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红细胞生成与铁稳态的相互作用在罕见遗传性贫血中的作用:打破平衡。

The Interplay between Drivers of Erythropoiesis and Iron Homeostasis in Rare Hereditary Anemias: Tipping the Balance.

机构信息

Department of Clinical Chemistry and Haematology, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands.

Van Creveldkliniek, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands.

出版信息

Int J Mol Sci. 2021 Feb 23;22(4):2204. doi: 10.3390/ijms22042204.

Abstract

Rare hereditary anemias (RHA) represent a group of disorders characterized by either impaired production of erythrocytes or decreased survival (i.e., hemolysis). In RHA, the regulation of iron metabolism and erythropoiesis is often disturbed, leading to iron overload or worsening of chronic anemia due to unavailability of iron for erythropoiesis. Whereas iron overload generally is a well-recognized complication in patients requiring regular blood transfusions, it is also a significant problem in a large proportion of patients with RHA that are not transfusion dependent. This indicates that RHA share disease-specific defects in erythroid development that are linked to intrinsic defects in iron metabolism. In this review, we discuss the key regulators involved in the interplay between iron and erythropoiesis and their importance in the spectrum of RHA.

摘要

罕见遗传性贫血症(RHA)是一组以红细胞生成受损或寿命缩短(即溶血)为特征的疾病。在 RHA 中,铁代谢和红细胞生成的调节通常会受到干扰,导致铁过载或由于缺乏用于红细胞生成的铁而导致慢性贫血恶化。虽然铁过载通常是需要定期输血的患者的一种公认并发症,但在很大一部分非输血依赖的 RHA 患者中也是一个严重问题。这表明 RHA 在红细胞生成方面存在特定于疾病的缺陷,这些缺陷与铁代谢的内在缺陷有关。在这篇综述中,我们讨论了铁与红细胞生成相互作用中涉及的关键调节剂及其在 RHA 谱中的重要性。

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