Trajectory of white matter hyperintensity burden preceding mild cognitive impairment
To determine the time of acceleration in white matter hyperintensity (WMH) burden, a common indicator of cerebrovascular pathology, in relation to conversion to mild cognitive impairment (MCI) in the elderly. A total of 181 cognitively intact elderly volunteers from the longitudinal, prospective, Or...
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Veröffentlicht in: | Neurology 2012-08, Vol.79 (8), p.741-747 |
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creator | SILBERT, Lisa C DODGE, Hiroko H PERKINS, Louie G SHERBAKOV, Lena LAHNA, David ERTEN-LYONS, Deniz WOLTJER, Randall SHINTO, Lynne KAYE, Jeffrey A |
description | To determine the time of acceleration in white matter hyperintensity (WMH) burden, a common indicator of cerebrovascular pathology, in relation to conversion to mild cognitive impairment (MCI) in the elderly.
A total of 181 cognitively intact elderly volunteers from the longitudinal, prospective, Oregon Brain Aging Study underwent yearly evaluations, including brain MRI, and cognitive testing. MRIs were analyzed for imaging markers of neurodegeneration: WMH and ventricular CSF (vCSF) volumes. The time before MCI, when the changes in WMH and vCSF burden accelerate, was assessed using a mixed-effects model with a change point for subjects who developed MCI during follow-up.
During a follow-up duration of up to 19.6 years, 134 subjects converted to MCI. Acceleration in %WMH volume increase occurred 10.6 years before MCI onset. On average, the annual rate of change in %WMH increased an additional 3.3% after the change point. Acceleration in %vCSF volume increase occurred 3.7 years before the onset of MCI. Out of 63 subjects who converted to MCI and had autopsy, only 28.5% had Alzheimer disease (AD) as the sole etiology of their dementia, while almost just as many (24%) had both AD and significant ischemic cerebrovascular disease present.
Acceleration in WMH burden, a common indicator of cerebrovascular disease in the elderly, is a pathologic change that emerges early in the presymptomatic phase leading to MCI. Longitudinal changes in WMH may thus be useful in determining those at risk for cognitive impairment and for planning strategies for introducing disease-modifying therapies prior to dementia onset. |
doi_str_mv | 10.1212/wnl.0b013e3182661f2b |
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A total of 181 cognitively intact elderly volunteers from the longitudinal, prospective, Oregon Brain Aging Study underwent yearly evaluations, including brain MRI, and cognitive testing. MRIs were analyzed for imaging markers of neurodegeneration: WMH and ventricular CSF (vCSF) volumes. The time before MCI, when the changes in WMH and vCSF burden accelerate, was assessed using a mixed-effects model with a change point for subjects who developed MCI during follow-up.
During a follow-up duration of up to 19.6 years, 134 subjects converted to MCI. Acceleration in %WMH volume increase occurred 10.6 years before MCI onset. On average, the annual rate of change in %WMH increased an additional 3.3% after the change point. Acceleration in %vCSF volume increase occurred 3.7 years before the onset of MCI. Out of 63 subjects who converted to MCI and had autopsy, only 28.5% had Alzheimer disease (AD) as the sole etiology of their dementia, while almost just as many (24%) had both AD and significant ischemic cerebrovascular disease present.
Acceleration in WMH burden, a common indicator of cerebrovascular disease in the elderly, is a pathologic change that emerges early in the presymptomatic phase leading to MCI. Longitudinal changes in WMH may thus be useful in determining those at risk for cognitive impairment and for planning strategies for introducing disease-modifying therapies prior to dementia onset.</description><identifier>ISSN: 0028-3878</identifier><identifier>EISSN: 1526-632X</identifier><identifier>DOI: 10.1212/wnl.0b013e3182661f2b</identifier><identifier>PMID: 22843262</identifier><identifier>CODEN: NEURAI</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Aged ; Aged, 80 and over ; Biological and medical sciences ; Brain - pathology ; Cerebrospinal Fluid - metabolism ; Cognitive Dysfunction - cerebrospinal fluid ; Cognitive Dysfunction - diagnosis ; Cognitive Dysfunction - pathology ; Disease Progression ; Early Diagnosis ; Female ; Geriatric Assessment - methods ; Humans ; Magnetic Resonance Imaging - methods ; Male ; Medical sciences ; Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis ; Nerve Fibers, Myelinated - pathology ; Neuroimaging - methods ; Neurology ; Time Factors</subject><ispartof>Neurology, 2012-08, Vol.79 (8), p.741-747</ispartof><rights>2015 INIST-CNRS</rights><rights>Copyright © 2012 by AAN Enterprises, Inc. 2012 AAN Enterprises, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c537t-1eb4018d759e74d449d626694160e6c979ef79a4dc98b098e8cbc93c6f88f9fe3</citedby><cites>FETCH-LOGICAL-c537t-1eb4018d759e74d449d626694160e6c979ef79a4dc98b098e8cbc93c6f88f9fe3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26286057$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22843262$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SILBERT, Lisa C</creatorcontrib><creatorcontrib>DODGE, Hiroko H</creatorcontrib><creatorcontrib>PERKINS, Louie G</creatorcontrib><creatorcontrib>SHERBAKOV, Lena</creatorcontrib><creatorcontrib>LAHNA, David</creatorcontrib><creatorcontrib>ERTEN-LYONS, Deniz</creatorcontrib><creatorcontrib>WOLTJER, Randall</creatorcontrib><creatorcontrib>SHINTO, Lynne</creatorcontrib><creatorcontrib>KAYE, Jeffrey A</creatorcontrib><title>Trajectory of white matter hyperintensity burden preceding mild cognitive impairment</title><title>Neurology</title><addtitle>Neurology</addtitle><description>To determine the time of acceleration in white matter hyperintensity (WMH) burden, a common indicator of cerebrovascular pathology, in relation to conversion to mild cognitive impairment (MCI) in the elderly.
