Chiang Chia-Hung, Huang Po-Hsun, Leu Hsin-Bang, Hsu Chien-Yi, Wang Ko-Fan, Chen Jaw-Wen, Lin Shing-Jong
Division of Cardiology, Department of Medicine, Taipei Veterans General Hospital, Hsinchu Branch, Hsinchu, Taiwan, ROC.
Cardiology. 2013;126(3):191-201. doi: 10.1159/000351973. Epub 2013 Sep 18.
The purpose of this study was to explore the relationship between endothelial progenitor cell (EPC) levels, heart failure with preserved ejection fraction (HFpEF) and heart failure with reduced ejection fraction (HFrEF).
A total of 44 HFpEF patients, 40 HFrEF patients and 69 age-, gender- and comorbidity-matched controls were enrolled after evaluating their clinical manifestations and echocardiography findings. Flow cytometry with quantification of three EPC markers in peripheral blood samples was used to assess the number of circulating EPCs.
HFpEF and HFrEF patients had significantly decreased circulating EPC levels compared to controls. Among heart failure patients, patients with New York Heart Association functional class (FC) IV had fewer circulating EPCs compared to those with FC II and FC III (p = 0.053). A simple linear regression analysis of data showed that high sensitivity C-reactive protein, left ventricular ejection fraction, left atrium diameter and the ratio of medial early filling to early diastolic mitral annular velocity all correlated with the EPC count. In multivariate Cox regression analyses, both HFpEF and HFrEF were found to be independent predictors of a decreased EPC number.
HFpEF and HFrEF patients have decreased circulating EPC numbers, which is an indication of impaired endothelial turnover.
本研究旨在探讨内皮祖细胞(EPC)水平与射血分数保留的心力衰竭(HFpEF)及射血分数降低的心力衰竭(HFrEF)之间的关系。
在评估44例HFpEF患者、40例HFrEF患者及69例年龄、性别和合并症相匹配的对照者的临床表现及超声心动图检查结果后,将他们纳入研究。采用流式细胞术对外周血样本中的三种EPC标志物进行定量分析,以评估循环EPC的数量。
与对照组相比,HFpEF和HFrEF患者的循环EPC水平显著降低。在心力衰竭患者中,纽约心脏协会心功能分级(FC)为IV级的患者循环EPC数量少于FC II级和FC III级的患者(p = 0.053)。对数据进行的简单线性回归分析显示,高敏C反应蛋白、左心室射血分数、左心房直径以及舒张早期二尖瓣环速度与EPC计数均相关。在多因素Cox回归分析中,发现HFpEF和HFrEF均为EPC数量减少的独立预测因素。
HFpEF和HFrEF患者的循环EPC数量减少,这表明内皮细胞更新受损。