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脑白质疏松既有神经退行性变的原因,也有血管性原因,可能主要是一种远端轴索性神经病。

Cerebral white matter rarefaction has both neurodegenerative and vascular causes and may primarily be a distal axonopathy.

机构信息

Banner Sun Health Research Institute, Sun City, Arizona, USA.

Department of Neurology, Mayo Clinic, Scottsdale, Arizona, USA.

出版信息

J Neuropathol Exp Neurol. 2023 May 25;82(6):457-466. doi: 10.1093/jnen/nlad026.

Abstract

Cerebral white matter rarefaction (CWMR) was considered by Binswanger and Alzheimer to be due to cerebral arteriolosclerosis. Renewed attention came with CT and MR brain imaging, and neuropathological studies finding a high rate of CWMR in Alzheimer disease (AD). The relative contributions of cerebrovascular disease and AD to CWMR are still uncertain. In 1181 autopsies by the Arizona Study of Aging and Neurodegenerative Disorders (AZSAND), large-format brain sections were used to grade CWMR and determine its vascular and neurodegenerative correlates. Almost all neurodegenerative diseases had more severe CWMR than the normal control group. Multivariable logistic regression models indicated that Braak neurofibrillary stage was the strongest predictor of CWMR, with additional independently significant predictors including age, cortical and diencephalic lacunar and microinfarcts, body mass index, and female sex. It appears that while AD and cerebrovascular pathology may be additive in causing CWMR, both may be solely capable of this. The typical periventricular pattern suggests that CWMR is primarily a distal axonopathy caused by dysfunction of the cell bodies of long-association corticocortical projection neurons. A consequence of these findings is that CWMR should not be viewed simply as "small vessel disease" or as a pathognomonic indicator of vascular cognitive impairment or vascular dementia.

摘要

脑白质疏松症(Cerebral White Matter Raefaction,CWMR)被 Binswanger 和 Alzheimer 认为是由于脑小动脉硬化所致。随着 CT 和 MRI 脑成像的出现,以及神经病理学研究发现阿尔茨海默病(AD)中 CWMR 的发生率很高,人们对其重新产生了关注。脑血管病和 AD 对 CWMR 的相对贡献仍不确定。在亚利桑那州老龄化和神经退行性疾病研究(Arizona Study of Aging and Neurodegenerative Disorders,AZSAND)的 1181 例尸检中,使用大格式脑切片来对 CWMR 进行分级,并确定其与血管和神经退行性变的相关性。几乎所有神经退行性疾病的 CWMR 都比正常对照组严重。多变量逻辑回归模型表明,Braak 神经纤维缠结分期是 CWMR 的最强预测因子,另外还有独立显著的预测因子包括年龄、皮质和间脑腔隙性和微梗死、体重指数和女性。似乎 AD 和脑血管病理可能在导致 CWMR 方面具有相加作用,但两者也可能单独具有这种作用。典型的脑室周围模式表明,CWMR 主要是由长距离皮质-皮质投射神经元细胞体功能障碍引起的远端轴索病。这些发现的结果是,CWMR 不应简单地视为“小血管疾病”,也不应将其视为血管性认知障碍或血管性痴呆的特征性指标。

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