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European Heart Journal Advance Access originally published online on December 21, 2007
European Heart Journal 2008 29(2):224-230; doi:10.1093/eurheartj/ehm587
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Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2007. For permissions please email: journals.permissions@oxfordjournals.org

Myeloperoxidase, but not C-reactive protein, predicts cardiovascular risk in peripheral arterial disease

Gregorio Brevetti1,*, Vittorio Schiano1, Eugenio Laurenzano1, Giuseppe Giugliano1, Mario Petretta1, Francesco Scopacasa2 and Massimo Chiariello1

1 Department of Clinical Medicine and Cardiovascular and Immunological Sciences, University of Naples ‘Federico II’, Via Pansini 5, Naples, Italy
2 Department of Laboratory Medicine, University of Naples ‘Federico II’, Via Pansini 5, Naples, Italy

Received 3 May 2007; revised 14 November 2007; accepted 22 November 2007; online publish-ahead-of-print 21 December 2007.

* Corresponding author: Via G. Iannelli 45/A, 80131 Napoli, Italy. Tel/Fax: +39 081 7462240, Email: brevetti{at}unina.it

See page 150 for the editorial comment on this article (doi:10.1093/eurheartj/ehm535)

Aims: The prognostic role of inflammation in peripheral arterial disease (PAD) remains to be conclusively established. Accordingly, in these patients we investigated the impact of myeloperoxidase (MPOx) and C-reactive protein on the incidence of myocardial infarction and stroke.

Methods and results: Of 156 PAD patients, 10 had a myocardial infarction and seven a stroke, during follow-up. We used the receiver operating characteristic curve analysis and the bootstrap approach to identify the MPOx, C-reactive protein, and ankle brachial index (ABI) threshold levels that provided the best cut-off to predict the outcome. For MPOx a cut-off ≥183.7 pM was independently associated with a poor outcome (HR = 6.80, 95% CI 1.20–38.69, P = 0.031). The result remained unmodified when MPOx was used as a continuous variable (HR = 1.03, 95% CI 1.01–1.05, P = 0.031). Conversely, C-reactive protein was not a prognostic determinant in our series (HR = 0.88, 95% CI 0.60–1.29, P = 0.514). Kaplan–Meier curves for the four groups of patients delineated according to ABI and MPOx values identified using the bootstrap approach showed that the addition of MPOx measurement to ABI improved the ability to identify patients at risk for myocardial infarction and stroke.

Conclusion: In PAD, MPOx, but not C-reactive protein, predicts an increased risk of major cardiovascular events, and adds to the prognostic value of ABI, currently the most powerful prognostic indicator in these patients.

Key Words: Peripheral arterial disease • Inflammation • C-reactive protein • Myeloperoxidase • Prognosis • Cardiovascular diseases


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