ME/CFS pathophysiology

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [2]


The pathogenesis or the mechanisms and processes of Chronic fatigue syndrome (CFS) are gradually being revealed through research, including physiological and epidemiological studies. In a basic overview of CFS for health professionals, the CDC states that "After more than 3,000 research studies, there is now abundant scientific evidence that CFS is a real physiological illness."[1]

Chronic fatigue syndrome (CFS) or (ME) has been described in a 2008 Toxicology journal article as, "a constellation of multi-system dysfunctions primarily involving the neurological (nervous system), endocrine (hormone system), and immune systems." The article states recent research suggests the potential that xenobiotic (chemicals), infectious agents, stress, and other insults in early-life may be a component of later-life CFS.[2]

Pathophysiology (1) Immune system, Infection

A 2007 article in the journal Autoimmunity summarised; “The current concept is that CFS pathogenesis is a multi factorial condition in which an infective agent cause an aberrant immune response characterized by a shift to Th-2 (cytokine) dominant response. When the response fails to be switched-off, a chronic immune activation occurs and is clinically expressed in the symptomatology of CFS." [3]

Immune dysfunction

When compared with CFS patients with normal natural killer cell activity, a 2006 study found those with lower levels reported less vigor, more daytime dysfunction, and more cognitive impairment; with the researchers suggesting this to be useful at subtyping.[4] A systematic review on the immunology of CFS (published in 2003) found an inverse association between study quality and findings of low levels of natural killer cells (suggesting that the association may be related to study methodology), although no such association was found with studies finding abnormalities in T cells and cytokine levels.[5] In 2006 an updated review on the phenomenology and pathophysiology of CFS found that, "immune system involvement in the pathogenesis of CFS seems certain but the findings on the specific mechanisms are still inconsistent."[6] There is also evidence that people with CFS have improper gene expression including both over expression and under expression of genes involved in the immune system (see the gene expression section).

RNase L deregulation

Several studies have detected an abnormal form and activity level of 2-5A synthetase/RNase L enzyme (antiviral immune response) in some CFS patients[7][8][9][10][11][12] that appears to correlate with a reduction in exercise capacity,[13][14][15][16] and daily functioning. [17] A review published in 2005 suggested that this impaired pathway is of clinical importance and that further studies addressing treatment of this deregulation are warranted.[18] A study found that elevated RNase L did not correlate with alpha-delta sleep.[19]

Hyperactive immunity

Autoimmune disorders, representing a hyperactive immune system, most likely through a cell-mediated process, have been suggested.[20][21] In July 2005, researchers in the UK reported significant gene changes in the white blood cells in CFS patients consistent with the theory of immune system activation, possibly by an antigen triggering a constant immune fatigue state. The study, led by Dr Jonathan Kerr, discovered that 35 white blood cell genes, out of a total of 9,522 genes scanned were demonstrating differential function. There was also suggestion of neuronal and mitochondrial dysfunction as a result.[22]

Allergies

Patients with CFS commonly develop additional problems with allergies or food intolerance.[23][24][25]

Immunodeficiency

Immunodeficiency disorders (underactive immune system) have been reported. In 1989, an Australian study documented a loss of immunological integrity in one hundred CFS sufferers.[26] The authors found disordered ratios of T-cell subsets and reduced levels of immunoglobulins specifically IgG 1 and IgG 3; there have since been other similar findings,[27][28][29][30] and a review[31] Most strikingly, using the French Multitest to measure the body's response to a variety of antigens, the Australian group found that 33% of the subjects were hypoallergic, meaning they had a reduced immune response to the tested antigens, while an additional 55% were completely anergic (no immune response to the antigens).

Cytokine pattern

Cytokine pattern; several studies[32][33][34][35] and a number of reviews[31][36][37][3] indicate there is a cytokine pattern of type 2 response including Th2 T helper cell, bias in CFS. This promotes the humoral immune system which stimulates B cells and increases antibody production. It is suggested that this explains some immune dysfunctions in CFS. A reduction in Th1 response has also been found in some CFS studies.[38][39][40] with implications for altered Th1/Th2 balance. Therapeutic interventions aimed at induction of a more favorable cytokine expression pattern and immune status are being investigated.[31][41]

Infections

Enteroviruses

Often, there is evidence of enteroviruses, e.g. the Coxsackie virus.[42] The type of enterovirus varies, which can affect symptoms. Polio virus is one enterovirus associated with ME, in earlier times of outbreaks, before polio vaccination was common, paresis (paralysis) was often found in ME patients; this is no longer the case. [25] Stomach biopsies of 80% of CFS patients showed the presence of enteroviruses in one study, as opposed to only 20% among controls, and nearly all biopsy specimens had microscopic evidence of mild chronic inflammation.[43] Hyde and others suggest that these enteroviruses had been latent to be awakened by another, triggering infection, after which the immune system stays chronically active to combat the enterovirus. [25]

Reviews report different laboratories from Europe and, recently, from the USA have found enteroviral RNA in the tissues, including peripheral blood mononuclear cells, muscles and stomach, of patients with CFS. Chronic viral persistence through the formation of stable doublestranded RNA reconciles the two opposing observations of the past two decades: – the absence of live virions in chronically infected patients and animals and – the presence of enteroviral RNA in the blood or other tissues of patients. [44] [45] [46] [47] [48] [49] [50] [51] [52] [53]

Epstein-Barr virus

For many years the ubiquitous Epstein-Barr virus, present in 90% of the population, that commonly causes infectious mononucleosis also called glandular fever, was the principal suspect based on abnormal immunologic responses observed in uncontrolled studies.[54][55] Subsequent studies using various types of controls have had mixed conclusions.[56][57][58] Recent reviews consider EBV a factor either as a post infectious causal factor, [59] [60] or in reactivation, in subsets of patients. [61]

Other viruses

Other implicated viruses include Ross river virus,[62] [63] Borna disease, [64] [65] Parvovirus B19 [66] [60] also herpes viruses Cytomegalovirus (HHV-5), [67] [68] [69] Human Herpesvirus Six (HHV-6) and HHV-7, [70] [71] [72] A review by Soto and Straus in 2000 states the evidence argues against an ongoing active herpes virus infection,[73] more recent reviews suggest these viruses may play a role in triggering or perpetuating CFS in subtypes. [74][75]

Bacterial

Bacterial infections associated with CFS include;

Q Fever (Coxiella burnetii ), can cause a post infectious fatigue syndrome following infection as indicated in reveiws [76] [60] [77] and from findings. [63] [78] [79] [80] Genetic polymorphism studies support the concept of different immune states in chronic Q fever, determined by genetic variations in host immune responses. [81]

Chlamydia pneumoniae Patients have been found in study to have higher rates of infection than controls. [82] in review [60]

Mycoplasma of several types and even multiple type infections have been found in high prevalence in CFS patients. [83] [84] [85] [86] One study tested persons with CFS identified in the general population and found no sign of infection. [87] A review concludes it is not clear whether mycoplasmas are associated with CFS/FMS as causal agents, cofactors, or opportunistic infections. [88] [89] Although multiple bacterial and/or viral co-infections (Mycoplasma, Chlamydia, HHV-6) in CFS patients have been associated with increased severity of signs and symptoms. [82]

Enterobacteria There have been findings of the involvement of gram-negative enterobacteria in the etiology of CFS and for the presence of an increased gut-intestinal permeability associated with severity of symptoms. [90]

Other immunological and infection findings

  • A study published in 1995 found that 3 immunological tests (protein A binding, Raji cell, or C3/C4) best discriminated CFS patients from fatigued controls.[91]
  • A study found that while exercise worsened symptoms in CFS patients, it also increased allergen challenge response only in the CFS group, regardless of allergy status.[92]
  • A study found that fatigue persists in a significant minority of patients for six months or more after infections, suggesting post-infective fatigue syndrome is a valid illness model for investigating CFS.[93]
  • In a study on people who had glandular fever (which is caused by the Epstein-Barr virus), no difference was found between the levels of virus in the blood from patients who recovered quickly when compared with those whose fatigue lasted more than six months, although the latter had an altered immune response. The scientists involved believed this suggests CFS can be caused by neurological damage done (during the acute infection phase) to parts of the brain which control perception of fatigue and pain.[94]
  • Other bacterial micro-organisms may be associated with CFS, a veterinary surgeon and his co-worker handling CFS animal cases associated with Staphylococcus spp. Bacteremia, contracted the illness and their CFS was diagnosed to CDC criteria. [95]

Pathophysiology (2) Nervous system

Chronic fatigue is a typical symptom of neurological diseases, including chronic fatigue syndrome, is also seen in diseases that affect the central, peripheral, and autonomic nervous systems (central fatigue). Enhanced perception of effort and limited endurance of sustained physical and mental activities are the main characteristics of central fatigue. Metabolic and structural lesions can cause muscle fatigability (peripheral fatigue) also disrupt the usual process of activation in pathways interconnecting the basal ganglia (peripheral nerves), thalamus, limbic system, and higher cortical centre are implicated in the pathophysiological process of central fatigue. A state of low cortisol might sensitise the HPA axis to development of persistent central fatigue after stress. [96]

Neurological abnormalities

Researchers have found evidence that CFS may involve distinct neurological abnormalities. MRI and SPECT scans show abnormalities within the brain.[97] Studies have shown that CFS patients have abnormalities in blood flow to the brain[98] possibly indicative of viral cause[99] and similar but not identical compared to patients with clinical depression.[100][101] A number of studies have shown that CFS patients have abnormal levels of neurotransmitters including increased serotonin[102][103] (the opposite of what is found in primary depression).[104] Reduced brain serotonin receptor sensitivity or number,[105] and high auto antibodies to serotonin have also been found.[106] Recent studies found altered gene expression in the brain’s serotonin and sympathetic nervous system pathways,[107] with altered responses of the HPA axis to serotonin.[108] Other reported neurotransmitter irregularities include glutamate,[109] acetylcholine sensitivity associated increased cutaneous microcirculation,[110] and autoantibodies to cholinergic receptors associated with central pain.[111] Beta-endorphin, a natural pain killer, has been found to be low in CFS patients, the opposite of what is found in primary depression.[112][113]

Dysautonomia

Dysautonomia is the disruption of the function of the autonomic nervous system (ANS). The ANS controls many aspects of homeostasis. The dysautonomia that evidences itself in CFS shows up mostly in problems of orthostatic intolerance - the inability to stand up without feeling dizzy, faint, nauseated, etc.[114] Research into the orthostatic intolerance found in CFS indicates it is very similar to that found in postural orthostatic tachycardia syndrome (POTS)[115] and hypocapnia.[116] POTS and CFS patients exhibit reduced blood flows to the heart upon standing that result in reduced blood flow to the brain. The reduced blood flows to the heart are believed to originate in blood pooling in the lower body upon standing. Many CFS patients report symptoms of orthostatic intolerance and low or lowered blood pressure.[117] [118] [119]

Inner-ear disorders

Problems such as Meniere's, also tumor in the inner ear, [120]or Benign Paroxysmal Positional Vertigo (BPPV) can cause dizziness, vertigo, and fatigue. Tinnitus is also quite common.[25] Antibodies associated with hearing loss have been found in CFS and FMS patients with inner ear disorders[121]

Orthostatic hypotension

Syndromes of orthostatic intolerance, in particular neurally mediated hypotension (NMH) and postural orthostatic tachycardia syndrome (POTS), have been shown to be associated with chronic fatigue syndrome.[122][123] These conditions, which reduce blood flow to the brain after periods of standing, can be diagnosed with a tilt table test. A clinical trial of fludrocortisone, a drug sometimes used to treat low blood pressure, showed little or no benefit for people with CFS.[124]

Psychiatric abnormalities

Depression

There is some overlap in symptoms between depression and CFS, and sometimes cases of CFS are mistakenly attributed to clinical depression. There are, however, many clinical differences between the two. [125]

Clinical depression often responds well to physical exercise, whereas CFS is characterised by exercise intolerance but with a willingness to be active. (See section on post-exertion symptom exacerbation.) Comorbid depression occurs in 10-15% of CFS patients and should be treated as usual, except that the patient’s energy level, cognitive dysfunction and drug sensitivity must be taken into account. [125] Comorbid depression may be a pre-existing condition, or the result of living with CFS.

