Does the Addenbrooke's Cognitive Examination-revised add to the Mini-Mental State Examination in established Alzheimer disease? Results from a national dementia research register

Objective To evaluate how much the Addenbrooke's Cognitive Examination‐revised (ACE‐R) improves the estimate of cognitive ability from the Mini‐Mental State Examination (MMSE) in people with Alzheimer disease (AD). Methods We examined itemized data in people with AD who were on the Scottish Dem...

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Veröffentlicht in:International journal of geriatric psychiatry 2013-04, Vol.28 (4), p.351-355
Hauptverfasser: Law, Emma, Connelly, Peter J., Randall, Emma, McNeill, Catriona, Fox, Helen C., Parra, Mario A., Hudson, Justine, Whyte, Leigh-Ann, Johnstone, Jane, Gray, Sarah, Starr, John M.
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container_issue 4
container_start_page 351
container_title International journal of geriatric psychiatry
container_volume 28
creator Law, Emma
Connelly, Peter J.
Randall, Emma
McNeill, Catriona
Fox, Helen C.
Parra, Mario A.
Hudson, Justine
Whyte, Leigh-Ann
Johnstone, Jane
Gray, Sarah
Starr, John M.
description Objective To evaluate how much the Addenbrooke's Cognitive Examination‐revised (ACE‐R) improves the estimate of cognitive ability from the Mini‐Mental State Examination (MMSE) in people with Alzheimer disease (AD). Methods We examined itemized data in people with AD who were on the Scottish Dementia Research Interest Register drawn from eight centres across Scotland, covering 75% of the Scottish population. ACE‐R items that comprise the MMSE and those that did not (non‐MMSE items) were summed separately. We residualized MMSE total on non‐MMSE total and vice versa to derive a measure of the variance unique to each. Results Five hundred and one (258 male, 243 female) participants, mean age 75.7 (range 52–94) years were on the register, of whom 329 (160 men, 169 women) had AD. Of those with AD, 309 had a mean MMSE of 20.5 and mean ACE‐R of 57.5 measured with Pearson r = 0.92 between MMSE and ACE‐R totals, and the regression equation ACE‐R score = 3.0 × MMSE − 4.1. The unique non‐MMSE items score correlated with ACE‐R total r = 0.40 (16% of ACE‐R variance). Conclusions The ACE‐R and MMSE total scores are highly correlated. In this clinical sample of people with established AD, for an MMSE score of 24, the predicted ACE‐R score was 67.9 with 95% confidence intervals of 61.6–75.4. The extra non‐MMSE ACE‐R items improve estimates of cognitive ability by 16%. Copyright © 2012 John Wiley & Sons, Ltd.
doi_str_mv 10.1002/gps.3828
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Results from a national dementia research register</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Law, Emma ; Connelly, Peter J. ; Randall, Emma ; McNeill, Catriona ; Fox, Helen C. ; Parra, Mario A. ; Hudson, Justine ; Whyte, Leigh-Ann ; Johnstone, Jane ; Gray, Sarah ; Starr, John M.</creator><creatorcontrib>Law, Emma ; Connelly, Peter J. ; Randall, Emma ; McNeill, Catriona ; Fox, Helen C. ; Parra, Mario A. ; Hudson, Justine ; Whyte, Leigh-Ann ; Johnstone, Jane ; Gray, Sarah ; Starr, John M.</creatorcontrib><description>Objective To evaluate how much the Addenbrooke's Cognitive Examination‐revised (ACE‐R) improves the estimate of cognitive ability from the Mini‐Mental State Examination (MMSE) in people with Alzheimer disease (AD). Methods We examined itemized data in people with AD who were on the Scottish Dementia Research Interest Register drawn from eight centres across Scotland, covering 75% of the Scottish population. ACE‐R items that comprise the MMSE and those that did not (non‐MMSE items) were summed separately. We residualized MMSE total on non‐MMSE total and vice versa to derive a measure of the variance unique to each. Results Five hundred and one (258 male, 243 female) participants, mean age 75.7 (range 52–94) years were on the register, of whom 329 (160 men, 169 women) had AD. Of those with AD, 309 had a mean MMSE of 20.5 and mean ACE‐R of 57.5 measured with Pearson r = 0.92 between MMSE and ACE‐R totals, and the regression equation ACE‐R score = 3.0 × MMSE − 4.1. The unique non‐MMSE items score correlated with ACE‐R total r = 0.40 (16% of ACE‐R variance). Conclusions The ACE‐R and MMSE total scores are highly correlated. In this clinical sample of people with established AD, for an MMSE score of 24, the predicted ACE‐R score was 67.9 with 95% confidence intervals of 61.6–75.4. The extra non‐MMSE ACE‐R items improve estimates of cognitive ability by 16%. 