Behavioral and cognitive markers of mild cognitive impairment: diagnostic value of saccadic eye movements and Simon task
Background Mild Cognitive Impairment (MCI) has been considered as a prodromal stage of Alzheimer disease (AD). Subtle changes in specific aspects of executive function like inhibitory control have been found in MCI. Aims We examined attentional and inhibitory control with the aim to distinguish betw...
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Veröffentlicht in: | Aging clinical and experimental research 2019-11, Vol.31 (11), p.1591-1600 |
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description | Background
Mild Cognitive Impairment (MCI) has been considered as a prodromal stage of Alzheimer disease (AD). Subtle changes in specific aspects of executive function like inhibitory control have been found in MCI.
Aims
We examined attentional and inhibitory control with the aim to distinguish between amnestic MCI patients and healthy controls.
Method
Using neuropsychological, behavioral, and oculomotor function experiments, we examined executive function in 59 normal control, 49, multiple domain amnestic MCI (a-MCI) subjects, and 21 early stage AD patients using eye tracking and Simon task as measures of attentional control, to determine which saccade and behavioral tasks were sensitive enough to identify a-MCI. Saccades were investigated in gap and overlap pro-saccade and anti-saccade tasks.
Results
Scores on the Simon task were inversely correlated with general cognitive status and can distinguish a-MCI from controls with excellent specificity (AUC = 0.65 for reaction time and 0.59 for false responses). More importantly, our results showed that saccadic gains were affected in a-MCI and were the most sensitive measures to distinguish a-MCI from normal participants AST gap task AUC = 0.7, PST gap task AUC = 0.63, AST overlap task (AUC = 0.73). Moreover, these parameters were strongly correlated with neuropsychological measures. Using tests in parallel model, improved sensitivity up to 0.97.
Conclusion
The present results enable us to suggest eye tracking along with behavioral data as a possible sensitive tools to detect a-MCI in preclinical stage. |
doi_str_mv | 10.1007/s40520-019-01121-w |
format | Article |
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Mild Cognitive Impairment (MCI) has been considered as a prodromal stage of Alzheimer disease (AD). Subtle changes in specific aspects of executive function like inhibitory control have been found in MCI.
Aims
We examined attentional and inhibitory control with the aim to distinguish between amnestic MCI patients and healthy controls.
Method
Using neuropsychological, behavioral, and oculomotor function experiments, we examined executive function in 59 normal control, 49, multiple domain amnestic MCI (a-MCI) subjects, and 21 early stage AD patients using eye tracking and Simon task as measures of attentional control, to determine which saccade and behavioral tasks were sensitive enough to identify a-MCI. Saccades were investigated in gap and overlap pro-saccade and anti-saccade tasks.
Results
Scores on the Simon task were inversely correlated with general cognitive status and can distinguish a-MCI from controls with excellent specificity (AUC = 0.65 for reaction time and 0.59 for false responses). More importantly, our results showed that saccadic gains were affected in a-MCI and were the most sensitive measures to distinguish a-MCI from normal participants AST gap task AUC = 0.7, PST gap task AUC = 0.63, AST overlap task (AUC = 0.73). Moreover, these parameters were strongly correlated with neuropsychological measures. Using tests in parallel model, improved sensitivity up to 0.97.
Conclusion
The present results enable us to suggest eye tracking along with behavioral data as a possible sensitive tools to detect a-MCI in preclinical stage.</description><identifier>ISSN: 1720-8319</identifier><identifier>ISSN: 1594-0667</identifier><identifier>EISSN: 1720-8319</identifier><identifier>DOI: 10.1007/s40520-019-01121-w</identifier><identifier>PMID: 30659514</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Aged ; Aged, 80 and over ; Aging ; Alzheimer Disease - diagnosis ; Alzheimer Disease - physiopathology ; Brain research ; Case-Control Studies ; Cognitive ability ; Cognitive Dysfunction - diagnosis ; Cognitive Dysfunction - physiopathology ; Dementia ; Executive Function - physiology ; Experiments ; Eye movements ; Female ; Geriatrics/Gerontology ; Humans ; Keyboards ; Male ; Medical research ; Medicine ; Medicine & Public Health ; Memory ; Mental disorders ; Mental health ; Middle Aged ; Neuropsychological Tests ; Original Article ; Reaction Time - physiology ; Rehabilitation ; Saccades - physiology</subject><ispartof>Aging clinical and experimental research, 2019-11, Vol.31 (11), p.1591-1600</ispartof><rights>Springer Nature Switzerland AG 2019</rights><rights>Aging Clinical and Experimental Research is a copyright of Springer, (2019). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-c0a1bd0a10f3d83b53e9df57a1dcd7831f84d9434feecfed0dcd350fb721ca1c3</citedby><cites>FETCH-LOGICAL-c375t-c0a1bd0a10f3d83b53e9df57a1dcd7831f84d9434feecfed0dcd350fb721ca1c3</cites><orcidid>0000-0001-8494-9747</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s40520-019-01121-w$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s40520-019-01121-w$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30659514$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chehrehnegar, Negin</creatorcontrib><creatorcontrib>Nejati, Vahid</creatorcontrib><creatorcontrib>Shati, Mohsen</creatorcontrib><creatorcontrib>Esmaeili, Mahdieh</creatorcontrib><creatorcontrib>Rezvani, Zahra</creatorcontrib><creatorcontrib>Haghi, Marjan</creatorcontrib><creatorcontrib>Foroughan, Mahshid</creatorcontrib><title>Behavioral and cognitive markers of mild cognitive impairment: diagnostic value of saccadic eye movements and Simon task</title><title>Aging clinical and experimental research</title><addtitle>Aging Clin Exp Res</addtitle><addtitle>Aging Clin Exp Res</addtitle><description>Background
Mild Cognitive Impairment (MCI) has been considered as a prodromal stage of Alzheimer disease (AD). Subtle changes in specific aspects of executive function like inhibitory control have been found in MCI.
