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Magnetic Resonance Derived Myocardial Strain Assessment Using Feature Tracking
Published on: February 12, 2011
Multichamber Strain Imaging and Biomarker Profiling for 1-Year Risk Stratification in Pediatric Dilated
Iolanda Muntean1,2, Asmaa-Carla Hagau3,4, Diana-Ramona Iurian2,3
1Department of Paediatrics III, George Emil Palade University of Medicine, Pharmacy, Science, and Technology of Targu Mures, 540142 Targu Mures, Romania.
Insights
This study found that multichamber strain imaging and NT-proBNP levels can help predict 1-year outcomes in children with dilated cardiomyopathy (DCM). These tools aid in identifying high-risk patients for advanced heart failure therapies.
Area of Science:
- Pediatric Cardiology
- Cardiovascular Imaging
- Biomarkers in Heart Disease
Background:
- Dilated cardiomyopathy (DCM) in children is rare but serious, often progressing to heart failure (HF) and heart transplant (HTx).
- Accurate short-term risk stratification is crucial for pediatric DCM patients, yet prognostic tools are limited.
- Early identification of high-risk children can guide timely intervention and management.
Purpose of the Study:
- To assess the 1-year prognostic value of multichamber speckle-tracking echocardiography (STE) and biomarkers in children with DCM.
- To evaluate age-adjusted N-terminal pro-B-type natriuretic peptide (NT-proBNP) and vitamin D as prognostic markers.
- To identify reliable markers for predicting major adverse events within one year.
Main Methods:
- A prospective cohort study involving 29 children with idiopathic DCM and 27 healthy controls.
- Standardized clinical, laboratory, and echocardiographic assessments, including multichamber STE.
- Primary endpoint: a 12-month composite of ICD implantation, LVAD, HTx, or all-cause mortality.
Main Results:
- 31% of DCM patients experienced major adverse events within 1 year.
- Impaired left ventricular global longitudinal strain (LVGLS), reduced right ventricular free wall strain (RVFWSL), and lower left atrial strain rate (LASr) were associated with adverse events.
- Elevated Z-score log NT-proBNP was significantly higher in the event group.
- LVGLS, Zlog NT-proBNP, and LASr demonstrated excellent discrimination for 1-year events (AUCs 0.91, 0.91, and 0.87).
Conclusions:
- Multichamber strain imaging (LVGLS, LASr) combined with age-adjusted NT-proBNP are promising exploratory markers for short-term risk stratification in pediatric DCM.
- These markers can support earlier follow-up intensification and timely referral for advanced heart failure therapies.
- Validation in larger, multicenter cohorts is warranted to confirm these findings.
Abstract:
Dilated cardiomyopathy (DCM) in children is rare, but carries a high risk of progression to advanced heart failure (HF) and heart transplant (HTx). Improved short-term risk stratification is essential; however, robust pediatric prognostic tools remain limited. We aimed to evaluate the 1-year prognostic value of multichamber speckle-tracking echocardiography (STE) and biomarkers, including age-adjusted N-terminal pro-B-type natriuretic peptide (NT-proBNP) and vitamin D, in children with DCM. In this single-centre prospective cohort study, 29 children with idiopathic DCM and 27 age- and sex-matched healthy controls underwent standardised clinical, laboratory, and echocardiographic assessment. The primary endpoint was a 12-month composite of implantation of an implantable cardioverter-defibrillator (ICD), left-ventricular assist device (LVAD), HTx, or all-cause mortality. During a 1-year follow-up, 9/29 (31%) DCM patients experienced major events. Compared with event-free patients and controls, children with events had more impaired LVGLS (-5.99 ± 2.45% vs. -13.44 ± 6.88% and -19.98 ± 3.25%), lower LASr (10.97 ± 7.67% vs. 25.36 ± 10.28% and 44.0 ± 11.43%), and reduced RVFWSL (-15.32 ± 5.24% vs. -23.13 ± 8.55% and -24.78 ± 4.45%; all p < 0.01). Zlog NT-proBNP was markedly higher in the event group (5.37 [5.00-6.08] vs. 2.28 [0.71-3.68] and 0.14 [-0.02-0.88]). LVGLS, Zlog NT-proBNP, and LASr showed excellent discrimination for 1-year events (AUC 0.91, 0.91, and 0.87, respectively), with clinically applicable cut-offs (LVGLS ≥ -8%, Zlog NT-proBNP ≥ 4.6, LASr ≤ 21%). In conclusion, multichamber strain imaging combined with age-adjusted NT-proBNP provides clinically relevant, exploratory markers for short-term risk stratification in pediatric DCM, supporting earlier intensification of follow-up and timely referral for advanced heart failure therapies. These findings warrant validation in larger multicenter cohorts.
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