Key result
Non-contrast BOOST CMR matches standard LGE and T2-STIR for quantifying myocardial injury.
Why the study?
Clinical adoption of CMR for risk stratification in STEMI is limited by long scan times, breath-holding requirements, and use of contrast agents.
Does a non-contrast, free-breathing 3D whole-heart T1/T2 CMR method (iT2prep-IR BOOST) provide comparable diagnostic accuracy to conventional contrast-enhanced CMR for assessing myocardial injury in STEMI patients?
Observational (n=64)
No
Does a non-contrast, free-breathing 3D whole-heart T1/T2 CMR method (iT2prep-IR BOOST) provide comparable diagnostic accuracy to conventional contrast-enhanced CMR for assessing myocardial injury in STEMI patients?
A rapid, non-contrast, free-breathing CMR sequence (iT2prep-IR BOOST) accurately identifies myocardial infarction and microvascular obstruction in STEMI patients, offering a viable alternative to contrast-dependent scans.
Answers are grounded in this paper and cite their sources.
May accelerate non-contrast CMR workflows in STEMI; leaves open whether accuracy suffices for routine risk stratification.
Background Clinical adoption of cardiovascular magnetic resonance (CMR) for risk stratification in ST-elevation myocardial infarction (STEMI) is often limited by long scan times and the requirement for breath-holding and contrast agents. Objectives This study aimed to validate a non-contrast, free-breathing 3D whole-heart T1/T2 CMR method (iT 2 prep-IR BOOST) for rapid assessment of myocardial injury in STEMI patients, hypothesizing that this technique provides promising diagnostic accuracy and quantitative assessment to conventional contrast-enhanced CMR. Methods A free-breathing 3D isotropic whole-heart iT 2 prep-IR BOOST sequence was performed with a scan time of <8 minutes. Sixty-four STEMI patients underwent CMR, including iT 2 prep-IR BOOST, clinical T2-STIR, late gadolinium enhancement (LGE) and T1/T2 mapping. The diagnostic performance of iT 2 prep-IR BOOST was evaluated against LGE and T2-STIR to assess myocardial infarction (MI), microvascular obstruction (MVO), and edema. Subgroup analyses further investigated the association between MVO detected by iT 2 prep-IR BOOST and left ventricular (LV) remodeling at 1-year follow-up. Results In 60 STEMI patients, the acquisition was completed in 7.2 ± 0.6 min as a single free-breathing 3D whole-heart scan. Patient-level analysis showed high sensitivity and specificity for MVO (100.0% / 87.5%) and segmental MVO detection (95.8% / 97.8%). T 2 prep-IR BOOST yielded robust image contrast for MI comparable to LGE, while offering comparable edema visualization to T2-STIR. Volumetric and transmurality quantifications of MVO, MI, and edema showed excellent agreement with reference standards (all r > 0.90, p < 0.001), supported by significant biophysical correlations with native T1/T2 values ( p < 0.001). Furthermore, in a 1-year follow-up cohort (n=51), baseline T 2 prep-IR BOOST-derived MVO volume was associated with adverse left ventricular remodeling, showing significant correlations with both ΔLVEDVI (r = 0.305, p = 0.029) and ΔLVESVI (r = 0.293, p = 0.037). Conclusions In this preliminary single-center study, iT 2 prep-IR BOOST showed promising diagnostic performance and close quantitative agreement with conventional LGE and T2-STIR in stable STEMI patients. Further prospective validation in larger, independent, and more heterogeneous cohorts, including patients unable to undergo contrast-enhanced CMR, is required before this technique can be considered an alternative to standard LGE and T2-weighted sequences.
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Liu et al. (2026) conducted an observational in ST-elevation myocardial infarction (STEMI) (n=64). iT2prep-IR BOOST CMR (non-contrast, free-breathing 3D whole-heart T1/T2 CMR) vs. Late gadolinium enhancement (LGE) and clinical T2-STIR was evaluated on Volumetric and transmurality quantifications of MVO, MI, and edema (r > 0.90, p=<0.001). Non-contrast iT2prep-IR BOOST CMR showed excellent agreement with standard LGE and T2-STIR for quantifying myocardial injury and high sensitivity for microvascular obstruction.
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