Predictive validity and diagnostic stability of mild cognitive impairment subtypes

Abstract Background Mild cognitive impairment (MCI) is subclassified into four subtypes by the presence of impairment in the memory domain (amnestic vs nonamnestic) and the number of impaired cognitive domains (single vs multiple). However, predictive validity for outcomes of these criteria and the...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Alzheimer's & dementia 2012-11, Vol.8 (6), p.553-559
Hauptverfasser: Han, Ji Won, Kim, Tae Hui, Lee, Seok Bum, Park, Joon Hyuk, Lee, Jung Jae, Huh, Yoonseok, Park, Jee Eun, Jhoo, Jin Hyeong, Lee, Dong Young, Kim, Ki Woong
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 559
container_issue 6
container_start_page 553
container_title Alzheimer's & dementia
container_volume 8
creator Han, Ji Won
Kim, Tae Hui
Lee, Seok Bum
Park, Joon Hyuk
Lee, Jung Jae
Huh, Yoonseok
Park, Jee Eun
Jhoo, Jin Hyeong
Lee, Dong Young
Kim, Ki Woong
description Abstract Background Mild cognitive impairment (MCI) is subclassified into four subtypes by the presence of impairment in the memory domain (amnestic vs nonamnestic) and the number of impaired cognitive domains (single vs multiple). However, predictive validity for outcomes of these criteria and the diagnostic stability of the subtypes are questionable. Methods We investigated the outcomes of 140 patients with MCI who participated in the baseline study of the Korean Longitudinal Study on Health and Aging and completed the 18-month follow-up evaluation (mean duration of follow-up = 1.57 ± 0.24 years). We evaluated the predictive validity of the criteria using multinomial logistic regression analyses, and the diagnostic stability of MCI subtypes using annual conversion rates between subtypes. Results Compared with the single-domain type (MCIs), the multiple-domain type (MCIm) had a lower chance of reversion to normal cognition (MCIm = 10.94%, MCIs = 43.42%) and higher risk of conversion to dementia (MCIm = 23.44%, MCIs = 5.26%). The difference in the reversion rate between the multiple- and single-domain type was statistically significant (odds ratio = 0.233, 95% confidence interval = 0.070–0.771, P = .017). However, neither the chance of reversion nor the risk of conversion was different between amnestic and nonamnestic subtypes. Among the 81 participants who neither converted to dementia nor reverted to normal cognition, 39 converted to different subtype (annual conversion rate = 17.74%). Conclusions The number of impaired cognitive domains, but not the presence of memory impairment, predicted poor outcomes in people with MCI. However, MCI subtype was diagnostically unstable.
doi_str_mv 10.1016/j.jalz.2011.08.007
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1323338906</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>1_s2_0_S1552526011029815</els_id><sourcerecordid>1272717307</sourcerecordid><originalsourceid>FETCH-LOGICAL-c6017-5e487d53f7bb04307918489a7c3a331677cc53879a02a15666c865aadd0a16e83</originalsourceid><addsrcrecordid>eNqNkktv1DAUhS0Eog_4AyxQlmwmXNvxIxJCGlVQqEYC8diwsRzbUzk4yWAng8Kvx2lKFywoG9uyv3vulc9B6BmGEgPmL9uy1eFXSQDjEmQJIB6gU8wY2TAi6od3Zw4n6CylFqACidljdEIoBoIJO0WfPkZnvRn90RVHHbz141zo3hbW6-t-SKM3RRp148PyMOyLzgdbmOG69zc1vjtoHzvXj0WamnE-uPQEPdrrkNzT2_0cfX375svFu83uw-X7i-1uYzhgsWGuksIyuhdNAxUFUWNZyVoLQzWlmAthDKNS1BqIxoxzbiRnWlsLGnMn6Tl6seoe4vBjcmlUnU_GhaB7N0xJYUoopbIGfj9KBBFY5CHuRzEhnFSZzyhZUROHlKLbq0P0nY6zwqAWh1SrFofU4pACqeBG__mt_tR0zt6V_LEkA9sV-OmDm_9DUm13366u8rLcgVybvFo1XP7_o3dRJeNdb7LV0ZlR2cH_e8bXf5Wb4HtvdPjuZpfaYYp9dlZhlYgC9XnJ2RKz3J7UOWH0NzUgyQ0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1122624727</pqid></control><display><type>article</type><title>Predictive