Progression of white matter lesions and hemorrhages in cerebral amyloid angiopathy
To determine the rate of progression of white matter lesions and hemorrhages in a cohort with cerebral amyloid angiopathy (CAA). The authors analyzed data from 26 patients with possible (3) or probable (23) CAA, diagnosed by the Boston Criteria. Brain maps of white matter hyperintensities, normalize...
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Veröffentlicht in: | Neurology 2006-07, Vol.67 (1), p.83-87 |
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description | To determine the rate of progression of white matter lesions and hemorrhages in a cohort with cerebral amyloid angiopathy (CAA).
The authors analyzed data from 26 patients with possible (3) or probable (23) CAA, diagnosed by the Boston Criteria. Brain maps of white matter hyperintensities, normalized to head size (nWMH), were created by blinded computer-assisted segmentation of MRI images obtained at baseline and after a median follow-up interval of 1.1 year.
There was a substantial nWMH volume increase over the interscan interval (median 0.5 mL/year, interquartile range 0.1 to 2.8, p < 0.001). The median yearly increase, expressed as a percentage of the baseline WMH volume, was 18%. The characteristic most strongly associated with nWMH volume increase was the baseline nWMH volume (r = 0.57, p = 0.002). The volume of nWMH progression was also associated with history of cognitive impairment (median 5.0 mL/year in cognitively impaired subjects vs 0.3 mL/year in cognitively unimpaired, p = 0.02) but not age or hypertension. This association remained present in an analysis stratified by baseline WMH volume. New hemorrhages, including asymptomatic microbleeds, were seen in 46% of subjects. The number of new MRI hemorrhages correlated strongly with baseline nWMH (r = 0.53, p = 0.005) but not with nWMH progression (r = 0.22, p = 0.28).
There is a progressive increase in white matter lesions in subjects with cerebral amyloid angiopathy. The association of white matter lesions with incident lobar hemorrhages suggests that white matter damage may reflect a progressive microangiopathy due to cerebral amyloid angiopathy. |
doi_str_mv | 10.1212/01.wnl.0000223613.57229.24 |
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The authors analyzed data from 26 patients with possible (3) or probable (23) CAA, diagnosed by the Boston Criteria. Brain maps of white matter hyperintensities, normalized to head size (nWMH), were created by blinded computer-assisted segmentation of MRI images obtained at baseline and after a median follow-up interval of 1.1 year.
There was a substantial nWMH volume increase over the interscan interval (median 0.5 mL/year, interquartile range 0.1 to 2.8, p < 0.001). The median yearly increase, expressed as a percentage of the baseline WMH volume, was 18%. The characteristic most strongly associated with nWMH volume increase was the baseline nWMH volume (r = 0.57, p = 0.002). The volume of nWMH progression was also associated with history of cognitive impairment (median 5.0 mL/year in cognitively impaired subjects vs 0.3 mL/year in cognitively unimpaired, p = 0.02) but not age or hypertension. This association remained present in an analysis stratified by baseline WMH volume. New hemorrhages, including asymptomatic microbleeds, were seen in 46% of subjects. The number of new MRI hemorrhages correlated strongly with baseline nWMH (r = 0.53, p = 0.005) but not with nWMH progression (r = 0.22, p = 0.28).
