Volume 18 Supplement 1

19th Annual SCMR Scientific Sessions

Open Access

Assessment of T1rho relaxation times after reperfused myocardial infarction

  • Marie Madden2,
  • Shahid Mohammed2,
  • Francisco Contijoch2,
  • James J Pilla2,
  • Joseph H Gorman1,
  • Yuchi Han3,
  • Robert C Gorman1 and
  • Walter R Witschey2
Journal of Cardiovascular Magnetic Resonance201618(Suppl 1):W13


Published: 27 January 2016


T1ρ MRI is an emerging method for high spatial resolution tissue characterization of myocardial infarct (MI), but the evolution of T1ρ in the first month after reperfused MI is uncertain. We conducted a study of reperfused MI in pigs to serially monitor T1ρ relaxation times at baseline, 1 and 4 weeks post-MI and correlated these results with T2, native T1, and histological findings.


13 pigs underwent 90 minutes of occlusion of the circumflex artery branches. T1ρ, T2 and native T1 MRI data were collected at terminal 1 week (n = 6) and 4 weeks (n = 7) post-MI studies. 2D T1ρ single-shot balanced steady-state free precession (bSSFP) sequences were performed using a spin echo, spin lock T1ρ pulse cluster (90x - SLy - 180y - SL-y - 90-x) with the following parameters: TSL = 2-50 ms, B1 = 500 Hz. T2 MRI was obtained 90x - 180y - 90-x using the same readout parameters. T1 maps were obtained with a modified Look-Locker sequence (MOLLI WIP sequence #448B, 5-3-3, Siemens), utilizing a single-shot acquisition with 8 inversion times. For LGE MRI, the animal received 0.1 mmol/kg intravenous injection of gadolinium contrast (MultiHance). Late-gadolinium enhanced (LGE) MRI was obtained using a 3D multishot phase-sensitive inversion recovery (PSIR) sequence with bSSFP spatial encoding. Ex vivo MRI and histology was performed at each terminal time point. Fibrotic tissue was assessed with trichrome staining. In vivo MRI was spatially correlated with ex vivo imaging and histopathology.


Infarct T1ρ increased 39.0 (1 week) and 32.1 ms (4 weeks) and T2 increased 21.0 ms (1 week) and 16.2 (4 weeks) after infarction. In vivo T1ρ was longer than T2 in normal (baseline), remote and infarcted tissue at 1 and 4 weeks (p < 0.05). Native T1 increased 288.0 and 212.4 ms at 1 and 4 weeks post-infarction (p < 0.05). The percent increase in T1ρ, T2 and T1 from baseline was 76, 48 and 24% at 1 week and 56, 36 and 21% at 4 weeks in the infarct region. T1ρ post-infarction area at 1 week was highly correlated with infarct fibrosis (p < 0.05).


T1ρ relaxation times were highly correlated with alterations in post-MI pathology at 1 and 4 weeks and therefore it may be a useful method for non-contrast enhanced imaging of infarction.

Figure 1

Authors’ Affiliations

Surgery, University of Pennsylvania
Radiology, University of Pennsylvania
Medicine, University of Pennsylvania


© Madden et al. 2016

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.