Cardiac Resynchronization by Cardiosphere-Derived Stem Cell Transplantation in an Experimental Model of Myocardial Infarction

Background: Cardiosphere-derived stem cell (CDC) transplantation can improve global left ventricular ejection fraction (LVEF) after myocardial infarction (MI). The aim of this study was to examine the effects of CDC transplantation on regional function and dyssynchrony after MI. Methods: Two million rat CDCs (n = 7) or phosphate-buffered saline (n = 7) was injected into the infarct regions of Wistar Kyoto rats. Infarct size and CDC localization were evaluated by positron emission tomography (n = 7). Two-dimensional and strain echocardiography were performed at 1 and 4 weeks after MI. LVEF, circumferential strain, and time to peak circumferential strain were measured in the basal and apical short-axis views. Dyssynchrony was defined as the maximal difference of time to peak circumferential strain of opposing segments in each short-axis view. Engraftment was measured by quantitative polymerase chain reaction. Results: Positron emission tomography revealed that infarct size was 15.4 +/- 3.6% of the left ventricle and that CDCs were localized to the infarct and border zone. CDC transplantation improved mean LVEF (45 +/- 8% to 52 +/- 7%, P = .02), mean circumferential strain (-7 +/- 2% to -10 +/- 1%, P = .02), and mean dyssynchrony (45 +/- 10 to 28 +/- 11 m sec, P = .04) of the infarct/peri-infarct zone from 1 to 4 weeks after MI, despite CDC engraftment of only 2.4 +/- 3%. In contrast, mean LVEF (48 +/- 5% to 40 +/- 4%, P = .03) and mean circumferential strain (-8 +/- 2% to -7 +/- 1%, P = .02) of the infarcted region deteriorated, with no significant change in dyssynchrony (42 +/- 12 vs 46 +/- 13 m sec, P = .60) in the saline group during the same time period. Change in LVEF was correlated with change in circumferential strain (r = -0.8, P = .002) and dyssynchrony (r = 0.6, P =.02) of the infarct/peri-infarct region at 4 weeks after MI. Conclusions: CDC therapy enhanced LVEF by improving circumferential strain and decreasing dyssynchrony of the infarct/peri-infarct region at 4 weeks, but not 1 week, after MI. Cellular resynchronization therapy using CDCs may be an alternative to traditional electrical cellular resynchronization therapy in post-MI dyssynchrony. (J Am Soc Echocardiogr 2011; 24: 808-14.)