Prognostic value and echocardiographic determinants of plasma myeloperoxidase levels in chronic heart failure

J Am Coll Cardiol. 2007 Jun 19;49(24):2364-70. doi: 10.1016/j.jacc.2007.02.053. Epub 2007 Jun 4.

Abstract

Objectives: The purpose of this study was to explore the relationship between myeloperoxidase (MPO) and cardiac structure, performance, and prognosis.

Background: 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.

Methods: 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).

Results: 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]).

Conclusions: 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.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Arabidopsis Proteins
  • Chronic Disease
  • Creatinine / metabolism
  • Cyclophilins
  • Female
  • Heart Failure / diagnostic imaging*
  • Heart Failure / enzymology*
  • Heart Failure / physiopathology
  • Humans
  • Leukocyte Count
  • Male
  • Middle Aged
  • Neutrophils
  • Peroxidase / blood*
  • Prognosis
  • Proportional Hazards Models
  • Stroke Volume
  • Ultrasonography
  • Ventricular Dysfunction, Left / enzymology
  • Ventricular Dysfunction, Right / enzymology

Substances

  • Arabidopsis Proteins
  • Creatinine
  • Peroxidase
  • Cyclophilins
  • ROC1 protein, Arabidopsis