Key result
3D single-frequency 140-Hz cardiac MRE at 3.0 T demonstrated excellent short-interval reproducibility for left ventricular myocardial stiffness quantification (ICC 0.979; 95% CI 0.966-0.987).
Why the study?
Cardiac magnetic resonance elastography non-invasively quantifies myocardial stiffness, but long-interval reproducibility data at 3.0 T single-frequency 140-Hz remain limited.
Does 3.0 T single-frequency cardiac MR elastography provide reproducible quantification of left ventricular myocardial stiffness?
Observational (n=69)
No
Does 3.0 T single-frequency cardiac MR elastography provide reproducible quantification of left ventricular myocardial stiffness?
Effect estimate: ICC 0.979 (95% CI 0.966-0.987)
p-value: p=< .001
3.0 T single-frequency 140-Hz cardiac MR elastography demonstrates excellent short- and long-interval reproducibility for quantifying left ventricular myocardial stiffness.
Background: Cardiac magnetic resonance elastography (MRE) allows the non-invasive quantification of myocardial stiffness, but long-interval reproducibility data at 3.0 T single-frequency 140-Hz remain limited. Purpose: To evaluate the short- and long-interval reproducibility of 3.0 T cardiac MRE for left ventricular (LV) myocardial stiffness across healthy volunteers and patients with conditions associated with elevated myocardial stiffness. Materials and Methods: This prospective single-center study included 69 participants: 60 healthy volunteers and 9 with cardiovascular disease (6 with aortic stenosis and 3 with long-standing hypertension). All participants underwent baseline cardiac MRE (scanner: Signa Premier 3.0 T, GE Healthcare, driver: Resoundant), an immediate short-interval rescan (SIR) within 5 minutes, and a long-interval rescan (LIR) after approximately 1 month. Left ventricular myocardial stiffness and octahedral shear strain signal-to-noise ratio were measured independently by 2 readers. Reproducibility was assessed using Bland-Altman analysis, intraclass correlation coefficients (ICCs), within-subject coefficient of variation, standard error of measurement, and smallest detectable change at the 95% confidence (SDC95) level. Results: < .001), respectively. Inter-reader agreement was excellent across all timepoints, with ICCs of 0.970 at baseline (95% CI, 0.953-0.982), 0.966 for SIR (95% CI, 0.945-0.979), and 0.962 for LIR (95% CI, 0.939-0.976). Within-reader scan-rescan reproducibility was also excellent. For Reader 1, stiffness ICC was 0.979 for the SIR (95% CI, 0.966-0.987) and 0.957 for the LIR (95% CI, 0.932-0.973), with SDC95 values of 0.616 kPa (95% CI, 0.528-0.741) and 0.869 kPa (95% CI, 0.744-1.044), respectively. Reader 2 showed excellent reproducibility, with ICCs ≤0.943. Conclusions: 3D single-frequency 140-Hz cardiac MRE at 3.0 T provides excellent short- and long-interval reproducibility for LV myocardial stiffness quantification. The SDC95 values may help distinguish true longitudinal stiffness changes from measurement variability.
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Wang et al. (2026) conducted an observational in Elevated myocardial stiffness (aortic stenosis, hypertension) (n=69). 3.0 T single-frequency 140-Hz cardiac MR elastography was evaluated on Reproducibility of left ventricular myocardial stiffness (short-interval rescan ICC for Reader 1) (ICC 0.979, 95% CI 0.966-0.987, p=< .001). 3D single-frequency 140-Hz cardiac MRE at 3.0 T demonstrated excellent short-interval reproducibility for left ventricular myocardial stiffness quantification (ICC 0.979; 95% CI 0.966-0.987).
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