Context: Cortisol secretion is related to ACTH concentration by a sigmoidal dose-response curve, in which high ACTH concentrations drive maximal cortisol secretion rates (CSR max). Objective:Wesought to estimate CSR max and free cortisol half-life in healthyhumans(n-21) using numerical methods applied to data acquired during cosyntropin (250 μg) stimulation. We also evaluated the effect of overnight dexamethasone (DEX; 1 mg) vs. placebo on estimates of CSR maxand free cortisol half-life. Design: This study was a double-blind, placebo-controlled, randomized order of overnight DEX vs. placebo, cosyntropin (250 μg) stimulation with frequent serum cortisol sampling and computer-assisted numerical analysis. Setting: The study was conducted at a single academic medical center. Participants: Twenty-one healthy adult subjects (15 females and six males), mean aged 46 yr, participated in the study. Intervention: Intervention in the study included DEX vs. placebo pretreatment, cosyntropin (250 μg) iv with frequent cortisol sampling. Main Outcome Measures: CSR max and free cortisol half-life estimates, R 2 for goodness of fit, were measured. Results: Mean-SD CSR max was 0.44 ± 0.13 nM/second, with free cortisol half-life of 2.2 ± 1.1 min. DEX did not significantly affect estimates of CSR max or free cortisol half-life. Our model accounts for most of the variability of measured cortisol concentrations (overall R 2-= 90.9 ± 11.0%) and was more accurate (P = 0.004) during DEX suppression (R 2 = 94.6 ± 4.6%) compared with placebo (R 2 = 87.2 ± 8.7%). Conclusions: Application of a mass-action model under conditions of cosyntropin stimulation provides a relatively simple method for estimation CSR max that accurately predicts measured cortisol concentrations. DEX administration did not significantly affect estimates of CSR max or free cortisol half-life. Copyright © 2012 by The Endocrine Society.
CITATION STYLE
Dorin, R. I., Qiao, Z., Qualls, C. R., & Urban, F. K. (2012). Estimation of maximal cortisol secretion rate in healthy humans. Journal of Clinical Endocrinology and Metabolism, 97(4), 1285–1293. https://doi.org/10.1210/jc.2011-2227
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