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Duke Conte Center for the Neuroscience of Depression in Late Life

Conte Centers for the Neuroscience of Depression

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00576875
Enrollment
795
Registered
2007-12-19
Start date
2006-08-31
Completion date
2011-07-31
Last updated
2012-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Major Depression

Keywords

Depression, Elderly, Neuroimaging, Postmortem, Knockout mouse

Brief summary

The proposed Silvio O. Conte Center for Neuroscience of Depression will focus on understanding the neurobiological mechanism of depression. A total of 5 projects are proposed. The center is focused on a single hypothesis. The first project examines localization of lesions, structural changes in critical regions subserving the circuit, alterations in the white matter tracts relevant to the circuit and changes in glutamate. The second project uses post mortem cell counting and cellular localization in serotonin receptors and assessment of the type of cell loss in the orbitofrontal cortex. The third project uses cognitive paradigms and functional MRI to probe the circuit and the role of brain lesions and serotonin on the functioning of this circuit. The fourth project uses transgenic and knockout mice to examine to role of norepinephrine and serotonin as it relates to the circuit. The final project is designed to assess in these transgenic mice using multielectrode array of single neuron recordings of the firing pattern of the circuit neurons in various states and tasks and the role of monoamines in modulating this circuit.

Detailed description

Three shared resources, administrative, research and assessment and data management/statistics are proposed to facilitate the conduct of these projects and to ensure integration at the conceptual, analytical and resource availability level, and flow to the various projects. Findings from the center should greatly enhance our understanding of the biology of depressive disorders and help improve the treatment of these disorders. In addition, the technological innovations developed in the context of this project are likely to be of major importance and relevant to other studies of brain function.

Interventions

None listed

Sponsors

University of Mississippi Medical Center
CollaboratorOTHER
Duke University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

For depressed group: 1. Age \> 60 years 2. Major depression, single episode or recurrent 3. Ability to read and write English 4. MMSE \>25 5. Willingness to participate in the follow-up study for at least two years. For non-depressed group: 1. Age \> 60 years 2. Ability to read and write English 3. MMSE \>25 4. Willingness to participate in the follow-up study for at least two years

Exclusion criteria

1. Lifetime alcohol or drug dependence 2. Conditions associated with MRI abnormalities such hydrocephalus, benign and cancerous brain tumors, epilepsy, Parkinson's disease, Huntington's chorea, dementia, demyelinating diseases, etc. 3. Endocrine disorder (other than diabetes mellitus) 4. Any physical or intellectual disability that may affect completion of self rating instruments 5. Established clinical diagnosis of dementia 6. Other primary psychiatric disorders, including panic disorder, social phobia, OCD, non-affective psychosis (including schizo-affective disorder), schizophrenia, bipolar disorder 7. Any metal or pacemaker in the body which precludes MRI.

Design outcomes

Primary

MeasureTime frame
Each of the projects in the Duke Conte Center has its own aims and primary outcomesUp to five years

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026