Javascript must be enabled to continue!
Abstract 15057: Electromechanical Discoordination is Present in Patients With Duchenne Muscular Dystrophy Independent of Tissue Fibrosis
View through CrossRef
Introduction:
Progressive ventricular dysfunction is a cardinal symptom in Duchenne Muscular Dystrophy (DMD). Some of the earliest signs of cardiomyopathy in DMD are myocardial fibrotic deposition and LV strain defects. Electromechanical discoordination, as measured by Systolic Stretch Fraction (SSF) and Diastolic Relaxation Fraction (DRF), has been shown to be a sensitive marker of ventricular dysfunction. The presence of this discoordination in relation to fibrotic deposition in DMD has yet to be elucidated.
Hypothesis:
Patients with DMD will have abnormal SSF and DRF on cardiac MRI (CMR) tissue tracking analysis and associated with fibrotic deposition.
Methods:
Patients with DMD (n=31)(mean age: 14 ± 4 yrs) and controls (n=20) (mean age: 15 ± 3 yrs) underwent CMR for volumetric and functional analysis as well as Gadolinium (Gd) enhancement to evaluate the presence of fibrosis. Circumferential strain and strain rate indices from each segment were used to calculate electromechanical discoordination. Strain rate data was used to calculate SSF and DRF.
Results:
Patients with DMD showed increased median LV SSF compared to controls [0.027 (IQR: 0.015-0.041) vs 0.007 (IQR:0.005-0.013), P = 0.002] as well as increased median LV DRF [0.371 (IQR: 0.310-0.473) vs 0.300 (IQR: 0.264-0.325), P < 0.001] (Figure). When comparing Gd(+) (n=14) vs Gd(-) (n=17) DMD patients, there was no difference between groups in either SSF [0.027 (IQR: 0.016-0.042) vs 0.026 (IQR: 0.008-0.040), P= 0.929] or DRF [0.371 (IQR: 0.309-0.537) vs 0.379 (IQR: 0.322-0.464), P= 0.931]. The SSF was associated with ESVi (R=0.71, P<0.001), EDVi (R=0.65, P< 0.001) and inversely associated with EF (R=-0.63, P<0.001).
Conclusion:
Patients with DMD showed increased levels of LV electromechanical discoordination independent of qualitative presence of fibrosis noted by Gd enhancement. This allows speculation that changes in electromechanical discoordination may precede visible fibrotic change in DMD.
Ovid Technologies (Wolters Kluwer Health)
Title: Abstract 15057: Electromechanical Discoordination is Present in Patients With Duchenne Muscular Dystrophy Independent of Tissue Fibrosis
Description:
Introduction:
Progressive ventricular dysfunction is a cardinal symptom in Duchenne Muscular Dystrophy (DMD).
Some of the earliest signs of cardiomyopathy in DMD are myocardial fibrotic deposition and LV strain defects.
Electromechanical discoordination, as measured by Systolic Stretch Fraction (SSF) and Diastolic Relaxation Fraction (DRF), has been shown to be a sensitive marker of ventricular dysfunction.
The presence of this discoordination in relation to fibrotic deposition in DMD has yet to be elucidated.
Hypothesis:
Patients with DMD will have abnormal SSF and DRF on cardiac MRI (CMR) tissue tracking analysis and associated with fibrotic deposition.
Methods:
Patients with DMD (n=31)(mean age: 14 ± 4 yrs) and controls (n=20) (mean age: 15 ± 3 yrs) underwent CMR for volumetric and functional analysis as well as Gadolinium (Gd) enhancement to evaluate the presence of fibrosis.
Circumferential strain and strain rate indices from each segment were used to calculate electromechanical discoordination.
Strain rate data was used to calculate SSF and DRF.
Results:
Patients with DMD showed increased median LV SSF compared to controls [0.
027 (IQR: 0.
015-0.
041) vs 0.
007 (IQR:0.
005-0.
013), P = 0.
002] as well as increased median LV DRF [0.
371 (IQR: 0.
310-0.
473) vs 0.
300 (IQR: 0.
264-0.
325), P < 0.
001] (Figure).
When comparing Gd(+) (n=14) vs Gd(-) (n=17) DMD patients, there was no difference between groups in either SSF [0.
027 (IQR: 0.
016-0.
042) vs 0.
026 (IQR: 0.
008-0.
040), P= 0.
929] or DRF [0.
371 (IQR: 0.
309-0.
537) vs 0.
379 (IQR: 0.
322-0.
464), P= 0.
931].
The SSF was associated with ESVi (R=0.
71, P<0.
001), EDVi (R=0.
65, P< 0.
001) and inversely associated with EF (R=-0.
63, P<0.
001).
Conclusion:
Patients with DMD showed increased levels of LV electromechanical discoordination independent of qualitative presence of fibrosis noted by Gd enhancement.
This allows speculation that changes in electromechanical discoordination may precede visible fibrotic change in DMD.
Related Results
Abstract 14479: Fontan Patients With Dominant Left Ventricular Morphology Have Severe Ventricular Electromechanical Discoordination Associated With Worse Exercise Capacity
Abstract 14479: Fontan Patients With Dominant Left Ventricular Morphology Have Severe Ventricular Electromechanical Discoordination Associated With Worse Exercise Capacity
Introduction:
Fontan patients with a single left ventricle (SLV) develop late systolic and diastolic dysfunction. The development of SLV dysfunction has been associated...
Role of Growth Factors and Apoptosis Proteins in Cognitive Disorder Development in Patients with Duchenne Muscular Dystrophy
Role of Growth Factors and Apoptosis Proteins in Cognitive Disorder Development in Patients with Duchenne Muscular Dystrophy
Duchenne muscular dystrophy (DMD) is a progressive neuromuscular disease; it occurs due to a mutation in the dystrophin protein gene; as a result, the protein is not synthesized an...
Duchenne De Boulogne: A Pioneer in Neurology and Medical Photography
Duchenne De Boulogne: A Pioneer in Neurology and Medical Photography
ABSTRACT:Guillaume-Benjamin-Amand Duchenne was born 200 years ago in Boulogne-sur-Mer (Pas-de-Calais, France). He studied medicine in Paris and became a physician in 1831. He pract...
The MRL Mitochondrial Genome Decreases Murine Muscular Dystrophy Severity
The MRL Mitochondrial Genome Decreases Murine Muscular Dystrophy Severity
It is well known that muscular dystrophy disease severity is controlled by genetic modifiers. The expectation is that by identifying these modifiers, we can illuminate additional t...
A Nonsense Variant in COL6A1 in Landseer Dogs with Muscular Dystrophy
A Nonsense Variant in COL6A1 in Landseer Dogs with Muscular Dystrophy
Abstract
A novel canine muscular dystrophy in Landseer dogs was observed. We had access to five affected dogs from two litters. The clinical signs started at a few w...
Vulvar Dystrophies: An Evaluation
Vulvar Dystrophies: An Evaluation
EDITORIAL COMMENT: This paper provides readers with a logical plan of treatment for patients presenting with pruritus, vulvitis or visible vulvar disease who are found on directed...
Duchenne Muscular Dystrophy: Clinical Characteristics, Molecular Mechanisms and Management
Duchenne Muscular Dystrophy: Clinical Characteristics, Molecular Mechanisms and Management
The dystrophinopathies encompass a range of X-linked muscle disorders varying from mild to severe, including Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), and...

