The Journal of Thoracic and Cardiovascular Surgery
Volume 133, Issue 6 , Pages 1604-1611.e1, June 2007

Effects of pyridoxal-5′-phosphate (MC-1) in patients undergoing high-risk coronary artery bypass surgery: Results of the MEND-CABG randomized study

  • Jean-Claude Tardif, MD

      Affiliations

    • Montreal Heart Institute, Montreal, Canada
    • Corresponding Author InformationAddress for reprints: Jean–Claude Tardif, MD, Montreal Heart Institute, 5000 Belanger Street, Montreal, H1T 1C8, Canada.
  • ,
  • Michel Carrier, MD

      Affiliations

    • Montreal Heart Institute, Montreal, Canada
  • ,
  • David E. Kandzari, MD

      Affiliations

    • Duke Clinical Research Institute, Durham, NC
  • ,
  • Robert Emery, MD

      Affiliations

    • Minnesota Heart and Vascular Center, Edina, Minn
  • ,
  • Robert Cote, MD

      Affiliations

    • Medicure, Winnipeg, Canada.
  • ,
  • Therese Heinonen, DVM

      Affiliations

    • Université de Montréal, the Montreal Heart Institute Coordinating Center, Montreal, Canada
  • ,
  • Marjorie Zettler, PhD

      Affiliations

    • Montreal General Hospital, Montreal, Canada
  • ,
  • Vic Hasselblad, PhD

      Affiliations

    • Duke Clinical Research Institute, Durham, NC
  • ,
  • Marie-Claude Guertin, PhD

      Affiliations

    • Université de Montréal, the Montreal Heart Institute Coordinating Center, Montreal, Canada
    • Medicure, Winnipeg, Canada.
  • ,
  • Robert A. Harrington, MD

      Affiliations

    • Duke Clinical Research Institute, Durham, NC
  • ,
  • MEND-CABG Investigators

Received 7 July 2006; received in revised form 21 December 2006; accepted 2 January 2007.

Objective

Coronary artery bypass graft surgery remains associated with significant postoperative cardiovascular morbidity and mortality in high-risk patients. MC-1 (pyridoxal-5′-phosphate monohydrate) inhibits purinergic receptors and intracellular influx of Ca2+, thereby reducing cellular injury during experimental ischemia and reperfusion. The MEND-CABG trial tested the hypothesis that MC-1 reduces cardiovascular morbidity and mortality after coronary artery bypass graft.

Methods

In a phase 2, double-blinded, placebo-controlled study, 901 patients scheduled for coronary artery bypass graft surgery with cardiopulmonary bypass and at high risk for subsequent cardiac or neurologic complications were randomly assigned to receive oral MC-1 (250 mg or 750 mg/d once daily) or placebo beginning 3 to 10 hours prior to surgery and continued to postoperative day 30.

Results

At 30 days, MC-1 250 mg (compared with placebo) reduced the composite of death, nonfatal cerebral infarction, and nonfatal myocardial infarction by 14.0% (P = .3124) with peak creatinine kinase–myocardial band ≥50 ng/mL (prespecified primary end point); 32.3% (P = .0349) with peak creatinine kinase–myocardial band ≥70 ng/mL; and 37.2% (P = .0283) with peak creatinine kinase–myocardial band ≥100 ng/mL. Myocardial infarctions with peak creatinine kinase–myocardial band≥100 ng/mL were reduced by 47.2% in the MC-1 250-mg group versus placebo (P = .0083). Greater efficacy was demonstrated with 250 mg than with the 750-mg dose of MC-1.

Conclusions

In high-risk patients undergoing coronary artery bypass graft, treatment with MC-1 did not significantly affect the prespecified primary end point but was associated with a significant reduction in perioperative myocardial infarction with creatinine kinase–myocardial band ≥100 ng/mL. A larger, well-powered trial is needed to evaluate the cardioprotective effects of MC-1.

CTSNet classification: 16

Abbreviations and Acronyms: ATP, adenosine triphosphate, CABG, coronary artery bypass graft, CEC, Clinical Endpoint Committee, CK-MB, creatinine kinase–myocardial band, ECG, electrocardiogram, MI, myocardial infarction, P-5′-P, pyridoxal-5′-phosphate monohydrate, PCI, percutaneous coronary intervention, POD, postoperative day

 

 Michel Carrier, David Kandzari, and Robert Harrington report grant support from Medicure; Robert Emery reports consulting fees from Medicure; Marjorie Zettler is an employee of Medicure. The study was sponsored by Medicure.

PII: S0022-5223(07)00293-0

doi:10.1016/j.jtcvs.2007.01.049

Refers to article:

  • Translational research: Is there a future?

    Edward Donald Verrier
    The Journal of Thoracic and Cardiovascular Surgery June 2007 (Vol. 133, Issue 6, Pages 1409-1411)

The Journal of Thoracic and Cardiovascular Surgery
Volume 133, Issue 6 , Pages 1604-1611.e1, June 2007