Skip to main content

Advertisement

Log in

Transplantation of progenitor cells after reperfused acute myocardial infarction: evaluation of perfusion and myocardial viability with FDG-PET and thallium SPECT

  • Original Article
  • Published:
European Journal of Nuclear Medicine and Molecular Imaging Aims and scope Submit manuscript

Abstract

Clinical outcome after myocardial infarction depends on the extent of irreversibly damaged myocardium. Implantation of bone marrow-/circulating blood-derived progenitor cells has been shown to improve contractile cardiac function after myocardial infarction in both experimental and initial clinical studies. In the present study, first observations of the effect of local intracoronary progenitor cell infusion on the regeneration of infarcted cardiac tissue after acute myocardial infarction was evaluated by means of 18F-fluorodeoxyglucose positron emission tomography (PET) and 201Tl single-photon emission computed tomography (SPECT). Twenty-six patients underwent intracoronary infusion of bone marrow-derived (BMCs) (15 patients) or circulating blood-derived endothelial progenitor cells (EPCs) (11 patients) 4±2 days after acute myocardial infarction. Based on a left ventricular segmentation model (17 segments), mean signal intensities as a parameter of viability and perfusion in the infarct zone and non-infarct areas were calculated quantitatively by PET and SPECT at baseline and at 4 months of follow-up. Transplantation of progenitor cells was associated with a significant increase in the mean signal intensity (MSI) in the infarct zone from 54.5% (25th and 75th percentiles: 47.7%, 60.0%) to 58.0% (52.7%, 66.7%) on PET (P=0.013) and from 58.0% (49.5%, 63.0%) to 61.5% (52.5%, 70.2%) on SPECT (P=0.005). Global left ventricular ejection fraction (LVEF) increased from 53.5% (42.6%, 60.0%) to 58.0% (53.0%, 65.8%) (P<0.001). In the five patients without an increase in MSI on PET, LVEF changed from 60.0% (50.0%, 64.0%) to 72.0% (64.0%, 75.5%) at follow-up. PET and SPECT did not show any significant changes in MSI in the non-infarct areas [from 73% (68.5%, 76.2%) to 73% (69.7%, 78.0%) for PET and from 72.0% (66.5%, 77.6%) to 73.0% (67.5%, 78.2%) for SPECT]. There were no significant differences in myocardial viability and perfusion between BMC and EPC infusion. These preliminary results show that coronary stenting and transplantation of progenitor cells result in a significant increase in myocardial viability and perfusion. Therapeutic effects can be reliably measured by PET and SPECT.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4A–D
Fig. 5

Similar content being viewed by others

References

  1. Orlic D, Kajstura J, Chimenti S, et al. Mobilized bone marrow cells repair the infarcted heart, improving function and survival. Proc Natl Acad Sci USA 2001; 98:10344–10349.

    CAS  PubMed  Google Scholar 

  2. Kocher AA, Schuster MD, Szabolcs MJ, et al. Neovascularization of ischemic myocardium by human bone-marrow-derived angioblasts prevents cardiomyocyte apoptosis, reduces remodeling and cardiac function. Nat Med 2001; 7:430–436.

    PubMed  Google Scholar 

  3. Fuchs S, Baffour R, Zhou YF, et al. Transendocardial delivery of autologous bone marrow enhances collateral perfusion and regional function in pigs with chronic experimental myocardial ischemia. J Am Coll Cardiol 2001; 37:1726–1732.

    Article  CAS  PubMed  Google Scholar 

  4. Kawamoto A, Baffour R, Zhou YF, et al. Therapeutic potential of ex vivo expanded endothelial progenitor cells for myocardial ischemia. Circulation 2001; 103:634–637.

    CAS  PubMed  Google Scholar 

  5. Orlic D, Kajstura J, Chimenti S, et al. Bone marrow cells regenerate infarcted myocardium. Nature 2001; 410:701–705.

    CAS  PubMed  Google Scholar 

  6. Strauer BE, Brehm M, Zeus T, et al. Repair of infarcted myocardium by autologous intracoronary mononuclear bone marrow cell transplantation in humans. Circulation 2002; 106:1913–1918.

