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J Am Coll Cardiol, 2001; 38:1782-1787
© 2001 by the American College of Cardiology Foundation
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REVIEW ARTICLE

Renal function: the Cinderella of cardiovascular risk profile

Luis M. Ruilope, MD*,*, Dirk J. van Veldhuisen, MD, PhD, FACC{dagger}, Eberhard Ritz, MD, FRCP, FACP{ddagger} and Thomas F. Luscher, MD, FRCP§

* Unidad de Hipertensión, Hospital 12 de Octubre, Madrid, Spain
{dagger} Department of Cardiology, Thoraxcenter, University Hospital, Groningen, The Netherlands
{ddagger} Department of Internal Medicine, Division of Nephrology, Rupert Karl University, Heidelberg, Germany
§ Abteilungsleiter Kardiologie, Universität Spital, Zürich, Switzerland

Manuscript received March 20, 2001; revised manuscript received July 24, 2001, accepted August 20, 2001.

* Reprint requests and correspondence: Luis M. Ruilope, Unidad de Hipertensión, Hospital 12 de Octubre, 28041 Madrid, Spain
Luis_M_Ruilope{at}teleline.es

The presence of an altered renal function in essential hypertension, advanced heart failure (HF) and after a myocardial infarction (MI) is associated with higher cardiovascular morbidity and mortality. Indices of altered renal function (e.g., microalbuminuria, increased serum creatinine concentrations, decrease in estimated creatinine clearance or overt proteinuria) are independent predictors of cardiovascular morbidity and mortality in any of the three clinical situations. These parameters should then be routinely evaluated in clinical practice. These facts have several therapeutic implications. First, although there is no evidence-based information on the level of blood pressure that confers optimal renal protection, levels substantially lower than past recommendations are advisable. Second, hypertensive kidney damage should be prevented by early treatment of hypertensive patients, particularly those with microalbuminuria. Finally, to avoid further aggravation of high cardiovascular risk, antihypertensive agents devoid of unwanted metabolic side effects should be used for the treatment of hypertensive vascular damage. In HF, the combination of an angiotensin-converting enzyme (ACE) inhibitor and a beta-blocker seem to be the most renoprotective. Renal outcome is also improved by ACE inhibition after an MI. Finally, renal and cardiovascular outcome seem to run in parallel in all these situations.

Abbreviations and Acronyms
  ACE = angiotensin-converting enzyme
  BP = blood pressure
  CHF = congestive heart failure
  GFR = glomerular filtration rate
  HF = heart failure
  LV = left ventricle, left ventricular
  LVEF = left ventricular ejection fraction
  MI = myocardial infarction
  SCr = serum creatinine




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