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Chronic Fatigue Syndrome

What Causes Chronic Fatigue Syndrome?


Date: 28/05/09
 
Despite lots of research, experts haven't been able to pinpoint Chronic Fatigue Syndrome (CFS) to one single cause. Some believe CFS (or CFS/ME) develops from multiple contributing factors which manifest as CFS/ME under the right conditions.

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What causes chronic fatigue syndrome (CFS/ME)?

Probably a question every CFS/ME sufferer asks their doctor and one that makes many doctors scratch their heads.

Besides the up-hill battle to get a proper diagnosis, when CFS/ME sufferers were asked about their biggest struggles resulting from this condition 33 per cent said education was a major concern. A further 13 per cent said dealing with a disbelieving doctor, 12 per cent said financial worries and dealing with the symptoms and 10 per cent said managing day-to-day. Isolation (44 per cent), losing relationships (31 per cent) and losing independence (20 per cent) were cited as their biggest quality of life issues.

CFS/ME: Difficult prognosis, difficult diagnosis

Despite lots of research, experts haven't been able to pinpoint CFS to one single cause. Some believe CFS (or CFS/ME) develops from multiple contributing factors which manifest as CFS/ME under the right conditions.

Contributing factors may include:

    * Genetic factors
    * Central nervous system and hormone abnormalities
    * A virus or other infection
    * Immune system abnormalities
    * Stressful conditions
    * Toxins

Not all the factors apply to everyone with CFS/ME. It’s more likely that sufferers have a combination of these factors which led to the condition. This in itself makes it very difficult for a doctor or specialist to diagnose CFS/ME.

Different combinations of these factors cause different symptoms and manifests in different ways in the body and for this reason you will find that no two sufferers experience CFS/ME in the same way. Each case of CFS/ME is as individual and unique as the person suffering from it.

Experts have now started to identify categories, or subgroups, of CFS/ME. Eventually, sub-grouping may help sufferers and their doctors to figure out the best way to treat each individual case.

CFS/ME: Genetic Factors & Chronic Fatigue Syndrome

Recent research links CFS/ME with genes involved in the hypothalamic-pituitary-adrenal (HPA) axis and the sympathetic nervous system.

The HPA axis controls your sleep, response to stress, and depression. Researchers looked at DNA that controls how your body reacts to trauma, injury and stress, and they found a common variation that could predict CFS/ME with 76 per cent accuracy. This research could be the first credible evidence of a biological basis for CFS/ME.

Other studies show genetic abnormalities in people with CFS/ME that influence immune function, cellular communication, and the ways cells generate energy.

This research suggests that some people may be genetically predisposed to CFS/ME.

CFS/ME: Central Nervous System & Hormone Abnormalities

Researchers are especially interested in some of the central-nervous-system chemicals and hormones controlled by the HPA axis:

* Neurotransmitter changes: Neurotransmitters are chemicals that communicate messages in your brain. Research has shown that some people with CFS/ME have abnormal fluctuating levels of serotonin and dopamine (both neurotransmitters).
* Stress hormone deficiencies: Research has shown the levels of the stress hormone cortisol are low in CFS/ME sufferers. This could make it hard to deal with stress, either physical (such as infection or exertion) or mental. Cortisol replacement has helped some CFS/ME sufferers. In a US study by the Centre of Disease Control showed that women with CFS/ME had low morning cortisol levels while men with CFS/ME did not, which could help explain why the condition is far more common in women.
* Disturbed circadian rhythms: Your circadian clock (part of the HPA axis) regulates your sleep-wake cycle. Evidence suggests that in some people with CFS/ME this clock is thrown off, possibly by a mentally or physically stressful event. The body is unable to re-established the proper rhythm. Sufferers appear to spend more time in the REM (rapid-eye movement) phase of sleep, which is when you're dreaming. People in this subgroup of CFS/ME get more help from sleep medications than people in other subgroups.
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CFS/ME: Infections

Many of the signs and symptoms of CFS/ME are similar to those of a lingering viral illness and it is possible that a viral-infection lies at the heart of CFS/ME. Researchers have examined three infection-related theories, though none has been proven:

1. A virus or bacteria infects the body and damages the immune system. The damage then continues to cause flu-like symptoms even after the virus or bacteria is gone.
2. After an infection, an abnormal action by the immune system triggers a virus that had become inactive to be reactivate.
3. A physiological response to viral infections occurs in people who are susceptible.

