Cognitive and functional progression of dementia in two longitudinal studies

Objectives Previous studies have identified several subgroups (ie, latent trajectories) with distinct disease progression among people with dementia. However, the methods and results were not always consistent. This study aims to perform a coordinated analysis of latent trajectories of cognitive and...

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Veröffentlicht in:International journal of geriatric psychiatry 2019-11, Vol.34 (11), p.1623-1632
Hauptverfasser: Wang, Yuwei, Haaksma, Miriam L., Ramakers, Inez H.G.B., Verhey, Frans R.J., Flier, Wiesje M., Scheltens, Philip, Maurik, Ingrid, Olde Rikkert, Marcel G.M., Leoutsakos, Jeannie‐Marie S., Melis, René J.F.
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container_end_page 1632
container_issue 11
container_start_page 1623
container_title International journal of geriatric psychiatry
container_volume 34
creator Wang, Yuwei
Haaksma, Miriam L.
Ramakers, Inez H.G.B.
Verhey, Frans R.J.
Flier, Wiesje M.
Scheltens, Philip
Maurik, Ingrid
Olde Rikkert, Marcel G.M.
Leoutsakos, Jeannie‐Marie S.
Melis, René J.F.
description Objectives Previous studies have identified several subgroups (ie, latent trajectories) with distinct disease progression among people with dementia. However, the methods and results were not always consistent. This study aims to perform a coordinated analysis of latent trajectories of cognitive and functional progression in dementia across two datasets. Methods Included and analyzed using the same statistical approach were 1628 participants with dementia from the US National Alzheimer's Coordinating Center (NACC) and 331 participants with dementia from the Dutch Clinical Course of Cognition and Comorbidity study (4C‐Study). Trajectories of cognition and instrumental activities of daily living (IADL) were modeled jointly in a parallel‐process growth mixture model. Results Cognition and IADL tended to decline in unison across the two samples. Slow decline in both domains was observed in 26% of the US sample and 74% of the Dutch sample. Rapid decline in cognition and IADL was observed in 7% of the US sample and 26% of the Dutch sample. The majority (67%) of the US sample showed moderate cognitive decline and rapid IADL decline. Conclusions Trajectories of slow and rapid dementia progression were identified in both samples. Despite using the same statistical methods, the number of latent trajectories was not replicated and the relative class sizes differed considerably across datasets. These results call for careful consideration when comparing progression estimates in the literature. In addition, the observed discrepancy between cognitive and functional decline stresses the need to monitor dementia progression across multiple domains.
doi_str_mv 10.1002/gps.5175
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However, the methods and results were not always consistent. This study aims to perform a coordinated analysis of latent trajectories of cognitive and functional progression in dementia across two datasets. Methods Included and analyzed using the same statistical approach were 1628 participants with dementia from the US National Alzheimer's Coordinating Center (NACC) and 331 participants with dementia from the Dutch Clinical Course of Cognition and Comorbidity study (4C‐Study). Trajectories of cognition and instrumental activities of daily living (IADL) were modeled jointly in a parallel‐process growth mixture model. Results Cognition and IADL tended to decline in unison across the two samples. Slow decline in both domains was observed in 26% of the US sample and 74% of the Dutch sample. Rapid decline in cognition and IADL was observed in 7% of the US sample and 26% of the Dutch sample. The majority (67%) of the US sample showed moderate cognitive decline and rapid IADL decline. Conclusions Trajectories of slow and rapid dementia progression were identified in both samples. Despite using the same statistical methods, the number of latent trajectories was not replicated and the relative class sizes differed considerably across datasets. These results call for careful consideration when comparing progression estimates in the literature. In addition, the observed discrepancy between cognitive and functional decline stresses the need to monitor dementia progression across multiple domains.</description><identifier>ISSN: 0885-6230</identifier><identifier>ISSN: 1099-1166</identifier><identifier>EISSN: 1099-1166</identifier><identifier>DOI: 10.1002/gps.5175</identifier><identifier>PMID: 31318090</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Activities of daily living ; Activities of Daily Living - psychology ; Aged ; Aged, 80 and over ; Alzheimer's disease ; cognition ; Cognition &amp; reasoning ; Cognitive ability ; Cognitive Dysfunction - psychology ; Comorbidity ; coordinated analysis ; daily functioning ; Dementia ; Dementia - physiopathology ; Dementia - psychology ; Dementia disorders ; dementia progression ; Disease Progression ; Female ; Geriatric psychiatry ; growth mixture model ; Humans ; Longitudinal Studies ; Male ; Middle Aged ; Neurodegenerative diseases ; Statistics ; trajectory</subject><ispartof>International journal of geriatric psychiatry, 2019-11, Vol.34 (11), p.1623-1632</ispartof><rights>2019 The Authors. International Journal of Geriatric Psychiatry published by John Wiley &amp; Sons Ltd</rights><rights>2019 The Authors. International Journal of Geriatric Psychiatry published by John Wiley &amp; Sons Ltd.