Prognostic value of plasma renin activity in heart failure patients with chronic kidney disease

Roberta Poletti1, Giuseppe Vergaro, Luc Zyw

  • 1Division of Cardiovascular Medicine, Fondazione G. Monasterio, CNR-Regione Toscana, Via Giuseppe Moruzzi 1, 56124 Pisa, Italy. poletti@ftgm.it

Insights

Plasma renin activity (PRA) independently predicts cardiac death in patients with chronic heart failure and chronic kidney disease (CKD). Combining PRA with NT-proBNP identifies high-risk patients needing intensified care targeting the renin-angiotensin system.

Area of Science:

  • Cardiology
  • Nephrology
  • Biomarkers

Background:

  • Kidney function impairment is common in chronic heart failure (CHF) and impacts prognosis.
  • Chronic kidney disease (CKD) in CHF patients is linked to worse clinical status and neurohormonal markers.
  • The prognostic significance of plasma renin activity (PRA) in CHF with CKD requires further investigation.

Purpose of the Study:

  • To determine the prognostic impact of plasma renin activity (PRA) in patients with chronic heart failure (CHF) and chronic kidney disease (CKD).
  • To identify independent predictors of cardiac death in this patient population.

Main Methods:

  • 996 consecutive CHF patients were enrolled, characterized clinically and neurohormonally.
  • Patients were followed for cardiac death over a median of 36 months.
  • Cox multivariate and ROC analyses were used to assess prognostic factors, including PRA and NT-proBNP.

Main Results:

  • 437 patients had stage ≥ 3 CKD, associated with worse outcomes.
  • In CKD patients, ejection fraction, NT-proBNP, and PRA were independent predictors of cardiac death.
  • A PRA cut-off of 3.29 ng/mL/h predicted prognosis; elevated PRA and NT-proBNP identified highest-risk patients.

Conclusions:

  • Plasma renin activity (PRA) is an independent prognostic marker in CHF patients with CKD.
  • The combination of PRA and NT-proBNP identifies high-risk patients who may benefit from intensified renin-angiotensin system antagonism therapy.
Abstract

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