Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas.
Department of Clinical Sciences, University of Texas Southwestern Medical Center, Dallas.
JAMA Cardiol. 2021 Feb 1;6(2):179-187. doi: 10.1001/jamacardio.2020.4939.
Higher coronary artery calcium (CAC) identifies individuals at increased atherosclerotic cardiovascular disease (ASCVD) risk. Whether it can also identify individuals likely to derive net benefit from aspirin therapy is unclear.
To examine the association between CAC, bleeding, and ASCVD and explore the net estimated effect of aspirin at different CAC thresholds.
DESIGN, SETTING, AND PARTICIPANTS: Prospective population-based cohort study of Dallas Heart Study participants, free from ASCVD and not taking aspirin at baseline. Data were analyzed between February 1, 2020, and July 15, 2020.
Coronary artery calcium score in the following categories: 0, 1-99, and 100 or higher.
Major bleeding and ASCVD events were identified from International Statistical Classification of Diseases and Related Health Problems, Ninth Revision codes. Meta-analysis-derived aspirin effect estimates were applied to observed ASCVD and bleeding rates to model the net effect of aspirin at different CAC thresholds.
A total of 2191 participants (mean [SD], age 44 [9.1] years, 1247 women [57%], and 1039 black individuals [47%]) had 116 major bleeding and 123 ASCVD events over a median follow-up of 12.2 years. Higher CAC categories (CAC 1-99 and ≥100 vs CAC 0) were associated with both ASCVD and bleeding events (hazard ratio [HR], 1.6; 95% CI, 1.1-2.4; HR, 2.6; 95% CI, 1.5-4.3; HR, 4.8; 95% CI, 2.8-8.2; P < .001; HR, 5.3; 95% CI, 3.6-7.9; P < .001), but the association between CAC and bleeding was attenuated after multivariable adjustment. Applying meta-analysis estimates, irrespective of CAC, aspirin use was estimated to result in net harm in individuals at low (<5%) and intermediate (5%-20%) 10-year ASCVD risk and net benefit in those at high (≥20%) ASCVD risk. Among individuals at lower bleeding risk, a CAC score of at least 100 identified individuals who would experience net benefit, but only in those at borderline or higher (≥5%) 10-year ASCVD risk. In individuals at higher bleeding risk, there would be net harm from aspirin irrespective of CAC and ASCVD risk.
Higher CAC is associated with both ASCVD and bleeding events, with a stronger association with ASCVD. A high CAC score identifies individuals estimated to derive net benefit from primary prevention aspirin therapy from those who would not, but only in the setting of lower bleeding risk and estimated ASCVD risk that is not low.
较高的冠状动脉钙(CAC)可识别出动脉粥样硬化性心血管疾病(ASCVD)风险增加的个体。但 CAC 是否也能识别出可能从阿司匹林治疗中获益的个体尚不清楚。
研究 CAC、出血和 ASCVD 之间的关联,并探讨不同 CAC 阈值下阿司匹林的净估计效果。
设计、地点和参与者:这是一项达拉斯心脏研究参与者的前瞻性基于人群的队列研究,参与者基线时无 ASCVD 且未服用阿司匹林。数据分析于 2020 年 2 月 1 日至 2020 年 7 月 15 日进行。
冠状动脉钙评分分为以下几类:0、1-99 和 100 或更高。
主要出血和 ASCVD 事件由国际疾病分类和相关健康问题第 9 次修订版代码确定。应用荟萃分析得出的阿司匹林效果估计值来模拟不同 CAC 阈值下阿司匹林的净效果,对观察到的 ASCVD 和出血率进行建模。
共有 2191 名参与者(平均[标准差]年龄 44[9.1]岁,1247 名女性[57%]和 1039 名黑人[47%])在中位随访 12.2 年后发生了 116 例主要出血和 123 例 ASCVD 事件。较高的 CAC 类别(CAC 1-99 和≥100 与 CAC 0)与 ASCVD 和出血事件均相关(风险比[HR],1.6;95%置信区间[CI],1.1-2.4;HR,2.6;95%CI,1.5-4.3;HR,4.8;95%CI,2.8-8.2;P<0.001;HR,5.3;95%CI,3.6-7.9;P<0.001),但 CAC 与出血之间的关联在多变量调整后减弱。应用荟萃分析估计值,无论 CAC 如何,阿司匹林的使用估计在低(<5%)和中(5%-20%)10 年 ASCVD 风险的个体中会导致净危害,在高(≥20%)ASCVD 风险的个体中会导致净获益。在出血风险较低的个体中,CAC 评分至少为 100 可识别出预计将从初级预防阿司匹林治疗中获益的个体,但仅在边缘或更高(≥5%)10 年 ASCVD 风险的个体中。在出血风险较高的个体中,无论 CAC 和 ASCVD 风险如何,阿司匹林的使用都会造成净危害。
较高的 CAC 与 ASCVD 和出血事件均相关,与 ASCVD 的相关性更强。高 CAC 评分可识别出预计将从初级预防阿司匹林治疗中获益的个体,而不是从那些不会获益的个体,但仅在出血风险较低且 ASCVD 风险不低的情况下才可以。