Assessment of Myocardial Contractile Function Using Global and Segmental Circumferential Strain following Intracoronary Stem Cell Infusion after Myocardial Infarction: MRI Feature Tracking Feasibility Study
Background. Magnetic resonance imaging (MRI) strain analysis is a sensitive method to assess myocardial function. Our objective was to define the feasibility of MRI circumferential strain ( ) analysis in assessing subtle changes in myocardial function following stem cell therapy. Methods and Results. Patients in the Amorcyte Phase I trial were randomly assigned to treatment with either autologous bone-marrow-derived stem cells infused into the infarct-related artery 5 to 11 days following primary PCI or control. MRI studies were obtained at baseline, 3, and 6 months. was measured in the short axis views at the base, mid and apical slices of the left ventricle (LV) for each patient (13 treatments and 10 controls). Mid-anterior LV improved between baseline ? and 3 months ? , . There were no significant changes in at 3 months and 6 months compared to baseline for other segments. There was excellent intraobserver and interobserver agreement for basal and mid circumferential strain. Conclusion. MRI segmental strain analysis is feasible in assessment of regional myocardial function following cell therapy with excellent intra- and inter-observer variability's. Using this method, a modest interval change in segmental was detected in treatment group. 1. Introduction Circumferential strain ( ) analysis is an established method to assess myocardial function. has been demonstrated to detect changes in myocardial contractility across a variety of cardiac conditions including hypertensive [1] or hypertrophic cardiomyopathy [2] and Duchenne muscular dystrophy [3] before changes in left ventricular ejection fraction (LVEF) are observed. Cell therapy offers a promising approach for regeneration of damaged vascular and cardiac tissue after acute myocardial infarction (MI) [4–8]. The Amorcyte trial evaluated effect of autologous bone marrow derived CD34+ cell therapy on LVEF and myocardial perfusion [9]. Significant improvement in myocardial perfusion and a trend towards improvement in LV ejection fraction were reported. Because the changes seen in systolic function are modest and by design regional, the more sensitive myocardial strain techniques offer an attractive option for analyzing these results. Accordingly, we evaluated the feasibility of MRI-derived segmental analysis in patients treated with cell therapy following primary intervention for ST-segment elevation myocardial infarction (STEMI), using the feature tracking (FT) technique. The FT technique was previously validated for assessment against harmonic phase imaging (HARP) [10] and subsequently utilized for
References
[1]
B. D. Rosen, M. F. Saad, S. Shea et al., “Hypertension and smoking are associated with reduced regional left ventricular function in asymptomatic individuals: the multi-ethnic study of atherosclerosis,” Journal of the American College of Cardiology, vol. 47, no. 6, pp. 1150–1158, 2006.
[2]
G. di Bella, F. Minutoli, A. Pingitore et al., “Endocardial and epicardial deformations in cardiac amyloidosis and hypertrophic cardiomyopathy-2-D feature strain echocardiography,” Circulation Journal, vol. 75, no. 5, pp. 1200–1208, 2011.
[3]
K. N. Hor, J. Wansapura, L. W. Markham et al., “Circumferential strain analysis identifies strata of cardiomyopathy in duchenne muscular dystrophy: a cardiac magnetic resonance tagging study,” Journal of the American College of Cardiology, vol. 53, no. 14, pp. 1204–1210, 2009.
[4]
T. Hosoda, J. Kajstura, A. Leri, and P. Anversa, “Mechanisms of myocardial regeneration,” Circulation Journal, vol. 74, no. 1, pp. 13–17, 2010.
[5]
R. Uemura, M. Xu, N. Ahmad, and M. Ashraf, “Bone marrow stem cells prevent left ventricular remodeling of ischemic heart through paracrine signaling,” Circulation Research, vol. 98, no. 11, pp. 1414–1421, 2006.
[6]
V. Sch?chinger, S. Erbs, A. Els?sser et al., “Improved clinical outcome after intracoronary administration of bone-marrow-derived progenitor cells in acute myocardial infarction: final 1-year results of the REPAIR-AMI trial,” European Heart Journal, vol. 27, no. 23, pp. 2775–2783, 2006.
[7]
M. B. Britten, N. D. Abolmaali, B. Assmus et al., “Infarct remodeling after intracoronary progenitor cell treatment in patients with acute myocardial infarction (TOPCARE-AMI): mechanistic insights from serial contrast-enhanced magnetic resonance imaging,” Circulation, vol. 108, no. 18, pp. 2212–2218, 2003.
[8]
E. Martin-Rendon, S. J. Brunskill, C. J. Hyde, S. J. Stanworth, A. Mathur, and S. M. Watt, “Autologous bone marrow stem cells to treat acute myocardial infarction: a systematic review,” European Heart Journal, vol. 29, no. 15, pp. 1807–1818, 2008.
[9]
A. A. Quyyumi, E. K. Waller, J. Murrow et al., “CD34+ cell infusion after ST elevation myocardial infarction is associated with improved perfusion and is dose dependent,” American Heart Journal, vol. 161, no. 1, pp. 98–105, 2011.
