<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Schwartz GG</submitter><funding>British Heart Foundation</funding><funding>American Heart Association-American Stroke Association</funding><funding>NHLBI NIH HHS</funding><pagination>1077-1084</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7171952</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>43(5)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>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.&lt;h4>Research design and methods&lt;/h4>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 A&lt;sub>1c&lt;/sub> 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 A&lt;sub>1c&lt;/sub> ?6.5%, or a combination of at least two measurements of serum glucose ?7.0 mmol/L (fasting) or ?11.1 mmol/L (random).&lt;h4>Results&lt;/h4>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; &lt;i>P&lt;/i> &lt; 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.&lt;h4>Conclusions&lt;/h4>In patients with a recent acute coronary syndrome, incident diabetes is common and is reduced substantially by treatment with dalcetrapib.</pubmed_abstract><journal>Diabetes care</journal><pubmed_title>Dalcetrapib Reduces Risk of New-Onset Diabetes in Patients With Coronary Heart Disease.</pubmed_title><pmcid>PMC7171952</pmcid><funding_grant_id>RE/13/1/30181</funding_grant_id><funding_grant_id>R01 HL134320</funding_grant_id><funding_grant_id>R01 HL098839</funding_grant_id><funding_grant_id>16GRNT30410012</funding_grant_id><pubmed_authors>Kallend D</pubmed_authors><pubmed_authors>McMurray JJV</pubmed_authors><pubmed_authors>Kittelson J</pubmed_authors><pubmed_authors>Ballantyne CM</pubmed_authors><pubmed_authors>Laghrissi-Thode F</pubmed_authors><pubmed_authors>Schwartz GG</pubmed_authors><pubmed_authors>Leiter LA</pubmed_authors><pubmed_authors>Preiss D</pubmed_authors><pubmed_authors>Black DM</pubmed_authors><pubmed_authors>Nicholls SJ</pubmed_authors><pubmed_authors>Tardif JC</pubmed_authors><pubmed_authors>Shah PK</pubmed_authors><pubmed_authors>Barter PJ</pubmed_authors><pubmed_authors>Leitersdorf E</pubmed_authors><pubmed_authors>Olsson AG</pubmed_authors></additional><is_claimable>false</is_claimable><name>Dalcetrapib Reduces Risk of New-Onset Diabetes in Patients With Coronary Heart Disease.</name><description>&lt;h4>Objective&lt;/h4>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.&lt;h4>Research design and methods&lt;/h4>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 A&lt;sub>1c&lt;/sub> 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 A&lt;sub>1c&lt;/sub> ?6.5%, or a combination of at least two measurements of serum glucose ?7.0 mmol/L (fasting) or ?11.1 mmol/L (random).&lt;h4>Results&lt;/h4>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; &lt;i>P&lt;/i> &lt; 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.&lt;h4>Conclusions&lt;/h4>In patients with a recent acute coronary syndrome, incident diabetes is common and is reduced substantially by treatment with dalcetrapib.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 May</publication><modification>2021-02-21T01:03:24Z</modification><creation>2020-05-22T19:18:56Z</creation></dates><accession>S-EPMC7171952</accession><cross_references><pubmed>32144166</pubmed><doi>10.2337/dc19-2204</doi></cross_references></HashMap>