.

Robert Edwards, PhD, is a clinical psychologist working in the Pain Management Center at Brigham and Women’s Hospital in Boston. He led the research team while he was at Johns Hopkins University.

“The focus is often on getting inflammatory processes under control and thinking that once that gets done, everything will be fine. It often means that pain in RA patients is not quite ignored, but it’s relatively under targeted as an important symptom,” Edwards explains.

For this study, researchers conducted a battery of pain tests involving pressure, heat and cold stimulation. Study participants had the power to stop the pain at any time. Scientists compared pain experiences and blood samples of 19 rheumatoid arthritis patients with similar data from 21 healthy individuals. Participants each had one testing session in which their responses to a variety of painful stimuli were recorded and blood samples were taken multiple times to test their reactivity to the stress hormone cortisol as well as interleukin-6 (IL-6) and tumor necrosis factor-alpha (TNF-alpha) chemicals.

The study found that people with rheumatoid arthritis had a fairly general increased sensitivity to pain and to mechanical and thermal stimuli across several body sites. They also complained of pain from heat and cold more quickly and felt it more intensely than those without rheumatoid arthritis. 

They felt pain from heat, for example, at a temperature about three to four degrees cooler than those without rheumatoid arthritis. 

“I’d estimate that in general and on average, RA patients are 20 percent more sensitive to a painful stimuli than the controls,” Edwards says.

The implications for daily life are obvious.

“If you are more sensitive to pain and you do something like stub your toe, it’s going to hurt worse and bother you more than it would someone who’s less pain sensitive,” he says.

And there may be other long-term, negative consequences to be more pain sensitive. For example, a good amount of literature now suggests that the more sensitive to pain you are, the more you are at risk for things like long-term post surgical pain.

People with rheumatoid arthritis and those in the control group had the same TNF-a in their blood stream before pain. But after scientists applied plain, the levels in people with rheumatoid arthritis went up by a factor of three or four, where as levels in the control group did not change. Edwards says it’s not clear how pain turns up inflammation.

Daniel Clauw, MD, is a professor of anesthesiology at the University of Michigan and serves as the Director of the Chronic Pain and Fatigue Research Center. He says several factors could be causing the pain. He points out that this study shows the pressure difference was most varied in the thumb, which is the area that is most likely to be closest to inflamed joints. He says that suggests in the future, researchers should look at precisely what regions have the increased pain sensitivity to see if it’s due to inflammation of the joints or something more widespread.

Until then, Edwards says there are things that people with rheumatoid arthritis can do to minimize their pain. 

“There’s pretty good evidence out there that the way a lot of people respond to pain is they wait until it gets really bad before they do anything about it. And at this point, there’s very good reason to think that even mild pain should be treated as early as possible,” he says.

Edwards also points out that there is evidence that regular exercise and alternative approaches like yoga, hypnosis and acupuncture may help to improve pain. “So I’d strongly encourage RA patients to take advantage of these.”

