Investigators of the Duke CRC/PE propose to continue and expand activities developed during the first five years of this award. The primary goal of the Duke Center is to define and validate a limited number of depressive subtypes in late life that are clinically relevant and prime for further study because of recent advances in neurosciences, psychometric assessment, nosology, epidemiology, biostatistics, as well as biologic approaches to therapy. Specifically, the Duke Center will continue to recruit approximately 160 subjects per year equally distributed between young/middle-aged (30-59) and elderly (60+) depressed inpatients and outpatients. Each subject recruited will undergo a baseline evaluation, including evaluation of both Axis I and Axis II DSM-III-R diagnoses, cognitive functioning, severity of depressive symptoms, baseline laboratory data, physical and social functioning. Subjects will be allocated, as appropriate, to three ongoing CRC Programs: 1) the Biological Markers Program; 2) the Brain MRI Program; and 3) the Effects of ECT in the Elderly Program. Subjects will also be allocated to four new pilot projects: 1) the Social Factors and Outcome of Major Depression Study; 2) the Natural History of Late Life Depression Study; 3) the Sleep Disorders and Depression Pilot; and 4) the Family History of Depression and Dementia Pilot. CRC investigators will pursue, among others, the following findings from previous CRC studies during the next five years to achieve the goal of subtyping depressive disorders: 1) nosological investigations that indicate longitudinal data and data on social functioning (improve prognosis); 2) the relevance of the receptor that bind tritiated imipramine (as a marker of depressive sub-types in the elderly; 3) the importance of family history in defining subtypes of late life depression (especially when depression is comorbid with dementia); 4) the relationship between late life depression and structural brain abnormalities, and 5) the effectiveness and side effects of ECT in the elderly.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Specialized Center (P50)
Project #
2P50MH040159-07
Application #
3107114
Study Section
Treatment Development and Assessment Research Review Committee (TDA)
Project Start
1984-09-30
Project End
1993-08-31
Budget Start
1990-09-01
Budget End
1991-08-31
Support Year
7
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Duke University
Department
Type
Schools of Medicine
DUNS #
071723621
City
Durham
State
NC
Country
United States
Zip Code
27705
Jamerson, Brenda D; Payne, Martha E; Garrett, Melanie E et al. (2013) Folate metabolism genes, dietary folate and response to antidepressant medications in late-life depression. Int J Geriatr Psychiatry 28:925-32
Beaulieu, Jean-Martin; Gainetdinov, Raul R; Caron, Marc G (2009) Akt/GSK3 signaling in the action of psychotropic drugs. Annu Rev Pharmacol Toxicol 49:327-47
Trone, R J; Weaver, K G; Steffens, D C et al. (2009) Glycemic index and glycemic load are not associated with brain lesions in the elderly. J Nutr Health Aging 13:117-20
Payne, Martha E; Jamerson, Brenda D; Potocky, Christopher F et al. (2009) Natural food folate and late-life depression. J Nutr Elder 28:348-58
Parker, R D; Flint, Elizabeth P; Bosworth, Hayden B et al. (2003) A three-factor analytic model of the MADRS in geriatric depression. Int J Geriatr Psychiatry 18:73-7
Steffens, D C; Rama Krishnan, K R (1998) Psychotherapeutic agents in older adults. Metabolism, bioavailability, and drug interactions. Clin Geriatr Med 14:17-31
Li, T; Yang, L; Wiese, C et al. (1994) No association between alleles or genotypes at the dopamine transporter gene and schizophrenia. Psychiatry Res 52:17-23
Hughes, D C; Turnbull, J E; Blazer, D G (1992) Family history of psychiatric disorder and low self-confidence: predictors of depressive symptoms at 12-month follow-up. J Affect Disord 25:197-212
Fremeau Jr, R T; Caron, M G; Blakely, R D (1992) Molecular cloning and expression of a high affinity L-proline transporter expressed in putative glutamatergic pathways of rat brain. Neuron 8:915-26
Blazer, D; Burchett, B; Service, C et al. (1991) The association of age and depression among the elderly: an epidemiologic exploration. J Gerontol 46:M210-5

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