American Journal of Cardiology
Volume 104, Issue 11 , Pages 1484-1489, 1 December 2009

Left Ventricular Mass and Volume With Telmisartan, Ramipril, or Combination in Patients With Previous Atherosclerotic Events or With Diabetes Mellitus (from the ONgoing Telmisartan Alone and in Combination With Ramipril Global Endpoint Trial [ONTARGET])

  • Brett R. Cowan, BE, MBChB

      Affiliations

    • Auckland MRI Research Group, University of Auckland, Auckland, New Zealand
  • ,
  • Alistair A. Young, PhD

      Affiliations

    • Auckland MRI Research Group, University of Auckland, Auckland, New Zealand
    • Corresponding Author InformationCorresponding author: Tel: 64-9-3737-599, ext 86115; fax: 64-9-3737-484
  • ,
  • Craig Anderson, MBBS, PhD

      Affiliations

    • Clinical Trials Research Unit, School of Population Health, University of Auckland, Auckland, New Zealand
    • The George Institute for International Health, University of Sydney and Royal Prince Alfred Hospital, Sydney, Australia
  • ,
  • Robert N. Doughty, MD

      Affiliations

    • Department of Medicine, University of Auckland, Auckland, New Zealand
  • ,
  • Rungroj Krittayaphong, MD

      Affiliations

    • Division of Cardiology, Department of Medicine, Siriraj Hospital, Bankok, Thailand
  • ,
  • Eva Lonn, MD, MSc

      Affiliations

    • Department of Medicine, Division of Cardiology and Population Health Research Institute, McMaster University, Hamilton, Ontario, Canada
  • ,
  • Thomas H. Marwick, MBBS, PhD

      Affiliations

    • Department of Medicine, University of Queensland, Brisbane, Australia
  • ,
  • Chris M. Reid, BA, DipEd, MSc, PhD

      Affiliations

    • Baker IDI Heart and Diabetes Institute, Melbourne, Australia
    • CCRE Therapeutics, Monash University, Melbourne, Australia
  • ,
  • John E. Sanderson, MD

      Affiliations

    • Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong
    • Department of Cardiovascular Medicine, University of Birmingham, Birmingham, United Kingdom
  • ,
  • Roland E. Schmieder, MD

      Affiliations

    • Department of Nephrology and Hypertension, Friedrich-Alexander-University Erlangen-Nürnberg, Erlangen, Germany
  • ,
  • Koon Teo, MB, PhD

      Affiliations

    • Department of Medicine, Division of Cardiology and Population Health Research Institute, McMaster University, Hamilton, Ontario, Canada
  • ,
  • Angela K. Wadham, BA

      Affiliations

    • Clinical Trials Research Unit, School of Population Health, University of Auckland, Auckland, New Zealand
  • ,
  • Stephen G. Worthley, MBBS, PhD

      Affiliations

    • Cardiovascular Investigation Unit, Royal Adelaide Hospital, Adelaide, Australia
  • ,
  • Cheuk-Man Yu, MD

      Affiliations

    • Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong
  • ,
  • Salim Yusuf, MD

      Affiliations

    • Department of Medicine, Division of Cardiology and Population Health Research Institute, McMaster University, Hamilton, Ontario, Canada
  • ,
  • Garry L. Jennings, MD

      Affiliations

    • Baker IDI Heart and Diabetes Institute, Melbourne, Australia
  • ,
  • ONTARGET Investigators

Received 6 May 2009; received in revised form 10 July 2009; accepted 10 July 2009. published online 16 October 2009.

The ONgoing Telmisartan Alone and in combination with Ramipril Global Endpoint Trial (ONTARGET) showed that the angiotensin receptor blocker telmisartan 80 mg was not inferior to the angiotensin-converting enzyme inhibitor ramipril 10 mg, and the combination no more effective than ramipril alone, in decreasing morbidity and mortality in patients with cardiovascular disease or high-risk diabetes. Although therapy targeting angiotensin II is known to decrease left ventricular (LV) mass and volume, the relative influence of angiotensin-converting enzyme inhibitor inhibitors and angiotensin receptor blocker, and their combination, on the heart remains unclear in this population. Magnetic resonance imaging was performed in 287 patients enrolled in ONTARGET, across 8 centers in 6 countries, at randomization and after 2-year treatment (90, 100, and 97 patients in the ramipril, telmisartan, and combination therapy groups, respectively). Baseline patient characteristics showed higher frequencies of coronary artery disease, Asian ethnicity, and use of statins and β blockers than the main ONTARGET trial. LV mass decreased in all groups (p <0.0001 for each), but there were no significant differences in change in LV mass or volume among groups, except that LV mass index decreased more on combination versus telmisartan (p = 0.04). Key determinants of LV mass decrease were a history of hypertension (p = 0.03), baseline mass (p <0.0001), and decrease in systolic blood pressure (p <0.0001). The best magnetic resonance imaging predictor of composite events was end-systolic volume (p <0.0001). In conclusion, telmisartan and ramipril had similar effects on LV mass and volume, and combination therapy was not more effective, in high-risk patients with cardiovascular disease. These results are consistent with the major outcome findings of the main ONTARGET study.

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 This work was supported by McMaster University, Hamilton, Ontario, Canada, and Boehringer Ingleheim, Ingleheim, Germany.

PII: S0002-9149(09)01355-1

doi:10.1016/j.amjcard.2009.07.018

American Journal of Cardiology
Volume 104, Issue 11 , Pages 1484-1489, 1 December 2009