- Meeting abstract
- Open Access
240 Blood oxygen-sensitive ssfp imaging for probing the myocardial perfusion reserves of patients with coronary artery disease: a feasibility study
© Dharmakumar et al; licensee BioMed Central Ltd. 2008
- Published: 22 October 2008
- Myocardial Perfusion
- Coronary Artery Stenosis
- Signal Intensity Ratio
- Myocardial Perfusion Reserve
- Significant Coronary Artery Stenosis
Myocardial oxygen deficits secondary to coronary artery stenosis may be detected with blood-oxygen-level-dependent (BOLD) MRI. Similar to the first-pass perfusion technique, BOLD MRI identifies functionally significant coronary artery stenosis based on regional myocardial signal intensity differences at stress (pharmocological vasodilation). While the advantages of BOLD MRI have been long recognized, long scan times, poor image quality and/or oxygen sensitivity have limited the clinical utility of this technique. BOLD MRI based on steady-state free precession (SSFP) is a promising approach to overcoming many of these obstacles. It has been used to detect regional myocardial oxygen differences in canine models with experimental coronary artery stenosis.
This work investigates whether SSFP BOLD MRI can detect regional myocardial perfusion deficits in patients who have been tested positive for coronary artery disease via x-ray angiography and Thallium SPECT.
Nine patients with coronary artery disease underwent CMR studies using procedures and protocols approved by our institution. Studies were performed using a Siemens Avanto 1.5 T scanner. Following whole-heart manual shim, a mid-ventricular slice was identified. This was followed by acquisitions of 2D SSFP images at mid-ventricle during rest and stress. First-pass perfusion scans at rest and stress, and late-enhancement scans covering the mid-ventricular slice of interest were also obtained. Adenosine studies were performed 3 minutes after starting an intravenous infusion of Adenosine (140 μg/kg body weight/min). Imaging parameters for 2D SSFP scans were: TR/TE = 5.8/2.9 ms; flip angle = 90°; single-breath hold (13–20 s) with retrospective gating (20 cardiac phases); and voxel size = 1.5 × 1.5 × 5 mm3.
End-systolic frames obtained before and during Adenosine were analyzed in a segmental fashion using the AHA 6-segment model. Based on Thallium SPECT, segments were classified as healthy, mildly affected, severely affected, or infarcted. Infarcted segments (fixed defect on SPECT and positive on late enhancement images) were excluded from further analysis. Segmental SSFP signal intensities at rest and stress were measured and the signal intensity ratio (Stress/Rest) was calculated. One-way ANOVA with Tukey post-hoc analysis was used to determine the statistical significance of regional differences.
In the absence of coronary artery stenosis, pharmacological stress is expected to increase basal myocardial perfusion and vascular oxygenation. The progression of coronary artery stenosis reduces this vasodilatory capacity, resulting in oxygenation changes in corresponding myocardial territories. Since SSFP signals are directly dependent on blood oxygenation, the signal intensity ratios between rest and stress conditions can be used to identify ischemic territories of the myocardium.
This work demonstrated that 2D SSFP CMR at 1.5 T may provide a robust non-contrast technique capable of identifying regional myocardial oxygen deficits in patients with known coronary artery stenosis. Further studies are warranted to establish the sensitivity and specificity of the technique.
This article is published under license to BioMed Central Ltd.