Validity of current clinical criteria for Alzheimer's disease, vascular dementia and dementia with Lewy bodies
Following the success of the NINCDS-ADRDA criteria for Alzheimer's disease, groups interested in vascular dementia and dementia with Lewy bodies have now adopted similar criteria. To assess whether the validity of these criteria are influenced by the prevalence of mixed pathologies or by the pr...
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Veröffentlicht in: | British journal of psychiatry 1999-01, Vol.174 (1), p.45-50 |
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creator | Holmes, Clive Cairns, Nigel Lantos, Peter L. Mann, Anthony |
description | Following the success of the NINCDS-ADRDA criteria for Alzheimer's disease, groups interested in vascular dementia and dementia with Lewy bodies have now adopted similar criteria.
To assess whether the validity of these criteria are influenced by the prevalence of mixed pathologies or by the prevalence rate.
A community based post-mortem study.
Mixed pathologies were common (33.8%). The high specificities obtained for the CDLB and NINDS-AIREN criteria (1.00 and 0.95, respectively) were associated with low sensitivities (0.22 and 0.43, respectively). Low prevalence and the presence of mixed pathologies had a deleterious effect on positive predictive values.
Current clinical diagnostic criteria are good at detecting pathology per se but not at detecting pure pathology. A large proportion of subjects from the general population fulfilling probable CDLB, probable NINCDS-ADRDA or probable NINDS-AIREN will have mixed pathologies. |
doi_str_mv | 10.1192/bjp.174.1.45 |
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To assess whether the validity of these criteria are influenced by the prevalence of mixed pathologies or by the prevalence rate.
A community based post-mortem study.
Mixed pathologies were common (33.8%). The high specificities obtained for the CDLB and NINDS-AIREN criteria (1.00 and 0.95, respectively) were associated with low sensitivities (0.22 and 0.43, respectively). Low prevalence and the presence of mixed pathologies had a deleterious effect on positive predictive values.
Current clinical diagnostic criteria are good at detecting pathology per se but not at detecting pure pathology. A large proportion of subjects from the general population fulfilling probable CDLB, probable NINCDS-ADRDA or probable NINDS-AIREN will have mixed pathologies.</description><identifier>ISSN: 0007-1250</identifier><identifier>EISSN: 1472-1465</identifier><identifier>DOI: 10.1192/bjp.174.1.45</identifier><identifier>PMID: 10211150</identifier><language>eng</language><publisher>Cambridge, UK: Cambridge University Press</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Alzheimer Disease - pathology ; Alzheimer's disease ; Autopsy ; Dementia ; Dementia disorders ; Dementia, Vascular - pathology ; Female ; Humans ; Lewy bodies ; Lewy Bodies - pathology ; Male ; Middle Aged ; Neurodegenerative diseases ; Pathology ; Predictive Value of Tests ; Sensitivity and Specificity ; Vascular dementia</subject><ispartof>British journal of psychiatry, 1999-01, Vol.174 (1), p.45-50</ispartof><rights>Copyright © 1999 The Royal College of Psychiatrists</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c379t-8082caff71906d2af3bdae05822f8f9c43b112c1e6e2ebd47147dbe5d38b1fe63</citedby><cites>FETCH-LOGICAL-c379t-8082caff71906d2af3bdae05822f8f9c43b112c1e6e2ebd47147dbe5d38b1fe63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.cambridge.org/core/product/identifier/S0007125000152006/type/journal_article$$EHTML$$P50$$Gcambridge$$H</linktohtml><link.rule.ids>164,314,776,780,12826,27903,27904,30978,55606</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10211150$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Holmes, Clive</creatorcontrib><creatorcontrib>Cairns, Nigel</creatorcontrib><creatorcontrib>Lantos, Peter L.</creatorcontrib><creatorcontrib>Mann, Anthony</creatorcontrib><title>Validity of current clinical criteria for Alzheimer's disease, vascular dementia and dementia with Lewy bodies</title><title>British journal of psychiatry</title><addtitle>Br J Psychiatry</addtitle><description>Following the success of the NINCDS-ADRDA criteria for Alzheimer's disease, groups interested in vascular dementia and dementia with Lewy bodies have now adopted similar criteria.
To assess whether the validity of these criteria are influenced by the prevalence of mixed pathologies or by the prevalence rate.
A community based post-mortem study.
