Guo Qi, Owen David R, Rabiner Eugenii A, Turkheimer Federico E, Gunn Roger N
1] Centre for Neuroimaging Sciences, Institute of Psychiatry, King's College London, London, UK [2] Imanova, Centre for Imaging Sciences, London, UK [3] Division of Brain Sciences, Department of Medicine, Imperial College London, London, UK.
Division of Brain Sciences, Department of Medicine, Imperial College London, London, UK.
J Cereb Blood Flow Metab. 2014 Jul;34(7):1162-8. doi: 10.1038/jcbfm.2014.65. Epub 2014 Apr 16.
Positron emission tomography (PET) radioligands for a reversible central nervous system (CNS) demand a high specific to nonspecific signal characterized by the binding potential (BPND). The quantification of BPND requires the determination of the nondisplaceable binding usually derived from a reference region devoid of the target of interest. However, for many CNS targets, there is no valid reference region available. In such cases, the total volume of distribution (VT) is often used as the outcome measure, which includes both the specific and nonspecific binding signals. Here we present a graphical method that allows for direct comparison of the binding potential of ligands using the regional VT data alone via linear regression. The method was first validated using literature data for five serotonin transporter ligands, for which a reference region exists, and then applied to two second generation 18 kDa translocator protein radioligands, namely [(11)C]PBR28 and [(18)F]PBR111. The analysis determined that [(11)C]PBR28 had a higher BPND than [(18)F]PBR111.
用于可逆性中枢神经系统(CNS)的正电子发射断层扫描(PET)放射性配体需要具有以结合潜力(BPND)为特征的高特异性与非特异性信号。BPND的定量需要确定通常源自缺乏感兴趣靶点的参考区域的不可置换结合。然而,对于许多CNS靶点,没有可用的有效参考区域。在这种情况下,分布总体积(VT)通常用作结果测量指标,其包括特异性和非特异性结合信号。在此,我们提出一种图形方法,该方法允许仅通过线性回归使用区域VT数据直接比较配体的结合潜力。该方法首先使用存在参考区域的五种5-羟色胺转运体配体的文献数据进行验证,然后应用于两种第二代18 kDa转位蛋白放射性配体,即[(11)C]PBR28和[(18)F]PBR111。分析确定[(11)C]PBR28的BPND高于[(18)F]PBR111。