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Heart Stiffening in Pediatric Dilated Cardiomyopathy: Causes of Severity
Noor Mohammad Noori1, Alireza Teimouri2
1Department of Pediatrics, School of Medicine, Children and Adolescents Health Research Center, Research Institute of Cellular and Molecular Sciences in Infectious Diseases, Ali Ibne Abitaleb Hospital, Zahedan University of Medical Sciences, Zahedan, Iran.
Insights
Children with dilated cardiomyopathy (DCM) show increased aortic stiffness and reduced distensibility. This indicates that aortic stiffness is a significant factor contributing to the severity of DCM in pediatric patients.
Area of Science:
- Pediatric Cardiology
- Cardiovascular Physiology
- Biomedical Engineering
Background:
- Cardiomyopathy can cause heart stiffness and lead to heart failure.
- Dilated cardiomyopathy (DCM) is a condition affecting heart muscle.
- Understanding aortic stiffness in pediatric DCM is crucial for assessing disease severity.
Purpose of the Study:
- To investigate aortic stiffness in children diagnosed with dilated cardiomyopathy (DCM).
- To determine the contribution of aortic stiffness to the overall severity of DCM in pediatric patients.
Main Methods:
- A case-control study comparing 48 children with DCM to 96 healthy controls.
- Measurements included aortic strain, stiffness index, distensibility, and pressure strain elastic modulus.
- Statistical analysis was performed using SPSS 18, with P<0.05 considered significant.
Main Results:
- Children with DCM demonstrated significantly reduced aortic distensibility (P=0.004) and elevated aortic stiffness (P=0.001).
- Aortic strain was reduced, and pressure strain elastic modulus was elevated in the DCM group.
- Aortic stiffness index varied with the Ross classification post-treatment.
Conclusions:
- Pediatric patients with DCM exhibit impaired aortic elasticity.
- Reduced aortic distensibility and increased aortic stiffness are characteristic of DCM in children.
- Aortic stiffness is a relevant factor in the pathophysiology of pediatric DCM.
Background:
Cardiomyopathy, characterized by heart stiffness, can lead to heart failure. This study aimed to investigate aortic stiffness in children with dilated cardiomyopathy (DCM) to better understand its contribution to disease severity.
Methods:
This case-control study compared 48 children with DCM with 96 healthy children over a 10-year period starting in 2011. Aortic strain, aortic stiffness index, aortic distensibility, and pressure strain elastic modulus were measured. These parameters, along with several echocardiographic measures, were compared between the DCM and control groups. Statistical analyses were performed using SPSS 18, with a significance threshold set at a P value below 0.05.
Results:
The participants included 57.6% boys, with 58.3% in the DCM group and 57.35% in the control group (χ2=0.014, P=0.905). The age range was 2 to 18 years, with mean ages of 11.08±4.63 years for the DCM group and 10.77±2.82 years for the control group (P=0.691). Significant differences between groups were observed in aortic distensibility (P=0.004), aortic stiffness β index (P=0.001), and pressure strain elastic modulus (P=0.004). Post-treatment analyses based on ejection fraction and fractional shortening cutoffs indicated no changes in elasticity parameters except for the aortic stiffness β index, which varied according to the Ross classification.
Conclusion:
Children with DCM exhibited reduced aortic strain and aortic distensibility, as well as elevated aortic stiffness β index and pressure strain elastic modulus.
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