Related Experiment Video
Updated: Jun 5, 2025

A Surgical Model of Heart Failure with Preserved Ejection Fraction in Tibetan Minipigs
Published on: February 18, 2022
Iron deficiency and heart failure with preserved ejection fraction
Tetyana M Ternushchak1, Marianna I Tovt-Korshynska1, Snizhana V Feysa1
1UZHHOROD NATIONAL UNIVERSITY, UZHHOROD, UKRAINE.
Insights
Iron deficiency (ID) is common in heart failure with preserved ejection fraction (HFpEF), affecting 63% of patients. This comorbidity significantly reduces functional capacity and quality of life.
Area of Science:
- Cardiology
- Internal Medicine
- Clinical Research
Background:
- Heart failure with preserved ejection fraction (HFpEF) is a complex condition with multiple comorbidities.
- Iron deficiency (ID) is increasingly recognized as a significant comorbidity in heart failure patients.
Purpose of the Study:
- To determine the prevalence of iron deficiency (ID) in patients diagnosed with HFpEF.
- To investigate the relationship between ID and functional capacity in HFpEF patients.
- To assess the impact of ID on the quality of life in individuals with HFpEF.
Main Methods:
- A cohort of 121 consecutive outpatients newly diagnosed with HFpEF were analyzed.
- Patients were evaluated for iron status using serum ferritin and transferrin saturation (TSAT).
- Functional capacity was assessed using the 6-minute walk test (6MWT), and quality of life was measured with the Minnesota Living with Heart Failure Questionnaire.
Main Results:
- Iron deficiency (ID) was prevalent in 63% of the HFpEF patients studied.
- Patients with ID exhibited more severe HF symptoms, higher NT-proBNP and hs CRP levels, and poorer diastolic function.
- HFpEF patients with ID demonstrated significantly reduced functional capacity and lower quality of life scores.
Conclusions:
- Iron deficiency (ID) is a highly prevalent comorbidity in patients with HFpEF.
- The presence of ID is strongly associated with impaired functional capacity and diminished quality of life in HFpEF.
- Addressing ID may be crucial for improving clinical outcomes in HFpEF management.
Objective:
Aim: We aimed to assess the prevalence of ID in patients HFpEF and its relation to functional capacity and quality of life.
Patients And Methods:
Materials and Methods: We included in the analysis 121 consecutive outpatients newly diagnosed of HFpEF and tested with iron-related parameters. Patients were subdivided in two groups according to the presence of ID (n = 76, mean age 65.3 ± 7.1 years) or without ID (n =45, mean age 61.6 ± 7.4 years). Physical examination, routine laboratory tests, serum ferritin, transferrin saturation (TSAT), hs CRP, N-terminal proB-type natriuretic peptide (NT-proBNP), standard transthoracic echocardiogram examinations, functional capacity and quality were performed and assessed.
Results:
Results: Among all tested patients with iron-related parameters, 63% (76) met the European Society of Cardiology criteria for ID. Additionally, 29% (22) were found to have coexisting anemia. Patients with ID had more pronounced HF symptoms, higher NT-pro-BNP, hs CRP, ferritin and lower TSAT values and more severe diastolic dysfunction. Patients with HFpEF and ID performed worse functional capacity during the 6MWT and had lower quality of life with Minnesota Living with Heart Failure Questionnaire.
Conclusion:
Conclusions: ID as one of the most common comorbidities in HFpEF significantly impairs the functional capacity and quality of life.
More Related Videos
09:20Lumped-Parameter and Finite Element Modeling of Heart Failure with Preserved Ejection Fraction
Published on: February 13, 2021
14:35Post-Myocardial Infarction Heart Failure in Closed-chest Coronary Occlusion/Reperfusion Model in Göttingen Minipigs and Landrace Pigs
Published on: April 17, 2021
Related Concept Videos
Pathophysiology of Heart Failure
Imbalances in Cardiac Output
CHF can occur due to the failure of either side of the heart. Left-side failure leads to pulmonary congestion—the right side continues to send...
Heart Failure Drugs: Diuretics
Mitral Regurgitation I: Introduction
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System
Heart Failure Drugs: Inotropic Agents