Scheen A J, Krzesinski J M
Université de Liège, Service de Diabétologie, Nutrition et Maladies métaboliques et Unité de Pharmacologie clinique, CHU Sart Tilman, Liège, Belgique.
Rev Med Liege. 2007 Oct;62(10):639-43.
The controlled ADVANCE trial compared the incidence of major macrovascular and microvascular complications in 5,569 type 2 diabetic patients randomised to a fixed combination of perindopril and indapamide and in 5,571 patients randomised to placebo, followed for a mean duration of 4.3 years. Compared with patients assigned placebo, those assigned active therapy had a mean reduction in systolic blood pressure of 5.6 mm Hg and diastolic blood pressure of 2.2 mm Hg, despite the fact physicians were allowed to adjust antihypertensive therapy ad libitum. The relative risk of a major macrovascular and microvascular event (primary endpoint) was reduced by 9% (p = 0.041) in the active group. The separate reductions in macrovascular and microvascular events were similar but were not independently statistically significant. The relative risk of death was significantly reduced by 14% (p = 0.025), essentially due to a lower death rate from cardiovascular diseases (-18%; p = 0.027). The incidence of any coronary event was also significantly reduced (-14 %; p = 0.020), while only a trend was observed for all cerebrovascular events. Finally, renal events were significantly less frequent (-21%; p < 0.0001) whereas all ocular events were only slightly reduced (-5%; NS) in the active group as compared to the placebo group. The fixed combination of perindopril and indapamide was well tolerated and easy to administer. Overall one death due to any cause would be averted among every 79 diabetic patients assigned active therapy for 5 years. There was no evidence that the effects of the study treatment differed by initial blood pressure level or concomitant use of other treatments at baseline.
在ADVANCE对照试验中,将5569例2型糖尿病患者随机分配至培哚普利吲达帕胺固定复方组,5571例患者随机分配至安慰剂组,平均随访4.3年,比较主要大血管和微血管并发症的发生率。与服用安慰剂的患者相比,尽管允许医生随意调整抗高血压治疗方案,但接受活性治疗的患者收缩压平均降低5.6 mmHg,舒张压平均降低2.2 mmHg。活性治疗组主要大血管和微血管事件(主要终点)的相对风险降低了9%(p = 0.041)。大血管和微血管事件的单独降低幅度相似,但无独立统计学意义。死亡相对风险显著降低14%(p = 0.025),主要原因是心血管疾病死亡率降低(-18%;p = 0.027)。任何冠状动脉事件的发生率也显著降低(-14%;p = 0.020),而所有脑血管事件仅观察到一种趋势。最后,与安慰剂组相比,活性治疗组肾脏事件显著减少(-21%;p < 0.0001),而所有眼部事件仅略有减少(-5%;无统计学意义)。培哚普利吲达帕胺固定复方耐受性良好且易于给药。总体而言,每79例接受活性治疗5年的糖尿病患者中可避免1例因任何原因导致的死亡。没有证据表明研究治疗的效果因初始血压水平或基线时同时使用其他治疗而有所不同。