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Native T1 mapping correlates with severity of microvascular dysfunction measured by coronary flow reserve (CFR) in acute myocardial infarction
© Dall'Armellina et al.; licensee BioMed Central Ltd. 2014
Published: 16 January 2014
Native T1 mapping cardiac magnetic resonance (CMR) imaging allows for quantitative assessment of myocardial oedema following acute myocardial infarction (MI). Coronary flow reserve (CFR) measures the maximum increase in intracoronary blood flow and it is a marker of microvascular dysfunction consequent to ischemic damage. The relation between increasingly higher native T1 values and the underlying severity of microvascular damage due to ischemic insult is not known.We hypothesise that T1 values measured in areas of injured myocardium, correlate to invasive measurements of CFR and microvascular dysfunction.
We recruited 20 ST elevation MI (STEMI) patients post primary percutaneous coronary intervention. At 24 hours post procedure the patients underwent a repeat coronary angiogram with CFR measurement, and a 3T CMR. Matching short axis slices with full left ventricle (LV) coverage were acquired using functional steady-state free precession (SSFP) imaging, native T1 mapping, oedema T2W imaging and late gadolinium enhancement (LGE). For the comparisons among acute T1-mapping, T2W and LGE, we excluded apical slices due to partial volume effects and slices with off-resonance artifacts. In order to minimise ambiguity over acutely injured myocardium with low signal intensity and low T1 due to microvascular obstruction (MVO), patients with MVO on LGE were excluded from analyses. Each slice was segmented in a 6 equiangular segment model with the RV-LV junction as reference point. Global and segmental injured fractions by LGE and oedema were assessed; segmental T1 values were calculated in the injured myocardial segments with an injured fraction of at least 50% as determined by oedema and/or LGE.
Increasingly higher native T1 values correlate with the severity of myocardial injury assessed by invasive CFR at 24 hours post STEMI.
Oxford Biomedical Research Centre.
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