The Causes of Chronic Fatigue Syndrome (ME/CFS)
While the cause or causes
of chronic fatigue syndrome (ME/CFS) are still unclear researchers have documented numerous abnormalities that
have sparked considerable speculation regarding its cause.
Overall, research
findings suggest chronic fatigue syndrome (ME/CFS) is a multi-systemic
disorder involving the immune, neuroendocrine and cardiovascular systems.
Triggering Chronic Fatigue Syndrome (ME/CFS): A wide variety of events including
infection, injury, physical or psychological stress and toxin exposure have been
reported to trigger chronic fatigue syndrome (ME/CFS). Not all patients
can identify a triggering event. How such a process occurs is still unclear but
researchers are increasingly focused on the central nervous system and the ways
that stressful events such as injury and infection can affect the functioning of
the brain.
Central Nervous System Dysfunction: Several models of
chronic fatigue syndrome (ME/CFS) begin with an external event (infection, toxin, physical or psychological
stressor) that ultimately translates into central nervous system damage. Abnormal
patterns of brain activity, reduced brain blood flows, reduced gray matter volume,
altered metabolic findings, and others suggest areas of the brain involved in the
stress response, energy production, concentration, motivation, fatigue and pain
are damaged in chronic fatigue syndrome (ME/CFS).
Immune Defects: The flu-like symptoms
chronic fatigue syndrome (ME/CFS) patients often experience at the diseases onset has made
the immune system an important research emphasis. Several immune abnormalities
could contribute to the problems patients face.
Chronic Fatigue Syndrome (ME/CFS): the Basics
-
Impaired Cellular Immune Response
– Two abnormalities
in the responses cells have to infection in the 'interferon pathway' have been documented.
An antiviral enzyme in this pathway called the RNase L has been shown to be
fragmented in many patients. A subset of chronic fatigue syndrome
(ME/CFS) patients also display increased activity of another enzyme called protein-kinase
R (PKR) that is involved in killing cells infected with pathogens. These problems
suggest the immune systems of chronic fatigue syndrome (ME/CFS)
patients could
have troubles finding pathogens and killing the cells they've infected.
-
Natural Killer
(NK) and T-cell Dysfunction – NK and T-cells are two other components of the immune response
to pathogens. A set of chronic fatigue syndrome (ME/CFS) patients have been shown
to have reduced NK cell numbers and poor NK and T-cell functioning. These problems
also could interfere with the ability of the immune system to find infected cells
and kill them. Intriguingly some researchers believe that chronic immune activation
due to an underlying chronic infection has caused these cells to 'burn out'.
-
Th1/Th2 Imbalance
– There are two general branches (Th1/Th2) of the immune system. Some patients appear
to have an over activation of the anti-inflammatory (Th2) branch and an under activation
of the pro-inflammatory (Th1) branch of the immune system. This could cause increased
rates of allergy and sensitivity on the one hand and difficulty fighting off pathogens
on the other.
An Undiagnosed Chronic Infection: Chronic fatigue
syndrome (ME/CFS) patients were recently reported to be 18’s more likely to harbor
a pathogen than healthy controls. The NK cell ‘burn-out’, increased T-cell activation
and increased rates of cell suicide (apoptosis) in CFS could be caused by a chronic
infection. Preliminary study results suggest that antiviral drug therapy may be
able to cure some
CFS patients.
Impaired Stress Response: A significant number of patients
have reduced hypothalamic-pituitary-adrenal (HPA) axis functioning and lowered cortisol
levels. Since the stress response is important in mobilizing the bodies energy stores
for activity an impaired stress response could contribute to the fatigue patients
experience. Because the HPA axis also plays an important role in down regulating
the immune response low HPA axis activity could also contribute to the chronic
immune activation believed present.
Increased Sympathetic and Decreased Parasympathetic Nervous System (SNS/PNS) Activation:
Increased SNS activity could result in narrowed blood vessels and the low
blood volume, reduced brain and muscle blood flows, heart abnormalities under stress
and other problems seen in chronic fatigue syndrome (ME/CFS). Reduced PNS activity
could also contribute to unrefreshing sleep.
Genetics: Most assessments of the genetic component of
chronic fatigue syndrome (ME/CFS) rate it as ‘moderately” important. While
chronic fatigue syndrome (ME/CFS) is not strictly hereditary some evidence suggests that
it runs in family. Several gene mutation studies have found increased rates of neuro-endocrine
and immune mutations in the disease.
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The Phoenix Rising website is compiled by a layman. It is not a substitute for
a physician and is for informational uses only. Please discuss any treatments in
these pages with your physician./em>
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Chronic Fatigue Syndrome A Biological Approach Ed. Patrick Englebienn,, Kenny DeMeirleir
M.D, Ph.D., CRC Press. Washington D.C. 2002
Chronic fatigue syndrome is associated with diminished intracellular perforin. Maher
KJ, Klimas NG, Fletcher MA. Clin Exp Immunol. 2005 Dec;142(3):505-11.
Chronic fatigue syndrome: probable pathogenesis and possible treatments. Drugs.
2002;62(17):2433-46. Review. Evengard B, Klimas N.
2007 IACFS Conference Summary: The Immune System, Gut, Pain and Sleep.
Polymorphisms in genes regulating the HPA axis associated with empirically delineated
classes of unexplained chronic fatigue. Smith AK, White PD, Aslakson E, Vollmer-Conna
U, Rajeevan MS. Pharmacogenomics. 2006 Apr;7(3):387-94.
Patients with chronic fatigue syndrome have reduced absolute cortical blood
flow. Yoshiuchi K, Farkas J, Natelson BH. Clin Physiol Funct Imaging. 2006 Mar;26(2):83-6.