神经炎症
生物标志物
疾病
医学
神经影像学
生物信息学
冲程(发动机)
成像生物标志物
氧化应激
认知障碍
病理
神经科学
内科学
磁共振成像
生物
放射科
工程类
机械工程
生物化学
作者
Liu‐Yun Wu,Yuek Ling Chai,Irwin K. Cheah,Richard Chia,Saima Hilal,Thiruma V. Arumugam,Christopher Chen,Mitchell K.P. Lai
标识
DOI:10.1016/j.arr.2024.102247
摘要
Age-associated cerebral small vessel disease (CSVD) represents a clinically heterogenous condition, arising from diverse microvascular mechanisms. These lead to chronic cerebrovascular dysfunction and carry a substantial risk of subsequent stroke and vascular cognitive impairment in aging populations. Owing to advances in neuroimaging, in vivo visualization of cerebral vasculature abnormities and detection of CSVD, including lacunes, microinfarcts, microbleeds and white matter lesions, is now possible, but remains a resource-, skills- and time-intensive approach. As a result, there has been a recent proliferation of blood-based biomarker studies for CSVD aimed at developing accessible screening tools for early detection and risk stratification. However, a good understanding of the pathophysiological processes underpinning CSVD is needed to identify and assess clinically useful biomarkers. Here, we provide an overview of processes associated with CSVD pathogenesis, including endothelial injury and dysfunction, neuroinflammation, oxidative stress, perivascular neuronal damage as well as cardiovascular dysfunction. Then, we review clinical studies of the key biomolecules involved in the aforementioned processes. Lastly, we outline future trends and directions for CSVD biomarker discovery and clinical validation.
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