Microvasculopathy is associated with the number of cerebrovascular lesions in hereditary cerebral hemorrhage with amyloidosis, Dutch type

Microvascular changes such as microaneurysms and fibrinoid necrosis have been found in the presence of cerebral amyloid angiopathy (CAA). These CAA-associated microvasculopathies (CAA-AM) may contribute to the development of CAA-associated hemorrhages and/or infarcts, hereafter referred to as "...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Stroke (1970) 1998-08, Vol.29 (8), p.1588-1594
Hauptverfasser: NATTE, R, VINTERS, H. V, MAAT-SCHIEMAN, M. L. C, BORNEBROEK, M, HAAN, J, ROOS, R. A. C, VAN DUINEN, S. G
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1594
container_issue 8
container_start_page 1588
container_title Stroke (1970)
container_volume 29
creator NATTE, R
VINTERS, H. V
MAAT-SCHIEMAN, M. L. C
BORNEBROEK, M
HAAN, J
ROOS, R. A. C
VAN DUINEN, S. G
description Microvascular changes such as microaneurysms and fibrinoid necrosis have been found in the presence of cerebral amyloid angiopathy (CAA). These CAA-associated microvasculopathies (CAA-AM) may contribute to the development of CAA-associated hemorrhages and/or infarcts, hereafter referred to as "cerebrovascular lesions." Hereditary cerebral hemorrhage with amyloidosis, Dutch type (HCHWA-D) is an autosomal dominant form of CAA, in which the amyloid angiopathy is pathologically and biochemically similar to sporadic CAA associated with aging and Alzheimer disease. To determine the significance of CAA-AM for CAA-associated cerebrovascular complications, we investigated the association between CAA-AM and cerebrovascular lesions in HCHWA-D patients. In a previous autopsy study we semiquantitatively scored CAA-AM in 29 HCHWA-D patients. In the present study we reviewed clinical charts and autopsy protocols of these same patients. We investigated whether CAA-AM was associated with age at death, number of cerebrovascular lesions, duration of clinical illness, hypertension, and atherosclerosis. An association was found between CAA-AM and the number of cerebrovascular lesions (P = 0.009). The presence of microaneurysmal degeneration was most strongly associated with the number of cerebrovascular lesions (P < 0.001). In addition, we found an association between atherosclerosis and the CAA-AM score (P = 0.047). Hypertension was not associated with CAA-AM. Our findings support previous reports suggesting an important role of secondary microvascular degenerative changes in CAA-associated cerebrovascular lesions and suggest an aggravating effect of systemic atherosclerosis, but not hypertension, on the evolution of CAA-AM. These findings may be of relevance to understanding cerebrovascular complications of sporadic or Alzheimer disease-associated CAA.
doi_str_mv 10.1161/01.STR.29.8.1588
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_73837504</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>73837504</sourcerecordid><originalsourceid>FETCH-LOGICAL-c401t-273df413a6f296c6ee4d69d65ebe4669bf55f085a9125ebdbecf6035b26d47773</originalsourceid><addsrcrecordid>eNo9kEuL1TAUx4Mo43V070bIQlzZmkeTJkuZ8QUjgo7rkCYnNtI216RV7kfwW5vh1lkd-L_g_BB6TklLqaRvCG2_3X5tmW5VS4VSD9CBCtY1nWTqIToQwnXDOq0foyel_CSEMK7EBbrQPempVgf093N0Of22xW1TOtp1POFYsC0luWhX8PhPXEe8joCXbR4g4xSwgwzD_5LNeIIS01JwXPBYLR9Xm097yk5Vm1POo_0B5zE7n6YUfSqxvMbX2-rq_ukIT9GjYKcCz_Z7ib6_f3d79bG5-fLh09Xbm8Z1hK4N67kPHeVWBqalkwCdl9pLAQN0UuohCBGIElZTVjU_gAuScDEw6bu-7_klenXePeb0a4OymjkWB9NkF0hbMT1XvBekq0FyDlZApWQI5pjjXF8zlJg7-oZQU-kbpo0yd_Rr5cW-vQ0z-PvCjrv6L3e_srNTyHZxsdzHGBdEccL_AW1gkP4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>73837504</pqid></control><display><type>article</type><title>Microvasculopathy is associated with the number of cerebrovascular lesions in hereditary cerebral hemorrhage with