Stress and trauma

The majority of people who experience stress/trauma do not develop CFS, but these factors (including infection) increase the likelihood of acquiring CFS within one year[126][127] and a genetic disposition to CFS has been demonstrated. Two studies suggest that self-reported childhood stress/trauma significantly increases the likelihood of acquiring CFS as an adult: A preliminary study found a 3 to 8 fold increase (depending on the trauma type).[128] A study involving participants from the Swedish Twin Registry found that in matched case-control analyses, higher emotional instability and self-reported stress were significant risk factors (odds ratios, 1.72 and 1.64, respectively), while in co-twin control analyses the risk of emotional instability decreased to 1.02 whereas that of stress increased to 5.81 (suggesting genetic influences); there was also no association between extraversion and fatigue.[129] Anxiety disorders have been associated with CFS in 5-15 year olds.[130]

The CDC stated in 2006, their studies found gene mutation and abnormal gene activity levels in CFS patients that relate to the function of the hypothalamus-pituitary-adrenal (HPA) axis, which helps regulate the body's stress response.[131] Earlier CFS research also found evidence that suggested abnormal stress response was associated with subtle dysfunction of the HPA axis. Questions remain about the pathophysiology of these findings.[132][133][134] The controversy surrounding CFS has caused some social issues for patients and may contribute to their stress (see the Social issues section).

Psychoneuroimmunological interactions

A 2006 review published in Current neurovascular research states that there is growing evidence of autoantibodies to neuronal or endothelial (interior surface of blood vessels) targets in psychiatric disorders and hypothesizes how autoantibodies can play a role in the psychiatric disorders present in CFS.[135] Researchers involved in a review examining an immunological basis for CFS concluded that neuropsychiatric symptoms in CFS patients may be more closely related to disordered cytokine production by glial cells within the central nervous system rather than to circulating cytokines.[136] In one study, autoantibodies for muscarinic cholinergic receptor had been found in over half of the CFS patients and seemed to correlate with the severity of the "feeling of muscle weakness".[137] Elevated levels of nitric oxide (not to be confused with nitrous oxide) has been found in some CFS patients.[13] One hypothesis is that elevated levels of nitric oxide may contribute to a "sensitization" of the nervous system that results in behavioral changes.[138]

Other findings

Pathophysiology (3) Endocrine system, Other

In a 2006 update in the journal Curr Opin Psychiatry it was said; “Recent advances in understanding the pathophysiology of chronic fatigue syndrome continue to demonstrate the involvement of the central nervous system. Hyperserotonergic state and hypoactivity of the hypothalamic-pituitary-adrenal axis (HPA axis) constitute other findings, but the question of whether these alterations are a cause or consequence of chronic fatigue syndrome still remains unanswered.” [139] Alterations in serotonin signaling can lead to physiologic and behavioral changes. A 2008 study of gene polymorphisms indicates genetic predisposition possibly resulting in enhanced activity of serotonin may be involved in the pathophysiology of CFS. [140]

Endocrine dysfunction

Thyroid and adrenal disorders can cause CFS-like symptoms, as can several other known endocrine disorders.

Hypothalamic-pituitary-adrenal axis (HPA axis)

The HPA axis controls levels of hormones such as cortisol in the body. It is activated in a circadian (daily) cycle and modulated by stress, digestion, illness and other factors, and is important in regulating energy metabolism, the immune system, stress responses and inflammation in the body.

The HPA axis has been much studied in CFS which has shown underactivation with low cortisol not caused by adrenal insufficiency.[141][142][143][144][145] enhanced sensitivity of the HPA axis to negative feedback, [146][147] and a possibly altered diurnal cortisol rhythm. [148] These results have not been replicated in all CFS patients, so it is not clear whether this is just a subset of patients. [149] [150] It is also not clear if the HPA axis abnormalities are a cause or a result of the illness. However, a review has concluded, that even if the HPA axis dysfunctions are secondary to other factors; they are a likely factor in symptom propagation in CFS.[143]

Gene expression

Gene expression is the process by which the inheritable information in a gene, such as the DNA sequence, is made into a functional gene product, such as protein or RNA. Research into CFS has found abnormalities in gene expression, and the CDC has conducted over twenty related studies itself.[151] [131] It has been found that patients with CFS have specific abnormalities in expression of multiple genes which are involved in the biological process of transport (both vesicle-mediated and protein transport) and this became accentuated when CFS patients exercise.[152] Another study found that "the differentially expressed genes imply fundamental metabolic perturbations", such as those involved in purine and pyrimidine metabolism, glycolysis, oxidative phosphorylation, and glucose metabolism.[153] Several other studies have also suggested a genetic component to CFS involving immune dysfunction;[154] T cell activation, perturbation of neuronal and mitochondrial function, possible links to organophosphate exposure and virus infection;[155] immune response, apoptosis, ion channel activity, signal transduction, cell-cell signaling, regulation of cell growth and neuronal activity;[156] some of which may be treatable with drugs that are already available.[157] Gene expression abnormalities have been found relating to the central nervous system, metabolism and immune system; and has been associated by the CDC with impaired response to physical and psychological stresses in people with CFS. [131] Linking genes to specific symptoms has been difficult, although is likely to be an important means to elucidate the pathogenesis of CFS.[158]Seven subtypes of CFS/ME patients with distinct clinical differences have been identied in several gene expression studies.[159] [160]

Genetic polymorphisms

Polymorphism in biology occurs when two or more clearly different types exist in the same population of the same species. Preliminary studies have suggested that the risk of developing CFS may be influenced by polymorphisms in genes affecting the central nervous,[140][161] endocrine,[162][163][164] immune,[165][166] and/or cardiovascular systems.[167] A review published in 2007 stated that certain genetic polymorphisms might be regarded as predisposing factors.[168]

Oxidative stress

Oxidative stress is an imbalance between the production of reactive oxygen and a biological system's ability to readily detoxify the reactive intermediates or easily repair the resulting damage. Several studies[169][170][171][172][173][174] and a review[175] have implicated oxidative stress in CFS symptoms; especially relating to fatigue, pain and postexertional malaise/exercise intolerance. According to research, the findings on oxidative stress and nitrosative stress (nitric oxide-related toxicity); are associated with an inflammatory response, seem consistent with abnormal 2-5A synthetase/RNase L enzyme (antiviral) activity and involves an immune response, against disrupted lipid membrane components, (by-products of lipid peroxidation ) and to nitric-oxide modified amino acids that have have become immunogenic; related to symptoms and severity in CFS.[176][16][177] Gene expression studies suggest a common link between oxidative stress, immune system dysfunction and potassium imbalance in CFS patients leading to impaired nerve balance strongly reflected in abnormal heart rate variability.[178]

Metabolic disorders

Metabolic disorders and mitochondrial disorders can cause symptoms that strongly resemble CFS.[179] Mitochondrial disturbances have been discovered in patients diagnosed with postviral fatigue syndrome.[180] and mitochondrial dysfunction is considered a factor in PVFS and CDC defined CFS patients.[181][61][182][183]

Folate deficiency (suspicion by elevated homocysteine and low serum folate) may mimic CFS symptoms.[184][185]

Essential fatty acid deficiencies

Essential fatty acid levels: Several studies published between 1990 a 2005 reported finding reduced levels of Omega-6 or Omega-3 essential fatty acids in cell membranes or serum in patients diagnosed with postviral fatigue syndrome or CDC defined CFS.[186][187][188][189][190]One study conducted in 1999 on Oxford criteria defined CFS patients (Warren et al.) found no significant differences in fatty acid levels between treatment and placebo groups.[191] There have also been two controlled systematic proton neurospectroscopy studies of CFS patients that found raised levels of choline in brain areas consistent with an abnormality of essential fatty acid and phospholipid metabolism in the brain in CFS patients.[192][193] These changes have been considered due to essential fatty acid deficiencies resulting from delta 6 desaturase (D6D) enzyme inhibition in CFS. Some researchers have suggested D6D inhibition is linked to a possible viral cause.[25][192][193][194] However, researchers at an Australian University of Newcastle who reported finding, in CDC criteria defined CFS patients; a dysregulation in D6D enzyme activity and fatty acid changes consistent with an inflammatory mediated event. Found that both gradual and sudden onset had the same fatty acid anomaly differentiaiting them from controls, the primary lipid changes were potentially non-viral induced. Whilst sudden onset CFS patients could be differentiated by a key post-viral modification to fatty acids.[195][196] Other studies have shown that altered ratios of fatty acids and decreased availability of omega-3 EFAs plays a role in CFS symptoms and severity and is related to findings of lowered zinc and immune dysfunction, including the lowered mitogen-stimulated activation of some T cells. The decreased cell markers are also indicators of increased inflammation and low natural killer cell activation.[190][197] The reduced EFA findings are considered indicative of; oxidative stress with reduced anti-oxidant status, [189] [198] [199][200]

Carnitine deficiency

Carnitine deficiency; is said to produce symptoms of fatigue and myalgia similar to PVFS, ME and CFS.[25][201][202] Several studies have reported finding carnitine abnormalities in CFS patients. including lower serum total carnitine, free carnitine and acylcarnitine levels.[203][204][202][205]The findings of reduced brain uptake of acetylcarnitine suggest that the levels of biosynthesis of neurotransmitters through acetylcarnitine might be reduced in some brain regions of CFS patients.[109][206] There has been a contradictory study that included Oxford criteria defined patients. Others report of finding reduced levels of carnitine together with reduced essential fatty acids in patients with CDC defined CFS.[207][208] Carnitine and its esters are considered to regulate the immune networks and inflammation, through carnitine-dependent; transfer of fatty acids into cells, and mitochondrial energy production from beta-oxidation of long-chain fatty acids. A gene expression study indicates altered; carnitine function, mitochondrial function, and fatty acid metabolism in PVFS. Also that profiles of plasma lipids in subgroups of CDC defined CFS patients suggest anomalies including beta-oxidation of fatty acids.[181][209][210][211] As carnitine is considered an anti-oxidant, the lower plasma acetylcarnitine level may indicate, consumption by the increased oxidative stress in CFS.[212]

