Visit-to-Visit Low-Density Lipoprotein Cholesterol Variability and Risk of Cardiovascular Outcomes

被引:186
作者
Bangalore, Sripal [1 ]
Breazna, Andrei [2 ]
DeMicco, David A. [2 ]
Wun, Chuan-Chuan [2 ]
Messerli, Franz H. [3 ]
机构
[1] NYU, Sch Med, Div Cardiol, New York, NY 10016 USA
[2] Pfizer, New York, NY USA
[3] St Lukes Roosevelt Hosp, Mt Sinai Sch Med, Div Cardiol, New York, NY 10025 USA
关键词
cardiovascular outcomes; LDL cholesterol; variability; SYSTOLIC BLOOD-PRESSURE; STATIN; ROSUVASTATIN; ATORVASTATIN; TOLERABILITY; EFFICACY; METAANALYSIS; PREVENTION; GUIDELINES; MANAGEMENT;
D O I
10.1016/j.jacc.2015.02.017
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Studies demonstrate that lowering low-density lipoprotein cholesterol (LDL-C) using a statin is associated with significant reduction in cardiovascular events. Whether visit-to-visit variability in LDL-C levels affects cardiovascular outcomes is unknown. OBJECTIVES This study sought to evaluate the role of visit-to-visit variability in LDL-C levels on cardiovascular outcomes. METHODS We evaluated patients with coronary artery disease and LDL-C <130 mg/dl enrolled in the TNT (Treating to New Targets) trial, randomly assigned to receive atorvastatin 80 mg/day versus 10 mg/day and with at least one post-baseline measurement of LDL-C. Visit-to-visit LDL-C variability was evaluated from 3 months into random assignment through the use of various measurements of LDL-C variability: SD, average successive variability (ASV), coefficient of variation, and variation independent of mean, with the first 2 measurements used as the primary measurements. Primary outcome was any coronary event, and secondary outcomes were any cardiovascular event, death, myocardial infarction, or stroke. RESULTS Among 9,572 patients, SD and ASV were significantly lower with atorvastatin 80 mg/day versus 10 mg/day (SD: 12.03 +/- 9.70 vs. 12.52 +/- 7.43; p = 0.005; ASV: 12.84 +/- 10.48 vs. 13.76 +/- 8.69; p < 0.0001). In the adjusted model, each 1-SD increase in LDL-C variability (by ASV) increased the risk of any coronary event by 16% (hazard ratio [HR]: 1.16; 95% confidence interval [CI]: 1.10 to 1.23; p < 0.0001), any cardiovascular event by 11% (HR: 1.11; 95% CI: 1.07 to 1.15; p < 0.0001), death by 23% (HR: 1.23; 95% CI: 1.14 to 1.34; p < 0.0001), myocardial infarction by 10% (HR: 1.10; 95% CI: 1.02 to 1.19; p = 0.02), and stroke by 17% (HR: 1.17; 95% CI: 1.04 to 1.31; p = 0.01), independent of treatment effect and achieved LDL-C levels. Results were largely consistent when adjusted for medication adherence. CONCLUSIONS In subjects with coronary artery disease, visit-to-visit LDL-C variability is an independent predictor of cardiovascular events. (C) 2015 by the American College of Cardiology Foundation.
引用
收藏
页码:1539 / 1548
页数:10
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