- Original article
- Open Access
Regional uptakes from early-frame amyloid PET and 18F-FDG PET scans are comparable independent of disease state
European Journal of Hybrid Imaging volume 6, Article number: 2 (2022)
Positron emission tomography (PET) imaging with amyloid-beta (Aβ) tracers and 2-[18F] fluoro-2-Deoxy-d-glucose (18F-FDG) is extensively employed in Alzheimer’s disease (AD) studies as biomarkers of AD pathology and neurodegeneration. To reduce cost and additional burdens to the patient, early-frame uptake during Aβ PET scanning has been proposed as a surrogate measure of regional glucose metabolism. Considering the disease state specific impact of AD on neurovascular coupling, we investigated to what extent the information captured in the early frames of an Aβ-PET (18F-florbetapir or 18F-florbetaben) scan is comparable to that of a 18F-FDG PET scan, independent of disease state.
A partial correlation was performed on early-frame 18F-florbetapir and 18F-FDG regional data from 100 participants. In a secondary analysis, we compared 92 18F-florbetapir and 21 18F-florbetaben early-frame Aβ scans from cognitively unimpaired and mild cognitive impairment participants to ascertain if regional early-frame information was similar across different Aβ-PET radioligands.
The partial correlation of early-frame 18F-florbetapir with 18F-FDG was significant in all 84 brain ROIs, with correlation values ranging from 0.61 to 0.94. There were no significant differences between early-frame 18F-florbetapir and 18F-florbetaben images.
Overall, we find that the regional uptake measurements from early-frame 18F-florbetapir are strongly correlated with regional glucose metabolism as measured in ground-truth 18F-FDG PET scans, regardless of disease state. Future studies should focus on longitudinal early-frame amyloid PET imaging studies to further assess the value of early-frame imaging as a marker of brain metabolic decline.
Alzheimer’s disease (AD), the most common form of dementia, is a debilitating neurodegenerative disease that affects approximately 14.5% of the American population (Rajan et al. 2019). AD is pathologically characterized by amyloid-beta (Aβ) plaques and tau pathology (neurofibrillary tangles) which can be detected with Aβ positron emission tomography (PET) scans and used to differentiate AD from other forms of dementia. These Aβ plaques can occur as many as 10–15 years prior to the onset of observable cognitive decline and are considered an important early biomarker for AD prevention (Rowe et al. 2010). Given the utility of Aβ PET imaging, there are now multiple radioligand tracers including 11C-labeled Pittsburgh Compound-B (C-PIB), 18F-florbetapir, and 18F-florbetaben that can be used for in vivo imaging (Klunk et al. 2004; Wong et al. 2010; Villemagne et al. 2011).
However, quantification of Aβ burden alone is not always sufficient in the diagnosis of AD and it is important to consider additional aspects of pathophysiology, including neurodegeneration which could be reflected as early changes in cerebral blood flow (perfusion) and glucose metabolism (Jack et al. 2018; Ahmad et al. 2020). Studies show that differences in perfusion exist between healthy controls and AD patients and may also be present long before clinical symptoms of AD are observed (Hays et al. 2016; Kisler et al. 2017). Many have shown the importance of evaluating glucose metabolism in the brains of patients at risk of or diagnosed with AD (Chen and Zhong 2013; Gaitán et al. 2019). In particular, hypometabolism in the precuneus, posterior cingulate, and hippocampus has been observed in AD consistently, and associated with changes in synaptic density and correlated with cognitive impairment (Friedland et al. 1983; Maldjian and Whitlow 2012; Minoshima et al. 1997; Calsolaro and Edison 2016).
Acquiring information on all these aspects of the disease currently requires multiple PET scans, which is expensive and exposes the patient to multiple doses of radiation. As a solution to this problem, researchers have started to investigate the degree to which the early frames of an amyloid scan can capture the information provided by PET scans administered to assess glucose metabolism.
