American Heart Journal
Volume 154, Issue 1 , Pages 78.e1-78.e7, July 2007

Trimetazidine added to combined hemodynamic antianginal therapy in patients with type 2 diabetes: a randomized crossover trial

  • Letícia Weiss Ribeiro, MD, MSc

      Affiliations

    • Cardiology Division, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil
  • ,
  • Jorge P. Ribeiro, MD, ScD

      Affiliations

    • Cardiology Division, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil
  • ,
  • Ricardo Stein, MD, ScD

      Affiliations

    • Cardiology Division, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil
  • ,
  • Cristiane Leitão, MD, MSc

      Affiliations

    • Endocrinology Division, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil
  • ,
  • Carísi Anne Polanczyk, MD, ScD

      Affiliations

    • Corresponding Author InformationReprint requests: Carísi Anne Polanczyk, MD, ScD, Hospital de Clínicas de Porto Alegre, Rua Ramiro Barcelos 2350, sala 2225, 90035-007—Porto Alegre, RS, Brazil
    • Cardiology Division, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil

Received 13 November 2006; accepted 11 April 2007. published online 23 May 2007.

Background

In nondiabetic patients with stable angina, combined treatment with hemodynamic agents and trimetazidine is well-tolerated and effective in controlling ischemia. This study aims to evaluate the antiischemic and metabolic effects of trimetazidine in patients with type 2 diabetes mellitus, not eligible for revascularization, who remained symptomatic despite the use of at least 2 antianginal agents.

Methods

A randomized, double-blind, crossover clinical trial was used. Ten patients were randomized to receive trimetazidine (20 mg, 3 times a day) or placebo for 6-week periods. At baseline and at the end of each 6-week intervention period, clinical and biochemical evaluations, exercise testing, 24-hour ambulatory blood pressure, and Holter monitoring were performed.

Results

During trimetazidine therapy, patients had significant improvement on angina functional class (P < .05), with decrease in the number of weekly angina episodes (1.5 ± 0.8 vs 0.4 ± 0.7, P < .01), and in sublingual nitrate doses (1.4 ± 0.7 mg vs 0.1 ± 0.3 mg, P < .001). Time to 1-mm ST-segment depression during exercise test was increased after trimetazidine use (229 ± 126 seconds at baseline, 276 ± 101 seconds after placebo, and 348 ± 145 seconds after trimetazidine, P < .001). No differences were observed between treatment periods on mean 24-hour blood pressure, heart rate, and rate-pressure product evaluated concomitantly with ambulatory blood pressure and Holter monitoring. Glycemic and lipid profiles were similar after trimetazidine and placebo use.

Conclusions

In patients with diabetes who remain symptomatic, the addition of trimetazidine improves symptoms and exercise responses without hemodynamic or metabolic changes. The present data suggest that trimetazidine may be an effective adjunct therapy for these patients, but further investigation is needed to confirm these findings.

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 Dr Ribeiro reports having received consulting and lecture fees and grant support from Laboratórios Servier do Brasil.

PII: S0002-8703(07)00347-X

doi:10.1016/j.ahj.2007.04.026

American Heart Journal
Volume 154, Issue 1 , Pages 78.e1-78.e7, July 2007