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

被引:30
作者
Natté, R
Vinters, HV
Maat-Schieman, MLC
Bornebroek, M
Haan, J
Roos, RAC
van Duinen, SG
机构
[1] Leiden Univ, Dept Pathol L1Q, Med Ctr, NL-2300 RC Leiden, Netherlands
[2] Leiden Univ, Dept Neurol, Med Ctr, NL-2300 RC Leiden, Netherlands
[3] Univ Calif Los Angeles, Med Ctr, Dept Pathol & Lab Med, Sect Neuropathol, Los Angeles, CA 90024 USA
[4] Rijnland Hosp, Dept Neurol, Leiderdorp, Netherlands
关键词
Alzheimer's disease; amyloid beta protein; cerebral amyloid angiopathy; cerebral aneurysm; cerebral hemorrhage;
D O I
10.1161/01.STR.29.8.1588
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose-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 CBA 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. Methods-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. Results-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. Conclusions-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.
引用
收藏
页码:1588 / 1594
页数:7
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