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使用单克隆 vs. 多克隆皮质醇检测评估肾上腺皮质功能减退的发生率。

Rates of adrenal insufficiency using a monoclonal vs. polyclonal cortisol assay.

机构信息

Department of Pediatrics, Division of Endocrinology, Diabetes, and Metabolism, Washington University School of Medicine/Saint Louis Children's Hospital, Saint Louis, MO, USA.

出版信息

J Pediatr Endocrinol Metab. 2021 Dec 13;35(3):313-317. doi: 10.1515/jpem-2021-0519. Print 2022 Mar 28.

Abstract

OBJECTIVES

The diagnosis of adrenal insufficiency relies on clear cut-offs and accurate measurement of cortisol levels. Newer monoclonal antibody assays may increase the rate of diagnosis of adrenal insufficiency if traditional cortisol cut-off levels <18 mcg/dL (500 nmol/L) are applied. We aimed to determine if the rate of diagnosis of adrenal insufficiency using a 1 mcg Cosyntropin stimulation test varied with the change in cortisol assay from a polyclonal to a monoclonal antibody assay.

METHODS

Cortisol levels obtained during the 1 mcg Cosyntropin stimulation test performed in the last semester of 2016 using a polyclonal antibody cortisol assay were compared to tests performed using a monoclonal antibody cortisol assay during the first semester of 2017. Cosyntropin tests included cortisol values obtained at baseline, 20 min and 30 min after IV administration of 1 mcg Cosyntropin. Peak cortisol cut-off value <18 mcg/dL was used to diagnose adrenal insufficiency.

RESULTS

Stimulated cortisol values after 1 mcg Cosyntropin using the monoclonal assay in 2017 (n=38) were significantly lower (33%) compared to those obtained with the polyclonal assay in 2016 (n=27) (p-value <0.001). The number of passing tests with a peak cortisol value >18 mcg/dL fell from 74% in 2016 (20 out of 27 tests) to 29% in 2017 (11 out of 38 tests).

CONCLUSIONS

The change in cortisol assay substantially increased the number of patients diagnosed with adrenal insufficiency after 1 mcg Cosyntropin stimulation testing. Standardization of cortisol assays and diagnostic criteria is critical for the accurate diagnosis of adrenal insufficiency.

摘要

目的

肾上腺功能不全的诊断依赖于明确的分界值和皮质醇水平的准确测量。如果应用传统的皮质醇界值<18μg/dL(500nmol/L),新型单克隆抗体检测可能会增加肾上腺功能不全的诊断率。我们旨在确定在使用 1μg 促皮质素兴奋试验时,使用单克隆抗体检测皮质醇替代多克隆抗体检测时,肾上腺功能不全的诊断率是否会发生变化。

方法

比较了 2016 年下半年使用多克隆抗体皮质醇检测进行的 1μg 促皮质素兴奋试验和 2017 年上半年使用单克隆抗体皮质醇检测进行的试验。促皮质素试验包括静脉注射 1μg 促皮质素后基线、20 分钟和 30 分钟时获得的皮质醇值。<18μg/dL 的峰值皮质醇界值用于诊断肾上腺功能不全。

结果

2017 年使用单克隆检测的 1μg 促皮质素后,刺激皮质醇值(n=38)明显低于 2016 年多克隆检测(n=27)(p 值<0.001)。皮质醇值>18μg/dL 的通过测试的数量从 2016 年的 74%(27 次试验中有 20 次通过)降至 2017 年的 29%(38 次试验中有 11 次通过)。

结论

皮质醇检测的改变大大增加了使用 1μg 促皮质素兴奋试验诊断肾上腺功能不全的患者数量。皮质醇检测和诊断标准的标准化对于准确诊断肾上腺功能不全至关重要。

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