Log on / register
BioMed Central home | Journals A-Z | Feedback | Support | My details
Open AccessHighly AccessResearch

Improvement of myocardial perfusion reserve detected by cardiovascular magnetic resonance after direct endomyocardial implantation of autologous bone marrow cells in patients with severe coronary artery disease

Carmen Wing-Sze Chan email, Yok-Lam Kwong email, Raymond Y Kwong email, Chu-Pak Lau email and Hung-Fat Tse email

Journal of Cardiovascular Magnetic Resonance 2010, 12:6doi:10.1186/1532-429X-12-6

Published: 25 January 2010

Abstract (provisional)

Background

Recent studies suggested that bone marrow (BM) cell implantation in patients with severe chronic coronary artery disease (CAD) resulted in modest improvement in symptoms and cardiac function. This study sought to investigate the functional changes that occur within the chronic human ischaemic myocardium after direct endomyocardial BM cells implantation by cardiovascular magnetic resonance (CMR). Methods and Results We compared the interval changes of left ventricular ejection fraction (LVEF), myocardial perfusion reserve and the extent of myocardial scar by using late gadolinium enhancement CMR in 12 patients with severe CAD. CMR was performed at baseline and at 6 months after catheter-based direct endomyocardial autologous BM cell (n=12) injection to viable ischaemic myocardium as guided by electromechanical mapping. In patients randomized to receive BM cell injection, there was significant decrease in percentage area of peri-infarct regions (-23.6%, P=0.04) and increase in global LVEF (+9.0%, P=0.02), the percentage of regional wall thickening (+13.1%, P= 0.04) and MPR (+0.25%, P=0.03) over the target area at 6-months compared with baseline.

Conclusions

Direct endomyocardial implantation of autologous BM cells significantly improved global LVEF, regional wall thickening and myocardial perfusion reserve, and reduced percentage area of peri-infarct regions in patients with severe CAD.

The complete article is available as a provisional PDF. The fully formatted PDF and HTML versions are in production.


© 1999-2010 BioMed Central Ltd unless otherwise stated. Part of Springer Science+Business Media.