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Critical New Piece of Fibromyalgia Puzzle Found?

by Rich Carson
September 10, 2007

Pieces of the Fibromyalgia puzzle are slowly falling into place, and researchers have been moving toward a unified theory that explains the etiology and pathogenesis of the disease.

While the conviction among the majority of Fibromyalgia researchers is that Fibromyalgia represents a significant sensitization of the brain and spinal cord, some leading researchers have formed a theory that takes the "Sensitization Theory" a step further, to what can be called the "Hippocampus Hypothesis" or "Dopamine Hypothesis." This fascinating theory states that FM is primarily a brain dysfunction resulting from stress-induced physiological changes to a part of the brain called the hippocampus and to the important neurotransmitter that it regulates - dopamine.

Specifically, the hippocampus is extremely sensitive to stress, and in fact is the brain organ that enables us to respond to environmental stressors in a way that helps us avoid danger. The best example of the beneficial stress response is when our ancestors crossed paths with a saber tooth tiger - an immediate "fight or flight" response was mandatory to ensure survival.

Studies have shown that chronic stress, however, can contribute to a disruption of normal hippocampus function. The hippocampus plays a major role in pain perception and memory formation, and it is involved in controlling the production of that crucial brain neurotransmitter, dopamine. Dopamine abnormalities have been linked to "restless legs syndrome," increased pain, and feelings of self doubt, anxiety, and problems with memory formation.

If the "Dopamine Hypothesis" is correct, then it is reasonable to assume that drugs that restore normal dopamine levels and activity in the brain should have a therapeutic effect when administered to Fibromyalgia patients.

And this is where the "Dopamine Hypothesis" picks up steam. Andrew Holman, MD, conducted a controlled, double blind study of the drug pramipexole with several Fibromyalgia patients. Pramipexole, sold under the brand name Mirapex™, is approved for treatment of Parkinson's disease - a primary dopamine disorder. Patients experienced significant improvement in their symptoms. Another drug that affects dopamine and has been approved by the FDA as a treatment for restless legs syndrome - ropinirole - also met with remarkable success in another Fibromyalgia study conducted by Dr. Holman.

All told, the Dopamine Hypothesis looks promising for several reasons. It ties in nicely to the pathogenesis of the disease - that the onset of Fibromyalgia frequently occurs during times of prolonged or intense emotional or physical stress, when the hippocampus may become overworked and become dysfunctional as a result. And it ties into the fact that dopamine, which is largely regulated by the hippocampus, may cause many of the symptoms of Fibromyalgia when its levels are unregulated.

I would like to acknowledge Patrick B. Wood, MD, and Dr. Holman for their brilliant work with brain imaging, neurotransmitter physiology, and creative pharmaceutical approaches to normalizing/regulating dopamine in Fibromyalgia. Their work has proven beneficial to many Fibromyalgia patients and may hold promise for treatment of millions more. I applaud their bold, creative, and compassionate work.

Dr. Wood explains the Dopamine Hypothesis in easy-to-understand language, using computer generated graphics and patient and doctor interviews in the acclaimed Fibromyalgia DVD "Fibromyalgia: Show Me Where It Hurts". To purchase a copy of this DVD, please visit the ProHealth store.

Wishing you health and hope,

Rich Carson
ProHealth Founder and ME/CFS Patient [Note: This Founder's Corner is repeated from a past issue of FM Treatment & Research News, by reader request.



