Ferreira João Pedro, Dewan Pooja, Jhund Pardeep S, Lorenzo-Almorós Ana, Duarte Kévin, Petrie Mark C, Carson Peter E, McKelvie Robert, Komajda Michel, Zile Michael, Zannad Faiez, McMurray John J V
BHF Cardiovascular Research Centre, University of Glasgow, 126 University Place, Glasgow, G12 8TA, UK.
National Institute of Health and Medical Research (INSERM), Center for Clinical Multidisciplinary Research 1433, INSERM U1116, French Clinical Research Infrastructure Network (F-CRIN) Investigation Network Initiative-Cardiovascular and Renal Clinical Trialists (INI-CRCT), University of Lorraine, Regional University Hospital of Nancy, Nancy, France.
Clin Res Cardiol. 2020 Nov;109(11):1358-1365. doi: 10.1007/s00392-020-01632-x. Epub 2020 Mar 25.
The CHARM-Preserved trial suggested that the renin-angiotensin system (RAS) inhibitor candesartan might have been beneficial in heart failure with preserved ejection fraction (HFpEF); however, this hypothesis was not supported by the findings of I-Preserve with irbesartan.
To re-analyse the results of I-Preserve, adjusting for imbalances in baseline variables that may have influenced the trial outcomes.
Cox proportional hazards models with covariate adjustment for baseline variables, including age, sex, medical history, physiological and laboratory variables.
In I-Preserve, 763 (37.0%) participants in the placebo group and 742 (35.9%) in the irbesartan group experienced the primary composite outcome (death from any cause or hospitalization for heart failure, myocardial infarction, unstable angina, arrhythmia, or stroke). The prespecified analysis of this outcome, stratifying for the use of ACEi at baseline, gave a hazard ratio (HR) of 0.95 (95% confidence interval, 0.86-1.05); p = 0.35. Adjusting the effect of treatment for key prognostic baseline variables, gave a HR of 0.89 (0.80-0.99); p = 0.033. Similar findings were observed for the composite of cardiovascular death or HF hospitalization.
Adjusting for imbalances in baseline variables that influence outcomes (or the response to therapy or both) can improve the power around the estimate of the effect of treatment and may alter its statistical significance. Along with the CHARM-Preserved results, these findings suggest that angiotensin-receptor blockers may have a modest effect in HFpEF.
CHARM-Preserved试验表明,肾素-血管紧张素系统(RAS)抑制剂坎地沙坦可能对射血分数保留的心力衰竭(HFpEF)有益;然而,伊贝沙坦的I-Preserve试验结果并未支持这一假设。
重新分析I-Preserve试验的结果,对可能影响试验结果的基线变量不平衡进行校正。
采用Cox比例风险模型,对包括年龄、性别、病史、生理和实验室变量在内的基线变量进行协变量校正。
在I-Preserve试验中,安慰剂组763名(37.0%)参与者和伊贝沙坦组742名(35.9%)参与者发生了主要复合结局(任何原因导致的死亡或因心力衰竭、心肌梗死、不稳定型心绞痛、心律失常或中风住院)。对这一结局进行预先设定的分析,根据基线时ACEi的使用情况进行分层,风险比(HR)为0.95(95%置信区间为0.86-1.05);p = 0.35。对关键预后基线变量的治疗效果进行校正后,HR为0.89(0.80-0.99);p = 0.033。对于心血管死亡或HF住院的复合结局,观察到了类似的结果。
对影响结局(或治疗反应或两者)的基线变量不平衡进行校正,可以提高治疗效果估计的效力,并可能改变其统计学意义。连同CHARM-Preserved试验的结果,这些发现表明血管紧张素受体阻滞剂可能对HFpEF有适度的疗效。