Pahor M, Psaty B M, Furberg C D
Department of Preventive Medicine, College of Medicine, University of Tennessee, Memphis 38105, USA.
J Cardiovasc Pharmacol. 1998;32 Suppl 2:S18-23. doi: 10.1097/00005344-199800004-00004.
Recent trials in hypertensive patients with type 2 diabetes reveal important differences in the risk for major cardiovascular events when individual agents are compared. In the Fosinopril Amlodipine Cardiovascular Events Trial (FACET), 380 patients with hypertension and type 2 diabetes were randomized to fosinopril or amlodipine and followed for up to 3.5 years to assess effects on serum lipids. Although both agents effectively controlled blood pressure, amlodipine caused a significantly greater decrease in systolic pressure. At the end of the trial, serum cholesterol, high-density lipoprotein cholesterol, triglycerides, HbA1c, serum glucose, plasma insulin, serum creatinine, and microalbuminuria were similar in both groups. The patients randomized to fosinopril were significantly less likely to experience the prospectively defined combined outcome of acute myocardial infarction (MI), hospitalized angina, or stroke compared to those randomized to amlodipine (RR 0.49; 95% CI 0.26-0.95). In the Appropriate Blood pressure Control in Diabetes (ABCD) trial, 470 patients with hypertension and type 2 diabetes who were randomized to long-acting nisoldipine had an adjusted sevenfold increased risk for acute MI compared to those randomized to enalapril (RR 7.0; 95% CI 2.3-21.4). In the Multicenter Isradipine Diuretic Atherosclerosis Study (MIDAS) trial, the patients with hypertension and above the median of HbA1c (> or =6.7%) randomized to isradipine had a threefold increased risk for major cardiovascular events compared to those randomized to hydrochlorothiazide (RR 2.81; 95% CI 1.09-7.26). These findings are supported by several observational studies. Therefore, evidence is emerging that angiotensin-converting enzyme inhibitors and low-dose diuretics may be more effective than calcium antagonists for prevention of cardiovascular events in hypertensive patients with diabetes or impaired glucose control.
近期针对2型糖尿病高血压患者的试验显示,在比较不同药物时,主要心血管事件风险存在重要差异。在福辛普利氨氯地平心血管事件试验(FACET)中,380例高血压合并2型糖尿病患者被随机分为福辛普利组或氨氯地平组,并随访长达3.5年以评估对血脂的影响。尽管两种药物均能有效控制血压,但氨氯地平导致收缩压显著下降幅度更大。试验结束时,两组的血清胆固醇、高密度脂蛋白胆固醇、甘油三酯、糖化血红蛋白、血糖、血浆胰岛素、血清肌酐和微量白蛋白尿水平相似。与随机分配至氨氯地平组的患者相比,随机分配至福辛普利组的患者发生急性心肌梗死(MI)、住院心绞痛或中风这一预先定义的联合结局的可能性显著更低(相对危险度0.49;95%置信区间0.26 - 0.95)。在糖尿病患者血压适宜控制(ABCD)试验中,与随机分配至依那普利组的患者相比,随机分配至长效尼索地平组的470例高血压合并2型糖尿病患者发生急性MI的风险经调整后增加了7倍(相对危险度7.0;95%置信区间2.3 - 21.4)。在多中心伊拉地平利尿剂动脉粥样硬化研究(MIDAS)试验中,与随机分配至氢氯噻嗪组的患者相比,随机分配至伊拉地平组的糖化血红蛋白高于中位数(≥6.7%)的高血压患者发生主要心血管事件的风险增加了3倍(相对危险度2.81;95%置信区间1.09 - 7.26)。这些发现得到了多项观察性研究的支持。因此,越来越多的证据表明,对于预防糖尿病或血糖控制受损的高血压患者发生心血管事件,血管紧张素转换酶抑制剂和低剂量利尿剂可能比钙拮抗剂更有效。