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Stress related
Posted by: njnorris
Sep 12, 2007
This is an interesting connection to stress. I am 60 now. Due to life's circumstances severe stress has been a constant companion since my earliest childhood memories. As a young and middle-aged adult, I sometimes wondered how the extreme anxiety and fear I was experiencing could exist without affecting me physically as well. I have chosen to live unmedicated for all but the most severe episodes of anxiety and fibromyalgia pain. While not diagnosed until 10 years ago, I recall vivid episodes of mild exertion followed by severe pain as early as age 18 - with peak problems in my late 20's. My son's service in Iraq and lingering injuries have escalated stress levels in the past 3 years. Now even the slightest change in my physical routine results in flattening pain and fatigue. It would be interesting to note the side effects of the drugs administered to those in the study, as all aspects must be considered to decide. Since the drugs are approved for other conditions, it should not be hard to have a doctor prescribe the medication as a trial.
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Stress Makes Sense
Posted by: suemorr
Sep 12, 2007
It makes perfect sense to me that it would relate to stress. I'm 55 and have had quite a few stressful experiences since my teen years. "Fight or flight" and I are old friends. I had read a previous article about dopamine being very helpful with FM symptoms. How wonderful that progress is being made, and someday soon our pain will be gone.
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Fibromyalgia and the brain
Posted by: Hamm40
Sep 12, 2007
It makes a great deal of sense to me that stress plays a very important role in Fibromyalgia. I have had my Mother to die of cancer. Then my Brother dropped dead of a heart attack, my Father has two types of cancer and I am his caregiver. I also have a shadow over my left breast and lymph node swelling in my armpit and I'm only 41.
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chronic stress
Posted by: suzetta
Sep 12, 2007
Can chronic stress be industrial related? Can this theory be used as valid findings in a court of law? Please respond. Thank you. Suzette
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Requip is wonderful
Posted by: bettemabry
Sep 12, 2007
Requip has been a part of my medications for over 7 years. In 1991 I was injured in an auto accident and among my injuries was the need to have 3 vertebrae fused in my neck. Next I developed FM. Other health issues developed including sjogrens, degenerative joint disorder in lower back, etc. I have suffered with restless leg since my 20's. As time went on it became worse. About 7 years ago I attended a support group meeting for people with restless leg syndrome. Some researchers from Emory University Medical school (in Atlanta, GA)spoke about requip being studied for RLS. I took the information sheets to my rheumatologist and asked if I could try the requip. Given our excellent patient-physician relationship, she agree to let me try it. After trying different dosages, I found relief with 1 mg three times a day. If I get off schedule, the rest of that day is difficult. I feel that this has also helped my FM, except for flare-up times with stress, injuries, other health issues such as sjogrens, hypothyroid, etc. I am glad to see this article, especially because of the experience I have had since attending the Emory researchers meeting. (As a side note, at that time they were doing lots of research about the issue in the island of Iceland.)
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Fatigue
Posted by: blueotter
Sep 12, 2007
I have had fibromyalgia for almost 24 years -- at least the extreme fatigue part has been with me that long, and the pain has been there longer, though I was told it was in my head because I was so young. When I search my memory, I can't say I've had severe stress, but then I suppose stress affects different people differently. These days I have a skin/apocrine gland problem that is highly affected by stress, and I can honestly say that everyday stresses Do Indeed have an impact! Who knew? My immune system is otherwise very healthy -- I take some very powerful supplements that seem to keep away colds, restless leg, and most of the skin problems -- but absolutely nothing has been able to touch the fatigue. I heard of a new drug that came out this summer (2007) that is given for fatigue (can't remember the name, sorry!), but haven't tried it yet. My doctor said she never heard of it, and won't prescribe something unknown to her, but then I am in the process of finding a new doctor who lives closer to me, anyway -- the fatigue tends me make me a Champion Procrastinator. As soon as I relocate the name of the drug and find a closer physician, I will try to post the name of it here. Is there hope?
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doesn't fit my case
