Volume 17 Supplement 1

Abstracts of the 18th Annual SCMR Scientific Sessions

Open Access

Prognostic significance of quantitative measures of myocardial infarct pathology using native T1 mapping, in survivors of ST-elevation myocardial infarction

  • David Carrick2, 1,
  • Caroline Haig3,
  • Samuli M Rauhalammi2,
  • Nadeem Ahmed2,
  • Ify Mordi2,
  • Margaret McEntegart1,
  • Mark Petrie1,
  • Hany Eteiba1,
  • Stuart Hood1,
  • Stuart Watkins1,
  • Mitchell Lindsay1,
  • Ahmed Marous1,
  • Aleksandra Radjenovic2,
  • Ian Ford3,
  • Niko Tzemos2,
  • Keith G Oldroyd2, 1 and
  • Colin Berry2, 1
Journal of Cardiovascular Magnetic Resonance201517(Suppl 1):O53


Published: 3 February 2015


Myocardial longitudinal relaxation time (T1, ms) is a fundamental magnetic property of tissue that is related to water content and mobility. The pathophysiological and prognostic importance of native myocardial T1 values in acute STEMI patients is unknown. We aimed to assess the clinical significance of infarct tissue characteristics using native T1 cardiac magnetic resonance (CMR).


We performed a prospective single center cohort study in reperfused STEMI patients who underwent CMR 2 days and 6 months post-MI. Native T1 CMR (MOLLI investigational prototype sequence: 3 (3) 3 (3) 5) was measured in myocardial regions-of-interest. The area-at-risk and infarct territory were depicted with T1 mapping and late gadolinium contrast enhancement imaging, respectively. All-cause death or heart failure hospitalization was a pre-specified outcome that was assessed during follow-up.


300 STEMI patients (mean±SD age 59±12 years, 74% male, 114 with anterior STEMI) gave informed consent and had CMR (14 July 2011 - 22 November 2012). Of these, 288 STEMI patients had evaluable T1 maps and follow-up assessments (median duration 845 days). Infarct size was 18 ±14% of left ventricular mass. Microvascular obstruction occurred in 160 (55.6%) patients. Native T1 within the area-at-risk (1097 ±52 ms) was higher than in the remote zone (961 ±25 ms; p<0.01) or infarct core (996.9 (57.3); p<0.01). In multivariable linear regression, native T1 in the area-at-risk was independently and negatively associated with age, initial systolic blood pressure and TIMI coronary flow grade at presentation (all p<0.05), independent of LVEF, left ventricular end-diastolic volume (LVEDV) or infarct size. Similar findings were observed for T1 core values, which were also independently associated with Killip class.

At 6 months, LVEDV change was available for 262 patients and was increased by ≥20% in 30 (11.5%) patients of whom 23 (76.7%) had microvascular obstruction at baseline. T1 in the infarct core was a multivariable predictor of adverse remodeling (-0.01 (-0.02, -0.00); p=0.048).

288 (100%) patients had longer term follow-up completed. The median duration of follow-up was 845 days. Thirty (10.4%) patients died or experienced a heart failure event and 13 (4.5%) of these patients died or experienced a heart failure hospitalization post-discharge. Native T1 in the area-at-risk was a predictor of all-cause death or heart failure post-discharge (hazard ratio 0.985, 95% CI 0.973, 0.997; p=0.012) including after adjustment for LVEF at baseline (p=0.018) and LVEDV at baseline (p=0.013).


In acute STEMI patients, infarct zone tissue characteristics predict left ventricular remodeling and long-term health outcomes, independent of infarct size and LV function.


Figure 1

Kaplan-Meier survival plot (n = 288) for all-cause death or heart failure hospitalisation by T1 injured median.

Authors’ Affiliations

Golden Jubilee National Hospital
Institute of Cardiovascular and Medical Sciences, University of Glasgow
Robertson Center for Biostatistics, University of Glasgow


© Carrick et al; licensee BioMed Central Ltd. 2015

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.