The Role of Hepcidin and an Oral Iron Absorption Test in Identifying the Root Cause of Iron-Restricted Anemia (Enter-Iron).

IF 1.7 4区 医学 Q3 HEMATOLOGY
Acta Haematologica Pub Date : 2024-01-01 Epub Date: 2023-11-16 DOI:10.1159/000535275
Roberta Loveikyte, Yascha van den Berg, Andrea Elisabeth van der Meulen-de Jong, Lodewijk Thomas Vlasveld
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引用次数: 0

Abstract

Introduction: Traditional iron parameters often fail to distinguish the cause of iron-restricted anemia in patients without an obvious underlying cause. We evaluated whether an oral iron absorption test (OIAT) and hepcidin measurement could be useful diagnostic tests in these patients.

Methods: We retrospectively analyzed data extracted from medical records of all patients who underwent an OIAT and hepcidin measurement, noting subsequent clinical diagnosis. Δ Iron >15 µmol/L during the OIAT and a hepcidin level below the median (or suppressed ≤0.5 nm) were considered appropriate.

Results: Thirty-nine adult patients were included in the study. Sixteen patients with adequate OIAT had suppressed hepcidin levels indicative of classical iron-deficiency anemia (IDA); 59% of patients had abnormal OIAT. In this group, most patients with low hepcidin levels had anemia associated with abnormalities in the gastrointestinal tract, whereas 83.3% patients with high hepcidin levels had iron-refractory iron-deficiency anemia (IRIDA), confirmed by genetic testing. Finally, transferrin/log ferritin ratio accurately identified patients with suppressed hepcidin: AUC 0.98 [95% CI: 0.95-1.02], p < 0.001.

Conclusion: OIAT differentiates between classical IDA and other types of anemia caused by abnormalities in iron absorption or systemic iron availability. Additionally, elevated hepcidin in patients with oral iron malabsorption could indicate IRIDA.

hepcidin和口服铁吸收试验在确定铁限制性贫血的根本原因中的作用。
在没有明显病因的患者中,传统的铁参数往往不能区分铁限制性贫血的病因。我们评估了口服铁吸收试验(OIAT)和hepcidin测定是否可以作为这些患者有用的诊断试验。方法:我们回顾性分析了所有接受OIAT和hepcidin测量的患者的病历资料,并记录了随后的临床诊断。Δ铁>15µmol/L在OIAT和hepcidin水平低于中位数(或抑制≤0.5 nM)被认为是合适的。结果:39例成人患者纳入研究。16例接受充足OIAT治疗的患者hepcidin水平受到抑制,表明典型缺铁性贫血(IDA);59%的患者OIAT异常。在该组中,大多数hepcidin水平低的患者有与胃肠道异常相关的贫血,而83.3%的hepcidin水平高的患者有铁难治性缺铁性贫血(IRIDA),经基因检测证实。最后,转铁蛋白/对数铁蛋白比值准确识别hepcidin抑制患者:AUC 0.98 [95% CI: 0.95-1.02], P < 0.001。结论:OIAT可区分经典IDA和其他类型的贫血,这些贫血是由铁吸收或全身铁可用性异常引起的。此外,口服铁吸收不良患者的hepcidin升高可能提示IRIDA。
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来源期刊
Acta Haematologica
Acta Haematologica 医学-血液学
CiteScore
4.90
自引率
0.00%
发文量
61
审稿时长
6-12 weeks
期刊介绍: ''Acta Haematologica'' is a well-established and internationally recognized clinically-oriented journal featuring balanced, wide-ranging coverage of current hematology research. A wealth of information on such problems as anemia, leukemia, lymphoma, multiple myeloma, hereditary disorders, blood coagulation, growth factors, hematopoiesis and differentiation is contained in first-rate basic and clinical papers some of which are accompanied by editorial comments by eminent experts. These are supplemented by short state-of-the-art communications, reviews and correspondence as well as occasional special issues devoted to ‘hot topics’ in hematology. These will keep the practicing hematologist well informed of the new developments in the field.
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