Correlations between atrophy of the entorhinal cortex and cognitive function in patients with Alzheimer's disease and mild cognitive impairment

Aims In order to confirm the utility of the voxel‐based specific regional analysis system for Alzheimer's disease (VSRAD) in assessing the atrophy of the entorhinal cortex, we investigated whether there were correlations between VSRAD and the scores of neuropsychological tests in the patients w...

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Veröffentlicht in:Psychiatry and clinical neurosciences 2012-12, Vol.66 (7), p.587-593
Hauptverfasser: Li, Xudong, Jiao, Jinsong, Shimizu, Satoru, Jibiki, Itsuki, Watanabe, Ken-ichiro, Kubota, Takashi
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container_title Psychiatry and clinical neurosciences
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creator Li, Xudong
Jiao, Jinsong
Shimizu, Satoru
Jibiki, Itsuki
Watanabe, Ken-ichiro
Kubota, Takashi
description Aims In order to confirm the utility of the voxel‐based specific regional analysis system for Alzheimer's disease (VSRAD) in assessing the atrophy of the entorhinal cortex, we investigated whether there were correlations between VSRAD and the scores of neuropsychological tests in the patients with Alzheimer's disease (AD) and mild cognitive impairment. Methods Thirty patients, including 18 AD and 12 mild cognitive impairment patients, were included in this study. VSRAD was performed to assess the atrophy of the entorhinal cortex. The patients were carefully screened with the neuropsychological tests, including Wechsler Adult Intelligence Scale‐III (WAIS‐III), the Wechsler Memory Scale‐Revised, the Alzheimer's Disease Assessment Scale‐Cognitive Part (ADAS‐cog) and the revised version of Hasegawa's Dementia Scale. Results All patients showed atrophy with different degrees in the entorhinal cortex except one case. Z‐scores had significant positive correlation with ADAS‐cog, and negative correlation with Information subset of WAIS‐III (respectively, P = 0.0129 and P = 0.0294). The revised version of Hasegawa's Dementia Scale and the Similarities subsets of the WAIS‐III had a tendency of negatively correlating with Z‐scores of VSRAD (respectively, P = 0.0532 and P = 0.0635). The Delayed Visual Reproduction subset of the Wechsler Memory Scale‐Revised was also found to have a weak negative correlation with Z‐scores (P = 0.0609). Conclusions Z‐scores of VSRAD were revealed to have a close relation with many neuropsychological tests, especially ADAS‐cog and the Information subset of WAIS‐III. The results meant that VSRAD was a useful indictor of early diagnosis of AD, closely correlating with the changes of cognitive functions and the progression of the disease.
doi_str_mv 10.1111/pcn.12002
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Methods Thirty patients, including 18 AD and 12 mild cognitive impairment patients, were included in this study. VSRAD was performed to assess the atrophy of the entorhinal cortex. The patients were carefully screened with the neuropsychological tests, including Wechsler Adult Intelligence Scale‐III (WAIS‐III), the Wechsler Memory Scale‐Revised, the Alzheimer's Disease Assessment Scale‐Cognitive Part (ADAS‐cog) and the revised version of Hasegawa's Dementia Scale. Results All patients showed atrophy with different degrees in the entorhinal cortex except one case. Z‐scores had significant positive correlation with ADAS‐cog, and negative correlation with Information subset of WAIS‐III (respectively, P = 0.0129 and P = 0.0294). The revised version of Hasegawa's Dementia Scale and the Similarities subsets of the WAIS‐III had a tendency of negatively correlating with Z‐scores of VSRAD (respectively, P = 0.0532 and P = 0.0635). The Delayed Visual Reproduction subset of the Wechsler Memory Scale‐Revised was also found to have a weak negative correlation with Z‐scores (P = 0.0609). Conclusions Z‐scores of VSRAD were revealed to have a close relation with many neuropsychological tests, especially ADAS‐cog and the Information subset of WAIS‐III. The results meant that VSRAD was a useful indictor of early diagnosis of AD, closely correlating with the changes of cognitive functions and the progression of the disease.