Sojkova Jitka, Goh Joshua, Bilgel Murat, Landman Bennett, Yang Xue, Zhou Yun, An Yang, Beason-Held Lori L, Kraut Michael A, Wong Dean F, Resnick Susan M
Laboratory of Behavioral Neuroscience, National Institute on Aging, NIH, Bethesda, Maryland.
Laboratory of Behavioral Neuroscience, National Institute on Aging, NIH, Bethesda, Maryland National Taiwan University, Taipei, Taiwan.
J Nucl Med. 2015 Jul;56(7):1042-7. doi: 10.2967/jnumed.114.151480. Epub 2015 May 14.
Quantification of β-amyloid (Aβ) in vivo is often accomplished using the distribution volume ratio (DVR), based on a simplified reference tissue model. We investigated the local relationships between DVR and cerebral blood flow (CBF), as well as relative CBF (R1), in nondemented older adults.
Fifty-five nondemented participants (mean age, 78.5 y) in the Baltimore Longitudinal Study of Aging underwent (15)O-H2O PET CBF and dynamic (11)C-PiB PET. (15)O-H2O PET images were normalized and smoothed using SPM. A simplified reference tissue model with linear regression and spatial constraints was used to generate parametric DVR images. The DVR images were regressed on CBF images on a voxel-by-voxel basis using robust biologic parametric mapping, adjusting for age and sex (false discovery rate, P = 0.05; spatial extent, 50 voxels). DVR images were also regressed on R1 images, a measure of the transport rate constant from vascular space to tissue. All analyses were performed on the entire sample, and on high and low tertiles of mean cortical DVR.
Voxel-based analyses showed that increased DVR is associated with increased CBF in the frontal, parietal, temporal, and occipital cortices. However, this association appears to spare regions that typically show early Aβ deposition. A more robust relationship between DVR and CBF was observed in the lower tertile of DVR, that is, negligible cortical Aβ load, compared with the upper tertile of cortical DVR and Aβ load. The spatial distributions of the DVR-CBF and DVR-R1 correlations showed similar patterns. No reliable negative voxelwise relationships between DVR and CBF or R1 were observed.
Robust associations between DVR and CBF at negligible Aβ levels, together with similar spatial distributions of DVR-CBF and DVR-R1 correlations, suggest that regional distribution of DVR reflects blood flow and tracer influx rather than pattern of Aβ deposition in those with minimal Aβ load. DVR-CBF associations in individuals with a higher DVR are more likely to reflect true associations between patterns of Aβ deposition and CBF or neural activity. These findings have important implications for analysis and interpretation of voxelwise correlations with external variables in individuals with varying amounts of Aβ load.
基于简化参考组织模型,体内β-淀粉样蛋白(Aβ)的定量通常使用分布容积比(DVR)来完成。我们研究了非痴呆老年人中DVR与脑血流量(CBF)以及相对脑血流量(R1)之间的局部关系。
巴尔的摩纵向衰老研究中的55名非痴呆参与者(平均年龄78.5岁)接受了(15)O-H2O PET脑血流量和动态(11)C-PiB PET检查。(15)O-H2O PET图像使用SPM进行归一化和平滑处理。使用具有线性回归和空间约束的简化参考组织模型生成参数化DVR图像。使用稳健的生物参数映射在逐体素基础上对DVR图像与CBF图像进行回归分析,并对年龄和性别进行校正(错误发现率,P = 0.05;空间范围,50个体素)。DVR图像还与R1图像进行回归分析,R1是从血管空间到组织的转运速率常数的一种测量指标。所有分析均在整个样本以及平均皮质DVR的高低三分位数上进行。
基于体素的分析表明,额叶、顶叶、颞叶和枕叶皮质中DVR增加与CBF增加相关。然而,这种关联似乎在通常显示早期Aβ沉积的区域中不存在。与皮质DVR和Aβ负荷的高分位数相比,在DVR的低分位数(即皮质Aβ负荷可忽略不计)中观察到DVR与CBF之间存在更强健的关系。DVR-CBF和DVR-R1相关性的空间分布显示出相似的模式。未观察到DVR与CBF或R1之间可靠的负体素级关系。
在Aβ水平可忽略不计的情况下,DVR与CBF之间存在强健的关联,以及DVR-CBF和DVR-R1相关性具有相似的空间分布,这表明DVR的区域分布反映的是血流量和示踪剂流入,而不是Aβ负荷最小者的Aβ沉积模式。DVR较高的个体中DVR-CBF关联更有可能反映Aβ沉积模式与CBF或神经活动之间的真实关联。这些发现对于分析和解释不同Aβ负荷个体中与外部变量的体素级相关性具有重要意义。