[10]
K. N. Hor, W. M. Gottliebson, C. Carson et al., “Comparison of magnetic resonance feature tracking for strain calculation with harmonic phase imaging analysis,” Journal of the American College of Cardiology, vol. 3, no. 2, pp. 144–151, 2010.
[11]
W. Szczeklik, T. Miszalski-Jamka, L. Mastalerz et al., “Multimodality assessment of cardiac involvement in Churg-Strauss syndrome patients in clinical remission,” Circulation Journal, vol. 75, no. 3, pp. 649–655, 2011.
[12]
A. Schuster, S. Kutty, A. Padiyath, et al., “Cardiovascular magnetic resonance myocardial feature tracking detects quantitative wall motion during dobutamine stress,” Journal of Cardiovascular Magnetic Resonance, vol. 13, no. 1, p. 58, 2011.
[13]
B. E. Strauer, M. Brehm, T. Zeus et al., “Repair of infarcted myocardium by autologous intracoronary mononuclear bone marrow cell transplantation in humans,” Circulation, vol. 106, no. 15, pp. 1913–1918, 2002.
[14]
A. Tugcu, O. Yildirimtürk, Y. Tayyareci, C. Demiroglu, and S. Aytekin, “Evaluation of subclinical right ventricular dysfunction in obstructive sleep apnea patients using velocity vector imaging,” Circulation Journal, vol. 74, no. 2, pp. 312–319, 2010.
[15]
K. Kusunose, H. Yamada, S. Nishio et al., “Validation of longitudinal peak systolic strain by speckle tracking echocardiography with visual assessment and myocardial perfusion SPECT in patients with regional asynergy,” Circulation Journal, vol. 75, no. 1, pp. 141–147, 2011.
[16]
J. D'Hooge, A. Heimdal, F. Jamal et al., “Regional strain and strain rate measurements by cardiac ultrasound: principles, implementation and limitations,” European Journal of Echocardiography, vol. 1, no. 3, pp. 154–170, 2000.
[17]
K. N. Hor, R. Baumann, G. Pedrizzetti et al., “Magnetic resonance derived myocardial strain assessment using feature tracking,” Journal of Visualized Experiments, no. 48, article 2356, 2010.
[18]
J. M. Bland and D. G. Altman, “Statistical methods for assessing agreement between two methods of clinical measurement,” The Lancet, vol. 1, no. 8476, pp. 307–310, 1986.
[19]
G. K. Shukla, “Some exact tests of hypotheses about Grubbs's estimators,” Biometrics, vol. 29, no. 2, pp. 373–377, 1973.
[20]
U. T. Truong, X. Li, C. S. Broberg et al., “Significance of mechanical alterations in single ventricle patients on twisting and circumferential strain as determined by analysis of strain from gradient cine magnetic resonance imaging sequences,” American Journal of Cardiology, vol. 105, no. 10, pp. 1465–1469, 2010.
[21]
L. Herbots, J. D'Hooge, E. Eroglu et al., “Improved regional function after autologous bone marrow-derived stem cell transfer in patients with acute myocardial infarction: a randomized, double-blind strain rate imaging study,” European Heart Journal, vol. 30, no. 6, pp. 662–670, 2009.
[22]
M. Plewka, M. Krzemińska-Paku?a, P. Lipiec et al., “Effect of intracoronary injection of mononuclear bone marrow stem cells on left ventricular function in patients with acute myocardial infarction,” American Journal of Cardiology, vol. 104, no. 10, pp. 1336–1342, 2009.
[23]
G. Karatasakis, E. Leontiadis, I. Peristeri et al., “Intracoronary infusion of selected autologous bone marrow stem cells improves longitudinal myocardial strain and strain rate in patients with old anterior myocardial infarction without recent revascularization,” European Journal of Echocardiography, vol. 11, no. 5, pp. 440–445, 2010.
[24]
E. Hopp, K. Lunde, S. Solheim et al., “Regional myocardial function after intracoronary bone marrow cell injection in reperfused anterior wall infarction—a cardiovascular magnetic resonance tagging study,” Journal of Cardiovascular Magnetic Resonance, vol. 13, article 22, 2011.
[25]
J. H. Traverse, T. D. Henry, and L. A. Moye', “Is the measurement of left ventricular ejection fraction the proper end point for cell therapy trials? An analysis of the effect of bone marrow mononuclear stem cell administration on left ventricular ejection fraction after ST-segment elevation myocardial infarction when evaluated by cardiac magnetic resonance imaging,” American Heart Journal, vol. 162, no. 4, pp. 671–677, 2011.
[26]
S. D. Roes, C. J. W. Borleffs, R. J. Van Der Geest et al., “Infarct tissue heterogeneity assessed with contrast-enhanced mri predicts spontaneous ventricular arrhythmia in patients with ischemic cardiomyopathy and implantable cardioverter-defibrillator,” Circulation: Cardiovascular Imaging, vol. 2, no. 3, pp. 183–190, 2009.