validity and diagnostic stability of mild cognitive impairment subtypes</title><source>Applied Social Sciences Index &amp; Abstracts (ASSIA)</source><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Han, Ji Won ; Kim, Tae Hui ; Lee, Seok Bum ; Park, Joon Hyuk ; Lee, Jung Jae ; Huh, Yoonseok ; Park, Jee Eun ; Jhoo, Jin Hyeong ; Lee, Dong Young ; Kim, Ki Woong</creator><creatorcontrib>Han, Ji Won ; Kim, Tae Hui ; Lee, Seok Bum ; Park, Joon Hyuk ; Lee, Jung Jae ; Huh, Yoonseok ; Park, Jee Eun ; Jhoo, Jin Hyeong ; Lee, Dong Young ; Kim, Ki Woong</creatorcontrib><description>Abstract Background Mild cognitive impairment (MCI) is subclassified into four subtypes by the presence of impairment in the memory domain (amnestic vs nonamnestic) and the number of impaired cognitive domains (single vs multiple). However, predictive validity for outcomes of these criteria and the diagnostic stability of the subtypes are questionable. Methods We investigated the outcomes of 140 patients with MCI who participated in the baseline study of the Korean Longitudinal Study on Health and Aging and completed the 18-month follow-up evaluation (mean duration of follow-up = 1.57 ± 0.24 years). We evaluated the predictive validity of the criteria using multinomial logistic regression analyses, and the diagnostic stability of MCI subtypes using annual conversion rates between subtypes. Results Compared with the single-domain type (MCIs), the multiple-domain type (MCIm) had a lower chance of reversion to normal cognition (MCIm = 10.94%, MCIs = 43.42%) and higher risk of conversion to dementia (MCIm = 23.44%, MCIs = 5.26%). The difference in the reversion rate between the multiple- and single-domain type was statistically significant (odds ratio = 0.233, 95% confidence interval = 0.070–0.771, P = .017). However, neither the chance of reversion nor the risk of conversion was different between amnestic and nonamnestic subtypes. Among the 81 participants who neither converted to dementia nor reverted to normal cognition, 39 converted to different subtype (annual conversion rate = 17.74%). Conclusions The number of impaired cognitive domains, but not the presence of memory impairment, predicted poor outcomes in people with MCI. However, MCI subtype was diagnostically unstable.</description><identifier>ISSN: 1552-5260</identifier><identifier>EISSN: 1552-5279</identifier><identifier>DOI: 10.1016/j.jalz.2011.08.007</identifier><identifier>PMID: 23102125</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Aged ; Aging ; Alzheimer's disease ; Baseline studies ; Cognition ; Cognitive ability ; Cognitive Dysfunction - classification ; Cognitive Dysfunction - diagnosis ; Cohort studies ; Conversion ; Dementia ; Dementia disorders ; Diagnostic stability ; Female ; Follow-Up Studies ; Humans ; Male ; Memory ; Mild cognitive impairment subtypes ; Neurodegenerative diseases ; Neurology ; Predictive validity ; Predictive Value of Tests ; Regression analysis ; Reversion ; Reversion to normal ; Risk factors ; Statistical analysis ; Subtypes</subject><ispartof>Alzheimer's &amp; dementia, 2012-11, Vol.8 (6), p.553-559</ispartof><rights>The Alzheimer's Association</rights><rights>2012 The Alzheimer's Association</rights><rights>Copyright © 2012 The Alzheimer's Association. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6017-5e487d53f7bb04307918489a7c3a331677cc53879a02a15666c865aadd0a16e83</citedby><cites>FETCH-LOGICAL-c6017-5e487d53f7bb04307918489a7c3a331677cc53879a02a15666c865aadd0a16e83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1016%2Fj.jalz.2011.08.007$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1016%2Fj.jalz.2011.08.007$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,30979,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23102125$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Han, Ji Won</creatorcontrib><creatorcontrib>Kim, Tae Hui</creatorcontrib><creatorcontrib>Lee, Seok Bum</creatorcontrib><creatorcontrib>Park, Joon Hyuk</creatorcontrib><creatorcontrib>Lee, Jung Jae</creatorcontrib><creatorcontrib>Huh, Yoonseok</creatorcontrib><creatorcontrib>Park, Jee Eun</creatorcontrib><creatorcontrib>Jhoo, Jin Hyeong</creatorcontrib><creatorcontrib>Lee, Dong Young</creatorcontrib><creatorcontrib>Kim, Ki Woong</creatorcontrib><title>Predictive validity and diagnostic stability of mild cognitive impairment subtypes</title><title>Alzheimer's &amp; dementia</title><addtitle>Alzheimers Dement</addtitle><description>Abstract Background Mild cognitive impairment (MCI) is subclassified into four subtypes by the presence of impairment in the memory domain (amnestic vs nonamnestic) and the number of impaired cognitive domains (single vs multiple). However, predictive validity for outcomes of these criteria and the diagnostic stability of the subtypes are questionable. Methods We investigated the outcomes of 140 patients with MCI who participated in the baseline study of the Korean Longitudinal Study on Health and Aging and completed the 18-month follow-up evaluation (mean duration of follow-up = 1.57 ± 0.24 years). We evaluated the predictive validity of the criteria using multinomial logistic regression analyses, and the diagnostic stability of MCI subtypes using annual conversion rates between subtypes. Results Compared with the single-domain type (MCIs), the multiple-domain type (MCIm) had a lower chance of reversion to normal cognition (MCIm = 10.94%, MCIs = 43.42%) and higher risk of conversion to dementia (MCIm = 23.44%, MCIs = 5.26%). The difference in the reversion rate between the multiple- and single-domain type was statistically significant (odds ratio = 0.233, 95% confidence interval = 0.070–0.771, P = .017). However, neither the chance of reversion nor the risk of conversion was different between amnestic and nonamnestic subtypes. Among the 81 participants who neither converted to dementia nor reverted to normal cognition, 39 converted to different subtype (annual conversion rate = 17.74%). Conclusions The number of impaired cognitive domains, but not the presence of memory impairment, predicted poor outcomes in people with MCI. However, MCI subtype was diagnostically unstable.</description><subject>Aged</subject><subject>Aging</subject><subject>Alzheimer's disease</subject><subject>Baseline studies</subject><subject>Cognition</subject><subject>Cognitive ability</subject><subject>Cognitive Dysfunction - classification</subject><subject>Cognitive Dysfunction - diagnosis</subject><subject>Cohort studies</subject><subject>Conversion</subject><subject>Dementia</subject><subject>Dementia disorders</subject><subject>Diagnostic stability</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Male</subject><subject>Memory</subject><subject>Mild cognitive impairment subtypes</subject><subject>Neurodegenerative diseases</subject><subject>Neurology</subject><subject>Predictive validity</subject><subject>Predictive Value of Tests</subject><subject>Regression analysis</subject><subject>Reversion</subject><subject>Reversion to normal</subject><subject>Risk factors</subject><subject>Statistical