Can 11 C-PiB-PET Relative Delivery R 1 or 11 C-PiB-PET Perfusion Replace 18 F-FDG-PET in the Assessment of Brain Neurodegeneration?

Abstract

Background:

Pittsburgh Compound B (PiB) positron emission tomography (PET) is used to visualize in vivo amyloid plaques in the brain. Frequently the PiB examinations are complemented with a fluorodeoxyglucose (FDG) PET scan to further assess neurodegeneration.

Objective:

Our goal is to identify alternative correlates of FDG images by assessing which kinetic methods originate PiB derived relative delivery ratio (R₁) images that can be correlated with the FDG images, and to compare them with PiB perfusion (pPiB) images obtained from the early-phase of PiB acquisition.

Methods:

We selected 52 patients with cognitive impairment who underwent a dynamic PiB and FDG acquisitions. To compute the R₁ images, two simplified reference tissue models (SRTM and SRTM2) and two multi-linear reference tissue models (MRTM and MRTM2) were used. The pPiB images were obtained in two different time intervals.

Results:

All six types of images were of good quality and highly correlated with the FDG images (mean voxelwise within-subjects r > 0.92). The higher correlation was found for FDG-R₁(MRTM). Regarding the voxelwise regional correlation, the higher mean all brain correlations was r = 0.825 for FDG-R₁(MRTM) and statistically significant in the whole brain analysis.

Conclusion:

All R₁ and pPiB images here tested have potential to assess the metabolic impact of neurodegeneration almost as reliably as the FDG images. However, this is not enough to validate these images for a single-subject analysis compared with the FDG image, and thus they cannot yet be used clinically to replace the FDG image before such evaluation.

Keywords

Alzheimer’s disease compartmental models neurodegeneration perfusion

INTRODUCTION

Positron emission tomography (PET) imaging with Pittsburgh Compound B (PiB) labeled with ¹¹C tracer has been increasingly used in many nuclear medicine centers to visualize in vivo amyloid plaques in the brain, which is a core molecular imaging feature of Alzheimer’s disease (AD) [1]. However, the presence of high levels of amyloid plaques in the brain does not directly imply concurrent neural degeneration. Thus, regional cerebral blood flow (rCBF) and regional cerebral glucose metabolism have been extensively used as indirect biomarkers of synaptic dysfunction and neurodegeneration. Previous studies have shown a tight coupling between rCBF and regional glucose metabolism [2]. This last one has frequently been assessed with fluorodeoxyglucose (FDG) labeled with ¹⁸F for PET systems.

Frequently, patients with cognitive impairments for whom a differential diagnosis is difficult to provide are requested to undergo double PET imaging: PiB (or other available amyloid tracer, as florbetaben or florbetapir) and FDG, to help solve such diagnostic difficulties. However, this has the potential drawback of cost and radiation exposure increase. Complementary surrogate measures that avoid these problems are therefore worth being investigated. As a possible alternative, if a dynamic PiB PET acquisition is performed, beyond the parametric binding potential (BP_ND) image, the relative regional cerebral blood flow $(R_{1} = K_{1} / k_{1}^{'})$ parametric image can be estimated for each brain voxel from pharmacokinetic analyses of PiB, thereby providing such type of alternative (Fig. 1).

Fig. 1

Two-tissue compartment model with reference region. C _F+NS is the concentration due to free and nonspecific binding, C _S is the concentration due to specific binding.

A previous study has suggested that there is a significant correlation between the FDG images and the R₁ images [3]. Two other studies also have found a significant correlation between the FDG and the PiB perfusion (pPiB) images [4, 5]. In addition, Chen and colleagues [6] showed that the relative delivery ratio R₁ of PiB is highly correlated with relative rCBF measured by ¹⁵O-water normalized to cerebellum. Other research groups have focused on these issues using other available markers of amyloid plaques. For instance, Daerr et al. [7] showed a good correlation of early acquisitions of [¹⁸F]-florbetaben (FBB) PET with FDG PET [7], and Lin et al. [8] showed that Mini-Mental State Examination (MMSE) scores are significantly associated with the degree of perfusion impairment as assessed by early phase of ¹⁸F-AV-45 PET on a dataset of patients with AD, mild cognitive impairment (MCI), and healthy controls (HC).

