2020
DOI: 10.1007/s10620-020-06652-1
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Importance of Hepcidin in the Etiopathogenesis of Anemia in Inflammatory Bowel Disease

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Cited by 4 publications
(7 citation statements)
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“…Further, the complement system has emerged as an attractive target for early and upstream intervention in inflammatory diseases [ 33 ]. In addition, there is evidence that anemia decreases immune function and induces inflammatory response [ 34 ]. Based on the above findings, we speculated that the complement system may affect hematopoietic function by regulating immunity and inflammation.…”
Section: Discussionmentioning
confidence: 99%
“…Further, the complement system has emerged as an attractive target for early and upstream intervention in inflammatory diseases [ 33 ]. In addition, there is evidence that anemia decreases immune function and induces inflammatory response [ 34 ]. Based on the above findings, we speculated that the complement system may affect hematopoietic function by regulating immunity and inflammation.…”
Section: Discussionmentioning
confidence: 99%
“…IBD can be associated with both IDA and anemia of chronic disease (ACD), also known as anemia of inflammation (Karaskova et al, 2021).…”
Section: Discussionmentioning
confidence: 99%
“…a) Forest plot shows the weighted mean difference (WMD) in serum hepcidin concentrations between participants with IBD and healthy control participants. (b) Forest plot show the standardized mean difference (SMD) in serum prohepcidin concentrations between participants with IBD and healthy control participants.arises from inflammatory conditions whereby the IL-6-hepcidin axis is triggered, leading to low serum iron levels but maintaining sufficient iron stores(Camaschella et al, 2019;Karaskova et al, 2021; …”
mentioning
confidence: 99%
“…It is indispensable for the metabolism of many substances in the body [ (Dutt et al, 2022); (Stallhofer et al, 2022)]. Iron in the digestive tract is mainly absorbed in the duodenum and upper jejunum in the form of Fe 2+ (Karaskova et al, 2021). Then, in the epithelial cells of small intestinal mucosa, Fe 2+ is oxidized to Fe 3+ , and part of Fe 3+ in the blood is further bound to the transported by transferrin (TF) and receptor (TFR) on the cell membrane and transported into the cell [ (Piskin et al, 2022); (Zhao et al, 2022)], which reacts with the metal reductase Six-transmembrane epithelial antigen of prostate 3 (STEAP3) in the endoplasmic reticulum to form Fe 2+ ; Fe 2+ is transported to cells through transferrin receptor protein 1 (TFR1).…”
Section: Iron Metabolism Affects the Ferroptosismentioning
confidence: 99%