Vinnes Erik Wilhelm, Røys Eirik Åsen, Renstrøm Renate, Karlsen Sletten Ida Sofie, Chakraborty Sutirtha
Department of Medical Biochemistry and Pharmacology, Haukeland University Hospital, Bergen, Norway; Department of Clinical Science, University of Bergen, Bergen, Norway.
Department of Medical Biochemistry and Pharmacology, Haukeland University Hospital, Bergen, Norway; Department of Clinical Science, University of Bergen, Bergen, Norway.
Clin Chim Acta. 2025 Jan 30;566:120024. doi: 10.1016/j.cca.2024.120024. Epub 2024 Nov 2.
Total IgE (tIgE) is a frequently requested analyte in patients presenting with symptoms of atopy. Although tIgE has limited clinical utility in the diagnosis of atopic diseases, it is still important that appropriate reference intervals are provided to the intepreting clinician. Concerns have recently been raised whether laboratories may be using outdated tIgE reference intervals. The aim of this study was therefore to perform the first systematic literature review of tIgE reference intervals to aid laboratories in choosing appropriate sources.
A search was performed in MEDLINE, Embase and the Cochrane Library from time of inception to July 2024. Eligible studies had to provide an estimate of paediatric and/or adult tIgE reference intervals using current generation immunoassays. The methodology followed PRISMA guidelines, and the study protocol was registered in the PROSPERO database (CRD42023396441).
A total of 1667 records were screened of which 20 studies remained after full text review. The studies included 23 910 individuals and covered 18 countries. Upper reference limits varied significantly, with participant selection (inclusion or exclusion of in vitro confirmed specific IgE sensitised individuals) and statistical methods identified as the most important factors influencing the upper reference limit.
This review emphasises the need for laboratories to carefully evaluate the participant selection criteria and employed statistical methods whilst determining which tIgE reference intervals are the most appropriate to report to clinicians. Further efforts must also be made to harmonise and improve the reporting of tIgE reference interval studies.
总免疫球蛋白E(tIgE)是有特应性症状患者常被检测的分析物。尽管tIgE在特应性疾病诊断中的临床应用有限,但为解读临床医生提供适当的参考区间仍然很重要。最近有人担心实验室是否在使用过时的tIgE参考区间。因此,本研究的目的是首次对tIgE参考区间进行系统的文献综述,以帮助实验室选择合适的来源。
从数据库建立至2024年7月在MEDLINE、Embase和Cochrane图书馆进行检索。符合条件的研究必须使用当代免疫测定法提供儿科和/或成人tIgE参考区间的估计值。方法遵循PRISMA指南,研究方案已在PROSPERO数据库(CRD42023396441)中注册。
共筛选了1667条记录,经过全文审查后保留了20项研究。这些研究包括23910名个体,覆盖18个国家。参考上限差异显著,参与者选择(纳入或排除体外确认的特异性IgE致敏个体)和统计方法被确定为影响参考上限的最重要因素。
本综述强调实验室在确定向临床医生报告的最合适的tIgE参考区间时,需要仔细评估参与者选择标准和所采用的统计方法。还必须进一步努力协调和改进tIgE参考区间研究的报告。