Posted by: applepansy
Sep 12, 2007
My FMS didn't first occur during a time of high stress. I believe that FMS can cause changes in the brain but I think it's a symptom and not the root cause. If mirapex can helps improve quality of life for some FMS patients that's great. . . I'll be surprised if it helps ALL fms patients. applepansy
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FM related to other autoimmune diseases
Posted by: Katrinakilledme
Sep 12, 2007
I'm 42, had thyroid cancer at 19 (Hashimoto's), and have had chronic pain and all the syptoms of FM since. I was also diagnosed with mixed connective tissue disorder with lupus being the most prevelant, but not as bad as my FM, and I can tell the difference. I read that autoimmune diseases often come together. How does the dopamine theory of FM explain its autoimmune capacity as well as how dopamine affects the brain with mixed connectived tissue disorder?
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Dopamine and FMS
Posted by: SunflowerJRT
Sep 12, 2007
While I think it's great that researchers are looking for answers, I find it extremely difficult to watch countless numbers of family, friends and even strangers that are suffering with diagnosed and undiagnosed symptoms of CFIDS and FMS. I personally have had this dilemma trying numerous conventional and alternative treatments for my own case of CFIDS/FMS without any success until I found the Marshall Protocol at www.marshallprotocol.com in July 2004. I am now much improved although I'm not well yet and I do believe I still have a long way to go on my road to recovery but I am so much better than ever before and I believe the answer has already been revealed in Dr Marshall's groundbreaking work!
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Mirapex
Posted by: leann_sweeney
Sep 12, 2007
I'm not sure I buy this theory. I believe fibromyalgia is a pain disorder--yes a neurological problem--but I'm not sure dopamine--a very very strong drug--is the answer. I was prescribed Mirapex and of course it is EXPENSIVE. I was supposed to be on a graduated dosage but I vomited immediately after the first tiny dose and said, "not for me." Neurontin, on the other hand, has a generic and I was taking a small dose. But now that I am taking a higher dose--gradually increasing it--I am feeling relief for the first time in fifteen years. Neurontin for fibro (in a dosage of 1200mg-1800 mg) has been shown in studies to be as effective as Lyrica, the again oh-so EXPENSIVE and single FDA approved treatment for fibro. I think the drug companies have discovered a giant market of people desperate for relief. I say beware of articles like this suggesting expensive treatments like Mirapex. It may work for some, but so many people with fibro are disabled. They can't afford this!
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Stress and Fibromyalgia
Posted by: swifter
Sep 12, 2007
I am a 56 year old female with Fibromyalgia, Hypothyrodism, Restless Leg Syndrome, Irritable Bowel, and on a Gluten & MSG free diet, plus other physical problems. I am agreement with the argument on Fibromyalgia being Stress related. My father was abusive to my mother and they split up when I was two. She married a man when I was 5, who it turned out did not want me and I was afraid of. We moved in with her father just before I turned six. He was strict and I was scared of him for a long time, but he never came close to abusing me, he just never showed any affection. I came down with Rheumatic Fever during first grade and spent a whole summer in bed. I have always had a low self esteem and ended up pregnant and married when I was 16. I ended up being slugged in the jaw once and the eye three times, threatened with a gun more than once and finally left after seven years, scared to death he would kill me. My second husband never hit me just treated me horribly and took his anger out on my first child, when I figured it out I left with three children ages 1,2 and 11. I stayed single for over seven years, but had a boyfriend who out the clear blue one night, he was irritated over something he had done, slugged me in the jaw. When I was 35 I re-married and at 36 I ended up having TMJ and had a 15 hour jaw surgery. My mouth was wired shut, my medicines had alcohol in them, I got sick and lost 15 pounds in a week and a half, and had my first round with Restless Legs. During the first 3 years we were married, 30 relatives and friends died. During the years I have had problems with tiredness, muscle aches (growing pains), Asthma (stressed induced?), pnuemonia of various types, Bronchitis and other illnesses. It was not until I was rear-ended, while sitting in traffic, in 1999 that I was diagnosed with Post-Traumatic Fibromyalgia, and of course most doctors and people did not believe in it then. The doctor I have now is great and we went back through my history and have decided that I probably have had Fibro since I was slugged in the jaw the first time in 1969. This is just a short history of my life, but I truly believe my Fibro is Stress-related.
