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Updated: Jan 19, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
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.
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.
Abstract:
Heart failure (HF) and chronic kidney disease (CKD) co-exist, and it is estimated that about 50% of HF patients suffer from CKD. Although studies have been performed on the association between CKD and HF with reduced ejection fraction (HFrEF), less is known about the link between CKD and heart failure with preserved ejection fraction (HFpEF). Approximately, 50% of all patients with HF suffer from HFpEF, and this percentage is projected to rise in the coming years. Therapies for HFrEF are long established and considered quite successful. In contrast, clinical trials for treatment of HFpEF have all shown negative or disputable results. This is likely due to the multifactorial character and the lack of pathophysiological knowledge of HFpEF. The typical co-existence of HFpEF and CKD is partially due to common underlying comorbidities, such as hypertension, dyslipidemia and diabetes. Macrovascular changes accompanying CKD, such as hypertension and arterial stiffening, have been described to contribute to HFpEF development. Furthermore, several renal factors have a direct impact on the heart and/or coronary microvasculature and may underlie the association between CKD and HFpEF. These factors include: (1) activation of the renin-angiotensin-aldosterone system, (2) anemia, (3) hypercalcemia, hyperphosphatemia and increased levels of FGF-23, and (4) uremic toxins. This review critically discusses the above factors, focusing on their potential contribution to coronary dysfunction, left ventricular stiffening, and delayed left ventricular relaxation. We further summarize the directions of novel treatment options for HFpEF based on the contribution of these renal drivers.
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