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The Effects of Pioglitazone in Reducing Atherosclerosis Progression and Neointima Volume in Type 2 Diabetic Patients: Prospective Randomized Study With Volumetric Intravascular Ultrasonography Analysis

  • You, Sung-Hye (Department of Cardiology, Cardiovascular Center, Korea University College of Medicine, Anam Hospital) ;
  • Kim, Beum-Suk (Department of Cardiology, Cardiovascular Center, Korea University College of Medicine, Anam Hospital) ;
  • Hong, Soon-Jun (Department of Cardiology, Cardiovascular Center, Korea University College of Medicine, Anam Hospital) ;
  • Ahn, Chul-Min (Department of Cardiology, Cardiovascular Center, Korea University College of Medicine, Anam Hospital) ;
  • Lim, Do-Sun (Department of Cardiology, Cardiovascular Center, Korea University College of Medicine, Anam Hospital)
  • Received : 2010.03.01
  • Accepted : 2010.05.08
  • Published : 2010.12.30

Abstract

Background and Objectives: Pioglitazone has been known for its anti-atherogenic effects. We compared the effects of pioglitazone in reducing atherosclerosis progression and neointima volume in type 2 diabetic patients. Subjects and Methods: This was a prospective, randomized single-blinded, 8-month follow-up study. Patients with significant coronary artery stenosis were randomly assigned to either pioglitazone (n=19) or placebo (n=18) following zotarolimus-eluting stent (ZES) implantation. Intravascular ultrasonography of the culprit vessel was performed from 20 mm distal and proximal to the stent at baseline. and at 8-month, and volumetric analysis was performed. Changes in inflammation markers, insulin resistance and lipid profile were compared. Results: Changes in atherosclerosis progression from baseline in the pioglitazone group was significantly lower than that of the placebo group (0.06${\pm}$0.73 vs. 1.16${\pm}$1.41 $mm^3$/mm, p=0.024, respectively), and neointima volume was significantly lower in the pioglitazone group compared to the placebo group (1.74${\pm}$0.93 vs. 2.42${\pm}$1.98 mm$^3$/mm, p=0.007, respectively). Homeostatic model assessment-index, interleukin-6, and tumor necrosis factor-${\alpha}$ levels were significantly lower in the pioglitazone group at 8 months. Adiponectin levels increased significantly only in the pioglitazone group. No significant differences in retinol binding protein-4 levels between the 2 groups were seen during the 8-month follow-up period. Conclusion: Compared to placebo, pioglitazone was associated with significant reduction in atherosclerosis progression and neointima formation in type 2 diabetic patients with ZES implantation.

Keywords

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