Simončič Urban, Zanotti-Fregonara Paolo
aJožef Stefan Institute, Ljubljana bThe Centre of Excellence for Biosensors, Instrumentation and Process Control - COBIK, Ajdovščina, Slovenia cUniversity of Bordeaux, CNRS, INCIA, UMR 5287, Talence, France dMolecular Imaging Branch, National Institute of Mental Health, National Institute of Health, Bethesda, Maryland, USA.
Nucl Med Commun. 2015 Feb;36(2):187-93. doi: 10.1097/MNM.0000000000000231.
Quantitative PET studies often require the cumbersome and invasive procedure of arterial cannulation to measure the input function. This study sought to minimize the number of necessary blood samples by developing a factor-analysis-based image-derived input function (IDIF) methodology for dynamic PET brain studies.
IDIF estimation was performed as follows: (a) carotid and background regions were segmented manually on an early PET time frame; (b) blood-weighted and tissue-weighted time-activity curves (TACs) were extracted with factor analysis; (c) factor analysis results were denoised and scaled using the voxels with the highest blood signal; (d) using population data and one blood sample at 40 min, whole-blood TAC was estimated from postprocessed factor analysis results; and (e) the parent concentration was finally estimated by correcting the whole-blood curve with measured radiometabolite concentrations. The methodology was tested using data from 10 healthy individuals imaged with (11)C-rolipram. The accuracy of IDIFs was assessed against full arterial sampling by comparing the area under the curve of the input functions and by calculating the total distribution volume (VT).
The shape of the image-derived whole-blood TAC matched the reference arterial curves well, and the whole-blood area under the curves were accurately estimated (mean error 1.0±4.3%). The relative Logan-V(T) error was -4.1±6.4%. Compartmental modeling and spectral analysis gave less accurate V(T) results compared with Logan.
A factor-analysis-based IDIF for (11)C-rolipram brain PET studies that relies on a single blood sample and population data can be used for accurate quantification of Logan-V(T) values.
定量PET研究通常需要进行繁琐且有创的动脉插管操作来测量输入函数。本研究旨在通过开发一种基于因子分析的图像衍生输入函数(IDIF)方法,用于动态PET脑研究,以尽量减少所需血样的数量。
IDIF估计按以下步骤进行:(a)在PET早期时间帧上手动分割颈动脉和背景区域;(b)通过因子分析提取血加权和组织加权时间-活度曲线(TAC);(c)使用血信号最高的体素对因子分析结果进行去噪和缩放;(d)利用群体数据和40分钟时的一份血样,根据后处理的因子分析结果估计全血TAC;(e)最后通过用测量的放射性代谢物浓度校正全血曲线来估计母体浓度。使用来自10名健康个体的(11)C-咯利普兰成像数据对该方法进行了测试。通过比较输入函数曲线下面积并计算总分布容积(VT),评估IDIF相对于全动脉采样的准确性。
图像衍生的全血TAC形状与参考动脉曲线匹配良好,曲线下全血面积估计准确(平均误差1.0±4.3%)。相对Logan-V(T)误差为-4.1±6.4%。与Logan相比,房室模型和频谱分析给出的V(T)结果准确性较低。
一种基于因子分析的(11)C-咯利普兰脑PET研究IDIF,依赖于一份血样和群体数据,可用于准确量化Logan-V(T)值。