Prediction of dementia in primary care patients

Current approaches for AD prediction are based on biomarkers, which are however of restricted availability in primary care. AD prediction tools for primary care are therefore needed. We present a prediction score based on information that can be obtained in the primary care setting. We performed a l...

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Veröffentlicht in:PloS one 2011-02, Vol.6 (2), p.e16852-e16852
Hauptverfasser: Jessen, Frank, Wiese, Birgitt, Bickel, Horst, Eiffländer-Gorfer, Sandra, Fuchs, Angela, Kaduszkiewicz, Hanna, Köhler, Mirjam, Luck, Tobias, Mösch, Edelgard, Pentzek, Michael, Riedel-Heller, Steffi G, Wagner, Michael, Weyerer, Siegfried, Maier, Wolfgang, van den Bussche, Hendrik
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container_start_page e16852
container_title PloS one
container_volume 6
creator Jessen, Frank
Wiese, Birgitt
Bickel, Horst
Eiffländer-Gorfer, Sandra
Fuchs, Angela
Kaduszkiewicz, Hanna
Köhler, Mirjam
Luck, Tobias
Mösch, Edelgard
Pentzek, Michael
Riedel-Heller, Steffi G
Wagner, Michael
Weyerer, Siegfried
Maier, Wolfgang
van den Bussche, Hendrik
description Current approaches for AD prediction are based on biomarkers, which are however of restricted availability in primary care. AD prediction tools for primary care are therefore needed. We present a prediction score based on information that can be obtained in the primary care setting. We performed a longitudinal cohort study in 3.055 non-demented individuals above 75 years recruited via primary care chart registries (Study on Aging, Cognition and Dementia, AgeCoDe). After the baseline investigation we performed three follow-up investigations at 18 months intervals with incident dementia as the primary outcome. The best set of predictors was extracted from the baseline variables in one randomly selected half of the sample. This set included age, subjective memory impairment, performance on delayed verbal recall and verbal fluency, on the Mini-Mental-State-Examination, and on an instrumental activities of daily living scale. These variables were aggregated to a prediction score, which achieved a prediction accuracy of 0.84 for AD. The score was applied to the second half of the sample (test cohort). Here, the prediction accuracy was 0.79. With a cut-off of at least 80% sensitivity in the first cohort, 79.6% sensitivity, 66.4% specificity, 14.7% positive predictive value (PPV) and 97.8% negative predictive value of (NPV) for AD were achieved in the test cohort. At a cut-off for a high risk population (5% of individuals with the highest risk score in the first cohort) the PPV for AD was 39.1% (52% for any dementia) in the test cohort. The prediction score has useful prediction accuracy. It can define individuals (1) sensitively for low cost-low risk interventions, or (2) more specific and with increased PPV for measures of prevention with greater costs or risks. As it is independent of technical aids, it may be used within large scale prevention programs.
doi_str_mv 10.1371/journal.pone.0016852
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AD prediction tools for primary care are therefore needed. We present a prediction score based on information that can be obtained in the primary care setting. We performed a longitudinal cohort study in 3.055 non-demented individuals above 75 years recruited via primary care chart registries (Study on Aging, Cognition and Dementia, AgeCoDe). After the baseline investigation we performed three follow-up investigations at 18 months intervals with incident dementia as the primary outcome. The best set of predictors was extracted from the baseline variables in one randomly selected half of the sample. This set included age, subjective memory impairment, performance on delayed verbal recall and verbal fluency, on the Mini-Mental-State-Examination, and on an instrumental activities of daily living scale. These variables were aggregated to a prediction score, which achieved a prediction accuracy of 0.84 for AD. The score was applied to the second half of the sample (test cohort). 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Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Meteorological &amp; Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</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>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jessen, Frank</au><au>Wiese, Birgitt</au><au>Bickel, Horst</au><au>Eiffländer-Gorfer, Sandra</au><au>Fuchs, Angela</au><au>Kaduszkiewicz, Hanna</au><au>Köhler, Mirjam</au><au>Luck, Tobias</au><au>Mösch, Edelgard</au><au>Pentzek, Michael</au><au>Riedel-Heller, Steffi G</au><au>Wagner, Michael</au><au>Weyerer, Siegfried</au><au>Maier, Wolfgang</au><au>van den Bussche, Hendrik</au><au>Deli, Maria</au><aucorp>AgeCoDe Study Group</aucorp><aucorp>for the AgeCoDe Study Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prediction of dementia in primary care patients</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2011-02-18</date><risdate>2011</risdate><volume>6</volume><issue>2</issue><spage>e16852</spage><epage>e16852</epage><pages>e16852-e16852</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Current approaches for AD prediction are based on biomarkers, which are however of restricted availability in primary care. AD prediction tools for primary care are therefore needed. We present a prediction score based on information that can be obtained in the primary care setting. We performed a longitudinal cohort study in 3.055 non-demented individuals above 75 years recruited via primary care chart registries (Study on Aging, Cognition and Dementia, AgeCoDe). After the baseline investigation we performed three follow-up investigations at 18 months intervals with incident dementia as the primary outcome. The best set of predictors was extracted from the baseline variables in one randomly selected half of the sample. This set included age, subjective memory impairment, performance on delayed verbal recall and verbal fluency, on the Mini-Mental-State-Examination, and on an instrumental activities of daily living scale. These variables were aggregated to a prediction score, which achieved a prediction accuracy of 0.84 for AD. The score was applied to the second half of the sample (test cohort). Here, the prediction accuracy was 0.79. With a cut-off of at least 80% sensitivity in the first cohort, 79.6% sensitivity, 66.4% specificity, 14.7% positive predictive value (PPV) and 97.8% negative predictive value of (NPV) for AD were achieved in the test cohort. At a cut-off for a high risk population (5% of individuals with the highest risk score in the first cohort) the PPV for AD was 39.1% (52% for any dementia) in the test cohort. The prediction score has useful prediction accuracy. It can define individuals (1) sensitively for low cost-low risk interventions, or (2) more specific and with increased PPV for measures of prevention with greater costs or risks. As it is independent of technical aids, it may be used within large scale prevention programs.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>21364746</pmid><doi>10.1371/journal.pone.0016852</doi><tpages>e16852</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1932-6203
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1932-6203
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subjects Activities of daily living
Advertising executives
Aged
Aged, 80 and over
Aging
Alzheimer's disease
Biomarkers
Cognition
Cognitive ability
Cohort Studies
Costs
Dementia
Dementia - diagnosis
Dementia - genetics
Dementia disorders
Disease prevention
Female
Genotype
Health care
Health Services Accessibility
Humans
Longitudinal Studies
Low cost
Male
Medical diagnosis
Medicine
Memory
Mental health
Neuropsychological Tests
Occupational health
Patients
Predictions
Prevention
Primary care
Primary Health Care - methods
Prognosis
Psychiatry
Risk
Sensitivity
Sensitivity and Specificity
Studies
title Prediction of dementia in primary care patients
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