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Gene Pattern Revealed in Pilot Study
Dr. Jonathan Kerr and colleagues at
St. George’s
University of
London reported in the July 27, 2005
issue of the Journal of Clinical
Pathology that a preliminary study of 25 CFS patients and 25 matched
healthy controls revealed abnormalities in 35 of 9,522 genes analyzed using
microarray technology. Polymerase chain reaction studies showed the same results for 16 of these genes.
The pattern of dysregulated genes reflects T cell activation
and disruption of neuronal and mitochondrial function, findings that are
consistent with other studies in the CFS literature. The authors suggest that
their results point to a role for organophosphate exposure or viral infection in
CFS. Of the 25 patients tested, 15 reported onset with a flu-like illness. All
patients met the CDC case definition and the researchers took care to enroll
patients representing a broad spectrum of illness severity, including subjects
who were mostly bedbound as well as others with milder symptoms. Sixteen were
female and the subjects’ mean age was 40.6. None had received previous treatment
for depression. The study did not compare CFS patients to patients with other
medical conditions.
The group is currently expanding its search for a gene profile
and treatments, studying 1,000 patients and controls and looking at 47,000 genes
in collaboration with several other centers throughout the
United Kingdom.
Their work attracted coverage in the July 21 issue of
New
Scientist, a leading weekly science and technology magazine. The story was
picked up by BBC News and other news services and it was reported in the Aug. 2,
2005 edition of the New York Times. The study was funded by the CFS Research
Foundation, a UK
charity dedicated to supporting high quality research.
Microarray technology is being used by Dr. Suzanne Vernon and
colleagues at the U.S. Centers for Disease Control and Prevention to detect gene
expression abnormalities and identify a biomarker for CFS. Dr. Vernon wrote
about her group’s work in the fall 2004 issue of
the CFIDS
Chronicle (see pages 18-21). Her group has reported irregularities in
the expression of
neuronal
genes in CFS. Dr. R. Powell of the
UK’s
Southampton
University
Hospital reported a pilot study using
differential display that found upregulation of
mitochondrial
genes in CFS. With further study, these methods may well yield a diagnostic
test for CFS, as well as improved understanding of the underlying biologic
processes and more effective treatments.
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