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The Impact of Reward-induced Dopamine Release on Functional Connectivity: a Combined PET/fMRI Study

2018年4月16日 更新者:David Hsu、Stony Brook University
The present study would be the first to investigate the relationship between reward- and or social stimuli-induced dopamine (DA) release and neural function using a combined PET/fMRI approach. Data from this project conducted in healthy subjects will provide preliminary data for a larger grant application to study patient populations with known abnormalities in DA including schizophrenia, major depressive, substance use, and eating disorders.

研究概览

地位

完全的

条件

详细说明

Aim 1. To test the relationship between reward-induced dopamine (DA) release on changes in resting state functional connectivity (RSFC) in healthy subjects. In 20 healthy adults, the investigators will examine DA release (measured using positron emission tomography, PET) in the ventral striatum, thalamus, and prefrontal cortex, as previously described. Before and after the task the investigators will examine RSFC (measured using functional magnetic resonance imaging, fMRI) between these structures, which have been shown to form functional pathways serving motivation and emotion regulation in rodents and nonhuman primates. The investigators hypothesize that DA release will impact the functional relationship between these and other structures as determined by changes in RSFC.

Aim 2. To examine the relationship between dopamine release and the Reward Positivity (RewP) potential. Subjects will be presented with the option to participate in an event-related potential (ERP) study. The investigators will correlate the amount of DA release with the amplitude of the RewP potential, an ERP that is enhanced in reward versus non-reward circumstances. Based on previous studies, the investigators hypothesize that RewP amplitude will positively correlate with dopamine release in the nucleus accumbens.

研究类型

观察性的

注册 (实际的)

5

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • New York
      • Stony Brook、New York、美国、11794
        • Health Sciences Center

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 45年 (成人)

接受健康志愿者

是的

有资格学习的性别

全部

取样方法

非概率样本

研究人群

20 subjects (ages 18-45 years) will be included. Male and female representation will be about equal. No ethnic/racial/gender group is excluded.

描述

Inclusion Criteria:

  1. Healthy men and women age 18-45 who have the capacity to consent to the protocol.
  2. Ability to understand and follow instructions and oriented to name, time, and place.
  3. A negative urine pregnancy and toxicology screen
  4. Willingness to abstain from using aspirin, NSAIDs, or anticoagulants during the study

Exclusion Criteria:

  1. Left-handed or ambidextrous
  2. History of seizures
  3. History of strokes
  4. Clinically significant, uncontrolled liver, kidney, cardiac, or pulmonary disease
  5. Terminal medical diagnosis consistent with survival < 1 year
  6. Serious mental impairment. Mini mental state exam of < 23/30
  7. Current or past DSM-IV Axis I or neurologic disorders
  8. Actively abusing substances, including alcohol (regular alcohol use during the past 6 months equal to or greater than 16 cans of beer per week or equivalent; use of street drugs or regular tobacco use during the past 6 months)
  9. Unstable medical condition (≥ 3 months), or serious medical illnesses during the past three months (e.g., serious infections)
  10. Unexplained loss of consciousness; history of traumatic brain injury involving loss of consciousness greater than 2 minutes
  11. Currently pregnant or breastfeeding, sexually active and of child-bearing potential and not using adequate contraceptive methods
  12. Childbirth or miscarriage during past 6 months, breastfeeding within 6 months of recruitment
  13. Allergic to latex and/or study pharmaceuticals
  14. Diabetes and/or unable to fast for up to 7 hours
  15. Unable to lie comfortably in the scanner for up to 4 consecutive hours
  16. Would receive a total of over 5 rems to a radiosensitive organ (bone marrow, gonads, lens of the eye) or 15 rems to any other organ or to the body as a whole during a 12 month period
  17. Contraindications for MRI including neurostimulators, implanted medical devices, metal in the body, claustrophobia, weight over 440 pounds, and girth size incompatible for scanner bore.
  18. Participation in a similar Social Feedback Task within 2 months of the start of the study.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Dopamine receptor binding potential
大体时间:1-3 weeks
changes in dopamine receptor binding potential will be measured during and after a reward task or social stimulus task
1-3 weeks
Resting state fMRI
大体时间:1-3 weeks
Resting state functional connectivity will be measured using fMRI
1-3 weeks
Event-related potential (ERP) during reward
大体时间:1-3 weeks
ERP during a reward task is measured
1-3 weeks

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2016年6月1日

初级完成 (实际的)

2017年12月1日

研究完成 (实际的)

2017年12月1日

研究注册日期

首次提交

2016年6月13日

首先提交符合 QC 标准的

2016年6月15日

首次发布 (估计)

2016年6月16日

研究记录更新

最后更新发布 (实际的)

2018年4月17日

上次提交的符合 QC 标准的更新

2018年4月16日

最后验证

2018年4月1日

更多信息

与本研究相关的术语

其他研究编号

  • PET/MR Pilot

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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