Suppr超能文献

卡格列净与 2 型糖尿病的心血管和肾脏事件。

Canagliflozin and Cardiovascular and Renal Events in Type 2 Diabetes.

机构信息

From the George Institute for Global Health, Faculty of Medicine, UNSW Sydney (B.N., V.P.), the Charles Perkins Centre (B.N.), and the Royal North Shore Hospital (V.P., G.F.), University of Sydney, and the Faculty of Medicine, University of New South Wales (B.N.) - all in Sydney; Imperial College London, London (B.N.), and the Oxford Centre for Diabetes, Endocrinology, and Metabolism and Harris Manchester College, University of Oxford, Oxford (D.R.M.) - both in the United Kingdom; the Stanford Center for Clinical Research, Department of Medicine, Stanford University School of Medicine, Stanford, CA (K.W.M.); the University Medical Center Groningen, University of Groningen, Groningen, the Netherlands (D.Z.); and Janssen Research and Development, Raritan, NJ (N.E., W.S., G.L., M.D.).

出版信息

N Engl J Med. 2017 Aug 17;377(7):644-657. doi: 10.1056/NEJMoa1611925. Epub 2017 Jun 12.

Abstract

Background Canagliflozin is a sodium-glucose cotransporter 2 inhibitor that reduces glycemia as well as blood pressure, body weight, and albuminuria in people with diabetes. We report the effects of treatment with canagliflozin on cardiovascular, renal, and safety outcomes. Methods The CANVAS Program integrated data from two trials involving a total of 10,142 participants with type 2 diabetes and high cardiovascular risk. Participants in each trial were randomly assigned to receive canagliflozin or placebo and were followed for a mean of 188.2 weeks. The primary outcome was a composite of death from cardiovascular causes, nonfatal myocardial infarction, or nonfatal stroke. Results The mean age of the participants was 63.3 years, 35.8% were women, the mean duration of diabetes was 13.5 years, and 65.6% had a history of cardiovascular disease. The rate of the primary outcome was lower with canagliflozin than with placebo (occurring in 26.9 vs. 31.5 participants per 1000 patient-years; hazard ratio, 0.86; 95% confidence interval [CI], 0.75 to 0.97; P<0.001 for noninferiority; P=0.02 for superiority). Although on the basis of the prespecified hypothesis testing sequence the renal outcomes are not viewed as statistically significant, the results showed a possible benefit of canagliflozin with respect to the progression of albuminuria (hazard ratio, 0.73; 95% CI, 0.67 to 0.79) and the composite outcome of a sustained 40% reduction in the estimated glomerular filtration rate, the need for renal-replacement therapy, or death from renal causes (hazard ratio, 0.60; 95% CI, 0.47 to 0.77). Adverse reactions were consistent with the previously reported risks associated with canagliflozin except for an increased risk of amputation (6.3 vs. 3.4 participants per 1000 patient-years; hazard ratio, 1.97; 95% CI, 1.41 to 2.75); amputations were primarily at the level of the toe or metatarsal. Conclusions In two trials involving patients with type 2 diabetes and an elevated risk of cardiovascular disease, patients treated with canagliflozin had a lower risk of cardiovascular events than those who received placebo but a greater risk of amputation, primarily at the level of the toe or metatarsal. (Funded by Janssen Research and Development; CANVAS and CANVAS-R ClinicalTrials.gov numbers, NCT01032629 and NCT01989754 , respectively.).

摘要

背景

卡格列净是一种钠-葡萄糖共转运蛋白 2 抑制剂,可降低糖尿病患者的血糖水平以及血压、体重和白蛋白尿。我们报告了卡格列净治疗对心血管、肾脏和安全性结局的影响。

方法

CANVAS 项目整合了两项共纳入 10142 例 2 型糖尿病和心血管高风险患者的试验数据。每项试验的参与者均被随机分配接受卡格列净或安慰剂治疗,并随访平均 188.2 周。主要结局为心血管原因死亡、非致死性心肌梗死或非致死性卒中的复合结局。

结果

参与者的平均年龄为 63.3 岁,35.8%为女性,糖尿病病程平均为 13.5 年,65.6%有心血管疾病史。卡格列净组的主要结局发生率低于安慰剂组(每 1000 患者-年分别为 26.9 例和 31.5 例;风险比,0.86;95%置信区间[CI],0.75 至 0.97;非劣效性 P<0.001;优效性 P=0.02)。尽管基于预设的假设检验序列,肾脏结局并未显示具有统计学意义,但结果显示卡格列净可能有益于白蛋白尿的进展(风险比,0.73;95%CI,0.67 至 0.79)和估计肾小球滤过率持续下降 40%、需要肾脏替代治疗或因肾脏原因死亡的复合结局(风险比,0.60;95%CI,0.47 至 0.77)。不良反应与先前报道的卡格列净相关风险一致,除了截肢风险增加(每 1000 患者-年分别为 6.3 例和 3.4 例;风险比,1.97;95%CI,1.41 至 2.75);截肢主要发生在脚趾或跖骨。

结论

在两项涉及 2 型糖尿病和心血管疾病风险升高的患者的试验中,接受卡格列净治疗的患者发生心血管事件的风险低于接受安慰剂的患者,但截肢风险增加,主要发生在脚趾或跖骨。(由杨森研发资助;CANVAS 和 CANVAS-R 临床试验.gov 编号,NCT01032629 和 NCT01989754)。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验