Cerebral Small Vessel Disease: a Review of the Pathophysiological Mechanisms.
Yousef HannawiPublished in: Translational stroke research (2023)
Cerebral small vessel disease (cSVD) refers to the age-dependent pathological processes involving the brain small vessels and leading to vascular cognitive impairment, intracerebral hemorrhage, and acute lacunar ischemic stroke. Despite the significant public health burden of cSVD, disease-specific therapeutics remain unavailable due to the incomplete understanding of the underlying pathophysiological mechanisms. Recent advances in neuroimaging acquisition and processing capabilities as well as findings from cSVD animal models have revealed critical roles of several age-dependent processes in cSVD pathogenesis including arterial stiffness, vascular oxidative stress, low-grade systemic inflammation, gut dysbiosis, and increased salt intake. These factors interact to cause a state of endothelial cell dysfunction impairing cerebral blood flow regulation and breaking the blood brain barrier. Neuroinflammation follows resulting in neuronal injury and cSVD clinical manifestations. Impairment of the cerebral waste clearance through the glymphatic system is another potential process that has been recently highlighted contributing to the cognitive decline. This review details these mechanisms and attempts to explain their complex interactions. In addition, the relevant knowledge gaps in cSVD mechanistic understanding are identified and a systematic approach to future translational and early phase clinical research is proposed in order to reveal new cSVD mechanisms and develop disease-specific therapeutics.
Keyphrases
- cognitive decline
- oxidative stress
- low grade
- public health
- cerebral blood flow
- cognitive impairment
- cerebral ischemia
- subarachnoid hemorrhage
- healthcare
- endothelial cells
- mild cognitive impairment
- small molecule
- traumatic brain injury
- blood pressure
- single cell
- intensive care unit
- liver failure
- white matter
- physical activity
- lipopolysaccharide induced
- ischemia reperfusion injury
- hepatitis b virus
- inflammatory response
- high glucose
- resting state
- body mass index
- dna methylation
- extracorporeal membrane oxygenation
- functional connectivity
- induced apoptosis
- respiratory failure