There is a progressive increase in white matter lesions in subjects with cerebral amyloid angiopathy. The association of white matter lesions with incident lobar hemorrhages suggests that white matter damage may reflect a progressive microangiopathy due to cerebral amyloid angiopathy.</description><identifier>ISSN: 0028-3878</identifier><identifier>EISSN: 1526-632X</identifier><identifier>DOI: 10.1212/01.wnl.0000223613.57229.24</identifier><identifier>PMID: 16832082</identifier><identifier>CODEN: NEURAI</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Aged ; Biological and medical sciences ; Brain - pathology ; Brain - physiopathology ; Cerebral Amyloid Angiopathy - pathology ; Cerebral Amyloid Angiopathy - physiopathology ; Cerebral Hemorrhage - physiopathology ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Disease Progression ; Female ; Humans ; Image Processing, Computer-Assisted - methods ; Longitudinal Studies ; Magnetic Resonance Imaging - methods ; Male ; Medical sciences ; Middle Aged ; Neurology ; Statistics as Topic ; Vascular diseases and vascular malformations of the nervous system</subject><ispartof>Neurology, 2006-07, Vol.67 (1), p.83-87</ispartof><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c454t-f2a641b5be72f6a464e0a2af8a293a8ac392a16a53e13dca3e6ea9799ab308b53</citedby><cites>FETCH-LOGICAL-c454t-f2a641b5be72f6a464e0a2af8a293a8ac392a16a53e13dca3e6ea9799ab308b53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18051873$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16832082$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>CHEN, Y. W</creatorcontrib><creatorcontrib>GUROL, M. E</creatorcontrib><creatorcontrib>ROSAND, J</creatorcontrib><creatorcontrib>VISWANATHAN, A</creatorcontrib><creatorcontrib>RAKICH, S. M</creatorcontrib><creatorcontrib>GROOVER, T. R</creatorcontrib><creatorcontrib>GREENBERG, S. M</creatorcontrib><creatorcontrib>SMITH, E. E</creatorcontrib><title>Progression of white matter lesions and hemorrhages in cerebral amyloid angiopathy</title><title>Neurology</title><addtitle>Neurology</addtitle><description>To determine the rate of progression of white matter lesions and hemorrhages in a cohort with cerebral amyloid angiopathy (CAA).
The authors analyzed data from 26 patients with possible (3) or probable (23) CAA, diagnosed by the Boston Criteria. Brain maps of white matter hyperintensities, normalized to head size (nWMH), were created by blinded computer-assisted segmentation of MRI images obtained at baseline and after a median follow-up interval of 1.1 year.
There was a substantial nWMH volume increase over the interscan interval (median 0.5 mL/year, interquartile range 0.1 to 2.8, p < 0.001). The median yearly increase, expressed as a percentage of the baseline WMH volume, was 18%. The characteristic most strongly associated with nWMH volume increase was the baseline nWMH volume (r = 0.57, p = 0.002). The volume of nWMH progression was also associated with history of cognitive impairment (median 5.0 mL/year in cognitively impaired subjects vs 0.3 mL/year in cognitively unimpaired, p = 0.02) but not age or hypertension. This association remained present in an analysis stratified by baseline WMH volume. New hemorrhages, including asymptomatic microbleeds, were seen in 46% of subjects. The number of new MRI hemorrhages correlated strongly with baseline nWMH (r = 0.53, p = 0.005) but not with nWMH progression (r = 0.22, p = 0.28).
There is a progressive increase in white matter lesions in subjects with cerebral amyloid angiopathy. The association of white matter lesions with incident lobar hemorrhages suggests that white matter damage may reflect a progressive microangiopathy due to cerebral amyloid angiopathy.</description><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Brain - pathology</subject><subject>Brain - physiopathology</subject><subject>Cerebral Amyloid Angiopathy - pathology</subject><subject>Cerebral Amyloid Angiopathy - physiopathology</subject><subject>Cerebral Hemorrhage - physiopathology</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted - methods</subject><subject>Longitudinal Studies</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neurology</subject><subject>Statistics as Topic</subject><subject>Vascular diseases and vascular malformations of the nervous