Diagnostic utility of zinc protoporphyrin to detect iron deficiency in Kenyan preschool children: a community-based survey.

Q2 Medicine
BMC Hematology Pub Date : 2017-07-27 eCollection Date: 2017-01-01 DOI:10.1186/s12878-017-0082-z
Emily M Teshome, Andrew M Prentice, Ayşe Y Demir, Pauline E A Andang'o, Hans Verhoef
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引用次数: 11

Abstract

Background: Zinc protoporphyrin (ZPP) has been used to screen and manage iron deficiency in individual children, but it has also been recommended to assess population iron status. The diagnostic utility of ZPP used in combination with haemoglobin concentration has not been evaluated in pre-school children. We aimed to a) identify factors associated with ZPP in children aged 12-36 months; b) assess the diagnostic performance and utility of ZPP, either alone or in combination with haemoglobin, to detect iron deficiency.

Methods: We used baseline data from 338 Kenyan children enrolled in a community-based randomised trial. To identify factors related to ZZP measured in whole blood or erythrocytes, we used bivariate and multiple linear regression analysis. To assess diagnostic performance, we excluded children with elevated plasma concentrations of C-reactive protein or α1-acid glycoprotein, and with Plasmodium infection, and we analysed receiver operating characteristics (ROC) curves, with iron deficiency defined as plasma ferritin concentration < 12 μg/L. We also developed models to assess the diagnostic utility of ZPP and haemoglobin concentration when used to screen for iron deficiency.

Results: Whole blood ZPP and erythrocyte ZPP were independently associated with haemoglobin concentration, Plasmodium infection and plasma concentrations of soluble transferrin receptor, ferritin, and C-reactive protein. In children without inflammation or Plasmodium infection, the prevalence of true iron deficiency was 32.1%, compared to prevalence of 97.5% and 95.1% when assessed by whole blood ZPP and erythrocyte ZPP with conventional cut-off points (70 μmol/mol and 40 μmol/mol haem, respectively). Addition of whole blood ZPP or erythrocyte ZPP to haemoglobin concentration increased the area-under-the-ROC-curve (84.0%, p = 0.003, and 84.2%, p = 0.001, respectively, versus 62.7%). A diagnostic rule (0.038689 [haemoglobin concentration, g/L] + 0.00694 [whole blood ZPP, μmol/mol haem] >5.93120) correctly ruled out iron deficiency in 37.4%-53.7% of children screened, depending on the true prevalence, with both specificity and negative predictive value ≥90%.

Conclusions: In young children, whole blood ZPP and erythrocyte ZPP have added diagnostic value in detecting iron deficiency compared to haemoglobin concentration alone. A single diagnostic score based on haemoglobin concentration and whole blood ZPP can rule out iron deficiency in a substantial proportion of children screened.

Trial registration: ClinicalTrials.gov NCT02073149 (25 February 2014).

Abstract Image

Abstract Image

原卟啉锌检测肯尼亚学龄前儿童缺铁的诊断效用:一项基于社区的调查。
背景:原卟啉锌(ZPP)已被用于筛查和管理个体儿童缺铁,但也被推荐用于评估人群铁状况。ZPP与血红蛋白浓度联合用于学龄前儿童的诊断效用尚未得到评估。我们的目标是a)确定与12-36个月儿童ZPP相关的因素;b)评估ZPP单独或与血红蛋白联合检测缺铁的诊断性能和效用。方法:我们使用了一项基于社区的随机试验中338名肯尼亚儿童的基线数据。为了确定与全血或红细胞ZZP测量相关的因素,我们使用了双变量和多元线性回归分析。为了评估诊断效果,我们排除了血浆c反应蛋白或α1-酸性糖蛋白浓度升高以及疟原虫感染的儿童,并分析了受试者工作特征(ROC)曲线,将缺铁定义为血浆铁蛋白浓度。全血ZPP和红细胞ZPP与血红蛋白浓度、疟原虫感染和血浆可溶性转铁蛋白受体、铁蛋白和c反应蛋白浓度独立相关。在没有炎症或疟原虫感染的儿童中,真正缺铁的患病率为32.1%,而采用常规截断点(血红素分别为70 μmol/mol和40 μmol/mol)全血和红细胞ZPP评估的患病率分别为97.5%和95.1%。在血红蛋白浓度中加入全血ZPP或红细胞ZPP增加了roc曲线下面积(分别为84.0%,p = 0.003和84.2%,p = 0.001,分别为62.7%)。诊断规则(0.038689[血红蛋白浓度,g/L] + 0.00694[全血ZPP, μmol/mol血红素]>5.93120)在37.4% ~ 53.7%的筛查儿童中正确排除缺铁,根据真实患病率,特异性和阴性预测值均≥90%。结论:在幼儿中,全血ZPP和红细胞ZPP与单独血红蛋白浓度相比,在检测缺铁方面具有更大的诊断价值。基于血红蛋白浓度和全血ZPP的单一诊断评分可以排除大部分筛查儿童的缺铁。试验注册:ClinicalTrials.gov NCT02073149(2014年2月25日)。
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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来源期刊
BMC Hematology
BMC Hematology Medicine-Hematology
CiteScore
4.10
自引率
0.00%
发文量
0
期刊介绍: BMC Hematology is an open access, peer-reviewed journal that considers articles on basic, experimental and clinical research related to hematology. The journal welcomes submissions on non-malignant and malignant hematological diseases, hemostasis and thrombosis, hematopoiesis, stem cells and transplantation.
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