Clinical Trials Directory

Trials / Completed

CompletedNCT01978132

Primary Hyperaldosteronism and Ischemia-reperfusion Injury

Primary Hyperaldosteronism and Endothelial Ischemia-reperfusion Injury

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Radboud University Medical Center · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Patients with primary hyperaldosteronism experience more cardiovascular events compared to patients with primary hypertension, independent of the blood pressure level. In this research we hypothesize that patients with primary hyperaldosteronism are more susceptible to ischemia-reperfusion injury.

Detailed description

Patients with PHA have an increased risk of cardiovascular events, independent of blood pressure level. Also in patients suffering a myocardial infarction, circulating aldosterone levels are associated with increased mortality. In animal models of myocardial infarction, the administration of exogenous aldosterone increased infarct size, although other studies did not report this effect. In similar models, antagonists of the mineralocorticoid receptor (MR) reduced infarct size, which was completely abolished in ecto-5'-nucleotidase (CD73, the enzyme that catalyses extracellular formation of the endogenous nucleoside adenosine) and adenosine receptor knock-out mice. Therefore, we hypothesize that patients with PHA have an increased susceptibility for ischemia-reperfusion (IR)-injury due to down-regulation of the enzyme CD73. We will use the reduction in brachial flow-mediated dilation (FMD) by forearm IR as a well-validated endpoint for (endothelial) IR-injury.

Conditions

Interventions

TypeNameDescription
PROCEDUREforearm ischemia and reperfusionboth arms will be subjected to 20 minutes of forearm ischemia and 20 minutes of reperfusion.

Timeline

Start date
2013-11-01
Primary completion
2017-05-01
Completion
2017-07-01
First posted
2013-11-07
Last updated
2017-10-12

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT01978132. Inclusion in this directory is not an endorsement.