Toxic agents

Insecticides have a possible effect on the cause and/or course of CFS.[213][214] [215] [182] [60]

Exercise findings

A large study found that higher levels of exercise in childhood is associated with a lower risk of developing CFS later on. It also found that the development of CFS was not associated with other childhood or maternal factors such as psychological problems, academic ability, allergic tendencies, birth weight, birth order or obesity.[216]

Abnormal lactic acid responses to exercise in some CFS patients,[217][218][51] has been suggested to be a factor in CFS because it is commonly believed to be responsible for muscle fatigue.[219] However, some scientists have found that lactic acid may actually help prevent muscle fatigue rather than cause it, by keeping muscles properly responding to nerve signals.[220]

Other findings

Other findings regarding CFS in general include:

  • Researchers compared 48 CFS patients with 29 controls and found that 10 of the CFS patients tested positive for enterovirus RNA (most closely to that of the coxsackie B virus) in their muscles while all of the 29 controls tested negative. 28 of the 48 CFS patients had an abnormal lactate response to exercise, including 9 of the 10 who tested positive for enterovirus RNA.[221]
  • Researchers have found that children and teenagers with CFS are several times more likely to have some hyperflexible joints[222] in an association with Ehlers-Danlos syndrome.

See also

Template:MECFS

References

  1. CDC - CFS Basic Overview (PDF file, 31 KB)
  2. Dietert, RR (2008 Feb 8). "Possible role for early-life immune insult including developmental immunotoxicity in chronic fatigue syndrome (CFS) or myalgic encephalomyelitis (ME)". Toxicology. PMID 18336982. Unknown parameter |coauthors= ignored (help); Check date values in: |date= (help)
  3. 3.0 3.1 Appel S, Chapman J, Shoenfeld Y (2007). "Infection and vaccination in chronic fatigue syndrome: myth or reality?". Autoimmunity. 40 (1): 48–53. doi:10.1080/08916930701197273. PMID 17364497.
  4. Siegel SD, Antoni MH, Fletcher MA, Maher K, Segota MC, Klimas N (2006). "Impaired natural immunity, cognitive dysfunction, and physical symptoms in patients with chronic fatigue syndrome: preliminary evidence for a subgroup?". J Psychosom Res. 60 (6): 559–66. doi:10.1016/j.jpsychores.2006.03.001. PMID 16731230.
  5. Lyall M, Peakman M, Wessely S (2003). "A systematic review and critical evaluation of the immunology of chronic fatigue syndrome". J Psychosom Res. 55 (2): 79–90. doi:10.1016/S0022-3999(02)00515-9. PMID 12932505.
  6. Cho HJ, Skowera A, Cleare A, Wessely S (2006). "Chronic fatigue syndrome: an update focusing on phenomenology and pathophysiology". Curr Opin Psychiatry. 19 (1): 67–73. doi:10.1097/01.yco.0000194370.40062.b0. PMID 16612182.
  7. Tiev KP, Demettre E, Ercolano P, Bastide L, Lebleu B, Cabane J (2003). "RNase L levels in peripheral blood mononuclear cells: 37-kilodalton/83-kilodalton isoform ratio is a potential test for chronic fatigue syndrome". Clin Diagn Lab Immunol. 10 (2): 315–6. doi:10.1128/CDLI.10.2.315-316.2003. PMID 12626460.
  8. Demettre E, Bastide L, D'Haese A, De Smet K, De Meirleir K, Tiev KP, Englebienne P, Lebleu B (2002). "Ribonuclease L proteolysis in peripheral blood mononuclear cells of chronic fatigue syndrome patients". J Biol Chem. 277 (38): 35746–51. doi:10.1074/jbc.M201263200. PMID 12118002.
  9. Shetzline SE, Martinand-Mari C, Reichenbach NL, Buletic Z, Lebleu B, Pfleiderer W, Charubala R, De Meirleir K, De Becker P, Peterson DL, Herst CV, Englebienne P, Suhadolnik RJ (2002). "Structural and functional features of the 37-kDa 2-5A-dependent RNase L in chronic fatigue syndrome". J Interferon Cytokine Res. 22 (4): 443–56. doi:10.1089/10799900252952235. PMID 12034027.
  10. Suhadolnik RJ, Peterson DL, O'Brien K, Cheney PR, Herst CV, Reichenbach NL, Kon N, Horvath SE, Iacono KT, Adelson ME, De Meirleir K, De Becker P, Charubala R, Pfleiderer W (1997). "Biochemical evidence for a novel low molecular weight 2-5A-dependent RNase L in chronic fatigue syndrome". J Interferon Cytokine Res. 17 (7): 377–85. PMID 9243369.
  11. Fremont M, El Bakkouri K, Vaeyens F, Herst CV, De Meirleir K, Englebienne P (2005). "2',5'-Oligoadenylate size is critical to protect RNase L against proteolytic cleavage in chronic fatigue syndrome". Exp Mol Pathol. 78 (3): 239–46. doi:10.1016/j.yexmp.2005.01.003. PMID 15924878.
  12. Suhadolnik RJ, Reichenbach NL, Hitzges P, Sobol RW, Peterson DL, Henry B, Ablashi DV, Muller WE, Schroder HC, Carter WA; et al. (1994). "Upregulation of the 2-5A synthetase/RNase L antiviral pathway associated with chronic fatigue syndrome". Clin Infect Dis. 18 (Suppl 1): S96–104. PMID 8148461.
  13. 13.0 13.1 Nijs J, De Meirleir K, Meeus M, McGregor NR, Englebienne P (2004). "Chronic fatigue syndrome: intracellular immune deregulations as a possible etiology for abnormal exercise response". Med Hypotheses. 62 (5): 759–65. doi:10.1016/j.mehy.2003.11.030. PMID 15082102.
  14. Snell CR, Vanness JM, Strayer DR, Stevens SR (2002). "Physical performance and prediction of 2-5A synthetase/RNase L antiviral pathway activity in patients with chronic fatigue syndrome". In Vivo. 16 (2): 107–9. PMID 12073768.
  15. Nijs J, Meeus M, McGregor NR, Meeusen R, de Schutter G, van Hoof E, de Meirleir K (2005). "Chronic fatigue syndrome: exercise performance related to immune dysfunction". Med Sci Sports Exerc. 37 (10): 1647–54. doi:10.1249/01.mss.0000181680.35503.ce. PMID 16260962.
  16. 16.0 16.1 Snell CR, Vanness JM, Strayer DR, Stevens SR (2005). "Exercise capacity and immune function in male and female patients with chronic fatigue syndrome (CFS)". In Vivo. 19 (2): 387–90. PMID 15796202.
  17. Meeus M, Nijs J, McGregor N; et al. (2008). "Unravelling intracellular immune dysfunctions in chronic fatigue syndrome: interactions between protein kinase R activity, RNase L cleavage and elastase activity, and their clinical relevance". In Vivo. 22 (1): 115–21. PMID 18396793.
  18. Nijs J, De Meirleir K (2005). "Impairments of the 2-5A synthetase/RNase L pathway in chronic fatigue syndrome". In Vivo. 19 (6): 1013–21. PMID 16277015.
  19. Van Hoof E, De Becker P, Lapp C, Cluydts R, De Meirleir K (2007). "Defining the occurrence and influence of alpha-delta sleep in chronic fatigue syndrome". Am J Med Sci. 333 (2): 78–84. doi:10.1097/00000441-200702000-00003. PMID 17301585.
  20. Kennedy G, Spence V, Underwood C, Belch JJ. Increased neutrophil apoptosis in chronic fatigue syndrome. J Clin Pathol. 2004 Aug;57(8):891-3.
  21. Patarca R, Klimas NG, Lugtendorf S, Antoni M, Fletcher MA. Dysregulated expression of tumor necrosis factor in chronic fatigue syndrome: interrelations with cellular sources and patterns of soluble immune mediator expression. Clin Infect Dis. 1994 Jan;18 Suppl 1:S147-53.
  22. Original Research Paper, from the Journal of Clinical Pathology http://www.cfids.org/cfidslink/2005/cfs-gene.pdf
  23. Food Intolerance in Chronic Fatigue Syndrome. Seattle WA: American Association for Chronic Fatigue Syndrome. Jan. 2001. pp. Conference Paper 15. Unknown parameter |coauthors= ignored (help); |first1= missing |last1= in Authors list (help); Check date values in: |date= (help)
  24. Logan AC, Wong C (2001). "Chronic fatigue syndrome: oxidative stress and dietary modifications". Alternative medicine review : a journal of clinical therapeutic. 6 (5): 450–9. PMID 11703165.
  25. 25.0 25.1 25.2 25.3 25.4 25.5 Nightingale Research Foundation; Goldstein, Jay E.; Byron M. Hyde (1992). The Clinical and scientific basis of myalgic encephalomyelitis/chronic fatigue syndrome. Ogdensburg, N.Y: Nightingale Research Foundation. pp. 521–538, chapter57, The Role of Food Intolerance in Chronic Fatigue Syndrome. ISBN 0-9695662-0-4.
  26. Lloyd A, Wakefield D, Boughton C, Dwyer J (1989). "Immunological abnormalities in the chronic fatigue syndrome". Med J Aust. 151 (3): 122–4. PMID 2787888.
  27. Peterson PK, Shepard J, Macres M; et al. (1990). "A controlled trial of intravenous immunoglobulin G in chronic fatigue syndrome". Am. J. Med. 89 (5): 554–60. PMID 2239975.
  28. Lloyd A, Hickie I, Wakefield D, Boughton C, Dwyer J (1990). "A double-blind, placebo-controlled trial of intravenous immunoglobulin therapy in patients with chronic fatigue syndrome". Am. J. Med. 89 (5): 561–8. PMID 2146875.
  29. Hilgers A, Frank J (1994). "[Chronic fatigue syndrome: immune dysfunction, role of pathogens and toxic agents and neurological and cardial changes]". Wien Med Wochenschr (in German). 144 (16): 399–406. PMID 7856214.
  30. Natelson BH, LaManca JJ, Denny TN; et al. (1998). "Immunologic parameters in chronic fatigue syndrome, major depression, and multiple sclerosis". Am. J. Med. 105 (3A): 43S–49S. PMID 9790481.
  31. 31.0 31.1 31.2 Patarca R (2001). "Cytokines and chronic fatigue syndrome". Ann. N. Y. Acad. Sci. 933: 185–200. PMID 12000020.
