Journal Article (Review Article) DZNE-2020-06521

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png
Understanding the role of the perivascular space in cerebral small vessel disease.

 ;  ;  ;  ;  ;  ;  ;  ;  ;

2018
Oxford University Press Oxford

Cardiovascular research 114(11), 1462-1473 () [10.1093/cvr/cvy113]

This record in other databases:    

Please use a persistent id in citations: doi:

Abstract: Small vessel diseases (SVDs) are a group of disorders that result from pathological alteration of the small blood vessels in the brain, including the small arteries, capillaries and veins. Of the 35-36 million people that are estimated to suffer from dementia worldwide, up to 65% have an SVD component. Furthermore, SVD causes 20-25% of strokes, worsens outcome after stroke and is a leading cause of disability, cognitive impairment and poor mobility. Yet the underlying cause(s) of SVD are not fully understood. Magnetic resonance imaging has confirmed enlarged perivascular spaces (PVS) as a hallmark feature of SVD. In healthy tissue, these spaces are proposed to form part of a complex brain fluid drainage system which supports interstitial fluid exchange and may also facilitate clearance of waste products from the brain. The pathophysiological signature of PVS and what this infers about their function and interaction with cerebral microcirculation, plus subsequent downstream effects on lesion development in the brain has not been established. Here we discuss the potential of enlarged PVS to be a unique biomarker for SVD and related brain disorders with a vascular component. We propose that widening of PVS suggests presence of peri-vascular cell debris and other waste products that form part of a vicious cycle involving impaired cerebrovascular reactivity, blood-brain barrier dysfunction, perivascular inflammation and ultimately impaired clearance of waste proteins from the interstitial fluid space, leading to accumulation of toxins, hypoxia, and tissue damage. Here, we outline current knowledge, questions and hypotheses regarding understanding the brain fluid dynamics underpinning dementia and stroke through the common denominator of SVD.

Keyword(s): Animals (MeSH) ; Blood-Brain Barrier: physiopathology (MeSH) ; Cerebral Small Vessel Diseases: diagnostic imaging (MeSH) ; Cerebral Small Vessel Diseases: pathology (MeSH) ; Cerebral Small Vessel Diseases: physiopathology (MeSH) ; Glymphatic System: diagnostic imaging (MeSH) ; Glymphatic System: pathology (MeSH) ; Glymphatic System: physiopathology (MeSH) ; Humans (MeSH) ; Magnetic Resonance Imaging (MeSH) ; Microvessels: diagnostic imaging (MeSH) ; Microvessels: pathology (MeSH) ; Microvessels: physiopathology (MeSH) ; Prognosis (MeSH)

Classification:

Contributing Institute(s):
  1. Clinical Dementia Research München (Clinical Dementia Research München)
Research Program(s):
  1. 344 - Clinical and Health Care Research (POF3-344) (POF3-344)

Appears in the scientific report 2018
Database coverage:
Medline ; BIOSIS Previews ; Clarivate Analytics Master Journal List ; Current Contents - Clinical Medicine ; Current Contents - Life Sciences ; Ebsco Academic Search ; IF >= 10 ; JCR ; NationallizenzNationallizenz ; SCOPUS ; Web of Science Core Collection
Click to display QR Code for this record

The record appears in these collections:
Document types > Articles > Journal Article
Institute Collections > M DZNE > M DZNE-AG Levin
Public records
Publications Database

 Record created 2020-02-18, last modified 2024-03-21


Rate this document:

Rate this document:
1
2
3
 
(Not yet reviewed)