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Results from a national dementia research register</title><title>International journal of geriatric psychiatry</title><addtitle>Int J Geriatr Psychiatry</addtitle><description>Objective To evaluate how much the Addenbrooke's Cognitive Examination‐revised (ACE‐R) improves the estimate of cognitive ability from the Mini‐Mental State Examination (MMSE) in people with Alzheimer disease (AD). Methods We examined itemized data in people with AD who were on the Scottish Dementia Research Interest Register drawn from eight centres across Scotland, covering 75% of the Scottish population. ACE‐R items that comprise the MMSE and those that did not (non‐MMSE items) were summed separately. We residualized MMSE total on non‐MMSE total and vice versa to derive a measure of the variance unique to each. Results Five hundred and one (258 male, 243 female) participants, mean age 75.7 (range 52–94) years were on the register, of whom 329 (160 men, 169 women) had AD. Of those with AD, 309 had a mean MMSE of 20.5 and mean ACE‐R of 57.5 measured with Pearson r = 0.92 between MMSE and ACE‐R totals, and the regression equation ACE‐R score = 3.0 × MMSE − 4.1. The unique non‐MMSE items score correlated with ACE‐R total r = 0.40 (16% of ACE‐R variance). Conclusions The ACE‐R and MMSE total scores are highly correlated. In this clinical sample of people with established AD, for an MMSE score of 24, the predicted ACE‐R score was 67.9 with 95% confidence intervals of 61.6–75.4. The extra non‐MMSE ACE‐R items improve estimates of cognitive ability by 16%. Copyright © 2012 John Wiley &amp; Sons, Ltd.</description><subject>Ability tests</subject><subject>Age</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Alzheimer disease</subject><subject>Alzheimer Disease - diagnosis</subject><subject>Alzheimer Disease - psychology</subject><subject>Alzheimer's disease</subject><subject>Biological and medical sciences</subject><subject>Brief Psychiatric Rating Scale</subject><subject>cognition</subject><subject>Cognition - physiology</subject><subject>Cognitive ability</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Dementia</subject><subject>Female</subject><subject>General aspects</subject><subject>Geriatric psychiatry</subject><subject>Geriatrics</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neurology</subject><subject>Neuropsychological Tests</subject><subject>Predictive Value of Tests</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. 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Results from a national dementia research register</title><author>Law, Emma ; Connelly, Peter J. ; Randall, Emma ; McNeill, Catriona ; Fox, Helen C. ; Parra, Mario A. ; Hudson, Justine ; Whyte, Leigh-Ann ; Johnstone, Jane ; Gray, Sarah ; Starr, John M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6568-dadbaf1a095b438ba020171d02ffeb8bbc8c43ad05a06c258e55bf4772987ac03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Ability tests</topic><topic>Age</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Alzheimer disease</topic><topic>Alzheimer Disease - diagnosis</topic><topic>Alzheimer Disease - psychology</topic><topic>Alzheimer's disease</topic><topic>Biological and medical sciences</topic><topic>Brief Psychiatric Rating Scale</topic><topic>cognition</topic><topic>Cognition - physiology</topic><topic>Cognitive ability</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Dementia</topic><topic>Female</topic><topic>General aspects</topic><topic>Geriatric psychiatry</topic><topic>Geriatrics</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neurology</topic><topic>Neuropsychological Tests</topic><topic>Predictive Value of Tests</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Regression analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Law, Emma</creatorcontrib><creatorcontrib>Connelly, Peter J.