While not everyone with CFS/ME shows signs of infection, many do. Research suggest that some cases of CFS/ME are caused at least in part by a virus:

Enterovirus connection: In a 2007 study, CFS/ME sufferers were four times more likely than healthy people to have evidence of enteroviruses in their stomach tissue. Enteroviruses cause stomach infections, and symptoms of CFS/ME frequently start after some kind of stomach infection.
Rnase L: Our bodies use the enzyme Rnase L to kill viruses that attack our cells. CFS/ME sufferers frequently have high levels of this enzyme present in their bodies, suggesting chronic immune activity.
Natural Killer (NK) Cells & T Cells: NK & T cells in your immune system attack virus-infected cells. CFS/ME sufferers frequently have low levels, suggesting chronic immune activity may be depleting them.
Antibodies: CFS/ME sufferers typically have high levels of antibodies to many infection-causing organisms that cause fatigue and other CFS/ME symptoms. These organisms include those that cause Lyme disease, candida (yeast), human herpesvirus type 6 (HHV-6), measles, parvovirus and Epstein-Barr. Researchers have not been able to show that any of these is a significant cause of CFS/ME.
Post-illness onset: Up to 80per cent of CFS/ME cases start suddenly after a flu-like condition.

Some researchers suggest that changes in normally harmless bacteria in the intestine may also play a role in the development of CFS/ME.

CFS/ME doesn't spread through direct content, sufferers aren’t contagious, and in spite of well-designed studies, researchers have not been able to link CFS/ME with any specific infections.

CFS/ME: Immune System Abnormalities

Several studies have shown irregularities in the immune systems of CFS/ME sufferers, but researchers have not found a consistent pattern of abnormalities. Among the most common are allergies and an overactive immune system.

Some studies have reported that a majority of CFS/ME sufferers are allergic to such things as pollen, certain foods and metals such as nickel and mercury. So in theory, allergens may trigger a series of immune abnormalities which then lead to CFS/ME. Another theory is that allergies, stress and infection combined may deplete a chemical called adenosine triphosphate (ATP), which stores energy in cells. CFS/ME sufferers typically have low ATP levels.

Some CFS/ME sufferers have high levels of a substance called cytokines, which researchers theorise could cause some of the symptoms of CFS/ME, including fatigue and muscle aches. Various studies have reported T cell imbalances in people with CFS/ME, but other studies have not confirmed the T cell and cytokine abnormalities.

While CFS/ME appears to have a few features in common with autoimmune diseases such as lupus or multiple sclerosis, in which the immune system mistakenly attacks healthy parts of the body, most researchers now believe CFS/ME is probably not caused by autoimmunity. Tests of CFS/ME sufferers do not show markers of the organ damage generally associated with autoimmune disease.

CFS/ME: Stressful Conditions

Researchers believe your psychological makeup, personality and social environment can determine whether you'll develop CFS/ME, but they don't yet fully understand the complex relationship between these factors and the cause of CFS/ME. While these factors are probably not a primary cause of CFS/ME, they're likely to play a role in making people susceptible.

It is important to understand that CFS/ME is not a psychological disease, nor does having it mean someone is psychologically weak or unable to cope with things. While it is sometimes linked to clinical depression, this likely has more to do with neuro-chemical imbalances and/or the impact of the illness.

CFS/ME: Chemicals & Environmental Toxins

Chronic fatigue and chronic pain are often associated with exposure to various harmful chemicals and environmental toxins. These can include solvents, pesticides or heavy metals. However, because most of us have been exposed to these types of chemicals at some point, it's difficult to track down which ones might be causing problems.

A condition called multiple chemical sensitivity (MCS) causes many of the same symptoms as CFS/ME, and the two are believed to be overlapping conditions.

In the next alert in this series, I will look at the treatment options for CFS/ME sufferers.

CFS/ME: Related reading

Understanding Chronic Fatigue Syndrome And Myalgic Encephalomyelitis

Diagnosing Chronic Fatigue Syndrome

Stepping In To The ‘Minefield’ Of Finding The Right Treatment For Chronic Fatigue Syndrome

Chronic Fatigue Syndrome: Natural Measures Can Help Combat This Debilitating Condition

Myalgic Encephalopathy

Exploring The Benefits Of Malic Acid

Myalgic Encephalopathy

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Sources:

‘What Causes Chronic Fatigue Syndrome’ By Adrienne Dellwo, published online 18.04.09, chronicfatigue.about.com

‘Chronic fatigue syndrome or myalgic encephalomyelitis’ published online, hcd2.bupa.co.uk

‘InterAction – The magazine of Action for ME’ Issue 68, Summer of 2009.

