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      Effect of age, ethnicity, sex, cognitive status and APOE genotype on amyloid load and the threshold for amyloid positivity

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          Abstract

          The threshold for amyloid positivity by visual assessment on PET has been validated by comparison to amyloid load measured histopathologically and biochemically at post mortem. As such, it is now feasible to use qualitative visual assessment of amyloid positivity as an in-vivo gold standard to determine those factors which can modify the quantitative threshold for amyloid positivity. We calculated quantitative amyloid load, measured as Standardized Uptake Value Ratios (SUVRs) using [18-F]florbetaben PET scans, for 159 Hispanic and non-Hispanic participants, who had been classified clinically as Cognitively Normal (CN), Mild Cognitive Impairment (MCI) or Dementia (DEM). PET scans were visually rated as amyloid positive (A+) or negative (A-), and these judgments were used as the gold standard with which to determine (using ROC analyses) the SUVR threshold for amyloid positivity considering factors such as age, ethnicity (Hispanic versus non-Hispanic), gender, cognitive status, and apolipoprotein E ε4 carrier status. Visually rated scans were A+ for 11% of CN, 39.0% of MCI and 70% of DEM participants. The optimal SUVR threshold for A+ among all participants was 1.42 (sensitivity = 94%; specificity = 92.5%), but this quantitative threshold was higher among E4 carriers (SUVR = 1.52) than non-carriers (SUVR = 1.31). While mean SUVRs did not differ between Hispanic and non-Hispanic participants;, a statistically significant interaction term indicated that the effect of E4 carrier status on amyloid load was greater among non-Hispanics than Hispanics. Visual assessment, as the gold standard for A+, facilitates determination of the effects of various factors on quantitative thresholds for amyloid positivity. A continuous relationship was found between amyloid load and global cognitive scores, suggesting that any calculated threshold for the whole group, or a subgroup, is artefactual and that the lowest calculated threshold may be optimal for the purposes of early diagnosis and intervention.

          Highlights

          • Demographic factors did not affect the threshold for amyloid positivity.

          • Cognitive status did not affect this threshold for amyloid positivity.

          • APOE4 carriers had a higher threshold for amyloid positivity than non-carriers.

          • Among APOE4 carriers, non-Hispanics had higher amyloid load than non- Hispanics.

          • There was a continuous relationship between amyloid load and cognitive status.

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          Most cited references38

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          Index for rating diagnostic tests.

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            Hopkins Verbal Learning Test ? Revised: Normative Data and Analysis of Inter-Form and Test-Retest Reliability

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              Defining imaging biomarker cut points for brain aging and Alzheimer's disease

              Our goal was to develop cut points for amyloid positron emission tomography (PET), tau PET, flouro-deoxyglucose (FDG) PET, and MRI cortical thickness.
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                Author and article information

                Contributors
                Journal
                Neuroimage Clin
                Neuroimage Clin
                NeuroImage : Clinical
                Elsevier
                2213-1582
                27 March 2019
                2019
                27 March 2019
                : 22
                : 101800
                Affiliations
                [a ]Florida ADRC, USA
                [b ]Mount Sinai Medical Center, Miami Beach, USA
                [c ]Miller School of Medicine, University of Miami, Miami, FL, USA
                [d ]College of Engineering and Computing, Florida International University, Miami, FL, USA
                [e ]Florida Atlantic University, USA
                [f ]University of Florida College of Medicine, Gainesville, FL, USA
                [g ]Mayo Clinic Florida, Department of Neurology, Jacksonville, FL, USA
                [h ]Mayo Clinic Florida, Department of Neuroscience, Jacksonville, FL, USA
                [i ]Life Molecular Imaging Inc, USA
                [j ]University of Florida, College of Public Health and Health Professions, USA
                [k ]Department of Medicine, University of Hong Kong, Hong Kong
                [l ]Robert Stempel College of Public Health & Social Work, Florida International University, Miami, FL, USA
                Author notes
                [* ]Corresponding author at: Wien Center for Alzheimer's Disease & Memory Disorder, Mount Sinai Medical Center, 4300 Alton Road, Miami Beach, FL 33140, USA. ranjan.duara@ 123456msmc.com
                Article
                S2213-1582(19)30150-0 101800
                10.1016/j.nicl.2019.101800
                6447735
                30991618
                f08ad091-7683-4319-8b65-f46cd56be1ec
                © 2019 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 22 June 2018
                : 8 February 2019
                : 26 March 2019
                Categories
                Regular Article

                amyloid,apoe,threshold,cognition,hispanic,suvr
                amyloid, apoe, threshold, cognition, hispanic, suvr

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