Kropholler Marc A, Boellaard Ronald, Schuitemaker Alie, Folkersma Hedy, van Berckel Bart N M, Lammertsma Adriaan A
Department of Nuclear Medicine & PET Research, VU University Medical Center, Amsterdam, The Netherlands.
J Cereb Blood Flow Metab. 2006 Nov;26(11):1431-41. doi: 10.1038/sj.jcbfm.9600289. Epub 2006 Mar 1.
(11)C-PK11195 is a marker of activated microglia, which can be used to measure inflammation in neurologic disorders. The purpose of the present study was to define the optimal reference tissue model based on a comparison with a validated plasma input model and using clinical studies and Monte Carlo simulations. Accuracy and reproducibility of reference tissue models were evaluated using Monte Carlo simulations. The effects of noise and variation in specific binding, nonspecific binding and blood volume were evaluated. Dynamic positron emission tomography scans were performed on 13 subjects, and radioactivity in arterial blood was monitored online. In addition, blood samples were taken to generate a metabolite corrected plasma input function. Both a (validated) two-tissue reversible compartment model with K(1)/k(2) fixed to whole cortex and various reference tissue models were fitted to the data. Finally, a simplified reference tissue model (SRTM) corrected for nonspecific binding using plasma input data (SRTM(pl_corr)) was investigated. Correlations between reference tissue models (including SRTM(pl_corr)) and the plasma input model were calculated. Monte Carlo simulations indicated that low-specific binding results in decreased accuracy and reproducibility. In this respect, the SRTM and SRTM(pl_corr) performed relatively well. Varying blood volume had no effect on performance. In the clinical evaluation, SRTM(pl_corr) and SRTM had the highest correlations with the plasma input model (R(2)=0.82 and 0.78, respectively). SRTM(pl_corr) is optimal when an arterial plasma input curve is available. Simplified reference tissue model is the best alternative when no plasma input is available.
[(11)C](R)-PK11195是活化小胶质细胞的标志物,可用于测量神经疾病中的炎症。本研究的目的是通过与经过验证的血浆输入模型进行比较,并利用临床研究和蒙特卡罗模拟来确定最佳参考组织模型。使用蒙特卡罗模拟评估参考组织模型的准确性和可重复性。评估了噪声以及特异性结合、非特异性结合和血容量变化的影响。对13名受试者进行了动态正电子发射断层扫描,并在线监测动脉血中的放射性。此外,采集血样以生成代谢物校正后的血浆输入函数。将K(1)/k(2)固定为全脑皮质的(经过验证的)双组织可逆隔室模型和各种参考组织模型都与数据进行拟合。最后,研究了使用血浆输入数据校正非特异性结合的简化参考组织模型(SRTM(pl_corr))。计算了参考组织模型(包括SRTM(pl_corr))与血浆输入模型之间的相关性。蒙特卡罗模拟表明,低特异性结合会导致准确性和可重复性降低。在这方面,SRTM和SRTM(pl_corr)表现相对较好。血容量变化对性能没有影响。在临床评估中,SRTM(pl_corr)和SRTM与血浆输入模型的相关性最高(R(2)分别为0.82和0.78)。当有动脉血浆输入曲线时,SRTM(pl_corr)是最佳选择。当没有血浆输入时,简化参考组织模型是最佳替代方案。