Visual associative learning to detect early episodic memory deficits and distinguish Alzheimer’s disease from other types of dementia

We investigated how well a visual associative learning task discriminates Alzheimer's disease (AD) dementia from other types of dementia and how it relates to AD pathology. 3,599 patients (63.9 ± 8.9 years old, 41% female) from the Amsterdam Dementia Cohort completed two sets of the Visual Asso...

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Veröffentlicht in:Journal of the International Neuropsychological Society 2024-07, Vol.30 (6), p.584-593
Hauptverfasser: Dubbelman, Mark A., Tomassen, Jori, van der Landen, Sophie M., Bakker, Els, Kamps, Suzie, van Unnik, Annemartijn A.J.M., van de Glind, Marie-Christine A.B.J., van der Vlies, Annelies E., Koene, Ted, Leeuwis, Anna E., Barkhof, Frederik, van Harten, Argonde C., Teunissen, Charlotte, van de Giessen, Elsmarieke, Lemstra, Afina W., Pijnenburg, Yolande A.L., Ponds, Rudolf W.H., Sikkes, Sietske A.M.
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container_issue 6
container_start_page 584
container_title Journal of the International Neuropsychological Society
container_volume 30
creator Dubbelman, Mark A.
Tomassen, Jori
van der Landen, Sophie M.
Bakker, Els
Kamps, Suzie
van Unnik, Annemartijn A.J.M.
van de Glind, Marie-Christine A.B.J.
van der Vlies, Annelies E.
Koene, Ted
Leeuwis, Anna E.
Barkhof, Frederik
van Harten, Argonde C.
Teunissen, Charlotte
van de Giessen, Elsmarieke
Lemstra, Afina W.
Pijnenburg, Yolande A.L.
Ponds, Rudolf W.H.
Sikkes, Sietske A.M.
description We investigated how well a visual associative learning task discriminates Alzheimer's disease (AD) dementia from other types of dementia and how it relates to AD pathology. 3,599 patients (63.9 ± 8.9 years old, 41% female) from the Amsterdam Dementia Cohort completed two sets of the Visual Association Test (VAT) in a single test session and underwent magnetic resonance imaging. We performed receiver operating curve analysis to investigate the VAT's discriminatory ability between AD dementia and other diagnoses and compared it to that of other episodic memory tests. We tested associations between VAT performance and medial temporal lobe atrophy (MTA), and amyloid status ( = 2,769, 77%). Patients with AD dementia performed worse on the VAT than all other patients. The VAT discriminated well between AD and other types of dementia (area under the curve range 0.70-0.86), better than other episodic memory tests. Six-hundred forty patients (17.8%) learned all associations on VAT-A, but not on VAT-B, and they were more likely to have higher MTA scores (odds ratios range 1.63 (MTA 0.5) through 5.13 for MTA ≥ 3, all < .001) and to be amyloid positive (odds ratio = 3.38, 95%CI = [2.71, 4.22], < .001) than patients who learned all associations on both sets. Performance on the VAT, especially on a second set administered immediately after the first, discriminates AD from other types of dementia and is associated with MTA and amyloid positivity. The VAT might be a useful, simple tool to assess early episodic memory deficits in the presence of AD pathology.
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We performed receiver operating curve analysis to investigate the VAT's discriminatory ability between AD dementia and other diagnoses and compared it to that of other episodic memory tests. We tested associations between VAT performance and medial temporal lobe atrophy (MTA), and amyloid status ( = 2,769, 77%). Patients with AD dementia performed worse on the VAT than all other patients. The VAT discriminated well between AD and other types of dementia (area under the curve range 0.70-0.86), better than other episodic memory tests. Six-hundred forty patients (17.8%) learned all associations on VAT-A, but not on VAT-B, and they were more likely to have higher MTA scores (odds ratios range 1.63 (MTA 0.5) through 5.13 for MTA ≥ 3, all &lt; .001) and to be amyloid positive (odds ratio = 3.38, 95%CI = [2.71, 4.22], &lt; .001) than patients who learned all associations on both sets. 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We performed receiver operating curve analysis to investigate the VAT's discriminatory ability between AD dementia and other diagnoses and compared it to that of other episodic memory tests. We tested associations between VAT performance and medial temporal lobe atrophy (MTA), and amyloid status ( = 2,769, 77%). Patients with AD dementia performed worse on the VAT than all other patients. The VAT discriminated well between AD and other types of dementia (area under the curve range 0.70-0.86), better than other episodic memory tests. Six-hundred forty patients (17.8%) learned all associations on VAT-A, but not on VAT-B, and they were more likely to have higher MTA scores (odds ratios range 1.63 (MTA 0.5) through 5.13 for MTA ≥ 3, all &lt; .001) and to be amyloid positive (odds ratio = 3.38, 95%CI = [2.71, 4.22], &lt; .001) than patients who learned all associations on both sets. 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subjects Aged
Alzheimer Disease - complications
Alzheimer Disease - diagnosis
Alzheimer Disease - physiopathology
Alzheimer's disease
Association Learning - physiology
Associative learning
Atrophy
Atrophy - pathology
Dementia
Dementia - diagnosis
Dementia - physiopathology
Dementia disorders
Diagnosis, Differential
Female
Humans
Magnetic Resonance Imaging
Male
Memory
Memory Disorders - diagnosis
Memory Disorders - etiology
Memory Disorders - physiopathology
Memory, Episodic
Mental task performance
Middle Aged
Neurodegenerative diseases
Neuropsychological Tests - standards
Pathology
Temporal lobe
Temporal Lobe - diagnostic imaging
Temporal Lobe - pathology
Temporal Lobe - physiopathology
Visual discrimination learning
title Visual associative learning to detect early episodic memory deficits and distinguish Alzheimer’s disease from other types of dementia
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