| Literature DB >> 33673530 |
Marleena Repo1,2, Markus Hannula3, Juha Taavela4, Jari Hyttinen3, Jorma Isola5, Pauliina Hiltunen1, Alina Popp6, Katri Kaukinen2,7, Kalle Kurppa1,8, Katri Lindfors2.
Abstract
Anemia is a frequent finding in children with celiac disease but the detailed pathophysiological mechanisms in the intestine remain obscure. One possible explanation could be an abnormal expression of duodenal iron transport proteins. However, the results have so far been inconsistent. We investigated this issue by comparing immunohistochemical stainings of duodenal cytochrome B (DCYTB), divalent metal transporter 1 (DMT1), ferroportin, hephaestin and transferrin receptor 1 (TfR1) in duodenal biopsies between 27 children with celiac disease and duodenal atrophy, 10 celiac autoantibody-positive children with potential celiac disease and six autoantibody-negative control children. Twenty out of these 43 subjects had anemia. The expressions of the iron proteins were investigated with regard to saturation and the percentage of the stained area or stained membrane length of the enterocytes. The results showed the stained area of ferroportin to be increased and the saturation of hephaestin to be decreased in celiac disease patients compared with controls. There were no differences in the transporter protein expressions between anemic and non-anemic patients. The present results suggest an iron status-independent alteration of ferroportin and hephaestin proteins in children with histologically confirmed celiac disease.Entities:
Keywords: anemia; celiac disease; iron transporter
Year: 2021 PMID: 33673530 PMCID: PMC7997288 DOI: 10.3390/nu13030776
Source DB: PubMed Journal: Nutrients ISSN: 2072-6643 Impact factor: 5.717