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Iron Homeostasis and Hepcidin Concentration in Patients With Acromegaly

Hepcidin is a protein responsible for maintaining iron (Fe) homeostasis. Data regarding the role of hepcidin in the pathomechanism of Fe balance disturbances associated with acromegaly (AG) are scarce. The aim of the study was to assess the impact of alterations in complete blood count parameters, F...

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Autores principales: Krygier, Aleksandra, Szczepanek-Parulska, Ewelina, Cieślewicz, Maja, Wrotkowska, Elżbieta, Chanaj-Kaczmarek, Justyna, Ruchała, Marek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8863047/
https://www.ncbi.nlm.nih.gov/pubmed/35211089
http://dx.doi.org/10.3389/fendo.2021.788247
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author Krygier, Aleksandra
Szczepanek-Parulska, Ewelina
Cieślewicz, Maja
Wrotkowska, Elżbieta
Chanaj-Kaczmarek, Justyna
Ruchała, Marek
author_facet Krygier, Aleksandra
Szczepanek-Parulska, Ewelina
Cieślewicz, Maja
Wrotkowska, Elżbieta
Chanaj-Kaczmarek, Justyna
Ruchała, Marek
author_sort Krygier, Aleksandra
collection PubMed
description Hepcidin is a protein responsible for maintaining iron (Fe) homeostasis. Data regarding the role of hepcidin in the pathomechanism of Fe balance disturbances associated with acromegaly (AG) are scarce. The aim of the study was to assess the impact of alterations in complete blood count parameters, Fe homeostasis, gonadal status and GH/IGF-1 on the level of hepcidin in AG patients. The study evaluated the differences in hepcidin concentration and iron homeostasis between patients newly diagnosed with AG in comparison to healthy control subjects (CS). We prospectively enrolled 25 adult patients newly diagnosed with AG and 25 healthy volunteers who served as CS. The level of hepcidin was measured using the Hepcidin 25 (bioactive) hs ELISA, which is a highly sensitive enzyme immunoassay for the quantitative in vitro diagnostic measurement (DRG Instruments GmbH, Germany). The median of hepcidin concentration in the serum of patients with AG was significantly lower 9.8 (6.2–18.2) ng/ml as compared to CS 21.3 (14.3–34.0) ng/ml (p = 0.003). In the AG group, a statistically significant negative correlation between hepcidin and IGF-1 (rho = −0.441) was observed. Our study demonstrated a decreased hepcidin level in AG patients in comparison to CS what may have a potentially protective effect against anemia through an increased bioavailability of Fe. Additionally, GH may have a positive direct or indirect effect on erythropoiesis. Further studies on larger patient groups are necessary in order to clarify the exact role of hepcidin in the regulation of erythropoiesis in the excess of GH/IGF-1.
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spelling pubmed-88630472022-02-23 Iron Homeostasis and Hepcidin Concentration in Patients With Acromegaly Krygier, Aleksandra Szczepanek-Parulska, Ewelina Cieślewicz, Maja Wrotkowska, Elżbieta Chanaj-Kaczmarek, Justyna Ruchała, Marek Front Endocrinol (Lausanne) Endocrinology Hepcidin is a protein responsible for maintaining iron (Fe) homeostasis. Data regarding the role of hepcidin in the pathomechanism of Fe balance disturbances associated with acromegaly (AG) are scarce. The aim of the study was to assess the impact of alterations in complete blood count parameters, Fe homeostasis, gonadal status and GH/IGF-1 on the level of hepcidin in AG patients. The study evaluated the differences in hepcidin concentration and iron homeostasis between patients newly diagnosed with AG in comparison to healthy control subjects (CS). We prospectively enrolled 25 adult patients newly diagnosed with AG and 25 healthy volunteers who served as CS. The level of hepcidin was measured using the Hepcidin 25 (bioactive) hs ELISA, which is a highly sensitive enzyme immunoassay for the quantitative in vitro diagnostic measurement (DRG Instruments GmbH, Germany). The median of hepcidin concentration in the serum of patients with AG was significantly lower 9.8 (6.2–18.2) ng/ml as compared to CS 21.3 (14.3–34.0) ng/ml (p = 0.003). In the AG group, a statistically significant negative correlation between hepcidin and IGF-1 (rho = −0.441) was observed. Our study demonstrated a decreased hepcidin level in AG patients in comparison to CS what may have a potentially protective effect against anemia through an increased bioavailability of Fe. Additionally, GH may have a positive direct or indirect effect on erythropoiesis. Further studies on larger patient groups are necessary in order to clarify the exact role of hepcidin in the regulation of erythropoiesis in the excess of GH/IGF-1. Frontiers Media S.A. 2022-02-08 /pmc/articles/PMC8863047/ /pubmed/35211089 http://dx.doi.org/10.3389/fendo.2021.788247 Text en Copyright © 2022 Krygier, Szczepanek-Parulska, Cieślewicz, Wrotkowska, Chanaj-Kaczmarek and Ruchała https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Krygier, Aleksandra
Szczepanek-Parulska, Ewelina
Cieślewicz, Maja
Wrotkowska, Elżbieta
Chanaj-Kaczmarek, Justyna
Ruchała, Marek
Iron Homeostasis and Hepcidin Concentration in Patients With Acromegaly
title Iron Homeostasis and Hepcidin Concentration in Patients With Acromegaly
title_full Iron Homeostasis and Hepcidin Concentration in Patients With Acromegaly
title_fullStr Iron Homeostasis and Hepcidin Concentration in Patients With Acromegaly
title_full_unstemmed Iron Homeostasis and Hepcidin Concentration in Patients With Acromegaly
title_short Iron Homeostasis and Hepcidin Concentration in Patients With Acromegaly
title_sort iron homeostasis and hepcidin concentration in patients with acromegaly
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8863047/
https://www.ncbi.nlm.nih.gov/pubmed/35211089
http://dx.doi.org/10.3389/fendo.2021.788247
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