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Comments

Peter Posted 27/05/2009

Chronic Fatigue in my opinion is associated with depleted glutathione levels. We all produce less Glutathione from the age of twenty but some people run low earlier. Toxins are sometimes associated with low levels because Glutathione is used up detoxifying the body. Any way taking Glutathione does not help because it is broken down in the digestive process. There are precursors that have been verified and quantified to increase Glutathione levels in our cells, it's wonderful. Glutathione is essential for cell health and all diseases start at some level of cellular dysfunction. Any how have a look at what Doctors say.

Duncan Playle Posted 27/05/2009

As an ME/CFS of nearly 10 years now I am so happy that an article like this confirms the physiological nature of the condition because it makes myself, and indeed other ME suffers, feel recognized and acknowledged as having a real condition which, in many cases, is completely life changing. Thanks for writing this and I look forward to future releases on this subject.

Duncan Playle Posted 27/05/2009

As an ME/CFS of nearly 10 years now I am so happy that an article like this confirms the physiological nature of the condition because it makes myself, and indeed other ME suffers, feel recognized and acknowledged as having a real condition which, in many cases, is completely life changing. Thank for writing this and I look forward to future releases on this subject.

Greg Timson Posted 27/05/2009

Another great article. Unfortunately it's the lack of knowledge as to what causes this condition that gives us no help in determining what the most appropriate treatments are. Your comprehensive article seems to have covered the most 'current' possible causes in an informative and accessible way! I am really enjoying this series of articles. Well done!

James Williams Posted 28/05/2009

I suffered from CFS for years until my brother talked me into taking Olive Leaf Extract. Within two weeks my CFS had vitually disappeared. I thoroughly recommend Olive Leaf Extract for CFS and colds. Buy the highest quality Olive Leaf Liquid Extract available with standardized ingredients.

John Posted 28/05/2009

I can't remember exactly when my CFS symptoms first started, but I never suffered any such-like symptoms until after I was really ill with suspected Glandular Fever. Although blood tests indicated that I didn't have Glandular Fever, I spent several days in bed completely exhausted and sweating prefusely. That for me was the catalyst for my CFS symptoms, and that's why I believe that the trigger for CFS is viral based.

Eileen Freeman Posted 28/05/2009

I thought I had ME many years ago and used aciphophillus to restore bowl flora. It made a difference. Many years later I was diagnosed with Coeliac (Celiac in America) Disease - cannot digest the gluten in wheat, barley, rye and oats. My symptoms were exhaustion. No iron stores but okay haemoglobin iron. The doctors in UK don't test for iron stores - ferritin levels - just haemoglobin. Good luck Now it appears I may have a thyroid problem or adrenal insufficiency problem and am undergoing tests. What I am trying to say is that there is always a cause - it's finding it.

Paul Blake MH Posted 31/05/2009

Hi, Autoimmune diseases are interesting there are approximately 80 to 100 with another 40 waiting for a name and if you get one you will get another and so on. Medical science cannot explain why we have this autoimmune epidemic or why you have even one of these diseases. You can trigger one of them just by having an auto accident, taking aspirin or medication or by starting a new exercise routine, even too much stress says latest research. Naturopathic medicine says, "Look for the root, it is in the basics beginning with what is on your fork, what toxins are in your body, what exercise do you do, what stress is in your life, what is your spiritual base". Scientific arrogance has led us down the wrong path we better stop and take a close look at what is happening. This month 150 new chemicals will be added to the 85,000 in the environment which are part of the autoimmune problem. They will be added too industry with no oversight control at all. Autoimmune disease is the worst kind of contradiction; for a sufferer you are attacking your body with your immune system, a world upside down. God bless you in your search. Sincerely Paul

Christine Standing Posted 01/06/2009

Thanks for this article on CFE/ME. It is in keeping with what I have found out about my illness. The onset was two years ago after returning to the UK on a longhaul flight. Toxins entered the cabin via the engines - result - aerotoxic syndrome. See more information about aerotoxic syndrome here I acquired brain damage and lung injury; the specialist has now acknowledged that I have aerotoxic syndrome... (two years it has taken me, and many skeptical doctors with resulting disappointment.) Keep it going! Christine

David McDonald Posted 25/02/2010

Thank you for this excellent series of articles. This is brilliant stuff.



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