van Boven Nick, Akkerhuis K Martijn, Anroedh Sharda S, Rizopoulos Dimitris, Pinto Yigal, Battes Linda C, Hillege Hans L, Caliskan Kadir C, Germans Tjeerd, Manintveld Olivier C, Cornel Jan-Hein, Constantinescu Alina A, Boersma Eric, Umans Victor A, Kardys Isabella
Cardiology, Medical Centre Alkmaar, Alkmaar, The Netherlands.
Cardiology, Erasmus Medical Centre, Rotterdam, The Netherlands.
Int J Cardiol. 2017 May 15;235:124-132. doi: 10.1016/j.ijcard.2017.02.078. Epub 2017 Feb 22.
Several studies have suggested circulating microRNAs (miRs) are associated with heart failure, but these studies were small, and limited to single miR measurements. We examined 7 miRs which were previously linked to heart failure, and tested whether their temporal expression level predicts prognosis in a prospective cohort of chronic heart failure (CHF) patients.
In 2011-2013, 263 CHF patients were included. At inclusion and subsequently every 3months, we measured 7miRs. The primary endpoint (PE) comprised heart failure hospitalization, cardiovascular mortality, cardiac transplantation and LVAD implantation. Associations between temporal miR patterns and the PE were investigated by joint modelling, which combines mixed models with Cox regression. Mean age was 67±13years, 72% were men and 27% NYHA classes III-IV. We obtained 873 blood samples (median 3 [IQR 2-5] per patient). The PE was reached in 41 patients (16%) during a median follow-up of 0.9 [0.6-1.4] years. The temporal pattern of miR-22-3p was independently associated with the PE (HR [95% CI] per doubling of level: 0.64 [0.47-0.77]). The instantaneous change in level (slope of the temporal miR pattern) of miR-22-3p was also independently associated with the PE (HR [95% CI] per doubling of slope: 0.33 [0.20-0.51]). These associations remained statistically significant after adjustment for temporal patterns of NT-proBNP, Troponin T and CRP.
The temporal pattern of circulating miR-22-3p contains important prognostic and independent information in CHF patients. This concept warrants further investigation in larger series with extended follow-up.
多项研究表明,循环微RNA(miR)与心力衰竭有关,但这些研究规模较小,且仅限于单一miR测量。我们检测了7种先前与心力衰竭相关的miR,并在前瞻性慢性心力衰竭(CHF)患者队列中测试了它们的时间表达水平是否可预测预后。
2011年至2013年,纳入了263例CHF患者。在纳入时及随后每3个月,我们测量了7种miR。主要终点(PE)包括心力衰竭住院、心血管死亡、心脏移植和左心室辅助装置植入。通过联合建模研究了miR时间模式与PE之间的关联,联合建模将混合模型与Cox回归相结合。平均年龄为67±13岁,72%为男性,27%为纽约心脏协会(NYHA)III-IV级。我们共采集了873份血样(每位患者中位数为3份[四分位间距2-5份])。在中位随访0.9[0.6-1.4]年期间,41例患者(16%)达到了PE。miR-22-3p的时间模式与PE独立相关(水平每增加一倍的风险比[95%置信区间]:0.64[0.47-0.77])。miR-22-3p水平的瞬时变化(miR时间模式的斜率)也与PE独立相关(斜率每增加一倍的风险比[95%置信区间]:0.33[0.20-0.51])。在对N末端脑钠肽前体(NT-proBNP)、肌钙蛋白T和C反应蛋白(CRP)的时间模式进行校正后,这些关联仍具有统计学意义。
循环miR-22-3p的时间模式在CHF患者中包含重要的预后和独立信息。这一概念值得在更大规模、更长随访期的系列研究中进一步探讨。