Blood-based biomarkers of cerebral small vessel disease

被引:15
作者
Wu, Liu-Yun [1 ,2 ]
Chai, Yuek Ling [1 ,2 ]
Cheah, Irwin K. [3 ,4 ]
Chia, Rachel S. L. [1 ,2 ]
Hilal, Saima [2 ,5 ]
Arumugam, Thiruma V. [6 ,7 ]
Chen, Christopher P. [1 ,2 ]
Lai, Mitchell K. P. [1 ,2 ]
机构
[1] Natl Univ Hlth Syst, Memory Aging & Cognit Ctr, Singapore City, Singapore
[2] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Pharmacol, Unit 09, 14 Med Dr,Kent Ridge S117599, Singapore City, Singapore
[3] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Biochem, Singapore City, Singapore
[4] Natl Univ Singapore, Ctr Life Sci, Neurobiol Programme, Singapore City, Singapore
[5] Natl Univ Singapore, Natl Univ Hlth Syst, Saw Swee Hock Sch Publ Hlth, Kent Ridge, Singapore City, Singapore
[6] Sungkyunkwan Univ, Sch Pharm, Suwon, South Korea
[7] La Trobe Univ, Ctr Cardiovasc Biol & Dis Res, Sch Agr Biomed & Environm, Dept Microbiol Anat Physiol & Pharmacol, Bundoora, Vic, Australia
基金
英国医学研究理事会;
关键词
Biomarkers; Cerebral small vessel disease; Dementia; Vascular cognitive decline; WHITE-MATTER HYPERINTENSITIES; C-REACTIVE PROTEIN; NEUROFILAMENT LIGHT-CHAIN; HEPATOCYTE GROWTH-FACTOR; NEURON-SPECIFIC ENOLASE; HEART-BRAIN CONNECTION; VASCULAR RISK-FACTORS; PLASMA AMYLOID-BETA; CEREBROVASCULAR-DISEASE; ALZHEIMERS-DISEASE;
D O I
10.1016/j.arr.2024.102247
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
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 timeintensive 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.
引用
收藏
页数:22
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