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Not so Sure...
Posted by: didders
Sep 12, 2007
I have severe FMS. Confirmed repeatedly. So why do any and all dopamine re-uptake inhibitors make me insane? I get the adjusting period is hard for many, but I never adapt. Just go nuts with weird ideation, hyperactivity, and anger - not me at all. This theory may be part of the answer but seriously doubt it's THE one.
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wellbutrin sr 150 mg twice daily
Posted by: hensue
Sep 14, 2007
This drug is dopamine related. It has saved my life. We have had to tweak and add other drugs for jitters. I have chronic fatigue and fibromyalgia all over horrible pain. Of course it is no cure. I still work but I have to rest, No more walking seems as if anything aerobic I do. I have a flare. So I dont work out or walk or swim as you know the day after or next you will be so fatigued and in pain. As the doctor said listen to your pain if it makes you hurt do not do it. Easy to say. This has helped me function and keep functioning, I have always thought it was some how dopamine related. I believe we are on the right road! Sounds very encouraging to me! Keep me posted Thanks Sue hensue@rose.net
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Mirapex; childhood sexual abuse as cause?
Posted by: annemargis
Sep 14, 2007
Mirapex has helped me more than any other treatment. I tried Neurontin for a year, and it didn't help at all. Lyrica didn't help either. I'd like to see a survey done on how many fibromyalgia sufferers were sexually abused as children. Seems like every sufferer I meet says yes.
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Thanks to all!!!
Posted by: didders
Sep 15, 2007
Hi Kids - Cinda here...Fibromyalgia Network News also noted that our brains seem to age faster especially in the hippocampus (dopamine producing?) area. And the article - different doc - did mention fibros' lessened dopamine. Perhaps the dosages in meds like Wellbutrin are too high for us and that's the problem. There's slight dopamine re-uptake action in Cymbalta, which works great for me. I am deeply grateful for your response to my post because the real story comes from the people who have used these meds - not the drug companies or doctors getting golf trips for pushing them on us. Hugs to all! Cinda
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stress related fibro
Posted by: acheybreakybody
Sep 21, 2007
I can see a definite correlation between stress and fibro and also injuries/surgeries. What was described in the article, and how my brain started going on me when I was at work, fits me to a tee. I ended up quitting work, I couldn't handle it anymore. I worked in a bank. I noticed the higher my position got, the worse I felt. (Stress) I was not sexually abused. The people I know who have fibro were not abused either. But that is definitely a stessor. I have not tried any of these drugs mentioned.
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fibromyalgia
Posted by: maryellenthier
Oct 25, 2007
I am not experienced with the new treatment of mirapex,however,I was diagnosed at age 12 with rhumatoid arthritis.Although I never had the typical swelling of joints or crippling affects.I was diagnosed with FMS 2 years ago at age 49 after 7 or 8 years of complaining.I truly belive this is all stress related.I had a father who was an alcoholic,although I was never physically abused there was much stress in the household.I married at age 18 and stayed in that marriage for 22 years.This was an emotionally abusive marriage and also much stress finacially.The jobs I had,most recent was in a bank was very stressful and I became sicker and had a lot of concentration problems.Thankfully I was able to take time off and was confirmed by 7 Drs.that I was suffering from FMS and was put on disability.I have a terrific husband and family now who understands and it helps so much to have that when I am having a "down" time.I really belive that the RA I was diagnsed with as a child was FMS-which was not recognized 40 years ago.I think we are all different and need our personlized treatment plan - nothing works for some and something works for others.I also belive mild exercise and less sugar help very much.I was put on methadone at one point--I took one dose.That was definately not for me! I am on Xanex and ibuprophen.So far,I am dealing with really bad hip pain with darvocett and skelaxin as needed.Usually only 2-3 times a week.I would rather not take medication at all,but sometimes am glad it is available.I have lost 40 pounds this year and that seems to have helped quite a bit.Best wishes to all who are suffering.Never give up! I am thankful for this message board and hope to find some friends in the same position as I am.
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