The early-frames of an amyloid scan provide information akin to perfusion, as the amyloid-binding tracer perfuses through various regions throughout the brain (Blomquist et al. 2008). This information, in turn, may be used as a measure of metabolism, given that vascular and metabolic coupling has been established in cognitively normal older adults and those with degenerative dementias (Silverman 2004). Current literature on the topic suggests that the agreement between amyloid scans and F-18 fluorodeoxyglucose (18F-FDG) scans is promising (Hsiao et al. 2012; Tiepolt et al. 2016). Specifically, in one study with 33 subjects [11 mild cognitive impairment (MCI), 22 dementia (11 AD)] comparing 18F-florbetaben amyloid scans with 18F-FDG scans, researchers reported highly significant correlations (ranging from 0.60 to 0.92), irrespective of the early-frame number or the brain region (Daerr et al. 2017). Another study with 52 MCI subjects compared both early frames and the relative rate of delivery (R1) of C-PIB PET scans to 18F-FDG scans and found high correlations between early-frame C-PIB and 18F-FDG (0.83 for frames 0–6 min and 0.4 for frames 1–8 min) (Oliveira et al. 2018). Although there is growing evidence for the role of early-frame amyloid images in differentiating between disease state or for detecting brain metabolism, the question of whether early-frame amyloid measures could be a surrogate marker of brain metabolism robustly across different disease states (given that the degree of neurovascular coupling might differ by disease state) remains to be answered. If true, this finding could be extremely beneficial in the context of a clinical trial that recruits across the AD spectrum and uses glucose metabolism as a measure of either treatment efficacy or illness progression. Furthermore, comparing different types of amyloid tracers (e.g. 18F-florbetaben vs 18F-florbetapir) and identifying their similarities and/or differences would allow for a greater understanding of influence of radioligand choice and potential interchangeability of early-frame amyloid scans in replacement of 18F-FDG PET scans.
The primary objective of this study was to assess the degree to which early-frame 18F-florbetapir scans capture information about glucose metabolism in ground-truth 18F-FDG scans in an observational cohort of individuals with and without cognitive impairment and dementia. Specifically, we assessed standardized uptake value ratio (SUVR) from early-frame 18F-florbetapir PET and 18F-FDG PET scans in 82 cerebral regions of interest and 2 two composite regions (see Additional file 1: Supplementary Table S6) and conducted partial correlations to assess the relationship between the two scan types and tested if these associations were modulated by clinical disease state. As a secondary objective, we compared 18F-florbetapir early-frame regional SUVR values with 18F-florbetaben early-frame SUVR values of non-demented individuals to assess the similarity of the information captured by each tracer type and ascertain if 18F-FDG PET scans can be replaced by either type of early-frame amyloid scan.
Data were obtained from the database of the Alzheimer’s Disease Neuroimaging Initiative (ADNI) (adni.loni.usc.edu). The National Institute of Aging, the National Institute of Biomedical Imaging and Bioengineering, the Food and Drug Administration, private pharmaceutical companies, and nonprofit organizations launched ADNI in 2004 as a public–private partnership. ADNI is a longitudinal multi-center natural history study designed to characterize clinical, neuropsychological, MRI and PET imaging, genetic, and biochemical biomarkers for early detection and tracking of AD (Jack et al. 2008). The principal investigator of ADNI is Michael Weiner, MD, VA Medical Center and University of California, San Francisco. For current information on ADNI, see www.adni-info.org.
Subjects of the main study were ADNI participants (CU, MCI, and Dementia) who underwent both early-frame 18F-florbetapir PET and 18F-FDG PET. Exclusion criteria for ADNI participants included any significant neurologic disease, such as Parkinson’s disease, multi-infarct dementia, Huntington’s disease, normal pressure hydrocephalus, progression supranuclear palsy, seizure disorder, subdural hematoma, multiple sclerosis, or history of significant head trauma followed by persistent neurologic deficits or known structural brain abnormalities. The time between the two scans was limited to less than 2.5 years. The cohort for the secondary objective was based on ADNI participants (CU and MCI only) who underwent early-frame 18F-florbetaben PET imaging augmented with age, sex, and diagnoses matched participants with early-frame 18F-florbetapir PET imaging. Selection was made a priori from all ADNI subjects based on the availability of complete data including cross-sectional imaging and longitudinal clinical and cognitive measures as of April 20th, 2021.