Our main goal is to assess which is the best solution to obtain an image from the PiB PET acquisitioncomparable with the FDG PET image, and thus to provide a proxy measure of synaptic dysfunction and neurodegeneration. We considered four models to obtain the R₁ images and two time periods to obtain the pPiB images. For the R₁ images, we used the simplified reference tissue model (SRTM), the multi-linear reference tissue model (MRTM), the SRTM with fixed $k'_{2}$ (SRTM2), and the MRTM with fixed $k'_{2}$ (MRTM2). To generate the pPiB images, we considered two time periods that have been considered to be optimal [4 , 10], one between 0 and 6 min (pPiB(0– 6)) and the other between 1 and 8 min (pPiB(1– 8)). A second goal is to validate the results obtained by Meyer and colleagues [3] but now using a different and larger dataset of patients.

MATERIALS AND METHODS

Patients

A total of 52 patients who underwent ¹¹C-PiB PET and ¹⁸F-FDG PET examinations were included in this study. We included all patients from Institute of Nuclear Science Applied to Health (ICNAS, University of Coimbra), except patients with head movements during the acquisitions above the scanner resolution. All patients gave written informed consent, as approved by the Ethics committee of the University of Coimbra. Demographic and clinical information are summarized in Table 1. The criteria for the diagnosis of the neurodegenerative disorders were: probable AD dementia according to NINCDS-ADRDA criteria [11], MCI due to AD following the NINCDS-ADRDA criteria [12], primary progressive aphasia according to the recommendations of Gorno-Tempini and colleagues [13], and the behavioral variant of frontotemporal dementia (FTD) according to the criteria of the International Behavioural Variant FTD Criteria Consortium [14].

Table 1

Synthesis of clinical and demographic data of the patients

Subjects	Number of	Age	Amyloid burden
	patients (M/F)	(mean±SD)	negative / low / high
AD	20 (6/14)	68±6	1 / 0 / 19
MCI	19 (8/11)	69±7	6 / 7 / 6
PPA	5 (3/2)	66±7	2 / 0 / 3
FTD	4 (1/3)	72±10	3 / 1 / 0
Other	4 (1/3)	54±10	4 / 0 / 0
Total	52 (19/33)	67±8	16 / 8 / 28

We also categorized PiB-PET images in three groups— amyloid negative, amyloid borderline/low burden, and high amyloid deposition—following our local classifier based on support vector machines (SVM), which uses the voxelwise brain grey matter standardized uptake value ratio (SUVR) computed from the PiB-PET images, and using the cerebellar grey matter as reference region.

PET acquisitions

All ¹¹C-PIB PET and ¹⁸F-FDG PET acquisitions were performed in the same scanner (Philips PET/CT Gemini GXL), preceded by a low-dose brain CT acquisition for attenuation correction. Except for one patient, both scans were acquired on the same day (¹⁸F-FDG was injected approximately 2 h after ¹¹C-PiB injection). For each acquisition, the patient’s head was restrained with a soft elastic tape. All patients fasted for at least 6 h before ¹⁸F-FDG injection.

The ¹¹C-PiB PET acquisitions were dynamic, lasted for 90 min (37 frames: 4×15 s + 8×30 s + 9×60 s + 2×180 s + 14×300 s) and started immediately after the intravenous bolus injection of approximately 555 MBq of ¹¹C-PiB. The ¹⁸F-FDG PET acquisitions were static, started approximately 30 min after the intravenous bolus injection of approximately 185 MBq of ¹⁸F-FDG and lasted for 30 min.

Both acquisitions were reconstructed using the LOR RAMLA algorithm (Philips PET/CT Gemini GXL) with attenuation and scatter correction. In both cases, an isotropic voxel size of 2 mm was defined.

Quantification of pPiB images and relative delivery ratio R₁ parametric images

Voxelwise pPiB(0– 6 min) and pPiB(1– 8 min) images were computed by cumulatively adding the frames in the time periods between 0 and 6 min and between 1 and 8 min after injection, respectively. These time intervals where chosen since they were found optimal in previous works.