</rights><rights>2019 John Wiley &amp; Sons, Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4385-d58c46e718dc535665571959870e8caaea6fb89c713451f6e1974e18fd0d54ad3</citedby><cites>FETCH-LOGICAL-c4385-d58c46e718dc535665571959870e8caaea6fb89c713451f6e1974e18fd0d54ad3</cites><orcidid>0000-0002-3518-9152 ; 0000-0002-1010-1046 ; 0000-0002-7863-4738 ; 0000-0002-1482-7039</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fgps.5175$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fgps.5175$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31318090$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Yuwei</creatorcontrib><creatorcontrib>Haaksma, Miriam L.</creatorcontrib><creatorcontrib>Ramakers, Inez H.G.B.</creatorcontrib><creatorcontrib>Verhey, Frans R.J.</creatorcontrib><creatorcontrib>Flier, Wiesje M.</creatorcontrib><creatorcontrib>Scheltens, Philip</creatorcontrib><creatorcontrib>Maurik, Ingrid</creatorcontrib><creatorcontrib>Olde Rikkert, Marcel G.M.</creatorcontrib><creatorcontrib>Leoutsakos, Jeannie‐Marie S.</creatorcontrib><creatorcontrib>Melis, René J.F.</creatorcontrib><title>Cognitive and functional progression of dementia in two longitudinal studies</title><title>International journal of geriatric psychiatry</title><addtitle>Int J Geriatr Psychiatry</addtitle><description>Objectives Previous studies have identified several subgroups (ie, latent trajectories) with distinct disease progression among people with dementia. However, the methods and results were not always consistent. This study aims to perform a coordinated analysis of latent trajectories of cognitive and functional progression in dementia across two datasets. Methods Included and analyzed using the same statistical approach were 1628 participants with dementia from the US National Alzheimer's Coordinating Center (NACC) and 331 participants with dementia from the Dutch Clinical Course of Cognition and Comorbidity study (4C‐Study). Trajectories of cognition and instrumental activities of daily living (IADL) were modeled jointly in a parallel‐process growth mixture model. Results Cognition and IADL tended to decline in unison across the two samples. Slow decline in both domains was observed in 26% of the US sample and 74% of the Dutch sample. Rapid decline in cognition and IADL was observed in 7% of the US sample and 26% of the Dutch sample. The majority (67%) of the US sample showed moderate cognitive decline and rapid IADL decline. Conclusions Trajectories of slow and rapid dementia progression were identified in both samples. Despite using the same statistical methods, the number of latent trajectories was not replicated and the relative class sizes differed considerably across datasets. These results call for careful consideration when comparing progression estimates in the literature. 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However, the methods and results were not always consistent. This study aims to perform a coordinated analysis of latent trajectories of cognitive and functional progression in dementia across two datasets. Methods Included and analyzed using the same statistical approach were 1628 participants with dementia from the US National Alzheimer's Coordinating Center (NACC) and 331 participants with dementia from the Dutch Clinical Course of Cognition and Comorbidity study (4C‐Study). Trajectories of cognition and instrumental activities of daily living (IADL) were modeled jointly in a parallel‐process growth mixture model. Results Cognition and IADL tended to decline in unison across the two samples. Slow decline in both domains was observed in 26% of the US sample and 74% of the Dutch sample. Rapid decline in cognition and IADL was observed in 7% of the US sample and 26% of the Dutch sample. The majority (67%) of the US sample showed moderate cognitive decline and rapid IADL decline. Conclusions Trajectories of slow and rapid dementia progression were identified in both samples. Despite using the same statistical methods, the number of latent trajectories was not replicated and the relative class sizes differed considerably across datasets. These results call for careful consideration when comparing progression estimates in the literature. In addition, the observed discrepancy between cognitive and functional decline stresses the need to monitor dementia progression across multiple domains.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31318090</pmid><doi>10.1002/gps.5175</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-3518-9152</orcidid><orcidid>https://orcid.org/0000-0002-1010-1046</orcidid><orcidid>https://orcid.org/0000-0002-7863-4738</orcidid><orcidid>https://orcid.org/0000-0002-1482-7039</orcidid><oa>free_for_read</oa></addata></record>
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subjects Activities of daily living
Activities of Daily Living - psychology
Aged
Aged, 80 and over
Alzheimer's disease
cognition
Cognition & reasoning
Cognitive ability
Cognitive Dysfunction - psychology
Comorbidity
coordinated analysis
daily functioning
Dementia
Dementia - physiopathology
Dementia - psychology
Dementia disorders
dementia progression
Disease Progression
Female
Geriatric psychiatry
growth mixture model
Humans
Longitudinal Studies
Male
Middle Aged
Neurodegenerative diseases
Statistics
trajectory
title Cognitive and functional progression of dementia in two longitudinal studies
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