Drüeke Tilman B, Locatelli Francesco, Clyne Naomi, Eckardt Kai-Uwe, Macdougall Iain C, Tsakiris Dimitrios, Burger Hans-Ulrich, Scherhag Armin
Inserm Unité 507 and Assistance Publique-Hôpitaux de Paris, Necker Hospital, Division of Nephrology, Paris, France.
N Engl J Med. 2006 Nov 16;355(20):2071-84. doi: 10.1056/NEJMoa062276.
Whether correction of anemia in patients with stage 3 or 4 chronic kidney disease improves cardiovascular outcomes is not established.
We randomly assigned 603 patients with an estimated glomerular filtration rate (GFR) of 15.0 to 35.0 ml per minute per 1.73 m2 of body-surface area and mild-to-moderate anemia (hemoglobin level, 11.0 to 12.5 g per deciliter) to a target hemoglobin value in the normal range (13.0 to 15.0 g per deciliter, group 1) or the subnormal range (10.5 to 11.5 g per deciliter, group 2). Subcutaneous erythropoietin (epoetin beta) was initiated at randomization (group 1) or only after the hemoglobin level fell below 10.5 g per deciliter (group 2). The primary end point was a composite of eight cardiovascular events; secondary end points included left ventricular mass index, quality-of-life scores, and the progression of chronic kidney disease.
During the 3-year study, complete correction of anemia did not affect the likelihood of a first cardiovascular event (58 events in group 1 vs. 47 events in group 2; hazard ratio, 0.78; 95% confidence interval, 0.53 to 1.14; P=0.20). Left ventricular mass index remained stable in both groups. The mean estimated GFR was 24.9 ml per minute in group 1 and 24.2 ml per minute in group 2 at baseline and decreased by 3.6 and 3.1 ml per minute per year, respectively (P=0.40). Dialysis was required in more patients in group 1 than in group 2 (127 vs. 111, P=0.03). General health and physical function improved significantly (P=0.003 and P<0.001, respectively, in group 1, as compared with group 2). There was no significant difference in the combined incidence of adverse events between the two groups, but hypertensive episodes and headaches were more prevalent in group 1.
In patients with chronic kidney disease, early complete correction of anemia does not reduce the risk of cardiovascular events. (ClinicalTrials.gov number, NCT00321919 [ClinicalTrials.gov].).
3期或4期慢性肾病患者贫血的纠正是否能改善心血管结局尚未明确。
我们将603例估算肾小球滤过率(GFR)为每分钟15.0至35.0 ml/1.73 m²体表面积且伴有轻至中度贫血(血红蛋白水平为每分升11.0至12.5 g)的患者随机分为两组,一组将血红蛋白目标值设定在正常范围(每分升13.0至15.0 g,第1组),另一组设定在低于正常范围(每分升10.5至11.5 g,第2组)。皮下注射促红细胞生成素(β-促红细胞生成素)在随机分组时开始(第1组),或仅在血红蛋白水平降至每分升10.5 g以下时开始(第2组)。主要终点是8种心血管事件的复合终点;次要终点包括左心室质量指数、生活质量评分以及慢性肾病的进展情况。
在为期3年的研究中,贫血的完全纠正并未影响首次发生心血管事件的可能性(第1组58例事件,第2组47例事件;风险比为0.78;95%置信区间为0.53至1.14;P = 0.20)。两组的左心室质量指数均保持稳定。第1组和第2组在基线时的平均估算GFR分别为每分钟24.9 ml和每分钟24.2 ml,每年分别下降3.6 ml和3.1 ml(P = 0.40)。第1组需要透析的患者比第2组多(127例对111例,P = 0.03)。总体健康和身体功能有显著改善(与第2组相比,第1组分别为P = 0.003和P < 0.001)。两组不良事件的合并发生率无显著差异,但第1组高血压发作和头痛更为常见。
在慢性肾病患者中,早期完全纠正贫血并不能降低心血管事件的风险。(临床试验注册号,NCT00321919 [ClinicalTrials.gov]。)