Rosiglitazone evaluated for cardiovascular outcomes--an interim analysis
- PMID: 17551159
- DOI: 10.1056/NEJMoa073394
Rosiglitazone evaluated for cardiovascular outcomes--an interim analysis
Abstract
Background: A recent meta-analysis raised concern regarding an increased risk of myocardial infarction and death from cardiovascular causes associated with rosiglitazone treatment of type 2 diabetes.
Methods: We conducted an unplanned interim analysis of a randomized, multicenter, open-label, noninferiority trial involving 4447 patients with type 2 diabetes who had inadequate glycemic control while receiving metformin or sulfonylurea, in which 2220 patients were assigned to receive add-on rosiglitazone (rosiglitazone group), and 2227 to receive a combination of metformin plus sulfonylurea (control group). The primary end point was hospitalization or death from cardiovascular causes.
Results: Because the mean follow-up was only 3.75 years, our interim analysis had limited statistical power to detect treatment differences. A total of 217 patients in the rosiglitazone group and 202 patients in the control group had the adjudicated primary end point (hazard ratio, 1.08; 95% confidence interval [CI], 0.89 to 1.31). After the inclusion of end points pending adjudication, the hazard ratio was 1.11 (95% CI, 0.93 to 1.32). There were no statistically significant differences between the rosiglitazone group and the control group regarding myocardial infarction and death from cardiovascular causes or any cause. There were more patients with heart failure in the rosiglitazone group than in the control group (hazard ratio, 2.15; 95% CI, 1.30 to 3.57).
Conclusions: Our interim findings from this ongoing study were inconclusive regarding the effect of rosiglitazone on the overall risk of hospitalization or death from cardiovascular causes. There was no evidence of any increase in death from either cardiovascular causes or all causes. Rosiglitazone was associated with an increased risk of heart failure. The data were insufficient to determine whether the drug was associated with an increase in the risk of myocardial infarction. (ClinicalTrials.gov number, NCT00379769 [ClinicalTrials.gov].).
Copyright 2007 Massachusetts Medical Society.
Comment in
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Rosiglitazone--continued uncertainty about safety.N Engl J Med. 2007 Jul 5;357(1):63-4. doi: 10.1056/NEJMe078118. Epub 2007 Jun 5. N Engl J Med. 2007. PMID: 17551160 No abstract available.
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Rosiglitazone and cardiotoxicity--weighing the evidence.N Engl J Med. 2007 Jul 5;357(1):64-6. doi: 10.1056/NEJMe078117. Epub 2007 Jun 5. N Engl J Med. 2007. PMID: 17551161 No abstract available.
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The record on rosiglitazone and the risk of myocardial infarction.N Engl J Med. 2007 Jul 5;357(1):67-9. doi: 10.1056/NEJMe078116. Epub 2007 Jun 5. N Engl J Med. 2007. PMID: 17551162 No abstract available.
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Rosiglitazone increased heart failure but did not differ from metformin plus sulfonylurea for other CV outcomes at interim analysis.ACP J Club. 2007 Nov-Dec;147(3):67. ACP J Club. 2007. PMID: 17975869 No abstract available.
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Rosiglitazone: possible complications and treatment of non-alcoholic steatohepatitis (NASH).J Hepatol. 2008 Jan;48(1):174-6. doi: 10.1016/j.jhep.2007.10.004. Epub 2007 Nov 5. J Hepatol. 2008. PMID: 18022724 No abstract available.
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Rosiglitazone increased heart failure but did not differ from metformin plus sulphonylurea for other CV outcomes at interim analysis.Evid Based Med. 2007 Dec;12(6):170. doi: 10.1136/ebm.12.6.170. Evid Based Med. 2007. PMID: 18063730 No abstract available.
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What are the long-term cardiovascular effects of treatment with rosiglitazone?Curr Diab Rep. 2008 Jun;8(3):201-2. doi: 10.1007/s11892-008-0034-x. Curr Diab Rep. 2008. PMID: 18625116 No abstract available.
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Don't mess with the DSMB.N Engl J Med. 2010 Jul 29;363(5):477-8. doi: 10.1056/NEJMe1007445. Epub 2010 Jul 7. N Engl J Med. 2010. PMID: 20647188 No abstract available.
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