Chronic Kidney Disease as a Risk Factor for Heart Failure With Preserved Ejection Fraction: A Focus on

Jens van de Wouw1, Michelle Broekhuizen1,2,3, Oana Sorop1

  • 1Division of Experimental Cardiology, Department of Cardiology, Erasmus MC University Medical Center, Rotterdam, Netherlands.

Frontiers in Physiology
|September 26, 2019
PubMed

Insights

Chronic kidney disease (CKD) significantly impacts heart failure with preserved ejection fraction (HFpEF) through factors like anemia and uremic toxins. Understanding these links is crucial for developing effective HFpEF treatments.

Area of Science:

  • Cardiology
  • Nephrology
  • Internal Medicine

Background:

  • Heart failure (HF) and chronic kidney disease (CKD) frequently co-exist in approximately 50% of HF patients.
  • While the link between CKD and HF with reduced ejection fraction (HFrEF) is studied, less is known about CKD's association with HF with preserved ejection fraction (HFpEF).
  • HFpEF affects about 50% of all HF patients, with rising prevalence, yet effective treatments remain elusive due to its complex nature.

Purpose of the Study:

  • To explore the pathophysiological links between CKD and HFpEF.
  • To identify key renal factors contributing to HFpEF development and progression.
  • To discuss potential novel therapeutic strategies for HFpEF based on these renal drivers.

Main Methods:

  • Review of existing literature on the co-existence of CKD and HFpEF.
  • Analysis of common comorbidities like hypertension, dyslipidemia, and diabetes.
  • Examination of specific renal factors: renin-angiotensin-aldosterone system, anemia, mineral metabolism (calcium, phosphate, FGF-23), and uremic toxins.

Main Results:

  • CKD contributes to HFpEF through macrovascular changes (hypertension, arterial stiffening) and direct renal factors.
  • Renal factors impacting the heart include RAAS activation, anemia, mineral imbalances, and uremic toxins.
  • These factors can lead to coronary dysfunction, left ventricular stiffening, and impaired relaxation in HFpEF patients.

Conclusions:

  • CKD plays a significant role in the development and progression of HFpEF.
  • Targeting renal-associated factors presents a promising avenue for novel HFpEF therapies.
  • Further research into these mechanisms is essential for improving HFpEF patient outcomes.

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