</description><identifier>ISSN: 1323-1316</identifier><identifier>EISSN: 1440-1819</identifier><identifier>DOI: 10.1111/pcn.12002</identifier><identifier>PMID: 23252925</identifier><language>eng</language><publisher>Richmond: Blackwell Publishing Ltd</publisher><subject>Adult and adolescent clinical studies ; Aged ; Aged, 80 and over ; Alzheimer Disease - pathology ; Alzheimer Disease - psychology ; Alzheimer's disease ; Atrophy ; Atrophy - pathology ; Biological and medical sciences ; Cognition - physiology ; Cognitive ability ; Cognitive Dysfunction - pathology ; Cognitive Dysfunction - psychology ; cognitive function ; Cortex (entorhinal) ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Dementia disorders ; entorhinal cortex ; Entorhinal Cortex - pathology ; Female ; Geriatrics ; Humans ; Intelligence ; Magnetic Resonance Imaging ; Male ; Medical sciences ; Memory ; Middle Aged ; mild cognitive impairment ; Neurodegenerative diseases ; Neurology ; Neuropsychological Tests ; Organic mental disorders. Neuropsychology ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Reproduction ; voxel-based specific regional analysis system for Alzheimer's disease</subject><ispartof>Psychiatry and clinical neurosciences, 2012-12, Vol.66 (7), p.587-593</ispartof><rights>2012 The Authors. Psychiatry and Clinical Neurosciences © 2012 Japanese Society of Psychiatry and Neurology</rights><rights>2015 INIST-CNRS</rights><rights>2012 The Authors. 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Methods Thirty patients, including 18 AD and 12 mild cognitive impairment patients, were included in this study. VSRAD was performed to assess the atrophy of the entorhinal cortex. The patients were carefully screened with the neuropsychological tests, including Wechsler Adult Intelligence Scale‐III (WAIS‐III), the Wechsler Memory Scale‐Revised, the Alzheimer's Disease Assessment Scale‐Cognitive Part (ADAS‐cog) and the revised version of Hasegawa's Dementia Scale. Results All patients showed atrophy with different degrees in the entorhinal cortex except one case. Z‐scores had significant positive correlation with ADAS‐cog, and negative correlation with Information subset of WAIS‐III (respectively, P = 0.0129 and P = 0.0294). The revised version of Hasegawa's Dementia Scale and the Similarities subsets of the WAIS‐III had a tendency of negatively correlating with Z‐scores of VSRAD (respectively, P = 0.0532 and P = 0.0635). The Delayed Visual Reproduction subset of the Wechsler Memory Scale‐Revised was also found to have a weak negative correlation with Z‐scores (P = 0.0609). Conclusions Z‐scores of VSRAD were revealed to have a close relation with many neuropsychological tests, especially ADAS‐cog and the Information subset of WAIS‐III. The results meant that VSRAD was a useful indictor of early diagnosis of AD, closely correlating with the changes of cognitive functions and the progression of the disease.