Four different approaches were used for quantification of relative delivery ratio R₁: MRTM, SRTM, MRTM2 and SRTM2. For all four methods, the cerebellar grey matter was used as reference region. This choice is based on the work of Thal et al. [15] where the authors showed that there is no amyloid deposition in the cerebellar grey matter before the phase 5 (advanced cases) and even in this phase the deposition is very small. This was confirmed using PiB PET by Klunk et al. [16].

SRTM and SRTM2

We implemented the SRTM [17] method using basis functions [18], since this solution is more stable than non-linear least squares method at the voxel level. The simplified operational equation is $C (t) = θ_{1} C^{'} (t) + θ_{2} C (t) \otimes e^{- θ_{s} t}$ where C is the concentration in the target region, is the concentration in the reference region and ⊗ is the convolution operator. We have considered 200 values for θ ₃ between 0.017 min^–1 and 0.137 min^–1 and, for each θ ₃, the other two parameters were estimated using linear least squares.

The SRTM2 is based on SRTM but implemented in two steps [19]. In the first one, the SRTM is applied to compute the BP_ND, R₁ and k ₂ at the voxel level [18]. Then, is derived as. Since should be the same for all brain voxels, it is estimated by computing the median of all obtained. Then, in the second step, it is fixed and the equation is rearranged, with only two parameters remaining to be optimized [19]. As for the SRTM, we implemented SRTM2 using basis functions and the same range of values for θ ₃. Since estimation is very sensitive to noise when computed at the voxel level, to compute it in the first step we have resampled the original dynamic images with voxels of 8×8×8 mm³ and only considered the values of when 0 < BP_ND < 3, k ₂> 0 and R₁ > 0.

MRTM and MRTM2

The MRTM implemented is based on the following multi-linear reference tissue model equation [20]: $C (T) = - \frac{V}{V^{'} b} \int_{0}^{T} C^{'} (t) d t + \frac{1}{b} \int_{0}^{T} C (t) d t - \frac{V}{V^{'} {k^{'}}_{2} b} C^{'} (T)$ which has three parameters to be optimized: $γ_{1} = - \frac{V}{V^{'} b}, γ_{2} = \frac{1}{b}, γ_{3} = \frac{V}{(V^{'} {k^{'}}_{2} b)}$ . It can be done efficiently using linear least squares. Then, ${BP}_{ND} = - (\frac{γ_{1}}{γ_{2}} + 1)$ , k ₂ = − γ ₂ and R₁ = γ ₃. In the experimental analysis we did, very noisy BP_ND images were obtained simultaneously with negative values of k ₂. Thus, we constrained the k ₂ as a minimum of 0.012 min^–1. This value was established experimentally based on the observation of the values of k ₂ obtained in a subset of the images considering 10 regions of interest (anterior cingulate, caudate, mesial temporal cortex, prefrontal cortex, posterior cingulate, putamen, precuneus, occipital cortex, parietal superior, and inferior cortex).

MRTM2 is a two-step implementation of the MRTM [20]. In the first step, the median of ${k^{'}}_{2}$ is estimated using MRTM and then fixed in the second step. By fixing, the equation can be rearranged to the following $C (T) = - \frac{V}{V^{'} b} ({\int^{}}_{T}^{0} C^{'} (t) d t + \frac{1}{k^{'}_{2}} C^{'} (T)) + \frac{1}{b} \int_{0}^{T} C (t) d t$ and thus obtaining $B P_{N D} = - (\frac{γ_{1}}{γ_{2}} + 1), R_{1} = \frac{γ_{1}}{{k^{'}}_{2}}$ , and k ₂ = − γ ₂.

Implementation of algorithms

For the computation of the R₁ and pPiB images, in the initial step a sum image was built using all frames and then the sum image was registered to the Montreal Neurological Institute (MNI) space using in-house made software using a deformable model based on cubic B-splines and a PiB sum image template as reference image. Next, all frames of the dynamic image were also registered using the same geometric transformation. Image registration algorithms were implemented using the Insight Toolkit (ITK) software library, version 3.20, and based on the optimization of the mutual information similarity measure [21]. Parameter optimization was done using the Vision Numerics Library (VNL) available in the ITK [21]. The sum PiB template is in the MNI space and was built in our institution using a set of normal PiB scans and with the help of the MRI of the subjects.

