Rosiglitazone could improve clinical outcomes after coronary stent implantation in nondiabetic patients with metabolic syndrome

被引:12
作者
Cao Zheng [1 ]
Zhou Yu-jie [1 ]
Zhao Ying-xin [1 ]
Liu Yu-yang [1 ]
Guo Yong-he [1 ]
Cheng Wan-jun [1 ]
机构
[1] Capital Univ Med Sci, Dept Cardiol, Beijing Anzhen Hosp, Beijing 100029, Peoples R China
关键词
stents; thiazolidinediones; coronary disease; metabolic syndrome;
D O I
10.1097/00029330-200607020-00006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Recent studies have shown that thiazolidinediones (TZDs) could reduce in-stent restenosis and improve clinical outcomes in patients with type 2 diabetes after coronary stent implantation. It remains unclear whether nondiabetic patients with metabolic syndrome after stenting could also benefit from the treatment with TZDs. Methods Three hundred and sixty patients with metabolic syndrome who underwent coronary stent implantation were randomly assigned to a rosiglitazone group (n=180) or a control group (n=180). Patients in the rosiglitazone treatment group were treated with rosiglitazone 1 day before coronary stenting (4 mg once daily) and treatment was continued until the 9 months follow-up; while in the control group, patients were treated with placebo 1 day before the procedure and until the 9 months follow-up. Adverse events were death, myocardial infarction and urgent target vessel revascularization within 9 months after coronary stenting. Results One hundred and fifty two patients in the rosiglitazone group and 145 patients in the control group survived during the follow-up. Baseline characteristics among patients in the two groups were well balanced. There was no significant difference in target vessels or the procedure of stent implantation. Compared with the control group, treatment with rosiglitazone was associated with a lower rate of death, myocardial infarction and urgent target vessel revascularization (7.2% vs 14.5 %, P=0.044). Conclusion Rosiglitazone could reduce the risk of the adverse cardiovascular event and improve clinical outcomes in nondiabetic patients with metabolic syndrome after coronary stent implantation.
引用
收藏
页码:1171 / 1175
页数:5
相关论文
共 22 条
[1]   Pioglitazone enhances cytokine-induced apoptosis in vascular smooth muscle cells and reduces intimal hyperplasia [J].
Aizawa, Y ;
Kawabe, J ;
Hasebe, N ;
Takehara, N ;
Kikuchi, K .
CIRCULATION, 2001, 104 (04) :455-460
[2]   Preventative effects of rosiglitazone on restenosis after coronary stent implantation in patients with type 2 diabetes [J].
Choi, D ;
Kim, SK ;
Choi, SH ;
Ko, YG ;
Ahn, CW ;
Jang, YS ;
Lim, SK ;
Lee, HC ;
Cha, BS .
DIABETES CARE, 2004, 27 (11) :2654-2660
[3]   Molecular basis of restenosis and drug-eluting stents [J].
Costa, MA ;
Simon, DI .
CIRCULATION, 2005, 111 (17) :2257-2273
[4]   Prevalence of the metabolic syndrome defined by the International Diabetes Federation among adults in the U.S [J].
Ford, ES .
DIABETES CARE, 2005, 28 (11) :2745-2749
[5]  
FREDERICK W, 2002, ARTERIOSCLER THROMB, V22, P1769
[6]   Insulin resistance, inflammation, and the prediabetic state [J].
Haffner, SM .
AMERICAN JOURNAL OF CARDIOLOGY, 2003, 92 (4A) :18J-26J
[7]   Markers of inflammation and cellular adhesion molecules in relation to insulin resistance in nondiabetic elderly: The Rotterdam study [J].
Hak, AE ;
Pols, HAP ;
Stehouwer, CDA ;
Meijer, J ;
Kiliaan, AJ ;
Hofman, A ;
Breteler, MMB ;
Witteman, JCM .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (09) :4398-4405
[8]  
JAMAL SR, 2005, AM HEART J, V150, P821
[9]   Endothelial dysfunction accompanies a pro-oxidant, pro-diabetic challenge in the insulin resistant, obese Zucker rat in vivo [J].
Laight, DW ;
Desai, KM ;
Anggård, EE ;
Carrier, MJ .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2000, 402 (1-2) :95-99
[10]   Evaluation of liver function in type 2 diabetic patients during clinical trials - Evidence that rosiglitazone does not cause hepatic dysfunction [J].
Lebovitz, HE ;
Kreider, M ;
Freed, MI .
DIABETES CARE, 2002, 25 (05) :815-821