Prognostic value of plasma myeloperoxidase concentration in patients with stable coronary artery disease

Background There are no studies yet on the usefulness of myeloperoxidase (MPO) as a prognostic tool in patients with stable coronary artery disease (CAD). Methods The study included 382 patients with clinical and angiographic confirmation of stable CAD. Blood samples for MPO measurement were taken b...

Full description

Saved in:
Bibliographic Details
Published inThe American heart journal Vol. 155; no. 2; pp. 356 - 360
Main Authors Stefanescu, Ada, Braun, Siegmund, MD, Ndrepepa, Gjin, MD, Koppara, Tobias, MD, Pavaci, Herribert, MD, Mehilli, Julinda, MD, Schömig, Albert, MD, Kastrati, Adnan, MD
Format Journal Article
LanguageEnglish
Published New York, NY Mosby, Inc 01.02.2008
Elsevier
Elsevier Limited
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Background There are no studies yet on the usefulness of myeloperoxidase (MPO) as a prognostic tool in patients with stable coronary artery disease (CAD). Methods The study included 382 patients with clinical and angiographic confirmation of stable CAD. Blood samples for MPO measurement were taken before angiography. Myeloperoxidase was determined using an enzyme immunoassay. The primary end point of the study was all-cause mortality. Results Patients were categorized into 2 groups: the high-MPO group included patients in the third tertile of MPO levels (>75.0 μg/L; 127 patients), and the low-MPO group included patients in the first (<52.6 μg/L) and second tertiles (52.6-75.0 μg/L) of MPO levels (255 patients). The median follow-up was 3.5 [3.3-4.8] years. There were 35 deaths (9.2%) during the follow-up. The MPO concentration was 60.1 [47.0; 83.8] μg/L in survivors and 72.7 [54.8; 105.1] μg/L in nonsurvivors ( P = .06). There were 17 deaths in the high-MPO level and 18 deaths in the low-MPO group: Kaplan-Meier estimates of mortality were 18.3% and 10.5% with an odds ratio of 1.96 (95% confidence interval [1.02-3.76], P = .04). The Cox proportional hazards model adjusting for correlates of mortality showed that plasma MPO was not an independent correlate of mortality (hazard ratio 1.06, 95% confidence interval [0.71-1.59], P = .77 for 1 SD increase in the log variable). Conclusion Although elevated plasma MPO concentration is associated with a more advanced cardiovascular risk profile, plasma MPO does not predict mortality independent of other cardiovascular risk factors in patients with stable CAD.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0002-8703
1097-6744
DOI:10.1016/j.ahj.2007.10.017