Aims
We examined attentional and inhibitory control with the aim to distinguish between amnestic MCI patients and healthy controls.
Method
Using neuropsychological, behavioral, and oculomotor function experiments, we examined executive function in 59 normal control, 49, multiple domain amnestic MCI (a-MCI) subjects, and 21 early stage AD patients using eye tracking and Simon task as measures of attentional control, to determine which saccade and behavioral tasks were sensitive enough to identify a-MCI. Saccades were investigated in gap and overlap pro-saccade and anti-saccade tasks.
Results
Scores on the Simon task were inversely correlated with general cognitive status and can distinguish a-MCI from controls with excellent specificity (AUC = 0.65 for reaction time and 0.59 for false responses). More importantly, our results showed that saccadic gains were affected in a-MCI and were the most sensitive measures to distinguish a-MCI from normal participants AST gap task AUC = 0.7, PST gap task AUC = 0.63, AST overlap task (AUC = 0.73). Moreover, these parameters were strongly correlated with neuropsychological measures. Using tests in parallel model, improved sensitivity up to 0.97.
Conclusion
The present results enable us to suggest eye tracking along with behavioral data as a possible sensitive tools to detect a-MCI in preclinical stage.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Aging</subject><subject>Alzheimer Disease - diagnosis</subject><subject>Alzheimer Disease - physiopathology</subject><subject>Brain research</subject><subject>Case-Control Studies</subject><subject>Cognitive ability</subject><subject>Cognitive Dysfunction - diagnosis</subject><subject>Cognitive Dysfunction - physiopathology</subject><subject>Dementia</subject><subject>Executive Function - physiology</subject><subject>Experiments</subject><subject>Eye movements</subject><subject>Female</subject><subject>Geriatrics/Gerontology</subject><subject>Humans</subject><subject>Keyboards</subject><subject>Male</subject><subject>Medical research</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Memory</subject><subject>Mental disorders</subject><subject>Mental health</subject><subject>Middle Aged</subject><subject>Neuropsychological Tests</subject><subject>Original Article</subject><subject>Reaction Time - physiology</subject><subject>Rehabilitation</subject><subject>Saccades - physiology</subject><issn>1720-8319</issn><issn>1594-0667</issn><issn>1720-8319</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kctOAyEUhonR2Fp9ARdmEjduRmEYpONOG29JExfqmlA4VNqZocJMa99eevESFy64nfOdHzg_QscEnxOM-UXIMctwikkRB8lIuthBXcJjqE9Jsftr30EHIUwwzkk87KMOxZesYCTvoo8beJNz67wsE1nrRLlxbRs7h6SSfgo-JM4klS1_Z2w1k9ZXUDdXibZyXLvQWJXMZdnCCg9SKaljBJZRxs1hhYa1_LOtXJ00MkwP0Z6RZYCj7dpDr3e3L4OHdPh0_zi4HqaKctakCksy0nHChuo-HTEKhTaMS6KV5vFvpp_rIqe5AVAGNI5hyrAZ8YwoSRTtobON7sy79xZCIyobFJSlrMG1QWSEF5RTynhET_-gE9f6Or5OZHTVYM5yFqlsQynvQvBgxMzb2KylIFisfBEbX0T0Rax9EYtYdLKVbkcV6O-SLyMiQDdAiKl6DP7n7n9kPwErt5tC</recordid><startdate>20191101</startdate><enddate>20191101</enddate><creator>Chehrehnegar, Negin</creator><creator>Nejati, Vahid</creator><creator>Shati, Mohsen</creator><creator>Esmaeili, Mahdieh</creator><creator>Rezvani, Zahra</creator><creator>Haghi, Marjan</creator><creator>Foroughan, Mahshid</creator><general>Springer International Publishing</general><general>Springer Nature B.V</general><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-8494-9747</orcidid></search><sort><creationdate>20191101</creationdate><title>Behavioral and cognitive markers of mild cognitive impairment: diagnostic value of saccadic eye movements and Simon task</title><author>Chehrehnegar, Negin ; Nejati, Vahid ; Shati, Mohsen ; Esmaeili, Mahdieh ; Rezvani, Zahra ; Haghi, Marjan ; Foroughan, Mahshid</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-c0a1bd0a10f3d83b53e9df57a1dcd7831f84d9434feecfed0dcd350fb721ca1c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Aging</topic><topic>Alzheimer Disease - diagnosis</topic><topic>Alzheimer Disease - physiopathology</topic><topic>Brain research</topic><topic>Case-Control Studies</topic><topic>Cognitive ability</topic><topic>Cognitive Dysfunction - diagnosis</topic><topic>Cognitive Dysfunction - physiopathology</topic><topic>Dementia</topic><topic>Executive