  32. Skowera A, Cleare A, Blair D, Bevis L, Wessely SC, Peakman M (2004). "High levels of type 2 cytokine-producing cells in chronic fatigue syndrome". Clin. Exp. Immunol. 135 (2): 294–302. PMID 14738459.
  33. Hanson SJ, Gause W, Natelson B (2001). "Detection of immunologically significant factors for chronic fatigue syndrome using neural-network classifiers". Clin. Diagn. Lab. Immunol. 8 (3): 658–62. doi:10.1128/CDLI.8.3.658-662.2001. PMID 11329477.
  34. Visser J, Graffelman W, Blauw B; et al. (2001). "LPS-induced IL-10 production in whole blood cultures from chronic fatigue syndrome patients is increased but supersensitive to inhibition by dexamethasone". J. Neuroimmunol. 119 (2): 343–9. PMID 11585638.
  35. Bennett AL, Chao CC, Hu S, Buchwald D, Fagioli LR, Schur PH, Peterson PK, Komaroff AL (1997). "Elevation of bioactive transforming growth factor-beta in serum from patients with chronic fatigue syndrome". J Clin Immunol. 17 (2): 160–6. doi:10.1023/A:1027330616073. PMID 9083892.
  36. Visser JT, De Kloet ER, Nagelkerken L (2000). "Altered glucocorticoid regulation of the immune response in the chronic fatigue syndrome". Ann. N. Y. Acad. Sci. 917: 868–75. PMID 11268418.
  37. Patarca-Montero R, Antoni M, Fletcher MA, Klimas NG (2001). "Cytokine and other immunologic markers in chronic fatigue syndrome and their relation to neuropsychological factors". Appl Neuropsychol. 8 (1): 51–64. PMID 11388124.
  38. Gaab J, Rohleder N, Heitz V; et al. (2005). "Stress-induced changes in LPS-induced pro-inflammatory cytokine production in chronic fatigue syndrome". Psychoneuroendocrinology. 30 (2): 188–98. doi:10.1016/j.psyneuen.2004.06.008. PMID 15471616.
  39. Visser J, Blauw B, Hinloopen B; et al. (1998). "CD4 T lymphocytes from patients with chronic fatigue syndrome have decreased interferon-gamma production and increased sensitivity to dexamethasone". J. Infect. Dis. 177 (2): 451–4. PMID 9466535.
  40. Klimas NG, Salvato FR, Morgan R, Fletcher MA (1990). "Immunologic abnormalities in chronic fatigue syndrome". J. Clin. Microbiol. 28 (6): 1403–10. PMID 2166084.
  41. Elenkov IJ, Wilder RL, Chrousos GP, Vizi ES (2000). "The sympathetic nerve--an integrative interface between two supersystems: the brain and the immune system". Pharmacol. Rev. 52 (4): 595–638. PMID 11121511.
  42. Ramsay MA (1986), "Postviral Fatigue Syndrome. The saga of Royal Free disease", Londen, ISBN 0-906923-96-4
  43. Chia JK, Chia AY (2007). "Chronic fatigue syndrome is associated with chronic enterovirus infection of the stomach". J Clin Pathol. Online preprint. doi:10.1136/jcp.2007.050054. PMID 17872383.
  44. Hooper M (2007). "Myalgic encephalomyelitis: a review with emphasis on key findings in biomedical research". J. Clin. Pathol. 60 (5): 466–71. doi:10.1136/jcp.2006.042408. PMID 16935967. Unknown parameter |month= ignored (help)
  45. Chia JK, Chia AY (2008). "Chronic fatigue syndrome is associated with chronic enterovirus infection of the stomach". J. Clin. Pathol. 61 (1): 43–8. doi:10.1136/jcp.2007.050054. PMID 17872383. Unknown parameter |month= ignored (help)
  46. "Medical News: Stomach Virus Associated with Chronic Fatigue Syndrome - in Rheumatology, General Rheumatology from MedPage Today".
  47. Kerr JR (2008). "Enterovirus infection of the stomach in chronic fatigue syndrome/myalgic encephalomyelitis". J. Clin. Pathol. 61 (1): 1–2. doi:10.1136/jcp.2007.051342. PMID 17873115. Unknown parameter |month= ignored (help)
  48. Chia JK (2005). "The role of enterovirus in chronic fatigue syndrome". J. Clin. Pathol. 58 (11): 1126–32. doi:10.1136/jcp.2004.020255. PMID 16254097. Unknown parameter |month= ignored (help)
  49. Douche-Aourik F, Berlier W, Féasson L; et al. (2003). "Detection of enterovirus in human skeletal muscle from patients with chronic inflammatory muscle disease or fibromyalgia and healthy subjects". J. Med. Virol. 71 (4): 540–7. doi:10.1002/jmv.10531. PMID 14556267. Unknown parameter |month= ignored (help)
  50. Fohlman J, Friman G, Tuvemo T (1997). "[Enterovirus infections in new disguise]". Lakartidningen (in Swedish). 94 (28–29): 2555–60. PMID 9254324. Unknown parameter |month= ignored (help)
  51. 51.0 51.1 Lane RJ, Soteriou BA, Zhang H, Archard LC (2003). "Enterovirus related metabolic myopathy: a postviral fatigue syndrome". J. Neurol. Neurosurg. Psychiatr. 74 (10): 1382–6. PMID 14570830. Unknown parameter |month= ignored (help)
  52. Dalakas MC (2003). "Enteroviruses in chronic fatigue syndrome: "now you see them, now you don't"". J. Neurol. Neurosurg. Psychiatr. 74 (10): 1361–2. PMID 14570825. Unknown parameter |month= ignored (help)
  53. Galbraith DN, Nairn C, Clements GB (1997). "Evidence for enteroviral persistence in humans". J. Gen. Virol. 78 ( Pt 2): 307–12. PMID 9018051. Unknown parameter |month= ignored (help)
  54. Jones J, Ray C, Minnich L, Hicks M, Kibler R, Lucas D (1985). "Evidence for active Epstein-Barr virus infection in patients with persistent, unexplained illnesses: elevated anti-early antigen antibodies". Ann Intern Med. 102 (1): 1–7. PMID 2578266.
  55. Straus S, Tosato G, Armstrong G, Lawley T, Preble O, Henle W, Davey R, Pearson G, Epstein J, Brus I (1985). "Persisting illness and fatigue in adults with evidence of Epstein-Barr virus infection". Ann Intern Med. 102 (1): 7–16. PMID 2578268.
  56. Holmes GP, Kaplan JE, Stewart JA, Hunt B, Pinsky PF, Schonberger LB (1987). "A cluster of patients with a chronic mononucleosis-like syndrome. Is Epstein-Barr virus the cause?". JAMA. 257 (17): 2297–302. PMID 3033337.
  57. Kawai K, Kawai A (1992). "Studies on the relationship between chronic fatigue syndrome and Epstein-Barr virus in Japan". Intern Med. 31 (3): 313–8. doi:10.2169/internalmedicine.31.313. PMID 1319246.
  58. Lerner A, Beqaj S, Deeter R, Fitzgerald J (2004). "IgM serum antibodies to Epstein-Barr virus are uniquely present in a subset of patients with the chronic fatigue syndrome". In Vivo. 18 (2): 101–6. PMID 15113035.
  59. Glaser R, Padgett DA, Litsky ML; et al. (2005). "Stress-associated changes in the steady-state expression of latent Epstein-Barr virus: implications for chronic fatigue syndrome and cancer". Brain Behav. Immun. 19 (2): 91–103. doi:10.1016/j.bbi.2004.09.001. PMID 15664781. Unknown parameter |month= ignored (help)
  60. 60.0 60.1 60.2 60.3 60.4 Devanur LD, Kerr JR (2006). "Chronic fatigue syndrome". J. Clin. Virol. 37 (3): 139–50. doi:10.1016/j.jcv.2006.08.013. PMID 16978917. Unknown parameter |month= ignored (help)
  61. 61.0 61.1 Klimas NG, Koneru AO (2007). "Chronic fatigue syndrome: inflammation, immune function, and neuroendocrine interactions". Curr Rheumatol Rep. 9 (6): 482–7. PMID 18177602. Unknown parameter |month= ignored (help)
  62. Selden SM, Cameron AS (1996). "Changing epidemiology of Ross River virus disease in South Australia". Med. J. Aust. 165 (6): 313–7. PMID 8862330.
  63. 63.0 63.1 Hickie I, Davenport T, Wakefield D; et al. (2006). "Post-infective and chronic fatigue syndromes precipitated by viral and non-viral pathogens: prospective cohort study". BMJ. 333 (7568): 575. doi:10.1136/bmj.38933.585764.AE. PMID 16950834.
  64. Li YJ, Wang DX, Zhang FM, Liu ZD, Yang AY, Ykuta K (2003). "[Detection of antibody against Borna disease virus-p24 in the plasma of Chinese patients with chronic fatigue syndrome by Western-blot analysis]". Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi (in Chinese). 17 (4): 330–3. PMID 15340544.
  65. Kitani T, Kuratsune H, Fuke I; et al. (1996). "Possible correlation between Borna disease virus infection and Japanese patients with chronic fatigue syndrome". Microbiol. Immunol. 40 (6): 459–62. PMID 8839433.
  66. Kerr JR (2005). "Pathogenesis of parvovirus B19 infection: host gene variability, and possible means and effects of virus persistence". J. Vet. Med. B Infect. Dis. Vet. Public Health. 52 (7–8): 335–9. doi:10.1111/j.1439-0450.2005.00859.x. PMID 16316396.
  67. Beqaj SH, Lerner AM, Fitzgerald JT (2007). "Immunoassay with cytomegalovirus early antigens from gene products p52 and CM2 (UL44 and UL57) detect active infection in patients with chronic fatigue syndrome". J Clin Pathol. doi:10.1136/jcp.2007.050633. PMID 18037660.
  68. Lerner AM, Beqaj SH, Deeter RG, Fitzgerald JT (2002). "IgM serum antibodies to human cytomegalovirus nonstructural gene products p52 and CM2 (UL44 and UL57) are uniquely present in a subset of patients with chronic fatigue syndrome". In Vivo. 16 (3): 153–9. PMID 12182109.
  69. Lerner AM, Dworkin HJ, Sayyed T; et al. (2004). "Prevalence of abnormal cardiac wall motion in the cardiomyopathy associated with incomplete multiplication of Epstein-barr Virus and/or cytomegalovirus in patients with chronic fatigue syndrome". In Vivo. 18 (4): 417–24. PMID 15369178.
  70. Chapenko S, Krumina A, Kozireva S; et al. (2006). "Activation of human herpesviruses 6 and 7 in patients with chronic fatigue syndrome". J. Clin. Virol. 37 Suppl 1: S47–51. doi:10.1016/S1386-6532(06)70011-7. PMID 17276369.
  71. Kondo K (2007). "[Chronic fatigue syndrome and herpesvirus reactivation]". Nippon Rinsho (in Japanese). 65 (6): 1043–8. PMID 17561695.
