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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
In vivo cardiac diffusion tensor imaging quantifies microstructural disorganization to distinguish hypertrophic
Yujie Liu1, Zhixiang Dong1, Gang Yin1
1Radiology Imaging Center, Fuwai Hospital, National Center for Cardiovascular Diseases, State Key Laboratory of Cardiovascular Disease, Chinese Academy of Medical Sciences and Peking Union Medical College, Beilishi Road No. 167, Xicheng District, Beijing, 100037, China.
Insights
Cardiac diffusion tensor imaging (cDTI) effectively distinguishes hypertrophic cardiomyopathy (HCM) from hypertensive heart disease (HHD). Specific cDTI parameters like E2A and FA show superior diagnostic performance for microstructural alterations in HCM.
Area of Science:
- Cardiovascular Imaging
- Biomarkers
- Medical Diagnostics
Background:
- Hypertrophic cardiomyopathy (HCM) and hypertensive heart disease (HHD) are common causes of cardiac hypertrophy.
- Differentiating between HCM and HHD is crucial for appropriate patient management.
- Microstructural alterations in the myocardium may offer unique diagnostic signatures.
Purpose of the Study:
- To assess the capability of cardiac diffusion tensor imaging (cDTI) to differentiate HCM from HHD.
- To identify specific cDTI-derived microstructural parameters for distinguishing these conditions.
- To compare the diagnostic performance of cDTI with conventional cardiac magnetic resonance (CMR) techniques.
Main Methods:
- Prospective enrollment of 40 HCM and 14 HHD patients.
- Utilized 3.0T CMR including cDTI, T1 mapping, and late gadolinium enhancement (LGE).
- Analyzed cDTI parameters (MD, E2A, HA, FA) and compared them across groups using ANCOVA, with ROC analysis for diagnostic performance.
Main Results:
- HCM patients exhibited greater LVWT, LGE extent, native T1, and ECV compared to HHD patients.
- cDTI revealed significant microstructural differences: reduced FA and elevated E2A in HCM.
- E2A (AUC=0.88) and FA (AUC=0.79) demonstrated superior diagnostic performance over native T1, ECV, and LGE for distinguishing HCM from HHD.
Conclusions:
- E2A and FA from cDTI are robust biomarkers of myocardial microstructural alterations.
- cDTI provides superior differentiation of HCM from HHD compared to conventional hypertrophy and fibrosis indices.
- cDTI holds significant potential for diagnosing ambiguous cases of cardiac hypertrophy.
Objectives:
To evaluate whether cardiac diffusion tensor imaging (cDTI) can discriminate hypertrophic cardiomyopathy (HCM) from hypertensive heart disease (HHD) based on microstructural alterations.
Materials And Methods:
This prospective study enrolled 40 HCM patients and 14 HHD patients who underwent 3.0T cardiac magnetic resonance (CMR), including cDTI, T1 mapping and late gadolinium enhancement (LGE). Parameters of cDTI (mean diffusivity [MD], secondary eigenvector [E2A], helix angel [HA)] and fractional anisotropy [FA]) were compared across groups using analysis of covariance. Diagnostic performance was assessed using receiver operating characteristic analysis. A subgroup analysis was performed in HCM patients with mild hypertrophy (left ventricular wall thickness [LVWT] 13-19 mm).
Results:
Compared to patients with HHD, those with HCM showed significantly greater LVWT, LGE extent, native T1 and extracellular volume fraction (ECV, all p < 0.05). cDTI revealed significant microstructural alterations in HCM, characterized by reduced FA (p = 0.001) and elevated E2A p < 0.001). Analysis of covariance confirmed these differences after adjusting for LVWT, native T1, and ECV. ROC analysis demonstrated that E2A (AUC = 0.88) and FA (AUC = 0.79) had superior diagnostic performance for distinguishing HCM from HHD, outperforming native T1 (AUC = 0.76), ECV (AUC = 0.75), and LGE extent (AUC = 0.67). In the HCM subgroup, E2A maintained the highest diagnostic performance (AUC = 0.86), followed by FA and ECV (both AUC = 0.73).
Conclusions:
E2A and FA derived from cDTI were robust biomarkers of microstructural alterations, enabling superior differentiation of HCM from HHD beyond conventional hypertrophy and fibrosis indices. These findings support the potential utility of cDTI in diagnosis of ambiguous hypertrophy.
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