Function - physiology</topic><topic>Experiments</topic><topic>Eye movements</topic><topic>Female</topic><topic>Geriatrics/Gerontology</topic><topic>Humans</topic><topic>Keyboards</topic><topic>Male</topic><topic>Medical research</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Memory</topic><topic>Mental disorders</topic><topic>Mental health</topic><topic>Middle Aged</topic><topic>Neuropsychological Tests</topic><topic>Original Article</topic><topic>Reaction Time - physiology</topic><topic>Rehabilitation</topic><topic>Saccades - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chehrehnegar, Negin</creatorcontrib><creatorcontrib>Nejati, Vahid</creatorcontrib><creatorcontrib>Shati, Mohsen</creatorcontrib><creatorcontrib>Esmaeili, Mahdieh</creatorcontrib><creatorcontrib>Rezvani, Zahra</creatorcontrib><creatorcontrib>Haghi, Marjan</creatorcontrib><creatorcontrib>Foroughan, Mahshid</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Aging clinical and experimental research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chehrehnegar, Negin</au><au>Nejati, Vahid</au><au>Shati, Mohsen</au><au>Esmaeili, Mahdieh</au><au>Rezvani, Zahra</au><au>Haghi, Marjan</au><au>Foroughan, Mahshid</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Behavioral and cognitive markers of mild cognitive impairment: diagnostic value of saccadic eye movements and Simon task</atitle><jtitle>Aging clinical and experimental research</jtitle><stitle>Aging Clin Exp Res</stitle><addtitle>Aging Clin Exp Res</addtitle><date>2019-11-01</date><risdate>2019</risdate><volume>31</volume><issue>11</issue><spage>1591</spage><epage>1600</epage><pages>1591-1600</pages><issn>1720-8319</issn><issn>1594-0667</issn><eissn>1720-8319</eissn><abstract>Background
Mild Cognitive Impairment (MCI) has been considered as a prodromal stage of Alzheimer disease (AD). Subtle changes in specific aspects of executive function like inhibitory control have been found in MCI.
Aims
We examined attentional and inhibitory control with the aim to distinguish between amnestic MCI patients and healthy controls.
Method
Using neuropsychological, behavioral, and oculomotor function experiments, we examined executive function in 59 normal control, 49, multiple domain amnestic MCI (a-MCI) subjects, and 21 early stage AD patients using eye tracking and Simon task as measures of attentional control, to determine which saccade and behavioral tasks were sensitive enough to identify a-MCI. Saccades were investigated in gap and overlap pro-saccade and anti-saccade tasks.
Results
Scores on the Simon task were inversely correlated with general cognitive status and can distinguish a-MCI from controls with excellent specificity (AUC = 0.65 for reaction time and 0.59 for false responses). More importantly, our results showed that saccadic gains were affected in a-MCI and were the most sensitive measures to distinguish a-MCI from normal participants AST gap task AUC = 0.7, PST gap task AUC = 0.63, AST overlap task (AUC = 0.73). Moreover, these parameters were strongly correlated with neuropsychological measures. Using tests in parallel model, improved sensitivity up to 0.97.
Conclusion
The present results enable us to suggest eye tracking along with behavioral data as a possible sensitive tools to detect a-MCI in preclinical stage.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>30659514</pmid><doi>10.1007/s40520-019-01121-w</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-8494-9747</orcidid></addata></record> |
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subjects | Aged Aged, 80 and over Aging Alzheimer Disease - diagnosis Alzheimer Disease - physiopathology Brain research Case-Control Studies Cognitive ability Cognitive Dysfunction - diagnosis Cognitive Dysfunction - physiopathology Dementia Executive Function - physiology Experiments Eye movements Female Geriatrics/Gerontology Humans Keyboards Male Medical research Medicine Medicine & Public Health Memory Mental disorders Mental health Middle Aged Neuropsychological Tests Original Article Reaction Time - physiology Rehabilitation Saccades - physiology |
title | Behavioral and cognitive markers of mild cognitive impairment: diagnostic value of saccadic eye movements and Simon task |
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