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Impact of Incident Diabetes and Incident Nonfatal Cardiovascular Disease on 18-Year Mortality

The Multiple Risk Factor Intervention Trial experience

  1. Lynn E. Eberly, PHD1,
  2. Jerome D. Cohen, MD2,
  3. Ronald Prineas, MD, PHD3,
  4. Lingfeng Yang, MS1 and
  5. For The Multiple Risk Factor Intervention Trial Research Group
  1. 1Division of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, Minnesota
  2. 2Saint Louis University School of Medicine, St. Louis, Missouri
  3. 3Department of Public Health Sciences, Wake Forest University School of Medicine, Winston-Salem, North Carolina. L.Y. is currently at the Department of Biostatistics and Epidemiology, School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania

    Abstract

    OBJECTIVE— To report long-term risks for total, cardiovascular disease (CVD), and coronary heart disease (CHD) mortality associated with incident diabetes (using current diagnostic criteria) and with incident nonfatal CVD (NF-CVD).

    RESEARCH DESIGN AND METHODS— A total of 11,645 participants without diabetes or CVD at baseline from the Multiple Risk Factor Intervention Trial who survived to the end of the trial were grouped by during-trial incident diabetes and/or NF-CVD events: neither diabetes nor NF-CVD, diabetes only, NF-CVD only, or both diabetes and NF-CVD. Incident diabetes was defined by use of hypoglycemic agents or fasting glucose ≥126 mg/dl at any time over the 6 trial years. Proportional hazards models tested group differences in mortality over 18 post-trial years.

    RESULTS— Among 3,859 total deaths were 1,846 from CVD and 1,277 from CHD, with death rates per 10,000 person-years of 203, 97, and 67, respectively. Multivariate-adjusted hazard ratios (HRs) for total mortality were 2.75 (P < 0.0001) for those with NF-CVD and diabetes both, 1.92 (P < 0.0001) for those with NF-CVD only, and 1.49 (P < 0.0001) for those with diabetes only, relative to neither diabetes nor NF-CVD. NF-CVD was associated with a higher hazard of death than diabetes for total (HR 1.29, P = 0.0004), CVD (HR 1.76, P < 0.0001), and CHD (HR 1.88, P < 0.0001) mortality. Only the subgroup of participants on hypoglycemic agents showed an equivalent risk of total mortality relative to participants with NF-CVD (HR 0.93, P = 0.54).

    CONCLUSIONS— Current diabetes diagnostic criteria conferred significantly increased total, CVD, and CHD mortality risks independent of the impact of NF-CVD. NF-CVD was more strongly predictive of mortality.

    Footnotes

    • Address correspondence and reprint requests to L.E. Eberly, Division of Biostatistics, School of Public Health, University of Minnesota, 420 Delaware St. SE, Mayo Mail Code 303, Minneapolis, MN 55455-0378. E-mail: lynn{at}biostat.umn.edu.

      Received for publication 7 August 2002 and accepted in revised form 7 November 2002.

      A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances.

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