</description><subject>Adult and adolescent clinical studies</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Alzheimer Disease - pathology</subject><subject>Alzheimer Disease - psychology</subject><subject>Alzheimer's disease</subject><subject>Atrophy</subject><subject>Atrophy - pathology</subject><subject>Biological and medical sciences</subject><subject>Cognition - physiology</subject><subject>Cognitive ability</subject><subject>Cognitive Dysfunction - pathology</subject><subject>Cognitive Dysfunction - psychology</subject><subject>cognitive function</subject><subject>Cortex (entorhinal)</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Dementia disorders</subject><subject>entorhinal cortex</subject><subject>Entorhinal Cortex - pathology</subject><subject>Female</subject><subject>Geriatrics</subject><subject>Humans</subject><subject>Intelligence</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Memory</subject><subject>Middle Aged</subject><subject>mild cognitive impairment</subject><subject>Neurodegenerative diseases</subject><subject>Neurology</subject><subject>Neuropsychological Tests</subject><subject>Organic mental disorders. Neuropsychology</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Reproduction</subject><subject>voxel-based specific regional analysis system for Alzheimer's disease</subject><issn>1323-1316</issn><issn>1440-1819</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNks1u1DAUhSMEoqWw4AWQJYRgk9bXTmxnWY2ggEalQgWWlse5IS6JE-yEYXgJXhnPDwWxwhsfy985kn1Plj0GegppnY3WnwKjlN3JjqEoaA4KqrtJc8Zz4CCOsgcx3lBKORdwPztinJWsYuVx9nMxhICdmdzgI1nhtEb0xExhGNsNGRoytUjQT0NonTcdsUOY8Dsxvk7ys3eT-4akmb3dBhDnyZiiEh_J2k0tOe9-tOh6DM8jqV1EE3Hn7V33d4DrR-NCn3wPs3uN6SI-Ouwn2YdXL68Xr_Plu4s3i_Nl7gpesbzgUq0KroxpTA1CrGRRWSVkbcv0NGGlBAMW6tKWqiosWgOVMqqWVKRjXfOT7MU-dwzD1xnjpHsXLXad8TjMUQOTnAmpaPE_KJNUVcAS-vQf9GaYQ_q3LcWrspQKykQ9OVDzqsdaj8H1Jmz076kk4NkBMNGargnGWxf_cEIKUSlI3NmeW7sON7f3QPW2FjrVQu9qoa8WlzuRHPne4WIa463DhC9aSC5L_enyQr-Fpbq6_gj6Pf8FDsy58g</recordid><startdate>201212</startdate><enddate>201212</enddate><creator>Li, Xudong</creator><creator>Jiao, Jinsong</creator><creator>Shimizu, Satoru</creator><creator>Jibiki, Itsuki</creator><creator>Watanabe, Ken-ichiro</creator><creator>Kubota, Takashi</creator><general>Blackwell Publishing Ltd</general><general>Wiley-Blackwell</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7TK</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201212</creationdate><title>Correlations between atrophy of the entorhinal cortex and cognitive function in patients with Alzheimer's disease and mild cognitive impairment</title><author>Li, Xudong ; Jiao, Jinsong ; Shimizu, Satoru ; Jibiki, Itsuki ; Watanabe, Ken-ichiro ; Kubota, Takashi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i4392-4378b438aafad166b749c867dc53256c771a1c1d5c5894ceca198a8d70694cdd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adult and adolescent clinical studies</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Alzheimer Disease - pathology</topic><topic>Alzheimer Disease - psychology</topic><topic>Alzheimer's disease</topic><topic>Atrophy</topic><topic>Atrophy - pathology</topic><topic>Biological and medical sciences</topic><topic>Cognition - physiology</topic><topic>Cognitive ability</topic><topic>Cognitive Dysfunction - pathology</topic><topic>Cognitive Dysfunction - psychology</topic><topic>cognitive function</topic><topic>Cortex (entorhinal)</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Dementia disorders</topic><topic>entorhinal cortex</topic><topic>Entorhinal Cortex - pathology</topic><topic>Female</topic><topic>Geriatrics</topic><topic>Humans</topic><topic>Intelligence</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Memory</topic><topic>Middle Aged</topic><topic>mild cognitive impairment</topic><topic>Neurodegenerative diseases</topic><topic>Neurology</topic><topic>Neuropsychological Tests</topic><topic>Organic mental disorders. Neuropsychology</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Reproduction</topic><topic>voxel-based specific regional analysis system for Alzheimer's disease</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Xudong</creatorcontrib><creatorcontrib>Jiao, Jinsong</creatorcontrib><creatorcontrib>Shimizu, Satoru</creatorcontrib><creatorcontrib>Jibiki, Itsuki</creatorcontrib><creatorcontrib>Watanabe, Ken-ichiro</creatorcontrib><creatorcontrib>Kubota, Takashi</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Psychiatry