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The value of 3T contrast-enhanced whole-heart Coronary MRA in a integrated assessment of Cardiac Magnetic Resonance Protocol for Detection of suspected or known Coronary Artery Disease
lijun zhang 1, Yi He1, Zhan ming Fan1, and Debiao Li2

1Radiology Department, Beijing Anzhen Hospital, Capital Medical University, Beijing, People's Republic of China, 2Cedars-Sinai Medical Center, Biomedical Imaging Research Institute,University of California, Los Angeles, United States

Synopsis

We try to evaluate the additive diagnostic value of a 3T whole-heart CE-MRCA integration into a CMR-MPI/LGE protocol for the detection of coronary artery disease A total of 38 subjects were examined by CMR (including CMR-MPI, MRCA, and LGE)[j1] and x-ray invasive coronary angiography (ICA). Diagnostic performances of MRCA, CMR-MPI/LGE, and MRCA+CMR-MPI/LGE integration were determined having XA as standard for coronary artery disease. In per-vessel analysis, integrated protocol (AUC=0.84) performed better than the isolated CMR-MPI/LGE (AUC=0.63). In this suspected or known coronary artery disease population, integration of CE-MRCA significantly improved per-vessel diagnostic accuracy of a comprehensive 3T CMR-MPI/LGE protocol.

Introduction/Purpose

First-pass myocardial MR perfusion(MPI) has become a reliable tool for the diagnosis of myocardial ischemia. Contrast-enhanced magnetic resonance coronary angiography (CE-MRCA) has been shown to be able to show the lesion and anatomy of the coronary artery, but its incremental value as part of a CMR protocol including MPI and late gadolinium enhancement (LGE) is not well established. The purpose of this study was to evaluate the additive diagnostic value of a 3-dimensional whole-heart CE-MRCA integration into a 3T CMR-MPI/LGE protocol for the coronary artery disease.

Method

Thirty-eight symptomatic patients (54.7±11.5 years; 74% men) with suspected or known coronary artery disease underwent CMR (including CMR-MPI, MRCA, and LGE) and x-ray invasive coronary angiography (ICA). CMR was performed on a 3.0T whole-body scanner (MAGNETOM Verio, Siemens Healthcare, Erlangen, Germany). A 32-element cardiac matrix coil was activated for data collection. For perfusion imaging, 3 short-axis slices (basal, midventricular, and apical) were acquired under maximal hyperemia achieved with 140 μg・kg−1・min−1 IV ATP infusion, during the first pass of a bolus of 0.05 mmol・kg−1 of gadolinium injected at 5 mL・s−1 through a dedicated right antecubital vein. Cine scans were performed between stress and rest perfusion acquisitions with a balanced SSFP sequence. A navigator-gated, ECG-triggered, fat-saturated, inversion-recovery prepared segmented 3D FLASH sequence was employed for whole heart coronary MRA with additional infusion of contrast medium (0.1mmol/kg at 2ml/s). LGE images were collected by phase sensitive inversion recovery sequence .The total acquisition time is 56.8min.

Result

Diagnostic performances of MRCA, CMR-MPI/LGE, and MRCA+CMR-MPI/LGE integration were determined having XA as standard for coronary artery disease (≥50% stenosis/occlusion in vessels>2 mm). In per-vessel analysis, integrated protocol (AUC=0.84) performed better than the isolated CMR-MPI/LGE (AUC=0.63) and similarly to the isolated MRCA(AUC=0.87). In per-vessel analysis, MRCA had 90% sensitivity, 85% specificity, 81% positive predictive value and 92% negative predictive value. CMR-MPI/LGE had 42% sensitivity, 85% specificity, 67% positive predictive value and 67% negative predictive value. Integration of MRCA with CMR-MPI/LGE further improved CMR performance to 94% sensitivity, 74% specificity, positive predictive value of 72%, and negative predictive value of 94%, with a global accuracy of 82%. On per-segment analysis, MRCA shows right coronary artery and left anterior descending branch well, but poorly for The distal segment of left circumflex branch and left circumflex branch.

Discussion/Conclusion

In this suspected or known Coronary Artery Disease population, integration of contrast-enhanced whole-heart MRCA significantly improved per-vessel diagnostic accuracy of a comprehensive 3-T stress-rest CMR-MPI/LGE protocol.

The use of 3T CE-MRCA integration into a CMR-MPI/LGE was not seen in the previous literature. In this study, we try to examine whether 3T CE-MRCA can improve the diagnostic efficacy of coronary heart disease. But the data is not large enough, so for the per-patient analysisis is not accurate enough.

Acknowledgements

Thanks for all people in our study.

References

1. Bettencourt N, Ferreira N, Chiribiri A,et al. Additive value of magnetic resonance coronary angiography in a comprehensive cardiacmagnetic resonance stress-rest protocol for detection of functionally significant coronary artery disease: a pilot study.Circ Cardiovasc Imaging. 2013 Sep;6(5):730-8.

2. Pereira E, Bettencourt N, Ferreira N,et al. Incremental value of adenosine stress cardiac magnetic resonance in coronary artery disease detection. Int J Cardiol. 2013 Oct 9;168(4):4160-7.

3.Qi Yang, Kuncheng Li, Xin Liu,et al.Contrast-Enhanced hole-Heart Coronary MRA at 3.0T: A Comparative Study with X-ray Angiography in a Single Center. J Am Coll Cardiol. 2009 June 30; 54(1): 69–76.

Figures

CE-MRCA and CAG, men, 63-year-old,CAG displayed LCX Occlusion and LAD Severe stenosis.CE- MRCA correctly identified significant stenoses .


The three pictures above : CMR stress perfusion show Left ventricular lateral wall myocardial ischemia.

The three pictures below: After 45 days, the same patient referred for CMR and CAG for recurrent chest pain. LGE show lateral wall infarction. CAG show distal stent in LCX occlusion.


AUC( for per-vessel analysis): CMR-MPI/LGE=0.63,MRCA=0.87, integrated protocol=0.84.

Accu. indicates accuracy; CAD , coronary artery disease; CMR-MPI/LGE, cardiac magnetic resonance myocardial perfusion imaging and late gadolinium enhancement; FN, false-negative; FP, false-positive; MRCA, magnetic resonance coronary angiography; NPV, negative predictive value; PPV, positive predictive value; sensit., sensitivity; Specif., specificity; TN, true-negative; TP, true-positive

Proc. Intl. Soc. Mag. Reson. Med. 25 (2017)
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