TY - JOUR
T1 - Cerebral small vessel disease
T2 - Pathological mechanisms and potential therapeutic targets
AU - Gao, Yue
AU - Li, Di
AU - Lin, Jianwen
AU - Thomas, Aline M.
AU - Miao, Jianyu
AU - Chen, Dong
AU - Li, Shen
AU - Chu, Chengyan
N1 - Funding Information:
This work was supported by the Fund Project of Central Government for Guiding Development of the Local Science and Technology (Free exploration for basic research), Dalian Municipal Medicine and Science Planning Project (2011005), and Dalian Municipal Medical Key Specialty Climbing Project (2022ZZ215).
Publisher Copyright:
Copyright © 2022 Gao, Li, Lin, Thomas, Miao, Chen, Li and Chu.
PY - 2022/8/12
Y1 - 2022/8/12
N2 - Cerebral small vessel disease (CSVD) represents a diverse cluster of cerebrovascular diseases primarily affecting small arteries, capillaries, arterioles and venules. The diagnosis of CSVD relies on the identification of small subcortical infarcts, lacunes, white matter hyperintensities, perivascular spaces, and microbleeds using neuroimaging. CSVD is observed in 25% of strokes worldwide and is the most common pathology of cognitive decline and dementia in the elderly. Still, due to the poor understanding of pathophysiology in CSVD, there is not an effective preventative or therapeutic approach for CSVD. The most widely accepted approach to CSVD treatment is to mitigate vascular risk factors and adopt a healthier lifestyle. Thus, a deeper understanding of pathogenesis may foster more specific therapies. Here, we review the underlying mechanisms of pathological characteristics in CSVD development, with a focus on endothelial dysfunction, blood-brain barrier impairment and white matter change. We also describe inflammation in CSVD, whose role in contributing to CSVD pathology is gaining interest. Finally, we update the current treatments and preventative measures of CSVD, as well as discuss potential targets and novel strategies for CSVD treatment.
AB - Cerebral small vessel disease (CSVD) represents a diverse cluster of cerebrovascular diseases primarily affecting small arteries, capillaries, arterioles and venules. The diagnosis of CSVD relies on the identification of small subcortical infarcts, lacunes, white matter hyperintensities, perivascular spaces, and microbleeds using neuroimaging. CSVD is observed in 25% of strokes worldwide and is the most common pathology of cognitive decline and dementia in the elderly. Still, due to the poor understanding of pathophysiology in CSVD, there is not an effective preventative or therapeutic approach for CSVD. The most widely accepted approach to CSVD treatment is to mitigate vascular risk factors and adopt a healthier lifestyle. Thus, a deeper understanding of pathogenesis may foster more specific therapies. Here, we review the underlying mechanisms of pathological characteristics in CSVD development, with a focus on endothelial dysfunction, blood-brain barrier impairment and white matter change. We also describe inflammation in CSVD, whose role in contributing to CSVD pathology is gaining interest. Finally, we update the current treatments and preventative measures of CSVD, as well as discuss potential targets and novel strategies for CSVD treatment.
KW - blood-brain barrier breakdown
KW - cerebral small vessel disease
KW - cognitive impairment
KW - endothelial dysfunction
KW - inflammation
KW - white matter change
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U2 - 10.3389/fnagi.2022.961661
DO - 10.3389/fnagi.2022.961661
M3 - Review article
C2 - 36034144
AN - SCOPUS:85136804174
SN - 1663-4365
VL - 14
JO - Frontiers in Aging Neuroscience
JF - Frontiers in Aging Neuroscience
M1 - 961661
ER -