Objectives—Atherosclerosis may be caused by increased endothelial damage and by a consumptive loss of endothelial repair capacity by endothelial progenitors. Arterial stiffness is a reliable marker of atherosclerosis and a positive correlate of endothelial damage. We investigated whether an increased ratio of CD31/CD42 microparticles to endothelial progenitors, a possible indicator of endothelial damage and impaired endothelium reparation, may contribute to aortic stiffness in hypercholesterolemia. We also studied the in vitro effect of microparticles from hypercholesterolemic patients on endothelial progenitor survival. Methods and Results—Circulating CD31/CD42 microparticles, endothelial progenitors, and aortic pulse wave velocity (aPWV), a measure of aortic stiffness, were measured in 50 patients with never-treated hypercholesterolemia and 50 normocholesterolemic controls. Hypercholesterolemic patients had more circulating CD31/CD42 microparticles, less endothelial progenitors, and a stiffer aorta than controls. aPWV was associated with CD31/CD42 microparticles (r=0.61; P0.001), endothelial progenitors (r=0.45, P0.001), and with cholesterol levels (r=0.51; P0.001). High plasma cholesterol and a high ratio of CD31/CD42 microparticles to endothelial progenitors independently predicted an increased aPWV. Microparticles from hypercholesterolemic patients caused a significant endothelial progenitor loss in vitro. Conclusions—Hypercholesterolemia-related aortic stiffness is promoted by plasma cholesterol directly, increased endothelial damage, and reduced endothelium repair capacity by endothelial progenitors. (Arterioscler Thromb Vasc Biol. 2006;26:2530-2535.)

Increased Ratio of CD31+/CD42- Microparticles to Endothelial Progenitors as a Novel Marker of Atherosclerosis in Hypercholesterolemia.

PIRRO, Matteo;SCHILLACI, Giuseppe;BAGAGLIA, FRANCESCO;MANNARINO, MASSIMO RAFFAELE;VELARDI, Andrea;MANNARINO, Elmo
2006

Abstract

Objectives—Atherosclerosis may be caused by increased endothelial damage and by a consumptive loss of endothelial repair capacity by endothelial progenitors. Arterial stiffness is a reliable marker of atherosclerosis and a positive correlate of endothelial damage. We investigated whether an increased ratio of CD31/CD42 microparticles to endothelial progenitors, a possible indicator of endothelial damage and impaired endothelium reparation, may contribute to aortic stiffness in hypercholesterolemia. We also studied the in vitro effect of microparticles from hypercholesterolemic patients on endothelial progenitor survival. Methods and Results—Circulating CD31/CD42 microparticles, endothelial progenitors, and aortic pulse wave velocity (aPWV), a measure of aortic stiffness, were measured in 50 patients with never-treated hypercholesterolemia and 50 normocholesterolemic controls. Hypercholesterolemic patients had more circulating CD31/CD42 microparticles, less endothelial progenitors, and a stiffer aorta than controls. aPWV was associated with CD31/CD42 microparticles (r=0.61; P0.001), endothelial progenitors (r=0.45, P0.001), and with cholesterol levels (r=0.51; P0.001). High plasma cholesterol and a high ratio of CD31/CD42 microparticles to endothelial progenitors independently predicted an increased aPWV. Microparticles from hypercholesterolemic patients caused a significant endothelial progenitor loss in vitro. Conclusions—Hypercholesterolemia-related aortic stiffness is promoted by plasma cholesterol directly, increased endothelial damage, and reduced endothelium repair capacity by endothelial progenitors. (Arterioscler Thromb Vasc Biol. 2006;26:2530-2535.)
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11391/152462
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 136
  • ???jsp.display-item.citation.isi??? 123
social impact