| NIH Announces Awards in Chronic Fatigue Syndrome Research
The Office of Research on Women’s Health (ORWH) and the
Trans-NIH Working Group for Research in Chronic Fatigue Syndrome
(CFSWG) of the National Institutes of Health (NIH) are pleased
to announce seven (7) awards in Chronic Fatigue Syndrome (CFS)
research. The proposed studies will help researchers understand
how the diverse symptoms in CFS are related to the interactions
between the immune and neurological systems — an important
step towards developing effective treatments for a disabling condition.
The awards were funded by ORWH, Office of the Director, and four
member institutes: The National Institute on Alcohol Abuse and
Alcoholism (NIAAA), the National Institute of Environmental Health
Sciences (NIEHS), the National Institute of Arthritis Musculoskeletal
and Skin Diseases (NIAMS), and the National Institute of Neurological
Disorders and Stroke (NINDS).
Katherine Light, Ph.D., University of Utah, St. Lake City, Utah,
plans to first explore in humans the suggested mechanisms for the
perception of pain and fatigue in CFS by assessing repeated patterns
in the immune and neurological systems that are present before,
during and immediately after mental and physical exertion. There
is a possibility that findings will lead to the development of
a biomarker for CFS. Her second pilot study will focus on identifying
family risk patterns in CFS using the Utah Family Data Base (large
genealogy data base) to explore the familial/genetic component
of CFS. Identifying a genetic predisposition to CFS will assist
in the development of more effective medications.
Theoharis Theoharides, M.D.,Ph.D., Tufts University, Boston, Massachusetts,
will explore the relationship of human mast cells (molecules released
in stress) in the brain, not only in explaining the development
of CFS but also in explaining the effects of antidepressants in
relieving symptoms in CFS patients. Dr. Theoharides will examine
the cellular changes that explain CFS symptoms using three different
classes of antidepressants: tricyclic, serotonin uptake inhibitors
and bupropion. Future studies will build on these findings to develop
clinical trials of select antidepressants or other molecules that
inhibit CFS.
Mary Ann Fletcher, Ph.D., University of Miami, Miami, Florida,
plans to study the role of specific peptides: neuropeptide Y (NPY)
and dipeptidyl-peptidase (CD26) in the development of CFS. These
peptides, formed from amino acids (the basic building blocks of
the body that are essential in combating illness), regulate many
physiological and disease processes in the cardiorespiratory, immune,
nervous and endocrine systems. This study will also examine aspects
of the relationship between different levels of peptides and the
severity of CFS symptoms and may lead to the development of biomarkers.
Dianne Lorton, Ph.D. at the Sun Health Research Institute in Sun
City, Arizona, will establish a tissue bank to make brain and spinal
cord tissue available to study CFS/FM (fibromyalga). She has gathered
an interdisciplinary research team that will determine the extent
to which chronic pain in these patients is associated with glial
(support cells of the nervous system) activation and resulting
cytokine production (compounds essential to engage the immune response).
While studies in rodents have shown this activation leads to inflammation
and chronic pain, Dr. Lorton will test the extent that this process
is involved in humans in order to target mechanisms to treat the
chronic pain associated with CFS.
James Baraniuk, M.D., Georgetown University, Washington D.C.,
has found that despite its diverse clinical syndromes, the CFS
proteome (the entire group of proteins in an organism or system)
is the same, suggesting a strong relationship with malfunctioning
of the central nervous system. Dr. Baraniuk developed the first
predictive model of CFS based solely on objective data and he now
proposes to recruit a new group of CFS and Healthy Control subjects
to determine if the proteins in their cerebrospinal fluid will
be a predictive marker of the spectrum of CFS symptoms. There is
a high probability that these methods and markers will be of diagnostic
value and will be useful for assessing changes over time in disease
severity and treatment effects.
Michael Antoni, Ph.D., at the University of Miami, Miami, Florida,
has demonstrated the positive effects of participation in group
cognitive behavioral stress management (CBSM) on quality of life,
perceived stress, fatigue, memory, muscle pain and post-exertional
malaise for CFS patients compared to those in a control condition.
Many CFS patients are too debilitated to attend regular therapy
sessions. Therefore, in the present study, he will test the physiological
effects of a telephone-based cognitive behavioral stress management
intervention to illuminate CFS patients’ neuroimmune mechanisms
in relation to stress and stress management. The correlation of
the neuroimmune parameters and the behavioral components promises
to identify a biologically useful marker for CFS.
Italo Biaggioni, M.D. at Vanderbilt University in Nashville, Tennessee,
will explicate the role of the sympathetic nervous system (SNS)
in the cardiovascular and inflammatory abnormalities in the subset
of patients with postural tachycardia (POTS) — increase in
heart rate and often decrease in blood pressure on standing. Preliminary
studies indicate a relationship between the mechanisms underlying
POTS and CFS symptoms. Dr. Baggioni will test these hypotheses
in a comprehensive set of experiments with appropriate controls.
“These innovative, interdisciplinary studies to help us
better understand the role of the central nervous system in the
origin and development of CFS; represent efforts of the Trans-NIH
Working Group for Research on Chronic Fatigue Syndrome, chaired
by the ORWH, to expand interest in CFS research. I am excited that
these efforts could lead to major advances in understanding the
disease processes of CFS and that they may also provide diagnostic
biomarkers that can be used to measure treatment effects. These
studies may also help us understand why some of the known treatments
are effective and lead to the development of newer and more targeted
remedies,” stated Dr. Vivian W. Pinn, M.D., Director of the
ORWH.
The Office of Research on Women’s Health (ORWH), Office
of the Director, National Institutes of Health (NIH) serves as
a focal point for women’s health research at the NIH. For
more information about NIH’s Office of Research on Women’s
Health, visit http://orwh.od.nih.gov/.
The National Institutes of Health (NIH) — The Nation's Medical Research
Agency — includes 27 Institutes and Centers and is a component of
the U.S. Department of Health and Human Services. It is the primary federal
agency for conducting and supporting basic, clinical and translational medical
research, and it investigates the causes, treatments, and cures for both common
and rare diseases. For more information about NIH and its programs, visit www.nih.gov. |