Author + information
- Received April 16, 2003
- Accepted June 4, 2003
- Published online December 17, 2003.
- Pieter C Smits, MD, PhD*,* (, )
- Robert-Jan M van Geuns, MD, PhD†,
- Don Poldermans, MD, PhD*,
- Manolis Bountioukos, MD*,
- Emile E.M Onderwater*,
- Chi Hang Lee, MD*,
- Alex P.W.M Maat, MD* and
- Patrick W Serruys, MD, PhD*
- ↵*Reprint requests and correspondence:
Dr. Pieter C. Smits, Department of Cardiology, Thorax Center, Room Bd 412, Erasmus Medical Center Rotterdam, Dr. Molewaterplein 40, 3015 GD Rotterdam, The Netherlands.
Objectives We report on the procedural and six-month results of the first percutaneous and stand-alone study on myocardial repair with autologous skeletal myoblasts.
Background Preclinical studies have shown that skeletal myoblast transplantation to injured myocardium can partially restore left ventricular (LV) function.
Methods In a pilot safety and feasibility study of five patients with symptomatic heart failure (HF) after an anterior wall infarction, autologous skeletal myoblasts were obtained from the quadriceps muscle and cultured in vitro for cell expansion. After a culturing process, 296 ± 199 million cells were harvested (positive desmin staining 55 ± 30%). With a NOGA-guided catheter system (Biosense-Webster, Waterloo, Belgium), 196 ± 105 million cells were transendocardially injected into the infarcted area. Electrocardiographic and LV function assessment was done by Holter monitoring, LV angiography, nuclear radiography, dobutamine stress echocardiography, and magnetic resonance imaging (MRI).
Results All cell transplantation procedures were uneventful, and no serious adverse events occurred during follow-up. One patient received an implantable cardioverter-defibrillator after transplantation because of asymptomatic runs of nonsustained ventricular tachycardia. Compared with baseline, the LV ejection fraction increased from 36 ± 11% to 41 ± 9% (3 months, p = 0.009) and 45 ± 8% (6 months, p = 0.23). Regional wall analysis by MRI showed significantly increased wall thickening at the target areas and less wall thickening in remote areas (wall thickening at target areas vs. 3 months follow-up: 0.9 ± 2.3 mm vs. 1.8 ± 2.4 mm, p = 0.008).
Conclusions This pilot study is the first to demonstrate the potential and feasibility of percutaneous skeletal myoblast delivery as a stand-alone procedure for myocardial repair in patients with post-infarction HF. More data are needed to confirm its safety.
☆ This study was partly financially supported by Bioheart Inc., Weston, Florida.
- Received April 16, 2003.
- Accepted June 4, 2003.
- American College of Cardiology Foundation