Participants were injected with 185 mBq (5 mCi) of 18F-FDG and a dynamic 3D scan of 6 5-min frames were acquired 30–60 min post injection. For each individual, an average of all frames was used in this analysis. Dynamic images were used as static images were not available.
Early-frame 18F-florbetapir/18F-florbetaben PET
Participants were injected with 370 mBq (10 mCi) of 18F-florbetapir or 300 mBq (8.1 mCi) of 18F-florbetaben with simultaneous initiation of the dynamic PET scan. The scan lasted 20 min and comprised the following sequence (4 × 15 s, 4 × 30 s, 3 × 60 s, 3 × 120 s, 2 × 240 s). An average of frames 4–11, i.e., average of 45 s to 6 min, as recommended by multiple studies were used in this analysis (Rostomian et al. 2011; Rodriguez-Vieitez et al. 2017).
3T multimodality MRI data included a 3D MP-RAGE or IR-SPGR T1-weighted (T1w) MRI, as described online (http://adni.loni.usc.edu/methods/documents/mri-protocols).
Image quality assurance
All images were visualized with MRIcron to check for outstanding artifacts and the overall quality of the acquisition.
A fully automated processing pipeline, Advanced Normalization Tools (ANTs) cortical thickness pipeline, was applied to each T1w scan and spatially normalized each image to a widely used T1w MRI template in stereotaxic space, the Montreal Neurological Institute/International Consortium for Brain Mapping (MNI-152) (Avants et al. 2011). Each anatomical MRI was segmented into N = 75 cortical and N = 7 subcortical regions-of-interest (ROIs) based on a previously published volumetric Hammers atlas (Hammers et al. 2003; Gousias et al. 2008).
Early-frame amyloid PET and 18F-FDG PET images were level 4 ADNI preprocessed data that had been smoothed to standard 8 FWHM, co-registered, standardized to a baseline image, averaged, and normalized (http://adni.loni.usc.edu/methods/pet-analysis-method/pet-analysis/). The averaged images were then rigid-aligned to corresponding T1w images, then spatially normalized to template space using the subject specific T1w image space to MNI space spatial normalization transformation. Standard uptake values for 82 regions of interest were then extracted from the registered PET images. The brainstem served as a reference region for both the early-frame 18F-florbetapir images and 18F-FDG images to estimate the regional standard uptake value ratio (SUVR) (Verger et al. 2021). Further, composite regions of interest comprising the average of the middle/inferior temporal, posterior cingulate cortex, and inferolateral remainder of the parietal lobe regions by hemisphere, as previously described in Landau et al. (2011), were also included.
All analyses were conducted with statistical software in R (R Core Team 2017). All ROI-based analyses were adjusted for multiple comparisons with the False Discovery Rate (FDR) method.
Comparison of early-frame 18F-florbetapir and 18F-FDG
A partial correlation between regional early-frame 18F-florbetapir and regional 18F-FDG SUVR was performed with time between scans as a covariate. Additionally, Bland–Altman plots were used to show graphically the agreement between the two modalities across all regions. To assess the effect of disease state (i.e., CU, MCI, Dementia) on the inter-modality (i.e., early-frame 18F-florbetapir versus 18F-FDG) associations, a linear regression analysis between regional early-frame 18F-florbetapir and 18F-FDG uptakes was performed with clinical disease state as an interaction term and time between scans as a covariate. The linear regression analysis was repeated with the clinical dementia rating (CDR) sum of boxes score (continuous) in lieu of disease state (categorical) to assess if the association between early-frame 18F-florbetapir and 18F-FDG PET regional SUVR is modulated by the symptom severity. Additionally, bias between the two modalities was calculated as the difference between the 18F-florbetapir mean and the 18F-FDG mean, divided by the 18F-FDG mean (ground truth for glucose metabolism), multiplied by 100.