¹⁸F-FDG image processing

The ¹⁸F-FDG images were first rigidly registered with the correspondent R₁(MRTM) image and then registered to the MNI space using the transformation found when the respective ¹¹C-PiB images were registered to the MNI space.

Statistics

Intensity normalization

The pPiB, R₁ and ¹⁸F-FDG registered images were smoothed with a Gaussian kernel with 8 mm full width at half maximum and then intensity normalized. The intensity normalization was done independently per each image by dividing each voxel value by the mean brain values of the respective image. The brain voxels were defined based on the MNI template.

Within-subjects correlation

For each subject, the mean Pearson correlation coefficients between the pairs FDG-pPiB(0– 6 min), FDG-pPiB(1– 8 min), FDG-R₁(MRTM), FDG-R₁(MRTM2), FDG-R₁(SRTM), and FDG-R₁(SRTM2) were computed. For each FDG image, all brain voxels were correlated with the correspondent voxels of the pPiB or R₁ image, yielding a correlation coefficient per pair of images per subject. Comparison of correlations was performed using repeated measures ANOVA.

To assess differences of the correlation among the amyloid burden groups (negative, low and high) the Kruskal-Wallis test was used. ANOVA and Kruskal-Wallis test were performed using the Statistical Package for the Social Sciences (SPSS, v20).

Voxelwise regional correlation

Since variations of cerebral blood flow and glucose metabolism coupling are not homogeneous across all brain regions [22], we assessed the regional correlation at voxel level. Per each voxel location, we computed the correlation between the group of the FDG images against the groups of pPiB or R₁ images. Thus, we obtained the whole-brain correlation distribution.

Correlation significance was assessed per each voxel using Benjamini-Hochberg false discovery rate (FDR) correction for multiple comparisons with α= 0.05. Differences in the mean whole brain voxelwise correlation were assessed using ANOVA.

RESULTS

Within-subjects correlation

Results of the Pearson linear correlation coefficient between FDG, R₁ and pPiB images are shown in Fig. 2. Mean±standard deviation values were 0.929±0.016, 0.924±0.020, 0.936±0.015, 0.933±0.016, 0.933±0.016, and 0.932±0.018, for the correlations FDG-R₁(SRTM), FDG-R₁(SRTM2), FDG-R₁(MRTM), FDG-R₁(MRTM2), FDG-pPiB(0– 6 min), and FDG-pPiB(1– 8 min), respectively. This means that the R₁ and pPiB images can explain about 85% of the content of the FDG images. Figure 3 shows two examples of the FDG, pPiB(1– 8 min), and R₁(MRTM) images of two patients where it is easy to visually identify asymmetric uptake, which very likely indicates hypometabolism in region with lower FDG, R₁ and pPiB values.

Fig. 2

Boxplot graph comparing the within subjects correlation coefficient between the FDG images and the R₁(SRTM), R₁(SRTM2), R₁(MRTM), R₁(MRTM2), pPiB(0– 6min) and pPiB(1– 8min) images.

Fig. 3

Two examples of the FDG, pPiB(1– 8min), and R₁(MRTM) images, respectively from the left to the right. The images on the top are from a patient with AD, and on the bottom from a patient with FTD. In the top there is an asymmetric uptake in the parietal cortex and on the bottom an asymmetric uptake in the frontal cortex. These patterns can be seen in the three types of images.

Repeated measures ANOVA with Greenhouse-Geisser correction shows that there is a statistically significant difference (F = 23.359, p < 0.001) among the correlation coefficients. Based on post hoc paired t-test with Bonferroni correction for multiple comparisons, it was observed that the correlation between the FDG and R₁(MRTM) images is significantly higher (p < 0.004) than the other correlations. Although statistically significant differences have been found among the mean computed correlations, the differences are low and with likely irrelevant biologically significance (lesser than 0.012).

