TY - JOUR
T1 - Right Ventricular Remodeling Assessed by MRI in Duchenne Muscular Dystrophy
AU - Brown, Nicholas K.
AU - Berhane, Haben
AU - Gambetta, Katheryn
AU - Markl, Michael
AU - Rigsby, Cynthia K.
AU - Robinson, Joshua D
AU - Husain, Nazia
N1 - Funding Information:
Research reported in this publication was supported by the National Heart, Lung, And Blood Institute of the National Institutes of Health under Award Number R01HL117888.
Publisher Copyright:
© 2022 International Society for Magnetic Resonance in Medicine.
PY - 2022
Y1 - 2022
N2 - Background: In Duchenne muscular dystrophy (DMD), the right ventricle (RV) tends to be relatively well preserved, but characterization remains difficult due to its complex architecture. Tissue phase mapping (TPM) is a phase contrast cine MRI technique that allows for multidirectional assessment of myocardial velocities. Purpose: To use TPM to elucidate relationships between myocardial structure, function, and clinical variables in DMD. Study Type: Retrospective. Subjects: A total of 20 patients with muscular dystrophy (median age: 16 years); 18 age-matched normal controls (median age: 15 years). Field Strength/Sequence: Three-directional velocity encoded cine gradient echo sequence (TPM) at 1.5 T, balanced steady-state free procession (bSSFP), T1 mapping with extracellular volume (ECV), and late gadolinium enhancement (LGE). Assessment: TPM in basal, mid, and apical short-axis planes was performed as part of a standard MRI study with collection of clinical data. Radial, circumferential, and longitudinal velocities (Vr, Vφ, and Vz, respectively) and corresponding time to peak (TTP) velocities were quantified from TPM and used to calculate RV twist as well as intraventricular and interventricular dyssynchrony. The correlations between TPM velocities, myocardial structure/function, and clinical variables were assessed. Statistical Test: Unpaired t-test, Wilcoxon rank-sum test, Bland–Altman analyses were used for comparisons between DMD patients and controls and between DMD subgroups. Pearson's test was used for correlations (r). Significance level: P < 0.05. Results: Compared to controls, DMD patients had preserved RV ejection fraction (RVEF 53% ± 8%) but significantly increased interventricular dyssynchrony (Vφ: 0.49 ± 0.21 vs. 0.72 ± 0.17). Within the DMD cohort, RV dyssynchrony significantly increased with lower LV ejection fraction (intraventricular Vr and Vz: r = −0.49; interventricular Vz: r = 0.48). In addition, RV intraventricular dyssynchrony significantly increased with older age (Vz: r = 0.67). Data Conclusion: RV remodeling in DMD occurs in the context of preserved RVEF. Within DMD, this abnormal RV deformation is associated with older age and decreased LVEF. Evidence Level: 4. Technical Efficacy: Stage 2.
AB - Background: In Duchenne muscular dystrophy (DMD), the right ventricle (RV) tends to be relatively well preserved, but characterization remains difficult due to its complex architecture. Tissue phase mapping (TPM) is a phase contrast cine MRI technique that allows for multidirectional assessment of myocardial velocities. Purpose: To use TPM to elucidate relationships between myocardial structure, function, and clinical variables in DMD. Study Type: Retrospective. Subjects: A total of 20 patients with muscular dystrophy (median age: 16 years); 18 age-matched normal controls (median age: 15 years). Field Strength/Sequence: Three-directional velocity encoded cine gradient echo sequence (TPM) at 1.5 T, balanced steady-state free procession (bSSFP), T1 mapping with extracellular volume (ECV), and late gadolinium enhancement (LGE). Assessment: TPM in basal, mid, and apical short-axis planes was performed as part of a standard MRI study with collection of clinical data. Radial, circumferential, and longitudinal velocities (Vr, Vφ, and Vz, respectively) and corresponding time to peak (TTP) velocities were quantified from TPM and used to calculate RV twist as well as intraventricular and interventricular dyssynchrony. The correlations between TPM velocities, myocardial structure/function, and clinical variables were assessed. Statistical Test: Unpaired t-test, Wilcoxon rank-sum test, Bland–Altman analyses were used for comparisons between DMD patients and controls and between DMD subgroups. Pearson's test was used for correlations (r). Significance level: P < 0.05. Results: Compared to controls, DMD patients had preserved RV ejection fraction (RVEF 53% ± 8%) but significantly increased interventricular dyssynchrony (Vφ: 0.49 ± 0.21 vs. 0.72 ± 0.17). Within the DMD cohort, RV dyssynchrony significantly increased with lower LV ejection fraction (intraventricular Vr and Vz: r = −0.49; interventricular Vz: r = 0.48). In addition, RV intraventricular dyssynchrony significantly increased with older age (Vz: r = 0.67). Data Conclusion: RV remodeling in DMD occurs in the context of preserved RVEF. Within DMD, this abnormal RV deformation is associated with older age and decreased LVEF. Evidence Level: 4. Technical Efficacy: Stage 2.
KW - Duchenne muscular dystrophy
KW - late gadolinium enhancement
KW - parametric mapping
KW - tissue phase mapping
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U2 - 10.1002/jmri.28521
DO - 10.1002/jmri.28521
M3 - Article
C2 - 36354274
AN - SCOPUS:85141818746
SN - 1053-1807
JO - Journal of Magnetic Resonance Imaging
JF - Journal of Magnetic Resonance Imaging
ER -