Skip to main content
Log in

Effects of Trimetazidine on Myocardial Perfusion and the Contractile Response of Chronically Dysfunctional Myocardium in Ischemic Cardiomyopathy

A 24-Month Study

  • Original Research Article
  • Published:
American Journal of Cardiovascular Drugs Aims and scope Submit manuscript

Abstract

Objective

The aim was to assess the long-term effect of trimetazidine on myocardial perfusion, using gated single photon emission computerized tomography (SPECT).

Methods

200 patients (aged 54.7 ² 12 years) with ischemic left ventricular dysfunction (LVD) and multivessel coronary artery disease were randomized to receive trimetazidine 20mg three times daily or a placebo for 24 months. At baseline and after 24 months of treatment, all patients underwent a symptom-limited cardiopulmonary exercise test concluded by the injection of 99mTc-MIBI (technetium-99m methoxy-isobutyl-isonitrile). Imaging of post-stress gated SPECT and resting gated SPECT were performed. Standard antianginal therapy was interrupted for 48 hours (nitrates for 6 hours) before the exercise tests and resumed immediately after testing.

Results

On initial evaluation, summed stress and rest scores (SSS and SRS, respectively), systolic wall thickness (SWT), and wall motion score index (WMI), heart rate, SBP, and rate pressure product were similar at rest and peak exercise in both groups. After 24 months, 91 % of patients in the trimetazidine group versus 22% in the placebo group showed a significant decrease of the frequency of anginal episodes per week (3.9 vs 5.7, p < 0.01). Weekly nitroglycerin (glyceryl trinitrate) tablet consumption was significantly lower with trimetazidine than with placebo at endpoint (2.3 ² 0.8 vs 6.1 ² 1.6, p < 0.01). This was supported by perfusion SPECT data. Compared with baseline values, SSS and SRS were significantly reduced with trimetazidine (from 19.8 ² 7.7 to 11.2 ² 6.1, p < 0.00001 and from 12.4 ² 8.7 to 5.8 ² 3.3, p < 0.00001, respectively). There was a nonsignificant decrease from baseline values in both SRS and SSS with placebo group (from 11.9 ² 8.3 to 11.2 ² 7.4 and 18.1²6.3 to 17.9 ² 9.2, respectively).

Duration of peak exercise increased significantly from baseline values with trimetazidine (from 4.6 to 5.8 minutes, p < 0.01) but not with placebo (from 5.4 to 5.8 minutes). Accordingly, mean maximum work at peak exercise improved by 1.2 metabolic equivalents with trimetazidine. This was proved by gated SPECT with an increase in SWT score of 89.5% (p < 0.00001) and in ejection fraction of 23% with trimetazidine (p < 0.001) without significant changes in hemodynamic parameters.

Conclusion

Trimetazidine improves ischemic attacks in patients with ischemic cardiomyopathy, clinically and objectively as seen in gated SPECT myocardial perfusion. The improvement in myocardial function with trimetazidine was not accompanied by hemodynamic changes.

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
Table I
Table II
Table III
Table IV
Fig. 2
Fig. 3
Table V

Similar content being viewed by others

References

  1. Birnbaum Y, Criger DA, Wagner GS, et al. Prediction of the extent and severity of left ventricular dysfunction in anterior acute myocardial infarction by the admission electrocardiogram. Am Heart J 2001; 141(6): 915–24.

    Article  PubMed  CAS  Google Scholar 

  2. Pfeffer MA, McMurray JJ, Velazquez EJ, et al. Valsartan, captopril, or both in myocardial infarction complicated by heart failure, left ventricular dysfunction, or both. N Engl J Med 2003; 349(20): 1893–906.

    Article  PubMed  CAS  Google Scholar 

  3. DiBianco R. Update on therapy for heart failure. Am J Med 2003; 115(6): 480–8.

    Article  PubMed  Google Scholar 

  4. McKee SP, Leslie SJ, LeMaitre JP, et al. Management of chronic heart failure due to systolic left ventricular dysfunction by cardiologist and non-cardiologist physicians. Eur J Heart Fail 2003; 5(4): 549–55.

    Article  PubMed  Google Scholar 

  5. McClellan KJ, Plosker GL. Trimetazidine: a review of its use in stable angina pectoris and other coronary conditions. Drugs 1999; 58: 143–57.

    Article  PubMed  CAS  Google Scholar 

  6. Marzilli M, Klein W. Efficacy and tolerability of trimetazidine in stable angina: a metaanalysis of randomized, double-blind, controlled trials. Coron Artery Dis 2003; 14: 171–9.

    Article  PubMed  Google Scholar 

  7. Cross HR. Trimetazidine for stable angina pectoris. Expert Opin Pharmacother 2001; 2(5): 857–75.

    Article  PubMed  CAS  Google Scholar 

  8. Lu C, Dabrowski P, Fragasso G, et al. Effects of trimetazidine on ischemic left ventricular dysfunction in patients with coronary artery disease. Am J Cardiol 1998; 82(7): 898–901.

    Article  PubMed  CAS  Google Scholar 

  9. Marzilli M. Cardioprotective effects of trimetazidine: a review. Curr Med Res Opin 2003; 19(7): 661–72.

    Article  PubMed  CAS  Google Scholar 

  10. Desideri A, Celegon L. Metabolic management of ischemic heart disease: clinical data with trimetazidine. Am J Cardiol 1998; 82(5A): 50K–3K.