A total of 181 cognitively intact elderly volunteers from the longitudinal, prospective, Oregon Brain Aging Study underwent yearly evaluations, including brain MRI, and cognitive testing. MRIs were analyzed for imaging markers of neurodegeneration: WMH and ventricular CSF (vCSF) volumes. The time before MCI, when the changes in WMH and vCSF burden accelerate, was assessed using a mixed-effects model with a change point for subjects who developed MCI during follow-up.
During a follow-up duration of up to 19.6 years, 134 subjects converted to MCI. Acceleration in %WMH volume increase occurred 10.6 years before MCI onset. On average, the annual rate of change in %WMH increased an additional 3.3% after the change point. Acceleration in %vCSF volume increase occurred 3.7 years before the onset of MCI. Out of 63 subjects who converted to MCI and had autopsy, only 28.5% had Alzheimer disease (AD) as the sole etiology of their dementia, while almost just as many (24%) had both AD and significant ischemic cerebrovascular disease present.
Acceleration in WMH burden, a common indicator of cerebrovascular disease in the elderly, is a pathologic change that emerges early in the presymptomatic phase leading to MCI. Longitudinal changes in WMH may thus be useful in determining those at risk for cognitive impairment and for planning strategies for introducing disease-modifying therapies prior to dementia onset.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>Brain - pathology</subject><subject>Cerebrospinal Fluid - metabolism</subject><subject>Cognitive Dysfunction - cerebrospinal fluid</subject><subject>Cognitive Dysfunction - diagnosis</subject><subject>Cognitive Dysfunction - pathology</subject><subject>Disease Progression</subject><subject>Early Diagnosis</subject><subject>Female</subject><subject>Geriatric Assessment - methods</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</subject><subject>Nerve Fibers, Myelinated - pathology</subject><subject>Neuroimaging - methods</subject><subject>Neurology</subject><subject>Time Factors</subject><issn>0028-3878</issn><issn>1526-632X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi0EokvhHyDkCxKXFH_FsS9IqCof0qq9LIKb5TjjXVeJE2xvq_33GHUp0EtPc5hn3pl3XoReU3JGGWXvb-N4RnpCOXCqmJTUs_4JWtGWyUZy9uMpWhHCVMNVp07Qi5yvCanNTj9HJ4wpwZlkK7TZJHsNrszpgGePb3ehAJ5sKZDw7rBACrFAzKEccL9PA0S8JHAwhLjFUxgH7OZtDCXcAA7TYkOaIJaX6Jm3Y4ZXx3qKvn262Jx_adZXn7-ef1w3ruVdaSj0glA1dK2GTgxC6EFWI1pQSUA63WnwnbZicFr1RCtQrneaO-mV8toDP0Uf7nSXfT_B4OrqZEezpDDZdDCzDeb_Tgw7s51vDBeM0pZXgXdHgTT_3EMuZgrZwTjaCPM-G8p0vaWjRD6OEt5SIup_KyruUJfmnBP4-4soMb-zM98v1-ZhdnXszb9u7of-hFWBt0fAZmdHn2x0If_lJFOStB3_Bfb3pbo</recordid><startdate>20120821</startdate><enddate>20120821</enddate><creator>SILBERT, Lisa C</creator><creator>DODGE, Hiroko H</creator><creator>PERKINS, Louie G</creator><creator>SHERBAKOV, Lena</creator><creator>LAHNA, David</creator><creator>ERTEN-LYONS, Deniz</creator><creator>WOLTJER, Randall</creator><creator>SHINTO, Lynne</creator><creator>KAYE, Jeffrey A</creator><general>Lippincott Williams & Wilkins</general><scope>IQODW</scope><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>7X8</scope><scope>7TK</scope><scope>5PM</scope></search><sort><creationdate>20120821</creationdate><title>Trajectory of white matter hyperintensity burden preceding mild cognitive impairment</title><author>SILBERT, Lisa C ; DODGE, Hiroko H ; PERKINS, Louie G ; SHERBAKOV, Lena ; LAHNA, David ; ERTEN-LYONS, Deniz ; WOLTJER, Randall ; SHINTO, Lynne ; KAYE, Jeffrey A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c537t-1eb4018d759e74d449d626694160e6c979ef79a4dc98b098e8cbc93c6f88f9fe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biological and medical sciences</topic><topic>Brain - pathology</topic><topic>Cerebrospinal Fluid - metabolism</topic><topic>Cognitive Dysfunction - cerebrospinal fluid</topic><topic>Cognitive Dysfunction - diagnosis</topic><topic>Cognitive Dysfunction - pathology</topic><topic>Disease Progression</topic><topic>Early Diagnosis</topic><topic>Female</topic><topic>Geriatric Assessment - methods</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</topic><topic>Nerve Fibers, Myelinated - pathology</topic><topic>Neuroimaging - methods</topic><topic>Neurology</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SILBERT, Lisa C</creatorcontrib><creatorcontrib>DODGE, Hiroko H</creatorcontrib><creatorcontrib>PERKINS, Louie G</creatorcontrib><creatorcontrib>SHERBAKOV, Lena</creatorcontrib><creatorcontrib>LAHNA, David</creatorcontrib><creatorcontrib>ERTEN-LYONS, Deniz</creatorcontrib><creatorcontrib>WOLTJER, Randall</creatorcontrib><creatorcontrib>SHINTO, Lynne</creatorcontrib><creatorcontrib>KAYE, Jeffrey A</creatorcontrib><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>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SILBERT, Lisa C</au><au>DODGE, Hiroko H</au><au>PERKINS, Louie G</au><au>SHERBAKOV, Lena</au><au>LAHNA, David</au><au>ERTEN-LYONS, Deniz</au><au>WOLTJER, Randall</au><au>SHINTO, Lynne</au><au>KAYE, Jeffrey A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Trajectory of white matter hyperintensity burden preceding mild cognitive impairment</atitle><jtitle>Neurology</jtitle><addtitle>Neurology</addtitle><date>2012-08-21</date><risdate>2012</risdate><volume>79</volume><issue>8</issue><spage>741</spage><epage>747</epage><pages>741-747</pages><issn>0028-3878</issn><eissn>1526-632X</eissn><coden>NEURAI</coden><abstract>To determine the time of acceleration in white matter hyperintensity (WMH) burden, a common indicator of cerebrovascular pathology, in relation to conversion to mild cognitive impairment (MCI) in the elderly.
A total of 181 cognitively intact elderly volunteers from the longitudinal, prospective, Oregon Brain Aging Study underwent yearly evaluations, including brain MRI, and cognitive testing. MRIs were analyzed for imaging markers of neurodegeneration: WMH and ventricular CSF (vCSF) volumes. The time before MCI, when the changes in WMH and vCSF burden accelerate, was assessed using a mixed-effects model with a change point for subjects who developed MCI during follow-up.
During a follow-up duration of up to 19.6 years, 134 subjects converted to MCI. Acceleration in %WMH volume increase occurred 10.6 years before MCI onset. On average, the annual rate of change in %WMH increased an additional 3.3% after the change point. Acceleration in %vCSF volume increase occurred 3.7 years before the onset of MCI. Out of 63 subjects who converted to MCI and had autopsy, only 28.5% had Alzheimer disease (AD) as the sole etiology of their dementia, while almost just as many (24%) had both AD and significant ischemic cerebrovascular disease present.
Acceleration in WMH burden, a common indicator of cerebrovascular disease in the elderly, is a pathologic change that emerges early in the presymptomatic phase leading to MCI. Longitudinal changes in WMH may thus be useful in determining those at risk for cognitive impairment and for planning strategies for introducing disease-modifying therapies prior to dementia onset.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>22843262</pmid><doi>10.1212/wnl.0b013e3182661f2b</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Aged, 80 and over Biological and medical sciences Brain - pathology Cerebrospinal Fluid - metabolism Cognitive Dysfunction - cerebrospinal fluid Cognitive Dysfunction - diagnosis Cognitive Dysfunction - pathology Disease Progression Early Diagnosis Female Geriatric Assessment - methods Humans Magnetic Resonance Imaging - methods Male Medical sciences Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis Nerve Fibers, Myelinated - pathology Neuroimaging - methods Neurology Time Factors |
title | Trajectory of white matter hyperintensity burden preceding mild cognitive impairment |
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