缺铁儿童血清hepcidin水平和铁参数。

The Korean Journal of Hematology Pub Date : 2012-12-01 Epub Date: 2012-12-24 DOI:10.5045/kjh.2012.47.4.286
Hyoung Soo Choi, Sang Hoon Song, Jae Hee Lee, Hee-Jin Kim, Hye Ran Yang
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引用次数: 71

摘要

背景:缺铁(ID)和缺铁性贫血(IDA)是儿童常见的营养失调。Hepcidin是肝脏产生的一种肽激素,是全身铁代谢的中枢调节剂。我们评估血清hepcidin水平是否可以诊断儿童ID。方法:59例儿童血清(男23例,女36例;5个月~ 17岁)的患者用ELISA检测hepcidin-25。根据血红蛋白水平和铁参数将患者分为:IDA (N=17)、ID (N=18)和control (N=24)。结果:血清hepcidin、铁蛋白、可溶性转铁蛋白受体(sTfR)、转铁蛋白饱和度、血红蛋白水平在两组间差异显著(p)。结论:血清hepcidin水平与铁状态有显著相关性,可作为ID的一个有用指标。需要进一步的研究来验证这些发现并确定儿童的可靠临界值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Serum hepcidin levels and iron parameters in children with iron deficiency.

Background: Iron deficiency (ID) and iron deficiency anemia (IDA) are common nutritional disorders in children. Hepcidin, a peptide hormone produced in the liver, is a central regulator of systemic iron metabolism. We evaluated whether serum hepcidin levels can diagnose ID in children.

Methods: Sera from 59 children (23 males and 36 females; 5 months to 17 years) were analyzed for hepcidin-25 by ELISA. Patients were classified according to hemoglobin level and iron parameters as: IDA, (N=17), ID (N=18), and control (N=24).

Results: Serum hepcidin, ferritin, soluble transferrin receptor (sTfR), transferrin saturation, and hemoglobin levels differed significantly between groups (P<0.0001). Serum hepcidin and ferritin levels (mean±SD) were 2.01±2.30 and 7.00±7.86, 7.72±8.03 and 29.35±24.01, 16.71±14.74 and 46.40±43.57 ng/mL in the IDA, ID, and control groups, respectively. The area under the receiver operating characteristic curve for serum hepcidin as a predictor of ID was 0.852 (95% CI, 0.755-0.950). Hepcidin ≤6.895 ng/mL had a sensitivity of 79.2% and specificity of 82.8% for the diagnosis of ID. Serum hepcidin levels were significantly correlated with ferritin, transferrin saturation, and hemoglobin levels and significantly negatively correlated with sTfR level and total iron binding capacity (P<0.0001).

Conclusion: Serum hepcidin levels are significantly associated with iron status and can be a useful indicator of ID. Further studies are necessary to validate these findings and determine a reliable cutoff value in children.

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