    Article  PubMed  CAS  Google Scholar 

  11. Kantor P, Lucien A, Kozak R, et al. The antianginal drug trimetazidine shifts cardiac energy metabolism from fatty acid oxidation to glucose oxidation by inhibiting mitochondrial long-chain 3-ketoacyl coenzyme A thiolase. Circ Res 2000; 86(5): 580–8.

    Article  PubMed  CAS  Google Scholar 

  12. Sellier P, Broustet J-P. Assessment of anti-ischemic and antianginal effect at trough plasma concentration and safety of trimetazidine MR 35mg in patients with stable angina pectoris: a multicenter, double-blind, placebo-controlled study. Am J Cardiovasc Drugs 2003; 3(5): 361–9.

    Article  PubMed  CAS  Google Scholar 

  13. Shlyakhto EV, Almazov VVA, Nifontov EM, et al. Antianginal effects of trimetazidine and left ventricular function improvement in patients with stable angina pectoris. Am J Cardiovasc Drugs 2002; 2(2): 119–24.

    Article  PubMed  CAS  Google Scholar 

  14. Kober G, Pennaforte S, Buck T, et al. Myocardial cytoprotection during percutaneous transluminal coronary angioplasty. Eur Heart J 1993; 14 Suppl. G: 6–11.

    Article  PubMed  Google Scholar 

  15. Birand A, Kudaiberdieva GZ, Batyraliev TA, et al. Effects of trimetazidine on heart rate variability and left ventricular systolic performance in patients with coronary artery disease after percutaneous transluminal angioplasty. Angiology 1997; 48(5): 413–22.

    Article  PubMed  CAS  Google Scholar 

  16. Polonski L, Dec I, Wojnar R, et al. Trimetazidine limits the effects of myocardial ischaemia during percutaneous coronary angioplasty. Curr Med Res Opin 2002; 18(7): 389–96.

    Article  PubMed  CAS  Google Scholar 

  17. Detry JM, Sellier P, Pennaforte S, et al. Trimetazidine: a new concept in the treatment of angina. Comparison with propranolol in patients with stable angina: Trimetazidine European Multicenter Study Group. Br J Clin Pharmacol 1994; 37(3): 279–88.

    Article  PubMed  CAS  Google Scholar 

  18. Szwed H, Sadowski Z, Elikowski W, et al. Trimpol II: combination treatment of stable effort angina using trimetazidine and metoprolol. Results of a randomised, double blind, multicentre study. Eur Heart J 2001; 22(2): 2267–74.

    Article  PubMed  CAS  Google Scholar 

  19. Dalla-Volta S, Maraglino G, Delia-Valentina P, et al. Comparison of trimetazidine with nifedipene in effort angina: a double-blind, crossover study. Cardiovasc Drugs Ther 1990; 4: 853–9.

    Article  PubMed  Google Scholar 

  20. Levy S. Combination therapy of trimetazidine with diltiazem in patients with coronary artery disease: Group of South of France Investigators. Am J Cardiol 1995; 76: 12B–6B.

    Article  PubMed  CAS  Google Scholar 

  21. Manchanda SC, Krishnaswani S. Combination treatment with trimetazidine and diltiazem in stable angina pectoris. Heart 1997; 78: 353–7.

    PubMed  CAS  Google Scholar 

  22. Dahlberg ST, Leppo JA. Myocardial kinetics of radiolabeled perfusion agents: basis for perfusion imaging. J Nucl Cardiol 1994; 1(2 Pt 1): 189–97.

    Article  PubMed  CAS  Google Scholar 

  23. Germano G, Erel J, Lewin H, et al. Automatic quantitation of regional myocardial wall motion and thickening from gated technetium-99m sestamibi myocardial perfusion single-photon emission computed tomography. J Am Coll Cardiol 1997; 30(5): 1360–7.

    Article  PubMed  CAS  Google Scholar 

  24. Germano G, Kiat H, Kavanagh PB, et al. Automatic quantification of ejection fraction from gated myocardial perfusion SPECT. J Nucl Med 1995; 36(11): 2138–47.

    PubMed  CAS  Google Scholar 

  25. Belardinelli R. Trimetazidine and the contractile response of dysfunctional myocardium in ischaemic cardiomyopathy. Rev Port Cardiol 2000; 19 Suppl. 5: V35–9.

    PubMed  Google Scholar 

  26. Belardinelli R, Purcaro A. Effects of trimetazidine on the contractile response of chronically dysfunctional myocardium to low-dose dobutamine in ischaemic cardiomyopathy. Eur Heart J 2001; 22(23): 2164–70.

    Article  PubMed  CAS  Google Scholar 

  27. Ciavolella M, Greco C, Tavolaro R, et al. Acute oral trimetazidine administration increases resting technetium 99m sestamibi uptake in hibernating myocardium. J Nucl Cardiol 1998; 5(2): 128–33.

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

The authors acknowledge the assistance of Servier Medical, Egypt and the Nuclear Cardiology staff at the National Heart Institute, Cairo University, Egypt.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Taher El-Kady.

Rights and permissions

Reprints and permissions

About this article

Cite this article

El-Kady, T., El-Sabban, K., Gabaly, M. et al. Effects of Trimetazidine on Myocardial Perfusion and the Contractile Response of Chronically Dysfunctional Myocardium in Ischemic Cardiomyopathy. Am J Cardiovasc Drugs 5, 271–278 (2005). https://doi.org/10.2165/00129784-200505040-00006

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.2165/00129784-200505040-00006

Keywords

Navigation