(Circulation. 2006;113:671-678.)
© 2006 American Heart Association, Inc.
Heart Failure |
From the University Medical Center Groningen, University of Groningen, the Netherlands (H.L.H., D.J.V.V.); Medical Statistics Unit, London School of Hygiene and Tropical Medicine, London, UK (D.N., S.P.); The Cardiovascular Division, Brigham and Womens Hospital, Boston, Mass (M.A.P.); Sahlgrenska University Hospital/Östra Göteborg, Sweden (K.S.); University of Glasgow, Glasgow, UK (J.J.V.M.); Hamilton Health Sciences and McMaster University, Hamilton, Ontario, Canada (S.Y.); Duke University Medical Center, Durham, NC (C.B.G.); AstraZeneca LP, Wilmington, Del (E.L.M.); Karolinska Hospital, Stockholm, Sweden (J.Ö.); Medisch Centrum Alkmaar, the Netherlands (J.H.C.); and the Department of Clinical Pharmacology, University of Groningen, the Netherlands (D.d.Z.).
Correspondence to Dr Hans L. Hillege, Department of Cardiology, Thoraxcenter, University Medical Center Groningen, University of Groningen, PO Box 30.001, 9700 RB Groningen, The Netherlands. E-mail h.hillege{at}tcc.umcg.nl
Received August 31, 2005; revision received November 4, 2005; accepted November 23, 2005.
Background Decreased renal function has been found to be an independent risk factor for cardiovascular outcomes in patients with chronic heart failure (CHF) with markedly reduced left ventricular ejection fraction (LVEF). The aim of this analysis was to evaluate the prognostic importance of renal function in a broader spectrum of patients with CHF.
Methods and Results The Candesartan in Heart Failure:Assessment of Reduction in Mortality and Morbidity (CHARM) program consisted of three component trials that enrolled patients with symptomatic CHF, based on use of ACE inhibitors and reduced (
40%) or preserved LVEF (>40%). Entry baseline creatinine was required to be below 3.0 mg/dL (265 µmol/L). Routine baseline serum creatinine assessments were done in 2680 North American patients. An analysis of the estimated glomerular filtration rate (eGFR), using the Modification of Diet in Renal Disease equation and LVEF on risk of cardiovascular death or hospitalization for heart failure, as well as on all-cause mortality, was conducted on these 2680 patients. The proportion of patients with eGFR <60 mL/min per 1.73 m2 was 36.0%; 42.6% for CHARM-Alternative, 33.0% for CHARM-Added, and 34.7% for CHARM-Preserved. During the median follow-up of 34.4 months (total 6493 person-years), the primary outcome of cardiovascular death or hospital admission for worsening CHF occurred in 950 of 2680 subjects. Both reduced eGFR and lower LVEF were found to be significant independent predictors of worse outcome after adjustment for major confounding baseline clinical characteristics. The risk for cardiovascular death or hospitalization for worsening CHF as well as the risk for all-cause mortality increased significantly below an eGFR of 60 mL/min per 1.73 m2 (adjusted hazard ratio, 1.54 for 45 to 60 mL/min per 1.73 m2 and 1.86 for <45 mL/min per 1.73 m2 for the primary outcome, both P<0.001, and hazard ratio of 1.50, P=0.006, and 1.91, P=0.001, respectively, for all-cause mortality). The prognostic value of eGFR was not significantly different among the three component trials. There was no significant interaction between renal function, the effect of candesartan, and clinical outcome.
Conclusions Impaired renal function is independently associated with heightened risk for death, cardiovascular death, and hospitalization for heart failure in patients with CHF with both preserved as well as reduced LVEF. There was no evidence that the beneficial effect of candesartan was modified by baseline eGFR.
Key Words: heart failure angiotensin kidney risk factors prognosis
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