Mechanisms of Depression and Anhedonia in Adolescents: Linking Sleep Duration and Timing to Reward- and Stress-Related Brain Function

青少年抑郁和快感缺失的机制：将睡眠持续时间和时间与奖励和压力相关的大脑功能联系起来

• 批准号: 10570250
• 负责人: Melynda D Casement
• 金额: $ 74.35万
• 依托单位: UNIVERSITY OF OREGON
• 依托单位国家: 美国
• 财政年份: 2022
• 资助国家: 美国
• 起止时间: 2022-02-10 至 2026-12-31
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10570250
• 关键词: 19 year old; Adolescence; Adolescent; Adult; Anhedonia; Behavioral; Biological Markers; Brain; Characteristics; Clinical; Development; Diagnosis; Endocrine; Etiology; Event; Experimental Designs; Exposure to; Goals; Growth; Hour; Incidence; Intervention; Laboratories; Licensing; Life; Link; Measurement; Measures; Medial; Mediating; Mental Depression; Mental Health; Mental health promotion; Modeling; Monitor; Morbidity - disease rate; National Institute of Mental Health; Observational Study; Participant; Patient Self-Report; Prefrontal Cortex; Prevalence; Prevention; Psychologist; Psychopathology; Randomized; Recommendation; Recurrence; Reporting; Research; Research Design; Research Personnel; Rewards; Risk; Risk Factors; Sampling; Series; Severities; Sleep; Sleep Deprivation; Sleep disturbances; Stress; Stressful Event; Symptoms; System; Testing; Time; Translating; Work; biobehavior; circadian; depression model; depression prevention; depressive symptoms; design; disability; experience; experimental study; high school; improved; improvement on sleep; modifiable risk; mortality; preventive intervention; recruit; response; single episode major depressive disorder; sleep behavior; sleep regulation; stressor; suicidal

7. PROJECT SUMMARY/ABSTRACT The long-term objectives of this proposal are: 1) to evaluate a biobehavioral model of depressive symptoms and anhedonia in adolescents, and 2) to leverage sleep and circadian function to promote mental health. These objectives are consistent with two key priorities of the National Institute of Mental Health (NIMH): 1) identify mechanisms of psychopathology, and 2) improve prevention and treatment for psychopathology. The proposed model of depression posits that sleep duration and/or timing moderate the effects of stressful events on depressive symptoms and anhedonia by disrupting reward- and stress-related brain function. The research approach uses two complementary study designs to evaluate the proposed model: 1) an observational study (n=150) that assesses the degree to which short and late sleep predict reward- and stress-related brain function and depressive symptoms and anhedonia, and 2) an experimental study (n=100) that assesses the extent to which sleep duration and timing impact reward- and stress-related brain function and depressive symptoms and anhedonia. The sample includes high-school adolescents (14-19 years of age) with enhanced risk for depressive symptoms based on exposure to lifetime stressful events and current depressive symptoms. Recruitment will be stratified to include adolescents with short and late sleep (weekday sleep duration ≤ 6 h & midpoint ≥ 4 am; n=100) versus long and early sleep (weekday sleep duration ≥ 8 h & midpoint ≤ 2:30 am; n=50). Both studies include measurement of daily sleep and stressful events for 2 weeks; laboratory measures of reward- and stress-related brain function and sleep and circadian characteristics; self-report measures of lifetime stressful events; and self-report measures of depressive symptoms and anhedonia during daily and weekly monitoring. The experimental study includes random assignment of adolescents with short and late sleep from the observational study to 2 weeks of either: 1) 90 min extension and advance of sleep opportunity and timing (n=50); or 2) typical sleep opportunity and timing (n=50). This research approach is designed to accomplish three specific aims: 1) Evaluate the extent to which sleep duration and/or timing predict reward- and stress-related brain function, and moderate the effects of stressful life events; 2) Establish the extent to which sleep duration and/or timing impact reward- and stress-related brain function, and moderate the effects of stressful life events; and 3) Determine the extent to which changes in reward- or stress-related brain function mediate the associations between sleep duration and/or timing and later depressive symptoms and anhedonia. The investigative team has expertise in the etiology and prevention of depression in adolescents, including specific expertise in the impact of sleep and stressful life events on the stress and reward systems that contribute to depression and anhedonia. All four investigators are also licensed clinical psychologists who are committed to translating research on the mechanisms of psychopathology to preventative interventions.

7. 项目总结/文摘