Study reveals elevated hepcidin levels in dogs with portosystemic shunt, indicating potential links to microcytosis.
Microcytosis and iron sequestration are commonly observed abnormalities in dogs with portosystemic shunt (PSS). The role of hepcidin - the main hormone regulating iron homeostasis - in this condition is still unclear. Our study is intended to determine the serum concentrations of known hepcidin isomers in canine patients with portosystemic shunt, compared to a healthy control group. Routine haematological and biochemical examinations were performed for 10 dogs diagnosed with PSS and for 18 healthy controls. And the serum concentrations of hepcidin-α and hepcidin-β isomers were determined by liquid chromatography-tandem mass spectrometry (LC/MS-MS) method. In this study, both serum hepcidin isomer concentrations were significantly (p < 0,05) higher in the PSS group compared to healthy dogs (hepcidin-α: 46.1 vs. 23.1 ng·mL-1, p = 0.014, hepcidin-β: 76.6 vs 48.4 ng·mL-1, p = 0.027). In dogs with PSS, there was a significant negative correlation between iron and hepcidin isomer concentrations (hepcidin-α: rho: -0.81, p = 0.007, hepcidin-β rho: -0.84, p = 0.0004). Our results suggest that elevated serum hepcidin concentration plays an important role in the development of microcytosis and iron sequestration observed in patients with PSS; however, further studies needed in large cohort of patients. Serum hepcidin could be used as a potential biomarker in patients with PSS-associated anaemia.
No takes yet. Share an insight, caveat, or question.
Vizi et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: