Division of Cardiology, San Francisco General Hospital and University of California at San Francisco, San Francisco, California 94114, USA.
J Am Coll Cardiol. 2013 Jan 15;61(2):148-52. doi: 10.1016/j.jacc.2012.09.042. Epub 2012 Dec 5.
The purpose of this study was to compare the incidence of new-onset diabetes (NOD) with cardiovascular (CV) event reduction at different levels of NOD risk.
Statins reduce the number of CV events but increase the incidence of NOD. We previously reported that 4 factors independently predicted NOD: fasting blood glucose >100 mg/dl, fasting triglycerides >150 mg/dl, body mass index >30 kg/m(2), and history of hypertension.
We compared NOD incidence with CV event reduction among 15,056 patients with coronary disease but without diabetes at baseline in the TNT (Treating to New Targets) (n = 7,595) and IDEAL (Incremental Decrease in Endpoints Through Aggressive Lipid Lowering) (n = 7,461) trials. CV events included coronary heart disease death, myocardial infarction, stroke, and resuscitated cardiac arrest.
Among 8,825 patients with 0 to 1 of the aforementioned NOD risk factors at baseline, NOD developed in 142 of 4,407 patients in the atorvastatin 80 mg group and in 148 of 4,418 in the atorvastatin 10 mg and simvastatin 20 to 40 mg groups (3.22% vs. 3.35%; hazard ratio [HR]: 0.97; 95% confidence intervals [CI]: 0.77 to 1.22). Among the remaining 6,231 patients with 2 to 4 NOD risk factors, NOD developed in 448 of 3,128 in the atorvastatin 80 mg group and in 368 of 3,103 in the lower-dose groups (14.3% vs. 11.9%; HR: 1.24; 95% CI: 1.08 to 1.42; p = 0.0027). The number of CV events was significantly reduced with atorvastatin 80 mg in both NOD risk groups.
Compared with lower-dose statin therapy, atorvastatin 80 mg/day did not increase the incidence of NOD in patients with 0 to 1 NOD risk factors but did, by 24%, among patients with 2 to 4 NOD risk factors. The number of CV events was significantly reduced with atorvastatin 80 mg in both NOD risk groups.
本研究旨在比较不同新发糖尿病(NOD)风险水平下,NOD 发病率与心血管(CV)事件减少之间的关系。
他汀类药物可降低 CV 事件的发生,但会增加 NOD 的发病率。我们之前的报告表明,4 个因素可独立预测 NOD:空腹血糖>100mg/dl、空腹甘油三酯>150mg/dl、体重指数>30kg/m²和高血压病史。
我们比较了 TNT(治疗至新目标)(n=7595)和 IDEAL(通过强化降脂进一步降低终点事件)(n=7461)试验中 15056 例基线时无糖尿病但患有冠心病患者的 NOD 发病率与 CV 事件减少之间的关系。CV 事件包括冠心病死亡、心肌梗死、卒中和复苏性心脏骤停。
在基线时有 0-1 个上述 NOD 危险因素的 8825 例患者中,阿托伐他汀 80mg 组有 142 例(4407 例中的 3.22%)和阿托伐他汀 10mg 联合辛伐他汀 20-40mg 组有 148 例(4418 例中的 3.35%)发生 NOD(危险比[HR]:0.97;95%置信区间[CI]:0.77 至 1.22)。在其余 6231 例有 2-4 个 NOD 危险因素的患者中,阿托伐他汀 80mg 组有 448 例(3128 例中的 14.3%)和低剂量组有 368 例(3103 例中的 11.9%)发生 NOD(HR:1.24;95%CI:1.08 至 1.42;p=0.0027)。在两个 NOD 风险组中,阿托伐他汀 80mg 均可显著减少 CV 事件的发生。
与低剂量他汀类药物治疗相比,阿托伐他汀 80mg/天在 NOD 风险因素为 0-1 的患者中并未增加 NOD 的发病率,但在 NOD 风险因素为 2-4 的患者中发病率增加了 24%。在两个 NOD 风险组中,阿托伐他汀 80mg 均可显著减少 CV 事件的发生。