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Clinical Care/Education/Nutrition

Secondary Prevention of Cardiovascular Events With Long-Term Pravastatin in Patients With Diabetes or Impaired Fasting Glucose

Results from the LIPID trial

  1. Anthony Keech, MBBS, FRACP1,
  2. David Colquhoun, MBBS, FRACP2,
  3. James Best, MD, FRACP3,
  4. Adrienne Kirby, MSC1,
  5. R. John Simes, MD, FRACP1,
  6. David Hunt, MD, FRACP4,
  7. Wendy Hague, MBBS, MBA1,
  8. Elaine Beller, MAPPSTAT1,
  9. Manjula Arulchelvam, MSC1,
  10. Jennifer Baker, MBBS, MSC1,
  11. Andrew Tonkin, MD, FRACP5 and
  12. for the LIPID Study Group
  1. 1National Health Medical Research Council Clinical Trials Centre, University of Sydney, Sydney, Australia
  2. 2Wesley Medical Centre, Brisbane, Australia
  3. 3St. Vincent’s Hospital, Melbourne, Australia
  4. 4Royal Melbourne Hospital, Melbourne, Australia
  5. 5National Heart Foundation, Melbourne, Australia
  1. Address correspondence and reprint requests to Professor Anthony Keech, NHMRC Clinical Trials Centre, Mallett Street Campus, University of Sydney, NSW 2006, Australia. E-mail: enquiry{at}ctc.usyd.edu.au
Diabetes Care 2003 Oct; 26(10): 2713-2721. https://doi.org/10.2337/diacare.26.10.2713
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  • Figure 1—
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    Figure 1—

    Numbers of patients in the LIPID study by baseline glucose status. During the trial, 23.8% of patients on placebo commenced cholesterol-lowering therapy.

  • Figure 2—
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    Figure 2—

    Changes in blood lipid levels with pravastatin therapy compared with placebo over 5 years in subgroups by glucose status in the LIPID study. ApoB, apolipoprotein B.

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    Figure 3—

    Effects of pravastatin on cardiovascular end points over a median of 6 years by glucose status. RRRs were derived from the Cox proportional hazards model. P for heterogeneity between end points = 0.7, within end points = 0.4. The lines show 95% CIs for each glucose group and the diamonds show 95% CIs for all patients. CABG, coronary artery bypass grafting; NNT, number needed to treat (based on the common RRR for the whole cohort); PTCA, percutaneous transluminal coronary angioplasty. *P < 0.001; †P = 0.048.

  • Figure 4—
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    Figure 4—

    Kaplan-Meier plots showing the effects of pravastatin on CHD events (CHD death or nonfatal myocardial infarction) and stroke by glucose status.

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    Figure 5—

    Meta-analysis of CHD secondary-prevention trials of effects of statin therapy in patients with a history of diabetes and patients with IFG or NFG: effects of statin drugs on CHD end points. Risk reductions and SEs were calculated using a fixed-effects model.

Tables

  • Figures
  • Table 1—

    Baseline characteristics of 9,014 patients in the LIPID study by glucose status

    CharacteristicDiabetesIFGNFG
    n1,0779406,997
    Age (years)64 (57–68)63 (55–67.5)62 (55–67)
    Age-group (years)
     ≥65454038
    Sex
     Female191517
    Qualifying event
     Myocardial infarction636264
     Unstable angina373836
    Coronary risk factors
     Current smoker9119
     History of hypertension524639
     Obesity322515
    Other vascular disease
     Claudication15109
     History of stroke663
    Drug use
     Insulin1000
     Oral hypoglycemic3800
    • Data are percent of median (interquartile range). * The differences in the proportions among the three groups were significant (χ2 test for heterogeneity P < 0.05) for all baseline characteristics.

  • Table 2—

    Baseline serum lipid and glucose levels (mmol/l) by glucose status

    LipidDiabetesIFGNFG
    n1,0779406,997
    Total cholesterol5.56 (4.98–6.10)5.62 (5.09–6.27)5.67 (5.09–6.22)
    LDL cholesterol3.70 (3.16–4.20)3.80 (3.33–4.38)3.91 (3.42–4.43)
    HDL cholesterol0.86 (0.75–1.01)0.90 (0.78–1.04)0.93 (0.80–1.09)
    Triglycerides1.90 (1.36–2.69)1.72 (1.26–2.40)1.53 (1.14–2.08)
    Total/HDL cholesterol ratio6.41 (5.38–7.53)6.26 (5.21–7.36)6.03 (5.09–7.05)
    Apolipoprotein B1.35 (1.19–1.53)1.34 (1.18–1.52)1.32 (1.16–1.49)
    Fasting glucose7.7 (6.9–9.4)6.3 (6.2–6.6)5.2 (4.9–5.5)
    • Data are median (interquartile range).

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Diabetes Care: 26 (10)

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October 2003, 26(10)
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Secondary Prevention of Cardiovascular Events With Long-Term Pravastatin in Patients With Diabetes or Impaired Fasting Glucose
Anthony Keech, David Colquhoun, James Best, Adrienne Kirby, R. John Simes, David Hunt, Wendy Hague, Elaine Beller, Manjula Arulchelvam, Jennifer Baker, Andrew Tonkin
Diabetes Care Oct 2003, 26 (10) 2713-2721; DOI: 10.2337/diacare.26.10.2713

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Secondary Prevention of Cardiovascular Events With Long-Term Pravastatin in Patients With Diabetes or Impaired Fasting Glucose
Anthony Keech, David Colquhoun, James Best, Adrienne Kirby, R. John Simes, David Hunt, Wendy Hague, Elaine Beller, Manjula Arulchelvam, Jennifer Baker, Andrew Tonkin
Diabetes Care Oct 2003, 26 (10) 2713-2721; DOI: 10.2337/diacare.26.10.2713
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