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普伐他汀对糖尿病合并慢性肾病患者的影响。

Effect of pravastatin in people with diabetes and chronic kidney disease.

作者信息

Tonelli Marcello, Keech Anthony, Shepherd Jim, Sacks Frank, Tonkin Andrew, Packard Chris, Pfeffer Marc, Simes John, Isles Chris, Furberg Curt, West Malcolm, Craven Tim, Curhan Gary

机构信息

Division of Nephrology, University of Alberta, Edmonton, Alberta, Canada.

出版信息

J Am Soc Nephrol. 2005 Dec;16(12):3748-54. doi: 10.1681/ASN.2005070779. Epub 2005 Oct 26.

Abstract

Although diabetes is a major cause of chronic kidney disease (CKD), limited data describe the cardiovascular benefit of hydroxymethyl glutaryl CoA reductase inhibitors (statins) in people with both of these conditions. This study sought to determine whether pravastatin reduced the incidence of first or recurrent cardiovascular events in people with non-dialysis-dependent CKD and concomitant diabetes, using data from three randomized trials of pravastatin 40 mg daily versus placebo. CKD was defined by estimated GFR <60 or 60 to 89.9 ml/min per 1.73 m2 with proteinuria. Of 19,737 patients, 4099 (20.8%) had CKD but not diabetes at baseline, 873 (4.4%) had diabetes but not CKD, and 571 (2.9%) had both conditions. The primary composite outcome was time to myocardial infarction, coronary death, or percutaneous/surgical coronary revascularization. Median follow-up was 64 mo. After adjustment for trial and random treatment assignment, the incidence of the primary outcome was lowest in individuals with neither CKD nor diabetes (15.2%), intermediate in individuals with only CKD (18.6%) or only diabetes (21.3%), and highest in individuals with both characteristics (27.0%). Pravastatin reduced the relative likelihood of the primary outcome to a similar extent in subgroups defined by the presence or absence of CKD and diabetes. For example, pravastatin was associated with a significant reduction in the relative risk of the primary outcome by 25% in patients with CKD and concomitant diabetes and by 24% in individuals with neither characteristic. However, the absolute reduction in the risk of the primary outcome as a result of pravastatin use was highest in patients with both CKD and diabetes (6.4%) and lowest in individuals with neither characteristic (3.5%). In conclusion, stage 2 or early stage 3 CKD and diabetes both are associated with higher cardiovascular risk, and pravastatin reduces cardiovascular event rates in people with neither, one, or both characteristics. Given the high absolute benefit of pravastatin in patient with diabetes and stage 2 or early stage 3 CKD, this population in particular should be targeted for widespread use of statins. Additional studies are needed to determine whether these benefits apply to patients with more severe CKD, and recruitment to such studies should be given high priority.

摘要

尽管糖尿病是慢性肾脏病(CKD)的主要病因,但关于羟甲基戊二酰辅酶A还原酶抑制剂(他汀类药物)对同时患有这两种疾病的患者心血管方面益处的数据有限。本研究旨在利用三项每日服用40 mg普伐他汀与安慰剂对比的随机试验数据,确定普伐他汀是否能降低非透析依赖型CKD合并糖尿病患者首次或复发性心血管事件的发生率。CKD的定义为估算肾小球滤过率(eGFR)<60或60至89.9 ml/min/1.73 m²且伴有蛋白尿。在19737例患者中,4099例(20.8%)在基线时患有CKD但无糖尿病,873例(4.4%)患有糖尿病但无CKD,571例(2.9%)同时患有这两种疾病。主要复合终点为发生心肌梗死、冠状动脉死亡或经皮/外科冠状动脉血运重建的时间。中位随访时间为64个月。在对试验和随机治疗分配进行调整后,主要终点发生率在既无CKD也无糖尿病的个体中最低(15.2%),在仅患有CKD(18.6%)或仅患有糖尿病(21.3%)的个体中处于中间水平,在同时具备这两种特征的个体中最高(27.0%)。在根据是否存在CKD和糖尿病定义的亚组中,普伐他汀降低主要终点相对可能性的程度相似。例如,在患有CKD合并糖尿病的患者中,普伐他汀使主要终点相对风险显著降低25%,在不具备这两种特征的个体中降低24%。然而,使用普伐他汀导致主要终点风险的绝对降低幅度在同时患有CKD和糖尿病的患者中最高(6.4%),在不具备这两种特征的个体中最低(3.5%)。总之,2期或3期早期CKD和糖尿病均与较高的心血管风险相关,普伐他汀可降低不具备、具备其中一种或同时具备这两种特征的人群的心血管事件发生率。鉴于普伐他汀对糖尿病合并2期或3期早期CKD患者有较高的绝对获益,尤其应针对这一人群广泛使用他汀类药物。需要进一步研究以确定这些益处是否适用于更严重CKD患者,并且应高度优先招募患者参与此类研究。

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