Plaque angiogenesis and intraplaque hemorrhage in atherosclerosis

Acute cardiovascular events, due to rupture or erosion of an atherosclerotic plaque, represent the major cause of morbidity and mortality in patients. Growing evidence suggests that plaque neovascularization is an important contributor to plaque growth and instability. The vessels’ immaturity, with...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:European journal of pharmacology Ročník 816; s. 107 - 115
Hlavní autoři: Parma, Laura, Baganha, Fabiana, Quax, Paul H.A., de Vries, Margreet R.
Médium: Journal Article
Jazyk:angličtina
Vydáno: Netherlands Elsevier B.V 05.12.2017
Témata:
Angiogenesis
Animals
Atherosclerosis
Hemorrhage - complications
Humans
Intraplaque hemorrhage
Molecular Imaging
Neovascularization, Pathologic - diagnostic imaging
Plaque neovessels
Plaque, Atherosclerotic - complications
Plaque, Atherosclerotic - diagnostic imaging
Plaque, Atherosclerotic - physiopathology
VEGF
Angiogenesis
Plaque neovessels
VEGF
Intraplaque hemorrhage
Atherosclerosis
ISSN:0014-2999, 1879-0712, 1879-0712
On-line přístup:Získat plný text
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!
Popis
Shrnutí:Acute cardiovascular events, due to rupture or erosion of an atherosclerotic plaque, represent the major cause of morbidity and mortality in patients. Growing evidence suggests that plaque neovascularization is an important contributor to plaque growth and instability. The vessels’ immaturity, with profound structural and functional abnormalities, leads to recurrent intraplaque hemorrhage. This review discusses new insights of atherosclerotic neovascularization, including the effects of leaky neovessels on intraplaque hemorrhage, both in experimental models and humans. Furthermore, modalities for in vivo imaging and therapeutic interventions to target plaque angiogenesis will be discussed.
Bibliografie:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
ObjectType-Review-3
content type line 23
ISSN:0014-2999
1879-0712
1879-0712
DOI:10.1016/j.ejphar.2017.04.028