  72. De Bolle L, Naesens L, De Clercq E (2005). "Update on human herpesvirus 6 biology, clinical features, and therapy". Clin. Microbiol. Rev. 18 (1): 217–45. doi:10.1128/CMR.18.1.217-245.2005. PMID 15653828.
  73. "Chronic Fatigue Syndrome and Herpesviruses: the Fading Evidence". Herpes. 7 (2): 46–50. 2000. PMID 11867001.
  74. Komaroff AL, Jacobson S, Ablashi DV, Yamanishi K (2006). "Highlights from 5th International Conference on HHV-6 and -7". Herpes. 13 (3): 81–2. PMID 17147913.
  75. Komaroff AL (2006). "Is human herpesvirus-6 a trigger for chronic fatigue syndrome?". J. Clin. Virol. 37 Suppl 1: S39–46. doi:10.1016/S1386-6532(06)70010-5. PMID 17276367.
  76. Parker NR, Barralet JH, Bell AM (2006). "Q fever". Lancet. 367 (9511): 679–88. doi:10.1016/S0140-6736(06)68266-4. PMID 16503466. Unknown parameter |month= ignored (help)
  77. Madariaga MG, Rezai K, Trenholme GM, Weinstein RA (2003). "Q fever: a biological weapon in your backyard". Lancet Infect Dis. 3 (11): 709–21. PMID 14592601. Unknown parameter |month= ignored (help)
  78. Ayres JG, Flint N, Smith EG; et al. (1998). "Post-infection fatigue syndrome following Q fever". QJM. 91 (2): 105–23. PMID 9578893. Unknown parameter |month= ignored (help)
  79. Ledina D, Bradarić N, Milas I, Ivić I, Brncić N, Kuzmicić N (2007). "Chronic fatigue syndrome after Q fever". Med. Sci. Monit. 13 (7): CS88–92. PMID 17599032. Unknown parameter |month= ignored (help)
  80. Ikuta K, Yamada T, Shimomura T; et al. (2003). "Diagnostic evaluation of 2', 5'-oligoadenylate synthetase activities and antibodies against Epstein-Barr virus and Coxiella burnetii in patients with chronic fatigue syndrome in Japan". Microbes Infect. 5 (12): 1096–102. PMID 14554250. Unknown parameter |month= ignored (help)
  81. Helbig K, Harris R, Ayres J; et al. (2005). "Immune response genes in the post-Q-fever fatigue syndrome, Q fever endocarditis and uncomplicated acute primary Q fever". QJM. 98 (8): 565–74. doi:10.1093/qjmed/hci086. PMID 15955794. Unknown parameter |month= ignored (help)
  82. 82.0 82.1 Nicolson GL, Gan R, Haier J (2003). "Multiple co-infections (Mycoplasma, Chlamydia, human herpes virus-6) in blood of chronic fatigue syndrome patients: association with signs and symptoms". APMIS. 111 (5): 557–66. PMID 12887507. Unknown parameter |month= ignored (help)
  83. Nijs J, Nicolson GL, De Becker P, Coomans D, De Meirleir K (2002). "High prevalence of Mycoplasma infections among European chronic fatigue syndrome patients. Examination of four Mycoplasma species in blood of chronic fatigue syndrome patients". FEMS Immunol. Med. Microbiol. 34 (3): 209–14. PMID 12423773. Unknown parameter |month= ignored (help)
  84. Nasralla M, Haier J, Nicolson GL (1999). "Multiple mycoplasmal infections detected in blood of patients with chronic fatigue syndrome and/or fibromyalgia syndrome". Eur. J. Clin. Microbiol. Infect. Dis. 18 (12): 859–65. PMID 10691196. Unknown parameter |month= ignored (help)
  85. Choppa PC, Vojdani A, Tagle C, Andrin R, Magtoto L (1998). "Multiplex PCR for the detection of Mycoplasma fermentans, M. hominis and M. penetrans in cell cultures and blood samples of patients with chronic fatigue syndrome". Mol. Cell. Probes. 12 (5): 301–8. doi:10.1006/mcpr.1998.0186. PMID 9778455. Unknown parameter |month= ignored (help)
  86. Vojdani A, Choppa PC, Tagle C, Andrin R, Samimi B, Lapp CW (1998). "Detection of Mycoplasma genus and Mycoplasma fermentans by PCR in patients with Chronic Fatigue Syndrome". FEMS Immunol. Med. Microbiol. 22 (4): 355–65. PMID 9879928. Unknown parameter |month= ignored (help)
  87. Vernon SD, Shukla SK, Reeves WC (2003). "Absence of Mycoplasma species DNA in chronic fatigue syndrome". J. Med. Microbiol. 52 (Pt 11): 1027–8. PMID 14532349. Unknown parameter |month= ignored (help)
  88. Endresen GK (2003). "Mycoplasma blood infection in chronic fatigue and fibromyalgia syndromes". Rheumatol. Int. 23 (5): 211–5. doi:10.1007/s00296-003-0355-7. PMID 12879275. Unknown parameter |month= ignored (help)
  89. Sairenji T, Nagata K (2007). "[Viral infections in chronic fatigue syndrome]". Nippon Rinsho (in Japanese). 65 (6): 991–6. PMID 17561687. Unknown parameter |month= ignored (help)
  90. Maes M, Mihaylova I, Leunis JC (2007). "Increased serum IgA and IgM against LPS of enterobacteria in chronic fatigue syndrome (CFS): indication for the involvement of gram-negative enterobacteria in the etiology of CFS and for the presence of an increased gut-intestinal permeability". J Affect Disord. 99 (1–3): 237–40. doi:10.1016/j.jad.2006.08.021. PMID 17007934. Unknown parameter |month= ignored (help)
  91. Natelson BH, Ellis SP, Braonain PJ, DeLuca J, Tapp WN (1995). "Frequency of deviant immunological test values in chronic fatigue syndrome patients". Clin Diagn Lab Immunol. 2 (2): 238–40. PMID 7697537.
  92. Sorensen B, Streib JE, Strand M, Make B, Giclas PC, Fleshner M, Jones JF (2003). "Complement activation in a model of chronic fatigue syndrome". J Allergy Clin Immunol. 112 (2): 397–403. doi:10.1067/mai.2003.1615. PMID 12897748.
  93. Hickie I, Davenport T, Wakefield D, Vollmer-Conna U, Cameron B, Vernon SD, Reeves WC, Lloyd A; Dubbo Infection Outcomes Study Group (2006). "Post-infective and chronic fatigue syndromes precipitated by viral and non-viral pathogens: prospective cohort study". BMJ. 333 (7568): 575. doi:10.1136/bmj.38933.585764.AE. PMID 16950834.
  94. Cameron B, Bharadwaj M, Burrows J, Fazou C, Wakefield D, Hickie I, Ffrench R, Khanna R, Lloyd A (2006). "Prolonged illness after infectious mononucleosis is associated with altered immunity but not with increased viral load". J Infect Dis. 193 (5): 664–71. doi:10.1086/500248. PMID 16453261.
  95. Tarello W (2001). "Chronic fatigue syndrome (CFS) associated with Staphylococcus spp. bacteremia, responsive to potassium arsenite 0.5% in a veterinary surgeon and his coworking wife, handling with CFS animal cases". Comp. Immunol. Microbiol. Infect. Dis. 24 (4): 233–46. PMID 11561958. Unknown parameter |month= ignored (help)
  96. Chaudhuri A, Behan PO (2004). "Fatigue in neurological disorders". Lancet. 363 (9413): 978–88. doi:10.1016/S0140-6736(04)15794-2. PMID 15043967.
  97. Schwartz RB, Garada BM, Komaroff AL; et al. (1994). "Detection of intracranial abnormalities in patients with chronic fatigue syndrome: comparison of MR imaging and SPECT". AJR. American journal of roentgenology. 162 (4): 935–41. PMID 8141020.
  98. Abu-Judeh HH, Levine S, Kumar M; et al. (1998). "Comparison of SPET brain perfusion and 18F-FDG brain metabolism in patients with chronic fatigue syndrome". Nuclear medicine communications. 19 (11): 1065–71. PMID 9861623.
  99. Schwartz RB, Komaroff AL, Garada BM; et al. (1994). "SPECT imaging of the brain: comparison of findings in patients with chronic fatigue syndrome, AIDS dementia complex, and major unipolar depression". AJR. American journal of roentgenology. 162 (4): 943–51. PMID 8141022.
  100. MacHale SM, Lawŕie SM, Cavanagh JT; et al. (2000). "Cerebral perfusion in chronic fatigue syndrome and depression". The British Journal of Psychiatry : the journal of mental science. 176: 550–6. PMID 10974961.
  101. Fischler B, D'Haenen H, Cluydts R; et al. (1996). "Comparison of 99m Tc HMPAO SPECT scan between chronic fatigue syndrome, major depression and healthy controls: an exploratory study of clinical correlates of regional cerebral blood flow". Neuropsychobiology. 34 (4): 175–83. PMID 9121617.
  102. Demitrack MA, Gold PW, Dale JK, Krahn DD, Kling MA, Straus SE (1992). "Plasma and cerebrospinal fluid monoamine metabolism in patients with chronic fatigue syndrome: preliminary findings". Biol. Psychiatry. 32 (12): 1065–77. PMID 1282370.
  103. Badawy AA, Morgan CJ, Llewelyn MB, Albuquerque SR, Farmer A (2005). "Heterogeneity of serum tryptophan concentration and availability to the brain in patients with the chronic fatigue syndrome". J. Psychopharmacol. (Oxford). 19 (4): 385–91. doi:10.1177/0269881105053293. PMID 15982993.
  104. Cleare AJ, Bearn J, Allain T; et al. (1995). "Contrasting neuroendocrine responses in depression and chronic fatigue syndrome". Journal of affective disorders. 34 (4): 283–9. PMID 8550954.
  105. Cleare AJ, Messa C, Rabiner EA, Grasby PM (2005). "Brain 5-HT1A receptor binding in chronic fatigue syndrome measured using positron emission tomography and [11C]WAY-100635". Biol. Psychiatry. 57 (3): 239–46. doi:10.1016/j.biopsych.2004.10.031. PMID 15691524.
  106. Klein R, Berg PA (1995). "High incidence of antibodies to 5-hydroxytryptamine, gangliosides and phospholipids in patients with chronic fatigue and fibromyalgia syndrome and their relatives: evidence for a clinical entity of both disorders". Eur. J. Med. Res. 1 (1): 21–6. PMID 9392689.
  107. Goertzel BN, Pennachin C, de Souza Coelho L, Gurbaxani B, Maloney EM, Jones JF (2006). "Combinations of single nucleotide polymorphisms in neuroendocrine effector and receptor genes predict chronic fatigue syndrome". Pharmacogenomics. 7 (3): 475–83. doi:10.2217/14622416.7.3.475. PMID 16610957.
