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Endothelial Function and Heart Rate Variability After Stenting

Endothelial Function and Heart Rate Variability After Stenting in Coronary Arteries

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00999323
Acronym
FUNKIS
Enrollment
100
Registered
2009-10-21
Start date
2007-07-31
Completion date
2009-10-31
Last updated
2015-07-28

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

Conditions

Restenosis or Adverse Cardiovascular Event

Brief summary

The objective of this study is to evaluate whether impaired endothelial function and low heart rate variability are associated with clinical restenosis after percutaneous coronary intervention with stent implantation in patients with angina or acute coronary syndrome. Furthermore, the study examines a potential correlation between biomarkers of endothelial cell activation and endothelial dysfunction.

Detailed description

Background Atherosclerosis is a chronic, systemic and diffusely distributed disease causing focal complications in different vascular beds. Impaired endothelial function is the initial step in the progressive course of atherosclerosis . Endothelial dysfunction is considered a systemic process and both coronary and peripheral endothelial dysfunction have been shown to be independently associated with cardiovascular events . Percutanenous coronary intervention (PCI) with implantation of stent is the treatment of choice in symptomatic stenotic coronary artyery disease (CAD), but in-stent restenosis and progression of disease remains its main limitation. Early identification of patients at risk of restenosis after PCI would therefore be of clinical value. There is only limited prospective data on the role of peripheral endothelial dysfunction after PCI predicting restenosis and cardiovascular events , , . Furthermore, it is unknown if peripheral endothelial dysfunction is associated with increased levels of biomarkers of endothelial cell activation in this population. There are conflicting data on inflammatory markers as high-sensitivity CRP with regard to endothelial function. Low heart rate variability (HRV) predicts automic dysfunction and is a strong and independent predictor of mortality in patients with coronary artery disease (CAD) . Clinical depression after myocardial infarction is associated with decreased HRV, linking depression to increased cardiac mortality in post-myocardial infarction patients . Whether decreased HRV is associated with endothelial dysfunction or restenosis is unknown. Objective The objective of this study is to evaluate whether impaired endothelial function and low HRV are associated with clinical restenosis. Furthermore, the study examines a potential correlation between biomarkers of endothelial cell activation and endothelial dysfunction. Another issue is depression after PCI and a potential association with impaired endothelial function and increased levels of makers for endothelial activation. Methods Subjects This prospective study includes consecutively patients with acute coronary syndromes undergoing PCI with stent implantation for significant single vessel disease at Stavanger University Hospital, Stavanger, Norway. Patients will be followed for at least 6 months. Exclusion criteria are multivessel disease, left ventricular dysfunction defined as ejection fraction (EF) \< 50%, former aortocoronary bypass-surgery, systemic inflammatory diseases other than atherosclerosis, cognitive impairement, severe psychiatric disorder, renal failure (kreatinin \> 250 mmol/l), refusion to participate.

Interventions

DEVICEstent implantation in coronary artery

Percuatenous Coronary Intervention with implanatation of a stent

Sponsors

Helse Stavanger HF
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Patients after successful revascularization by percutaneous coronary intervention with stent implantation for single coronary artery disease

Exclusion criteria

* Multivessel coronary artery disease * Left ventricular dysfunction defined as ejection fraction (EF) \< 50% * Former aortocoronary bypass-surgery * Systemic inflammatory diseases other than atherosclerosis * inability to give informed consent * Renal failure (kreatinin \> 250 mmol/l) * Refusion to participate

Design outcomes

Primary

MeasureTime frame
clinical restenosis, major cardiovascular event12 months

Secondary

MeasureTime frame
endothelial function, heart rate variability12 months

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026