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 "...
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Veröffentlicht in: | Stroke (1970) 1998-08, Vol.29 (8), p.1588-1594 |
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container_title | Stroke (1970) |
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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 |
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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.</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 & 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&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 < 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. 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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 < 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 & Wilkins</pub><pmid>9707198</pmid><doi>10.1161/01.STR.29.8.1588</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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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 |
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