Patient Stratification and Treatment Response Prediction in Neuropharmacotherapy Using Hybrid Positron Emmission Tomography/Magnetic Resconance Imaging (PET/MR)
试验速览
- 阶段
- 4 期
- 入组人数
- 80
- 试验地点
- 2
- 主要终点
- Hamilton Depression Scale (HDRS)
研究概览
简要总结
Selective serotonin reuptake inhibitors (SSRIs) raise serotonin (5-HT) in the synaptic cleft and are the current first line of pharmacological antidepressive treatment. Yet, there is a missing link between this first molecular step in their mechanism of action and observed clinical improvement. We have determined to establish a framework combining genuine molecular and functional imaging, i.e. hybrid pharmaco-PET/MR imaging, of the human serotonergic system in order to predict antidepressant treatment response.
Objectives:
- To predict antidepressant treatment response from data obtained using hybrid PET/MR with acute pharmacological challenge.
- To discriminate healthy from depressed subjects using this paradigm.
- To establish models connecting regional changes in occupancy of serotonin transporters (5-HTT) following citalopram infusion, with changes in brain activation and connectivity of major resting-state hub networks.
Design: Randomized, double-blind, placebo-controlled, cross-over mono-center study.
Materials and methods:
40 major depressed (MDD) and 40 healthy subjects will undergo 2 PET/MR scans on a 3T SIEMENS mMR Biograph scanner: 1. challenge with citalopram 8mg 2. placebo (saline). After structural imaging, functional MRI will be continuously acquired. [11C]DASB will be applied using a bolus + constant infusion paradigm to probe 5-HTT binding potentials and monitor 5-HTT occupancy with drug challenge, applied after 70min, in a single session. Scanning will be terminated 80min after challenge. MDD patients will receive subsequent escitalopram treatment with repeated evaluation of response for 3 months.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Basic Science
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 18 Years 至 55 Years(Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •General health based on medical history, physical examination and structured clinical interview for DSM-IV (SCID)
- •HAM-D≥18 (patients)
- •Willingness and competence to sign the informed consent form
- •Age 18 to 55 years
排除标准
- •Any medical, psychiatric or neurological illness (other than MDD)
- •Current or former psychopharmacological treatment
- •Current or former substance abuse
- •Pregnancy
- •Any implant or stainless steel graft or any other contraindications for MRI
- •Failure to comply with the study protocol or to follow the instructions of the investigating team
- •Participation in studies involving radiation exposure in the past 10 years.
- •Body mass index <17 or >30
结局指标
主要结局
Hamilton Depression Scale (HDRS)
时间窗: 12 weeks
次要结局
未报告次要终点
研究者
Rupert Lanzenberger
Head of the Neuroimaging Labs
Medical University of Vienna
