Duodenal expression of iron transport molecules in patients with hereditary hemochromatosis or iron deficiency

Disturbances of iron metabolism are observed in chronic liver diseases. In the present study, we examined gene expression of duodenal iron transport molecules and hepcidin in patients with hereditary hemochromatosis (HHC) (treated and untreated), involving various genotypes (genotypes which represen...

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Main Authors: Dostalikova-Cimburova, Marketa, Kratka, Karolina, Balusikova, Kamila, Chmelikova, Jitka, Hejda, Vaclav, Hnanicek, Jan, Neubauerova, Jitka, Vranova, Jana, Kovar, Jan, Horak, Jiri
Format: Online
Language:English
Published: Blackwell Publishing Ltd 2012
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822694/
id pubmed-3822694
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spelling pubmed-38226942015-03-27 Duodenal expression of iron transport molecules in patients with hereditary hemochromatosis or iron deficiency Dostalikova-Cimburova, Marketa Kratka, Karolina Balusikova, Kamila Chmelikova, Jitka Hejda, Vaclav Hnanicek, Jan Neubauerova, Jitka Vranova, Jana Kovar, Jan Horak, Jiri Original Articles Disturbances of iron metabolism are observed in chronic liver diseases. In the present study, we examined gene expression of duodenal iron transport molecules and hepcidin in patients with hereditary hemochromatosis (HHC) (treated and untreated), involving various genotypes (genotypes which represent risk for HHC were examined), and in patients with iron deficiency anaemia (IDA). Gene expressions of DMT1, ferroportin, Dcytb, hephaestin, HFE and TFR1 were measured in duodenal biopsies using real-time PCR and Western blot. Serum hepcidin levels were measured using ELISA. DMT1, ferroportin and TFR1 mRNA levels were significantly increased in post-phlebotomized hemochromatics relative to controls. mRNAs of all tested molecules were significantly increased in patients with IDA compared to controls. The protein expression of ferroportin was increased in both groups of patients but not significantly. Spearman rank correlations showed that DMT1 versus ferroportin, Dcytb versus hephaestin and DMT1 versus TFR1 mRNAs were positively correlated regardless of the underlying cause, similarly to protein levels of ferroportin versus Dcytb and ferroportin versus hephaestin. Serum ferritin was negatively correlated with DMT1 mRNA in investigated groups of patients, except for HHC group. A decrease of serum hepcidin was observed in IDA patients, but this was not statistically significant. Our data showed that although untreated HHC patients do not have increased mRNA levels of iron transport molecules when compared to normal subjects, the expression is relatively increased in relation to body iron stores. On the other hand, post-phlebotomized HHC patients had increased DMT1 and ferroportin mRNA levels possibly due to stimulated erythropoiesis after phlebotomy. Blackwell Publishing Ltd 2012-08 2012-07-29 /pmc/articles/PMC3822694/ /pubmed/21973163 http://dx.doi.org/10.1111/j.1582-4934.2011.01458.x Text en Copyright © 2012 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Dostalikova-Cimburova, Marketa
Kratka, Karolina
Balusikova, Kamila
Chmelikova, Jitka
Hejda, Vaclav
Hnanicek, Jan
Neubauerova, Jitka
Vranova, Jana
Kovar, Jan
Horak, Jiri
spellingShingle Dostalikova-Cimburova, Marketa
Kratka, Karolina
Balusikova, Kamila
Chmelikova, Jitka
Hejda, Vaclav
Hnanicek, Jan
Neubauerova, Jitka
Vranova, Jana
Kovar, Jan
Horak, Jiri
Duodenal expression of iron transport molecules in patients with hereditary hemochromatosis or iron deficiency
author_facet Dostalikova-Cimburova, Marketa
Kratka, Karolina
Balusikova, Kamila
Chmelikova, Jitka
Hejda, Vaclav
Hnanicek, Jan
Neubauerova, Jitka
Vranova, Jana
Kovar, Jan
Horak, Jiri
author_sort Dostalikova-Cimburova, Marketa
title Duodenal expression of iron transport molecules in patients with hereditary hemochromatosis or iron deficiency
title_short Duodenal expression of iron transport molecules in patients with hereditary hemochromatosis or iron deficiency
title_full Duodenal expression of iron transport molecules in patients with hereditary hemochromatosis or iron deficiency
title_fullStr Duodenal expression of iron transport molecules in patients with hereditary hemochromatosis or iron deficiency
title_full_unstemmed Duodenal expression of iron transport molecules in patients with hereditary hemochromatosis or iron deficiency
title_sort duodenal expression of iron transport molecules in patients with hereditary hemochromatosis or iron deficiency
description Disturbances of iron metabolism are observed in chronic liver diseases. In the present study, we examined gene expression of duodenal iron transport molecules and hepcidin in patients with hereditary hemochromatosis (HHC) (treated and untreated), involving various genotypes (genotypes which represent risk for HHC were examined), and in patients with iron deficiency anaemia (IDA). Gene expressions of DMT1, ferroportin, Dcytb, hephaestin, HFE and TFR1 were measured in duodenal biopsies using real-time PCR and Western blot. Serum hepcidin levels were measured using ELISA. DMT1, ferroportin and TFR1 mRNA levels were significantly increased in post-phlebotomized hemochromatics relative to controls. mRNAs of all tested molecules were significantly increased in patients with IDA compared to controls. The protein expression of ferroportin was increased in both groups of patients but not significantly. Spearman rank correlations showed that DMT1 versus ferroportin, Dcytb versus hephaestin and DMT1 versus TFR1 mRNAs were positively correlated regardless of the underlying cause, similarly to protein levels of ferroportin versus Dcytb and ferroportin versus hephaestin. Serum ferritin was negatively correlated with DMT1 mRNA in investigated groups of patients, except for HHC group. A decrease of serum hepcidin was observed in IDA patients, but this was not statistically significant. Our data showed that although untreated HHC patients do not have increased mRNA levels of iron transport molecules when compared to normal subjects, the expression is relatively increased in relation to body iron stores. On the other hand, post-phlebotomized HHC patients had increased DMT1 and ferroportin mRNA levels possibly due to stimulated erythropoiesis after phlebotomy.
publisher Blackwell Publishing Ltd
publishDate 2012
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822694/
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