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Effect of Different Reconstruction Algorithms on the Dynamics and Modeling Parameters of 18F-Galacto-RGD in mice

机译:不同重建算法对小鼠18F-吡酰-RGD动力学和建模参数的影响

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So far FBP (Filtered Back Projection) is still the standard reconstruction method for kinetic modeling of PET data. Iterative reconstruction algorithms, such as OSEM (Ordered Subsets Expectation Maximization) or MAP (Maximum A Posteriori) create images with better signal-to-noise ratios and less streak artifacts. This is of special interest in the short-time frames with low statistics at the beginning of a dynamic acquisition. To determine if iteratively reconstructed PET data could be used for kinetic modeling of pre-clinical data, we compared OSEM2D and OSEM3D/MAP data with FBP data using microPET data. Nude mice (n=6) bearing a human melanoma tumor were imaged over 90 minutes with a FOCUS 120 microPET. We applied 18F-Galacto-RGD via a tail vein catheter into the animal (9-19 MBq). 18F-Galacto-RGD is used for imaging the α{sub}vβ{sub}3 expression during angiogenesis and on specific tumor cells. Each list mode dataset was binned into 19 frames and reconstructed with FBP, OSEM2D and OSEM3D/MAP. The data was not corrected for scatter and attenuation. Volumes of interest (VOIs) were drawn on the heart and tumor tissue. No corrections for spillover and partial volume effect were applied. For the kinetic modeling of the tumor data a standard 2-tissue-compartment model with reversible binding was used (fitting parameters: K{sub}1, k{sub}2, k{sub}3, k{sub}4 (rate constants) and D{sub}v (vascular blood fraction)). The input function TACs of the iteratively reconstructed data showed no considerable difference to the FBP data. Only the OSEM3D/MAP TACs for the tumor VOIs were clearly and consistently higher for all datasets than the corresponding FBP and OSEM2D TACs. Kinetic modeling shows negligible parameter changes for K{sub}1, k{sub}2, k{sub}3 and k{sub}4 for all reconstruction algorithms. The higher OSEM3D/MAP tumor values are compensated only with an overestimated D{sub}v (D{sub}v(FBP)=2.2%, D{sub}v(OSEM3D/MAP)=3.3%). Further work needs to be done on optimizing the iteration settings for the OSEM3D/MAP.
机译:到目前为止FBP(过滤后投影)仍是PET数据的动力学建模的标准重建方法。迭代重建算法,例如OSEM(有序的子集期望最大化)或地图(最大后验)创建具有更好的信噪比比和较少的条纹伪像的图像。这对动态采集开始时具有低统计数据的短时间帧的特殊兴趣。为了确定迭代重建的PET数据,可用于预临床数据的动力学建模,我们使用Micropet数据与FBP数据进行比较了OSEM2D和OSEM3D / MAP数据。携带人黑色素瘤肿瘤的裸鼠(n = 6)在90分钟内成像,焦点120微量焦点成像。我们通过尾部静脉导管施加18°F-Galacto-RGD进入动物(9-19 MBQ)。 18F-加乳酸RGD用于在血管生成期和特异性肿瘤细胞期间对α{亚vβ{亚} 3表达进行成像。每个列表模式数据集都被列入19帧,并用FBP,OSEM2D和OSEM3D / MAP重建。数据没有纠正散射和衰减。感兴趣的毛卷(vois)被绘制在心脏和肿瘤组织上。没有应用溢出和部分体积效应的校正。对于肿瘤数据的动力学建模,使用具有可逆绑定的标准2组织隔室模型(拟合参数:K {Sub} 1,K {Sub} 2,K {Sub} 3,K {Sub} 4(速率常数)和d {亚} v(血管血液分数))。迭代重建数据的输入功能TAC显示对FBP数据没有相当大的差异。对于肿瘤VoIS的OSEM3D / MAP TAC,对于所有数据集比相应的FBP和OSEM2D TACs显然且始终如一。动力学建模显示了所有重建算法的k {sub} 1,k {sub} 2,k {sub} 3和k {sub} 4的可忽略的参数变化。较高的OSEM3D / MAP肿瘤值仅通过高估D {SUB} V(D {SUB} V(FBP)= 2.2%,D {SUB} V(OSEM3D / MAP)= 3.3%)来补偿。需要在优化OSEM3D / MAP的迭代设置上进行进一步的工作。

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