Tang W H Wilson, Tong Wilson, Troughton Richard W, Martin Maureen G, Shrestha Kevin, Borowski Allen, Jasper Sue, Hazen Stanley L, Klein Allan L
Section of Heart Failure and Cardiac Transplantation Medicine, Department of Cardiovascular Medicine, Cleveland Clinic, Cleveland, Ohio 44195, USA.
J Am Coll Cardiol. 2007 Jun 19;49(24):2364-70. doi: 10.1016/j.jacc.2007.02.053. Epub 2007 Jun 4.
The purpose of this study was to explore the relationship between myeloperoxidase (MPO) and cardiac structure, performance, and prognosis.
Myeloperoxidase is an inflammatory marker that is elevated in patients with heart failure (HF) and cardiac dysfunction, with mechanistic links to plaque vulnerability and left ventricular (LV) remodeling.
We evaluated plasma MPO levels (CardioMPO, PrognostiX, Inc., Cleveland, Ohio) in 140 patients with chronic systolic HF (LV ejection fraction <35%) and examined the plasma MPO levels' relationships with echocardiographic indexes of systolic and diastolic performance, as well as long-term clinical outcomes (death, cardiac transplantation, or HF hospitalization).
Within the overall cohort, increasing plasma MPO levels were associated with increasing likelihood of more advanced HF (restrictive diastolic stage, right ventricular systolic dysfunction > or =3+, and tricuspid regurgitation area > or =1.8 cm2). Plasma MPO levels were predictive of long-term clinical outcomes (risk ratio [95% confidence interval] = 3.35 [1.52 to 8.86]), even after adjustment for age, LV ejection fraction, plasma B-type natriuretic peptide (BNP), creatinine clearance, or diastolic stage. In receiver-operator characteristic curve analyses, addition of MPO to BNP testing augmented the predictive accuracy of future adverse clinical events (area under the curve 0.66 for BNP only [chi-square test = 12.9, p = 0.0003], and 0.70 for BNP plus MPO [chi-square test = 15.87, p = 0.0004]).
In chronic systolic HF, elevated plasma MPO levels are associated with an increased likelihood of more advanced HF. Moreover, elevated plasma MPO levels within a HF subject seem to be predictive of increased adverse clinical outcomes.
本研究旨在探讨髓过氧化物酶(MPO)与心脏结构、功能及预后之间的关系。
髓过氧化物酶是一种炎症标志物,在心力衰竭(HF)和心脏功能障碍患者中升高,与斑块易损性和左心室(LV)重塑存在机制联系。
我们评估了140例慢性收缩性HF患者(左心室射血分数<35%)的血浆MPO水平(CardioMPO,PrognostiX公司,俄亥俄州克利夫兰),并研究了血浆MPO水平与收缩和舒张功能的超声心动图指标以及长期临床结局(死亡、心脏移植或HF住院)之间的关系。
在整个队列中,血浆MPO水平升高与更晚期HF(限制性舒张期、右心室收缩功能障碍>或=3+、三尖瓣反流面积>或=1.8 cm2)的可能性增加相关。即使在调整年龄、左心室射血分数、血浆B型利钠肽(BNP)、肌酐清除率或舒张期后,血浆MPO水平仍可预测长期临床结局(风险比[95%置信区间]=3.35[1.52至8.86])。在受试者工作特征曲线分析中,将MPO添加到BNP检测中可提高未来不良临床事件的预测准确性(仅BNP时曲线下面积为0.66[卡方检验=12.9,p=0.0003],BNP加MPO时为0.70[卡方检验=15.87,p=0.0004])。
在慢性收缩性HF中,血浆MPO水平升高与更晚期HF的可能性增加相关。此外,HF患者体内血浆MPO水平升高似乎可预测不良临床结局增加。