Progression of CAC Score and Risk of Incident CVD

被引:51
作者
Radford, Nina B. [1 ]
DeFina, Laura F. [2 ]
Barlow, Carolyn E. [2 ]
Lakoski, Susan G. [3 ]
Leonard, David [2 ]
Paixao, Andre R. M. [4 ]
Khera, Amit [5 ]
Levine, Benjamin D. [5 ,6 ,7 ]
机构
[1] Cooper Clin, Dallas, TX USA
[2] Cooper Inst, Dallas, TX USA
[3] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[4] Emory Univ, Div Cardiol, Dept Med, Atlanta, GA 30322 USA
[5] Univ Texas Southwestern Med Ctr Dallas, Div Cardiol, Dept Med, Dallas, TX 75390 USA
[6] Texas Hlth Presbyterian Hosp, Inst Exercise & Environm Med, Dallas, TX USA
[7] Univ Texas Southwestern Med Ctr Dallas, Dallas, TX 75390 USA
关键词
imaging; outcomes; subclinical atherosclerosis; CORONARY-ARTERY CALCIUM; HEART-DISEASE EVENTS; ASYMPTOMATIC ADULTS; COMPUTED-TOMOGRAPHY; PHYSICAL-ACTIVITY; STATIN THERAPY; CALCIFICATION; ATHEROSCLEROSIS; TRENDS; MEN;
D O I
10.1016/j.jcmg.2016.03.010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES The authors sought to determine the relative contributions of baseline coronary artery calcification (CAC), follow-up CAC, and CAC progression on incident cardiovascular disease (CVD). BACKGROUND Repeat CAC scanning has been proposed as a method to track progression of total atherosclerotic burden. However, whether CAC progression is a useful predictor of future CVD events remains unclear. METHODS This was a prospective observational study of 5,933 participants free of CVD who underwent 2 examinations, including CAC scores, and subsequent CVD event assessment. CAC progression was calculated using the square root method. The primary outcome was total CVD events (CVD death, nonfatal myocardial infarction, nonfatal atherosclerotic stroke, coronary artery bypass surgery, percutaneous coronary intervention). Secondary outcomes included hard CVD events, total coronary heart disease (CHD) events, and hard CHD events. RESULTS CAC was detected at baseline in 2,870 individuals (48%). The average time between scans was 3.5 +/- 2.0 years. After their second scan, 161 individuals experienced a total CVD event during a mean follow-up of 7.3 years. CAC progression was significantly associated with total CVD events (hazard ratio: 1.14, 95% confidence interval: 1.01 to 1.30 per interquartile range; p = 0.042) in the model including baseline CAC, but the contribution of CAC progression was small relative to baseline CAC (chi-square 4.16 vs. 65.92). Furthermore, CAC progression was not associated with total CVD events in the model including follow-up CAC instead of baseline CAC (hazard ratio: 1.05, 95% confidence interval: 0.92 to 1.21; p = 0.475). A model that included follow-up CAC alone performed as well as the model that included baseline CAC and CAC progression. CONCLUSIONS Although CAC progression was independently, but modestly, associated with CVD outcomes, this relationship was no longer significant when including follow-up CAC in the model. These findings imply that if serial CAC scanning is performed, the latest scan should be used for risk assessment, and in this context, CAC progression provides no additional prognostic information. (C) 2016 by the American College of Cardiology Foundation.
引用
收藏
页码:1420 / 1429
页数:10
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