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...
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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 |
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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 & 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 & 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 & Abstracts (ASSIA)</collection><jtitle>Alzheimer's & 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 & 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> |
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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 |
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