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 |
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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. |
doi_str_mv | 10.1017/S1355617724000079 |
format | Article |
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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.</description><identifier>ISSN: 1355-6177</identifier><identifier>ISSN: 1469-7661</identifier><identifier>EISSN: 1469-7661</identifier><identifier>DOI: 10.1017/S1355617724000079</identifier><identifier>PMID: 38389489</identifier><language>eng</language><publisher>New York, USA: Cambridge University Press</publisher><subject>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</subject><ispartof>Journal of the International Neuropsychological Society, 2024-07, Vol.30 (6), p.584-593</ispartof><rights>The Author(s), 2024. Published by Cambridge University Press on behalf of International Neuropsychological Society</rights><rights>The Author(s), 2024. Published by Cambridge University Press on behalf of International Neuropsychological Society. This work is licensed under the Creative Commons Attribution License This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited. (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c368t-9154b497d447847be164665bf966b3abd69b11d9f967c1e56f2c3991c15de1c13</cites><orcidid>0000-0002-5708-4925</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.cambridge.org/core/product/identifier/S1355617724000079/type/journal_article$$EHTML$$P50$$Gcambridge$$Hfree_for_read</linktohtml><link.rule.ids>164,314,776,780,27901,27902,55603</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38389489$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dubbelman, Mark A.</creatorcontrib><creatorcontrib>Tomassen, Jori</creatorcontrib><creatorcontrib>van der Landen, Sophie M.</creatorcontrib><creatorcontrib>Bakker, Els</creatorcontrib><creatorcontrib>Kamps, Suzie</creatorcontrib><creatorcontrib>van Unnik, Annemartijn A.J.M.</creatorcontrib><creatorcontrib>van de Glind, Marie-Christine A.B.J.</creatorcontrib><creatorcontrib>van der Vlies, Annelies E.</creatorcontrib><creatorcontrib>Koene, Ted</creatorcontrib><creatorcontrib>Leeuwis, Anna E.</creatorcontrib><creatorcontrib>Barkhof, Frederik</creatorcontrib><creatorcontrib>van Harten, Argonde C.</creatorcontrib><creatorcontrib>Teunissen, Charlotte</creatorcontrib><creatorcontrib>van de Giessen, Elsmarieke</creatorcontrib><creatorcontrib>Lemstra, Afina W.</creatorcontrib><creatorcontrib>Pijnenburg, Yolande A.L.</creatorcontrib><creatorcontrib>Ponds, Rudolf W.H.</creatorcontrib><creatorcontrib>Sikkes, Sietske A.M.</creatorcontrib><title>Visual associative learning to detect early episodic memory deficits and distinguish Alzheimer’s disease from other types of dementia</title><title>Journal of the International Neuropsychological Society</title><addtitle>J Int Neuropsychol Soc</addtitle><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.</description><subject>Aged</subject><subject>Alzheimer Disease - complications</subject><subject>Alzheimer Disease - diagnosis</subject><subject>Alzheimer Disease - physiopathology</subject><subject>Alzheimer's disease</subject><subject>Association Learning - physiology</subject><subject>Associative learning</subject><subject>Atrophy</subject><subject>Atrophy - pathology</subject><subject>Dementia</subject><subject>Dementia - diagnosis</subject><subject>Dementia - physiopathology</subject><subject>Dementia disorders</subject><subject>Diagnosis, Differential</subject><subject>Female</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Memory</subject><subject>Memory Disorders - diagnosis</subject><subject>Memory Disorders - etiology</subject><subject>Memory Disorders - physiopathology</subject><subject>Memory, Episodic</subject><subject>Mental task performance</subject><subject>Middle Aged</subject><subject>Neurodegenerative diseases</subject><subject>Neuropsychological Tests - standards</subject><subject>Pathology</subject><subject>Temporal lobe</subject><subject>Temporal Lobe - diagnostic imaging</subject><subject>Temporal Lobe - pathology</subject><subject>Temporal Lobe - physiopathology</subject><subject>Visual discrimination learning</subject><issn>1355-6177</issn><issn>1469-7661</issn><issn>1469-7661</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>IKXGN</sourceid><sourceid>EIF</sourceid><recordid>eNp1kc2OFCEUhStG44yjD-DGkLhxU8ptKCiWk4l_ySQu_NlWKLg1zaQoWi5l0q7c-Qy-nk8i7bSaaGQBF853DoTbNA-BPwUO-tlbEF2nQOuN5HVoc6s5BalMq5WC27WucnvQT5p7RNecgwDO7zYnohe9kb05bb5-CLTamVmi5IIt4ROyGW1ewnLFSmIeC7rC6sm8Z7gLlHxwLGJMeV_FKbhQiNnFMx-oVNMaaMvO589bDBHz9y_f6KCgJWRTTpGlssXMyn6HxNJUIyIuJdj7zZ3JzoQPjutZ8_7F83cXr9rLNy9fX5xftk6ovrQGOjlKo72Uupd6RFBSqW6cjFKjsKNXZgTwpu61A-zUtHHCGHDQeayzOGue3OTucvq4IpUhBnI4z3bBtNIgAISWwHtd0cd_oddpzUt93U-q29Tf5ZWCG8rlRJRxGnY5RJv3A_Dh0KXhny5Vz6Nj8jpG9L8dv9pSAXEMtXHMwV_hn7v_H_sDyvCefA</recordid><startdate>20240701</startdate><enddate>20240701</enddate><creator>Dubbelman, Mark A.