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Gadolinium-Free Cardiac MR Stress T1-Mapping to Distinguish Epicardial From Microvascular Coronary Disease
Authors:Alexander Liu  Rohan S. Wijesurendra  Joanna M. Liu  Andreas Greiser  Michael Jerosch-Herold  John C. Forfar  Keith M. Channon  Stefan K. Piechnik  Stefan Neubauer  Rajesh K. Kharbanda  Vanessa M. Ferreira
Affiliation:1. Oxford Centre for Clinical Magnetic Resonance Research, Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, United Kingdom;2. Siemens Healthcare GmbH, Erlangen, Germany;3. Brigham and Women’s Hospital, Radiology, Cardiovascular Imaging, Boston, Massachusetts;4. Oxford Heart Centre, John Radcliffe Hospital, Oxford, United Kingdom;5. Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, United Kingdom
Abstract:

Background

Novel cardiac magnetic resonance (CMR) stress T1 mapping can detect ischemia and myocardial blood volume changes without contrast agents and may be a more comprehensive ischemia biomarker than myocardial blood flow.

Objectives

This study describes the performance of the first prospective validation of stress T1 mapping against invasive coronary measurements for detecting obstructive epicardial coronary artery disease (CAD), defined by fractional flow reserve (FFR <0.8), and coronary microvascular dysfunction, defined by FFR ≥0.8 and the index of microcirculatory resistance (IMR ≥25 U), compared with first-pass perfusion imaging.

Methods

Ninety subjects (60 patients with angina; 30 healthy control subjects) underwent CMR (1.5- and 3-T) to assess left ventricular function (cine), ischemia (adenosine stress/rest T1 mapping and perfusion), and infarction (late gadolinium enhancement). FFR and IMR were assessed ≤7 days post-CMR. Stress and rest images were analyzed blinded to other information.

Results

Normal myocardial T1 reactivity (ΔT1) was 6.2 ± 0.4% (1.5-T) and 6.2 ± 1.3% (3-T). Ischemic viable myocardium downstream of obstructive CAD showed near-abolished T1 reactivity (ΔT1 = 0.7 ± 0.7%). Myocardium downstream of nonobstructive coronary arteries with microvascular dysfunction showed less-blunted T1 reactivity (ΔT1 = 3.0 ± 0.9%). Stress T1 mapping significantly outperformed gadolinium-based first-pass perfusion, including absolute quantification of myocardial blood flow, for detecting obstructive CAD (area under the receiver-operating characteristic curve: 0.97 ± 0.02 vs. 0.91 ± 0.03, respectively; p < 0.001). A ΔT1 of 1.5% accurately detected obstructive CAD (sensitivity: 93%; specificity: 95%; p < 0.001), whereas a less-blunted ΔT1 of 4.0% accurately detected microvascular dysfunction (area under the receiver-operating characteristic curve: 0.95 ± 0.03; sensitivity: 94%; specificity: 94%: p < 0.001).

Conclusions

CMR stress T1 mapping accurately detected and differentiated between obstructive epicardial CAD and microvascular dysfunction, without contrast agents or radiation.
Keywords:adenosine stress  cardiac magnetic resonance  coronary artery disease  myocardial ischemia  T1 mapping  AUC  area under the receiver-operating characteristic curve  CAD  coronary artery disease  CI  confidence interval  CMD  coronary microvascular dysfunction  CMR  cardiac magnetic resonance  GBCA  gadolinium-based contrast agents  FFR  fractional flow reserve  IMR  index of microcirculatory resistance  LGE  late gadolinium enhancement  ROC  receiver-operating characteristic
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