Sleep and Healthy Aging Research on Depression for Younger Women
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Non-social (Monetary) Reward Response (Reward Learning and Sensitivity)
研究概览
简要总结
Compelling evidence indicates inflammation plays a role in depression, but potential mechanisms linking inflammation to depression, such as dysregulated reward processing, are poorly understood. This study comprehensively evaluates effects of inflammation on reward across dimensions (e.g., anticipating versus receiving a reward) and types (e.g., money vs. smiling faces) in younger and older women. Characterizing how inflammation shapes the dynamic and multidimensional reward system, and how this may differ by age, may give insight into risk factors for depression and help identify critical points for intervention.
详细描述
This study will use an inflammatory challenge (i.e., endotoxin) to assess effects of inflammation on the behavioral response to social and non-social rewards, using tasks that assess reward motivation, sensitivity, and learning. Both elevated inflammation and reward dysregulation are associated with depression and have been shown to predict depression onset; understanding how inflammation alters the reward system in the laboratory setting may provide insight into risk factors and help identify potential areas for intervention. In this placebo-controlled, randomized, double-blind study of low dose endotoxin in 40 adult premenopausal women (25-44 y), the investigators will examine effects of endotoxin on reward responsiveness across dimensions (i.e., motivation, sensitivity, learning) and reward types (e.g., social and non-social). The investigators hypothesize that as compared to placebo, endotoxin will 1) decrease non-social reward responses across reward dimensions; 2) decrease "general" social reward responses across reward dimensions; 3) increase "close" social reward responses across reward dimensions; 4) decrease resting eye blink rate (EBR); EBR will be correlated with learning and motivation for non-social reward. The second component of the study is to examine whether effects of endotoxin on reward differ as a function of age; in particular it is hypothesized that effects will be more robust in younger compared to older women. In order to test for age differences, this study will use data from 40 older women (65+ y) participating in a parallel ongoing randomized controlled trial (ClinicalTrials.gov Identifier: NCT03256760). Thus, the investigation aims to: 1) Evaluate effects of inflammation on non-social reward as a function of age; 2) Evaluate effects of inflammation on general and close social reward as a function of age; 3) Examine changes in dopaminergic activity as a mechanism linking effects of inflammation on non-social reward processing as a function of age.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- Triple (Participant, Care Provider, Outcomes Assessor)
盲法说明
Blinded infusion
入排标准
- 年龄范围
- 25 Years 至 44 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Participants will be required to be in good general health (as evaluated during the phone and in-person baseline session)
- •Participants will be biologically female and premenopausal (as evaluated by self report).
- •Participants will 25-44 years of age.
排除标准
- •Presence of chronic mental or physical illness
- •History of allergies, autoimmune, liver, or other severe chronic diseases,
- •Current and regular use of prescription medications such as steroids, non-steroid anti-inflammatory drugs, aspirin, immune modifying drugs, opioid analgesics, statins, antihypertensive drugs, anti-arrhythmic drugs, and antidepressant medications (none in the last 6 months).
- •Nightshift work or time zone shifts (> 3hrs) within the previous 6 weeks
- •Previous history of fainting during blood draws.
- •Presence of co-morbid medical conditions not limited to but including cardiovascular (e.g., history of acute coronary event, stroke) and neurological diseases (e.g., Parkinson's disease), as well as pain disorders;
- •Presence of comorbid inflammatory disorders such as rheumatoid arthritis or other autoimmune disorders;
- •Presence of an uncontrolled medical condition that is deemed by the investigators to interfere with the proposed study procedures, or to put the study participant at undue risk;
- •Presence of chronic infection, which may elevate proinflammatory cytokines;
- •Presence of an acute infectious illness in the two weeks prior to an experimental session.
- •Current Axis I psychiatric disorders as determined by the Research Version of the Structured Clinical Interview including a current major depressive disorder and substance dependence
- •Lifetime history of suicide attempt or inpatient psychiatric admission.
- •Current history of sleep apnea or nocturnal myoclonus; Phase-shift disorder, which will be identified by the Structured Clinical Interview and the Duke Structured Interview for Sleep Disorders
- •Current smoking or excessive caffeine use (>600 mg/day) because of the known effects on proinflammatory cytokine levels;
- •Evidence of recreational drug use from urine test.
