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老年人脑淀粉样血管病:临床病理特征、发病机制及危险因素

Cerebral amyloid angiopathy in the elderly: the clinicopathological features, pathogenesis, and risk factors.

作者信息

Itoh Y, Yamada M

机构信息

Department of Neurology, Faculty of Medicine, Tokyo Medical and Dental University, Japan.

出版信息

J Med Dent Sci. 1997 Mar;44(1):11-9.

PMID:9385038
Abstract

Cerebral amyloid angiopathy (CAA) is known to be associated with intracerebral hemorrhage in the elderly. In this study we demonstrated that, among 101 cases with intracerebral hemorrhages found in 1000 consecutive autopsied cases (average age, 82.9 years) at a geriatric hospital, CAA accounted for 10.9% of them (31.0% of lobar and 14.3% of cerebellar hemorrhages). Immunohistochemically, the cerebrovascular amyloid was positive for beta/A4 peptide, and less intensely for cystatin C. The CAA-related hemorrhages were characteristically located near the cortical surface and ruptured into the subarachnoid space. No mutation of the amyloid precursor protein gene or the cystatin C gene was detected in these cases. From the observation of 500 serial sections containing amyloid-laden vessels of a patient with CAA-related hemorrhage, it was suggested that the hemorrhage occurred at microaneurysms with fibrinoid necrosis, which were found in small arteries in the cerebral cortex. The spatial distribution of CAA was closely associated with that of subpial beta/A4 peptide deposits in the brain, raising the possibility that the cerebrovascular amyloid originates from the brain parenchyma. Finally, the severity of CAA did not seem to be influenced by the inheritance of the epsilon 4 allele of the apolipoprotein E gene, which is known as a risk factor for dementia of the Alzheimer type.

摘要

脑淀粉样血管病(CAA)已知与老年人脑出血有关。在本研究中,我们证明,在一家老年医院连续1000例尸检病例(平均年龄82.9岁)中发现的101例脑出血病例中,CAA占其中的10.9%(脑叶出血的31.0%,小脑出血的14.3%)。免疫组织化学显示,脑血管淀粉样蛋白对β/A4肽呈阳性,对胱抑素C的阳性强度较低。与CAA相关的出血特征性地位于皮质表面附近,并破入蛛网膜下腔。在这些病例中未检测到淀粉样前体蛋白基因或胱抑素C基因的突变。通过观察一名患有CAA相关出血患者的500个连续切片,其中含有淀粉样蛋白沉积的血管,提示出血发生在脑皮质小动脉中出现的伴有纤维蛋白样坏死的微动脉瘤处。CAA的空间分布与脑软膜下β/A4肽沉积的分布密切相关,这增加了脑血管淀粉样蛋白起源于脑实质的可能性。最后,CAA的严重程度似乎不受载脂蛋白E基因ε4等位基因遗传的影响,该等位基因是阿尔茨海默病型痴呆的已知危险因素。

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