Literature DB >> 29174474

Iron overload in hematological disorders.

Eitan Fibach1, Eliezer A Rachmilewitz2.   

Abstract

While most common symptom of impairment of iron homeostasis is iron deficiency anemia, some hematological disorders are associated with iron overload (IO). These disorders are related mainly to chronic severe hemolytic anemia, where red blood cells (RBC) or their precursors are destroyed prematurely (hemolyzed), leading to anemia that cannot be compensated by increased production of new RBC. In such cases, IO is mainly due to repeated RBC transfusions and/or increased uptake of iron in the gastrointestinal tract. Normally, iron is present in the plasma and in the cells bound to compounds that render it redox inactive. Iron overload leaves a fraction of the iron free (labile iron pool) and redox active, leading to the generation of excess free radicals such as the reactive oxygen species. This condition upsets the cellular redox balance between oxidants and antioxidants, leading to oxidative stress. The free radicals bind to various cellular components, thereby becoming toxic to vital organs. Oxidative stress may also affect blood cells, such as RBC, platelets and neutrophils, exacerbating the anemia, and causing recurrent infections and thrombotic events, respectively. The toxic effect of IO can be decreased by treating the patients with iron chelators that enter cells, bind free iron and remove it from the body through the urine and feces. Iron toxicity may be also ameliorated by treatment with anti-oxidants that scavenge free radicals and/or correct their damage. The use of iron chelators is widely accepted when started in young patients with severe chronic anemia, but is still debatable as a therapeutic modality for older patients suffering from IO due to myelodysplastic syndromes. It should be noted that in addition to preventing iron toxicity, some compounds with iron chelator activity may also benefit other aspects of hematological disorders. These aspects include stimulation of platelet production, inhibition of leukemic cell proliferation and induction of their differentiation. Compounds with such multiple activities may prove beneficial for at least some patients with leukemia and myelodysplastic syndromes.
Copyright © 2017 Elsevier Masson SAS. All rights reserved.

Entities:  

Mesh:

Year:  2017        PMID: 29174474     DOI: 10.1016/j.lpm.2017.10.007

Source DB:  PubMed          Journal:  Presse Med        ISSN: 0755-4982            Impact factor:   1.228


  16 in total

1.  A Genome-Wide Association Study Identifies Blood Disorder-Related Variants Influencing Hemoglobin A1c With Implications for Glycemic Status in U.S. Hispanics/Latinos.

Authors:  Jee-Young Moon; Tin L Louie; Deepti Jain; Tamar Sofer; Claudia Schurmann; Jennifer E Below; Chao-Qiang Lai; M Larissa Aviles-Santa; Gregory A Talavera; Caren E Smith; Lauren E Petty; Erwin P Bottinger; Yii-Der Ida Chen; Kent D Taylor; Martha L Daviglus; Jianwen Cai; Tao Wang; Katherine L Tucker; José M Ordovás; Craig L Hanis; Ruth J F Loos; Neil Schneiderman; Jerome I Rotter; Robert C Kaplan; Qibin Qi
Journal:  Diabetes Care       Date:  2019-06-18       Impact factor: 19.112

Review 2.  Oxidative Stress in β-Thalassemia.

Authors:  Eitan Fibach; Mutaz Dana
Journal:  Mol Diagn Ther       Date:  2019-04       Impact factor: 4.074

3.  Iron chelating properties of Eltrombopag: Investigating its role in thalassemia-induced osteoporosis.

Authors:  Francesca Punzo; Chiara Tortora; Maura Argenziano; Maddalena Casale; Silverio Perrotta; Francesca Rossi
Journal:  PLoS One       Date:  2018-12-03       Impact factor: 3.240

4.  Excessive Reactive Iron Impairs Hematopoiesis by Affecting Both Immature Hematopoietic Cells and Stromal Cells.

Authors:  Hirokazu Tanaka; J Luis Espinoza; Ryosuke Fujiwara; Shinya Rai; Yasuyoshi Morita; Takashi Ashida; Yuzuru Kanakura; Itaru Matsumura
Journal:  Cells       Date:  2019-03-08       Impact factor: 6.600

Review 5.  Erythropoiesis In Vitro-A Research and Therapeutic Tool in Thalassemia.

Authors:  Eitan Fibach
Journal:  J Clin Med       Date:  2019-12-02       Impact factor: 4.241

Review 6.  Role of Heme Oxygenase as a Modulator of Heme-Mediated Pathways.

Authors:  J Catharina Duvigneau; Harald Esterbauer; Andrey V Kozlov
Journal:  Antioxidants (Basel)       Date:  2019-10-11

Review 7.  Pathophysiology and treatment of patients with beta-thalassemia - an update.

Authors:  Eitan Fibach; Eliezer A Rachmilewitz
Journal:  F1000Res       Date:  2017-12-20

8.  α-Lipoic Acid Reduces Iron-induced Toxicity and Oxidative Stress in a Model of Iron Overload.

Authors:  Giuseppina Camiolo; Daniele Tibullo; Cesarina Giallongo; Alessandra Romano; Nunziatina L Parrinello; Giuseppe Musumeci; Michelino Di Rosa; Nunzio Vicario; Maria V Brundo; Francesco Amenta; Margherita Ferrante; Chiara Copat; Roberto Avola; Giovanni Li Volti; Antonio Salvaggio; Francesco Di Raimondo; Giuseppe A Palumbo
Journal:  Int J Mol Sci       Date:  2019-01-31       Impact factor: 5.923

9.  Reactive oxygen species, glutathione, and vitamin E concentrations in dogs with hemolytic or nonhemolytic anemia.

Authors:  Andrew D Woolcock; Priscila B S Serpa; Andrea P Santos; John A Christian; George E Moore
Journal:  J Vet Intern Med       Date:  2020-10-13       Impact factor: 3.333

Review 10.  The Role of Fe, Zn, and Cu in Pregnancy.

Authors:  Konrad Grzeszczak; Sebastian Kwiatkowski; Danuta Kosik-Bogacka
Journal:  Biomolecules       Date:  2020-08-12
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.