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Comparison of low-dose and high-dose cosyntropin stimulation testing in children
Ayse Pinar Cemeroglu1, Lora Kleis, Daniel C Postellon
1Helen DeVos Children's Hospital, Spectrum Health Medical Group, Michigan State University, Pediatric Endocrinology and Diabetes Clinic, Grand Rapids, Michigan, USA. ayse.cemeroglu@devoschildrens.org
Insights
Low-dose (LD) cosyntropin testing for adrenal insufficiency in children requires cautious interpretation. A lower cut-off of 14 µg/dL for LD testing can help avoid false positives while still identifying impaired hypothalamic-pituitary-adrenal axis function.
Area of Science:
- Pediatric Endocrinology
- Endocrinology
- Adrenal Insufficiency Testing
Background:
- Lack of consensus exists regarding low-dose (LD) versus high-dose (HD) cosyntropin testing for secondary/tertiary adrenal insufficiency in children.
- This study evaluates the efficacy of LD and HD cosyntropin stimulation tests in pediatric patients.
Purpose of the Study:
- To compare LD and HD cosyntropin stimulation testing in children for hypothalamic-pituitary-adrenal axis (HPAA) evaluation.
- To propose a new peak cortisol cut-off value for LD cosyntropin testing to minimize false-positive results.
Main Methods:
- Retrospective analysis of 36 children undergoing LD (1 µg) and HD (249 µg) cosyntropin testing during growth hormone (GH) stimulation tests.
- Patients were divided into two groups: Group A (intact HPAA) and Group B (impaired HPAA or steroid use).
Main Results:
- In children with intact HPAA (Group A), mean peak cortisol was 18.5 ± 2.4 µg/dL for LD and 24.8 ± 3.1 µg/dL for HD testing.
- In children with impaired HPAA (Group B), mean peak cortisol was 15.7 ± 6.1 µg/dL for LD and 21.7 ± 7.9 µg/dL for HD testing.
- Using a standard 18 µg/dL cut-off, 37% of patients with intact HPAA showed a false-positive result with LD testing; a 14 µg/dL cut-off eliminated these false positives.
Conclusions:
- LD cosyntropin stimulation testing requires careful interpretation to prevent unnecessary long-term treatment.
- A lower cut-off value (≥14 µg/dL) for LD cosyntropin testing appears effective in avoiding false positives while still detecting most cases of impaired HPAA in children.
Background:
There is no consensus among pediatric endocrinologists in using low-dose (LD) versus high-dose (HD) cosyntropin to test for secondary/tertiary adrenal insufficiency. This paper compares LD and HD cosyntropin stimulation testing in children for evaluation of hypothalamic-pituitary-adrenal axis (HPAA) and suggests a new peak cortisol cut-off value for LD stimulation testing to avoid false positivity.
Methods:
Data of 36 children receiving LD (1 µg) and HD (249 µg) cosyntropin consecutively during growth hormone (GH) stimulation testing were analyzed in two groups. Group A were patients who passed GH stimulation testing and were not on oral, inhaled or intranasal steroids (intact hypothalamic-pituitary axis, n= 19). Group B were patients who failed GH stimulation testing and/or were on oral, inhaled or intranasal steroids (impaired hypothalamic-pituitary axis, n= 17).
Results:
In group A, the mean peak cortisol response in LD cosyntropin was 18.5 ± 2.4 µg/dL and that for the HD cosyntropin was 24.8 ± 3.1 µg/dL (r: 0.76, P≤ 0.05). In group B, the mean peak cortisol response in LD cosyntropin was 15.7 ± 6.1 µg/dL and that for HD cosyntropin was 21.7 ± 7.9 µg/dL (r: 0.98, P≤ 0.05). When a standard cut-off of 18 µg/dL was used, 37% of the patients with intact HPAA failed LD cosyntropin testing, but a cut-off of 14 µg/dL eliminated false positive results.
Conclusions:
LD cosyntropin stimulation testing results should be interpreted cautiously when used alone to prevent unnecessary long-term treatment. Using a lower cut-off for LD (≥14 µg/dL) seems to avoid false positive results and still detects most cases of impaired HPAA.
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