analysis</subject><subject>Subtypes</subject><issn>1552-5260</issn><issn>1552-5279</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>7QJ</sourceid><recordid>eNqNkktv1DAUhS0Eog_4AyxQlmwmXNvxIxJCGlVQqEYC8diwsRzbUzk4yWAng8Kvx2lKFywoG9uyv3vulc9B6BmGEgPmL9uy1eFXSQDjEmQJIB6gU8wY2TAi6od3Zw4n6CylFqACidljdEIoBoIJO0WfPkZnvRn90RVHHbz141zo3hbW6-t-SKM3RRp148PyMOyLzgdbmOG69zc1vjtoHzvXj0WamnE-uPQEPdrrkNzT2_0cfX375svFu83uw-X7i-1uYzhgsWGuksIyuhdNAxUFUWNZyVoLQzWlmAthDKNS1BqIxoxzbiRnWlsLGnMn6Tl6seoe4vBjcmlUnU_GhaB7N0xJYUoopbIGfj9KBBFY5CHuRzEhnFSZzyhZUROHlKLbq0P0nY6zwqAWh1SrFofU4pACqeBG__mt_tR0zt6V_LEkA9sV-OmDm_9DUm13366u8rLcgVybvFo1XP7_o3dRJeNdb7LV0ZlR2cH_e8bXf5Wb4HtvdPjuZpfaYYp9dlZhlYgC9XnJ2RKz3J7UOWH0NzUgyQ0</recordid><startdate>201211</startdate><enddate>201211</enddate><creator>Han, Ji Won</creator><creator>Kim, Tae Hui</creator><creator>Lee, Seok Bum</creator><creator>Park, Joon Hyuk</creator><creator>Lee, Jung Jae</creator><creator>Huh, Yoonseok</creator><creator>Park, Jee Eun</creator><creator>Jhoo, Jin Hyeong</creator><creator>Lee, Dong Young</creator><creator>Kim, Ki Woong</creator><general>Elsevier Inc</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>7X8</scope><scope>7TK</scope><scope>7QJ</scope></search><sort><creationdate>201211</creationdate><title>Predictive validity and diagnostic stability of mild cognitive impairment subtypes</title><author>Han, Ji Won ; Kim, Tae Hui ; Lee, Seok Bum ; Park, Joon Hyuk ; Lee, Jung Jae ; Huh, Yoonseok ; Park, Jee Eun ; Jhoo, Jin Hyeong ; Lee, Dong Young ; Kim, Ki Woong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6017-5e487d53f7bb04307918489a7c3a331677cc53879a02a15666c865aadd0a16e83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Aged</topic><topic>Aging</topic><topic>Alzheimer's disease</topic><topic>Baseline studies</topic><topic>Cognition</topic><topic>Cognitive ability</topic><topic>Cognitive Dysfunction - classification</topic><topic>Cognitive Dysfunction - diagnosis</topic><topic>Cohort studies</topic><topic>Conversion</topic><topic>Dementia</topic><topic>Dementia disorders</topic><topic>Diagnostic stability</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Male</topic><topic>Memory</topic><topic>Mild cognitive impairment subtypes</topic><topic>Neurodegenerative diseases</topic><topic>Neurology</topic><topic>Predictive validity</topic><topic>Predictive Value of Tests</topic><topic>Regression analysis</topic><topic>Reversion</topic><topic>Reversion to normal</topic><topic>Risk factors</topic><topic>Statistical analysis</topic><topic>Subtypes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Han, Ji Won</creatorcontrib><creatorcontrib>Kim, Tae Hui</creatorcontrib><creatorcontrib>Lee, Seok Bum</creatorcontrib><creatorcontrib>Park, Joon Hyuk</creatorcontrib><creatorcontrib>Lee, Jung Jae</creatorcontrib><creatorcontrib>Huh, Yoonseok</creatorcontrib><creatorcontrib>Park, Jee Eun</creatorcontrib><creatorcontrib>Jhoo, Jin Hyeong</creatorcontrib><creatorcontrib>Lee, Dong Young</creatorcontrib><creatorcontrib>Kim, Ki Woong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><collection>Applied Social Sciences Index &amp; Abstracts (ASSIA)</collection><jtitle>Alzheimer's &amp; dementia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Han, Ji Won</au><au>Kim, Tae Hui</au><au>Lee, Seok Bum</au><au>Park, Joon Hyuk</au><au>Lee, Jung Jae</au><au>Huh, Yoonseok</au><au>Park, Jee Eun</au><au>Jhoo, Jin Hyeong</au><au>Lee, Dong Young</au><au>Kim, Ki Woong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Predictive validity and diagnostic stability of mild cognitive impairment