  108. Dinan TG, Majeed T, Lavelle E, Scott LV, Berti C, Behan P (1997). "Blunted serotonin-mediated activation of the hypothalamic-pituitary-adrenal axis in chronic fatigue syndrome". Psychoneuroendocrinology. 22 (4): 261–7. PMID 9226729.
  109. 109.0 109.1 Kuratsune H, Yamaguti K, Lindh G; et al. (2002). "Brain regions involved in fatigue sensation: reduced acetylcarnitine uptake into the brain". Neuroimage. 17 (3): 1256–65. PMID 12414265.
  110. Spence VA, Khan F, Kennedy G, Abbot NC, Belch JJ (2004). "Acetylcholine mediated vasodilatation in the microcirculation of patients with chronic fatigue syndrome". Prostaglandins Leukot. Essent. Fatty Acids. 70 (4): 403–7. doi:10.1016/j.plefa.2003.12.016. PMID 15041034.
  111. Tanaka S, Kuratsune H, Hidaka Y; et al. (2003). "Autoantibodies against muscarinic cholinergic receptor in chronic fatigue syndrome". Int. J. Mol. Med. 12 (2): 225–30. PMID 12851722.
  112. Conti F, Pittoni V, Sacerdote P, Priori R, Meroni PL, Valesini G (1998). "Decreased immunoreactive beta-endorphin in mononuclear leucocytes from patients with chronic fatigue syndrome". Clin. Exp. Rheumatol. 16 (6): 729–32. PMID 9844768.
  113. Panerai AE, Vecchiet J, Panzeri P; et al. (2002). "Peripheral blood mononuclear cell beta-endorphin concentration is decreased in chronic fatigue syndrome and fibromyalgia but not in depression: preliminary report". The Clinical journal of pain. 18 (4): 270–3. PMID 12131069.
  114. Goldstein DS, Robertson D, Esler M, Straus SE, Eisenhofer G (2002). "Dysautonomias: clinical disorders of the autonomic nervous system". Ann. Intern. Med. 137 (9): 753–63. PMID 12416949.
  115. Galland BC, Jackson PM, Sayers RM, Taylor BJ (2008). "A matched case control study of orthostatic intolerance in children/adolescents with chronic fatigue syndrome". Pediatr. Res. 63 (2): 196–202. doi:10.1203/PDR.0b013e31815ed612. PMID 18091356.
  116. Natelson BH, Intriligator R, Cherniack NS, Chandler HK, Stewart JM (2007). "Hypocapnia is a biological marker for orthostatic intolerance in some patients with chronic fatigue syndrome". Dyn Med. 6: 2. doi:10.1186/1476-5918-6-2. PMID 17263876.
  117. Newton JL, Okonkwo O, Sutcliffe K, Seth A, Shin J, Jones DE (2007). "Symptoms of autonomic dysfunction in chronic fatigue syndrome". QJM. 100 (8): 519–26. doi:10.1093/qjmed/hcm057. PMID 17617647.
  118. Tanaka H (2007). "[Autonomic function and child chronic fatigue syndrome]". Nippon Rinsho (in Japanese). 65 (6): 1105–12. PMID 17561705.
  119. Stewart JM, Gewitz MH, Weldon A, Arlievsky N, Li K, Munoz J (1999). "Orthostatic intolerance in adolescent chronic fatigue syndrome". Pediatrics. 103 (1): 116–21. PMID 9917448.
  120. Godefroy WP, Hastan D, van der Mey AG (2007). "Translabyrinthine surgery for disabling vertigo in vestibular schwannoma patients". Clin Otolaryngol. 32 (3): 167–72. doi:10.1111/j.1365-2273.2007.01427.x. PMID 17550503.
  121. Heller U, Becker EW, Zenner HP, Berg PA (1998). "[Incidence and clinical relevance of antibodies to phospholipids, serotonin and ganglioside in patients with sudden deafness and progressive inner ear hearing loss]". HNO (in German). 46 (6): 583–6. PMID 9677490.
  122. Tolan R, Stewart J. "Chronic Fatigue Syndrome", eMedicine, August 17 2006, retrieved November 9 2006.
  123. Rowe, PC. "General Information Brochure on Orthostatic Intolerance and its Treatment", Chronic Fatigue Clinic, Johns Hopkins Children's Center, February 2003, retrieved November 9 2006.
  124. Rowe P, Calkins H, DeBusk K, McKenzie R, Anand R, Sharma G, Cuccherini B, Soto N, Hohman P, Snader S, Lucas K, Wolff M, Straus S (2001). "Fludrocortisone acetate to treat neurally mediated hypotension in chronic fatigue syndrome: a randomized controlled trial". JAMA. 285 (1): 52–9. doi:10.1001/jama.285.1.52. PMID 11150109.
  125. 125.0 125.1 Stein E (2001), "How to differentiate CFS from Psychiatric Disorder", Presented at The Alison Hunter Memorial Foundation Third International Clinical and Scientific Conference, Sydney, Australia
  126. Salit IE (1997). "Precipitating factors for the chronic fatigue syndrome". J Psychiatr Res. 31 (1): 59–65. doi:10.1016/S0022-3956(96)00050-7. PMID 9201648.
  127. Theorell T, Blomkvist V, Lindh G, Evengard B. "Critical life events, infections, and symptoms during the year preceding chronic fatigue syndrome (CFS): an examination of CFS patients and subjects with a nonspecific life crisis". Psychosom Med. 61 (3): 304–10. PMID 10367610.
  128. Heim C, Wagner D, Maloney E, Papanicolaou DA, Solomon L, Jones JF, Unger ER, Reeves WC (2006). "Early adverse experience and risk for chronic fatigue syndrome: results from a population-based study". Arch Gen Psychiatry. 63 (11): 1258–66. doi:10.1001/archpsyc.63.11.1258. PMID 17088506.
  129. Kato K, Sullivan PF, Evengard B, Pedersen NL (2006). "Premorbid predictors of chronic fatigue". Arch Gen Psychiatry. 63 (11): 1267–72. doi:10.1001/archpsyc.63.11.1267. PMID 17088507.
  130. T Chalder, R Goodman, S Wessely, M Hotopf, H Meltzer (2003). "Epidemiology of chronic fatigue syndrome and self reported myalgic encephalomyelitis in 5-15 year olds: cross sectional study". BMJ. 327: 654–655. doi:10.1136/bmj.327.7416.654.
  131. 131.0 131.1 131.2 Reeves W (April 20, 2006). "Press Briefing on Chronic Fatigue Syndrome" (HTM). Centers for Disease Control and Prevention. Retrieved 2008-01-27. Unknown parameter |coauthors= ignored (help)
  132. Roberts AD, Wessely S, Chalder T, Papadopoulos A, Cleare AJ (2004). "Salivary cortisol response to awakening in chronic fatigue syndrome". Br J Psychiatry. 184: 136–41. doi:10.1192/bjp.184.2.136. PMID 14754825.
  133. Gaab J, Huster D, Peisen R, Engert V, Heitz V, Schad T, Schurmeyer TH, Ehlert U (2002). "Hypothalamic-pituitary-adrenal axis reactivity in chronic fatigue syndrome and health under psychological, physiological, and pharmacological stimulation". Psychosom Med. 64 (6): 951–62. doi:10.1097/01.PSY.0000038937.67401.61. PMID 12461200.
  134. Gaab J, Engert V, Heitz V, Schad T, Schurmeyer TH, Ehlert U (2004). "Associations between neuroendocrine responses to the Insulin Tolerance Test and patient characteristics in chronic fatigue syndrome". J Psychosom Res. 56 (4): 419–24. doi:10.1016/S0022-3999(03)00625-1. PMID 15094026.
  135. Margutti P, Delunardo F, Ortona E (2006). "Autoantibodies associated with psychiatric disorders". Curr Neurovasc Res. 3 (2): 149–57. doi:10.2174/156720206776875894. PMID 16719797.
  136. Vollmer-Conna U, Lloyd A, Hickie I, Wakefield D (1998). "Chronic fatigue syndrome: an immunological perspective". Aust N Z J Psychiatry. 32 (4): 523–7. PMID 9711366.
  137. Tanaka S, Kuratsune H, Hidaka Y, Hakariya Y, Tatsumi KI, Takano T, Kanakura Y, Amino N (2003). "Autoantibodies against muscarinic cholinergic receptor in chronic fatigue syndrome". Int J Mol Med. 12 (2): 225–30. PMID 12851722.
  138. Nijs J, Van de Velde B, De Meirleir K (2005). "Pain in patients with chronic fatigue syndrome: does nitric oxide trigger central sensitisation?". Med Hypotheses. 64 (3): 558–62. doi:10.1016/j.mehy.2004.07.037. PMID 15617866.
  139. Cho HJ, Skowera A, Cleare A, Wessely S (2006). "Chronic fatigue syndrome: an update focusing on phenomenology and pathophysiology". Curr Opin Psychiatry. 19 (1): 67–73. doi:10.1097/01.yco.0000194370.40062.b0. PMID 16612182.
  140. 140.0 140.1 Smith AK, Dimulescu I, Falkenberg VR; et al. (2008). "Genetic evaluation of the serotonergic system in chronic fatigue syndrome". Psychoneuroendocrinology. 33 (2): 188–97. doi:10.1016/j.psyneuen.2007.11.001. PMID 18079067.
  141. Demitrack MA, Dale JK, Straus SE; et al. (1991). "Evidence for impaired activation of the hypothalamic-pituitary-adrenal axis in patients with chronic fatigue syndrome". J. Clin. Endocrinol. Metab. 73 (6): 1224–34. PMID 1659582.
  142. Cleare AJ (2003). "The neuroendocrinology of chronic fatigue syndrome". Endocr. Rev. 24 (2): 236–52. PMID 12700181.
  143. 143.0 143.1 Van Den Eede F, Moorkens G, Van Houdenhove B, Cosyns P, Claes SJ (2007). "Hypothalamic-pituitary-adrenal axis function in chronic fatigue syndrome". Neuropsychobiology. 55 (2): 112–20. doi:10.1159/000104468. PMID 17596739.
  144. Jerjes WK, Cleare AJ, Wessely S, Wood PJ, Taylor NF (2005). "Diurnal patterns of salivary cortisol and cortisone output in chronic fatigue syndrome". J Affect Disord. 87 (2–3): 299–304. doi:10.1016/j.jad.2005.03.013. PMID 15922454. Unknown parameter |month= ignored (help)
  145. Nater UM, Maloney E, Boneva RS; et al. (2008). "Attenuated morning salivary cortisol concentrations in a population-based study of persons with chronic fatigue syndrome and well controls". J. Clin. Endocrinol. Metab. 93 (3): 703–9. doi:10.1210/jc.2007-1747. PMID 18160468. Unknown parameter |month= ignored (help)
