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European Heart Journal 2003 24(5):412-420; doi:10.1016/S0195-668X(02)00526-2
Copyright © 2003 by the European Society of Cardiology.
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Accelerated decline and prognostic impact of renal function after myocardial infarction and the benefits of ACE inhibition: the CATS randomized trial

H.L. Hillegea,*, W.H. van Gilsta,b, D.J. van Veldhuisena, G. Navisc, D.E. Grobbeed, P.A. de Graeffb,e and D. de Zeeuwb

a Trial Coordination Center/Department of Cardiology/Thoraxcenter, University Hospital Groningen, Hanzeplein 1, 9700 Groningen, The Netherlands
b Department of Clinical Pharmacology, State University Groningen, Groningen, The Netherlands
c Division of Nephrology, Department of Internal Medicine, University Hospital Groningen, Groningen, The Netherlands
d Julius Center for Patient Oriented Research, University Medical Center, Utrecht, The Netherlands
e Department of Internal Medicine, University Hospital Groningen, Groningen, The Netherlands

* Corresponding author. Tel.: +31-50-361-8066; fax: +31-50-361-8062
E-mail address: h.hillege{at}tcc.azg.nl

Received 31 May 2002; revised 15 July 2002; accepted 24 July 2002

Aims Information regarding the cardiorenal axis in patients after a myocardial infarction (MI) is limited. We examined the change in renal function after a first MI, the protective effect of angiotensin converting enzyme (ACE) inhibition and the prognostic value of baseline renal function.

Methods and results The study population consisted of 298 patients with a first anterior wall MI who were randomized to the ACE inhibitor captopril or placebo after completion of streptokinase infusion. Renal function, by means of glomerular filtration rate (GFR), was calculated using the Cockroft–Gault equation (GFRc). In the placebo group, renal function (GFRc) declined by 5.5mlmin–1within 1 year, vs only 0.5mlmin–1in the ACE inhibitor group . This beneficial effect of captopril was most pronounced in patients with the most compromised renal function at baseline. The incidence of chronic heart failure (CHF) within 1 year increased significantly with decreasing GFRc(divided into tertiles: 24.0, 28.9, and 41.2%; ). The risk-ratio for GFRc<81mlmin–1vs >103mlmin–1was 1.86 (95% CI 1.11–3.13; ).

Conclusions Renal function markedly deteriorates after a first MI, but is significantly preserved by ACE inhibition. Furthermore, an impaired baseline renal function adds to the prognostic risk of developing CHF in patients after a first anterior MI.

Key Words: Renal function • Myocardial infarction • Prognosis • Angiotensin converting enzyme inhibitors


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