Solveig Henneicke, Sven Günther Meuth, Stefanie Schreiber
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引用次数: 0
Abstract
Sporadic cerebral small vessel disease determines age- and vascular-risk-factor-related processes of the small brain vasculature. The underlying pathology develops in a stage-dependent manner - probably over decades - often already starting in midlife. Endothelial and pericyte activation precedes blood-brain barrier leaks, extracellular matrix remodeling and neuroinflammation, which ultimately result in bleeds, synaptic and neural dysfunction. Hemodynamic compromise of the small vessel walls promotes perivascular drainage failure and accumulation of neurotoxic waste products in the brain. Clinical diagnosis is mainly based on magnetic resonance imaging according to the Standards for Reporting Vascular Changes on Neuroimaging 2. Cerebral amyloid angiopathy is particularly stratified according to the Boston v2.0 criteria. Small vessel disease of the brain could be clinically silent, or manifested through a heterogeneous spectrum of diseases, where cognitive decline and stroke-related symptoms are the most common ones. Prevention and therapy are centered around vascular risk factor control, physically and cognitively enriched life style and, presumably, maintenance of a good sleep quality, which promotes sufficient perivascular drainage. Prevention of ischemic stroke through anticoagulation that carries at the same time an increased risk for large brain hemorrhages - particularly in the presence of disseminated cortical superficial siderosis - remains one of the main challenges. The cerebral small vessel disease field is rapidly evolving, focusing on the establishment of early disease stage imaging and biofluid biomarkers of neurovascular unit remodeling and the compromise of perivascular drainage. New prevention and therapy strategies will correspondingly center around the dedicated targeting of, e. g., cellular small vessel wall and perivascular tissue structures. Growing knowledge about brain microvasculature bridging neuroimmunological, neurovascular and neurodegenerative fields might lead to a rethink about apparently separate disease entities and the development of overarching concepts for a common line of prevention and treatment for several diseases.
零星脑小血管疾病决定了脑小血管与年龄和血管风险因素相关的过程。潜在的病理变化以阶段依赖的方式发展,可能持续数十年,通常在中年就已经开始。在血脑屏障渗漏、细胞外基质重塑和神经炎症发生之前,内皮和周细胞就已被激活,最终导致出血、突触和神经功能失调。小血管壁的血流动力学受损会导致血管周围引流失败,神经毒性废物在脑内积聚。临床诊断主要依据《神经影像学血管病变报告标准》(Standards for Reporting Vascular Changes on Neuroimaging 2)的磁共振成像。脑淀粉样血管病尤其要根据波士顿 v2.0 标准进行分层。脑部小血管疾病在临床上可能是无症状的,也可能表现为多种疾病,其中认知能力下降和中风相关症状最为常见。预防和治疗的核心是控制血管风险因素、丰富身体和认知能力的生活方式,以及保持良好的睡眠质量,从而促进血管周围充分排水。通过抗凝治疗预防缺血性中风仍是主要挑战之一,因为抗凝治疗同时会增加大面积脑出血的风险,尤其是在存在播散性皮质浅层蛛网膜病变的情况下。脑小血管疾病领域正在迅速发展,重点是建立早期疾病阶段的成像和神经血管单元重塑的生物流体生物标志物,以及血管周围引流的损害。新的预防和治疗策略将相应地以专门针对小血管壁和血管周围组织结构等为中心。人们对连接神经免疫学、神经血管和神经退行性疾病领域的脑微血管的认识不断加深,这可能会促使人们重新思考表面上相互独立的疾病实体,并为多种疾病的共同预防和治疗制定总体概念。
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