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U researcher helps explain chronic fatigue

By Deborah Rafferty

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Published: Wednesday, September 16, 2009

Updated: Wednesday, September 16, 2009

ChronicFatigueRGB.jpg

Lennie Mahler

Alan Light, a research professor in the anesthesiology department, explains recent findings about Chronic Fatigue Syndrome patients.

Alan Light’s new research into what causes fatigue has done anything but exhaust him.

Excited over the findings in his work, he animatedly described the intricacies of all the genes splashed across the cover of the Journal of Pain that published his findings. The more a person exercises, the more a newly understood gene everyone has tells the body’s muscles they are too tired to keep working­—some to a debilitating degree, he said.

“It is surprising at the half-hour mark how much the gene increases in patients with chronic fatigue syndrome,” said Light, an anesthesiology research professor, pointing to the differences between normal patients and patients with the disorder.

This research will allow patients with CFS to better understand what is happening to them and hopefully prove to the scientific world that it is an actual disease, not an excuse for what can be percieved as lazy behavior. It will also give physicians a test to determine if patients have CFS and how to provide proper treatment to help them get better.

Light and his team of researchers identified a number of genes that increase during exercise in a ground-breaking discovery­—especially for patients with CFS. These genes produce a protein, which tells the muscles they are tired and to stop exercising.
The experiments were first conducted using mouse models. However, the problem with the mice is that they cannot tell you whether they are in pain or are tired.

In human trials, Light had two separate groups—people with and without CFS—do a simple arm and leg movement exercise for 25 minutes, which takes the same amount of energy as walking up stairs, Light said. Then they drew white blood cells from the patients at various points during the next 24 hours.

For the normal group, the patients had little trouble doing the exercise. However, the patients with CFS had extreme difficulty even finishing. Light said patients with CFS have trouble having enough energy to do everyday tasks and often do not leave the house. It’s as though someone is screaming at you, and after a while, you stop listening, Light said.
“Imagine that you have really beaten yourself doing an exercise you haven’t done in a while,” Light said. “Imagine what you feel like the next day. Now imagine feeling like that all the time. That’s what patients with CFS feel like.”

After analyzing the data from the trials, Light and his researchers found that exercise increases the amount of the proteins that tell the muscles they are tired. Normal patients show very little change, but in patients with CFS there is a tremendous amount of proteins, which could explain why the patients are tired all the time, Light said. Most of the genes Light identified were sensory, which tell the brain what the rest of the body is feeling.
For Light, the research has only just begun. He would like to analyze more what fatigue is and the difference between mental and physical fatigue. However, testing mental fatigue would be difficult because researchers could not extract brain cells because the cells do not grow back.

“What is fatigue? To most of the world, it is a sensation, something a little like pain,” Light said. “It makes you want to stop what you are doing. Fatigue is a system in place to protect us from overusing our body and brain to prevent irreversible damage.”
 

d.rafferty@chronicle.utah.edu
 

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6 comments

Your name
Wed Oct 14 2009 14:07
This is very interesting, together along with the latest information on the XMRV virus. Finally we may be getting some answers, but we need funding for research. The CDC use a definition of the illness which is too vague. I would like to ask Alan Light how his work relates to the private UK tests for mitochondrial dysfunction and ADP/ATP recycling. Does he think it is related?
Kurt with CFS in Utah
Mon Sep 21 2009 11:19
Thanks for this article, but one point needs to be cleared up. The only people who think CFS is lazy behavior are those in the public who do not realize that CFS is not the same as having ordinary fatigue. The CDC, the scientific community, and any medical personnel who are up to date on modern medical issues are already convinced that CFS is a serious and very real disease. The CDC ran a publicity campaign more than a year ago trying to help the public understand that CFS is disabling and disrupts lives and families. The PSA spots ran on television stations all over the US, including in Utah (remember the ad with the women in slow-motion trying to get out of bed while her family's life ran on around her? that was from the CDC about CFS). Hundreds of studies of CFS have shown that CFS involves a large number of physical abnormalities, but CFS research is poorly funded and a complete understanding of this disabling illness remains elusive. The fact that CFS has been a serious public health problem for decades now and a full understanding of its cause or pathophysiology is still lacking is a black mark on the political-medical-media establishment.

Over 1 million Americans have CFS, and many are totally disabled by the condition. The CDC has identified many genetic traits common in CFS and compares CFS with having late stage cancer, heart disease or multiple sclerosis. CFS has appeared in clusters suggesting an infectious or environmental component. CFS first appeared in large numbers in the 1980s during the early years of the AIDS epidemic and was systematically blocked from serious public attention due to political resistance to a second public health problem at that time. This was documented in the book " Ossler's Web."

The CFS epidemic affects more people and costs the economy more than the AIDS epidemic in the US, yet spending for AIDS research remains a thousand times more than spending for CFS. Public attention to CFS also continues to lag far behind attention to far lesser health problems, which is partly due to lack of interest by the media. A lengthy media campaign to raise awareness for CFS is sorely needed.

Regarding this study, CFS is a complicated disorder and researchers produce a new theory every few months. This research is not the first to show physical problems in CFS, but this is certainly a new and very interesting finding. I hope this paper and others will continue to pay attention to the plague of CFS that has swept the US the past 25 years or so.

Adam
Mon Sep 21 2009 07:15
It is caused by Electromagnetic Radiation. Sufferers who move away from electricity and all forms of airborn transmissions always improve.
Laurel
Thu Sep 17 2009 10:53
The problem with this illness is that we don't look sick. It's like taking a still photograph at any given point in time, especially because we are only seen in public between naps, when we are most rested. But if you were to follow us all day with a video camera, and saw just how much time every day we have to spend in bed, you would be shocked. So I'm all for gaining legitimacy in the eyes of the medical community by objective testing.
Your name
Wed Sep 16 2009 23:35
Imagine moving through life with weights strapped to your arms and legs, and with a constant infusion of sleeping pills. Thank you, Professor Light for pursuing this disease. Hopefully, identification of the cause can lead to a cure!
Your name
Wed Sep 16 2009 21:24
Finally! Something quantitative! Maybe now all the medical professionals who have poo-poo'd us for years will give us a little respect! Heck, maybe my FAMILY will give me a little respect.






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