amyloidosis, Dutch type</title><source>MEDLINE</source><source>American Heart Association Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Journals@Ovid Complete</source><source>Alma/SFX Local Collection</source><creator>NATTE, R ; VINTERS, H. V ; MAAT-SCHIEMAN, M. L. C ; BORNEBROEK, M ; HAAN, J ; ROOS, R. A. C ; VAN DUINEN, S. G</creator><creatorcontrib>NATTE, R ; VINTERS, H. V ; MAAT-SCHIEMAN, M. L. C ; BORNEBROEK, M ; HAAN, J ; ROOS, R. A. C ; VAN DUINEN, S. G</creatorcontrib><description>Microvascular changes such as microaneurysms and fibrinoid necrosis have been found in the presence of cerebral amyloid angiopathy (CAA). These CAA-associated microvasculopathies (CAA-AM) may contribute to the development of CAA-associated hemorrhages and/or infarcts, hereafter referred to as "cerebrovascular lesions." Hereditary cerebral hemorrhage with amyloidosis, Dutch type (HCHWA-D) is an autosomal dominant form of CAA, in which the amyloid angiopathy is pathologically and biochemically similar to sporadic CAA associated with aging and Alzheimer disease. To determine the significance of CAA-AM for CAA-associated cerebrovascular complications, we investigated the association between CAA-AM and cerebrovascular lesions in HCHWA-D patients. In a previous autopsy study we semiquantitatively scored CAA-AM in 29 HCHWA-D patients. In the present study we reviewed clinical charts and autopsy protocols of these same patients. We investigated whether CAA-AM was associated with age at death, number of cerebrovascular lesions, duration of clinical illness, hypertension, and atherosclerosis. An association was found between CAA-AM and the number of cerebrovascular lesions (P = 0.009). The presence of microaneurysmal degeneration was most strongly associated with the number of cerebrovascular lesions (P &lt; 0.001). In addition, we found an association between atherosclerosis and the CAA-AM score (P = 0.047). Hypertension was not associated with CAA-AM. Our findings support previous reports suggesting an important role of secondary microvascular degenerative changes in CAA-associated cerebrovascular lesions and suggest an aggravating effect of systemic atherosclerosis, but not hypertension, on the evolution of CAA-AM. These findings may be of relevance to understanding cerebrovascular complications of sporadic or Alzheimer disease-associated CAA.</description><identifier>ISSN: 0039-2499</identifier><identifier>EISSN: 1524-4628</identifier><identifier>DOI: 10.1161/01.STR.29.8.1588</identifier><identifier>PMID: 9707198</identifier><identifier>CODEN: SJCCA7</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams &amp; Wilkins</publisher><subject>Age Factors ; Aged ; Aged, 80 and over ; Arteriosclerosis - complications ; Arteriosclerosis - pathology ; Biological and medical sciences ; Brain - blood supply ; Capillaries - pathology ; Cerebral Amyloid Angiopathy - genetics ; Cerebral Amyloid Angiopathy - mortality ; Cerebral Amyloid Angiopathy - pathology ; Cerebral Hemorrhage - genetics ; Cerebral Hemorrhage - mortality ; Cerebral Hemorrhage - pathology ; Cerebrovascular Disorders - etiology ; Cerebrovascular Disorders - genetics ; Cerebrovascular Disorders - pathology ; Female ; Humans ; Hypertension - complications ; Hypertension - pathology ; Intracranial Aneurysm - complications ; Intracranial Aneurysm - pathology ; Male ; Medical sciences ; Microcirculation ; Middle Aged ; Neurology ; Vascular diseases and vascular malformations of the nervous system</subject><ispartof>Stroke (1970), 1998-08, Vol.29 (8), p.1588-1594</ispartof><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c401t-273df413a6f296c6ee4d69d65ebe4669bf55f085a9125ebdbecf6035b26d47773</citedby><cites>FETCH-LOGICAL-c401t-273df413a6f296c6ee4d69d65ebe4669bf55f085a9125ebdbecf6035b26d47773</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3687,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=2350830$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9707198$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>NATTE, R</creatorcontrib><creatorcontrib>VINTERS, H. V</creatorcontrib><creatorcontrib>MAAT-SCHIEMAN, M. L. C</creatorcontrib><creatorcontrib>BORNEBROEK, M</creatorcontrib><creatorcontrib>HAAN, J</creatorcontrib><creatorcontrib>ROOS, R. A. C</creatorcontrib><creatorcontrib>VAN DUINEN, S. G</creatorcontrib><title>Microvasculopathy is associated with the number of cerebrovascular lesions in hereditary cerebral hemorrhage with amyloidosis, Dutch type</title><title>Stroke (1970)</title><addtitle>Stroke</addtitle><description>Microvascular changes such as microaneurysms and fibrinoid necrosis have been found in the presence of cerebral amyloid angiopathy (CAA). These CAA-associated microvasculopathies (CAA-AM) may contribute to the development of CAA-associated hemorrhages and/or infarcts, hereafter referred to as "cerebrovascular lesions." Hereditary cerebral hemorrhage with amyloidosis, Dutch type (HCHWA-D) is an autosomal dominant form of CAA, in which the amyloid angiopathy is pathologically and biochemically similar to sporadic CAA associated with aging and Alzheimer disease. To determine the significance of CAA-AM for CAA-associated cerebrovascular complications, we investigated the association between CAA-AM and cerebrovascular lesions in HCHWA-D patients. In a previous autopsy study we semiquantitatively scored CAA-AM in 29 HCHWA-D patients. In the present study we reviewed clinical charts and autopsy protocols of these same patients. We investigated whether CAA-AM was associated with age at death, number of cerebrovascular lesions, duration of clinical illness, hypertension, and atherosclerosis. An association was found between CAA-AM and the number of cerebrovascular lesions (P = 0.009). The presence of microaneurysmal degeneration was most strongly associated with the number of cerebrovascular lesions (P &lt; 0.001). In addition, we found an association between atherosclerosis and the CAA-AM score (P = 0.047). Hypertension was not associated with CAA-AM. Our findings support previous reports suggesting an important role of secondary microvascular degenerative changes in CAA-associated cerebrovascular lesions and suggest an aggravating effect of systemic atherosclerosis, but not hypertension, on the evolution of CAA-AM. These findings may be of relevance to understanding cerebrovascular complications of sporadic or Alzheimer disease-associated CAA.</description><subject>Age Factors</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Arteriosclerosis - complications</subject><subject>Arteriosclerosis - pathology</subject><subject>Biological and medical sciences</subject><subject>Brain - blood supply</subject><subject>Capillaries - pathology</subject><subject>Cerebral Amyloid Angiopathy - genetics</subject><subject>Cerebral Amyloid Angiopathy - mortality</subject><subject>Cerebral Amyloid Angiopathy - pathology</subject><subject>Cerebral Hemorrhage - genetics</subject><subject>Cerebral Hemorrhage - mortality</subject><subject>Cerebral Hemorrhage - pathology</subject><subject>Cerebrovascular Disorders - etiology</subject><subject>Cerebrovascular Disorders - genetics</subject><subject>Cerebrovascular Disorders - pathology</subject><subject>Female</subject><subject>Humans</subject><subject>Hypertension - complications</subject><subject>Hypertension - pathology</subject><subject>Intracranial Aneurysm - complications</subject><subject>Intracranial Aneurysm - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microcirculation</subject><subject>Middle Aged</subject><subject>Neurology</subject><subject>Vascular diseases and vascular