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In Vivo Quantitative Assessment of Myocardial Structure, Function, Perfusion and Viability Using Cardiac Micro-computed Tomography
Published on: February 16, 2016
Prognostic Value of MRI-Based Left Ventricular Trabecular Complexity for Sudden Cardiac Death in Hypertrophic
Jinquan Zhang1, Mengdi Yu1, Lutong Pu1
1Department of Cardiology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Insights
Left ventricular fractal dimension (FD) predicts sudden cardiac death (SCD) in hypertrophic cardiomyopathy (HCM) patients. Elevated FD, particularly in the apex, indicates higher risk and correlates with MYBPC3 genetic variants.
Area of Science:
- Cardiology
- Medical Imaging
- Genetics
Background:
- Hypertrophic cardiomyopathy (HCM) is a primary cause of sudden cardiac death (SCD).
- Accurate risk stratification is crucial for timely intervention in HCM patients.
Purpose of the Study:
- To validate left ventricular (LV) myocardial trabecular complexity using fractal dimension (FD) for SCD prediction.
- To investigate the association between LV FD and sarcomere variants in a large HCM cohort.
Main Methods:
- Prospective study of 835 HCM patients using 3T cardiac MRI with SSFP cine sequences.
- Independent analysis of LV global and apical FD by two blinded cardiologists.
- Cox regression and Kaplan-Meier analyses for SCD prediction; Welch's t-test for genetic variant comparisons.
Main Results:
- Global and apical LV FD independently predicted SCD, improving risk stratification models.
- Higher FD values were observed in MYBPC3 variant carriers compared to other sarcomere variant carriers.
- LV FD measurements demonstrated incremental prognostic value beyond established risk predictors.
Conclusions:
- LV global and apical FD are valuable independent predictors of SCD in HCM.
- Trabecular complexity, quantified by FD, is linked to specific genetic variants like MYBPC3.
- FD analysis offers a novel approach for risk assessment in HCM.
Background:
Hypertrophic cardiomyopathy (HCM) is a leading cause of sudden cardiac death (SCD). Early identification of high-risk patients is important for guiding preventive measures.
Purpose:
To validate left ventricular (LV) myocardial trabecular complexity using fractal dimension (FD) for SCD prediction in a larger cohort and investigate its relationship with sarcomere variants.
Study Type:
Prospective.
Population:
835 HCM patients (506 men; 50.7 ± 14.4 years).
Field Strength/Sequence:
Steady-state free precession (SSFP) cine sequence at 3 T.
Assessment:
Two cardiologists, blinded to clinical outcomes, independently analyzed assigned cardiac MRI cases. Biventricular function, late gadolinium enhancement, and LV FD were measured with fracAnalyse. The endpoint was SCD or aborted SCD. Sarcomere variants were classified by the American College of Medical Genetics and Genomics criteria, and their associations with FD were assessed.
Statistical Tests:
Cox regression assessed associations with SCD. Kaplan-Meier analysis and log-rank test were used to compare SCD incidence. Harrell's C-index assessed model discrimination. Welch's t-test compared FD between variant groups. Two-sided p < 0.05 indicated significance.
Results:
Global FD (hazard ratio [HR] per 0.01 increase, 1.07, 95% CI: 1.01-1.15) and maximal apical FD (HR, 1.08, 95% CI: 1.02-1.14) independently predicted SCD after adjustment for European Society of Cardiology and American Heart Association risk predictors. High global FD (≥ 1.256) or maximal apical FD (≥ 1.352) improved model discrimination (C-index: 0.779-0.803, 0.77-0.791). MYBPC3 carriers had significantly higher maximal apical FD (1.35 ± 0.05 vs. 1.33 ± 0.07), maximal basal FD (1.35 ± 0.05 vs. 1.32 ± 0.06), and mean basal FD (1.28 ± 0.06 vs. 1.25 ± 0.07) than other sarcomere variant carriers.
Data Conclusion:
LV global and apical FDs provide independent and incremental prognostic value for predicting SCD. MYBPC3 variant carriers exhibited elevated FD values, linking trabecular complexity with genetic variants in HCM.
Evidence Level:
2.
Technical Efficacy:
Stage 3.
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