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HFpEF Diagnosis: A Challenge in CKD with Current Algorithms
Anca E Stefan1,2, Maria A Covic1,3, Gianina Dodi1
1Grigore T. Popa University of Medicine and Pharmacy Iasi, 700115 Iasi, Romania.
Insights
Diagnosing heart failure with preserved ejection fraction (HFpEF) in chronic kidney disease (CKD) patients is complex. NT-proBNP levels vary, necessitating CKD-specific diagnostic strategies for accurate HFpEF assessment.
Area of Science:
- Cardiology
- Nephrology
- Biomarkers
Background:
- Chronic kidney disease (CKD) significantly increases cardiovascular remodeling and heart failure with preserved ejection fraction (HFpEF) risk.
- Diagnosing HFpEF in CKD is challenging due to coexisting structural cardiac abnormalities and elevated NT-proBNP levels.
Purpose of the Study:
- To evaluate HFpEF classification in ambulatory CKD patients using a modified HFA-PEFF approach.
- To assess the impact of NT-proBNP thresholds on HFpEF diagnosis in CKD.
- To explore NT-proBNP's relationship with diastolic dysfunction and cardiac structure in CKD.
Main Methods:
- Cross-sectional study of CKD stages G3-G4 patients with NYHA II dyspnea.
- Comprehensive clinical, metabolic, vascular, and echocardiographic assessments.
- Modified HFA-PEFF algorithm application for HFpEF assessment, including NT-proBNP threshold analysis.
Main Results:
- High prevalence of cardiometabolic burden (74.9%) and structural cardiac abnormalities.
- HFpEF identified in 52.9% using the modified algorithm; 86.7% fell into intermediate probability without biomarker domain.
- A cohort-adapted NT-proBNP threshold of 700 pg/mL identified 19.8% of patients with HFpEF.
Conclusions:
- CKD G3-G4 patients show significant cardiovascular abnormalities, often undiagnosed.
- HFpEF classification is sensitive to NT-proBNP thresholds, indicating limited discriminatory power for diastolic dysfunction.
- Development of CKD-sensitive HFpEF diagnostic approaches is crucial for this population.
Background:
Chronic kidney disease (CKD) is associated with a high burden of cardiovascular remodeling and increased risk of heart failure with preserved ejection fraction (HFpEF). However, the interpretation of natriuretic peptide-based HFpEF diagnostic remains challenging in CKD populations, where structural cardiac abnormalities and elevated NT-proBNP levels frequently coexist.
Methods:
We conducted a cross-sectional study including ambulatory patients with CKD stages G3-G4 and NYHA II dyspnea. Clinical, metabolic, vascular, and echocardiographic assessments were performed. HFpEF was assessed using a modified HFA-PEFF-based approach derived from the ESC-recommended diagnostic algorithm. We evaluated the impact of NT-proBNP thresholds on HFpEF classification and explored the relationship between NT-proBNP, echocardiographic diastolic dysfunction, and structural cardiac abnormalities.
Results:
The cohort displayed a high cardiometabolic burden (74.9%), and structural cardiac abnormalities were highly prevalent. Using a modified HFA-PEFF diagnostic algorithm, HFpEF was identified in 52.9% of patients. However, when the biomarker domain was excluded, 86.7% of patients remained within the intermediate-probability range. In an exploratory analysis, a cutoff of 700 pg/mL was identified as the cohort-adapted threshold with the best diagnostic balance and identified 19.8% patients as having HFpEF.
Conclusions:
Patients with CKD G3-G4 exhibited substantial structural and functional cardiovascular abnormalities despite no prior diagnosis of heart failure. HFpEF classification varied according to the NT-proBNP threshold applied, while NT-proBNP demonstrated limited discriminatory performance for echocardiographic diastolic dysfunction. These findings support the need for more refined and CKD-sensitive approaches for HFpEF characterization in this population.
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