subtypes</atitle><jtitle>Alzheimer's &amp; dementia</jtitle><addtitle>Alzheimers Dement</addtitle><date>2012-11</date><risdate>2012</risdate><volume>8</volume><issue>6</issue><spage>553</spage><epage>559</epage><pages>553-559</pages><issn>1552-5260</issn><eissn>1552-5279</eissn><abstract>Abstract Background Mild cognitive impairment (MCI) is subclassified into four subtypes by the presence of impairment in the memory domain (amnestic vs nonamnestic) and the number of impaired cognitive domains (single vs multiple). However, predictive validity for outcomes of these criteria and the diagnostic stability of the subtypes are questionable. Methods We investigated the outcomes of 140 patients with MCI who participated in the baseline study of the Korean Longitudinal Study on Health and Aging and completed the 18-month follow-up evaluation (mean duration of follow-up = 1.57 ± 0.24 years). We evaluated the predictive validity of the criteria using multinomial logistic regression analyses, and the diagnostic stability of MCI subtypes using annual conversion rates between subtypes. Results Compared with the single-domain type (MCIs), the multiple-domain type (MCIm) had a lower chance of reversion to normal cognition (MCIm = 10.94%, MCIs = 43.42%) and higher risk of conversion to dementia (MCIm = 23.44%, MCIs = 5.26%). The difference in the reversion rate between the multiple- and single-domain type was statistically significant (odds ratio = 0.233, 95% confidence interval = 0.070–0.771, P = .017). However, neither the chance of reversion nor the risk of conversion was different between amnestic and nonamnestic subtypes. Among the 81 participants who neither converted to dementia nor reverted to normal cognition, 39 converted to different subtype (annual conversion rate = 17.74%). Conclusions The number of impaired cognitive domains, but not the presence of memory impairment, predicted poor outcomes in people with MCI. However, MCI subtype was diagnostically unstable.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>23102125</pmid><doi>10.1016/j.jalz.2011.08.007</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1552-5260
ispartof Alzheimer's & dementia, 2012-11, Vol.8 (6), p.553-559
issn 1552-5260
1552-5279
language eng
recordid cdi_proquest_miscellaneous_1323338906
source Applied Social Sciences Index & Abstracts (ASSIA); MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Aged
Aging
Alzheimer's disease
Baseline studies
Cognition
Cognitive ability
Cognitive Dysfunction - classification
Cognitive Dysfunction - diagnosis
Cohort studies
Conversion
Dementia
Dementia disorders
Diagnostic stability
Female
Follow-Up Studies
Humans
Male
Memory
Mild cognitive impairment subtypes
Neurodegenerative diseases
Neurology
Predictive validity
Predictive Value of Tests
Regression analysis
Reversion
Reversion to normal
Risk factors
Statistical analysis
Subtypes
title Predictive validity and diagnostic stability of mild cognitive impairment subtypes
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T04%3A20%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Predictive%20validity%20and%20diagnostic%20stability%20of%20mild%20cognitive%20impairment%20subtypes&rft.jtitle=Alzheimer's%20&%20dementia&rft.au=Han,%20Ji%20Won&rft.date=2012-11&rft.volume=8&rft.issue=6&rft.spage=553&rft.epage=559&rft.pages=553-559&rft.issn=1552-5260&rft.eissn=1552-5279&rft_id=info:doi/10.1016/j.jalz.2011.08.007&rft_dat=%3Cproquest_cross%3E1272717307%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1122624727&rft_id=info:pmid/23102125&rft_els_id=1_s2_0_S1552526011029815&rfr_iscdi=true