</creator><creator>Tomassen, Jori</creator><creator>van der Landen, Sophie M.</creator><creator>Bakker, Els</creator><creator>Kamps, Suzie</creator><creator>van Unnik, Annemartijn A.J.M.</creator><creator>van de Glind, Marie-Christine A.B.J.</creator><creator>van der Vlies, Annelies E.</creator><creator>Koene, Ted</creator><creator>Leeuwis, Anna E.</creator><creator>Barkhof, Frederik</creator><creator>van Harten, Argonde C.</creator><creator>Teunissen, Charlotte</creator><creator>van de Giessen, Elsmarieke</creator><creator>Lemstra, Afina W.</creator><creator>Pijnenburg, Yolande A.L.</creator><creator>Ponds, Rudolf W.H.</creator><creator>Sikkes, Sietske A.M.</creator><general>Cambridge University Press</general><scope>IKXGN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5708-4925</orcidid></search><sort><creationdate>20240701</creationdate><title>Visual associative learning to detect early episodic memory deficits and distinguish Alzheimer’s disease from other types of dementia</title><author>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.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-9154b497d447847be164665bf966b3abd69b11d9f967c1e56f2c3991c15de1c13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Aged</topic><topic>Alzheimer Disease - complications</topic><topic>Alzheimer Disease - diagnosis</topic><topic>Alzheimer Disease - physiopathology</topic><topic>Alzheimer's disease</topic><topic>Association Learning - physiology</topic><topic>Associative learning</topic><topic>Atrophy</topic><topic>Atrophy - pathology</topic><topic>Dementia</topic><topic>Dementia - diagnosis</topic><topic>Dementia - physiopathology</topic><topic>Dementia disorders</topic><topic>Diagnosis, Differential</topic><topic>Female</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Memory</topic><topic>Memory Disorders - diagnosis</topic><topic>Memory Disorders - etiology</topic><topic>Memory Disorders - physiopathology</topic><topic>Memory, Episodic</topic><topic>Mental task performance</topic><topic>Middle Aged</topic><topic>Neurodegenerative diseases</topic><topic>Neuropsychological Tests - standards</topic><topic>Pathology</topic><topic>Temporal lobe</topic><topic>Temporal Lobe - diagnostic imaging</topic><topic>Temporal Lobe - pathology</topic><topic>Temporal Lobe - physiopathology</topic><topic>Visual discrimination learning</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dubbelman, Mark A.</creatorcontrib><creatorcontrib>Tomassen, Jori</creatorcontrib><creatorcontrib>van der Landen, Sophie M.</creatorcontrib><creatorcontrib>Bakker, Els</creatorcontrib><creatorcontrib>Kamps, Suzie</creatorcontrib><creatorcontrib>van Unnik, Annemartijn A.J.M.</creatorcontrib><creatorcontrib>van de Glind, Marie-Christine A.B.J.</creatorcontrib><creatorcontrib>van der Vlies, Annelies E.</creatorcontrib><creatorcontrib>Koene, Ted</creatorcontrib><creatorcontrib>Leeuwis, Anna E.</creatorcontrib><creatorcontrib>Barkhof, Frederik</creatorcontrib><creatorcontrib>van Harten, Argonde C.</creatorcontrib><creatorcontrib>Teunissen, Charlotte</creatorcontrib><creatorcontrib>van de Giessen, Elsmarieke</creatorcontrib><creatorcontrib>Lemstra, Afina W.</creatorcontrib><creatorcontrib>Pijnenburg, Yolande A.L.</creatorcontrib><creatorcontrib>Ponds, Rudolf W.H.</creatorcontrib><creatorcontrib>Sikkes, Sietske A.M.</creatorcontrib><collection>Cambridge Journals Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the International Neuropsychological Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dubbelman, Mark A.</au><au>Tomassen, Jori</au><au>van der Landen, Sophie M.</au><au>Bakker, Els</au><au>Kamps, Suzie</au><au>van Unnik, Annemartijn A.J.M.</au><au>van de Glind, Marie-Christine A.B.J.</au><au>van der Vlies, Annelies E.</au><au>Koene, Ted</au><au>Leeuwis, Anna E.</au><au>Barkhof, Frederik</au><au>van Harten, Argonde C.</au><au>Teunissen, Charlotte</au><au>van de Giessen, Elsmarieke</au><au>Lemstra, Afina W.</au><au>Pijnenburg, Yolande A.L.</au><au>Ponds, Rudolf W.H.</au><au>Sikkes, Sietske A.M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Visual associative learning to detect early episodic memory deficits and distinguish Alzheimer’s disease from other types of dementia</atitle><jtitle>Journal of the International Neuropsychological Society</jtitle><addtitle>J Int Neuropsychol Soc</addtitle><date>2024-07-01</date><risdate>2024</risdate><volume>30</volume><issue>6</issue><spage>584</spage><epage>593</epage><pages>584-593</pages><issn>1355-6177</issn><issn>1469-7661</issn><eissn>1469-7661</eissn><abstract>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.</abstract><cop>New York, USA</cop><pub>Cambridge University Press</pub><pmid>38389489</pmid><doi>10.1017/S1355617724000079</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-5708-4925</orcidid><oa>free_for_read</oa></addata></record> |
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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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