and clinical neurosciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Xudong</au><au>Jiao, Jinsong</au><au>Shimizu, Satoru</au><au>Jibiki, Itsuki</au><au>Watanabe, Ken-ichiro</au><au>Kubota, Takashi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Correlations between atrophy of the entorhinal cortex and cognitive function in patients with Alzheimer's disease and mild cognitive impairment</atitle><jtitle>Psychiatry and clinical neurosciences</jtitle><addtitle>Psychiatry Clin Neurosci</addtitle><date>2012-12</date><risdate>2012</risdate><volume>66</volume><issue>7</issue><spage>587</spage><epage>593</epage><pages>587-593</pages><issn>1323-1316</issn><eissn>1440-1819</eissn><abstract>Aims In order to confirm the utility of the voxel‐based specific regional analysis system for Alzheimer's disease (VSRAD) in assessing the atrophy of the entorhinal cortex, we investigated whether there were correlations between VSRAD and the scores of neuropsychological tests in the patients with Alzheimer's disease (AD) and mild cognitive impairment. Methods Thirty patients, including 18 AD and 12 mild cognitive impairment patients, were included in this study. VSRAD was performed to assess the atrophy of the entorhinal cortex. The patients were carefully screened with the neuropsychological tests, including Wechsler Adult Intelligence Scale‐III (WAIS‐III), the Wechsler Memory Scale‐Revised, the Alzheimer's Disease Assessment Scale‐Cognitive Part (ADAS‐cog) and the revised version of Hasegawa's Dementia Scale. Results All patients showed atrophy with different degrees in the entorhinal cortex except one case. Z‐scores had significant positive correlation with ADAS‐cog, and negative correlation with Information subset of WAIS‐III (respectively, P = 0.0129 and P = 0.0294). The revised version of Hasegawa's Dementia Scale and the Similarities subsets of the WAIS‐III had a tendency of negatively correlating with Z‐scores of VSRAD (respectively, P = 0.0532 and P = 0.0635). The Delayed Visual Reproduction subset of the Wechsler Memory Scale‐Revised was also found to have a weak negative correlation with Z‐scores (P = 0.0609). Conclusions Z‐scores of VSRAD were revealed to have a close relation with many neuropsychological tests, especially ADAS‐cog and the Information subset of WAIS‐III. The results meant that VSRAD was a useful indictor of early diagnosis of AD, closely correlating with the changes of cognitive functions and the progression of the disease.</abstract><cop>Richmond</cop><pub>Blackwell Publishing Ltd</pub><pmid>23252925</pmid><doi>10.1111/pcn.12002</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Freely Accessible Japanese Titles; Wiley Online Library Journals Frontfile Complete; Wiley Online Library Free Content; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Adult and adolescent clinical studies
Aged
Aged, 80 and over
Alzheimer Disease - pathology
Alzheimer Disease - psychology
Alzheimer's disease
Atrophy
Atrophy - pathology
Biological and medical sciences
Cognition - physiology
Cognitive ability
Cognitive Dysfunction - pathology
Cognitive Dysfunction - psychology
cognitive function
Cortex (entorhinal)
Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
Dementia disorders
entorhinal cortex
Entorhinal Cortex - pathology
Female
Geriatrics
Humans
Intelligence
Magnetic Resonance Imaging
Male
Medical sciences
Memory
Middle Aged
mild cognitive impairment
Neurodegenerative diseases
Neurology
Neuropsychological Tests
Organic mental disorders. Neuropsychology
Psychology. Psychoanalysis. Psychiatry
Psychopathology. Psychiatry
Reproduction
voxel-based specific regional analysis system for Alzheimer's disease
title Correlations between atrophy of the entorhinal cortex and cognitive function in patients with Alzheimer's disease and mild cognitive impairment
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