Skip to main navigation Skip to search Skip to main content

The risk of developing coronary artery disease or congestive heart failure, and overall mortality, in type 2 diabetic patients receiving rosiglitazone, pioglitazone, metformin, or sulfonylureas: A retrospective analysis

  • Kevin M. Pantalone
  • , Michael W. Kattan
  • , Changhong Yu
  • , Brian J. Wells
  • , Susana Arrigain
  • , Anil Jain
  • , Ashish Atreja
  • , Robert S. Zimmerman

Research output: Contribution to journalArticlepeer-review

124 Scopus citations

Abstract

Oral anti-diabetic agents have been associated with adverse cardiovascular events in type 2 diabetes (DM2). We investigated the risk of coronary artery disease (CAD), congestive heart failure (CHF), and mortality using multivariable Cox models in a retrospective cohort of 20,450 DM2 patients from our electronic health record (EHR). We observed no differences in CAD risk among the agents. Metformin was associated with a reduced risk of CHF (HR 0.76, 95% CI 0.64-0.91) and mortality (HR 0.54, 95% CI 0.46-0.64) when compared to sulfonylurea. Pioglitazone was also associated with a lower risk of mortality when compared to sulfonylurea (HR 0.59, 95% CI 0.43-0.81). No other significant differences were found between the oral agents. In conclusions, our results did not identify an increased CAD risk with rosiglitazone in clinical practice. However, the results do reinforce a possible increased risk of adverse events in DM2 patients prescribed sulfonylureas.

Original languageEnglish
Pages (from-to)145-154
Number of pages10
JournalActa Diabetologica
Volume46
Issue number2
DOIs
StatePublished - Jun 2009
Externally publishedYes

Keywords

  • Antidiabetic agents
  • Congestive heart failure
  • Coronary artery disease
  • Hypoglycemic agents
  • Mortality
  • Rosiglitazone
  • Thiazolidinediones

Fingerprint

Dive into the research topics of 'The risk of developing coronary artery disease or congestive heart failure, and overall mortality, in type 2 diabetic patients receiving rosiglitazone, pioglitazone, metformin, or sulfonylureas: A retrospective analysis'. Together they form a unique fingerprint.

Cite this