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射血分数降低的心力衰竭患者心肌损伤、炎症和肾功能生物标志物的评估:VICTORIA 生物标志物子研究。

Assessment of Biomarkers of Myocardial injury, Inflammation, and Renal Function in Heart Failure With Reduced Ejection Fraction: The VICTORIA Biomarker Substudy.

机构信息

Inova Heart and Vascular Institute, Falls Church, Virginia.

Canadian VIGOUR Centre, University of Alberta, Edmonton, Alberta, Canada.

出版信息

J Card Fail. 2023 Apr;29(4):448-458. doi: 10.1016/j.cardfail.2022.12.013. Epub 2023 Jan 9.

Abstract

BACKGROUND

Circulating biomarkers may be useful in understanding prognosis and treatment efficacy in heart failure with reduced ejection fraction. In the VICTORIA (Vericiguat Global Study in Subjects with Heart Failure with Reduced Ejection Fraction) trial, vericiguat, a soluble guanylate cyclase stimulator, decreased the primary outcome of cardiovascular death or heart failure hospitalization in heart failure with reduced ejection fraction. We evaluated biomarkers of cardiac injury, inflammation, and renal function for associations with outcomes and vericiguat treatment effect.

METHODS AND RESULTS

High-sensitivity cardiac troponin T (hs-cTnT), growth differentiation factor-15 (GDF-15), interleukin-6 (IL-6), high-sensitivity C-reactive protein (hs-CRP), and cystatin C were measured at baseline and 16 weeks. Associations of biomarkers with the primary outcome and its components were estimated. Interaction with study treatment was tested. Changes in biomarkers over time were examined by study treatment. One or more biomarkers were measured in 4652 (92%) of 5050 participants at baseline and 4063 (81%) at 16 weeks. After adjustment, higher values of hs-cTnT, growth differentiation factor-15, and interleukin-6 were associated with the primary outcome, independent of N-terminal pro-B-type natriuretic peptide. Higher hs-cTnT values were associated with a hazard ratio per log standard deviation of 1.21 (95% confidence interval 1.14-1.27). A treatment interaction with vericiguat was evident with hs-cTnT and cardiovascular death (P = .04), but not HF hospitalization (P = .38). All biomarkers except cystatin C decreased over 16 weeks and no relationship between treatment assignment and changes in biomarker levels was observed.

CONCLUSIONS

hs-cTnT, growth differentiation factor-15, and interleukin-6 levels were associated with risk of the primary outcome in VICTORIA (Vericiguat Global Study in Subjects with Heart Failure with Reduced Ejection Fraction). Uniquely, lower hs-cTnT was associated with a lower rate of cardiovascular death but not HF hospitalization after treatment with vericiguat.

摘要

背景

循环生物标志物可能有助于了解射血分数降低的心力衰竭患者的预后和治疗效果。在 VICTORIA(降低射血分数的心力衰竭患者的可溶性鸟苷酸环化酶刺激剂全球研究)试验中,可溶性鸟苷酸环化酶刺激剂维立西胍降低了射血分数降低的心力衰竭患者的主要心血管死亡或心力衰竭住院的结局。我们评估了心脏损伤、炎症和肾功能的生物标志物与结局和维立西胍治疗效果的关系。

方法和结果

在基线和 16 周时测量高敏心肌肌钙蛋白 T(hs-cTnT)、生长分化因子 15(GDF-15)、白细胞介素 6(IL-6)、高敏 C 反应蛋白(hs-CRP)和胱抑素 C。估计生物标志物与主要结局及其组成部分的相关性。测试了与研究治疗的相互作用。通过研究治疗检查随时间变化的生物标志物。在基线时,5050 名参与者中有 4652 名(92%)和 16 周时,有 4063 名(81%)测量了一个或多个生物标志物。调整后,hs-cTnT、生长分化因子-15 和白细胞介素-6 的较高值与主要结局相关,与 N 末端前 B 型利钠肽无关。每 log 标准差的 hs-cTnT 值增加与危险比为 1.21(95%置信区间为 1.14-1.27)。hs-cTnT 和心血管死亡与维立西胍治疗存在明显的相互作用(P=0.04),但心力衰竭住院无相互作用(P=0.38)。除胱抑素 C 外,所有生物标志物在 16 周内均下降,未观察到治疗分配与生物标志物水平变化之间的关系。

结论

hs-cTnT、生长分化因子-15 和白细胞介素-6 水平与 VICTORIA(降低射血分数的心力衰竭患者的可溶性鸟苷酸环化酶刺激剂全球研究)的主要结局风险相关。独特的是,在用维立西胍治疗后,hs-cTnT 较低与心血管死亡率较低相关,但与心力衰竭住院无关。

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