malformations of the nervous system</subject><issn>0039-2499</issn><issn>1524-4628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kEuL1TAUx4Mo43V070bIQlzZmkeTJkuZ8QUjgo7rkCYnNtI216RV7kfwW5vh1lkd-L_g_BB6TklLqaRvCG2_3X5tmW5VS4VSD9CBCtY1nWTqIToQwnXDOq0foyel_CSEMK7EBbrQPempVgf093N0Of22xW1TOtp1POFYsC0luWhX8PhPXEe8joCXbR4g4xSwgwzD_5LNeIIS01JwXPBYLR9Xm097yk5Vm1POo_0B5zE7n6YUfSqxvMbX2-rq_ukIT9GjYKcCz_Z7ib6_f3d79bG5-fLh09Xbm8Z1hK4N67kPHeVWBqalkwCdl9pLAQN0UuohCBGIElZTVjU_gAuScDEw6bu-7_klenXePeb0a4OymjkWB9NkF0hbMT1XvBekq0FyDlZApWQI5pjjXF8zlJg7-oZQU-kbpo0yd_Rr5cW-vQ0z-PvCjrv6L3e_srNTyHZxsdzHGBdEccL_AW1gkP4</recordid><startdate>19980801</startdate><enddate>19980801</enddate><creator>NATTE, R</creator><creator>VINTERS, H. V</creator><creator>MAAT-SCHIEMAN, M. L. C</creator><creator>BORNEBROEK, M</creator><creator>HAAN, J</creator><creator>ROOS, R. A. C</creator><creator>VAN DUINEN, S. G</creator><general>Lippincott Williams &amp; 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></search><sort><creationdate>19980801</creationdate><title>Microvasculopathy is associated with the number of cerebrovascular lesions in hereditary cerebral hemorrhage with amyloidosis, Dutch type</title><author>NATTE, R ; VINTERS, H. V ; MAAT-SCHIEMAN, M. L. C ; BORNEBROEK, M ; HAAN, J ; ROOS, R. A. C ; VAN DUINEN, S. G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c401t-273df413a6f296c6ee4d69d65ebe4669bf55f085a9125ebdbecf6035b26d47773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Age Factors</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Arteriosclerosis - complications</topic><topic>Arteriosclerosis - pathology</topic><topic>Biological and medical sciences</topic><topic>Brain - blood supply</topic><topic>Capillaries - pathology</topic><topic>Cerebral Amyloid Angiopathy - genetics</topic><topic>Cerebral Amyloid Angiopathy - mortality</topic><topic>Cerebral Amyloid Angiopathy - pathology</topic><topic>Cerebral Hemorrhage - genetics</topic><topic>Cerebral Hemorrhage - mortality</topic><topic>Cerebral Hemorrhage - pathology</topic><topic>Cerebrovascular Disorders - etiology</topic><topic>Cerebrovascular Disorders - genetics</topic><topic>Cerebrovascular Disorders - pathology</topic><topic>Female</topic><topic>Humans</topic><topic>Hypertension - complications</topic><topic>Hypertension - pathology</topic><topic>Intracranial Aneurysm - complications</topic><topic>Intracranial Aneurysm - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microcirculation</topic><topic>Middle Aged</topic><topic>Neurology</topic><topic>Vascular diseases and vascular malformations of the nervous system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>NATTE, R</creatorcontrib><creatorcontrib>VINTERS, H. V</creatorcontrib><creatorcontrib>MAAT-SCHIEMAN, M. L. C</creatorcontrib><creatorcontrib>BORNEBROEK, M</creatorcontrib><creatorcontrib>HAAN, J</creatorcontrib><creatorcontrib>ROOS, R. A. C</creatorcontrib><creatorcontrib>VAN DUINEN, S. G</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><jtitle>Stroke (1970)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>NATTE, R</au><au>VINTERS, H. V</au><au>MAAT-SCHIEMAN, M. L. C</au><au>BORNEBROEK, M</au><au>HAAN, J</au><au>ROOS, R. A. C</au><au>VAN DUINEN, S. G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microvasculopathy is associated with the number of cerebrovascular lesions in hereditary cerebral hemorrhage with amyloidosis, Dutch type</atitle><jtitle>Stroke (1970)</jtitle><addtitle>Stroke</addtitle><date>1998-08-01</date><risdate>1998</risdate><volume>29</volume><issue>8</issue><spage>1588</spage><epage>1594</epage><pages>1588-1594</pages><issn>0039-2499</issn><eissn>1524-4628</eissn><coden>SJCCA7</coden><abstract>Microvascular changes such as microaneurysms and fibrinoid necrosis have been found in the presence of cerebral