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11C-氘代l-司来吉兰与11C-匹兹堡化合物B早期PET评估阿尔茨海默病脑灌注的比较

Comparison of Early-Phase 11C-Deuterium-l-Deprenyl and 11C-Pittsburgh Compound B PET for Assessing Brain Perfusion in Alzheimer Disease.

作者信息

Rodriguez-Vieitez Elena, Carter Stephen F, Chiotis Konstantinos, Saint-Aubert Laure, Leuzy Antoine, Schöll Michael, Almkvist Ove, Wall Anders, Långström Bengt, Nordberg Agneta

机构信息

Division of Translational Alzheimer Neurobiology, Center for Alzheimer Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden.

Division of Translational Alzheimer Neurobiology, Center for Alzheimer Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden Wolfson Molecular Imaging Centre, Institute of Brain, Behaviour and Mental Health, University of Manchester, Manchester, United Kingdom.

出版信息

J Nucl Med. 2016 Jul;57(7):1071-7. doi: 10.2967/jnumed.115.168732. Epub 2016 Feb 16.

Abstract

UNLABELLED

The PET tracer (11)C-deuterium-L-deprenyl ((11)C-DED) has been used to visualize activated astrocytes in vivo in patients with Alzheimer disease (AD). In this multitracer PET study, early-phase (11)C-DED and (11)C-Pittsburgh compound B ((11)C-PiB) (eDED and ePiB, respectively) were compared as surrogate markers of brain perfusion, and the extent to which (11)C-DED binding is influenced by brain perfusion was investigated.

METHODS

(11)C-DED, (11)C-PiB, and (18)F-FDG dynamic PET scans were obtained in age-matched groups comprising AD patients (n = 8), patients with mild cognitive impairment (n = 17), and healthy controls (n = 16). A modified reference Patlak model was used to quantify (11)C-DED binding. A simplified reference tissue model was applied to both (11)C-DED and (11)C-PiB to measure brain perfusion relative to the cerebellar gray matter (R1) and binding potentials. (11)C-PiB retention and (18)F-FDG uptake were also quantified as target-to-pons SUV ratios in 12 regions of interest (ROIs).

RESULTS

The strongest within-subject correlations with the corresponding R1 values (R1,DED and R1,PiB, respectively) and with (18)F-FDG uptake were obtained when the eDED and ePiB PET data were measured 1-4 min after injection. The optimum eDED/ePiB intervals also showed strong, significant ROI-based intersubject Pearson correlations with R1,DED/R1,PiB and with (18)F-FDG uptake, whereas (11)C-DED binding was largely independent of brain perfusion, as measured by eDED. Corresponding voxelwise correlations confirmed the ROI-based results. Temporoparietal eDED or ePiB brain perfusion measurements were highly discriminative between patient and control groups, with discriminative ability statistically comparable to that of temporoparietal (18)F-FDG glucose metabolism. Hypometabolism extended over wider regions than hypoperfusion in patient groups compared with controls.

CONCLUSION

The 1- to 4-min early-frame intervals of (11)C-DED or (11)C-PiB are suitable surrogate measures for brain perfusion. (11)C-DED binding is independent of brain perfusion, and thus (11)C-DED PET can provide information on both functional (brain perfusion) and pathologic (astrocytosis) aspects from a single PET scan. In comparison with glucose metabolism, early-phase (11)C-DED and (11)C-PiB perfusion appear to provide complementary rather than redundant information.

摘要

未标记

正电子发射断层显像(PET)示踪剂(11)C - 氘 - L - 司来吉兰((11)C - DED)已用于在体可视化阿尔茨海默病(AD)患者体内活化的星形胶质细胞。在这项多示踪剂PET研究中,比较了早期(11)C - DED和(11)C - 匹兹堡化合物B((11)C - PiB)(分别为eDED和ePiB)作为脑灌注的替代标志物,并研究了脑灌注对(11)C - DED结合的影响程度。

方法

在年龄匹配的组中进行了(11)C - DED、(11)C - PiB和(18)F - FDG动态PET扫描,这些组包括AD患者(n = 8)、轻度认知障碍患者(n = 17)和健康对照者(n = 16)。使用改良的参考Patlak模型对(11)C - DED结合进行定量。将简化参考组织模型应用于(11)C - DED和(11)C - PiB,以测量相对于小脑灰质的脑灌注(R1)和结合潜能。(11)C - PiB滞留和(18)F - FDG摄取也在12个感兴趣区域(ROI)中定量为靶区与脑桥的标准化摄取值(SUV)比。

结果

当在注射后1 - 4分钟测量eDED和ePiB PET数据时,获得了与相应R1值(分别为R1,DED和R1,PiB)以及与(18)F - FDG摄取的最强受试者内相关性。最佳eDED/ePiB间隔还显示出与R1,DED/R1,PiB以及与(18)F - FDG摄取基于ROI的受试者间强且显著的Pearson相关性,而通过eDED测量,(11)C - DED结合在很大程度上独立于脑灌注。相应的体素级相关性证实了基于ROI的结果。颞顶叶eDED或ePiB脑灌注测量在患者组和对照组之间具有高度鉴别性,其鉴别能力在统计学上与颞顶叶(18)F - FDG葡萄糖代谢相当。与对照组相比,患者组中代谢减低区域比灌注减低区域更广泛。

结论

(11)C - DED或(11)C - PiB的1至4分钟早期帧间隔是脑灌注的合适替代测量指标。(11)C - DED结合独立于脑灌注,因此(11)C - DED PET可从单次PET扫描中提供关于功能(脑灌注)和病理(星形细胞增生)方面的信息。与葡萄糖代谢相比,早期(11)C - DED和(11)C - PiB灌注似乎提供互补而非冗余信息。

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