Reproducibility of in-vivo diffusion tensor cardiovascular magnetic resonance in hypertrophic cardiomyopathy
Author(s)
Type
Journal Article
Abstract
Background: Myocardial disarray is an important histological feature of hypertrophic cardiomyopathy (HCM) which
has been studied post-mortem, but its in-vivo prevalence and extent is unknown. Cardiac Diffusion Tensor Imaging
(cDTI) provides information on mean intravoxel myocyte orientation and potentially myocardial disarray. Recent
technical advances have improved in-vivo cDTI, and the aim of this study was to assess the interstudy
reproducibility of quantitative in-vivo cDTI in patients with HCM.
Methods and results: A stimulated-echo single-shot-EPI sequence with zonal excitation and parallel imaging was
implemented. Ten patients with HCM were each scanned on 2 different days. For each scan 3 short axis
mid-ventricular slices were acquired with cDTI at end systole. Fractional anisotropy (FA), mean diffusivity (MD), and
helix angle (HA) maps were created using a cDTI post-processing platform developed in-house. The mean ± SD
global FA was 0.613 ± 0.044, MD was 0.750 ± 0.154 × 10-3 mm2
/s and HA was epicardium −34.3 ± 7.6°,
mesocardium 3.5 ± 6.9° and endocardium 38.9 ± 8.1°. Comparison of initial and repeat studies showed global
interstudy reproducibility for FA (SD = ± 0.045, Coefficient of Variation (CoV) = 7.2%), MD (SD = ± 0.135 × 10-3 mm2
/s,
CoV = 18.6%) and HA (epicardium SD = ± 4.8°; mesocardium SD = ± 3.4°; endocardium SD = ± 2.9°). Reproducibility
of FA was superior to MD (p = 0.003). Global MD was significantly higher in the septum than the reference lateral
wall (0.784 ± 0.188 vs 0.750 ± 0.154 x10-3 mm2
/s, p < 0.001). Septal HA was significantly lower than the reference
lateral wall in all 3 transmural layers (from −8.3° to −10.4°, all p < 0.001).
Conclusions: To the best of our knowledge, this is the first study to assess the interstudy reproducibility of DTI in
the human HCM heart in-vivo and the largest cDTI study in HCM to date. Our results show good reproducibility of
FA, MD and HA which indicates that current technology yields robust in-vivo measurements that have potential
clinical value. The interpretation of regional differences in the septum requires further investigation
has been studied post-mortem, but its in-vivo prevalence and extent is unknown. Cardiac Diffusion Tensor Imaging
(cDTI) provides information on mean intravoxel myocyte orientation and potentially myocardial disarray. Recent
technical advances have improved in-vivo cDTI, and the aim of this study was to assess the interstudy
reproducibility of quantitative in-vivo cDTI in patients with HCM.
Methods and results: A stimulated-echo single-shot-EPI sequence with zonal excitation and parallel imaging was
implemented. Ten patients with HCM were each scanned on 2 different days. For each scan 3 short axis
mid-ventricular slices were acquired with cDTI at end systole. Fractional anisotropy (FA), mean diffusivity (MD), and
helix angle (HA) maps were created using a cDTI post-processing platform developed in-house. The mean ± SD
global FA was 0.613 ± 0.044, MD was 0.750 ± 0.154 × 10-3 mm2
/s and HA was epicardium −34.3 ± 7.6°,
mesocardium 3.5 ± 6.9° and endocardium 38.9 ± 8.1°. Comparison of initial and repeat studies showed global
interstudy reproducibility for FA (SD = ± 0.045, Coefficient of Variation (CoV) = 7.2%), MD (SD = ± 0.135 × 10-3 mm2
/s,
CoV = 18.6%) and HA (epicardium SD = ± 4.8°; mesocardium SD = ± 3.4°; endocardium SD = ± 2.9°). Reproducibility
of FA was superior to MD (p = 0.003). Global MD was significantly higher in the septum than the reference lateral
wall (0.784 ± 0.188 vs 0.750 ± 0.154 x10-3 mm2
/s, p < 0.001). Septal HA was significantly lower than the reference
lateral wall in all 3 transmural layers (from −8.3° to −10.4°, all p < 0.001).
Conclusions: To the best of our knowledge, this is the first study to assess the interstudy reproducibility of DTI in
the human HCM heart in-vivo and the largest cDTI study in HCM to date. Our results show good reproducibility of
FA, MD and HA which indicates that current technology yields robust in-vivo measurements that have potential
clinical value. The interpretation of regional differences in the septum requires further investigation
Date Issued
2012-12-24
Date Acceptance
2012-12-19
Citation
Journal of Cardiovascular Magnetic Resonance, 2012, 14, pp.86-86
ISSN
1097-6647
Publisher
BioMed Central
Start Page
86
End Page
86
Journal / Book Title
Journal of Cardiovascular Magnetic Resonance
Volume
14
Copyright Statement
© 2012 The Author(s)
Identifier
https://jcmr-online.biomedcentral.com/articles/10.1186/1532-429X-14-86
Subjects
Science & Technology
Life Sciences & Biomedicine
Cardiac & Cardiovascular Systems
Radiology, Nuclear Medicine & Medical Imaging
Cardiovascular System & Cardiology
Hypertrophic cardiomyopathy
Diffusion tensor imaging
Diffusion weighted imaging
Cardiovascular magnetic resonance
Disarray
MUSCLE CELL DISORGANIZATION
MYOCARDIAL FIBER DISARRAY
LEFT-VENTRICULAR MYOCARDIUM
ENGINEERING MECHANICS
DIASTOLIC FUNCTION
SUCCESSIVE STATES
TASK-FORCE
DIAGNOSIS
WALL
ARCHITECTURE
Aged
Cardiomyopathy, Hypertrophic
Contrast Media
Diffusion Tensor Imaging
Female
Fibrosis
Humans
Male
Middle Aged
Myocardium
Observer Variation
Predictive Value of Tests
Prospective Studies
Reproducibility of Results
Stroke Volume
Ventricular Function, Left
Myocardium
Humans
Cardiomyopathy, Hypertrophic
Fibrosis
Contrast Media
Observer Variation
Stroke Volume
Prospective Studies
Reproducibility of Results
Predictive Value of Tests
Ventricular Function, Left
Aged
Middle Aged
Female
Male
Diffusion Tensor Imaging
Nuclear Medicine & Medical Imaging
1102 Cardiorespiratory Medicine and Haematology
Publication Status
Published
Article Number
1