| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Original Articles |
Divisions of Endocrinology of the Department of Pediatrics (G.P.B.K., N.M.D.) and Internal Medicine (R.P.F.D.), Isotopenlaboratorium (J.J.P.), Central Laboratory for Clinical Chemistry (B.G.W.), University Hospital Groningen, 9700 RB Groningen; and Center for High Performance Computing (R.d.B.), University of Groningen, 9700 AV, Groningen, The Netherlands.
Address all correspondence and requests for reprints to: G. P. B. Kraan, Ph.D., van Houtenlaan 206, 9722 GZ, Groningen, The Netherlands.
Abstract
We have measured the urinary cortisol production rate (uCPR)
simultaneously with the serum cortisol production rate (sCPR) in four
healthy men within a period of 3 days. uCPR, determined by isotope
dilution of 11-oxoetiocholanolone was compared with sCPR, which was
measured in three different ways (a, b, c). Blood was sampled at 10-min
intervals for 24 h, and deconvolution analysis was applied to the
cortisol concentrations. The daily serum cortisol production per liter,
multiplied by the distribution volume yielded sCPR. The measurement
methods are characterized as follows: a) the secretion and elimination
terms were free; b) like method a, but with the input of the rate
constants
and ß into the elimination function; c) the average
24-h cortisol concentration was multiplied by the metabolic clearance
rate. uCPR was 25.4 ± 4.7 [range: 21.331.4]
µmol/(m2·day), sCPR (method a) was 28.8 ± 4.5
[range: 23.534.3] µmol/(m2·day), sCPR (method b)
was 27.9 ± 8.1 [range: 18.537.7]
µmol/(m2·day), and sCPR (method c) was 29.3 ± 4.8
[range: 22.733.2] µmol/(m2·day). uCPR did not
significantly differ from each of the 3 sCPR values
(P > 0.30; >0.46; and >0.06, respectively). The
patterns of the cortisol secretory rates in the present and previous
studies do not necessarily represent the physiological process of the
secretory bursts. We conclude that the estimated CPR, being 2530
µmol/(m2·day) [911 mg/(m2·day)], can
serve as a guideline for glucocorticoid replacement dose and that the
urinary route to measure CPR is preferred because of its relative ease.
This article has been cited by other articles:
![]() |
S. A. Wudy, M. F. Hartmann, and T. Remer Sexual dimorphism in cortisol secretion starts after age 10 in healthy children: urinary cortisol metabolite excretion rates during growth Am J Physiol Endocrinol Metab, October 1, 2007; 293(4): E970 - E976. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Heckmann, M. F. Hartmann, B. Kampschulte, H. Gack, R.-H. Bodeker, L. Gortner, and S. A. Wudy Cortisol Production Rates in Preterm Infants in Relation to Growth and Illness: A Noninvasive Prospective Study Using Gas Chromatography-Mass Spectrometry J. Clin. Endocrinol. Metab., October 1, 2005; 90(10): 5737 - 5742. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. M. Keenan, F. Roelfsema, and J. D. Veldhuis Endogenous ACTH concentration-dependent drive of pulsatile cortisol secretion in the human Am J Physiol Endocrinol Metab, October 1, 2004; 287(4): E652 - E661. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. J. Inder and P. J. Hunt Glucocorticoid Replacement in Pituitary Surgery: Guidelines for Perioperative Assessment and Management J. Clin. Endocrinol. Metab., June 1, 2002; 87(6): 2745 - 2750. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Picard-Hagen, V. Gayrard, M. Alvinerie, H. Smeyers, R. Ricou, A. Bousquet-Melou, and P. L. Toutain A nonlabeled method to evaluate cortisol production rate by modeling plasma CBG-free cortisol disposition Am J Physiol Endocrinol Metab, November 1, 2001; 281(5): E946 - E956. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. G. Langendonk, J. D. Veldhuis, J. Burggraaf, R. C. Schoemaker, A. F. Cohen, A. Edo Meinders, and H. Pijl Estimation of growth hormone secretion rate: impact of kinetic assumptions intrinsic to the analytical approach Am J Physiol Regulatory Integrative Comp Physiol, January 1, 2001; 280(1): R225 - R232. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Bergendahl, A. Iranmanesh, C. Pastor, W. S. Evans, and J. D. Veldhuis Homeostatic Joint Amplification of Pulsatile and 24-Hour Rhythmic Cortisol Secretion by Fasting Stress in Midluteal Phase Women: Concurrent Disruption of Cortisol-Growth Hormone, Cortisol-Luteinizing Hormone, and Cortisol-Leptin Synchrony J. Clin. Endocrinol. Metab., November 1, 2000; 85(11): 4028 - 4035. [Abstract] [Full Text] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Endocrinology | Endocrine Reviews | J. Clin. End. & Metab. |
| Molecular Endocrinology | Recent Prog. Horm. Res. | All Endocrine Journals |