Pursnani Amit, Massaro Joseph M, D'Agostino Ralph B, O'Donnell Christopher J, Hoffmann Udo
Cardiac MR PET CT Program, Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Boston2Cardiology Division, NorthShore University Health System, Evanston, Illinois.
Department of Biostatistics, Boston University School of Public Health, Boston, Massachusetts4The Framingham Heart Study of the National Heart, Lung and Blood Institute and Boston University, Framingham, Massachusetts.
JAMA. 2015 Jul 14;314(2):134-41. doi: 10.1001/jama.2015.7515.
The 2013 American College of Cardiology/American Heart Association (ACC/AHA) guidelines for cholesterol management defined new eligibility criteria for statin therapy. However, it is unclear whether this approach improves identification of adults at higher risk of cardiovascular events.
To determine whether the ACC/AHA guidelines improve identification of individuals who develop incident cardiovascular disease (CVD) and/or have coronary artery calcification (CAC) compared with the National Cholesterol Education Program's 2004 Updated Third Report of the Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (ATP III) guidelines.
DESIGN, SETTING, AND PARTICIPANTS: Longitudinal community-based cohort study, with participants for this investigation drawn from the offspring and third-generation cohorts of the Framingham Heart Study. Participants underwent multidetector computed tomography for CAC between 2002 and 2005 and were followed up for a median of 9.4 years for incident CVD.
Statin eligibility was determined based on Framingham risk factors and low-density lipoprotein thresholds for ATP III, whereas the pooled cohort calculator was used for ACC/AHA.
The primary outcome was incident CVD (myocardial infarction, death due to coronary heart disease [CHD], or ischemic stroke). Secondary outcomes were CHD and CAC (as measured by the Agatston score).
Among 2435 statin-naive participants (mean age, 51.3 [SD, 8.6] years; 56% female), 39% (941/2435) were statin eligible by ACC/AHA compared with 14% (348/2435) by ATP III (P < .001). There were 74 incident CVD events (40 nonfatal myocardial infarctions, 31 nonfatal ischemic strokes, and 3 fatal CHD events). Participants who were statin eligible by ACC/AHA had increased hazard ratios for incident CVD compared with those eligible by ATP III: 6.8 (95% CI, 3.8-11.9) vs 3.1 (95% CI, 1.9-5.0), respectively (P<.001). Similar results were seen for CVD in participants with intermediate Framingham Risk Scores and for CHD. Participants who were newly statin eligible (n = 593 [24%]) had an incident CVD rate of 5.7%, yielding a number needed to treat of 39 to 58. Participants with CAC were more likely to be statin eligible by ACC/AHA than by ATP III: CAC score >0 (n = 1015): 63% vs 23%; CAC score >100 (n = 376): 80% vs 32%; and CAC score >300 (n = 186): 85% vs 34% (all P < .001). A CAC score of 0 identified a low-risk group among ACC/AHA statin-eligible participants (306/941 [33%]) with a CVD rate of 1.6%.
In this community-based primary prevention cohort, the ACC/AHA guidelines for determining statin eligibility, compared with the ATP III, were associated with greater accuracy and efficiency in identifying increased risk of incident CVD and subclinical coronary artery disease, particularly in intermediate-risk participants.
2013年美国心脏病学会/美国心脏协会(ACC/AHA)胆固醇管理指南定义了他汀类药物治疗的新适用标准。然而,尚不清楚这种方法是否能改善对心血管事件高风险成年人的识别。
确定与美国国家胆固醇教育计划专家小组2004年《成人高血胆固醇检测、评估和治疗第三次报告》(ATP III)指南相比,ACC/AHA指南在识别发生心血管疾病(CVD)和/或有冠状动脉钙化(CAC)的个体方面是否更具优势。
设计、地点和参与者:基于社区的纵向队列研究,本研究的参与者来自弗雷明汉心脏研究的后代和第三代队列。参与者在2002年至2005年间接受了用于检测CAC的多排螺旋CT检查,并对发生CVD的情况进行了中位数为9.4年的随访。
根据ATP III的弗雷明汉风险因素和低密度脂蛋白阈值确定他汀类药物的适用情况,而使用合并队列计算器来确定ACC/AHA的适用情况。
主要结局是发生CVD(心肌梗死、冠心病[CHD]死亡或缺血性中风)。次要结局是CHD和CAC(通过阿加斯顿评分测量)。
在2435名未服用过他汀类药物的参与者中(平均年龄51.3[标准差8.6]岁;56%为女性),根据ACC/AHA标准,39%(941/2435)符合他汀类药物治疗条件,而根据ATP III标准这一比例为14%(348/2435)(P<0.001)。共发生74例CVD事件(40例非致命性心肌梗死、31例非致命性缺血性中风和3例致命性CHD事件)。与根据ATP III标准符合他汀类药物治疗条件的参与者相比,根据ACC/AHA标准符合条件的参与者发生CVD的风险比增加:分别为6.8(95%CI,3.8 - 11.9)和3.1(95%CI,1.9 - 5.0)(P<0.001)。在弗雷明汉风险评分中等的参与者中,CVD以及CHD的情况也得到了类似结果。新符合他汀类药物治疗条件的参与者(n = 593[24%])发生CVD的发生率为5.7%,需治疗人数为39至58。与ATP III相比,有CAC的参与者更有可能根据ACC/AHA标准符合他汀类药物治疗条件:CAC评分>0(n = 1015):63%对23%;CAC评分>100(n = 376):80%对32%;CAC评分>300(n = 186):85%对34%(均P<0.001)。CAC评分为0在ACC/AHA符合他汀类药物治疗条件的参与者中识别出一个低风险组(306/941[33%]),其CVD发生率为1.6%。
在这个基于社区的一级预防队列中,与ATP III相比,ACC/AHA确定他汀类药物治疗条件的指南在识别CVD和亚临床冠状动脉疾病风险增加方面具有更高的准确性和效率,特别是在中等风险参与者中。