|
|
Home
Search
Study Topics
Glossary
|
 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||||||||||||||||||||||||||||||
| Sponsored by: |
National Institute of Mental Health (NIMH) |
|---|---|
| Information provided by: | National Institutes of Health Clinical Center (CC) |
| ClinicalTrials.gov Identifier: | NCT00001415 |
Purpose
A variety of hormones and immune system processes are responsible for how the body responds to illness. This study concentrates on how the hormone cortisol effects the release of immune system factors called cytokines.
Cortisol is a hormone produced in the adrenal glands as a response to stimulation from the pituitary gland. Abnormal levels of cortisol have been seen in several diseases such as depression and multiple sclerosis.
Cytokines are factors produced by certain white blood cells. They act by changing the cells that produce them (autocrine effect), altering other cells close to them (paracrine), and effecting cells throughout the body (endocrine effect). Cytokines are important in controlling inflammation processes.
In this study researchers would like to determine if changes in levels of hormones in the blood are associated with changes in cytokine levels. In addition, researchers would like to learn more about how cytokines respond to hormones in certain diseases.
| Condition |
|---|
|
Depressive Disorder Fatigue Syndrome, Chronic Fibromyalgia Healthy Inflammation |
| Study Type: | Observational |
| Official Title: | Glucocorticoid Effects on Cellular Cytokine Release |
| Estimated Enrollment: | 130 |
| Study Start Date: | May 1994 |
| Estimated Study Completion Date: | July 2000 |
Many of the biochemical alterations observed in people suffering from major depression are changes in the concentrations and activity of components of the generalized stress response. These include the principal hypothalamic stimulus of pituitary-adrenal activation (corticotropin releasing hormone) and the locus ceruleus/norepinephrine system. The current study attempts to provide a clearer picture of the stability of changes during the acute illness, the treatment phase and the recovery process. We particularly wish to determine whether abnormalities in HPA axis perturbability in the well-state can be demonstrated, and if so how these are related to the acutely-ill state, since this information could provide a quantifiable phenotypic marker for depression.
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Healthy volunteers.
Depressed patients.
Fibromyalgia patients.
Chronic fatigue patients.
Subjects must not have been treated with steroids for more than two weeks during the previous year.
Subjects must not be on chronic medications.
Subjects must not have known medical problems or any condition which interferes with their immune system's ability to respond to infections (talk with your physician if you are not sure about a particular situation).
Contacts and Locations More Information
| Study ID Numbers: | 940146, 94-M-0146 |
| Study First Received: | November 3, 1999 |
| Last Updated: | March 3, 2008 |
| ClinicalTrials.gov Identifier: | NCT00001415 |
| Health Authority: | United States: Federal Government |
|
IL-1 IL-6 Immune Response Inflammation Steroids |
Chronic Fatigue Syndrome Depression Fibromyalgia Normal Volunteer |
|
Fatigue Depression Myalgic encephalomyelitis Fibromyalgia Myofascial Pain Syndromes Central Nervous System Diseases Encephalomyelitis Pain Healthy Rheumatic Diseases |
Fatigue Syndrome, Chronic Depressive Disorder Inflammation Behavioral Symptoms Virus Diseases Muscular Diseases Neuromuscular Diseases Musculoskeletal Diseases Mental Disorders Mood Disorders |
|
Disease Pathologic Processes Syndrome Nervous System Diseases |