system</subject><issn>0028-3878</issn><issn>1526-632X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkV-r1DAQxYMo3vXqV5Ag6FtrMmnS1AdBLv6DC4oo-Bam2ek20jZr0vWy395c7-JqXgZyfnNmmMPYMylqCRJeClnfLFMtygNQRqpatwBdDc09tpEaTGUUfL_PNkW3lbKtvWCPcv4hRBHb7iG7kMYqEBY27MvnFHeJcg5x4XHgN2NYic-4rpT4RLffmeOy5SPNMaURd5R5WLinRH3CieN8nGLYFmYX4h7X8fiYPRhwyvTkVC_Zt3dvv159qK4_vf949ea68o1u1moANI3sdU8tDAYb05BAwMEidAotetUBSoNakVRbj4oMYdd2HfZK2F6rS_b6znd_6GfaelrWspDbpzBjOrqIwf2vLGF0u_jLSV3u1phi8OJkkOLPA-XVzSF7miZcKB6yM9ZAK3RXwFd3oE8x50TD3yFSuNtInJCuROLOkbg_kThoSvPTf9c8t54yKMDzE4DZ4zQkXHzIZ84KLW2r1G9uQZh5</recordid><startdate>20060711</startdate><enddate>20060711</enddate><creator>CHEN, Y. W</creator><creator>GUROL, M. E</creator><creator>ROSAND, J</creator><creator>VISWANATHAN, A</creator><creator>RAKICH, S. M</creator><creator>GROOVER, T. R</creator><creator>GREENBERG, S. M</creator><creator>SMITH, E. E</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>5PM</scope></search><sort><creationdate>20060711</creationdate><title>Progression of white matter lesions and hemorrhages in cerebral amyloid angiopathy</title><author>CHEN, Y. W ; GUROL, M. E ; ROSAND, J ; VISWANATHAN, A ; RAKICH, S. M ; GROOVER, T. R ; GREENBERG, S. M ; SMITH, E. 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Prion diseases</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Humans</topic><topic>Image Processing, Computer-Assisted - methods</topic><topic>Longitudinal Studies</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neurology</topic><topic>Statistics as Topic</topic><topic>Vascular diseases and vascular malformations of the nervous system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CHEN, Y. W</creatorcontrib><creatorcontrib>GUROL, M. E</creatorcontrib><creatorcontrib>ROSAND, J</creatorcontrib><creatorcontrib>VISWANATHAN, A</creatorcontrib><creatorcontrib>RAKICH, S. M</creatorcontrib><creatorcontrib>GROOVER, T. R</creatorcontrib><creatorcontrib>GREENBERG, S. M</creatorcontrib><creatorcontrib>SMITH, E. 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E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Progression of white matter lesions and hemorrhages in cerebral amyloid angiopathy</atitle><jtitle>Neurology</jtitle><addtitle>Neurology</addtitle><date>2006-07-11</date><risdate>2006</risdate><volume>67</volume><issue>1</issue><spage>83</spage><epage>87</epage><pages>83-87</pages><issn>0028-3878</issn><eissn>1526-632X</eissn><coden>NEURAI</coden><abstract>To determine the rate of progression of white matter lesions and hemorrhages in a cohort with cerebral amyloid angiopathy (CAA).
The authors analyzed data from 26 patients with possible (3) or probable (23) CAA, diagnosed by the Boston Criteria. Brain maps of white matter hyperintensities, normalized to head size (nWMH), were created by blinded computer-assisted segmentation of MRI images obtained at baseline and after a median follow-up interval of 1.1 year.
There was a substantial nWMH volume increase over the interscan interval (median 0.5 mL/year, interquartile range 0.1 to 2.8, p < 0.001). The median yearly increase, expressed as a percentage of the baseline WMH volume, was 18%. The characteristic most strongly associated with nWMH volume increase was the baseline nWMH volume (r = 0.57, p = 0.002). The volume of nWMH progression was also associated with history of cognitive impairment (median 5.0 mL/year in cognitively impaired subjects vs 0.3 mL/year in cognitively unimpaired, p = 0.02) but not age or hypertension. This association remained present in an analysis stratified by baseline WMH volume. New hemorrhages, including asymptomatic microbleeds, were seen in 46% of subjects. The number of new MRI hemorrhages correlated strongly with baseline nWMH (r = 0.53, p = 0.005) but not with nWMH progression (r = 0.22, p = 0.28).
There is a progressive increase in white matter lesions in subjects with cerebral amyloid angiopathy. The association of white matter lesions with incident lobar hemorrhages suggests that white matter damage may reflect a progressive microangiopathy due to cerebral amyloid angiopathy.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>16832082</pmid><doi>10.1212/01.wnl.0000223613.57229.24</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Biological and medical sciences Brain - pathology Brain - physiopathology Cerebral Amyloid Angiopathy - pathology Cerebral Amyloid Angiopathy - physiopathology Cerebral Hemorrhage - physiopathology Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Disease Progression Female Humans Image Processing, Computer-Assisted - methods Longitudinal Studies Magnetic Resonance Imaging - methods Male Medical sciences Middle Aged Neurology Statistics as Topic Vascular diseases and vascular malformations of the nervous system |
title | Progression of white matter lesions and hemorrhages in cerebral amyloid angiopathy |
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