Neuropathology of microbleeds in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

被引:4
|
作者
Magaki, Shino [1 ,2 ,9 ,10 ]
Chen, Zesheng [1 ,2 ,8 ]
Severance, Alyscia [1 ,2 ]
Williams, Christopher K. [1 ,2 ]
Diaz, Ramiro [1 ,2 ]
Fang, Chuo [3 ]
Khanlou, Negar [1 ,2 ]
Yong, William H. [1 ,2 ,7 ]
Paganini-Hill, Annlia [3 ]
Kalaria, Rajesh N. [4 ]
Vinters, Harry V. [1 ,2 ,5 ,6 ]
Fisher, Mark [3 ,7 ]
机构
[1] Ronald Reagan UCLA Med Ctr, Dept Pathol & Lab Med, Sect Neuropathol, Los Angeles, CA 90095 USA
[2] David Geffen Sch Med, Los Angeles, CA 90095 USA
[3] Univ Calif Irvine, Sch Med, Dept Neurol, Irvine, CA USA
[4] Newcastle Univ, Translat & Clin Res Inst, Campus Ageing & Vital, Newcastle Upon Tyne, England
[5] Ronald Reagan UCLA Med Ctr, Dept Neurol, Los Angeles, CA 90095 USA
[6] Ronald Reagan UCLA Med Ctr, Brain Res Inst, Los Angeles, CA 90095 USA
[7] Univ Calif Irvine, Sch Med, Dept Pathol & Lab Med, Irvine, CA USA
[8] Ctr Hosp Univ St Justine, Montreal, PQ, Canada
[9] Ronald Reagan UCLA Med Ctr, Dept Pathol & Lab Med, Rm 1P-250,10833 Le Conte Ave, Los Angeles, CA 90095 USA
[10] David Geffen Sch Med, Ctr Hlth Sci, Rm 1P-250,10833 Le Conte Ave, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
Aging; CADASIL; Cerebral microbleed; Hemosiderin; Immunohistochemistry; Small vessel disease; GRANULAR OSMIOPHILIC MATERIAL; SMALL VESSEL DISEASE; CEREBROVASCULAR PATHOLOGY; INTRACEREBRAL HEMORRHAGE; NOTCH3; ECTODOMAIN; IRON DEPOSITION; ISCHEMIC-STROKE; BASAL GANGLIA; MRI; TRANSFERRIN;
D O I
10.1093/jnen/nlad004
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Cerebral microbleeds (CMBs) detected on magnetic resonance imaging are common in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). The neuropathologic correlates of CMBs are unclear. In this study, we characterized findings relevant to CMBs in autopsy brain tissue of 8 patients with genetically confirmed CADASIL and 10 controls within the age range of the CADASIL patients by assessing the distribution and extent of hemosiderin/iron deposits including perivascular hemosiderin leakage (PVH), capillary hemosiderin deposits, and parenchymal iron deposits (PID) in the frontal cortex and white matter, basal ganglia and cerebellum. We also characterized infarcts, vessel wall thickening, and severity of vascular smooth muscle cell degeneration. CADASIL subjects had a significant increase in hemosiderin/iron deposits compared with controls. This increase was principally seen with PID. Hemosiderin/iron deposits were seen in the majority of CADASIL subjects in all brain areas. PVH was most pronounced in the frontal white matter and basal ganglia around small to medium sized arterioles, with no predilection for the vicinity of vessels with severe vascular changes or infarcts. CADASIL subjects have increased brain hemosiderin/iron deposits but these do not occur in a periarteriolar distribution. Pathogenesis of these lesions remains uncertain.
引用
收藏
页码:333 / 344
页数:12
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