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铁调素和口服铁吸收试验在确定缺铁性贫血(肠源性铁)根本病因中的作用。

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

机构信息

Department of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands.

Department of Gastroenterology and Hepatology, University Medical Center Groningen, Groningen, The Netherlands.

出版信息

Acta Haematol. 2024;147(4):402-412. doi: 10.1159/000535275. Epub 2023 Nov 16.

DOI:10.1159/000535275
PMID:37972576
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11296559/
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.

摘要

简介

传统的铁参数往往无法区分无明显潜在病因的缺铁性贫血患者的病因。我们评估了口服铁吸收试验(OIAT)和铁调素测量是否可以作为这些患者的有用诊断测试。

方法

我们回顾性分析了所有接受 OIAT 和铁调素测量的患者的病历数据,并记录了随后的临床诊断。OIAT 期间Δ铁>15 μmol/L 和铁调素水平低于中位数(或抑制≤0.5 nmol/L)被认为是合适的。

结果

研究纳入 39 名成年患者。16 名 OIAT 充分的患者铁调素水平受到抑制,提示为经典缺铁性贫血(IDA);59%的患者 OIAT 异常。在这组患者中,大多数铁调素水平较低的患者伴有胃肠道异常导致的贫血,而 83.3%铁调素水平较高的患者患有铁难治性缺铁性贫血(IRIDA),通过基因检测得到证实。最后,转铁蛋白/铁蛋白比值准确识别铁调素受抑制的患者:AUC 0.98[95%CI:0.95-1.02],p<0.001。

结论

OIAT 可区分经典 IDA 和由铁吸收或全身铁可用性异常引起的其他类型贫血。此外,口服铁吸收不良患者铁调素升高可能提示 IRIDA。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af00/11296559/840b9ab105e4/aha-2024-0147-0004-535275_F01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af00/11296559/840b9ab105e4/aha-2024-0147-0004-535275_F01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af00/11296559/840b9ab105e4/aha-2024-0147-0004-535275_F01.jpg

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