Yu Jie, Arnott Clare, Neuen Brendon L, Heersprink Hiddo L, Mahaffey Kenneth W, Cannon Christopher P, Khan Sadiya S, Baldridge Abigail S, Shah Sanjiv J, Huang Yuli, Li Chao, Figtree Gemma A, Perkovic Vlado, Jardine Meg J, Neal Bruce, Huffman Mark D
The George Institute for Global Health, UNSW Sydney, Sydney, Australia.
Department of Cardiology, Peking University Third Hospital, Beijing, China.
ESC Heart Fail. 2021 Apr;8(2):1482-1493. doi: 10.1002/ehf2.13236. Epub 2021 Feb 17.
The CANVAS Program identified the effect of canagliflozin on major adverse cardiovascular events (MACE) differed according to whether participants were using diuretics at study commencement. We sought to further evaluate this finding related to baseline differences, treatment effects, safety, and risk factor changes.
The CANVAS Program enrolled 10 142 participants with type 2 diabetes mellitus and high cardiovascular risk. Participants were randomized to canagliflozin or placebo and followed for a mean of 188 weeks. The primary outcome was major cardiovascular events, a composite of cardiovascular death, nonfatal myocardial infarction, or nonfatal stroke. Secondary outcomes included multiple cardiovascular, renal, and safety events. In this post hoc subgroup analysis, participants were categorized according to baseline use of any diuretic. The effect on outcomes was compared using Cox proportional hazards models, while risk factor changes were compared using mixed-effect models. At baseline, 4490 (44.3%) participants were using a diuretic. Compared with those not using a diuretic, participants using a diuretic were more likely to be older (mean age ± standard deviation, 64.3 ± 8.0 vs. 62.5 ± 8.3), be female (38.9% vs. 33.4%), and have heart failure (19.6% vs. 10.3%) (all P < 0.0001). The effect of canagliflozin on major cardiovascular events was greater for those using diuretic at baseline than for those who were not [adjusted hazard ratio 0.65 (95% confidence interval 0.54-0.78) vs. adjusted hazard ratio 1.13 (95% confidence interval 0.93-1.36), P < 0.0001]. Changes in most risk factors, including blood pressure, body weight, and urine albumin-to-creatinine ratio, were similar between groups (all P > 0.11), although the effect of canagliflozin on haemoglobin A1c reduction was slightly weaker in participants using compared with not using diuretics at baseline (-0.52% vs. -0.64%, P = 0.0007). Overall serious adverse events and key safety outcomes, including adverse renal events, were also similar (all P > 0.07).
Participants on baseline diuretics derived a greater benefit for major cardiovascular events from canagliflozin, which was not fully explained by differences in participant characteristics nor risk factor changes.
CANVAS研究项目发现,根据参与者在研究开始时是否使用利尿剂,卡格列净对主要不良心血管事件(MACE)的影响有所不同。我们试图进一步评估这一发现与基线差异、治疗效果、安全性和危险因素变化的关系。
CANVAS研究项目招募了10142名患有2型糖尿病且心血管风险较高的参与者。参与者被随机分配至卡格列净组或安慰剂组,平均随访188周。主要结局为主要心血管事件,即心血管死亡、非致死性心肌梗死或非致死性卒中的复合事件。次要结局包括多种心血管、肾脏和安全性事件。在这项事后亚组分析中,参与者根据基线时是否使用任何利尿剂进行分类。使用Cox比例风险模型比较对结局的影响,同时使用混合效应模型比较危险因素的变化。基线时,4490名(44.3%)参与者正在使用利尿剂。与未使用利尿剂的参与者相比,使用利尿剂的参与者更可能年龄较大(平均年龄±标准差,64.3±8.0岁对62.5±8.3岁)、为女性(38.9%对33.4%)且患有心力衰竭(19.6%对10.3%)(所有P<0.0001)。基线时使用利尿剂的参与者,卡格列净对主要心血管事件的影响大于未使用利尿剂的参与者[调整后风险比0.65(95%置信区间0.54 - 0.78)对调整后风险比1.13(95%置信区间0.93 - 1.36),P<0.0001]。两组间大多数危险因素的变化,包括血压、体重和尿白蛋白肌酐比值,均相似(所有P>0.11),尽管与基线时未使用利尿剂的参与者相比,卡格列净对使用利尿剂的参与者糖化血红蛋白降低的作用稍弱(-0.52%对-0.64%,P = 0.0007)。总体严重不良事件和关键安全性结局,包括不良肾脏事件,也相似(所有P>0.07)。
基线使用利尿剂的参与者从卡格列净中获得了更大的主要心血管事件获益,这不能完全由参与者特征差异或危险因素变化来解释。