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Published on: September 7, 2018
Altered Iron Metabolism in Dogs with Naturally Occurring Cardiac Disease
Carolina Frizzo-Ramos1, Pavlos Doulidis1, Ursula S Kolm1
1Small Animal Internal Medicine, Department for Companion Animals and Horses, University of Veterinary Medicine Vienna, 1210 Vienna, Austria.
This study reveals that dogs with cardiac disease exhibit altered iron metabolism, including reduced iron levels and impaired iron transport, independent of anemia. These changes are linked to inflammation and disease severity, suggesting a potential role for iron management in canine heart health.
Area of Science:
- Veterinary Cardiology
- Canine Internal Medicine
- Iron Metabolism
Background:
- Cardiac disease is a leading cause of death in dogs.
- Iron deficiency in humans with heart disease worsens symptoms and quality of life, independent of anemia.
- Iron metabolism in dogs with heart disease is poorly understood, often only considered in relation to anemia.
Purpose of the Study:
- To investigate iron metabolism and its regulatory pathways in dogs with cardiac disease.
- To determine if dogs with cardiac disease exhibit an iron-restricted phenotype.
- To assess the relationship between iron handling, inflammation, and cardiac disease severity in dogs.
Main Methods:
- Evaluated hematologic indices, serum iron, iron-binding capacity (TIBC, UIBC), ferritin, hepcidin, ceruloplasmin, C-reactive protein, and albumin in 61 dogs.
- Included healthy controls, dogs with compensated cardiac disease (CCD), and dogs with acute decompensated congestive heart failure (ADCHF).
Main Results:
- Dogs with cardiac disease showed systemic inflammation, reduced hematocrit, increased red blood cell distribution width, and decreased circulating iron.
- Both cardiac groups had reduced total and unsaturated iron-binding capacity (TIBC, UIBC), indicating decreased iron transport.
- Hepcidin levels were lower in CCD dogs and not elevated in ADCHF dogs, suggesting atypical iron regulation.
- In ADCHF dogs, iron-binding capacity correlated with cardiac remodeling, and inflammation markers linked to iron parameters.
Conclusions:
- Dogs with cardiac disease display systemic inflammation and altered iron metabolism, characterized by reduced iron availability and transport capacity, irrespective of anemia.
- Iron dysregulation in canine cardiac disease appears complex, with hepcidin regulation not following a typical inflammatory pattern.
- Findings suggest a significant interaction between inflammation, iron handling, and cardiac disease severity in dogs, highlighting potential therapeutic targets.
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