Dalcetrapib
dal-OUTCOMES secondary analysis: dalcetrapib cuts new-onset diabetes by 23% after acute coronary syndrome, NNT of 40 (Diabetes Care 2020)
Original title: Dalcetrapib Reduces Risk of New-Onset Diabetes in Patients With Coronary Heart Disease
In the dal-OUTCOMES trial, 15,871 patients with a recent acute coronary syndrome were randomised to dalcetrapib 600 mg daily or placebo, of whom 10,645 (67%) had no diabetes at baseline. Over a median follow-up of 30 months, incident diabetes occurred in 7.6% of the 5,326 patients assigned dalcetrapib versus 9.7% of the 5,319 assigned placebo, an absolute risk reduction of 2.1 percentage points and a hazard ratio of 0.77 (95% CI, 0.68 to 0.88, P < 0.001), corresponding to a number needed to treat of 40 for 3 years to prevent one case of diabetes, falling to 25 among those with prediabetes at baseline. Dalcetrapib also reduced progression from normoglycaemia to prediabetes and increased regression from diabetes back to no diabetes. Despite the neutral primary cardiovascular result of dal-OUTCOMES, this secondary analysis shows dalcetrapib substantially reduced incident diabetes in a population where new-onset diabetes carries an adverse prognosis.
Original abstract
Objective: Incident type 2 diabetes is common among patients with recent acute coronary syndrome and is associated with an adverse prognosis. Some data suggest that cholesteryl ester transfer protein (CETP) inhibitors reduce incident type 2 diabetes. We compared the effect of treatment with the CETP inhibitor dalcetrapib or placebo on incident diabetes in patients with recent acute coronary syndrome.
Research Design And Methods: In the dal-OUTCOMES trial, 15,871 patients were randomly assigned to treatment with dalcetrapib 600 mg daily or placebo, beginning 4-12 weeks after an acute coronary syndrome. Absence of diabetes at baseline was based on medical history, no use of antihyperglycemic medication, and hemoglobin A1c and serum glucose levels below diagnostic thresholds. Among these patients, incident diabetes after randomization was defined by any diabetes-related adverse event, new use of antihyperglycemic medication, hemoglobin A1c ≥6.5%, or a combination of at least two measurements of serum glucose ≥7.0 mmol/L (fasting) or ≥11.1 mmol/L (random).
Results: At baseline, 10,645 patients (67% of the trial cohort) did not have diabetes. During a median follow-up of 30 months, incident diabetes was identified in 403 of 5,326 patients (7.6%) assigned to dalcetrapib and in 516 of 5,319 (9.7%) assigned to placebo, corresponding to absolute risk reduction of 2.1%, hazard ratio of 0.77 (95% CI 0.68-0.88; P < 0.001), and a need to treat 40 patients for 3 years to prevent 1 incident case of diabetes. Considering only those with prediabetes at baseline, the number needed to treat for 3 years to prevent 1 incident case of diabetes was 25. Dalcetrapib also decreased the number of patients who progressed from normoglycemia to prediabetes and increased the number who regressed from diabetes to no diabetes.
Conclusions: In patients with a recent acute coronary syndrome, incident diabetes is common and is reduced substantially by treatment with dalcetrapib.
dalcetrapibdiabetesoutcomes trials
Summary written by cetpinhibition.org from the published abstract; figures as published. Page updated 18 August 2026. Methods.