Normative Cognitive Decline in Old Age

Objective To characterize trajectories of normative cognitive aging. Methods Older persons without dementia at study enrollment (n = 1,010) had annual cognitive testing for up to 24 years (mean = 9.9 years, standard deviation = 5.0), died, and underwent a neuropathologic examination to quantify 9 po...

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Veröffentlicht in:Annals of neurology 2020-06, Vol.87 (6), p.816-829
Hauptverfasser: Wilson, Robert S., Wang, Tianhao, Yu, Lei, Bennett, David A., Boyle, Patricia A.
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container_end_page 829
container_issue 6
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container_title Annals of neurology
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creator Wilson, Robert S.
Wang, Tianhao
Yu, Lei
Bennett, David A.
Boyle, Patricia A.
description Objective To characterize trajectories of normative cognitive aging. Methods Older persons without dementia at study enrollment (n = 1,010) had annual cognitive testing for up to 24 years (mean = 9.9 years, standard deviation = 5.0), died, and underwent a neuropathologic examination to quantify 9 postmortem markers of common neurodegenerative and cerebrovascular conditions. To accommodate the heterogeneity in cognitive trajectories, we used functional mixed effects models, which allow individuals to have different patterns of cognitive decline under a unified model structure. Results In a functional mixed effects model, postmortem markers (Alzheimer disease pathology, Lewy bodies, transactive response DNA‐binding protein 43 pathology, hippocampal sclerosis, atherosclerosis, gross infarcts) were associated with global cognitive decline. Residual global cognitive decline after adjustment for neuropathologic burden was weakly related to age at death; it occurred in only about one‐third of participants, mostly proximate to death. Results were comparable after eliminating the initial cognitive assessments to minimize retest learning or controlling for frailty proximate to death. Analyses were also conducted with composite measures of episodic memory and perceptual speed. Residual decline not attributable to neuropathologic burden was confined to a subset for each outcome and was most evident proximate to death. Age at death was unrelated to residual decline in episodic memory but was related to residual decline in perceptual speed. Interpretation Late life cognitive loss mainly reflects non‐normative pathologic and mortality‐related processes rather than normative age‐related processes. ANN NEUROL 2020;87:816–829
doi_str_mv 10.1002/ana.25711
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Methods Older persons without dementia at study enrollment (n = 1,010) had annual cognitive testing for up to 24 years (mean = 9.9 years, standard deviation = 5.0), died, and underwent a neuropathologic examination to quantify 9 postmortem markers of common neurodegenerative and cerebrovascular conditions. To accommodate the heterogeneity in cognitive trajectories, we used functional mixed effects models, which allow individuals to have different patterns of cognitive decline under a unified model structure. Results In a functional mixed effects model, postmortem markers (Alzheimer disease pathology, Lewy bodies, transactive response DNA‐binding protein 43 pathology, hippocampal sclerosis, atherosclerosis, gross infarcts) were associated with global cognitive decline. Residual global cognitive decline after adjustment for neuropathologic burden was weakly related to age at death; it occurred in only about one‐third of participants, mostly proximate to death. Results were comparable after eliminating the initial cognitive assessments to minimize retest learning or controlling for frailty proximate to death. Analyses were also conducted with composite measures of episodic memory and perceptual speed. Residual decline not attributable to neuropathologic burden was confined to a subset for each outcome and was most evident proximate to death. Age at death was unrelated to residual decline in episodic memory but was related to residual decline in perceptual speed. Interpretation Late life cognitive loss mainly reflects non‐normative pathologic and mortality‐related processes rather than normative age‐related processes. ANN NEUROL 2020;87:816–829</description><identifier>ISSN: 0364-5134</identifier><identifier>EISSN: 1531-8249</identifier><identifier>DOI: 10.1002/ana.25711</identifier><identifier>PMID: 32144793</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley &amp; Sons, Inc</publisher><subject>Age ; Aged ; Aged, 80 and over ; Aging ; Aging - psychology ; Alzheimer's disease ; Arteriosclerosis ; Atherosclerosis ; Autopsy ; Biomarkers ; Cerebrovascular Disorders - pathology ; Cerebrovascular Disorders - psychology ; Cognitive ability ; Cognitive Dysfunction - psychology ; Death ; Dementia disorders ; Deoxyribonucleic acid ; DNA ; Educational Status ; Female ; Frailty - psychology ; Heterogeneity ; Hippocampus ; Humans ; Lewy bodies ; Longitudinal Studies ; Male ; Markers ; Memory ; Memory, Episodic ; Mortality ; Neurodegenerative diseases ; Neurodegenerative Diseases - pathology ; Neurodegenerative Diseases - psychology ; Neurologic Examination ; Neuropathology ; Neuropsychological Tests ; Older people ; Pathology ; Reaction Time ; Reference Values</subject><ispartof>Annals of neurology, 2020-06, Vol.87 (6), p.816-829</ispartof><rights>2020 American Neurological Association</rights><rights>2020 American Neurological Association.