amyloid angiopathy (CAA). These CAA-associated microvasculopathies (CAA-AM) may contribute to the development of CAA-associated hemorrhages and/or infarcts, hereafter referred to as "cerebrovascular lesions." Hereditary cerebral hemorrhage with amyloidosis, Dutch type (HCHWA-D) is an autosomal dominant form of CAA, in which the amyloid angiopathy is pathologically and biochemically similar to sporadic CAA associated with aging and Alzheimer disease. To determine the significance of CAA-AM for CAA-associated cerebrovascular complications, we investigated the association between CAA-AM and cerebrovascular lesions in HCHWA-D patients. In a previous autopsy study we semiquantitatively scored CAA-AM in 29 HCHWA-D patients. In the present study we reviewed clinical charts and autopsy protocols of these same patients. We investigated whether CAA-AM was associated with age at death, number of cerebrovascular lesions, duration of clinical illness, hypertension, and atherosclerosis. An association was found between CAA-AM and the number of cerebrovascular lesions (P = 0.009). The presence of microaneurysmal degeneration was most strongly associated with the number of cerebrovascular lesions (P &lt; 0.001). In addition, we found an association between atherosclerosis and the CAA-AM score (P = 0.047). Hypertension was not associated with CAA-AM. Our findings support previous reports suggesting an important role of secondary microvascular degenerative changes in CAA-associated cerebrovascular lesions and suggest an aggravating effect of systemic atherosclerosis, but not hypertension, on the evolution of CAA-AM. These findings may be of relevance to understanding cerebrovascular complications of sporadic or Alzheimer disease-associated CAA.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams &amp; Wilkins</pub><pmid>9707198</pmid><doi>10.1161/01.STR.29.8.1588</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0039-2499
ispartof Stroke (1970), 1998-08, Vol.29 (8), p.1588-1594
issn 0039-2499
1524-4628
language eng
recordid cdi_proquest_miscellaneous_73837504
source MEDLINE; American Heart Association Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Journals@Ovid Complete; Alma/SFX Local Collection
subjects Age Factors
Aged
Aged, 80 and over
Arteriosclerosis - complications
Arteriosclerosis - pathology
Biological and medical sciences
Brain - blood supply
Capillaries - pathology
Cerebral Amyloid Angiopathy - genetics
Cerebral Amyloid Angiopathy - mortality
Cerebral Amyloid Angiopathy - pathology
Cerebral Hemorrhage - genetics
Cerebral Hemorrhage - mortality
Cerebral Hemorrhage - pathology
Cerebrovascular Disorders - etiology
Cerebrovascular Disorders - genetics
Cerebrovascular Disorders - pathology
Female
Humans
Hypertension - complications
Hypertension - pathology
Intracranial Aneurysm - complications
Intracranial Aneurysm - pathology
Male
Medical sciences
Microcirculation
Middle Aged
Neurology
Vascular diseases and vascular malformations of the nervous system
title Microvasculopathy is associated with the number of cerebrovascular lesions in hereditary cerebral hemorrhage with amyloidosis, Dutch type
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T19%3A23%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Microvasculopathy%20is%20associated%20with%20the%20number%20of%20cerebrovascular%20lesions%20in%20hereditary%20cerebral%20hemorrhage%20with%20amyloidosis,%20Dutch%20type&rft.jtitle=Stroke%20(1970)&rft.au=NATTE,%20R&rft.date=1998-08-01&rft.volume=29&rft.issue=8&rft.spage=1588&rft.epage=1594&rft.pages=1588-1594&rft.issn=0039-2499&rft.eissn=1524-4628&rft.coden=SJCCA7&rft_id=info:doi/10.1161/01.STR.29.8.1588&rft_dat=%3Cproquest_cross%3E73837504%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=73837504&rft_id=info:pmid/9707198&rfr_iscdi=true