There is not a statistically significant difference in the correlation between groups of patients, amyloid positive, amyloid doubtful or amyloid negative, per any type of images (Kruskal-Wallis test, p≥0.180), suggesting that their biological correlates remain the same across groups.

Voxelwise regional correlation

A summary of the results for all brain voxels Pearson correlation coefficients is shown in Table 2. Voxelwise correlations between FDG and R₁ or pPiB were statistically significant in all brain voxels, except for the R₁(SRTM2) where it was nevertheless significant in more than 99.9% of the brain voxels. There is a statistically significant difference among the mean voxelwise whole-brain magnitude of correlations between the six types of images; however the difference of the mean is very low (maximum difference of the mean is 0.023). As can be seen in Table 2, the median of the Pearson correlation coefficient is higher than 0.81, which means the correlation is strong or very strong in most of the brain voxels, irrespective of the particular model, suggesting that this proxy-based approach is relatively model independent.

Table 2

Voxelwise regional Pearson correlation coefficient between the FDG and R₁ or pPiB images

Images	Median	Mean±SD	Range (min - max)
R₁(SRTM)	0.826	0.809±0.093	0.247– 0.972
R₁(SRTM2)	0.819	0.802±0.097	0.194– 0.977
R₁(MRTM)	0.841	0.825±0.090	0.345– 0.981
R₁(MRTM2)	0.838	0.820±0.094	0.267– 0.980
pPiB(0– 6min)	0.827	0.809±0.097	0.276– 0.984
pPiB(1– 8min)	0.838	0.817±0.097	0.285– 0.981

Figure 4 shows the voxelwise correlation between the FDG images and the correspondent set of R₁(MRTM) images. As can be seen, the correlation is strong or very strong (r ≥ 0.7) in most of the brain. The regions where the correlation is not as robust are mainly in the transition between the grey and white matter. The distributions of the brain correlation between the FDG and the other R₁ or pPiB images are similar.

Fig. 4

Mean voxelwise correlation between the set of FDG images and the correspondent set of R₁(MRTM) images. The correlation image is overlapping the template MRI image.

DISCUSSION

In this work we performed a voxelwise analysis of the correlation between the FDG-PET images with the R₁ or pPiB images computed from PiB-PET dynamic acquisitions. Results show a very high (r > 0.9) mean within-subject Pearson correlation coefficient of the FDG images with the pPiB and R₁ images. A significantly higher correlation was found for the FDG-R₁(MRTM) against the correlation of the other pairs, however the difference had a very small effect size, and is therefore of likely irrelevant biological significance.

A previous study, Meyer et al. [3], also studied the correlation between R₁-PiB and FDG images, but using only the SRTM2 kinetic model and a small dataset of 22 patients, while we tested four kinetic models for the computation of the R₁ and used a dataset of 52 patients. Moreover, we further computed the correlation between the FDG and pPiB images using two time intervals and compared them with the correlation obtained between the R₁ and FDG images. They found a slightly inferior within-subject correlation of approximately r = 0.79 between the FDG and R₁ generated by the SRTM2 [19], using a similar protocol acquisition. We think there are two main reasons that may explain our superior results. First, different datasets were used; second, the implementation of the algorithms, both the kinetic models and the image processing. As in Meyer et al. [3], we did not find a statistically significant difference in the correlation among groups of patients (amyloid negative versus amyloid borderline versus high amyloid deposition) for the R₁ images. The same occurred for the pPiB images, suggesting that the use of these proxy measures is robust and independent of the used analysis method.

Regarding the regional voxelwise correlation of the FDG images with the pPiB and R₁ images, a high median voxelwise correlation correlation was found for the six types of images (r≥0.82). The regions with lesser correlation are mostly in the border between the grey and white matter. We think this can be partially explained by the image registration imperfections, since the uptake difference is higher from the grey matter to the white matter than within the grey matter or white matter.

We have opted to use the R₁, pPiB and FDG images after intensity normalization since the standardized uptake value (SUV) of the FDG images are highly dependent on the several factors that are not related to the cerebral glucose metabolism, for instance, the blood glucose levels, insulin levels or anemia; and the R₁ images depend on the free and non-specific binding in the cerebellar grey matter of each patient. Thus, after intensity normalization the variability of the uptake due to brain external factors is reduced, which is important for the computation of the voxelwise regional correlation. However, it is important to stress out that this normalization has no influence in the within-subject correlation, since the correlation is independent on scale factors.

