Membrane microparticles are submicron fragments of membrane vesicles shed from various cell types. Circulating endothelial microparticles have been proposed as markers of endothelial injury. However, which mechanical forces contribute to their release is not clear.
In a first series subjects (50% hypertensives) with and without arterial hypertension and no Coronary Artery Disease (CAD) (n=50) will be recruited. MP subpopulations will be discriminated by flow cytometry according to the expression of established surface antigens including CD31+/41-, CD144+, and CD62e+. Besides office and ambulatory 24h blood pressure measurements, pulse wave analysis will be performed to determine central blood pressure, augmentation index (AIX), and pulse wave velocity. Endothelial function (Flow-mediated dilation, FMD), arterial pulsatile stretch (fractional diameter changes, FDC), and wall-shear-stress (WSS) will be measured in the same segment of the brachial artery (BA) by ultrasound. In a second series, the investigators will take measurements in subjects with hypertensive crises (SBP\>180 mmHg) (n=20) before and after 4h and normalization of arterial BP by urapidil. In a third series, the investigators will take measurement in subjects with stable CAD (n=10) before and after transfemoral coronary diagnostic angiography.
Study Type
OBSERVATIONAL
Enrollment
80
Division of Cardiology, Pulmonology and Vascular Medicine Duesseldorf,
Düsseldorf, North Rhine-Westphalia, Germany
endothelial function
endothelial function measured by flow-mediated dilation (FMD) for Subgroup 1 and 2
Time frame: Baseline
Changes in endothelial function
endothelial function measured by flow-mediated dilation (FMD) for Subgroup 3
Time frame: Baseline and after 4 hours
Changes in endothelial function
endothelial function measured by flow-mediated dilation (FMD) for Subgroup 4 before and after transfemoral coronary diagnostic angiography
Time frame: Baseline and 4 hours after procedure
Microparticle
Microparticles (CD31+/41-, CD144+, and CD62e+) will be discriminated by flow cytometry for Subgroup 1 and 2
Time frame: Baseline
Changes in Microparticle
Microparticles (CD31+/41-, CD144+, and CD62e+) will be discriminated by flow cytometry for Subgroup 3
Time frame: Baseline and after 4 hours
Changes Microparticle
Microparticles (CD31+/41-, CD144+, and CD62e+) will be discriminated by flow cytometry for Subgroup 4 before and after transfemoral coronary diagnostic angiography
Time frame: Baseline and 4 hours after procedure
Wall Shear Stress
measured by ultrasound in brachial artery for Subgroup 1 and 2
Time frame: Baseline
Changes in Wall Shear Stress
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measured by ultrasound in brachial artery for Subgroup 3
Time frame: Baseline and 4 hours
Changes in Wall Shear Stress
measured by ultrasound in brachial artery for Subgroup 4 before and after transfemoral coronary diagnostic angiography
Time frame: Baseline and 4 hours after procedure
changes in fractional diameter (FDC)
measured by ultrasound in brachial artery for Subgroup 1 and 2
Time frame: Baseline
changes in fractional diameter (FDC)
measured by ultrasound in brachial artery for Subgroup 3
Time frame: Baseline and after 4 hours
Changes in fractional diameter (FDC)
measured by ultrasound in brachial artery for Subgroup 4 before and after transfemoral coronary diagnostic angiography
Time frame: Baseline and 4 hours after procedure
pulse wave velocity
measured for Subgroup 1 and 2
Time frame: Baseline
Changes in pulse wave velocity
measured for Subgroup 3
Time frame: Baseline and after 4 hours
Changes in pulse wave velocity
measured for Subgroup 4 before and after transfemoral coronary diagnostic angiography
Time frame: Baseline and 4 hours after procedure
augmentation index
measured for Subgroup 1 and 2
Time frame: baseline
Changes in augmentation index
measured for Subgroup 3
Time frame: Baseline and after 4 hours
Changes in augmentation index
measured for Subgroup 4 before and after transfemoral coronary diagnostic angiography
Time frame: Baseline and 4 hours after procedure