Comparison of early-frame 18F-florbetapir and 18F-florbetaben
We first compared the whole brain early-frame 18F-florbetapir and early-frame 18F-florbetaben patterns by taking the SUVRs of 82 cerebral regions per subject as vectors and computing cosine similarities between every pair of vectors. Linear regressions by region with covariates of age, diagnosis, and CDR sum of boxes score between early-frame 18F-florbetapir and early-frame 18F-florbetaben SUVR values were also conducted.
Early-frame 18F-florbetapir versus 18F-FDG
Out of 103 cases with early-frame 18F-florbetapir and 18F-FDG PET scans available as of April 20, 2021, three cases (two CU and one MCI) were removed due to a T1 to PET registration error. Based on the clinical assessment done closest in time to the early-frame 18F-florbetapir PET visit, the final study cohort was composed of 52 CU individuals, 33 individuals with MCI, and 15 individuals with dementia. Demographic and clinical characteristics of these participants are displayed in Table 1 and sample images of structural MRI, early-frame 18F-florbetapir and 18F-FDG PET scans are available in Fig. 1.
Early-frame 18F-florbetapir versus 18F-florbetaben
Out of 144 cases (122 18F-florbetapir, 22 18F-florbetaben) available as of April 20, 2021, one participant with an 18F-florbetaben scan was removed following an outlier detection criterion of 3 absolute z-scores from the mean of the distribution from patients (divided by diagnosis) for each ROI. An additional 30 18F-florbetapir cases were removed to ensure that the mean age between groups was not statistically significantly different. Based on the clinical assessment done closest in time to the early-frame 18F-florbetapir PET visit, the final cohort for this objective was composed of 77 CU individuals and 36 individuals with MCI. This cohort was limited to CU and MCI due to an insufficient number of available AD cases (N = 2) with early-frame 18F-florbetaben scan. Demographic and clinical characteristics of these are displayed in Table 2.
Association between early-frame 18F-florbetapir and FDG regional SUVRs
The partial correlation between early-frame 18F-florbetapir and 18F-FDG PET SUVRs was significant in all 82 cerebral regions and 2 composite regions, ranging from 0.61 to 0.94 (mean = 0.74) as displayed in Fig. 2. The highest correlation between the early-frame 18F-florbetapir and 18F-FDG data within cortical regions was in the anterior temporal lobe (left: r = 0.85, p < 2e−16; right: r = 0.85, p < 2e−16). Figure 3 provides a graphical comparison of the left posterior cingulate gyrus (r = 0.70), a region often observed in clinical trials, and the left middle frontal gyrus (r = 0.61), which exhibited the lowest partial correlation. The average 18F-FDG SUVR for the whole brain was 1.21 while the average early-frame 18F-florbetapir SUVR was 1.07. Figure 4 visualizes the measurement bias between early-frame 18F-florbetapir and 18F-FDG PET when using F-FDG as the gold-standard (also reported in Additional file 1: Supplementary Table S1). As displayed in the figure, there is a regional variance such that the difference between early-frame 18F-florbetapir SUVR and 18F-FDG SUVR is greater in frontoparietal regions compared to temporal regions. Partial correlations for all 82 cerebral regions and 2 composite regions are reported in Additional file 1: Supplementary Table S2. The Bland–Altman plots demonstrated that regional early-frame 18F-florbetapir and 18F-FDG SUVR are quite concordant, largely showing no change in residual variance with increasing 18F-FDG SUVR (Fig. 5, Additional file 1: Supplementary Table S3, Additional file 1: Supplementary Fig. S1).
