Publication: Hfpef diagnosis: a challenge in CKD with current algorithms
Program
KU-Authors
KU Authors
Co-Authors
Stefan, A. E.
Covic, M. A.
Dodi, G.
Avanu, A. E.
Bîrgoan, S.
Moroșanu, C.
Sascau, R. A.
Covic, A. C.
Bazyani, Amin
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Compiler & Affiliation
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Date
Language
eng
Type
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N/A
Journal Title
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Volume Title
Alternative Title
Abstract
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.
Source
Publisher
MDPI
Subject
Health sciences, Medicine, Cardiology and cardiovascular medicine, Endocrinology, Diabetes and metabolism
Citation
Has Part
Source
Life
Book Series Title
Edition
DOI
10.3390/life16060944
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Creative Commons license
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