Depression, Involutional Clinical Trial
Official title:
Neurocardiac Control in Major Depression
This study will examine how depression may influence the way the brain regulates heart
function. Some researchers believe that depression may be a risk factor for some forms of
heart disease.
Right-handed healthy volunteers and patients with major depressive disorder who are between
18 and 50 years of age may be eligible for this study. Female candidates must be
premenopausal. Patients must currently be experiencing a major depressive episode. All
candidates are screened with a medical history and physical examination, electrocardiogram,
and blood and urine tests. They are interviewed about their psychiatric and medical history,
current emotional state and sleep pattern, and family history of psychiatric disorders. They
complete symptoms ratings scales for depression, anxiety, and negative thinking; history of
alcohol and tobacco use; level of physical activity; socioeconomic status; overall level of
functioning; and, for depressed patients, their depression type. Women candidates have their
menstrual phase determined by the timing of their recent menstrual cycles and may undergo
testing to determine the time of their ovulation.
Participants undergo the following tests and procedures:
- 12-minute walk/run test - This test measures the subject's general level of
cardiorespiratory fitness. In a gymnasium in the NIH Clinical Center, the subject walks
or runs as far as he or she can in 12 minutes. Blood pressure is measured before and
after the exercise test, and heart rate is measured during exercise with a monitor worn
around the chest.
- Magnetic resonance imaging (MRI) - A brain MRI scan is done to obtain pictures of the
brain anatomy. Electrocardiogram leads are placed on the subject's chest to measure the
electrical activity of the heart during the scanning session. The subject lies on a
narrow bed in the scanner, which is a narrow metal cylinder about 6 feet long. The
scanning session takes up to 90 minutes.
- Positron emission tomography (PET) - PET scanning produces images of the brain's blood
flow. The subject is injected with a radiotracer (small amount of drug labeled with a
radioactive substance) that is detected by a special camera to trace blood flow. During
the scanning session, the subject lies still on a table. EKG leas are placed on the
subject's chest to measure the electrical activity of the heart during the scan. A mask
with holes for the eyes, ears, and mouth is placed over the subject's face to keep the
head f...
The presence of major depression, with or without pre-existing coronary artery disease,
predicts increased mortality from myocardial infarction (MI) and sudden cardiac death (SCD).
Decreased parasympathetic vagal outflow, especially in the presence of elevated cardiac
sympathetic tone, has been proposed as a mechanism for the increased risk of SCD. Multiple
lines of evidence suggests that fronto-limbic areas are actively engaged in the robust
optimization of autonomic balance between sympathetic and parasympathetic cardiac outflow
over a broad range of cognitive and physical demands. We propose that dysfunction of these
forebrain neurocardiac networks in MDD mediates maladaptive cardiac autonomic control and the
increased risk of cardiovascular mortality. In this model, neurocardiac control networks
exhibit a systemic bias toward increased sympathetic relative to parasympathetic outflow.
Increased amygdalar activity in MDD will promote this imbalance. Additionally, dysfunction in
posterior orbitofrontal cortex (OFC) and ventral anterior cingulated cortex (ACC), areas
associated with abnormal histopathological changes in MDD, will lead to reduced capacity for
generating adaptive levels of cardioinhibitory, parasympathetic tone. This reduced capacity
in depressives will be evidenced by abnormally large withdrawals of parasympathetic outflow,
compared to healthy controls, as cognitive or physical demands increase. This dynamic model
is potentially consistent with functional neuroimaging and post mortem histopathological
findings in MDD and the knowledge gained through testing this protocol may ultimately
elucidate how brain dysfunction in MDD mediates significantly increased clinical risk of
spontaneous ventricular arrhythmias and sudden cardiac death.
We propose to combine H (2) (15) O positron emission tomography (PET) and analysis of heart
rate variability (HRV) in order to study in vivo the neural structures underlying normal
forebrain control of cardiac autonomic function. We further aim to show whether regional
functional abnormalities in amygdala, ventral anterior cingulate cortex, and orbitofrontal
cortex-areas in which functional abnormalities have been identified in previous neuroimaging
studies of major depressives-are associated with impaired modulation of cardiac autonomic
function during major depression.
;
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