- •Body mass index > 35 because of the effects of obesity on proinflammatory cytokine activity
- •Any clinically significant abnormality on screening laboratory tests
- •Clinically significant abnormalities in electrocardiogram
研究组 & 干预措施
Endotoxin
Endotoxin 0.8 ng/kg body weight; 1 infusion
干预措施: Endotoxin (Biological)
Placebo
same volume of 0.9% saline
干预措施: Placebo (Biological)
结局指标
主要结局
Non-social (Monetary) Reward Response (Reward Learning and Sensitivity)
时间窗: Baseline and post-injection (2.25 hrs)
Implicit reward learning and sensitivity to monetary reward is assessed with the probabilistic reward task (PRT) a behavioral computer task; change in the magnitude of response bias from baseline to post-injection is the outcome measure. More positive response bias indicates a bias towards the more frequently reward stimuli (a better outcome); more negative response bias indicates a bias towards the less frequently reward stimuli (a worse outcome). This is not a standardized scale with minimum and maximum values. Response bias is calculated using a formula from signal detection theory and is a logarithmic ratio derived from choice frequencies. The formula is log b=1/2log((Rich-correct+.5) \*(Lean-incorrect+.5)/(rich-incorrect+.5) \* (lean-incorrect+.5)), where rich refers to the more frequently rewarded option and lean refers to the less frequently rewarded option.
Non-social (Monetary) Reward Response (Reward Motivation)
时间窗: Baseline and post-injection (2.1 hrs)
Motivation for monetary reward is assessed with a 10-minute version of the Effort Expenditure for Rewards Task (EEfRT), a behavioral computer task; change in the amount of hard trials chosen (relative to total trials) from baseline to post-injection is the outcome measure. The task is analyzed using generalized estimating equations (GEE) with a binary outcome; outcome values at each timepoint therefore range from 0 to 1, with higher numbers indicating higher motivation (a better outcome). The predictor for the GEE model is a time (coded as 0 and 1) by condition (coded as 0 and 1) interaction term. A negative result in the boxes below for each condition separately indicates a pre-to post-injection decrease in the proportion of hard trials chosen.
Non-social (Monetary) Reward Response (Reward Sensitivity)
时间窗: Baseline and post-injection (2.1 hrs)
Sensitivity for monetary reward is assessed with a 10-minute version of the Effort Expenditure for Rewards Task (EEfRT) a behavioral computer task, tested as the strength of the association between increases in potential monetary reward for hard trials and selection of hard (vs) easy trials during the task. This is tested using generalized estimating equations, with condition (LPS vs. placebo) by time (pre vs post-injection) by reward magnitude (ranges from $1-$4.12) predicting hard (vs easy) trial choice. More positive values indicate higher reward sensitivity ( a better outcome), and lower values indicate lower reward sensitivity. The unit of measurement for the task is the proportion of hard trials chosen; the unit of measurement for the reward sensitivity outcome is a beta coefficient. For example, a positive coefficient for reward magnitude in the GEE output means that as the reward amount increases by one unit (e.g., $1), the odds of choosing the high-effort option increase.
General Social Reward Response (Reward Sensitivity Via Emotional Dot Probe)
时间窗: Baseline and post-injection (2.7 hrs)
Sensitivity to general social reward cues (i.e., response to positive emotional faces) assessed as positive attentional bias with an emotional dot probe task. Attentional bias is assessed by measuring reaction times to targets that appear in the same location as emotional (e.g., happy faces) versus neutral cues (e.g., neutral faces). Outcomes are change from baseline to post-injection in attentional bias towards positive vs neutral faces. Higher positive attentional bias scores indicate higher sensitivity to reward; negative attentional bias score indicate less sensitivity to reward. A score of 0 indicates no bias. The attentional bias score is derived by subtracting the reaction time in ms on congruent trials (dot replaces an emotional face) from the reaction time on incongruent trials (dot replaces the neutral face).
General Social Reward Response (Reward Sensitivity Via Face Morphing Task)
时间窗: Baseline and post-injection (2.8 hrs)
Sensitivity to general social reward cues (i.e., response to positive emotional faces) assessed as positive emotion detection with a face morphing task. The outcome is the absolute change from baseline to post-injection in the percent of accurate responses. Higher accuracy is an indicator of higher sensitivity to reward and lower accuracy is an indicator of lower sensitivity to reward.
General Social Reward Response (Social Reward Motivation)
时间窗: Baseline and post-injection (2 hrs)
Motivation for general social reward is assessed via self-report; participants rate their desire to engage in 3 different activities, one of which is social, on a 1 (not at all) to 10 (extremely) Likert scale.; change in desire for the social activity from baseline to post-injection is the outcome variable. Higher values indicate higher motivation.
次要结局
- Depressed Mood Subscale of the Profile of Mood States (POMS)(Hourly, from pre-injection (T0) to 9 hours later (T9))
- Close Social Reward Response(Post-injection (2.9 hrs))
- Consummatory Daily Reward Response(14 days (7 days pre-injection; 7 days post-injection).)
- Dopaminergic Activity(Baseline and post-injection (1.9 hrs))
- Anticipatory Daily Reward Response(14 days (7 days pre-injection; 7 days post-injection).)
研究者
Chloe Boyle, PhD
Postdoctoral Fellow
University of California, Los Angeles