The origin of ferritin reference intervals: a systematic review.

IF 15.4 1区 医学 Q1 HEMATOLOGY
Judy Truong, Kanza Naveed, Daniel Beriault, David Lightfoot, Michael Fralick, Michelle Sholzberg
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引用次数: 0

Abstract

Iron deficiency is a highly prevalent condition, which contributes to unnecessary morbidity, mortality, and health inequity. A serum ferritin concentration of less than 30 μg/L has a high specificity and sensitivity for diagnosing iron deficiency in adults, but the laboratory reported lower limit of normal (LLN) is typically lower. These LLNs might not be rooted in rigorous scientific evidence and might be contributing to structural underdiagnosis of iron deficiency. A systematic review was done per systematic reviews and meta-analysis guidelines with the use of medical literature databases from inception of each database to Nov 30, 2021, to identify studies that determined ferritin reference intervals in healthy adults and grey literature search for the five most common ferritin assays (registration number CRD42022268844). The objectives were to systematically summarise the ferritin reference intervals and to do a methodological quality assessment of the included studies. 2306 studies were screened and 61 full texts were included. 37 studies were eligible for analysis of the ferritin LLN in the general population. The population the sample was comprised of was a total of 21 882 females and 23 650 males participants. The ferritin LLN was a median of 8 μg/L (IQR 5-15) and mean of 9 μg/L (SD 11) in females and a median of 25 μg/L (IQR 16-44) and mean of 25 μg/L (SD 29) in males. 30 (49%) of 61 studies did not explicitly screen for patients at risk of iron deficiency, and 32 (52%) did not refer to a reference interval establishment guideline (eg, guideline recommended by Clinical and Laboratory Standards Institute). The five most used commercial ferritin laboratory assays reported reference intervals with a median LLN of 11 (IQR 9-12) and mean of 9 μg/L (SD 4) for females and median of 22 (IQR 22-24) and mean of 23 μg/L (SD 4) for males. In the literature, serum ferritin reference intervals in healthy adults consistently report a LLN of less than 30 μg/L. Data driving these ferritin reference intervals are at high risk of bias, given no exclusion of individuals at risk for iron deficiency in the presumed normal population sample and no adherence to reference interval establishment standards. We suggest the use of evidence-based laboratory clinical decision limits to diagnose iron deficiency.

铁蛋白参考区间的起源:系统综述。
缺铁是一种高发疾病,会导致不必要的发病率、死亡率和健康不公平。血清铁蛋白浓度低于 30 μg/L 对诊断成人铁缺乏症具有较高的特异性和敏感性,但实验室报告的正常值下限(LLN)通常更低。这些正常值下限可能没有严格的科学依据,可能会导致铁缺乏症的结构性诊断不足。根据系统综述和荟萃分析指南,我们使用医学文献数据库进行了系统综述,从每个数据库开始到 2021 年 11 月 30 日,以确定健康成人铁蛋白参考区间的研究,并对五种最常见的铁蛋白测定进行了灰色文献检索(注册号 CRD42022268844)。目的是系统总结铁蛋白参考区间,并对纳入的研究进行方法学质量评估。共筛选了 2306 项研究,并纳入了 61 篇全文。37 项研究符合分析普通人群铁蛋白 LLN 的条件。样本人群包括 21 882 名女性和 23 650 名男性参与者。女性铁蛋白 LLN 的中位数为 8 μg/L(IQR 5-15),平均值为 9 μg/L(SD 11);男性铁蛋白 LLN 的中位数为 25 μg/L(IQR 16-44),平均值为 25 μg/L(SD 29)。61 项研究中有 30 项(49%)未明确筛查缺铁风险患者,32 项(52%)未参考参考区间建立指南(如临床和实验室标准协会推荐的指南)。五种最常用的商业铁蛋白实验室测定报告的参考区间为:女性 LLN 中位数为 11(IQR 9-12),平均值为 9 μg/L(SD 4);男性 LLN 中位数为 22(IQR 22-24),平均值为 23 μg/L(SD 4)。在文献中,健康成人的血清铁蛋白参考区间一致报告为 LLN 小于 30 μg/L。由于在假定的正常人群样本中没有排除缺铁风险个体,也没有遵守参考区间建立标准,因此这些铁蛋白参考区间的数据存在很大的偏差风险。我们建议使用循证实验室临床决策限制来诊断铁缺乏症。
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
Lancet Haematology
Lancet Haematology HEMATOLOGY-
CiteScore
26.00
自引率
0.80%
发文量
323
期刊介绍: Launched in autumn 2014, The Lancet Haematology is part of the Lancet specialty journals, exclusively available online. This monthly journal is committed to publishing original research that not only sheds light on haematological clinical practice but also advocates for change within the field. Aligned with the Lancet journals' tradition of high-impact research, The Lancet Haematology aspires to achieve a similar standing and reputation within its discipline. It upholds the rigorous reporting standards characteristic of all Lancet titles, ensuring a consistent commitment to quality in its contributions to the field of haematology.
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