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Depressed Mood is Not a Risk Factor for Incident Dementia in a Community-Based Cohort
Objectives: To determine the relationship between depressed mood and the development of Alzheimer disease in cognitively normal individuals. Design: Longitudinal and observational. Setting: Community-based cohort study. Participants: A total of 288 participants in the Cardiovascular Health Study-Cog...
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Published in: | The American journal of geriatric psychiatry 2009-08, Vol.17 (8), p.653-663 |
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creator | Becker, James T., Ph.D Chang, Yue-Fang, Ph.D Lopez, Oscar L., M.D Dew, Mary Amanda, Ph.D Sweet, Robert A., M.D Barnes, Deborah, Ph.D Yaffe, Kristine, M.D Young, Jeffrey, B.A Kuller, Lewis, M.D Reynolds, Charles F., M.D |
description | Objectives: To determine the relationship between depressed mood and the development of Alzheimer disease in cognitively normal individuals. Design: Longitudinal and observational. Setting: Community-based cohort study. Participants: A total of 288 participants in the Cardiovascular Health Study-Cognition Study (mean age: 77.52, SD = 3.65, range: 70–89). All of the participants were adjudicated as cognitively normal in 1998/1999, and all had at least three visits before 1998/1999 with measures of cognition and mood state. The mean length of follow-up from 1998–1999 to 2007 was 7.1 years (range: 1–9 years, median = 9 years). Measurements: The Center for Epidemiological Studies-Depression Scale (CESD) was used to index mood state, and the Modified Mini-Mental State Examination (3MSE) was the index of cognitive function among participants before 1998/1999. These measures were considered in two ways: participants were classified according to: 1) whether they showed a high-negative correlation between their CESD and 3MSE scores (i.e., indicating that greater depression was linked to poorer cognition) and 2) whether they showed persistently elevated CESD scores. The study outcome, development of dementia (N = 48), was based on consensus classifications, which was based on detailed neuropsychological and neurological exams. Results: The authors could find no consistent relationship between mood state, either alone or in relation to cognitive status, and the subsequent development of dementia. Those individuals whose cognitive functions were highly correlated with their mood state were no more likely to develop dementia than other participants. Those who had persistently depressed mood were also no more likely to develop dementia than those without persistently depressed mood. Conclusion: Within the confines of this prospective, community-based study of elderly adults, the authors could not find strong evidence to support the hypothesis that mood disturbance was linked with the development of dementia. |
doi_str_mv | 10.1097/JGP.0b013e3181aad1fe |
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Design: Longitudinal and observational. Setting: Community-based cohort study. Participants: A total of 288 participants in the Cardiovascular Health Study-Cognition Study (mean age: 77.52, SD = 3.65, range: 70–89). All of the participants were adjudicated as cognitively normal in 1998/1999, and all had at least three visits before 1998/1999 with measures of cognition and mood state. The mean length of follow-up from 1998–1999 to 2007 was 7.1 years (range: 1–9 years, median = 9 years). Measurements: The Center for Epidemiological Studies-Depression Scale (CESD) was used to index mood state, and the Modified Mini-Mental State Examination (3MSE) was the index of cognitive function among participants before 1998/1999. These measures were considered in two ways: participants were classified according to: 1) whether they showed a high-negative correlation between their CESD and 3MSE scores (i.e., indicating that greater depression was linked to poorer cognition) and 2) whether they showed persistently elevated CESD scores. The study outcome, development of dementia (N = 48), was based on consensus classifications, which was based on detailed neuropsychological and neurological exams. Results: The authors could find no consistent relationship between mood state, either alone or in relation to cognitive status, and the subsequent development of dementia. Those individuals whose cognitive functions were highly correlated with their mood state were no more likely to develop dementia than other participants. Those who had persistently depressed mood were also no more likely to develop dementia than those without persistently depressed mood. Conclusion: Within the confines of this prospective, community-based study of elderly adults, the authors could not find strong evidence to support the hypothesis that mood disturbance was linked with the development of dementia.