Relationship between thiazolidinedione use and cardiovascular outcomes and all-cause mortality among patients with diabetes: a time-updated propensity analysis

被引:38
作者
Habib, Zeina A. [3 ]
Tzogias, Leonidas [3 ]
Havstad, Suzanne L. [2 ]
Wells, Karen [2 ]
Divine, George [2 ]
Lanfear, David E. [3 ]
Tang, Jeffrey [3 ]
Krajenta, Richard [2 ]
Pladevall, Martel
Williams, L. Keoki [1 ,2 ,3 ]
机构
[1] Henry Ford Hlth Syst, Ctr Hlth Serv Res, Henry Ford Hosp, Detroit, MI 48202 USA
[2] Henry Ford Hosp, Dept Biostat & Res Epidemiol, Detroit, MI 48202 USA
[3] Henry Ford Hosp, Dept Internal Med, Detroit, MI 48202 USA
基金
美国国家卫生研究院;
关键词
thiazolidinediones; coronary heart disease; congestive heart failure; cerebrovascular accident; mortality; CONGESTIVE-HEART-FAILURE; MYOCARDIAL-INFARCTION; CYCLOOXYGENASE-2; INHIBITORS; INHALED CORTICOSTEROIDS; FLUID RETENTION; CLINICAL-TRIAL; ROSIGLITAZONE; RISK; EVENTS; PIOGLITAZONE;
D O I
10.1002/pds.1722
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Purpose To investigate the association of the thiazolidinediones (TZDs), rosiglitazone, and pioglitazone, together and individually on the risk of cardiovascular outcomes and all-cause mortality, using time-updated propensity score adjusted analysis. Methods We conducted a retrospective cohort study in a large vertically integrated health system in southeast Michigan. Cohort inclusion criteria included adult patients with diabetes treated with oral medications and followed longitudinally within the health system between I January 2000 and I December 2006. The primary outcome was fatal and non-fatal acute myocardial infarction (AMI). Secondary outcomes included hospitalizations for congestive heart failure (CHF), fatal, and non-fatal cerebrovascular accidents (CVA) and transient ischemic attacks (TIA), combined coronary heart disease (CHD) events, and all-cause mortality. Results 19 171 patients were included in this study. Use of TZDs (adjusted hazard ratio (aHR) with propensity adjustment (PA), 0.92; 95% confidence interval (CI) 0.73-1.17), rosiglitazone (aHR with PA, 1.06; 95%CI 0.66-1.70), and pioglitazone (aHR with PA, 0.91; 95%CI 0.69-1.21) was not associated with a higher risk of AMI. However, pioglitazone use was associated with a reduction in all-cause mortality (aHR with PA, 0.60; 95%CI 0.42-0.96). Compared with rosiglitazone, pioglitazone use was associated with a lower risk of all outcomes assessed, particularly CHF (p = 0.013) and combined CHD events (p = 0.048). Conclusions Our findings suggest that pioglitazone may have a more favorable risk profile when compared to rosiglitazone, arguing against a singular effect for TZDs on cardiovascular outcomes. Copyright (C) 2009 John Wiley & Sons, Ltd.
引用
收藏
页码:437 / 447
页数:11
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