4.7 Article

Cardiac stress T1-mapping response and extracellular volume stability of MOLLI-based T1-mapping methods

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SCIENTIFIC REPORTS
卷 11, 期 1, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/s41598-021-92923-4

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资金

  1. British Heart Foundation Clinical Research Training Fellowship [FS/19/65/34692]
  2. British Heart Foundation (BHF Chair Award) [CH/16/1/32013]
  3. British Heart Foundation Centre of Research Excellence in Oxford [RE/18/3/34214]
  4. National Institute for Health Research (NIHR) Oxford Biomedical Research Centre at The Oxford University Hospitals NHS Foundation Trust, University of Oxford, UK
  5. University of Oxford John Fell Fund [0009047]
  6. Oxford University Scholars funding

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This study compared two commonly used T1 mapping approaches in terms of stress T1 response and ECV measurement stability. The results showed that ShMOLLI demonstrated a greater stress T1 response, strong correlation with increased MBF, and higher ECV stability compared to the MOLLI variants tested.
Stress and rest T1-mapping may assess for myocardial ischemia and extracellular volume (ECV). However, the stress T1 response is method-dependent, and underestimation may lead to misdiagnosis. Further, ECV quantification may be affected by time, as well as the number and dosage of gadolinium (Gd) contrast administered. We compared two commonly available T1-mapping approaches in their stress T1 response and ECV measurement stability. Healthy subjects (n=10, 50% female, 35 +/- 8 years) underwent regadenoson stress CMR (1.5 T) on two separate days. Prototype ShMOLLI 5(1)1(1)1 sequence was used to acquire consecutive mid-ventricular T1-maps at rest, stress and post-Gd contrast to track the T1 time evolution. For comparison, standard MOLLI sequences were used: MOLLI 5(3)3 Low (256 matrix) & High (192 matrix) Heart Rate (HR) to acquire rest and stress T1-maps, and MOLLI 4(1)3(1)2 Low & High HR for post-contrast T1-maps. Stress and rest myocardial blood flow (MBF) maps were acquired after IV Gd contrast (0.05 mmol/kg each). Stress T1 reactivity (delta T1) was defined as the relative percentage increase in native T1 between rest and stress. Myocardial T1 values for delta T1 (dT1) and ECV were calculated. Residuals from the identified time dependencies were used to assess intra-method variability. ShMOLLI achieved a greater stress T1 response compared to MOLLI Low and High HR (peak dT1=6.4 +/- 1.7% vs. 4.8 +/- 1.3% vs. 3.8 +/- 1.0%, respectively; both p<0.0001). ShMOLLI dT1 correlated strongly with stress MBF (r=0.77, p<0.001), compared to MOLLI Low HR (r=0.65, p<0.01) and MOLLI High HR (r=0.43, p=0.07). ShMOLLI ECV was more stable to gadolinium dose with less time drift (0.006-0.04% per minute) than MOLLI variants. Overall, ShMOLLI demonstrated less intra-individual variability than MOLLI variants for stress T1 and ECV quantification. Power calculations indicate up to a fourfold (stress T1) and 7.5-fold (ECV) advantage in sample-size reduction using ShMOLLI. Our results indicate that ShMOLLI correlates strongly with increased MBF during regadenoson stress and achieves a significantly higher stress T1 response, greater effect size, and greater ECV measurement stability compared with the MOLLI variants tested.

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