Abstract
Background
CMR feature tracking (CMR-FT) is a method of assessing strain from routinely acquired steady- state free precession (SSFP) cine images similar to echocardiographic speckle tracking. However, its application to determine myocardial twist and untwist has never previously been explored. We sought to determine the feasibility of measuring twist and untwist from routine cine images in healthy volunteers at rest and during inotropic stimulation.
Methods
Ten healthy volunteers had routine SSFP cine images acquired at rest and after inotropic stimulation (10 and 20 micrograms of dobutamine). The rotation of the basal and apical slices, both subendocardial and subepicardial, was measured and global LV twist θ was calculated as the difference between the counter-clockwise (positive) rotation at the apex (φapex) and clockwise rotation at the base (viewed from apex), θ = φapex- φbase. Peak twist and untwist-rate and the respective times to peak were calculated using MATLAB software for both the subepicardial and subendocardial layers and compared between rest and stress.
Results
The peak and time to peak myocardial twist and untwist-rate are displayed at the endocardial (Table 1) and epicardial levels (Table 2). Twist and untwist-rate significantly increased with faster time to peak during dobutamine stimulation at the endocardial level (p < 0.05, significance measured with a paired t-test after logarithmic transformation of the sample). These changes were paralleled by a trend towards increased twist at the epicardial level and significantly increased untwist-rate associated with faster time to peak twist and untwist-rate during dobutamine stimulation (table 2).
Conclusions
It is feasible to derive myocardial twist and untwist and respective times to peak, both at rest and dobutamine stress using CMR-FT. Application of these new measures of deformation by CMR-FT should next be explored in disease states.
CMR feature tracking (CMR-FT) is a method of assessing strain from routinely acquired steady- state free precession (SSFP) cine images similar to echocardiographic speckle tracking. However, its application to determine myocardial twist and untwist has never previously been explored. We sought to determine the feasibility of measuring twist and untwist from routine cine images in healthy volunteers at rest and during inotropic stimulation.
Methods
Ten healthy volunteers had routine SSFP cine images acquired at rest and after inotropic stimulation (10 and 20 micrograms of dobutamine). The rotation of the basal and apical slices, both subendocardial and subepicardial, was measured and global LV twist θ was calculated as the difference between the counter-clockwise (positive) rotation at the apex (φapex) and clockwise rotation at the base (viewed from apex), θ = φapex- φbase. Peak twist and untwist-rate and the respective times to peak were calculated using MATLAB software for both the subepicardial and subendocardial layers and compared between rest and stress.
Results
The peak and time to peak myocardial twist and untwist-rate are displayed at the endocardial (Table 1) and epicardial levels (Table 2). Twist and untwist-rate significantly increased with faster time to peak during dobutamine stimulation at the endocardial level (p < 0.05, significance measured with a paired t-test after logarithmic transformation of the sample). These changes were paralleled by a trend towards increased twist at the epicardial level and significantly increased untwist-rate associated with faster time to peak twist and untwist-rate during dobutamine stimulation (table 2).
Conclusions
It is feasible to derive myocardial twist and untwist and respective times to peak, both at rest and dobutamine stress using CMR-FT. Application of these new measures of deformation by CMR-FT should next be explored in disease states.
Original language | English |
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Article number | P14 |
Journal | Journal of cardiovascular magnetic resonance |
Volume | 16 |
Issue number | S1 |
DOIs | |
Publication status | Published - 16 Jan 2014 |