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首页> 外文期刊>Journal of the American College of Cardiology >Effect of serelaxin on cardiac, renal, and hepatic biomarkers in the relaxin in acute heart failure (RELAX-AHF) development program: Correlation with outcomes
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Effect of serelaxin on cardiac, renal, and hepatic biomarkers in the relaxin in acute heart failure (RELAX-AHF) development program: Correlation with outcomes

机译:在急性心力衰竭(RELAX-AHF)发展计划中,丝氨蛋白对松弛素中心脏,肾脏和肝脏生物标志物的影响:与预后的关系

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Objectives: The aim of this study was to assess the effects of serelaxin on short-term changes in markers of organ damage and congestion and relate them to 180-day mortality in patients with acute heart failure. Background: Hospitalization for acute heart failure is associated with high post-discharge mortality, and this may be related to organ damage. Methods: The Pre-RELAX-AHF (Relaxin in Acute Heart Failure) phase II study and RELAX-AHF phase III study were international, multicenter, double-blind, placebo-controlled trials in which patients hospitalized for acute heart failure were randomized within 16 h to intravenous placebo or serelaxin. Each patient was followed daily to day 5 or discharge and at days 5, 14, and 60 after enrollment. Vital status was assessed through 180 days. In RELAX-AHF, laboratory evaluations were performed daily to day 5 and at day 14. Plasma levels of biomarkers were measured at baseline and days 2, 5, and 14. All-cause mortality was assessed as a safety endpoint in both studies. Results: Serelaxin reduced 180-day mortality, with similar effects in the phase II and phase III studies (combined studies: N = 1,395; hazard ratio: 0.62; 95% confidence interval: 0.43 to 0.88; p = 0.0076). In RELAX-AHF, changes in markers of cardiac (high-sensitivity cardiac troponin T), renal (creatinine and cystatin-C), and hepatic (aspartate transaminase and alanine transaminase) damage and of decongestion (N-terminal pro-brain natriuretic peptide) at day 2 and worsening heart failure during admission were associated with 180-day mortality. Serelaxin administration improved these markers, consistent with the prevention of organ damage and faster decongestion. Conclusions: Early administration of serelaxin was associated with a reduction of 180-day mortality, and this occurred with fewer signs of organ damage and more rapid relief of congestion during the first days after admission. ? 2013 American College of Cardiology Foundation.
机译:目的:本研究的目的是评估serelaxin对急性器官衰竭患者器官损伤和充血指标短期变化的影响,并将其与180天死亡率相关联。背景:急性心力衰竭住院与出院后死亡率高相关,这可能与器官损害有关。方法:RELAX-AHF(急性心力衰竭中的松弛素)II期研究和RELAX-AHF III期研究是国际性,多中心,双盲,安慰剂对照试验,其中急性心力衰竭住院患者随机分为16个h给予静脉安慰剂或serelaxin。每天随访至第5天或出院,并在入组后第5、14和60天。通过180天评估生命状态。在RELAX-AHF中,每天至第5天和第14天进行实验室评估。在基线和第2、5和14天测量血浆生物标志物水平。在这两项研究中,将全因死亡率评估为安全终点。结果:Serelaxin降低了180天的死亡率,在II期和III期研究中具有相似的作用(联合研究:N = 1,395;危险比:0.62; 95%置信区间:0.43至0.88; p = 0.0076)。在RELAX-AHF中,心脏(高敏感性心脏肌钙蛋白T),肾脏(肌酐和半胱氨酸蛋白酶抑制剂C)和肝(天冬氨酸转氨酶和丙氨酸转氨酶)标记和充血(N末端前脑利钠肽)的改变)在第2天和入院期间心力衰竭加重与180天死亡率有关。 Serelaxin给药改善了这些标志物,与预防器官损伤和更快的充血相一致。结论:早期给予serelaxin可以减少180天的死亡率,并且在入院后的第一天出现较少的器官损伤迹象和更迅速的充血缓解。 ? 2013美国心脏病学会基金会。

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