Late-life depression (LLD) is a common mental disorder in the elderly, with high prevalence rates ranging from 1 to 5% (Byers et al., 2010). Recent evidence suggest that LLD is linked to age-related negative health outcomes, such as cerebrovascular disease, increased risk of Alzheimer?s disease, vascular dementia, and mortality. The mechanisms of LLD are complex and involve the dysregulation of different biological pathways. Based on past research conducted in our group, we identified dysregulation of proteostasis control as a potential pathophysiologic mechanism of LLD. Loss of proteostasis control can play a significant role in neuronal and axonal dysfunction, revealed by diffusion-tensor imaging, in LLD. Based on preliminary data and the current literature, this study proposes to evaluate the association between a newly developed proteostasis control (PC) index, clinical phenotypes (severity of depressive symptoms and cognitive impairment), and microstructural white matter abnormalities in older adults with depression. Our hypotheses are that LLD individuals will show a significantly higher PC index (i.e. indicating a greater proteostasis dysregulation) compared to age- and gender-matched never-depressed control subjects. Also, PC dysregulation will be associated with greater cognitive impairment, and decreased fractional anisotropy and increased radial diffusivity in LLD. To our knowledge, this will be the first study to examine the association between circulating proteostasis markers, microstructural changes and clinical characteristics in LLD. By gaining a better understanding of the molecular basis of structural changes in LLD, we can identify novel therapeutic targets and critical periods for intervention to treat depression in older adults.

Public Health Relevance

Depression in older adults is a common mental disorder and associated worse quality of life, more functional disability, negative health outcomes, elevated direct and indirect costs. Given its high prevalence, its negative impact on individual health, and its negative long term prognosis, it is a condition of great public health relevance. This study aims to identify novel pathophysiological mechanisms in depression and how leads to brain structural changes in this condition. We will also be able to identify novel potential targets to the development of interventions aiming not only the treatment of depression in the elderly, but also aiming the prevention of the negative outcomes related to this condition.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Small Research Grants (R03)
Project #
1R03MH115212-01
Application #
9434051
Study Section
Neural Basis of Psychopathology, Addictions and Sleep Disorders Study Section (NPAS)
Program Officer
Evans, Jovier D
Project Start
2017-11-09
Project End
2018-11-08
Budget Start
2017-11-09
Budget End
2018-11-08
Support Year
1
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Texas Health Science Center Houston
Department
Psychiatry
Type
Schools of Medicine
DUNS #
800771594
City
Houston
State
TX
Country
United States
Zip Code
77030