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缩短扫描间隔对 L-[1-11C]亮氨酸 PET 法测定脑蛋白质合成区域性速率的影响。

Effects of shortened scanning intervals on calculated regional rates of cerebral protein synthesis determined with the L-[1-11C]leucine PET method.

机构信息

Section on Neuroadaptation & Protein Metabolism, National Institute of Mental Health, Bethesda, Maryland, United States of America.

Department of Neuroimaging, IoPPN, King's College London, London, United Kingdom.

出版信息

PLoS One. 2018 Apr 16;13(4):e0195580. doi: 10.1371/journal.pone.0195580. eCollection 2018.

DOI:10.1371/journal.pone.0195580
PMID:29659612
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5901930/
Abstract

To examine effects of scan duration on estimates of regional rates of cerebral protein synthesis (rCPS), we reanalyzed data from thirty-nine previously reported L-[1-11C]leucine PET studies. Subjects consisted of 12 healthy volunteers studied twice, awake and under propofol sedation, and 15 subjects with fragile X syndrome (FXS) studied once under propofol sedation. All scans were acquired on a high resolution scanner. We used a basis function method for voxelwise estimation of parameters of the kinetic model of L-[1-11C]leucine and rCPS over the interval beginning at the time of tracer injection and ending 30, 45, 60, 75 or 90 min later. For each study and scan interval, regional estimates in nine regions and whole brain were obtained by averaging voxelwise estimates over all voxels in the region. In all three groups rCPS was only slightly affected by scan interval length and was very stable between 60 and 90 min. Furthermore, statistical comparisons of rCPS between awake and sedated healthy volunteers provided almost identical results when they were based on 60 min scan data as when they were based on data from the full 90 min interval. Statistical comparisons between sedated healthy volunteers and sedated subjects with FXS also yielded almost identical results when based on 60 and 90 min scan intervals. We conclude that, under the conditions of our studies, scan duration can be shortened to 60 min without loss of precision.

摘要

为了检验扫描时间对脑蛋白质合成率(rCPS)区域估计值的影响,我们重新分析了之前报道的 39 项 L-[1-11C]亮氨酸 PET 研究的数据。研究对象包括 12 名健康志愿者,他们分别在清醒状态和异丙酚镇静状态下接受了两次扫描,以及 15 名脆性 X 综合征(FXS)患者,他们在异丙酚镇静状态下接受了一次扫描。所有扫描均在高分辨率扫描仪上进行。我们使用基函数方法对 L-[1-11C]亮氨酸和 rCPS 的动力学模型参数进行体素估计,扫描区间从示踪剂注射开始,持续 30、45、60、75 或 90 分钟。对于每个研究和扫描区间,通过对区域内所有体素的体素估计值进行平均,获得了 9 个区域和整个大脑的区域估计值。在所有三组中,rCPS 仅受到扫描区间长度的轻微影响,在 60 至 90 分钟之间非常稳定。此外,当基于 60 分钟扫描数据进行统计比较时,清醒和镇静状态下的健康志愿者之间的 rCPS 结果几乎与基于完整 90 分钟区间数据的结果完全相同。当基于 60 和 90 分钟扫描区间进行统计比较时,镇静状态下的健康志愿者和镇静状态下的 FXS 患者之间的 rCPS 结果也几乎相同。我们得出结论,在我们研究的条件下,可以将扫描时间缩短至 60 分钟,而不会降低精度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2695/5901930/6fb53d7d2230/pone.0195580.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2695/5901930/f5ab28744c49/pone.0195580.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2695/5901930/15eaf2cefd35/pone.0195580.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2695/5901930/6e0393355c3e/pone.0195580.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2695/5901930/6fb53d7d2230/pone.0195580.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2695/5901930/f5ab28744c49/pone.0195580.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2695/5901930/15eaf2cefd35/pone.0195580.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2695/5901930/6e0393355c3e/pone.0195580.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2695/5901930/6fb53d7d2230/pone.0195580.g004.jpg

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Impact of tissue kinetic heterogeneity on PET quantification: case study with the L-[1-C]leucine PET method for cerebral protein synthesis rates.组织动力学异质性对 PET 定量的影响:以 L-[1-C]亮氨酸 PET 方法测量脑蛋白质合成率为例。
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Altered cerebral protein synthesis in fragile X syndrome: studies in human subjects and knockout mice.脆性 X 综合征患者大脑蛋白合成改变:在人类受试者和基因敲除小鼠中的研究。
J Cereb Blood Flow Metab. 2013 Apr;33(4):499-507. doi: 10.1038/jcbfm.2012.205. Epub 2013 Jan 9.
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Use of spectral analysis with iterative filter for voxelwise determination of regional rates of cerebral protein synthesis with L-[1-11C]leucine PET.
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Neurobiol Dis. 2020 Sep;143:104978. doi: 10.1016/j.nbd.2020.104978. Epub 2020 Jun 20.
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Modelling Protein Synthesis as A Biomarker in Fragile X Syndrome Patient-Derived Cells.将蛋白质合成建模为脆性X综合征患者来源细胞中的生物标志物。
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4
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5
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J Cereb Blood Flow Metab. 2009 Jul;29(7):1317-31. doi: 10.1038/jcbfm.2009.52. Epub 2009 May 13.
6
Propofol anesthesia does not alter regional rates of cerebral protein synthesis measured with L-[1-(11)C]leucine and PET in healthy male subjects.在健康男性受试者中,丙泊酚麻醉不会改变用L-[1-(11)C]亮氨酸和正电子发射断层扫描(PET)测量的局部脑蛋白合成速率。
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J Neurosci. 2005 May 18;25(20):5087-95. doi: 10.1523/JNEUROSCI.0093-05.2005.
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