
The aim of this review is to highlight novel findings in 2019 in the area of neurovascular disease. Experimental studies have provided insight into disease development, molecular determinants of pathology, and putative novel therapeutic targets. Studies in genetic experimental models as well as monogenic forms of human cerebrovascular diseases identified pathogenic molecules that may also be relevant to sporadic cases. There have been advances in understanding the development of cerebral cavernous angiomas and arteriovenous malformations, and putative curative treatments have been suggested from experimental models. Key pathogenic pathways involved in vessel calcification and stiffness have also been identified. At the cellular level, studies showed that proper function of endothelial and mural cells, particularly pericytes, is crucial to ensure full endothelial differentiation and blood-brain barrier integrity. Moreover, recent discoveries support the existence of a homeostatic crosstalk between vascular cells and other neural cells, including neurons. Cerebrovascular diseases are strongly associated with inflammation. Beyond pathogenic roles of specific components of the inflammatory response, new discoveries showed interesting interactions between inflammatory molecules and regulators of vascular function. Clinical investigation on cerebrovascular diseases has progressed by combining advanced imaging and genome-wide association studies. Finally, vascular cognitive impairment and dementia are receiving increasing attention. Recent findings suggest that high-salt intake may cause cerebrovascular dysfunction and cognitive impairment independent of hypoperfusion and hypertension. These and other recent reports will surely inspire further research in the field of cerebrovascular disease that will hopefully contribute to improved prevention and treatment.
Supported by the Spanish Ministry of Science, In-novation and Universities (SAF2017-87459-R)
Peer reviewed
Endothelial cells, Cavernous angioma, Cerebrovascular diseases, Neurosciences. Biological psychiatry. Neuropsychiatry, CADASIL, Small vessel disease, Arteriovenous malformation, Neurovascular disease, Cerebral amyloid angiopathy, Pericytes, Neuropathology, RC321-571
Endothelial cells, Cavernous angioma, Cerebrovascular diseases, Neurosciences. Biological psychiatry. Neuropsychiatry, CADASIL, Small vessel disease, Arteriovenous malformation, Neurovascular disease, Cerebral amyloid angiopathy, Pericytes, Neuropathology, RC321-571
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