By John DeLuca, PhD
UMDNJ-New Jersey Medical
School
Studies assessing structural and
functional neuroimaging, autonomic
activity and neuroendocrine abnormalities all point to neuro-pathology in chronic fatigue syndrome (CFS)
patients. While the nature and the extent of neuropathologic involvement in CFS is still unclear, neurocognitive
studies make up a very large body of CFS research.
This is an important area for clinicians to
familiarize themselves with, as cognitive problems have been cited as one of the most disruptive and functionally
disabling symptoms of CFS, with up to 85% of patients reporting impairments in attention, concentration
and memory abilities.1
This article provides an overview of neurocognitive findings
in CFS patients and the possible underlying structural changes in the brain.
Cognitive
problems observed
Neuropsychological testing confirms cognitive abnormalities, although the data
is not consistent as to their nature and testing abnormalities may be subtle in contrast to patients’
descriptions of day-to-day problems.
Several formal neuropsychological studies report impairments
in attention, verbal memory, visual memory, reaction time and complex auditory information processing.2-5
However, others have not found memory or attentional deficits.6-7
Despite metholology
limitations, research with CFS patients is fairly consistent in showing that neuropsychological impairments
are primarily in the area of complex information processing. Whether the complaints of difficulties in
learning and memory result from slowed information processing efficiency, verbal processing difficulties
or susceptibility to interference are important questions that were addressed in a recent study. Patients
were found to be susceptible to brief distraction, which resulted in impaired immediate and delayed recall.8
Another
important question for neuropsychological research in CFS is the relationship between self-reported fatigue,
perceived cognitive impairment, and objective neuropsychological performance. Some research findings have
demonstrated that fatigue brought about by mental challenges did not universally impair performance.
A
study at the NIH-funded New Jersey Cooperative Research Center found that after exhaustive treadmill exercise,
CFS patients demonstrated impaired cognitive processing compared to healthy controls, suggesting that
physical fatigue may be a crucial variable in explaining impaired cognition.9 Several other
studies have arrived at similar conclusions.
It is important to note that the impaired cognition
experienced by many CFS patients may not necessarily be explained by an underlying psychiatric condition.
In at least one study, CFS patients without psychiatric comorbidity were impaired relative to controls
and patients without CFS with concurrent psychiatric disease on tests of memory, attention and information
processing.10
Neuroimaging study findings
It has been postulat-ed
that some of the symptoms
of CFS, such as impaired cognition, may result from brain abnormalities. Several studies have reported
significantly more abnormalities on MRI among CFS subjects relative to controls.
Overall, MRI studies
are generally consistent in demonstrating T2 signal hyperintensities in the subcortical white matter,
often in the frontal lobes. One study found that CFS patients without depression had a significantly larger
number of small, punctate subcortical white matter hyperintensities compared to CFS patients with depression
or sedentary controls.11
Another approach to neuroimaging is assessing cerebral blood
flow via single-photon emission computed tomography (SPECT). Most SPECT studies have shown significantly
decreased blood flow. This technique has demonstrated changes in some patients’ brains that were not apparent
on MRI.
In one study, decreases in regional cerebral blood flow throughout the brain have been
reported on SPECT in a CFS group relative to healthy controls, and abnormalities were observed in 80%
of the CFS patients. CFS patients could be distinguished from controls with unipolar depression based
on the pattern of SPECT abnormalities.12
In addition, significant brain stem hypoperfusion
on SPECT was found in patients with CFS relative to controls and depressed patients.13
At
least one research group reported a positive correlation between frontal blood flow (on SPECT) and cognitive
impairment. They hypothesized that the blood flow abnormalities may play a pathophysiological role in
cognitive impairment and physical activity limitations in CFS patients.14
There have
been few published reports of positron emission tomography (PET) scans in CFS patients. One research group
reported hypometabolism on PET in the brain stem of 18 CFS patients, which was not found in six depression
patients or six healthy controls.15
How does CFS differ from depression?
CFS symptoms
rely on subjective report,
which fuels the controversy over an organic versus emotional etiology of the illness. Some practitioners
confuse clinical depression, which may also cause difficulty in cognitive processing, with CFS.
High
diagnosis rates of depression in CFS patients may result from overlapping symptomatology, reaction to
disability imposed by fatigue or viral/immune changes in the brain. However, as has already been pointed
out, studies have shown that some of the brain abnormalities found in CFS may be differentiated from patients
who are psychiatrically depressed. However, this research is in its infancy, and more studies are needed.
In addition, one recent study showed that the pattern of depressive symptoms in CFS patients is
dissimilar to that observed in clinically depressed patients and more closely resembles the pattern observed
in patients with multiple sclerosis (MS).16
Implications for treatment
Much of the data on
brain abnormalities in CFS is
still too preliminary to use in practice. Although the MRI and SPECT findings of the brain in CFS patients
are intriguing, more carefully designed and controlled studies still need to be undertaken.
However,
physicians and other health care professionals could still make use of the information that neuroimaging
provides. Some patients with apparent CFS and brain lesions on MRI may actually have mild presentation
of other neurologic illnesses, such as MS.
Clinicians should also keep in mind that patients’ diminished
neurocogni-tive processing can be addressed through rehabilitation (see article this issue).
Clinicians should
also take patients’ impaired
cognition into account during office visits. Patients may need assistance in completing complex tasks,
such as filling out medical forms.
They may also have difficulty expressing themselves verbally
and understanding questions during exams. One way to help patients is to make questions very specific
and to state them one at a time, rather than as an uninterrupted series, since slowed processing speed
is a major problem in patients with CFS.
References
- Grafman J. In : Struas SE, ed. Chronic Fatigue Syndrome. NY: Marcel Deckker,
1994: 263-84.
- DeLuca, J et al. J Neurol Neurosurg Psych. 1995; 58:38-43.
- Riccio M et al. Brit J Clin Psych. 1992; 31: 111-120.
- Grafman J et al. J Neurol Neurosurg Psych. 1993: 56: 684-9.
- Scheffers MK et al. Neurol. 1992; 42: 1667-75.
- Johnson SK et al. Clin Infect Dis. 1994; 18: S84-S85.
- Krupp LB et al. Arch Neurol. 1994; 51: 705-10.
- Johnson SK et al. Cog Neuropsych. 1998; 3:269-85.
- LaManca J et al. Am J Med. 1998; 105: 59S-65S.
- LeLuca J et al. J Neurol Neurosurg Psych. 1997; 62:151-55.
- Natelson BH et al. J Neurol Sci. 1993; 120: 213-7.
- Ichise M et al. Nuclear Med Commun. 1992; 13: 767-72.
- Costa DC et al. Quarterly J Med. 1995; 88: 767-73.
- Fischler B et al. Neuropsychobiol. 1996; 34: 175-83.
- Tirelli U et al. Am J Med. 1998; 105: 54S-58S.
-
Johnson SK et al. J Affect Dis. 1996; 39: 21-30.
Dr. DeLuca is Director of Neuroscience Research, Kessler
Medical Rehabilitation and Education
Corporation, and Professor of Physical Medicine, Rehabilitation and Neurosciences, University of Medicine
and Dentistry of New Jersey (UMDNJ)-New Jersey Medical School.