Benzodiazepine Receptor in PTSD

PTSD 中的苯二氮卓受体

• 批准号: 7492635
• 负责人: James Douglas Bremner
• 金额: $ 17.21万
• 依托单位: EMORY UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-09-01 至 2011-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7492635
• 关键词: Amygdaloid structure; Animals; Anxiety; Benzodiazepine Receptor; Benzodiazepines; Binding; Brain; Brain imaging; Caring; Chronic; Consensus; Development; Disease; Early Intervention; Flumazenil; Freedom; Funding; Grant; Hippocampus (Brain); Human; Image; Iraq; Knowledge; Lead; Life; Measures; Medial; Mediating; Mental Health; Methods; National Center for Research Resources; Neurobiology; Operative Surgical Procedures; Outcome; Patients; Phase; Pilot Projects; Play; Positron-Emission Tomography; Post-Traumatic Stress Disorders; Prefrontal Cortex; Productivity; Publishing; Regulation; Research; Resolution; Resources; Role; Scanning; Sensory Receptors; Soldier; Source; Stress; Structure; Symptoms; System; Testing; Time; Trauma; Traumatic Stress Disorders; USA Georgia; Veterans; Vietnam; War; Western Asia Georgia; Work; design; health care service utilization; neurochemistry; novel; programs; receptor binding; single photon emission computed tomography; tool

DESCRIPTION (provided by applicant): Over 150,000 soldiers are currently deployed in Iraq as part of Operation Iraqi Freedom (OIF), and 12% of returning OIF soldiers have posttraumatic stress disorder (PTSD). 389,100 soldiers developed chronic PTSD from the Vietnam War, requiring a life-time of mental health care, with a loss of work productivity and greater utilization of health care resources. Research from our group and others showed changes in a functional circuit including hippocampus, medial prefrontal cortex, and amygdala. However these studies used global measures of brain function and structure; little is known about specific neurochemical systems in the brain that mediate PTSD symptoms. The benzodiazepine system mediates an inhibitory effect on brain function. Studies in animals show that stress results in a decrease in benzodiazepine receptor binding in the hippocampus and medial prefrontal cortex. In the only published neuroreceptor study in PTSD to our knowledge we showed a decrease in benzodiazepine receptor binding in medial prefrontal cortex with single photon emission computed tomography (SPECT) in veterans with chronic combat-related PTSD. We now have much higher resolution imaging (2 mm versus 13 mm with SPECT) with a grant funded by the NCRR to the PI for a High Resolution Research Tomograph (HRRT), which has been in place for two years. We have scanned several patients using PET HRRT and [C-11]flumazenil, a neuroreceptor compound that binds to the benzodiazepine receptor and can be used to image benzodiazepine receptor binding in the living human brain. Studies of the neurobiology of PTSD have been primarily performed in patients with long standing and chronic PTSD. There is currently a consensus that early phases of PTSD are different than chronic and long-standing PTSD, and that early interventions before the disorder becomes chronic and unremitting may offer a better opportunity for treatment. The PI is working in the Operation Iraqi Freedom (OIF) Trauma Program at the Atlanta VA, and there over 1000 soldiers returning to the state of Georgia each month, so there are ample sources of recruitment for research on early PTSD. This is a pilot study to measure benzodiazepine receptor binding in returning OIF veterans with and without PTSD, and non combat exposed comparison subjects with PET HRRT [C-11]flumazenil in OIF combat veterans with and without PTSD and non-combat exposed subjects. We hypothesize decreased benzodiazepine receptor binding in the prefrontal cortex in PTSD compared to the other two groups. We will also assess the ability of benzodiazepine binding to predict long-term outcome. We predict decreased prefrontal binding will be associated with progression to chronic PTSD at one year post assessment. Secondary aims are to assess the relationship between PTSD symptoms and benzodiazepine binding in the prefrontal cortex. This project is designed to examine binding of the benzodiazepine receptor in Iraq combat veterans with posttraumatic stress disorder (PTSD) and to see if this measure can be used to predict which returning veterans will progress to the development of chronic PTSD. The benzodiazepine system plays an important role in the regulation of anxiety. Understanding changes in the benzodiazepine system may lead to new treatments for Iraq combat veterans with PTSD; this project also proposes a novel method of testing whether brain imaging can be used to predict outcomes, which could provide an important tool for identifying veterans in need of early intervention.

描述（由申请人提供）：作为伊拉克自由行动（OIF）的一部分，目前有超过15万名士兵部署在伊拉克，12%的返回OIF士兵患有创伤后应激障碍（PTSD）。389，100名士兵在越南战争中患上了慢性创伤后应激障碍，需要终生的心理健康护理，工作效率降低，医疗资源利用率提高。我们小组和其他人的研究表明，包括海马体、内侧前额叶皮层和杏仁核在内的功能回路发生了变化。然而，这些研究使用了大脑功能和结构的整体测量;对大脑中介导PTSD症状的特定神经化学系统知之甚少。苯二氮卓系统介导对脑功能的抑制作用。对动物的研究表明，压力会导致海马体和内侧前额叶皮层中苯二氮卓受体结合的减少。据我们所知，在唯一发表的PTSD神经受体研究中，我们发现患有慢性战斗相关PTSD的退伍军人的单光子发射计算机断层扫描（SPECT）显示内侧前额叶皮质中苯二氮卓类受体结合减少。我们现在有更高的分辨率成像（2毫米与13毫米的SPECT）与赠款由NCRR资助的PI的高分辨率研究断层扫描仪（HRRT），这已经到位了两年。我们已经扫描了几个病人使用PET高分辨RT和[C-11]氟马西尼，一种神经受体化合物，结合到苯二氮卓类受体，可用于成像苯二氮卓类受体结合在活的人脑。PTSD的神经生物学研究主要在长期和慢性PTSD患者中进行。目前有一个共识，即PTSD的早期阶段不同于慢性和长期的PTSD，并且在疾病变成慢性和持续性之前的早期干预可能提供更好的治疗机会。PI正在亚特兰大VA的伊拉克自由行动（OIF）创伤计划中工作，每个月有超过1000名士兵返回格鲁吉亚州，因此有充足的招募来源用于早期创伤后应激障碍的研究。这是一项初步研究，旨在测量返回的OIF退伍军人（伴和不伴PTSD）和非战斗暴露受试者中苯二氮卓类受体结合率，并在OIF退伍军人（伴和不伴PTSD）和非战斗暴露受试者中进行PET HRRT [C-11]氟马西尼比较。我们假设与其他两组相比，PTSD患者前额叶皮层中苯二氮卓类受体结合减少。我们还将评估苯二氮卓类药物结合预测长期结局的能力。我们预测，在评估后一年，前额叶结合减少将与慢性PTSD的进展相关。第二个目的是评估PTSD症状与前额叶皮质中苯二氮卓类结合之间的关系。该项目旨在研究苯二氮卓类受体在伊拉克战斗退伍军人与创伤后应激障碍（PTSD）的结合，并看看这种措施是否可以用来预测哪些返回的退伍军人将进展到慢性PTSD的发展。苯二氮卓系统在焦虑的调节中起着重要的作用。了解苯二氮卓类系统的变化可能会为患有创伤后应激障碍的伊拉克退伍军人带来新的治疗方法;该项目还提出了一种新的方法来测试大脑成像是否可以用于预测结果，这可能为识别需要早期干预的退伍军人提供重要工具。