Effect of clinical disease stage on the associations between early-frame 18F-florbetapir and FDG regional SUVRs
Compared to CU participants, the early-frame 18F-florbetapir versus 18F-FDG uptake association in MCI and Dementia participants was significantly stronger only in the right thalamus (MCI: β = 0.37, p = 0.016; Dementia: β = 0.37, p = 0.025). In all other regions, clinical disease stage did not have a significant effect on the association. In the linear regression analysis accounting for disease stage differences by including CDR-SB instead of categorical clinical diagnosis as a linear interaction term the CDR sum of boxes score did not have statistically significant (p < 0.05 FDR corrected) modulation effect on the association between early-frame 18F-florbetapir and 18F-FDG uptake. This second linear regression analysis did however reiterate a significant correlation between 18F-florbetapir and 18F-FDG uptake (Additional file 1: Supplementary Table S4).
Association between early-frame 18F-florbetapir and early-frame 18F-florbetaben regional SUVRs
Figure 6a displays the average early-frame 18F-florbetapir brain profile with the average early-frame 18F-florbetaben profile with confidence bounds calculated as two standard deviations from the mean. Regional averages are displayed as a continuous line to help visualize a SUVR brain profile for each tracer and to easily compare between the two. As displayed in the cosine similarity matrix in Fig. 6b, similarities between and within tracer type were largely the same, ranging from 0.96 to 1.00 in this example. A visual comparison of the magnitude of similarity between and within tracer type can be found in Additional file 1: Supplementary Fig. S2. Given the large overlap between these two groups and the high similarity measures, we find that the two tracers did not differ statistically in the relative regional information collected. The results of the linear regression by region (covariates: age, diagnosis, and CDR sum of boxes score) between early-frame 18F-florbetapir and 18F-florbetaben scans can be found in Additional file 1: Supplementary Table S5.
In this study, we compared early-frame 18F-florbetapir PET and 18F-FDG PET scans from 100 cognitively diverse (CU, MCI, and Dementia) participants in 84 different cerebral regions-of-interest to assess the degree to which early-frame amyloid scans can capture information about cerebral glucose metabolism typically measured by 18F-FDG PET scans. We found that the correlation between early-frame 18F-florbetapir scans and 18F-FDG scans was moderate to strong across all ROIs and disease states, with the exception of the right thalamus where the strength of the inter-modality association was modulated in MCI and Dementia participants relative to CU. The strength of the correlation was also confirmed with a separate analysis that used CDR-SB scores instead of disease state, and also found no significant effect of score on the association between early-frame amyloid and 18F-FDG. Another major finding of our analyses was that early-frame 18F-florbetapir and 18F-florbetaben regional SUVRs do not significantly differ. Taken together, these results suggest that regional SUVR from early-frame amyloid scans, regardless of the tracer used, is well-correlated with regional SUVR from 18F-FDG PET scans and could potentially be used for diagnostic purposes in individuals along the AD spectrum.
The first major finding that the correlation between early-frame 18F-florbetapir and 18F-FDG regional SUVRs is significant and moderate to high (i.e., between 0.61 and 0.94) is consistent with previous studies that investigated a similar question using different amyloid tracers (i.e., C-PIB) or the addition of the R1 measure from amyloid scans (Daerr et al. 2017; Oliveira et al. 2018; Rostomian et al. 2011). Our finding is also of importance because it validates this correlation in a sample size roughly 2–3 times larger than in previous studies. Furthermore, we included a composite of temporoparietal regions that would be likely examined in an AD treatment trial and found the partial correlation between early-frame 18F-florbetapir and 18F-FDG was moderate and significant. Our observation that these inter-modality correlations are moderate to strong regardless of disease state also has important implications for the potential replacement of 18F-FDG scans with early-frame amyloid scans for more efficient study designs without loss of sensitivity. Specifically, it suggests that early-frame amyloid scans could be used as a surrogate measure to help quantify glucose metabolism in participants across the cognitive spectrum without concern of the correlation fluctuating between diagnoses. While this would be particularly beneficial for Alzheimer’s clinical trials that recruit participants with a wide range of clinical stages and participants that might convert between different disease states during the trial, we believe that these results should be replicated in a larger, more balanced cohort prior to making these claims.
