- Poster presentation
- Open Access
Cardiac dyssynchrony in a Becker cohort: preliminary results
© Gilles et al; licensee BioMed Central Ltd. 2015
- Published: 3 February 2015
- Lateral Segment
- Cardiac Motion
- Short Axis Slice
- Magnetom Trio
- Dyssynchrony Index
We previously reported the early detection of cardiac motion dyssynchrony in GRMD dogs (a model for Duchenne myopathy with cardiac involvement). In this new work, we applied the same dyssynchrony index in a cohort of 88 Becker patients of various age (38,7 ±13,6 years; range from 18 to 68) and disease burden (number of segment count with any Gd late enhancement : 4,37 ± 3,14 ; range from 0 to 12). We compared the data obtained to those in 10 control subjects.
Images were acquired on a Siemens Magnetom Trio 3T® and analyzed using Segment® software (Medviso AB). For each segment (AHA classification) of the two most basal short axis slices studied on MR cine true-FISP images, we assess the standard deviation of the mean position of the inner heart border. The mean for all phases of the cardiac cycle and both slices equals the global dyssynchrony index (DI). At this point, we do not dissociate systolic and diastolic dyssynchrony.
We found no correlation between the dyssynchrony index and the presence of Gd late enhancement in all segments (r=0,24) or in the lateral segments (r=0,07). We investigated the lateral segments more specifically because it is known from previous studies that the lateral wall is an early target of Gd late enhancement in Becker's disease.
Dyssynchrony in cardiac motion is globally higher in Becker patients compared to controls. Although part of the anomaly is probably driven by systolic asynchrony in very low EF patients, some patients with normal EF show dyssynchrony as well. We found no correlation between the dyssynchrony index and the presence of Gd late enhancement.
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