Related Experiment Video
Updated: Jun 3, 2026

Fecal Glucocorticoid Analysis: Non-invasive Adrenal Monitoring in Equids
Published on: April 25, 2016
Avoiding false-positive adrenal insufficiency diagnoses in children: insights from cortisol kinetics during pediatric
Derya Tepe1, Sirmen Kızılcan Çetin2, İrem Gökdemir1
1Department of Pediatric Endocrinology, Ankara Bilkent City Hospital, Bilkent, Ankara, Turkey.
Insights
The low-dose ACTH stimulation test (LDST) for pediatric adrenal insufficiency can be improved by extending sampling to 45 minutes and using time-specific cortisol thresholds. This reduces misdiagnoses and improves accuracy in diagnosing HPA axis dysfunction.
Area of Science:
- Pediatric Endocrinology
- Endocrinology
- Clinical Chemistry
Background:
- The low-dose ACTH stimulation test (LDST) is standard for assessing pediatric hypothalamic-pituitary-adrenal (HPA) axis function.
- Controversies exist regarding optimal cortisol sampling times and interpretation, potentially leading to false-positive adrenal insufficiency (AI) diagnoses.
Purpose of the Study:
- To characterize peak cortisol response timing during LDST in children without AI.
- To evaluate the diagnostic benefits of extended sampling and time-specific cortisol thresholds.
Main Methods:
- Retrospective analysis of 177 pediatric patients undergoing LDST for suspected central AI.
- Cortisol measurements at baseline, 15, 30, 45, and 60 minutes post-ACTH injection.
- Evaluation of peak timing, predictors, diagnostic contribution of extended points, and false-positive rates.
Main Results:
- Peak cortisol response most frequently occurred at 15 minutes (48.6%), followed by 30 minutes (28.8%).
- Terminating testing at 30 minutes risked misclassifying 11.9% of patients.
- Extending to 45 minutes offered significant diagnostic improvement; extension to 60 minutes yielded marginal benefit.
- Time-specific thresholds reduced false-positive AI diagnoses fivefold at 30 minutes compared to a uniform cutoff.
Conclusions:
- Pediatric LDST cortisol responses exhibit significant interindividual variability in peak timing.
- Extending sampling to 45 minutes and employing time-specific interpretation thresholds enhance diagnostic accuracy.
- These strategies effectively reduce false-positive AI diagnoses in pediatric practice.
Abstract:
The low-dose ACTH stimulation test (LDST) is widely used to evaluate hypothalamic-pituitary-adrenal (HPA) axis function in children; however, optimal cortisol sampling times and interpretation strategies remain controversial. Reliance on early or single time-point measurements may lead to false-positive diagnoses of adrenal insufficiency (AI). The aim of the study is. to characterize the timing of peak cortisol responses during LDST in children without AI and to assess the incremental diagnostic contribution of extended sampling and time-specific cortisol thresholds. We retrospectively analyzed 177 pediatric patients who underwent LDST for suspected central adrenal insufficiency at a single tertiary center. Serum cortisol was measured at baseline and at 15, 30, 45, and 60 min following intravenous administration of 1 µg ACTH. Adrenal sufficiency was defined as a peak cortisol ≥ 18 µg/dL(497 nmol/L). Peak timing distribution, basal predictors, incremental diagnostic contribution of additional time points, number needed to test (NNT), and false-positive rates using fixed versus time-specific cutoffs were evaluated. Peak cortisol occurred most frequently at 15 min (48.6%), followed by 30 min (28.8%), baseline (10.7%), 45 min (9.0%), and 60 min (2.8%). Termination of testing at 30 min would have misclassified 11.9% of patients as insufficient despite normal later responses. Extension to 45 min provided meaningful diagnostic improvement, whereas routine extension to 60 min presented only marginal additional benefit (NNT = 30). Higher basal cortisol levels were independently associated with earlier peak responses (p = 0.021), while demographic and auxological factors showed no association. Application of time-specific, percentile-based cortisol thresholds reduced false-positive classifications nearly fivefold at 30 min compared with a uniform 18 µg/dL cut-off.
Conclusion:
LDST cortisol responses in children show substantial interindividual variability in peak timing. Extension of sampling to 45 min and use of time-specific interpretation thresholds significantly improve diagnostic accuracy and reduce false-positive AI diagnoses in pediatric practice.
What Is Known:
• The low-dose ACTH stimulation test (LDST) is widely used to evaluate HPA axis function in children, but optimalcortisol sampling times and interpretation strategies remain controversial. • Reliance on early or single time-point cortisol measurements can lead to false-positive diagnoses of adrenal in sufficiency.
What Is New:
• Peak cortisol timing varies substantially between children, and terminating the LDST at 30 min would misclassify~12% of patients as insufficient despite normal later responses; higher basal cortisol independently predicts earlier peaks. • Extending sampling to 45 min and applying time-specific, percentile-based cortisol thresholds markedly improve diagnostic accuracy, reducing false-positive classifications nearly fivefold at 30 min compared with a uniform 18μg/dL cut-off.
Related Concept Videos
Cushing Syndrome II: Pathophysiology
Cushing Syndrome I: Introduction
Adrenal Gland Disorders
Adrenal insufficiency, characterized by insufficient cortisol and aldosterone production, leads to conditions like Addison's disease. This disorder, affecting the adrenal cortex, exhibits symptoms such as skin bronzing, dehydration, low blood pressure, fatigue, and weight loss. Congenital adrenal hyperplasia, a genetic ailment causing...
Hormones of the Adrenal Glands
The adrenal cortex, a powerhouse of hormone synthesis, generates over two dozen corticosteroid hormones. The zona glomerulosa produces mineralocorticoids, exemplified by aldosterone, influencing the electrolyte composition of body fluids. The synthesis of glucocorticoids such as cortisol and corticosterone...
Hypothalamic-Pituitary Axis
Pharmacokinetics in Pediatric Patients: Drug Metabolism