Differences between disease states in the right thalamus were subtle—the correlation between early frames and 18F-FDG PET was positive for all three disease states, with dementia and MCI groups exhibiting slightly stronger (more positive) correlations. However, there is no biological reason to expect this region to vary by disease state and this finding needs to be replicated in future datasets before any conclusions can be drawn from this observation.
While partial correlations between early-frame 18F-florbetapir and 18F-FDG PET SUVR were relatively strong in temporal regions and some central structures, we observed that the strength of the correlations was weaker in some frontal and occipital regions (Fig. 4 and Additional file 1: Supplementary Table S1). Specifically, we see that 18F-FDG SUVR tends to be higher than early-frame 18F-florbetapir SUVR in these regions. This is not an unexpected result, as we know that the coupling between perfusion and glucose metabolism is not always consistent throughout the brain (Tosun et al. 2016). For example, hypoperfusion of frontal regions in patients with AD has been previously reported (Kataoka et al. 2010; Thomas et al. 2015), while hypometabolism is not consistently found in these regions (Kato et al. 2016). Lower correlations between the two modalities in the occipital lobe were also reported by Hsiao et al. (2012). We acknowledge that while the two imaging modalities are not identical, they are similar enough (as evidenced by the correlations in Additional file 1: Supplementary Table S2) for certain applications, such as patient diagnosis and detection of treatment effect.
As a second major finding, we observed that within early frame amyloid scans, tracer type has no significant effect on standard uptake values in CU and MCI patients. With cosine similarity measures between and within tracer type ranging from 0.96 to 1.00, we believe that replacing one tracer with the other will not affect clinical decisions. By extension, these findings indicate that 18F-florbetapir and 18F-florbetaben early-frame amyloid scans could replace 18F-FDG scans in the measurement of cerebral glucose metabolism. Given the relatively small sample size of 18F-florbetaben scans (N = 21), it would be beneficial to replicate this analysis in a larger cohort. Additionally, it would be important to ascertain if early-frame 18F-florbetapir and 18F-florbetaben data is comparable in patients with advanced cognitive impairment (i.e., dementia).
There are a few limitations to this study worth mentioning. First, there are multiple components of an early-frame amyloid scan that can be considered for comparison with 18F-FDG. Many current studies suggest that early-frame amyloid and 18F-FDG are the most comparable when using the R1 measure of early frame scans, which represents the relative delivery rate of the tracer. In this analysis, we chose to focus on a simpler comparison with 18F-FDG that did not require kinetic modeling which yielded robust correlations between early-frame amyloid and 18F-FDG in this study. Additionally, the role of blood perfusion in this association between early-frame amyloid and 18F-FDG PET scans should be assessed in future studies as more arterial spin labeled (ASL) MRI data becomes available in early-frame studies. Second, we recognize that the early-frame 18F-florbetapir and 18F-florbetaben comparison would have been more complete with a partial correlation analysis between SUVRs from each early-frame image and a corresponding 18F-FDG image. However, 18F-FDG scans were not available for many ADNI participants selected for the early-frame 18F-florbetaben study. Comparing the partial correlation coefficients of early-frame 18F-florbetapir and 18F-FDG to those of 18F-florbetaben and 18F-FDG would be a worthwhile future analysis to further expand on the findings in this study.
