Seronde Marie-France, Vausort Mélanie, Gayat Etienne, Goretti Emeline, Ng Leong L, Squire Iain B, Vodovar Nicolas, Sadoune Malha, Samuel Jane-Lise, Thum Thomas, Solal Alain Cohen, Laribi Said, Plaisance Patrick, Wagner Daniel R, Mebazaa Alexandre, Devaux Yvan
Department of Cardiology, EA3920, University Hospital, Besançon, France.
UMRS 942 Inserm, University Paris Diderot, Paris, France.
PLoS One. 2015 Nov 18;10(11):e0142237. doi: 10.1371/journal.pone.0142237. eCollection 2015.
The biomarker value of circulating microRNAs (miRNAs) has been extensively addressed in patients with acute coronary syndrome. However, prognostic performances of miRNAs in patients with acute heart failure (AHF) has received less attention.
A test cohort of 294 patients with acute dyspnea (236 AHF and 58 non-AHF) and 44 patients with stable chronic heart failure (CHF), and an independent validation cohort of 711 AHF patients, were used. Admission levels of miR-1/-21/-23/-126/-423-5p were assessed in plasma samples.
In the test cohort, admission levels of miR-1 were lower in AHF and stable CHF patients compared to non-AHF patients (p = 0.0016). Levels of miR-126 and miR-423-5p were lower in AHF and in non-AHF patients compared to stable CHF patients (both p<0.001). Interestingly, admission levels of miR-423-5p were lower in patients who were re-admitted to the hospital in the year following the index hospitalization compared to patients who were not (p = 0.0001). Adjusted odds ratio [95% confidence interval] for one-year readmission was 0.70 [0.53-0.93] for miR-423-5p (p = 0.01). In the validation cohort, admission levels of miR-423-5p predicted 1-year mortality with an adjusted odds ratio [95% confidence interval] of 0.54 [0.36-0.82], p = 0.004. Patients within the lowest quartile of miR-423-5p were at high risk of long-term mortality (p = 0.02).
In AHF patients, low circulating levels of miR-423-5p at presentation are associated with a poor long-term outcome. This study supports the value of miR-423-5p as a prognostic biomarker of AHF.
循环微小RNA(miRNA)的生物标志物价值在急性冠状动脉综合征患者中已得到广泛研究。然而,miRNA在急性心力衰竭(AHF)患者中的预后表现受到的关注较少。
使用了一个由294例急性呼吸困难患者(236例AHF和58例非AHF)以及44例稳定的慢性心力衰竭(CHF)患者组成的测试队列,和一个由711例AHF患者组成的独立验证队列。在血浆样本中评估miR-1/-21/-23/-126/-423-5p的入院水平。
在测试队列中,与非AHF患者相比,AHF和稳定CHF患者的miR-1入院水平较低(p = 0.0016)。与稳定CHF患者相比,AHF和非AHF患者的miR-126和miR-423-5p水平较低(均p<0.001)。有趣的是,与未在索引住院后一年内再次入院的患者相比,再次入院患者的miR-423-5p入院水平较低(p = 0.0001)。miR-423-5p的一年再入院调整优势比[95%置信区间]为0.70[0.53 - 0.93](p = 0.01)。在验证队列中,miR-423-5p的入院水平预测1年死亡率的调整优势比[95%置信区间]为0.54[0.36 - 0.82],p = 0.004。miR-423-5p处于最低四分位数的患者长期死亡风险较高(p = 0.02)。
在AHF患者中,就诊时循环miR-423-5p水平低与长期预后不良相关。本研究支持miR-423-5p作为AHF预后生物标志物的价值。