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Hypertension and Injury

Hypertension, Endothelial Microparticle Release, and Endothelial Function: Role of Pressure, Shear, and Stretch

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02795377
Enrollment
80
Registered
2016-06-10
Start date
2016-04-30
Completion date
2017-11-30
Last updated
2017-11-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arterial Hypertension, CAD

Keywords

arterial hypertension, microparticle, endothelial function

Brief summary

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.

Detailed description

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.

Interventions

None listed

Sponsors

Klinik für Kardiologie, Pneumologie und Angiologie
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
50 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* male subjects with or without arterial hypertension, hypertensive crises, stable CAD * written informed consent

Exclusion criteria

* subjects with manifest peripheral artery, or cerebrovascular disease, acute inflammation (CRP\>0.6 mg/dl), malignancies, arrhythmias

Design outcomes

Primary

MeasureTime frameDescription
endothelial functionBaselineendothelial function measured by flow-mediated dilation (FMD) for Subgroup 1 and 2
Changes in endothelial functionBaseline and after 4 hoursendothelial function measured by flow-mediated dilation (FMD) for Subgroup 3

Secondary

MeasureTime frameDescription
Changes MicroparticleBaseline and 4 hours after procedureMicroparticles (CD31+/41-, CD144+, and CD62e+) will be discriminated by flow cytometry for Subgroup 4 before and after transfemoral coronary diagnostic angiography
Wall Shear StressBaselinemeasured by ultrasound in brachial artery for Subgroup 1 and 2
Changes in Wall Shear StressBaseline and 4 hoursmeasured by ultrasound in brachial artery for Subgroup 3
changes in fractional diameter (FDC)Baselinemeasured by ultrasound in brachial artery for Subgroup 1 and 2
MicroparticleBaselineMicroparticles (CD31+/41-, CD144+, and CD62e+) will be discriminated by flow cytometry for Subgroup 1 and 2
pulse wave velocityBaselinemeasured for Subgroup 1 and 2
Changes in pulse wave velocityBaseline and after 4 hoursmeasured for Subgroup 3
augmentation indexbaselinemeasured for Subgroup 1 and 2
Changes in augmentation indexBaseline and after 4 hoursmeasured for Subgroup 3
Changes in fractional diameter (FDC)Baseline and 4 hours after proceduremeasured by ultrasound in brachial artery for Subgroup 4 before and after transfemoral coronary diagnostic angiography
Changes in MicroparticleBaseline and after 4 hoursMicroparticles (CD31+/41-, CD144+, and CD62e+) will be discriminated by flow cytometry for Subgroup 3

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026