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5101-f1f264547f56441e506f0dcb45f8bc999ce17794c43e2573c095d5c16b54cc43</citedby><cites>FETCH-LOGICAL-c5101-f1f264547f56441e506f0dcb45f8bc999ce17794c43e2573c095d5c16b54cc43</cites><orcidid>0000-0001-9592-0333 ; 0000-0002-0237-8758</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%2Fana.25711$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fana.25711$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32144793$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wilson, Robert S.</creatorcontrib><creatorcontrib>Wang, Tianhao</creatorcontrib><creatorcontrib>Yu, Lei</creatorcontrib><creatorcontrib>Bennett, David A.</creatorcontrib><creatorcontrib>Boyle, Patricia A.</creatorcontrib><title>Normative Cognitive Decline in Old Age</title><title>Annals of neurology</title><addtitle>Ann Neurol</addtitle><description>Objective To characterize trajectories of normative cognitive aging. Methods Older persons without dementia at study enrollment (n = 1,010) had annual cognitive testing for up to 24 years (mean = 9.9 years, standard deviation = 5.0), died, and underwent a neuropathologic examination to quantify 9 postmortem markers of common neurodegenerative and cerebrovascular conditions. To accommodate the heterogeneity in cognitive trajectories, we used functional mixed effects models, which allow individuals to have different patterns of cognitive decline under a unified model structure. Results In a functional mixed effects model, postmortem markers (Alzheimer disease pathology, Lewy bodies, transactive response DNA‐binding protein 43 pathology, hippocampal sclerosis, atherosclerosis, gross infarcts) were associated with global cognitive decline. Residual global cognitive decline after adjustment for neuropathologic burden was weakly related to age at death; it occurred in only about one‐third of participants, mostly proximate to death. Results were comparable after eliminating the initial cognitive assessments to minimize retest learning or controlling for frailty proximate to death. Analyses were also conducted with composite measures of episodic memory and perceptual speed. Residual decline not attributable to neuropathologic burden was confined to a subset for each outcome and was most evident proximate to death. Age at death was unrelated to residual decline in episodic memory but was related to residual decline in perceptual speed. Interpretation Late life cognitive loss mainly reflects non‐normative pathologic and mortality‐related processes rather than normative age‐related processes. ANN NEUROL 2020;87:816–829</description><subject>Age</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Aging</subject><subject>Aging - psychology</subject><subject>Alzheimer's disease</subject><subject>Arteriosclerosis</subject><subject>Atherosclerosis</subject><subject>Autopsy</subject><subject>Biomarkers</subject><subject>Cerebrovascular Disorders - pathology</subject><subject>Cerebrovascular Disorders - psychology</subject><subject>Cognitive ability</subject><subject>Cognitive Dysfunction - psychology</subject><subject>Death</subject><subject>Dementia disorders</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Educational Status</subject><subject>Female</subject><subject>Frailty - psychology</subject><subject>Heterogeneity</subject><subject>Hippocampus</subject><subject>Humans</subject><subject>Lewy bodies</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Markers</subject><subject>Memory</subject><subject>Memory, Episodic</subject><subject>Mortality</subject><subject>Neurodegenerative diseases</subject><subject>Neurodegenerative Diseases - pathology</subject><subject>Neurodegenerative Diseases - psychology</subject><subject>Neurologic Examination</subject><subject>Neuropathology</subject><subject>Neuropsychological Tests</subject><subject>Older people</subject><subject>Pathology</subject><subject>Reaction Time</subject><subject>Reference Values</subject><issn>0364-5134</issn><issn>1531-8249</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kF1LwzAUhoMobk4v_ANSEEQvuuXkq8uVlPkJY7vZfWjTdGa06Wy3yf69cZ1DBa8SkofnvOdF6BJwHzAmg8QlfcIjgCPUBU4hHBImj1EXU8FCDpR10FnTLDDGUgA-RR1KgLFI0i66mVR1mazsxgSjau7s7vZgdGGdCawLpkUWxHNzjk7ypGjMxf7sodnT42z0Eo6nz6-jeBxqDhjCHHIiGGdRzgVjYDgWOc50yng-TLWUUhuIIsk0o8YHphpLnnENIuVM-8ceum-1y3Vamkwbt6qTQi1rWyb1VlWJVb9_nH1T82qjfA2UYy684XZvqKv3tWlWqrSNNkWROFOtG0VoxCj3GcCj13_QRbWunV9PEYY5wSAo9dRdS-m6apra5Ic0gL_GEuXbV7v2PXv1M_6B_K7bA4MW-LCF2f5vUvEkbpWfW4GLfg</recordid><startdate>202006</startdate><enddate>202006</enddate><creator>Wilson, Robert S.</creator><creator>Wang, Tianhao</creator><creator>Yu, Lei</creator><creator>Bennett, David A.</creator><creator>Boyle, Patricia A.</creator><general>John Wiley &amp; Sons, Inc</general><general>Wiley Subscription Services, Inc</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>7TK</scope><scope>7U7</scope><scope>C1K</scope><scope>K9.