  146. Jerjes WK, Taylor NF, Wood PJ, Cleare AJ (2007). "Enhanced feedback sensitivity to prednisolone in chronic fatigue syndrome". Psychoneuroendocrinology. 32 (2): 192–8. doi:10.1016/j.psyneuen.2006.12.005. PMID 17276605. Unknown parameter |month= ignored (help)
  147. Van Den Eede F, Moorkens G, Hulstijn W; et al. (2007). "Combined dexamethasone/corticotropin-releasing factor test in chronic fatigue syndrome". Psychol Med: 1–11. doi:10.1017/S0033291707001444. PMID 17803834. Unknown parameter |month= ignored (help)
  148. Nater UM, Youngblood LS, Jones JF; et al. (2008). "Alterations in diurnal salivary cortisol rhythm in a population-based sample of cases with chronic fatigue syndrome". Psychosom Med. 70 (3): 298–305. doi:10.1097/PSY.0b013e3181651025. PMID 18378875. Unknown parameter |month= ignored (help)
  149. Jerjes WK, Taylor NF, Peters TJ, Wessely S, Cleare AJ (2006). "Urinary cortisol and cortisol metabolite excretion in chronic fatigue syndrome". Psychosom Med. 68 (4): 578–82. doi:10.1097/01.psy.0000222358.01096.54. PMID 16868267.
  150. Jerjes WK, Peters TJ, Taylor NF, Wood PJ, Wessely S, Cleare AJ (2006). "Diurnal excretion of urinary cortisol, cortisone, and cortisol metabolites in chronic fatigue syndrome". J Psychosom Res. 60 (2): 145–53. doi:10.1016/j.jpsychores.2005.07.008. PMID 16439267. Unknown parameter |month= ignored (help)
  151. [1] The Centers For Disease Control and Prevention (website): CFS Home > Publications > Molecular Epidemiology Program - Date: July 25 2005 - Content source: National Center for Infectious Diseases
  152. Whistler T, Jones JF, Unger ER, Vernon SD (2005). "Exercise responsive genes measured in peripheral blood of women with chronic fatigue syndrome and matched control subjects". BMC Physiol. 5 (1): 5. doi:10.1186/1472-6793-5-5. PMID 15790422.
  153. Whistler T, Unger ER, Nisenbaum R, Vernon SD (2003). "Integration of gene expression, clinical, and epidemiologic data to characterize Chronic Fatigue Syndrome". J Transl Med. 1 (1): 10. doi:10.1186/1479-5876-1-10. PMID 14641939.
  154. Vernon SD, Unger ER, Dimulescu IM, Rajeevan M, Reeves WC (2002). "Utility of the blood for gene expression profiling and biomarker discovery in chronic fatigue syndrome". Dis Markers. 18 (4): 193–9. PMID 12590173.
  155. Kaushik N, Fear D, Richards SC, McDermott CR, Nuwaysir EF, Kellam P, Harrison TJ, Wilkinson RJ, Tyrrell DA, Holgate ST, Kerr JR (2005). "Gene expression in peripheral blood mononuclear cells from patients with chronic fatigue syndrome". J Clin Pathol. 58 (8): 826–32. doi:10.1136/jcp.2005.025718. PMID 16049284.
  156. Fang H, Xie Q, Boneva R, Fostel J, Perkins R, Tong W (2006). "Gene expression profile exploration of a large dataset on chronic fatigue syndrome". Pharmacogenomics. 7 (3): 429–40. doi:10.2217/14622416.7.3.429. PMID 16610953.
  157. BBC News (28 May 2005) - Scientists 'unlock ME genetics' (study still in its early stages)
  158. Fostel J, Boneva R, Lloyd A (2006). "Exploration of the gene expression correlates of chronic unexplained fatigue using factor analysis". Pharmacogenomics. 7 (3): 441–54. doi:10.2217/14622416.7.3.441. PMID 16610954.
  159. Kerr J, Burke B, Petty R; et al. (2007). "Seven genomic subtypes of Chronic Fatigue Syndrome / Myalgic Encephalomyelitis (CFS/ME): a detailed analysis of gene networks and clinical phenotypes". J Clin Pathol. doi:10.1136/jcp.2007.053553. PMID 18057078.
  160. Kerr JR, Petty R, Burke B; et al. (2008). "Gene expression subtypes in patients with chronic fatigue syndrome/myalgic encephalomyelitis". J. Infect. Dis. 197 (8): 1171–84. doi:10.1086/533453. PMID 18462164. Unknown parameter |month= ignored (help)
  161. Narita M, Nishigami N, Narita N, Yamaguti K, Okado N, Watanabe Y, Kuratsune H (2003). "Association between serotonin transporter gene polymorphism and chronic fatigue syndrome". Biochem. Biophys. Res. Commun. 311 (2): 264–6. doi:10.1016/j.bbrc.2003.09.207. PMID 14592408.
  162. Goertzel BN, Pennachin C, de Souza Coelho L, Gurbaxani B, Maloney EM, Jones JF (2006). "Combinations of single nucleotide polymorphisms in neuroendocrine effector and receptor genes predict chronic fatigue syndrome". Pharmacogenomics. 7 (3): 475–83. doi:10.2217/14622416.7.3.475. PMID 16610957.
  163. Smith AK, White PD, Aslakson E, Vollmer-Conna U, Rajeevan MS (2006). "Polymorphisms in genes regulating the HPA axis associated with empirically delineated classes of unexplained chronic fatigue". Pharmacogenomics. 7 (3): 387–94. doi:10.2217/14622416.7.3.387. PMID 16610949.
  164. Torpy DJ, Bachmann AW, Gartside M, Grice JE, Harris JM, Clifton P, Easteal S, Jackson RV, Whitworth JA (2004). "Association between chronic fatigue syndrome and the corticosteroid-binding globulin gene ALA SER224 polymorphism". Endocr. Res. 30 (3): 417–29. doi:10.1081/ERC-200035599. PMID 15554358.
  165. Kerr JR (2005). "Pathogenesis of parvovirus B19 infection: host gene variability, and possible means and effects of virus persistence". J. Vet. Med. B Infect. Dis. Vet. Public Health. 52 (7–8): 335–9. PMID 16316396.
  166. Carlo-Stella N, Badulli C, De Silvestri A, Bazzichi L, Martinetti M, Lorusso L, Bombardieri S, Salvaneschi L, Cuccia M (2006). "A first study of cytokine genomic polymorphisms in CFS: Positive association of TNF-857 and IFNgamma 874 rare alleles". Clin. Exp. Rheumatol. 24 (2): 179–82. PMID 16762155.
  167. Vladutiu GD, Natelson BH (2004). "Association of medically unexplained fatigue with ACE insertion/deletion polymorphism in Gulf War veterans". Muscle Nerve. 30 (1): 38–43. doi:10.1002/mus.20055. PMID 15221876.
  168. Wyller VB (2007). "The chronic fatigue syndrome - an update". Acta Neurol Scand Suppl. 187: 7–14. doi:10.1111/j.1600-0404.2007.00840.x. PMID 17419822.
  169. Kennedy G, Spence VA, McLaren M, Hill A, Underwood C, Belch JJ (2005). "Oxidative stress levels are raised in CFS and are associated with clinical symptoms". Free Radic Biol Med. 39 (5): 584–9. doi:10.1016/j.freeradbiomed.2005.04.020. PMID 16085177.
  170. Jammes Y, Steinberg JG, Mambrini O, Bregeon F, Delliaux S (2005). "Chronic fatigue syndrome: assessment of increased oxidative stress and altered muscle excitability in response to incremental exercise". J Intern Med. 257 (3): 299–310. doi:10.1111/j.1365-2796.2005.01452.x. PMID 15715687.
  171. Richards RS, Wang L, Jelinek H (2007). "Erythrocyte oxidative damage in chronic fatigue syndrome". Arch Med Res. 38 (1): 94–8. doi:10.1016/j.arcmed.2006.06.008. PMID 17174731.
  172. Vecchiet J, Cipollone F, Falasca K, Mezzetti A, Pizzigallo E, Bucciarelli T, De Laurentis S, Affaitati G, De Cesare D, Giamberardino MA (2003). "Relationship between musculoskeletal symptoms and blood markers of oxidative stress in patients with chronic fatigue syndrome". Neurosci Lett. 335 (3): 151–4. doi:10.1016/S0304-3940(02)01058-3. PMID 12531455.
  173. Fulle S, Mecocci P, Fano G, Vecchiet I, Vecchini A, Racciotti D, Cherubini A, Pizzigallo E, Vecchiet L, Senin U, Beal MF (2000). "Specific oxidative alterations in vastus lateralis muscle of patients with the diagnosis of chronic fatigue syndrome". Free Radic Biol Med. 29 (12): 1252–9. doi:10.1016/S0891-5849(00)00419-6. PMID 11118815.
  174. Richards RS, Roberts TK, McGregor NR, Dunstan RH, Butt HL (2000). "Blood parameters indicative of oxidative stress are associated with symptom expression in chronic fatigue syndrome". Redox Rep. 5 (1): 35–41. PMID 10905542.
  175. Nijs J, Meeus M, De Meirleir K (2006). "Chronic musculoskeletal pain in chronic fatigue syndrome: recent developments and therapeutic implications". Man Ther. 11 (3): 187–91. doi:10.1016/j.math.2006.03.008. PMID 16781183.
  176. Maes M, Mihaylova I, Bosmans E (2007). "Not in the mind of neurasthenic lazybones but in the cell nucleus: patients with chronic fatigue syndrome have increased production of nuclear factor kappa beta". Neuro Endocrinol. Lett. 28 (4): 456–62. PMID 17693979.
  177. Maes M, Mihaylova I, Leunis JC (2006). "Chronic fatigue syndrome is accompanied by an IgM-related immune response directed against neopitopes formed by oxidative or nitrosative damage to lipids and proteins". Neuro Endocrinol. Lett. 27 (5): 615–21. PMID 17159817.
  178. Broderick G, Craddock RC, Whistler T, Taylor R, Klimas N, Unger ER (2006). "Identifying illness parameters in fatiguing syndromes using classical projection methods". Pharmacogenomics. 7 (3): 407–19. doi:10.2217/14622416.7.3.407. PMID 16610951.
  179. van de Glind G, de Vries M, Rodenburg R, Hol F, Smeitink J, Morava E (2007). "Resting muscle pain as the first clinical symptom in children carrying the MTTK A8344G mutation". Eur. J. Paediatr. Neurol. 11 (4): 243–6. doi:10.1016/j.ejpn.2007.01.004. PMID 17293137.
  180. Behan WM, More IA, Behan PO (1991). "Mitochondrial abnormalities in the postviral fatigue syndrome". Acta Neuropathol. 83 (1): 61–5. PMID 1792865.
  181. 181.0 181.1 Vernon SD, Whistler T, Cameron B, Hickie IB, Reeves WC, Lloyd A (2006). "Preliminary evidence of mitochondrial dysfunction associated with post-infective fatigue after acute infection with Epstein Barr virus". BMC Infect. Dis. 6: 15. doi:10.1186/1471-2334-6-15. PMID 16448567.
