Jing Xu1, Zhao Shihua1, and Minjie Lu1
1Chinese Academy of Medical Sciences & Peking Union Medical College Fuwai Hospital, Beijing, China
Synopsis
Keywords: Myocardium, Heart
ATP can cause a pronounced positive
inotropic effect on human heart. CMR-FT even at rest provides an excellent negative
predictive value for myocardial ischemia and infarction in patients with CAD. CMR-FT
is easy to perform without the need for dedicated acquisition and complex
post-processing which can
be applied to standard CMR cine sequences. Rest myocardial strain might be a noninvasive option
serving as an additional gatekeeper for CAD patients with a needle-free test. Human
studies are needed to validate these findings in a multicenter setting and to
test whether CMR-FT can be incorporated into clinical guidelines.
Introduction/Purpose
It is still
challenging for cardiac magnetic resonance (CMR) to detect myocardial ischemia and infarction without the
use of gadolinium contrast. The aim of this study is to evaluate the potential value of adenosine triphosphate (ATP) stress myocardial strain derived from CMR-feature tracking (CMR-FT) as a novel option for the detection of myocardial ischemia and infarction in swine model. We hypothesized that the abnormality of
myocardial motion after ischemia within the progressive coronary artery
stenosis can be detected by CMR-FT at rest and during ATP stress.Method
Progressive obstructive coronary artery
disease (POCAD) model was constructed using Ameroid constrictor.
Rest and ATP stress cines, conventional myocardial rest and ATP stress
perfusion imaging and late gadolinium enhancement (LGE) were scanned and
analyzed. Rest and ATP stress myocardial strain, fully absolute myocardial
perfusion and LGE quantitation were analyzed among the normal, remote,
ischemic, and infarcted myocardium. Associations between myocardial strain and conventional
contrast myocardial perfusion and further diagnostic performance of strain were
evaluated by receiver operating characteristic (ROC) curves.Results
A total of 20 healthy male Chinese miniature swine were prospectively enrolled in this study (10 normal control and 10 POCAD swine. All rest and ATP stress
strain parameters were reduced significantly in ischemic segments compared with
normal segments (all p<0.05); rest and ATP stress circumferential strain
(CS) and radial strain (RS) were significantly different among remote,
ischemic, and infarcted myocardium (all p<0.001). The areas under ROC curve
for detecting ischemic and infarcted myocardium were 0.777 (95%CI 0.702, 0.853)
and 0.940 (95%CI 0.900, 0.979) for stress RS, and 0.744 (95%CI 0.645, 0.843)
and 0.935 (95%CI 0.886, 0.983) for rest RS (all p<0.001). Heat map
visualization illustrated that RS and CS showed good correlations with perfusion
parameters especially in infarcted segments. Normal controls showed significant
higher absolute global CS and RS during ATP stress in comparison with baseline
(-48.6%±9.5% vs. -41.6%±3.3% and 86.4%±9.0% vs.71.8%±10.3%, respectively, both p<0.05),
without significant global longitudinal strain (LS) reactivity (-32.0%±3.9% vs.
-29.8%±4.4%, p=0.132).
Discussion
In
this proof-of-principle study, we used myocardial strain parameters to
quantitatively estimate myocardial motion
and deformation in normal and IHD swine, and we found that
ATP could cause distinctive PIE on myocardium,
which can be detected by CMR-FT without gadolinium contrast. To the best
of our knowledge, this was the first study to evaluate CAD using ATP stress
myocardial strain by CMR-FT.Conclusions
ATP can cause a
pronounced PIE in left ventricle which can be quantitatively detected by
CMR-FT. Stress RS was the most powerful parameter to
distinguish non-ischemic, ischemic and infarcted myocardium. Significantly reduced rest RS could make the same
differentiation comparable to stress RS. Therefore, CMR-FT even at rest
held promise for CAD evaluation without the need of gadolinium contrast. Such a
noninvasive parameter might be a noninvasive option serving as an additional
gatekeeper for IHD patients with a needle-free test.Acknowledgements
No acknowledgement found.References
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