Absolute Quantification of Coronary Flow Reserve by Stress Perfusion MRI

The main hypothesis the investigators will test is that changes in myocardial blood volume, under physiologic stress, correlate with myocardial flow reserve as measured in low spatial resolution nuclear SPECT scans. Secondary hypothesis is that stress perfusion as quantified with bolus height corrected gadofosveset trisodium images, better correlate with SPECT perfusion than uncorrected, relative perfusion values.

The investigators propose implementing the scan protocol using a 1.5T or 3.0T MRI scanner. The investigators will scan a series of 20 patients recruited from the nuclear stress lab at Northwestern Memorial Hospital. These subjects will be approached and enrolled into a HIPPA Compliant, IRB approved research study to assess the effectiveness of myocardial perfusion and blood volume images to measure myocardial blood volume. Subjects will be scanned with a modified version of the clinical stress-perfusion protocol. Correlation analysis will be used to test the hypothesis that quantitative blood volume is an indicator of myocardial flow reserve.

Inclusion criteria

Under an Institutional Committee on Human Research board approved protocol, 20 patients with a suspected myocardial ischemic disease with positive stress nuclear medicine test laboratory will be recruited in this prospective study. All subjects will be screened for GFR within 24 hours before the exam. All patients must have a GFR > 30 mL/min/1.73m2 to be included in the study.

All subjects will be selected following the Nephrogenic Systemic Fibrosis (NSF) guidelines. All dialysis patients or end-stage renal disease patients with a creatinine clearance of < 30mL/min will not be selected for the study to avoid NSF.

Exclusion criteria

• Age 18 to 89 years;
• Known contraindication to MR imaging (such as pacemaker placement, magnetic implants, etc);
• Claustrophobia;
• Inability to perform an adequate breath-hold for imaging,
• Inability to provide informed consent;
• all subjects will be will be screened for GFR within 24 hours before the exam and subjects presenting with GFR < 60 ml/min will be excluded;
• Pregnant and lactating women;
• Patients with hypersensitivity to gadolinium contrast agents, metoprolol, adenosine, or nitroglycerin;

• Contra indication for Regadenoson

• 2nd- or 3rd-degree AV block (except in patients with a functioning artificial pacemaker)
• Sinus node disease (except in patients with a functioning artificial pacemaker)
• Unstable angina
• Acute myocardial infarction
• Known or suspected bronchoconstrictive or bronchospastic lung disease (e.g., asthma)
• Hypersensitivity to adenosine
• Caffeine within 12-24 hours
• Theophylline and Dipyridamole products within 24 hours