</description><identifier>ISSN: 1064-7481</identifier><identifier>EISSN: 1545-7214</identifier><identifier>DOI: 10.1097/JGP.0b013e3181aad1fe</identifier><identifier>PMID: 19634208</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>Aged ; Aged, 80 and over ; Aging ; Alzheimer Disease - epidemiology ; Cognition Disorders - diagnosis ; Cognition Disorders - epidemiology ; Cognition Disorders - psychology ; dementia ; Dementia - diagnosis ; Dementia - epidemiology ; Dementia - psychology ; depression ; Depression - diagnosis ; Depression - epidemiology ; Depression - psychology ; Female ; Follow-Up Studies ; Humans ; Incidence ; Internal Medicine ; Longitudinal Studies ; Magnetic Resonance Imaging ; Male ; Mental Status Schedule ; Prospective Studies ; Psychiatric Status Rating Scales - statistics & numerical data ; Residence Characteristics ; Risk Factors</subject><ispartof>The American journal of geriatric psychiatry, 2009-08, Vol.17 (8), p.653-663</ispartof><rights>American Association for Geriatric Psychiatry</rights><rights>2009 American Association for Geriatric Psychiatry</rights><rights>Copyright Lippincott Williams & Wilkins Aug 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c594t-e44e14b2fe481b12b3074d6363357ba19d64e3968b60cc3355c22747bc8232023</citedby><cites>FETCH-LOGICAL-c594t-e44e14b2fe481b12b3074d6363357ba19d64e3968b60cc3355c22747bc8232023</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/195986376/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/195986376?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>230,314,780,784,885,3549,21394,27924,27925,33611,33612,43733,45780,74221</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19634208$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Becker, James T., Ph.D</creatorcontrib><creatorcontrib>Chang, Yue-Fang, Ph.D</creatorcontrib><creatorcontrib>Lopez, Oscar L., M.D</creatorcontrib><creatorcontrib>Dew, Mary Amanda, Ph.D</creatorcontrib><creatorcontrib>Sweet, Robert A., M.D</creatorcontrib><creatorcontrib>Barnes, Deborah, Ph.D</creatorcontrib><creatorcontrib>Yaffe, Kristine, M.D</creatorcontrib><creatorcontrib>Young, Jeffrey, B.A</creatorcontrib><creatorcontrib>Kuller, Lewis, M.D</creatorcontrib><creatorcontrib>Reynolds, Charles F., M.D</creatorcontrib><title>Depressed Mood is Not a Risk Factor for Incident Dementia in a Community-Based Cohort</title><title>The American journal of geriatric psychiatry</title><addtitle>Am J Geriatr Psychiatry</addtitle><description>Objectives: To determine the relationship between depressed mood and the development of Alzheimer disease in cognitively normal individuals. Design: Longitudinal and observational. Setting: Community-based cohort study. Participants: A total of 288 participants in the Cardiovascular Health Study-Cognition Study (mean age: 77.52, SD = 3.65, range: 70–89). All of the participants were adjudicated as cognitively normal in 1998/1999, and all had at least three visits before 1998/1999 with measures of cognition and mood state. The mean length of follow-up from 1998–1999 to 2007 was 7.1 years (range: 1–9 years, median = 9 years). Measurements: The Center for Epidemiological Studies-Depression Scale (CESD) was used to index mood state, and the Modified Mini-Mental State Examination (3MSE) was the index of cognitive function among participants before 1998/1999. These measures were considered in two ways: participants were classified according to: 1) whether they showed a high-negative correlation between their CESD and 3MSE scores (i.e., indicating that greater depression was linked to poorer cognition) and 2) whether they showed persistently elevated CESD scores. The study outcome, development of dementia (N = 48), was based on consensus classifications, which was based on detailed neuropsychological and neurological exams. Results: The authors could find no consistent relationship between mood state, either alone or in relation to cognitive status, and the subsequent development of dementia. Those individuals whose cognitive functions were highly correlated with their mood state were no more likely to develop dementia than other participants. Those who had persistently depressed mood were also no more likely to develop dementia than those without persistently depressed mood. Conclusion: Within the confines of this prospective, community-based study of elderly adults, the authors could not find strong evidence to support the hypothesis that mood disturbance was linked with the development of dementia.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Aging</subject><subject>Alzheimer Disease - epidemiology</subject><subject>Cognition Disorders - diagnosis</subject><subject>Cognition Disorders - epidemiology</subject><subject>Cognition Disorders - psychology</subject><subject>dementia</subject><subject>Dementia - diagnosis</subject><subject>Dementia - epidemiology</subject><subject>Dementia - psychology</subject><subject>depression</subject><subject>Depression - diagnosis</subject><subject>Depression - epidemiology</subject><subject>Depression - psychology</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Incidence</subject><subject>Internal Medicine</subject><subject>Longitudinal Studies</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Mental Status Schedule</subject><subject>Prospective Studies</subject><subject>Psychiatric Status Rating Scales - 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epidemiology</topic><topic>Cognition Disorders - diagnosis</topic><topic>Cognition Disorders - epidemiology</topic><topic>Cognition Disorders - psychology</topic><topic>dementia</topic><topic>Dementia - diagnosis</topic><topic>Dementia - epidemiology</topic><topic>Dementia - psychology</topic><topic>depression</topic><topic>Depression - diagnosis</topic><topic>Depression - epidemiology</topic><topic>Depression - psychology</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Incidence</topic><topic>Internal Medicine</topic><topic>Longitudinal Studies</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Mental Status Schedule</topic><topic>Prospective Studies</topic><topic>Psychiatric Status Rating Scales - statistics & numerical data</topic><topic>Residence Characteristics</topic><topic>Risk Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Becker, James T., Ph.D</creatorcontrib><creatorcontrib>Chang, Yue-Fang, Ph.D</creatorcontrib><creatorcontrib>Lopez, Oscar L., M.D</creatorcontrib><creatorcontrib>Dew, Mary Amanda, Ph.D</creatorcontrib><creatorcontrib>Sweet, Robert A., M.D</creatorcontrib><creatorcontrib>Barnes, Deborah, Ph.D</creatorcontrib><creatorcontrib>Yaffe, Kristine, M.D</creatorcontrib><creatorcontrib>Young, Jeffrey, B.A</creatorcontrib><creatorcontrib>Kuller, Lewis, M.D</creatorcontrib><creatorcontrib>Reynolds, Charles F., M.D</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Social Sciences Premium Collection【Remote access available】</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Social Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Social Science Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Social Science 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>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The American journal of geriatric psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Becker, James T., Ph.D</au><au>Chang, Yue-Fang, Ph.D</au><au>Lopez, Oscar L., M.D</au><au>Dew, Mary Amanda, Ph.D</au><au>Sweet, Robert A., M.D</au><au>Barnes, Deborah, Ph.D</au><au>Yaffe, Kristine, M.D</au><au>Young, Jeffrey, B.A</au><au>Kuller, Lewis, M.D</au><au>Reynolds, Charles F., M.D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Depressed Mood is Not a Risk Factor for Incident Dementia in a Community-Based Cohort</atitle><jtitle>The American journal of geriatric psychiatry</jtitle><addtitle>Am J Geriatr Psychiatry</addtitle><date>2009-08-01</date><risdate>2009</risdate><volume>17</volume><issue>8</issue><spage>653</spage><epage>663</epage><pages>653-663</pages><issn>1064-7481</issn><eissn>1545-7214</eissn><abstract>Objectives: To determine the relationship between depressed mood and the development of Alzheimer disease in cognitively normal individuals. Design: Longitudinal and observational. Setting: Community-based cohort study. Participants: A total of 288 participants in the Cardiovascular Health Study-Cognition Study (mean age: 77.52, SD = 3.65, range: 70–89). All of the participants were adjudicated as cognitively normal in 1998/1999, and all had at least three visits before 1998/1999 with measures of cognition and mood state. The mean length of follow-up from 1998–1999 to 2007 was 7.1 years (range: 1–9 years, median = 9 years). Measurements: The Center for Epidemiological Studies-Depression Scale (CESD) was used to index mood state, and the Modified Mini-Mental State Examination (3MSE) was the index of cognitive function among participants before 1998/1999. These measures were considered in two ways: participants were classified according to: 1) whether they showed a high-negative correlation between their CESD and 3MSE scores (i.e., indicating that greater depression was linked to poorer cognition) and 2) whether they showed persistently elevated CESD scores. The study outcome, development of dementia (N = 48), was based on consensus classifications, which was based on detailed neuropsychological and neurological exams. Results: The authors could find no consistent relationship between mood state, either alone or in relation to cognitive status, and the subsequent development of dementia. Those individuals whose cognitive functions were highly correlated with their mood state were no more likely to develop dementia than other participants. Those who had persistently depressed mood were also no more likely to develop dementia than those without persistently depressed mood. Conclusion: Within the confines of this prospective, community-based study of elderly adults, the authors could not find strong evidence to support the hypothesis that mood disturbance was linked with the development of dementia.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>19634208</pmid><doi>10.1097/JGP.0b013e3181aad1fe</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Aged, 80 and over Aging Alzheimer Disease - epidemiology Cognition Disorders - diagnosis Cognition Disorders - epidemiology Cognition Disorders - psychology dementia Dementia - diagnosis Dementia - epidemiology Dementia - psychology depression Depression - diagnosis Depression - epidemiology Depression - psychology Female Follow-Up Studies Humans Incidence Internal Medicine Longitudinal Studies Magnetic Resonance Imaging Male Mental Status Schedule Prospective Studies Psychiatric Status Rating Scales - statistics & numerical data Residence Characteristics Risk Factors |
title | Depressed Mood is Not a Risk Factor for Incident Dementia in a Community-Based Cohort |
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