TY - JOUR
T1 - Comparison of strain measurement from multimodality tissue tracking with strain-encoding MRI and harmonic phase MRI in pulmonary hypertension
AU - Ohyama, Yoshiaki
AU - Ambale-Venkatesh, Bharath
AU - Chamera, Elzbieta
AU - Shehata, Monda L.
AU - Corona-Villalobos, Celia P.
AU - Zimmerman, Stefan L.
AU - Hassoun, Paul M.
AU - Bluemke, David Alan
AU - Lima, Joao A.C.
N1 - Funding Information:
This research was supported by grants NIH1P50HL084946 from National Institutes of Health .
Publisher Copyright:
© 2014 Elsevier Ireland Ltd. © 2015 Elsevier B.V. All rights reserved.
PY - 2015/3/1
Y1 - 2015/3/1
N2 - Background Pixel-based multimodality tissue tracking (MTT) is a new noninvasive method for the quantification of cardiac deformation from cine image of MRI. The aim of this study is to validate bi-ventricular strain measurement by MTT compared to strain-encoding (SENC) MRI and harmonic phase (HARP) MRI in pulmonary hypertension (PH) patients. Methods In 45 subjects (30 PH patients and 15 normal subjects), RV and LV peak global longitudinal strains (Ell) were measured from long axis 4 chamber view using MTT. LV peak global circumferential strains (Ecc) by MTT were measured from short axis. For validation, RV and LV Ell by MTT were compared to measures by SENC-MRI from short axis, and LV Ecc by MTT was compared to measures by short axis tagged MRI analysis (HARP). Reproducibility of MTT was also determined. Results MTT quantified RV Ell correlated closely to those of SENC (r = 0.72, p < 0.001), with good limits of agreement. LV Ell quantified by MTT showed moderate correlation with SENC (r = 0.57, p = 0.001), and LV Ecc by MTT also showed moderate correlation with HARP (- 16.9 ± 4.1 vs - 14.3 ± 3.5, p < 0.001 for all, r = 0.60, p < 0.001). RV Ell negatively correlated with RVEF (r = - 0.53, p = 0.001) and also positively correlated with mean PAP in PH patients (r = 0.60, p = 0.001). Strain measurement by MTT showed high reproducibility. Conclusions We demonstrate that MTT is a reproducible tool for quantification of cardiac deformation using cine images in PH patients. Hence, it could serve as a new rapid and comprehensive technique for clinical assessment of regional cardiac function.
AB - Background Pixel-based multimodality tissue tracking (MTT) is a new noninvasive method for the quantification of cardiac deformation from cine image of MRI. The aim of this study is to validate bi-ventricular strain measurement by MTT compared to strain-encoding (SENC) MRI and harmonic phase (HARP) MRI in pulmonary hypertension (PH) patients. Methods In 45 subjects (30 PH patients and 15 normal subjects), RV and LV peak global longitudinal strains (Ell) were measured from long axis 4 chamber view using MTT. LV peak global circumferential strains (Ecc) by MTT were measured from short axis. For validation, RV and LV Ell by MTT were compared to measures by SENC-MRI from short axis, and LV Ecc by MTT was compared to measures by short axis tagged MRI analysis (HARP). Reproducibility of MTT was also determined. Results MTT quantified RV Ell correlated closely to those of SENC (r = 0.72, p < 0.001), with good limits of agreement. LV Ell quantified by MTT showed moderate correlation with SENC (r = 0.57, p = 0.001), and LV Ecc by MTT also showed moderate correlation with HARP (- 16.9 ± 4.1 vs - 14.3 ± 3.5, p < 0.001 for all, r = 0.60, p < 0.001). RV Ell negatively correlated with RVEF (r = - 0.53, p = 0.001) and also positively correlated with mean PAP in PH patients (r = 0.60, p = 0.001). Strain measurement by MTT showed high reproducibility. Conclusions We demonstrate that MTT is a reproducible tool for quantification of cardiac deformation using cine images in PH patients. Hence, it could serve as a new rapid and comprehensive technique for clinical assessment of regional cardiac function.
KW - Abbreviations PH pulmonary hypertension
KW - Ecc circumferential strain.
KW - Ell longitudinal strain
KW - HARP harmonic phase analysis
KW - LV left ventricle
KW - MTT multimodality tissue tracking
KW - RV right ventricle
KW - SENC strain-encoding
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U2 - 10.1016/j.ijcard.2015.01.016
DO - 10.1016/j.ijcard.2015.01.016
M3 - Article
C2 - 25590963
AN - SCOPUS:84947202794
SN - 0167-5273
VL - 182
SP - 342
EP - 348
JO - International Journal of Cardiology
JF - International Journal of Cardiology
ER -