Laboratory diagnosis of iron deficiency: IRON DEFICIENCY ASSESSMENT

Á. Remacha, M. Sardá, M. C. Fernández, M. Murga
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引用次数: 9

Abstract

SUMMARY Worldwide, iron deficiency (ID) is the leading risk factor for disability and mortality, affecting both developing and developed countries with major consequences for human health as well as social and economic development. ID results from any situation in which dietary iron intake does not balance iron demands because of increased iron requirements, limited external supply and/or increased blood loss. In absolute ID, ferritin stores are progressively diminished; the supply of iron to transferrin is compromised, and as a consequence transferrin saturation is decreased. In functional ID (FID), iron stores cannot be mobilized as fast as necessary from the repleted macrophages of the reticuloendothelial system to the bone marrow. This condition is typical of the anemia of chronic diseases (ACD) because of inflammation-induced increased hepcidin levels. Both absolute and functional ID may evolve to ID anemia (IDA). The diagnosis of ACD + IDA remains challenging. In addition to a soluble transferrin receptor (sTfR)/log ferritin ratio > 2, there are several important hematological indices that may help in the diagnosis of absolute ID in ACD, such as the reticulocyte hemoglobin content and the percentage of hypochromic red blood cells. In this paper we review the causes of ID, the different laboratory tests available and how to combine them to establish a correct diagnosis of ID, FID, IDA, ACD and ACD + IDA.
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缺铁的实验室诊断:缺铁评估
在世界范围内,缺铁是导致残疾和死亡的主要风险因素,影响到发展中国家和发达国家,对人类健康以及社会和经济发展造成重大后果。缺铁症是由于铁需求增加、外部供应有限和/或失血增加而导致膳食铁摄入不能平衡铁需求的任何情况引起的。在绝对ID中,铁蛋白储存逐渐减少;铁对转铁蛋白的供应受到损害,因此转铁蛋白饱和度降低。在功能性ID (FID)中,铁储存不能像必要时那样快速地从网状内皮系统的巨噬细胞转移到骨髓。这种情况是典型的慢性疾病(ACD)贫血,因为炎症引起的hepcidin水平升高。绝对ID和功能性ID都可能发展为ID贫血(IDA)。ACD + IDA的诊断仍然具有挑战性。除了可溶性转铁蛋白受体(sTfR)/对数铁蛋白比值bbb2外,还有一些重要的血液学指标可能有助于ACD绝对ID的诊断,如网织红细胞血红蛋白含量和低色红细胞百分比。本文综述了ID的病因,不同的实验室检测方法,以及如何结合它们来建立ID、FID、IDA、ACD和ACD + IDA的正确诊断。
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