Face Name Associative Memory Exam and biomarker status in the ARMADA study: Advancing reliable measurement in Alzheimer's disease and cognitive aging

Abstract The Face Name Associative Memory Exam (FNAME) was introduced into the NIH Toolbox as part of the ARMADA study and establishes normative data for diverse participants, ages 64 to 85+, and proposes cutoff scores between biomarker positive versus negative (+/−) groups. The FNAME was administer...

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Main Authors: Dorene M. Rentz, Hannah M. Klinger, Aubryn Samaroo, Colleen Fitzpatrick, Olivia R. Schneider, Saki Amagai, John Devin Peipert
Format: Article
Language:English
Published: Wiley 2023-07-01
Series:Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring
Subjects:
Online Access:https://doi.org/10.1002/dad2.12473
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author Dorene M. Rentz
Hannah M. Klinger
Aubryn Samaroo
Colleen Fitzpatrick
Olivia R. Schneider
Saki Amagai
John Devin Peipert
author_facet Dorene M. Rentz
Hannah M. Klinger
Aubryn Samaroo
Colleen Fitzpatrick
Olivia R. Schneider
Saki Amagai
John Devin Peipert
author_sort Dorene M. Rentz
collection DOAJ
description Abstract The Face Name Associative Memory Exam (FNAME) was introduced into the NIH Toolbox as part of the ARMADA study and establishes normative data for diverse participants, ages 64 to 85+, and proposes cutoff scores between biomarker positive versus negative (+/−) groups. The FNAME was administered to 257 participants across the clinical spectrum with 122 having amyloid biomarkers. Linear regression explored the association between demographics and FNAME and between amyloid (+/−) groups. Receiver operating characteristic curves (ROC) identified performance thresholds that best discriminated between biomarker (+/−) individuals. Lower FNAME scores occurred in males, older ages, Black/African Americans, Hispanics, and biomarker‐positive participants. ROC analyses demonstrated acceptable accuracy (0.73 to 0.77) but only when combined with clinical status. The diagnostic discrimination of amyloid positivity was acceptable but not excellent, suggesting the FNAME may be a better screening indicator of clinical status rather than amyloid deposition in cognitively normal individuals. Normative data are provided.
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spelling doaj.art-4def25d74ed34b009e1e1dfdacec61c32023-09-27T11:20:33ZengWileyAlzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring2352-87292023-07-01153n/an/a10.1002/dad2.12473Face Name Associative Memory Exam and biomarker status in the ARMADA study: Advancing reliable measurement in Alzheimer's disease and cognitive agingDorene M. Rentz0Hannah M. Klinger1Aubryn Samaroo2Colleen Fitzpatrick3Olivia R. Schneider4Saki Amagai5John Devin Peipert6Departments of Neurology Massachusetts General Hospital Brigham and Women's Hospital Harvard Medical School Boston Massachusetts USADepartments of Neurology Massachusetts General Hospital Brigham and Women's Hospital Harvard Medical School Boston Massachusetts USAPraxis Precision Medicines Boston Massachusetts USADepartments of Neurology Massachusetts General Hospital Brigham and Women's Hospital Harvard Medical School Boston Massachusetts USAAlbany Medical College Albany New York USANorthwestern University Feinberg School of Medicine Chicago Illinois USANorthwestern University Feinberg School of Medicine Chicago Illinois USAAbstract The Face Name Associative Memory Exam (FNAME) was introduced into the NIH Toolbox as part of the ARMADA study and establishes normative data for diverse participants, ages 64 to 85+, and proposes cutoff scores between biomarker positive versus negative (+/−) groups. The FNAME was administered to 257 participants across the clinical spectrum with 122 having amyloid biomarkers. Linear regression explored the association between demographics and FNAME and between amyloid (+/−) groups. Receiver operating characteristic curves (ROC) identified performance thresholds that best discriminated between biomarker (+/−) individuals. Lower FNAME scores occurred in males, older ages, Black/African Americans, Hispanics, and biomarker‐positive participants. ROC analyses demonstrated acceptable accuracy (0.73 to 0.77) but only when combined with clinical status. The diagnostic discrimination of amyloid positivity was acceptable but not excellent, suggesting the FNAME may be a better screening indicator of clinical status rather than amyloid deposition in cognitively normal individuals. Normative data are provided.https://doi.org/10.1002/dad2.12473Alzheimer's diseasecognitiondementiamild cognitive impairmentneuropsychologyNIH Toolbox
spellingShingle Dorene M. Rentz
Hannah M. Klinger
Aubryn Samaroo
Colleen Fitzpatrick
Olivia R. Schneider
Saki Amagai
John Devin Peipert
Face Name Associative Memory Exam and biomarker status in the ARMADA study: Advancing reliable measurement in Alzheimer's disease and cognitive aging
Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring
Alzheimer's disease
cognition
dementia
mild cognitive impairment
neuropsychology
NIH Toolbox
title Face Name Associative Memory Exam and biomarker status in the ARMADA study: Advancing reliable measurement in Alzheimer's disease and cognitive aging
title_full Face Name Associative Memory Exam and biomarker status in the ARMADA study: Advancing reliable measurement in Alzheimer's disease and cognitive aging
title_fullStr Face Name Associative Memory Exam and biomarker status in the ARMADA study: Advancing reliable measurement in Alzheimer's disease and cognitive aging
title_full_unstemmed Face Name Associative Memory Exam and biomarker status in the ARMADA study: Advancing reliable measurement in Alzheimer's disease and cognitive aging
title_short Face Name Associative Memory Exam and biomarker status in the ARMADA study: Advancing reliable measurement in Alzheimer's disease and cognitive aging
title_sort face name associative memory exam and biomarker status in the armada study advancing reliable measurement in alzheimer s disease and cognitive aging
topic Alzheimer's disease
cognition
dementia
mild cognitive impairment
neuropsychology
NIH Toolbox
url https://doi.org/10.1002/dad2.12473
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