Document details

Serum Growth Differentiation Factor 15 (GDF15) Levels Reflect Ischemic Etiology in Heart Failure Patients with Iron Deficiency

Author(s): Tajes, Marta ; Ras-Jiménez, Maria del Mar ; Girona, Josefa ; Ramos-Polo, Raúl ; Guardiola, Montse ; García-Pinilla, José Manuel ; Ribalta, Josep ; Cobo-Marcos, Marta ; Masana, Lluís ; de Juan-Bagudá, Javier ; Fonseca, Cândida ; Enjuanes, Cristina ; Vázquez-Carrera, Manuel ; Comin-Colet, Josep ; Rodríguez-Calvo, Ricardo

Date: 2025

Persistent ID: http://hdl.handle.net/10362/189439

Origin: Repositório Institucional da UNL

Subject(s): GDF15; heart failure; iron deficiency; ischemic etiology; Biochemistry; Molecular Biology


Description

Funding Information: This research was funded by CIBER (Consorcio Centro de Investigaci\u00F3n Biom\u00E9dica en Red) (CB07/08/0028) and the Department of Research and Universities of the Generalitat of Catalonia (SGR-00815). Publisher Copyright: © 2025 by the authors.

Heart failure (HF), particularly of an ischemic etiology, is steadily increasing worldwide. Non-anemic iron deficiency (ID) is highly prevalent among HF patients, and it has been related to worse outcomes. Growth differentiation factor 15 (GDF15) has been related to atherosclerotic cardiovascular (CV) disease, HF and iron pathophysiology. Nevertheless, the specific potential role of GDF15 in HF patients with ID has not been fully explored. In this cross-sectional study we determined serum GDF15 levels in 60 HF patients with ID from the IRON-PATH II study. The discriminative capacity of GDF15 in logistic regression models for classifying these patients according to ischemic etiology was defined as the primary endpoint. Additionally, relationships between GDF15 levels and impaired right ventricle function, impaired functional capacity and HF were included as secondary endpoints. GDF15 was inversely related to tricuspid annular plane systolic excursion (TAPSE) and the six-minute walking test (6MWT), and positively related to hallmarks of HF [i.e., N-terminal prohormone of brain natriuretic peptide (NT-proBNP)] and other molecules influenced by HF progression [i.e., creatinine and ferritin]. Moreover, GDF15 was inversely related to hemoglobin, suggesting a potential link to iron homeostasis. Furthermore, GDF15 showed good classification capacity and improved the accuracy of a logistic regression model for ischemic HF classification in patients with ID. Overall, the findings of this study propose serum GDF15 levels as a potential tool for the classification of HF patients with ID according to the ischemic etiology.

Document Type Journal article
Language English
Contributor(s) NOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM); RUN
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