Mixed pathologies were common (33.8%). The high specificities obtained for the CDLB and NINDS-AIREN criteria (1.00 and 0.95, respectively) were associated with low sensitivities (0.22 and 0.43, respectively). Low prevalence and the presence of mixed pathologies had a deleterious effect on positive predictive values.
Current clinical diagnostic criteria are good at detecting pathology per se but not at detecting pure pathology. A large proportion of subjects from the general population fulfilling probable CDLB, probable NINCDS-ADRDA or probable NINDS-AIREN will have mixed pathologies.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Alzheimer Disease - pathology</subject><subject>Alzheimer's disease</subject><subject>Autopsy</subject><subject>Dementia</subject><subject>Dementia disorders</subject><subject>Dementia, Vascular - pathology</subject><subject>Female</subject><subject>Humans</subject><subject>Lewy bodies</subject><subject>Lewy Bodies - pathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neurodegenerative diseases</subject><subject>Pathology</subject><subject>Predictive Value of Tests</subject><subject>Sensitivity and Specificity</subject><subject>Vascular dementia</subject><issn>0007-1250</issn><issn>1472-1465</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>7QJ</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptkcuLFDEQxoMo7rh68ywBwb1st6l0utN9XBZXhQEv6jXkUdnO0I8x6d5h_OuNzMAuInUoCn711eMj5C2wEqDjH81uX4IUJZSifkY2ICQvQDT1c7JhjMkCeM0uyKuUdrmsBJcvyQUwDgA125Dppx6CC8uRzp7aNUacFmqHMAWrB2pjWDAGTf0c6c3wu8cwYrxK1IWEOuE1fdDJroOO1OGYWzOqJ_dYHMLS0y0ejtTMLmB6TV54PSR8c86X5Mfdp--3X4rtt89fb2-2ha1ktxQta7nV3kvoWOO49pVxGlndcu5b31lRGQBuARvkaJyQ-WpnsHZVa8BjU12SDyfdfZx_rZgWNYZkcRj0hPOaVNPJ_BvRZfD9P-BuXuOUd1O8artKihyZuj5RNs4pRfRqH8Oo41EBU39dUNkFlV1QoESd8Xdn0dWM6J7Ap7dngJ6APtz3hxBRRbtPR9s_1SjPI_VoYnD3-LjZf4f-AZvInio</recordid><startdate>199901</startdate><enddate>199901</enddate><creator>Holmes, Clive</creator><creator>Cairns, Nigel</creator><creator>Lantos, Peter L.</creator><creator>Mann, Anthony</creator><general>Cambridge University Press</general><general>RCP</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>0-V</scope><scope>3V.</scope><scope>7QJ</scope><scope>7TK</scope><scope>7XB</scope><scope>88G</scope><scope>88J</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ALSLI</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HEHIP</scope><scope>M2M</scope><scope>M2O</scope><scope>M2R</scope><scope>M2S</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>199901</creationdate><title>Validity of current clinical criteria for Alzheimer's disease, vascular dementia and dementia with Lewy bodies</title><author>Holmes, Clive ; 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To assess whether the validity of these criteria are influenced by the prevalence of mixed pathologies or by the prevalence rate.
A community based post-mortem study.
Mixed pathologies were common (33.8%). The high specificities obtained for the CDLB and NINDS-AIREN criteria (1.00 and 0.95, respectively) were associated with low sensitivities (0.22 and 0.43, respectively). Low prevalence and the presence of mixed pathologies had a deleterious effect on positive predictive values.
Current clinical diagnostic criteria are good at detecting pathology per se but not at detecting pure pathology. A large proportion of subjects from the general population fulfilling probable CDLB, probable NINCDS-ADRDA or probable NINDS-AIREN will have mixed pathologies.</abstract><cop>Cambridge, UK</cop><pub>Cambridge University Press</pub><pmid>10211150</pmid><doi>10.1192/bjp.174.1.45</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Aged Aged, 80 and over Alzheimer Disease - pathology Alzheimer's disease Autopsy Dementia Dementia disorders Dementia, Vascular - pathology Female Humans Lewy bodies Lewy Bodies - pathology Male Middle Aged Neurodegenerative diseases Pathology Predictive Value of Tests Sensitivity and Specificity Vascular dementia |
title | Validity of current clinical criteria for Alzheimer's disease, vascular dementia and dementia with Lewy bodies |
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