    Google Scholar 

  7. Assmus B, Schächinger V, Teupe C, et al. Transplantation of progenitor cells and regeneration enhancement in acute myocardial infarction. Circulation 2002; 106:3009–3017.

    Article  PubMed  Google Scholar 

  8. Matsunari I, Taki J, Nakajima K, et al. Myocardial viability assessment using nuclear imaging. Ann Nucl Med 2003; 17:169–179.

    CAS  PubMed  Google Scholar 

  9. Schwaiger M, Hicks R. The clinical role of metabolic imaging of the heart by positron emission tomography. J Nucl Med 1991; 32:565–578.

    CAS  PubMed  Google Scholar 

  10. Bax JJ, Maddahi J, Poldermans D, et al. Preoperative comparison of different noninvasive strategies for predicting improvement in left ventricular function after coronary artery bypass grafting. Am J Cardiol 2003; 92:1–4.

    Article  Google Scholar 

  11. Maddahi J, Schelbert H, Brunken R, et al. Role of thallium-201 and PET imaging in evaluation of myocardial viability and management of patients with coronary artery disease and left ventricular dysfunction. J Nucl Med 1994; 35:707–715.

    CAS  PubMed  Google Scholar 

  12. Bax JJ, Veening MA, Visser FC, et al. Optimal metabolic conditions during fluorine-18 fluorodeoxyglucose imaging; a comparative study using different protocols. Eur J Nucl Med 1997; 24:35–41.

    CAS  PubMed  Google Scholar 

  13. Dodge HT, Sandler H, Ballew DW, et al. The use of biplane angiography for the measurement of left ventricular volume in man. Eur Heart J 1960; 60:762–776.

    CAS  Google Scholar 

  14. Melin JA, Becker LC. Quantitative relationship between global left ventricular thallium uptake and blood flow: effects of propranolol, ouabain, dipyridamole, and coronary artery occlusion. J Nucl Med 1986; 27:641–652.

    CAS  PubMed  Google Scholar 

  15. Lewis P, Nunan T, Dynes A, et al. The use of low-dose intravenous insulin in clinical myocardial F-18 FDG PET scanning. Clin Nucl Med 1996; 21:15–18.

    CAS  PubMed  Google Scholar 

  16. Cerqueira MD, Weissman NJ, Dilsizian V, et al. Standardized myocardial segmentation and nomenclature for tomographic imaging of the heart. Circulation 2002; 105:539–542.

    Google Scholar 

  17. Segall G. Assessment of myocardial viability by positron emission tomography. Nucl Med Commun 2002; 23:323–330.

    Article  PubMed  Google Scholar 

  18. Schafers M, Matheja P, Hasfeld M, et al. The clinical impact of thallium-201 reinjection for the detection of myocardial hibernation. Eur J Nucl Med 1996; 23:407–413.

    CAS  PubMed  Google Scholar 

  19. Mesotten L, Maes A, Herregods MC, et al. PET “reversed mismatch pattern” early after acute myocardial infarction: follow-up of flow, metabolism and function. Eur J Nucl Med 2001; 28:466–471.

    CAS  PubMed  Google Scholar 

  20. Di Carli MF, Prcevski P, Singh TP, et al. Myocardial blood flow, function, and metabolism in repetitive stunning. J Nucl Med 2000; 41:1227–1234.

    PubMed  Google Scholar 

Download references

Acknowledgements

This work was supported by the DFG (Di 600/4-1 and FOR 501-1).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Natascha Döbert.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Döbert, N., Britten, M., Assmus, B. et al. Transplantation of progenitor cells after reperfused acute myocardial infarction: evaluation of perfusion and myocardial viability with FDG-PET and thallium SPECT. Eur J Nucl Med Mol Imaging 31, 1146–1151 (2004). https://doi.org/10.1007/s00259-004-1490-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00259-004-1490-4

Keywords

Navigation