</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9592-0333</orcidid><orcidid>https://orcid.org/0000-0002-0237-8758</orcidid></search><sort><creationdate>202006</creationdate><title>Normative Cognitive Decline in Old Age</title><author>Wilson, Robert S. ; Wang, Tianhao ; Yu, Lei ; Bennett, David A. ; Boyle, Patricia A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5101-f1f264547f56441e506f0dcb45f8bc999ce17794c43e2573c095d5c16b54cc43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Age</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Aging</topic><topic>Aging - psychology</topic><topic>Alzheimer's disease</topic><topic>Arteriosclerosis</topic><topic>Atherosclerosis</topic><topic>Autopsy</topic><topic>Biomarkers</topic><topic>Cerebrovascular Disorders - pathology</topic><topic>Cerebrovascular Disorders - psychology</topic><topic>Cognitive ability</topic><topic>Cognitive Dysfunction - psychology</topic><topic>Death</topic><topic>Dementia disorders</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Educational Status</topic><topic>Female</topic><topic>Frailty - psychology</topic><topic>Heterogeneity</topic><topic>Hippocampus</topic><topic>Humans</topic><topic>Lewy bodies</topic><topic>Longitudinal Studies</topic><topic>Male</topic><topic>Markers</topic><topic>Memory</topic><topic>Memory, Episodic</topic><topic>Mortality</topic><topic>Neurodegenerative diseases</topic><topic>Neurodegenerative Diseases - pathology</topic><topic>Neurodegenerative Diseases - psychology</topic><topic>Neurologic Examination</topic><topic>Neuropathology</topic><topic>Neuropsychological Tests</topic><topic>Older people</topic><topic>Pathology</topic><topic>Reaction Time</topic><topic>Reference Values</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wilson, Robert S.</creatorcontrib><creatorcontrib>Wang, Tianhao</creatorcontrib><creatorcontrib>Yu, Lei</creatorcontrib><creatorcontrib>Bennett, David A.</creatorcontrib><creatorcontrib>Boyle, Patricia A.</creatorcontrib><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>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Annals of neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wilson, Robert S.</au><au>Wang, Tianhao</au><au>Yu, Lei</au><au>Bennett, David A.</au><au>Boyle, Patricia A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Normative Cognitive Decline in Old Age</atitle><jtitle>Annals of neurology</jtitle><addtitle>Ann Neurol</addtitle><date>2020-06</date><risdate>2020</risdate><volume>87</volume><issue>6</issue><spage>816</spage><epage>829</epage><pages>816-829</pages><issn>0364-5134</issn><eissn>1531-8249</eissn><abstract>Objective To characterize trajectories of normative cognitive aging. Methods Older persons without dementia at study enrollment (n = 1,010) had annual cognitive testing for up to 24 years (mean = 9.9 years, standard deviation = 5.0), died, and underwent a neuropathologic examination to quantify 9 postmortem markers of common neurodegenerative and cerebrovascular conditions. To accommodate the heterogeneity in cognitive trajectories, we used functional mixed effects models, which allow individuals to have different patterns of cognitive decline under a unified model structure. Results In a functional mixed effects model, postmortem markers (Alzheimer disease pathology, Lewy bodies, transactive response DNA‐binding protein 43 pathology, hippocampal sclerosis, atherosclerosis, gross infarcts) were associated with global cognitive decline. Residual global cognitive decline after adjustment for neuropathologic burden was weakly related to age at death; it occurred in only about one‐third of participants, mostly proximate to death. Results were comparable after eliminating the initial cognitive assessments to minimize retest learning or controlling for frailty proximate to death. Analyses were also conducted with composite measures of episodic memory and perceptual speed. Residual decline not attributable to neuropathologic burden was confined to a subset for each outcome and was most evident proximate to death. Age at death was unrelated to residual decline in episodic memory but was related to residual decline in perceptual speed. Interpretation Late life cognitive loss mainly reflects non‐normative pathologic and mortality‐related processes rather than normative age‐related processes. ANN NEUROL 2020;87:816–829</abstract><cop>Hoboken, USA</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>32144793</pmid><doi>10.1002/ana.25711</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0001-9592-0333</orcidid><orcidid>https://orcid.org/0000-0002-0237-8758</orcidid><oa>free_for_read</oa></addata></record>
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subjects Age
Aged
Aged, 80 and over
Aging
Aging - psychology
Alzheimer's disease
Arteriosclerosis
Atherosclerosis
Autopsy
Biomarkers
Cerebrovascular Disorders - pathology
Cerebrovascular Disorders - psychology
Cognitive ability
Cognitive Dysfunction - psychology
Death
Dementia disorders
Deoxyribonucleic acid
DNA
Educational Status
Female
Frailty - psychology
Heterogeneity
Hippocampus
Humans
Lewy bodies
Longitudinal Studies
Male
Markers
Memory
Memory, Episodic
Mortality
Neurodegenerative diseases
Neurodegenerative Diseases - pathology
Neurodegenerative Diseases - psychology
Neurologic Examination
Neuropathology
Neuropsychological Tests
Older people
Pathology
Reaction Time
Reference Values
title Normative Cognitive Decline in Old Age
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