- Poster presentation
- Open Access
Comparison of cardiovascular magnetic resonance to single-photon emission computed tomography in women with suspected coronary artery disease: a CE-MARC sub-study
© Greenwood et al; licensee BioMed Central Ltd. 2013
- Published: 30 January 2013
- Diagnostic Accuracy
- Cardiovascular Magnetic Resonance
- Myocardial Perfusion Imaging
- Late Gadolinium Enhancement
- Suspected Coronary Artery Disease
Coronary artery disease (CAD) is the leading cause of death in women and under-diagnosis contributes to their high mortality. Breast attenuation and smaller heart size can make myocardial perfusion imaging with SPECT particularly challenging in women.This study compared the gender-specific diagnostic performance of CMR and SPECT in the CE-MARC study.
CE-MARC was a prospective study of 752 patients with suspected angina. All patients were scheduled for CMR, SPECT and X-ray coronary angiography. Multi-parametric CMR comprised adenosine stress/rest perfusion, cine imaging, late gadolinium enhancement and MR coronary angiography. Gated adenosine stress/rest SPECT was performed using 99mTc-tetrofosmin. The primary outcome was the diagnostic accuracy of multi-parametric CMR and SPECT to detect CAD in female and male subgroups. A secondary outcome was a comparison of the perfusion-only components of CMR and SPECT in both sexes according to LV mass and disease extent, and in females according to bra size.
In both sexes, CMR has greater sensitivity than SPECT but similar specificity. Unlike SPECT, there are no significant gender differences in the diagnostic performance of CMR. The major challenge for SPECT in females appears to be the smaller heart size rather than breast attenuation artefacts. CMR may be less susceptible to these effects due to its inherent higher spatial resolution. These findings plus an absence of ionising radiation exposure, mean CMR should be considered the preferred non-invasive test for females with suspected CAD.
CE-MARC was funded by the British Heart Foundation (BHF). JPG and SP receive an educational research grant from Philips Healthcare. SP is funded by a BHF fellowship (FS/1062/28409).
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.