Johns Hopkins Ciccarone Center for the Prevention of Cardiovascular Disease, Johns Hopkins School of Medicine, Baltimore, MD (A.W.P., Z.A.D., R.S.B., O.D., O.H.O., S.M.I.U., M.B.M., M.J.Blaha).
Division of Cardiovascular Prevention and Wellness, Houston Methodist DeBakey Heart and Vascular Center, Center for Outcomes Research, Houston Methodist Hospital, TX (K.N.).
Circulation. 2021 Apr 20;143(16):1571-1583. doi: 10.1161/CIRCULATIONAHA.120.050545. Epub 2021 Mar 2.
There are limited data on the unique cardiovascular disease (CVD), non-CVD, and mortality risks of primary prevention individuals with very high coronary artery calcium (CAC; ≥1000), especially compared with rates observed in secondary prevention populations.
Our study population consisted of 6814 ethnically diverse individuals 45 to 84 years of age who were free of known CVD from MESA (Multi-Ethnic Study of Atherosclerosis), a prospective, observational, community-based cohort. Mean follow-up time was 13.6±4.4 years. Hazard ratios of CAC ≥1000 were compared with both CAC 0 and CAC 400 to 999 for CVD, non-CVD, and mortality outcomes with the use of Cox proportional hazards regression adjusted for age, sex, and traditional risk factors. Using a sex-adjusted logarithmic model, we calculated event rates in MESA as a function of CAC and compared them with those observed in the placebo group of stable secondary prevention patients in the FOURIER clinical trial (Further Cardiovascular Outcomes Research With PCSK9 Inhibition in Subjects With Elevated Risk).
Compared with CAC 400 to 999, those with CAC ≥1000 (n=257) had a greater mean number of coronary vessels with CAC (3.4±0.5), greater total area of CAC (586.5±275.2 mm), similar CAC density, and more extensive extracoronary calcification. After full adjustment, CAC ≥1000 demonstrated a 4.71- (3.63-6.11), 7.57- (5.50-10.42), 4.86-(3.32-7.11), and 1.94-fold (1.57-2.41) increased risk for all CVD events, all coronary heart disease events, hard coronary heart disease events, and all-cause mortality, respectively, compared with CAC 0 and a 1.65- (1.25-2.16), 1.66- (1.22-2.25), 1.51- (1.03-2.23), and 1.34-fold (1.05-1.71) increased risk compared with CAC 400 to 999. With increasing CAC, hazard ratios increased for all event types, with no apparent upper CAC threshold. CAC ≥1000 was associated with a 1.95- (1.57-2.41) and 1.43-fold (1.12-1.83) increased risk for a first non-CVD event compared with CAC 0 and CAC 400 to 999, respectively. CAC 1000 corresponded to an annualized 3-point major adverse cardiovascular event rate of 3.4 per 100 person-years, similar to that of the total FOURIER population (3.3) and higher than those of the lower-risk FOURIER subgroups.
Individuals with very high CAC (≥1000) are a unique population at substantially higher risk for CVD events, non-CVD outcomes, and mortality than those with lower CAC, with 3-point major adverse cardiovascular event rates similar to those of a stable treated secondary prevention population. Future guidelines should consider a less distinct stratification algorithm between primary and secondary prevention patients in guiding aggressive preventive pharmacotherapy.
在原发性预防个体中,具有极高的冠状动脉钙(CAC;≥1000),特别是与二级预防人群观察到的比率相比,心血管疾病(CVD)、非 CVD 和死亡率的风险数据有限。
我们的研究人群由来自 MESA(动脉粥样硬化多民族研究)的 6814 名年龄在 45 至 84 岁之间、无已知心血管疾病的种族多样化个体组成,这是一个前瞻性、观察性、基于社区的队列。平均随访时间为 13.6±4.4 年。使用 Cox 比例风险回归调整年龄、性别和传统危险因素,比较 CAC≥1000 与 CAC 0 和 CAC 400 至 999 的 CVD、非 CVD 和死亡率结果的风险比。使用性别调整的对数模型,我们计算了 MESA 中 CAC 作为函数的事件发生率,并将其与 FOURIER 临床试验(在高危人群中用 PCSK9 抑制进一步心血管结果研究)中稳定二级预防患者安慰剂组观察到的发生率进行了比较。
与 CAC 400 至 999 相比,CAC≥1000(n=257)的冠状动脉 CAC 数量更多(3.4±0.5),总 CAC 面积更大(586.5±275.2mm),CAC 密度相似,并且存在更多的冠状动脉外钙化。在充分调整后,与 CAC 0 相比,CAC≥1000 分别显示出 4.71-(3.63-6.11)、7.57-(5.50-10.42)、4.86-(3.32-7.11)和 1.94 倍(1.57-2.41)的所有 CVD 事件、所有冠心病事件、硬冠心病事件和全因死亡率风险增加,与 CAC 400 至 999 相比,分别为 1.65-(1.25-2.16)、1.66-(1.22-2.25)、1.51-(1.03-2.23)和 1.34 倍(1.05-1.71)。随着 CAC 的增加,所有事件类型的危险比均增加,没有明显的 CAC 上限。与 CAC 0 和 CAC 400 至 999 相比,CAC≥1000 与首次非 CVD 事件的 1.95-(1.57-2.41)和 1.43 倍(1.12-1.83)风险相关。CAC 1000 对应的每年 3 点主要不良心血管事件发生率为 3.4/100 人年,与 FOURIER 总人群(3.3)相似,高于 FOURIER 较低风险亚组。
具有极高 CAC(≥1000)的个体具有明显更高的 CVD 事件、非 CVD 结果和死亡率风险,与 CAC 较低的个体相比,风险比明显更高,3 点主要不良心血管事件发生率与稳定的治疗二级预防人群相似。未来的指南应该考虑在指导积极的预防性药物治疗时,在原发性和继发性预防患者之间使用不太明显的分层算法。