Lowering the Triglyceride/High-Density Lipoprotein Cholesterol Ratio Is Associated With the Beneficial Impact of Pioglitazone on Progression of Coronary Atherosclerosis in Diabetic Patients Insights From the PERISCOPE (Pioglitazone Effect on Regression of Intravascular Sonographic Coronary Obstruction Prospective Evaluation) Study

被引:94
作者
Nicholls, Stephen J. [1 ,2 ,3 ]
Tuzcu, E. Murat [1 ]
Wolski, Kathy [1 ]
Bayturan, Ozgur [1 ]
Lavoie, Andrea [1 ]
Uno, Kiyoko [1 ]
Kupfer, Stuart [4 ]
Perez, Alfonso [4 ]
Nesto, Richard [5 ]
Nissen, Steven E. [1 ]
机构
[1] Cleveland Clin, Dept Cardiovasc Med, Cleveland, OH 44195 USA
[2] Cleveland Clin, Dept Cell Biol, Cleveland, OH 44195 USA
[3] Cleveland Clin, Ctr Cardiovasc Diagnost & Prevent, Cleveland, OH 44195 USA
[4] Takeda Pharmaceut, Deerfield, IL USA
[5] Lahey Clin Med Ctr, Dept Cardiovasc Med, Burlington, MA 01803 USA
关键词
atherosclerosis; diabetes; intravascular ultrasonography; INTIMA-MEDIA THICKNESS; CARDIOVASCULAR-DISEASE; MYOCARDIAL-INFARCTION; GLYCEMIC CONTROL; GLUCOSE CONTROL; TYPE-2; MORTALITY; MELLITUS; THERAPY; COMPLICATIONS;
D O I
10.1016/j.jacc.2010.06.055
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives The purpose of this study was to determine the factors associated with the favorable effect of pioglitazone on atheroma progression. Background Diabetes mellitus is associated with accelerated coronary atheroma progression. Pioglitazone slowed progression compared with glimepiride in this population. Methods In all, 360 diabetic patients with coronary artery disease were treated with pioglitazone or glimepiride for 18 months in the PERISCOPE (Pioglitazone Effect on Regression of Intravascular Sonographic Coronary Obstruction Prospective Evaluation) study. Coronary atheroma progression was evaluated by serial intravascular ultrasound. The relationship between changes in biochemical parameters, percent atheroma volume, and total atheroma volume was investigated. Results Pioglitazone-treated patients demonstrated greater increases in high-density lipoprotein cholesterol (HDL-C) and reductions in glycated hemoglobin, triglycerides, and C-reactive protein. Significant correlations were observed between changes in percent atheroma volume and triglycerides (r = 0.15, p = 0.04), triglyceride/HDL-C ratio (r = 0.16, p = 0.03), and glycated hemoglobin (r = 0.16, p = 0.03) with pioglitazone, and changes in low-density lipoprotein cholesterol (r = - 0.15, p = 0.05), apolipoprotein B (r = -0.16, p = 0.04), and apolipoprotein A-I (r = -0.20, p = 0.01) with glimepiride. Substantial atheroma regression, compared to progression, was associated with greater relative increases in HDL-C (14.2% vs. 7.8%, p = 0.04), relative decreases in triglycerides (-13.3% vs. -1.9%, p = 0.045), triglyceride/HDL-C ratio (-22.5 vs. -9.9%, p = 0.05), and decrease in glycated hemoglobin (-0.6% vs. -0.3%, p = 0.01). Multivariable analysis revealed that pioglitazone-induced effects on triglyceride/HDL-C were associated with changes in percent atheroma volume (p = 0.03) and total atheroma volume (p = 0.02). Conclusions Favorable effects of pioglitazone on the triglyceride/HDL-C ratio correlated with delayed atheroma progression in diabetic patients. This finding highlights the potential importance of targeting atherogenic dyslipidemia in diabetic patients with coronary artery disease. (J Am Coll Cardiol 2011;57:153-9) (C) 2011 by the American College of Cardiology Foundation
引用
收藏
页码:153 / 159
页数:7
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