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Updated: May 14, 2026

Measurements of Motor Function and Other Clinical Outcome Parameters in Ambulant Children with Duchenne Muscular Dystrophy
Published on: January 12, 2019
Abnormal circumferential strain is present in young Duchenne muscular dystrophy patients
Thomas D Ryan1, Michael D Taylor, Wojciech Mazur
1Division of Pediatric Cardiology, The Heart Institute, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, MLC 2003, Cincinnati, OH 45229-3039, USA. thomas.ryan@cchmc.org
Insights
Cardiac dysfunction in Duchenne muscular dystrophy (DMD) is detectable in young patients using strain (ε) measurements, even when standard tests like fractional shortening (FS) appear normal. This early detection of myocardial abnormalities in DMD is crucial for timely intervention.
Area of Science:
- Cardiology
- Pediatrics
- Genetics
Background:
- Duchenne muscular dystrophy (DMD) management has improved, making cardiac disease the leading cause of mortality.
- Standard echocardiographic measures like fractional shortening (FS) and ejection fraction (EF) often show normal results in young DMD patients.
- Early detection of cardiac dysfunction is critical for improving outcomes in DMD.
Purpose of the Study:
- To assess regional ventricular function using strain (ε) in young DMD patients.
- To compare transthoracic echocardiogram (TTE) strain parameters between DMD patients and healthy controls.
- To determine if strain analysis can detect cardiac abnormalities before global dysfunction is evident.
Main Methods:
- Retrospective review of TTE data from DMD patients (<8 years) and controls.
- Utilized feature tracking analysis software to measure total and segmental circumferential strain (ε cc).
- Compared LV ε cc and segmental ε cc (American Society of Echocardiography 16-segment model) between groups.
Main Results:
- No significant differences in FS were observed between DMD patients and controls.
- Absolute values for LV ε cc at the mid-chamber level were decreased in DMD patients.
- Segmental ε cc abnormalities were found in the anteroseptal, inferior, and inferolateral segments of DMD patients.
Conclusions:
- Young DMD patients exhibit abnormal total and segmental LV ε cc at the mid-chamber level, despite normal FS.
- Strain analysis (ε cc) can identify myocardial dysfunction in DMD patients earlier than standard global measures.
- These findings highlight the utility of strain echocardiography for early cardiac assessment in DMD.
Abstract:
Advances in management of non-cardiac issues in Duchenne muscular dystrophy (DMD) have improved such that DMD-associated cardiac disease has become the leading cause of death for such patients. Cardiac dysfunction measured by standard transthoracic echocardiographic methods, e.g., fractional shortening (FS) and ejection fraction (EF), is rarely present during the first decade of life. The current study used transthoracic echocardiogram (TTE) to assess strain (ε), an indicator of regional ventricular function, in young DMD patients. A retrospective review of the TTE database was performed. TTE results from DMD patients <8 years (n = 63) performed during 2009 to 2010 were compared with TTE results from an unaffected control group (n = 61). Feature tracking analysis software was used to measure total circumferential strain (ε cc) as well as segmental ε cc based on the American Society of Echocardiography 16-segment model. Although there were no differences in FS, the absolute value for left-ventricular (LV) ε cc at the mid-chamber level was decreased in DMD (-21.7 % ± 3.8 % vs. -19.8 % ± 4.2 %, p < 0.01; unaffected vs. DMD). Segmental ε(cc) was similarly affected in the anteroseptal segment (-23.0 % ± 6.1 % vs. -18.9 % ± 7.0 %, p = 0.001; controls vs. DMD), the inferior segment (-20.7 % ± 5.16 % vs. -17.7 % ± 6.1 %, p = 0.003; controls vs. DMD), and the inferolateral segment (-18.3 % ± 6.2 % vs. -15.9 % ± 6.7 %, p = 0.04; controls vs. DMD). In the present study we demonstrate both total and segmental LV ε cc (anteroseptal, inferior, and inferolateral segments) abnormalities at the mid-chamber level in a large group of young DMD patients with normal FS. These novel findings substantiate that the disease process is present and results in abnormal myocardial function before standard measures detect global dysfunction.
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