Assessment of Coronary Plaque Composition Using Optical Coherence Tomography
Coronary Atherosclerosis, Endothelial Dysfunction, Coronary Small Vessel Disease
About this trial
This is an interventional basic science trial for Coronary Atherosclerosis
Eligibility Criteria
Inclusion Criteria:
- age > 18 years and < 85 years
- referred to our cardiac catheterization laboratory for coronary vasomotion testing
- are found to have coronary endothelial dysfunction.
Exclusion Criteria:
- these include heart failure
- ejection fraction < 40%
- unstable angina
- myocardial infarction or angioplasty within 6 months prior to entry into the study
- use of investigational agents within 1 month of entry into the study,
- patients who require treatment with positive inotropic agents other than digoxin during the study
- patients with cerebrovascular accident within 6 months prior to entry the study
- significant endocrine, hepatic or renal, disorders
- local or systemic infectious disease within 4 weeks prior to entry into study
- pregnancy or lactation
- mental instability
- Federal Medical Center inmates
Sites / Locations
- Mayo Clinic
Arms of the Study
Arm 1
Arm 2
Other
Other
OCT at baseline
OCT following 6 month Lp-PLa2 inhibition
Subjects enrolled in the NIH funded and IRB approved (08-008161) protocol "Lp-PLA2 and Coronary Atherosclerosis in Humans" with a positive diagnosis of coronary artery endothelial dysfunction will be studied using Optical Coherence Tomography during the angiogram at baseline.
Subjects who are enrolled in IRB 10-000044 "Lp-PLA2 and Coronary Atherosclerosis in Humans Aim III" a study in which the investigators are examining the impact of long-term inhibition of Lp-PLA2, with a specific novel inhibitor or placebo, on Lp-PLA2 activity and improvement in coronary endothelial function will be studied using Optical Coherence Tomography during the 6 month return angiogram.