JACC:高剂量他汀治疗存在两难抉择
2013-04-11 晓东 编译 医学论坛网
近日《美国心脏病学会杂志》在线发表的一项研究表明,对于糖尿病风险较高的患者[合并2-4个新发糖尿病(NOD)危险因素],每日服用高剂量阿托伐他汀(80mg/日)时或应考虑降低剂量。 研究显示,对于NOD风险较低者(合并0-1个NOD危险因素),每日服用高剂量阿托伐他汀(80mg/日)不会增加NOD发生率。然而若患者糖尿病发生风险较高,合并了2-4个NOD危险因素,则每日服用高剂量比低剂量(1
近日《美国心脏病学会杂志》在线发表的一项研究表明,对于糖尿病风险较高的患者[合并2-4个新发糖尿病(NOD)危险因素],每日服用高剂量阿托伐他汀(80mg/日)时或应考虑降低剂量。
研究显示,对于NOD风险较低者(合并0-1个NOD危险因素),每日服用高剂量阿托伐他汀(80mg/日)不会增加NOD发生率。然而若患者糖尿病发生风险较高,合并了2-4个NOD危险因素,则每日服用高剂量比低剂量(10mg/日)者NOD风险增加24%。无论剂量高低,服用阿托伐他汀均可降低心血管事件风险。
他汀可以降低心血管事件例数,但同时可增加NOD的发生。研究者、旧金山总医院心脏科Waters DD等人既往报道过4项危险因素可独立预测NOD:空腹血糖水平>100mg/dl,空腹甘油三酯水平>150mg/dl,体质指数>30kg/m2,既往有高血压史。
这项研究中,研究者选取TNT(treating to new targets)试验(n=7595)和IDEAL (Incremental Decrease in Endpoints Through Aggressive Lipid Lowering)试验(n=7461)中的15056例基线时有冠脉疾病但无糖尿病的患者,对其NOD发生与心血管事件降低进行比较。心血管事件包括冠脉死亡、心梗、卒中与心脏骤停复苏幸存。
在基线时没有或只有1项NOD危险因的8825例患者当中,阿托伐他汀80mg组4407例患者发生NOD者142例;阿托伐他汀10mg组4418例患者中发生148例((3.22% 对. 3.35%; 危害比[HR]: 0.97; 95% 可信区间[CI]: 0.77 -1.22)。
其余6231例患者基线时合并2-4个NOD危险因素:阿托伐他汀80mg组3128例患者中出现448例NOD;低剂量(10mg)组3103例中患者出现368例NOD(14.3% vs. 11.9%; HR: 1.24; 95% CI: 1.08 to 1.42; p = 0.0027)。无论合并多少NOD危险因素,服用80mg阿托伐他汀的患者心血管事件均显著下降。
Cardiovascular event reduction versus new-onset diabetes during atorvastatin therapy: effect of baseline risk factors for diabetes.
OBJECTIVES
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.
BACKGROUND
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.
METHODS
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.
RESULTS
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.
CONCLUSIONS
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.
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