We should note that the current study is based on a convenience cohort where the degree of true population representation is not known. Most notable, due to strict exclusion of participants with vascular pathology etiologies in ADNI studies, vascular disease burden was overall low in our study cohort compared to the general population. Although strong evidence suggests that vascular disease influences glucose metabolism and regional cerebral perfusion, the degree to which cerebral perfusion and glucose metabolism correlate in the general population might impact the generalizability of findings in this study (Pascual et al. 2010; Leuzy et al. 2018; Yan et al. 2018). Furthermore, we recognize the limitation of exploring this correlation in a cross-sectional cohort. A very important aspect of investigating disease pathophysiology is to track its progression over time, which can only be accomplished through a longitudinal data set. Ideally, it would be important to identify whether changes in glucose metabolism over time could be detected in early-frame amyloid scans as they are in 18F-FDG scans. Put more simply, does this correlation between early-frame amyloid and 18F-FDG scans remain significant over time? The finding from this study that the correlation between early-frame amyloid and 18F-FDG scans is robust across disease states may indicate that the correlation would be preserved over the course of the disease, although this would need to be confirmed in a longitudinal dataset. Lastly, we acknowledge that our findings should be taken cautiously given the small number of individuals with dementia included in this analysis (15 out of 100).
Here, we showed that within a diverse cohort of individuals (cognitively unimpaired, have mild cognitive impairment, or dementia), early-frame 18F-florbetapir and 18F-FDG PET regional SUVRs are moderately to strongly correlated. Overall, this study will likely have significant implications for researchers studying biomarkers related to glucose metabolism in Alzheimer’s disease in a cohort of participants with a wide range of clinical stages, especially for those who may convert between disease states during the study period.
Availability of data and material
The datasets generated during and/or analyzed during the current study are not publicly available due to rules set forth by the Alzheimer’s Disease Neuroimaging Initiative, but are available from the corresponding author on reasonable request.
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Data collection and sharing for this project was funded by the Alzheimer's Disease Neuroimaging Initiative (ADNI) (National Institutes of Health Grant U01 AG024904). ADNI is funded by the National Institute on Aging, the National Institute of Biomedical Imaging and Bioengineering, and through generous contributions from the following: AbbVie, Alzheimer’s Association; Alzheimer’s Drug Discovery Foundation; Araclon Biotech; BioClinica, Inc.; Biogen; Bristol-Myers Squibb Company; CereSpir, Inc.; Cogstate; Eisai Inc.; Elan Pharmaceuticals, Inc.; Eli Lilly and Company; EuroImmun; F. Hoffmann-La Roche Ltd and its affiliated company Genentech, Inc.; Fujirebio; GE Healthcare; IXICO Ltd.; Janssen Alzheimer Immunotherapy Research & Development, LLC.; Johnson & Johnson Pharmaceutical Research & Development LLC.; Lumosity; Lundbeck; Merck & Co., Inc.; Meso Scale Diagnostics, LLC.; NeuroRx Research; Neurotrack Technologies; Novartis Pharmaceuticals Corporation; Pfizer Inc.; Piramal Imaging; Servier; Takeda Pharmaceutical Company; and Transition Therapeutics. The Canadian Institutes of Health Research is providing funds to support ADNI clinical sites in Canada. Private sector contributions are facilitated by the Foundation for the National Institutes of Health (www.fnih.org). The grantee organization is the Northern California Institute for Research and Education, and the study is coordinated by the Alzheimer’s Therapeutic Research Institute at the University of Southern California. ADNI data are disseminated by the Laboratory for Neuro Imaging at the University of Southern California.
Data used in preparation of this article were obtained from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database (adni.loni.usc.edu). As such, the investigators within the ADNI contributed to the design and implementation of ADNI and/or provided data but did not participate in analysis or writing of this report. A complete listing of ADNI investigators can be found at: http://adni.loni.usc.edu/wp-content/uploads/how_to_apply/ADNI_Acknowledgement_List.pdf.
This work is funded by the National Institutes of Health Grant U01 AG024904.
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Myoraku, A., Klein, G., Landau, S. et al. Regional uptakes from early-frame amyloid PET and 18F-FDG PET scans are comparable independent of disease state. European J Hybrid Imaging 6, 2 (2022). https://doi.org/10.1186/s41824-021-00123-0
- Early-frame imaging
- Alzheimer’s disease