白质
血管性痴呆
痴呆
医学
病理
神经学
高强度
移植
神经科学
疾病
内科学
心理学
磁共振成像
精神科
放射科
作者
S. Thomas Carmichael,Irene L. Llorente
出处
期刊:Neurotherapeutics
[Springer Science+Business Media]
日期:2023-01-01
卷期号:20 (1): 39-47
被引量:2
标识
DOI:10.1007/s13311-022-01322-8
摘要
White matter injury is a progressive vascular disease that leads to neurological deficits and vascular dementia. It comprises up to 30% of all diagnosed strokes, though up to ten times as many events go undiagnosed in early stages. There are several pathologies that can lead to white matter injury. While some studies suggest that white matter injury starts as small infarcts in deep penetrating blood vessels in the brain, others point to the breakdown of endothelial function or the blood–brain barrier as the primary cause of the disease. Whether due to local endothelial or BBB dysfunction, or to local small infarcts (or a combination), white matter injury progresses, accumulates, and expands from preexisting lesions into adjacent white matter to produce motor and cognitive deficits that present as vascular dementia in the elderly. Vascular dementia is the second leading cause of dementia, and white matter injury–attributed vascular dementia represents 40% of all diagnosed dementias and aggravates Alzheimer’s pathology. Despite the advances in the last 15 years, there are few animal models of progressive subcortical white matter injury or vascular dementia. This review will discuss recent progress in animal modeling of white matter injury and the emerging principles to enhance glial function as a means of promoting repair and recovery.
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