4.7 Article

Determining Amyloid-beta Positivity Using F-18-AZD4694 PET Imaging

Journal

JOURNAL OF NUCLEAR MEDICINE
Volume 62, Issue 2, Pages 247-252

Publisher

SOC NUCLEAR MEDICINE INC
DOI: 10.2967/jnumed.120.245209

Keywords

Alzheimer disease; amyloid-beta; PET; F-18-AZD4694

Funding

  1. McGill University's Faculty of Medicine Scholarship
  2. Canadian Institutes of Health Research (CIHR) [MOP-11-51-3]
  3. Alzheimer's Association [NIRG-12-92090, NIRP-12-259245]
  4. Fonds de Recherche du Quebec-Sante [2020-VICO-279314]
  5. Swedish Research Council [2018-02532, 2017-00915]
  6. European Research Council [681712]
  7. Swedish State Support for Clinical Research [ALFGBG-720931]
  8. Alzheimer Drug Discovery Foundation (ADDF) [201809-2016862, RDAPB-201809-2016615]
  9. UK Dementia Research Institute at UCL
  10. Swedish Alzheimer Foundation [AF-742881, FO2017-0243]
  11. Swedish government
  12. ALF-agreement [ALFGBG-715986]
  13. European Union Joint Program for Neurodegenerative Disorders [JPND2019-466-236]

Ask authors/readers for more resources

This study assessed multiple methods for determining an optimal cutoff for F-18-AZD4694 PET positivity, with good convergence among different approaches. The findings suggest that a threshold of 1.55 SUVR may have reliable discriminative accuracy for amyloid-beta positivity on PET imaging.
Amyloid-beta deposition into plaques is a pathologic hallmark of Alzheimer disease appearing years before the onset of symptoms. Although cerebral amyloid-8 deposition occurs on a continuum, dichotomization into positive and negative groups has advantages for diagnosis, clinical management, and population enrichment for clinical trials. F-18-AZD4694 (also known as F-18-NAV4694) is an amyloid-beta imaging ligand with high affinity for amyloid-beta plaques. Despite being used in multiple academic centers, no studies have assessed a quantitative cutoff for amyloid-8 positivity using F-18-AZD4694 PET. Methods: We assessed 176 individuals [young adults (n = 22), cognitively unimpaired elderly (n = 89), and cognitively impaired (n = 65)] who underwent amyloid-8 PET with F-18-AZD4694, lumbar puncture, structural MRI, and genotyping for APOE epsilon 4. F-18-AZD4694 values were normalized using the cerebellar gray matter as a reference region. We compared 5 methods for deriving a quantitative threshold for F-18-AZD4694 PET positivity: comparison with young control SUV ratios (SUVRs), receiver-operating-characteristic (ROC) curves based on clinical classification of cognitively unimpaired elderly versus Alzheimer disease dementia, ROC curves based on visual A8-positive/A8-negative classification, gaussian mixture modeling, and comparison with cerebrospinal fluid measures of amyloid-8, specifically the A842/A840 ratio. Results: We observed good convergence among the 4 methods: ROC curves based on visual classification (optimal cut point, 1.55 SUVR), ROC curves based on clinical classification (optimal cut point, 1.56 SUVR) gaussian mixture modeling (optimal cut point, 1.55 SUVR), and comparison with cerebrospinal fluid measures of amyloid-8 (optimal cut point, 1.51 SUVR). Means and 2 SDs from young controls resulted in a lower threshold (1.33 SUVR) that did not agree with the other methods and labeled most elderly individuals as A8 positive. Conclusion: Good convergence was obtained among several methods for determining an optimal cutoff for F-18-AZD4694 PET positivity. Despite conceptual and analytic idiosyncrasies linked with dichotomization of continuous variables, an F-18-AZD4694 threshold of 1.55 SUVR had reliable discriminative accuracy. Although clinical use of amyloid PET is currently by visual inspection of scans, quantitative thresholds may be helpful to arbitrate disagreement among raters or in borderline cases.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available