- Poster presentation
- Open Access
The native T1 in remote myocardium of patients with prior chronic infarction is not normal
https://doi.org/10.1186/1532-429X-18-S1-P102
© Bellm et al. 2016
- Published: 27 January 2016
Keywords
- Late Gadolinium Enhancement
- Coronary Artery Disease Patient
- Leave Ventricular Remodel
- Prior Myocardial Infarction
- Remote Myocardium
Background
Global left ventricular (LV) remodeling after myocardial infarction frequently occurs. Late Gadolinium Enhancement (LGE) CMR allows imaging of focal myocardial scar with areas remote from scar having no hyperenhancement. Myocardial T1 mapping allows quantification of interstitial fibrosis and may be a surrogate for LV remodeling. We sought to determine if there were T1 abnormalities in remote regions (no LGE positive areas) in patients with prior myocardial infarction.
Methods
In a prospective IRB-approved study, 12 patients with a history of coronary artery disease (CAD) and chronic myocardial infarction (61 ± 9 years, 9 males) and 10 healthy subjects (52 ± 10 years, 8 males) were recruited to undergo CMR scans. All subjects were in sinus rhythm during CMR study. We assessed native T1 mapping using the slice interleaved T1 sequence in 5 short axis-slices (from apical to basal). The sequence was acquired in a free-breathing ECG-triggered slice-selective bSSFP. T1 mapping of each scan was estimated by voxel-wise curve fitting using a 2-paramter fit model. All images were corrected for in-plane motion between different T1 weighted scans. Native myocardial T1 in healthy subjects were measured over the three mid-ventricular slices by manually drawing epicardial and endocardial contours. The native T1 times of the remote myocardium of the CAD patients were measured by manually drawing a region of interest (ROI) on the three mid-ventricular slices and excluding the infarct area. An unpaired-samples T-test analysis was used to test for statistically significant differences between the two groups.
Results
Subject characteristics of CAD patients and healthy cohorts with p-values of comparison.
CAD Patients (N = 12) | Healthy Cohorts (N = 10) | Comparison (p-value) | |
|---|---|---|---|
Male, % | 75% (N = 9) | 80% (N = 8) | |
Age, years | 61 ± 9 | 52 ± 10 | 0.029 |
Height, cm | 174 ± 8 | 174 ± 8 | 0.936 |
Weight, kg | 82 ± 18 | 81 ± 17 | 0.893 |
Hypertension, % | 75% (N = 9) | ||
Type 2 Diabetes, % | 25% (N = 4) | ||
BSA, m2 | 1.99 ± 0.24 | 1.98 ± 0.25 | 0.918 |
SBP, mmHg | 115 ± 16 | 112 ± 14 | 0.63 |
DBP, mmHg | 64 ± 12 | 61 ± 11 | 0.633 |
HR, beats per minute | 64 ± 11 | 58 ± 9 | 0.188 |
EDV-Cine, ml | 231 ± 61 | 175 ± 27 | 0.011 |
ESV-Cine, ml | 146 ± 52 | 73 ± 19 | 0.0001 |
SV-Cine, ml | 84 ± 24 | 102 ± 9.5 | 0.033 |
EF-Cine, % | 37 ± 9 | 59 ± 5 | 0.0001 |
LV-mass, grams | 128 ± 32 | 102 ± 14 | 0.022 |
boxplot with mean (line in box), interquartile range (box) and complete range (whisker) of native T1 time in remote myocardium of CAD patients and healthy cohorts (p = 0.0005).
Conclusions
Our data suggest there are diffuse changes in remote/normal myocardium resulting in abnormal/higher native T1 times in CAD patients with prior myocardial infarction. Further studies are needed to assess the prognostic value of an abnormal native T1 in the remote region among CAD patients.
Authors’ Affiliations
Copyright
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.