Debra
06 Jan 2010, 09:35
I have been diagnosed with RA and Lupus fpr the past 26 years and feel that the last few years pain has become harder to tolerate. Just five years ago I was also diagnosed with MS and that condition has given me quite a few new set of issues and problems now it seems pain,fatigue are a constant part of life. Research into pain for RA paitents is welcome as it would hopefully carry through to other autoimmune disease pain reaserch someday.
Karen
01 Jan 2010, 14:26
I was diagnosed with RA 16 years ago. I was on very strong meds in the beginning, but the side effects were almost as bad as the disease itself. So I decided to look elsewhere. I have since learned that I can control the bulk of my RA symptoms by avoiding the nightshades and all food preservatives. About 2 to 3 weeks after I eliminated these things from my diet, I noticed a remarkable difference. I have been medication free now for 10 years.
Patt
24 Jun 2009, 17:50
I have had an ankylosing spondylitic variant of RA and OA for 42 yrs and am very sensitive to cold. I have had many surgeries and have pretty much learned to live with pain, but not the fatigue. You can make up your mind to function in spite of pain...but it is virtually impossible to overlook the fatigue. If you force yourself to function anyway, you're just setting your self up for total exhaustion. This is one area that my doctors have not been able to help me with. Exercising makes me feel even worse!
Lynne MacDonald
21 Jun 2009, 13:10
The pain from the cold that some of you are mentioning is probably due to Raynaud's Disease which is often seen in patients with RA.I have had RA for more than half of my life, 27 yrs to be exact, and have both diseases. The sensitivity to cold can be very debilitating and painful.
vickie smith
19 Jun 2009, 12:01
I have had RA. for a little over five years. I'am on Enbrel shots 25mg. twice a week. I'am on predisone 7mg. a day and also on Arava, and I still suffer everyday with pain. Is there anything at all that will really control the pain to where I could be able to function better.
Cindy
17 Jun 2009, 20:16
I was diagnosed 10 years ago with RA and I definitely notice when I bump into something, especially my hands and feet, the pain is very bad and takes longer to ease up. I am doing well but agree with Dawn above, the fatigue is tough!
Beth
14 Jun 2009, 19:36
It took about three years for drs. to agree that I had RA. During that time I was treated by my GP with steroids which was slight help with inflammation and caused me to gain nearly 15 pounds. When I finally could get an appointment - it took more than a year to get in with one because there are so few in Alaska - with a Rheumatologist and travel more than 250 miles (one-way) to begin more effective treatment it took about a year to get the symptoms tolerable - I had spent weeks at a time in so much pain that I was beginning to wonder if I would ever be able to function normally again. I have been in "maintenance mode" for about two years, but I have noticed an increasing response to pain, that requires greater time to overcome than it did even four or five years ago. Even with prescription and OTC anti-inflammatories I am easily sent into overload with inflammation and pain. If researchers want the truth of symptoms and long-term management of diseases they are to be commended for actually including those who suffer with the disease in their research and being completely open-minded about the results. Thankfully this is a premise being applied in recent years and we can anticipate an effect that will improve our lives as we try to live with RA.
Katherine S
11 Jun 2009, 17:20
I have had RA for 22 years and have had 10 surgeries related to it. I thought I had a high tolerance for pain and have only used pain medication at the very beginning of recovery from surgery, not ongoing. However, in 2007 my knee was replaced. The pain was beyond what I had ever experienced. I was on pain meds for 6 weeks - My doctor begrudgingly gave them to me and quite honestly, made me feel like a failure. I did my exercises faithfully to get full range of motion, fortunately he let me do it in water, I couldn't do anything else. But, my knee still hurts all the time (I haven't told my doctor this). The other one needs replaced too, but I won't go there until I can't walk anymore. Thanks for this study, it helps me feel a little better.
Mary M.
11 Jun 2009, 14:13
I was diagnosed with RA a year & a half ago. However, years ago I noticed that my fingers would get cold and hurt when I went skiing despite wearing good ski gloves. I know I was much more sensitive to cold than my husband, who doesn't have RA. I am feeling better now, and faithfully take my meds and supplements, including calcium, which has helped my back pain a lot.
Cecile
11 Jun 2009, 13:26
I was diagnosed with RA 8 years ago. I am 5'2", 100 lbs, slender but strong. Three years before my RA was diagnosed, I tore my R. knee medial meniscus & had arthroscopic surgery. My Orthopedic Surgeon told me I would walk in 2 weeks. I was surprised at the amount of pain & inflammation I had, the pain was unbearable. I had to learn to walk in warm water, slowly, & I did 6 mo's of physical therapy before I was able to walk again without crutches or cane. The therapists & my surgeon couldn't explain why my recuperation from surgery took so long. I have come to fear surgery because of the amount of time I was unable to walk normal. I knew something was different about me.

Even though I had subclinical RA at that time, the symptoms your study found today were definitely there for me in 1997.

Also, even earlier than 1997, I used to experience tremendous pain in my finger joints, if I hit them on something, and the pain always used to surprise me, because I do have a high tolerance of pain. My joint would immediately swell & even change color. Again, your study lines up with my perception of pain upon trauma.

Thank you for conducting these tests. Now I know these observations were not just in my head.
Dawn
11 Jun 2009, 12:32
that article suprizes me because I have been diagnosed with RA and Gout. I feel having them and knowing I will more than likely have pain I have a higher tollerance to pain because I know I just have to accept it and carry on with life I don't find myself dwelling on the pain. Now the fatigue is another story.
christine
11 Jun 2009, 11:32
I have been diagnosed with RA. I have been doing pretty well. I find that exercise eating a healthy diet and achieving a healthy weight has helped improve my RA condition.
Cathy B.
11 Jun 2009, 10:44
I have been diagnosed with RA and Fibromyalgia. My cardiologist told me that in his opinion, that fibromyalgia was a symptom of RA, not a separate condition.

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