Attainment of goal/desirable lipid levels in patients with mixed dyslipidemia after 12 weeks of treatment with fenofibric acid and rosuvastatin combination therapy: A pooled analysis of controlled studies

被引:0
作者
Roth, Eli M. [1 ]
Rosenson, Robert S. [2 ]
Jones, Peter H. [3 ]
Davidson, Michael H. [4 ]
Kelly, Maureen T. [5 ]
Setze, Carolyn M. [5 ]
Lele, Aditya [5 ]
Thakker, Kamlesh [5 ]
机构
[1] Sterling Res Grp, Cincinnati, OH 45219 USA
[2] Mt Sinai Sch Med, New York, NY USA
[3] Baylor Coll Med, Houston, TX 77030 USA
[4] Univ Chicago, Pritzker Sch Med, Chicago, IL 60637 USA
[5] Abbott, Abbott Pk, IL USA
关键词
Fenofibric acid; Rosuvastatin; Combination therapy; Mixed dyslipidemia; Lipoproteins; CORONARY-HEART-DISEASE; DENSITY LIPOPROTEIN CHOLESTEROL; CARDIOVASCULAR-DISEASE; CARDIOMETABOLIC RISK; SECONDARY PREVENTION; APOLIPOPROTEIN-B; MANAGEMENT; SAFETY; EFFICACY; SIMVASTATIN;
D O I
10.1016/j.jacl.2012.02.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
BACKGROUND: Goal/desirable lipid levels are underachieved in patients with mixed dyslipidemia. These patients may have substantial residual risk of cardiovascular disease even while receiving optimal LDL-C-lowering therapy and may require additional therapy to improve multiple lipid/lipoprotein levels. OBJECTIVE: To evaluate attainment of goal/desirable levels of lipids/lipoproteins after 12-week treatment with combination rosuvastatin + fenofibric acid versus rosuvastatin monotherapy. METHODS: This was a post hoc analysis of patients with mixed dyslipidemia who enrolled in one of two randomized controlled trials, and were treated (N = 2066) with rosuvastatin (5, 10, or 20 mg), fenofibric acid 135 mg, or rosuvastatin + fenofibric acid for 12 weeks. Data were pooled across doses of rosuvastatin as monotherapy and combination therapy. RESULTS: Compared with rosuvastatin monotherapy, combination therapy had comparable effects in achieving risk-stratified LDL-C goals; however, measures of total atherogenic burden were improved because significantly greater percentages of patients attained non-HDL-C goal in high- (62.9% vs 50.4%, P = .006) and moderate-risk groups (87.6% vs 80.4%, P = .016) and apolipoprotein B (ApoB) <90 mg/dL in high-risk group (59.8% vs 43.8%, P < .001). In the overall population, more patients treated with the combination therapy achieved desirable levels of HDL-C >40/50 mg/dL in men/women (P < .001), triglycerides <150 mg/dL (P < .001), and ApoB <90 mg/dL (P < .001), compared with rosuvastatin monotherapy. Furthermore, combination therapy resulted in significantly greater percentages of patients achieving simultaneous specified levels of LDL-C + non-HDL-C (P < .015); LDL-C + HDL-C + TG (P < .001); and LDL-C + HDL-C + triglycerides + non-HDL-C + ApoB (P < .001), compared with rosuvastatin monotherapy. CONCLUSION: Rosuvastatin + fenofibric acid may be more efficacious than rosuvastatin alone in patients with mixed dyslipidemia. (C) 2012 National Lipid Association. All rights reserved.
引用
收藏
页码:534 / 544
页数:11
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