In:
American Journal of Hypertension, Oxford University Press (OUP), Vol. 32, No. 10 ( 2019-09-24), p. 953-959
Kurzfassung:
Endothelial function is an independent predictor of coronary artery disease (CAD) and is regulated by a number of factors, including blood pressure. Objectives The current study was designed to test the hypothesis that intra-arterial invasive central blood pressure is strongly associated with endothelial function in patients with CAD. Methods In patient with CAD (diameter stenosis ≥30%), invasive central (aortic) and left peripheral (brachial) blood pressures were determined during transradial coronary angiography. The endothelial function was evaluated by way of flow-mediated dilatation (FMD) of the brachial artery. Results We enrolled 413 consecutive patients. There were 260 patients with significant CAD (sCAD, diameter stenosis ≥50%) and 153 patients with nonsignificant CAD (nsCAD, diameter stenosis & lt;50% and ≤30%). FMD was significantly and inversely correlated with central and peripheral parameters in terms of systolic blood pressure, mean arterial pressure, and pulse pressure (PP) (r = −0.332, r = −0.184, and r = −0.407, respectively, all P & lt; 0.001) and (r = −0.303, r = −0.190, and r = −0.319, respectively, all P & lt; 0.001). Compared with sCAD, there was closer correlation between central PP with FMD in nsCAD (r = −0.548 vs. r = −0.345, both P & lt; 0.001). After adjusting potential confounders such as age, body mass index and high-sensitivity C-reactive protein, multivariate analysis showed that FMD remained independently associated with central PP, degree of coronary artery stenosis, and brachial-ankle pulse wave velocity in all patients. In patients with nsCAD, the multivariate analysis showed that only central PP was independently correlated with FMD. Conclusions In patients with stable CAD, a decline in endothelial function is most closely associated with invasive central pulse pressure.
Materialart:
Online-Ressource
ISSN:
0895-7061
,
1941-7225
Sprache:
Englisch
Verlag:
Oxford University Press (OUP)
Publikationsdatum:
2019
ZDB Id:
1479505-X
