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Updated: Jan 16, 2026

Ultrasonic Assessment of Myocardial Microstructure
Published on: January 14, 2014
Early Detection of Subclinical Myocardial Dysfunction in Familial Dilated Cardiomyopathy Using Myocardial Work
Apostolos Vrettos1, Ricardo Prista Monteiro1, Miltiadis Triantafyllou2
1Barts Heart Centre, St Bartholomew's Hospital, Barts Health NHS Trust, London EC1A 7BE, UK.
Myocardial work analysis, using global wasted work (GWW) and global work efficiency (GWE), detects early heart dysfunction in asymptomatic familial dilated cardiomyopathy (DCM) gene carriers. This method aids in the early detection and management of DCM.
Area of Science:
- Cardiology
- Genetics
- Medical Imaging
Background:
- Early detection of familial dilated cardiomyopathy (DCM) is critical for timely intervention.
- Myocardial work (MW) analysis integrates strain imaging and blood pressure to detect subclinical cardiac disease.
Purpose of the Study:
- To evaluate the utility of MW analysis in identifying early myocardial changes in asymptomatic relatives of DCM patients with a positive genotype (G+) compared to genotype-negative (G-) controls.
Main Methods:
- Seventy-seven asymptomatic relatives of DCM patients were divided into G+ (n=39) and G- (n=38) groups based on genetic testing.
- Comprehensive echocardiographic evaluation including MW parameters (GWI, GCW, GWW, GWE) was performed.
- Statistical analyses compared MW parameters between groups and assessed their predictive value for genotype status.
Main Results:
- G+ individuals showed significantly reduced global work efficiency (GWE) and increased global wasted work (GWW) compared to G- controls.
- GWE and GWW were significant predictors of gene carrier status in multivariable analysis.
- Increased baseline GWW and reduced GWE correlated with the development of cardiomyopathy phenotype during follow-up.
Conclusions:
- Myocardial work analysis, specifically GWE and GWW, effectively identifies early myocardial dysfunction in asymptomatic carriers of genetic variants for DCM.
- MW analysis shows potential to complement traditional imaging for early detection and management of familial DCM.
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