</creatorcontrib><creatorcontrib>Randall, Emma</creatorcontrib><creatorcontrib>McNeill, Catriona</creatorcontrib><creatorcontrib>Fox, Helen C.</creatorcontrib><creatorcontrib>Parra, Mario A.</creatorcontrib><creatorcontrib>Hudson, Justine</creatorcontrib><creatorcontrib>Whyte, Leigh-Ann</creatorcontrib><creatorcontrib>Johnstone, Jane</creatorcontrib><creatorcontrib>Gray, Sarah</creatorcontrib><creatorcontrib>Starr, John M.</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>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of geriatric psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Law, Emma</au><au>Connelly, Peter J.</au><au>Randall, Emma</au><au>McNeill, Catriona</au><au>Fox, Helen C.</au><au>Parra, Mario A.</au><au>Hudson, Justine</au><au>Whyte, Leigh-Ann</au><au>Johnstone, Jane</au><au>Gray, Sarah</au><au>Starr, John M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Does the Addenbrooke's Cognitive Examination-revised add to the Mini-Mental State Examination in established Alzheimer disease? Results from a national dementia research register</atitle><jtitle>International journal of geriatric psychiatry</jtitle><addtitle>Int J Geriatr Psychiatry</addtitle><date>2013-04</date><risdate>2013</risdate><volume>28</volume><issue>4</issue><spage>351</spage><epage>355</epage><pages>351-355</pages><issn>0885-6230</issn><eissn>1099-1166</eissn><coden>IJGPES</coden><abstract>Objective To evaluate how much the Addenbrooke's Cognitive Examination‐revised (ACE‐R) improves the estimate of cognitive ability from the Mini‐Mental State Examination (MMSE) in people with Alzheimer disease (AD). Methods We examined itemized data in people with AD who were on the Scottish Dementia Research Interest Register drawn from eight centres across Scotland, covering 75% of the Scottish population. ACE‐R items that comprise the MMSE and those that did not (non‐MMSE items) were summed separately. We residualized MMSE total on non‐MMSE total and vice versa to derive a measure of the variance unique to each. Results Five hundred and one (258 male, 243 female) participants, mean age 75.7 (range 52–94) years were on the register, of whom 329 (160 men, 169 women) had AD. Of those with AD, 309 had a mean MMSE of 20.5 and mean ACE‐R of 57.5 measured with Pearson r = 0.92 between MMSE and ACE‐R totals, and the regression equation ACE‐R score = 3.0 × MMSE − 4.1. The unique non‐MMSE items score correlated with ACE‐R total r = 0.40 (16% of ACE‐R variance). Conclusions The ACE‐R and MMSE total scores are highly correlated. In this clinical sample of people with established AD, for an MMSE score of 24, the predicted ACE‐R score was 67.9 with 95% confidence intervals of 61.6–75.4. The extra non‐MMSE ACE‐R items improve estimates of cognitive ability by 16%. Copyright © 2012 John Wiley &amp; Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley &amp; Sons, Ltd</pub><pmid>22556006</pmid><doi>10.1002/gps.3828</doi><tpages>5</tpages></addata></record>
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subjects Ability tests
Age
Aged
Aged, 80 and over
Alzheimer disease
Alzheimer Disease - diagnosis
Alzheimer Disease - psychology
Alzheimer's disease
Biological and medical sciences
Brief Psychiatric Rating Scale
cognition
Cognition - physiology
Cognitive ability
Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
Dementia
Female
General aspects
Geriatric psychiatry
Geriatrics
Humans
Male
Medical sciences
Middle Aged
Neurology
Neuropsychological Tests
Predictive Value of Tests
Psychology. Psychoanalysis. Psychiatry
Psychopathology. Psychiatry
Regression analysis
title Does the Addenbrooke's Cognitive Examination-revised add to the Mini-Mental State Examination in established Alzheimer disease? Results from a national dementia research register
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