In clinical practice, the R₁ and pPiB images should not be normalized, neither spatially nor intensity. The spatial normalization may introduce distortions that difficult the clinical analysis and the SUV of the pPiB images may have clinical implications.

In a previous study, the SRTM2 and the MRTM2 methods were found as the best options to compute the BP_ND for clinical studies [23]. These two methods have shown to be less affected by noise, producing BP_ND images with better contrast than the images obtained from the other tested methods, and also because they provided the best accuracies in simulated studies. In our implementation, SRTM2 and MRTM2 originated BP_ND images with less noise than the SRTM and MRTM methods, respectively; however, the R₁ images had higher level of noise.

Intriguingly, SRTM and MRTM originated better quality R₁ images than their two steps version SRTM2 and MRTM2, respectively. This was not expected, since SRTM2 and MRTM2 have been used in previous studies and have originated high quality R₁ and BP_ND images [3 , 23]. In fact, in our implementation, the BP_ND obtained using the SRTM2 and MRTM2 are of better quality than the BP_ND obtained using the SRTM and MRTM, however the same did not happen for the R₁ parametric images.

In terms of pPiB images, our results are as expected, since they confirm previous works where a significant correlation between the FDG and the PiB perfusion (pPiB) images was found [4, 5].

We have shown that there is high whole-brain within-subject correlation between R₁ or pPiB and FDG measures (Fig. 2), however this is not enough to validate the R₁ or pPiB images for a single-subject analysis compared with the FDG image [24], and thus these images cannot be used clinically to replace the FDG image before such evaluation. Other limitation of this study is that we cannot ascertain that the small differences found between the normalized R₁ or pPiB images and the normalized FDG images do not hide some information related with neuronal injury. In any case, the work of Lin et al. [8] showed that the MMSE scores are significantly associated with the degree of perfusion impairment, which we believe is solid evidence for the usefulness of the R₁ and pPiB images.

In conclusion, the results show that both R₁ and pPiB images can explain about 85% of the content of the FDG images, and thus they may be of great importance to assess the synaptic dysfunction and neurodegeneration when the FDG images are not available. The higher correlation with the FDG images was found for the R₁(MRTM). However, the differences for the others R₁ and pPiB images are rather small.

The pPiB images have originated results which are very close to the best R₁ images and are easier to compute, with shorter acquisition time. Thus they are probably the best choice to be computed routinely in the busy nuclear medicine centers. On the other hand, in centers where the BP_ND images are computed for helping in the differential diagnosis, the R₁ images may be the best choice, since they can be obtained simultaneously with the BP_ND images.

Footnotes

ACKNOWLEDGMENTS

This work was supported by the following grants: Strategic project FCT-UID/NEU/04539/2013 – COMPETE, POCI-01-0145-FEDER-007440, BIGDATIMAGE, CENTRO-01-0145-FEDER-000016, Centro 2020 FEDER, COMPETE, PAC – MEDPERSYST, POCI-01- 0145-FEDER-016428.

Authors’ disclosures available online ().

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Can 11 C-PiB-PET Relative Delivery R 1 or 11 C-PiB-PET Perfusion Replace 18 F-FDG-PET in the Assessment of Brain Neurodegeneration?

Abstract

Background:

Objective:

Methods:

Results:

Conclusion:

Keywords

INTRODUCTION

MATERIALS AND METHODS

Patients

PET acquisitions

Quantification of pPiB images and relative delivery ratio R1 parametric images

SRTM and SRTM2

MRTM and MRTM2

Implementation of algorithms

18F-FDG image processing

Statistics

Intensity normalization

Within-subjects correlation

Voxelwise regional correlation

RESULTS

Within-subjects correlation

Voxelwise regional correlation

DISCUSSION

Footnotes

ACKNOWLEDGMENTS

References

Quantification of pPiB images and relative delivery ratio R₁ parametric images

¹⁸F-FDG image processing