Peak Serum Cortisol Cutoffs to Diagnose Adrenal Insufficiency Across Different Cortisol Assays in Children


Journal

Journal of clinical research in pediatric endocrinology
ISSN: 1308-5735
Titre abrégé: J Clin Res Pediatr Endocrinol
Pays: Turkey
ID NLM: 101519456

Informations de publication

Date de publication:
22 11 2023
Historique:
medline: 28 11 2023
pubmed: 23 5 2023
entrez: 23 5 2023
Statut: ppublish

Résumé

Current peak serum cortisol cutoffs for the diagnosis of adrenal insufficiency (AI) after Cosyntropin stimulation have been established using polyclonal antibody (pAb) immunoassays. However, new and highly specific cortisol monoclonal antibody (mAb) immunoassays are being used more widely, which can potentially yield higher false positive rates. Thus, this study aimed to redefine the biochemical diagnostic cutoff points for AI in children when using a highly specific cortisol mAb immunoassay and liquid chromatography tandem mass spectrometry (LC/MS) to avoid unnecessary steroid use. Cortisol levels from 36 children undergoing 1 mcg Cosyntropin stimulation tests to rule out AI were measured using pAb immunoassay (Roche Elecsys Cortisol I), mAB immunoassay (Roche Elecsys Cortisol II), and LC/MS. Logistic regression was used to predict AI using the pAB as the reference standard. A receiver operator characteristic curve, area under the curve (AUC), sensitivity, specificity, and kappa agreement were also calculated. Using a peak serum cortisol cutoff value of 12.5 μg/dL for the mAb immunoassay provided 99% sensitivity and 94% specificity for diagnosing AI, when compared to the historical pAb immunoassay cutoff of 18 μg/dL (AUC=0.997). Likewise, a cutoff of value of 14 μg/dL using the LC/MS, provided 99% sensitivity and 88% specificity when compared to the pAb immunoassay (AUC=0.995). To prevent overdiagnosis of AI in children undergoing 1 mcg Cosyntropin stimulation test, our data support using a new peak serum cortisol cutoff of 12.5 μg/dL and 14 μg/dL to diagnose AI when using mAb immunoassays and LC/MS in children, respectively.

Identifiants

pubmed: 37218135
doi: 10.4274/jcrpe.galenos.2023.2023-2-3
pmc: PMC10683551
doi:

Substances chimiques

Hydrocortisone WI4X0X7BPJ
Cosyntropin 16960-16-0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

375-379

Subventions

Organisme : NIDDK NIH HHS
ID : P30 DK020579
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002345
Pays : United States

Informations de copyright

©Copyright 2023 by Turkish Society for Pediatric Endocrinology and Diabetes / The Journal of Clinical Research in Pediatric Endocrinology published by Galenos Publishing House.

Déclaration de conflit d'intérêts

Conflict of interest: None declared

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Auteurs

Samuel Cortez (S)

Washington University School of Medicine; St. Louis Children’s Hospital, Department of Pediatrics, Division of Endocrinology, Diabetes, and Metabolism, Missouri, USA

Ana Maria Arbeláez (AM)

Washington University School of Medicine; St. Louis Children’s Hospital, Department of Pediatrics, Division of Endocrinology, Diabetes, and Metabolism, Missouri, USA

Michael Wallendorf (M)

Washington University in St. Louis, Clinic of Biostatistics, Missouri, USA

Kyle McNerney (K)

Washington University School of Medicine; St. Louis Children’s Hospital, Department of Pediatrics, Division of Endocrinology, Diabetes, and Metabolism, Missouri, USA

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Classifications MeSH