  182. 182.0 182.1 Kaushik N, Fear D, Richards SC; et al. (2005). "Gene expression in peripheral blood mononuclear cells from patients with chronic fatigue syndrome". J. Clin. Pathol. 58 (8): 826–32. doi:10.1136/jcp.2005.025718. PMID 16049284.
  183. Pieczenik SR, Neustadt J (2007). "Mitochondrial dysfunction and molecular pathways of disease". Exp. Mol. Pathol. 83 (1): 84–92. doi:10.1016/j.yexmp.2006.09.008. PMID 17239370.
  184. Lundell K, Qazi S, Eddy L, Uckun FM. Clinical activity of folinic acid in patients with chronic fatigue syndrome. Arzneimittelforschung. 2006;56(6):399-404.
  185. Jacobson W, Saich T, Borysiewicz LK, Behan WM, Behan PO, Wreghitt TG. Serum folate and chronic fatigue syndrome. Neurology 1993 Dec;43(12):2645-7.
  186. Horrobin, David F. (1990). Omega-6 essential fatty acids: pathophysiology and roles in clinical medicine. New York: Wiley-Liss. pp. 275–282. ISBN 0-471-56693-4.
  187. Behan PO, Behan WM, Horrobin D (1990). "Effect of high doses of essential fatty acids on the postviral fatigue syndrome". Acta Neurol. Scand. 82 (3): 209–16. PMID 2270749.
  188. Ogawa R, Toyama S, Matsumoto H. (1992). "Chronic fatigue syndrome--cases in the Kanebo Memorial Hospital". Nippon Rinsho. 50 (11): 2648–52. PMID 1337561.
  189. 189.0 189.1 Liu Z, Wang D, Xue Q; et al. (2003). "Determination of fatty acid levels in erythrocyte membranes of patients with chronic fatigue syndrome". Nutritional neuroscience. 6 (6): 389–92. PMID 14744043.
  190. 190.0 190.1 Maes M, Mihaylova I, Leunis JC (2005). "In chronic fatigue syndrome, the decreased levels of omega-3 poly-unsaturated fatty acids are related to lowered serum zinc and defects in T cell activation". Neuro Endocrinol. Lett. 26 (6): 745–51. PMID 16380690.
  191. Warren G, McKendrick M, Peet M (1999). "The role of essential fatty acids in chronic fatigue syndrome. A case-controlled study of red-cell membrane essential fatty acids (EFA) and a placebo-controlled treatment study with high dose of EFA". Acta Neurol. Scand. 99 (2): 112–6. PMID 10071170.
  192. 192.0 192.1 Puri BK (2007). "Long-chain polyunsaturated fatty acids and the pathophysiology of myalgic encephalomyelitis (chronic fatigue syndrome)". J. Clin. Pathol. 60 (2): 122–4. doi:10.1136/jcp.2006.042424. PMID 16935966.
  193. 193.0 193.1 Puri BK (2004). "The use of eicosapentaenoic acid in the treatment of chronic fatigue syndrome". Prostaglandins Leukot. Essent. Fatty Acids. 70 (4): 399–401. doi:10.1016/j.plefa.2003.12.015. PMID 15041033.
  194. Carruthers, BM (2003). "Myalgic Encephomyelitis / Chronic fatigue Syndrome: Clinical Working Case Definition, Diagnostic and Treatment Protocols (a Consensus Document)". Journal of Chronic Fatigue Syndrome. 11 (1): 66. Unknown parameter |coauthors= ignored (help)
  195. McGregor N.R. Dunstan H.R. et al. 1998 “Alterations in Plasma Lipid Composition in Patients with CFS” presented at Conference; The Clinical and Scientific Basis of CFS, Sydney 1998, P38
  196. McGregor N.R. Dunstan H.R. et al. 1998 “Assessment of Lipid Homeostasis in Sudden and Gradual Onset CFS Patients” presented at Conference; The Clinical and Scientific Basis of CFS, Sydney 1998, P39
  197. Mihaylova I, DeRuyter M, Rummens JL, Bosmans E, Maes M (2007). "Decreased expression of CD69 in chronic fatigue syndrome in relation to inflammatory markers: evidence for a severe disorder in the early activation of T lymphocytes and natural killer cells". Neuro Endocrinol. Lett. 28 (4): 477–83. PMID 17693977.
  198. Fulle S, Mecocci P, Fanó G; et al. (2000). "Specific oxidative alterations in vastus lateralis muscle of patients with the diagnosis of chronic fatigue syndrome". Free Radic. Biol. Med. 29 (12): 1252–9. PMID 11118815.
  199. Kennedy G, Spence VA, McLaren M, Hill A, Underwood C, Belch JJ (2005). "Oxidative stress levels are raised in chronic fatigue syndrome and are associated with clinical symptoms". Free Radic. Biol. Med. 39 (5): 584–9. doi:10.1016/j.freeradbiomed.2005.04.020. PMID 16085177.
  200. Richards RS, Roberts TK, McGregor NR, Dunstan RH, Butt HL (2000). "Blood parameters indicative of oxidative stress are associated with symptom expression in chronic fatigue syndrome". Redox Rep. 5 (1): 35–41. PMID 10905542.
  201. Jenkins, Rachel; Mowbray, James F. (1991). Post-viral fatigue syndrome (Myalgic encephalomyelitis). New York: Wiley. ISBN 0-471-92846-1. Unknown parameter |Chapter= ignored (|chapter= suggested) (help)
  202. 202.0 202.1 Kuratsune H, Yamaguti K, Takahashi M, Misaki H, Tagawa S, Kitani T (1994). "Acylcarnitine deficiency in chronic fatigue syndrome". Clin. Infect. Dis. 18 Suppl 1: S62–7. PMID 8148455.
  203. Plioplys AV, Plioplys S (1995). "Serum levels of carnitine in chronic fatigue syndrome: clinical correlates". Neuropsychobiology. 32 (3): 132–8. PMID 8544970.
  204. Kuratsune H, Yamaguti K, Lindh G; et al. (1998). "Low levels of serum acylcarnitine in chronic fatigue syndrome and chronic hepatitis type C, but not seen in other diseases". Int. J. Mol. Med. 2 (1): 51–6. PMID 9854142.
  205. Kuratsune H, Yamaguti K, Hattori H; et al. (1992). "[Symptoms, signs and laboratory findings in patients with chronic fatigue syndrome]". Nippon Rinsho (in Japanese). 50 (11): 2665–72. PMID 1337562.
  206. Miwa S, Takikawa O (2007). "[Chronic fatigue syndrome and neurotransmitters]". Nippon Rinsho (in Japanese). 65 (6): 1005–10. PMID 17561689.
  207. Jones MG, Goodwin CS, Amjad S, Chalmers RA (2005). "Plasma and urinary carnitine and acylcarnitines in chronic fatigue syndrome". Clin. Chim. Acta. 360 (1–2): 173–7. doi:10.1016/j.cccn.2005.04.029. PMID 15967423.
  208. Li YJ, Wang DX, Bai XL; et al. (2005). "[Clinical characteristics of patients with chronic fatigue syndrome: analysis of 82 cases]". Zhonghua Yi Xue Za Zhi (in Chinese). 85 (10): 701–4. PMID 15932738.
  209. McGregor N.R. Dunstan H.R. et al. 1998 “Classification of CFS Patients by Assessing Plasma lipid Homeostasis” presented at Conference; The Clinical and Scientific Basis of CFS, Sydney 1998, P40
  210. Famularo G, De Simone C, Trinchieri V, Mosca L (2004). "Carnitines and its congeners: a metabolic pathway to the regulation of immune response and inflammation". Ann. N. Y. Acad. Sci. 1033: 132–8. doi:10.1196/annals.1320.012. PMID 15591010.
  211. Saheki T (1999). "[Carnitine as a vitamin-like biofactor]". Nippon Rinsho (in Japanese). 57 (10): 2270–5. PMID 10540873.
  212. Vermeulen RC, Scholte HR (2006). "Azithromycin in chronic fatigue syndrome (CFS), an analysis of clinical data". J Transl Med. 4 issue=: 34. doi:10.1186/1479-5876-4-34. PMID 16911783.
  213. Fernández-Solà J, Lluís Padierna M, Nogué Xarau S, Munné Mas P (2005). "[Chronic fatigue syndrome and multiple chemical hypersensitivity after insecticide exposure]". Med Clin (Barc) (in Spanish; Castilian). 124 (12): 451–3. PMID 15826581.
  214. Dunstan RH, Donohoe M, Taylor W; et al. (1995). "A preliminary investigation of chlorinated hydrocarbons and chronic fatigue syndrome". Med. J. Aust. 163 (6): 294–7. PMID 7565234.
  215. Kennedy G, Abbot NC, Spence V, Underwood C, Belch JJ (2004). "The specificity of the CDC-1994 criteria for chronic fatigue syndrome: comparison of health status in three groups of patients who fulfill the criteria". Ann Epidemiol. 14 (2): 95–100. doi:10.1016/j.annepidem.2003.10.004. PMID 15018881.
  216. Viner R, Hotopf M (2003). "Childhood predictors of self reported chronic fatigue syndrome/myalgic encephalomyelitis in adults: national birth cohort study". BMJ. 329 (7472): 941. doi:10.1136/bmj.38258.507928.55. PMID 15469945.
  217. Lane RJ, Barrett MC, Taylor DJ, Kemp GJ, Lodi R (1998). "Heterogeneity in chronic fatigue syndrome: evidence from magnetic resonance spectroscopy of muscle". Neuromuscul. Disord. 8 (3–4): 204–9. PMID 9631403.
  218. Lane RJ, Barrett MC, Woodrow D, Moss J, Fletcher R, Archard LC (1998). "Muscle fibre characteristics and lactate responses to exercise in chronic fatigue syndrome". J. Neurol. Neurosurg. Psychiatr. 64 (3): 362–7. PMID 9527150.
  219. Lamb GD, Stephenson DG (2006). "Point: lactic acid accumulation is an advantage during muscle activity". J. Appl. Physiol. 100 (4): 1410–2, discussion 1414. doi:10.1152/japplphysiol.00023.2006. PMID 16540714.
  220. Pedersen TH, Nielsen OB, Lamb GD, Stephenson DG (2004). "Intracellular acidosis enhances the excitability of working muscle". Science. 305 (5687): 1144–7. doi:10.1126/science.1101141. PMID 15326352.
  221. Lane RJ, Soteriou BA, Zhang H, Archard LC (2003). "Enterovirus related metabolic myopathy: a postviral fatigue syndrome". J Neurol Neurosurg Psychiatry. 74 (10): 1382–6. doi:10.1136/jnnp.74.10.1382. PMID 14570830.
  222. Barron DF, Cohen BA, Geraghty MT, Violand R, Rowe PC (2002). "Joint hypermobility is more common in children with chronic fatigue syndrome than in healthy controls". J Pediatr. 141 (3): 421–5. doi:10.1067/mpd.2002.127496. PMID 12219066.


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