PET/MRI定量脊髓FDG。

IF 1.4
Eve Lennie, Steven Sourbron, Nigel Hoggard, Thomas Jenkins, Charalampos Tsoumpas
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引用次数: 0

摘要

背景:在本研究中,我们研究了MRI衍生衰减图和有限检测器分辨率对PET/MRI期间脊髓正电子发射断层扫描(PET)活动摄取量化的影响。这是通过模拟[18 F]颈部和胸部的FDG PET数据,然后修改衰减图以去除骨骼特征来实现的。然后,我们将有序子集期望最大化重建的图像与完全衰减校正的图像进行了比较。该模拟在2.1和4.4 mm两种探测器分辨率下进行。然后使用临床研究的数据来评估点扩散函数(PSF)建模和飞行时间(TOF)校正的能力,如SIGNA PET/MR扫描仪(GE HealthCare)所实现的,以纠正这些量化错误。为了比较,在沿脊髓的每个椎体位置测量感兴趣区域的平均摄取。结果:模拟结果显示从颈脊髓到胸脊髓的摄取呈递减模式。当骨不包括在衰减校正中,平均摄取下降了3%-10.4%。在代表临床PET/MRI扫描仪的探测器分辨率下模拟的图像中,测量到的摄取差异为6.4%-23.9%。在探测器分辨率为4.4 mm时,与2.1 mm模拟相比,测量到摄取减少了32.2%。在患者资料中,将椎体骨引入衰减校正伪ct导致脊髓的SUV平均值差异为1.8%-18.3%。应用PSF模型没有导致任何统计学上显著的变化。TOF校正将有椎体骨和无椎体骨校正的数据衰减之间的SUV平均值的差异减小到4.3%-7%。当beta = 100时,衰减校正方法之间的差异最小,为0.6% ~ 5.2%。结论:在PET/MRI图像重建中忽略骨会降低脊髓量化时测量到的活度;然而,在低分辨率数据中,部分体积效应对减少测量的吸收量有更大的影响。虽然飞行时间校正在一定程度上解决了这些量化误差,但部分体积校正仍需进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Quantification of FDG in the spinal cord using PET/MRI.

Quantification of FDG in the spinal cord using PET/MRI.

Quantification of FDG in the spinal cord using PET/MRI.

Quantification of FDG in the spinal cord using PET/MRI.

Background: In this study, we investigate the impact of MR-derived attenuation maps and limited detector resolution on the quantification of positron emission tomography (PET) activity uptake in the spinal cord during PET/MRI. This was performed by simulating [ 18 F]FDG PET data in the neck and thorax and then modifying the attenuation map to remove bone features. We then compared Ordered Subset Expectation Maximisation-reconstructed images to those with full attenuation correction. This simulation was performed at two detector resolutions of 2.1 and 4.4 mm. Acquisitions from a clinical study were then used to assess the ability of point spread function (PSF) modelling and time-of-flight (TOF) corrections, as implemented on the SIGNA PET/MR scanner (GE HealthCare), to correct for these quantification errors. For comparison, mean uptake was measured in regions of interest at each vertebral position along the spinal cord.

Results: Simulation results showed a decreasing pattern of uptake from the cervical to the thoracic spinal cord. When bone was not included in attenuation correction, the mean uptake decreased by 3%-10.4%. This difference in measured uptake was 6.4%-23.9% in images simulated at a detector resolution representative of a clinical PET/MRI scanner. At a detector resolution of 4.4 mm, a 32.2% decrease in uptake was measured compared to the 2.1 mm simulation. In patient data, introducing vertebral bone to the attenuation correction pseudo-CT led to a 1.8%-18.3% difference in SUV mean in the spinal cord. Applying PSF modelling did not lead to any statistically significant changes. TOF correction reduces the difference in SUV mean between data attenuation corrected with and without vertebral bone to 4.3%-7%. TOF Q.Clear images with beta = 100 showed the smallest difference between attenuation correction approaches at 0.6%-5.2%.

Conclusion: Ignoring bone during image reconstruction in PET/MRI reduces the activity measured during quantification of the spinal cord; however, the partial volume effect has a greater impact on reducing measured uptake in lower-resolution data. While time-of-flight correction goes somewhat resolves these quantification errors, further research is needed into partial volume correction.

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