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Am J Physiol Endocrinol Metab 285: E1118-E1126, 2003. First published July 29, 2003; doi:10.1152/ajpendo.00562.2002
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A statistical model of diurnal variation in human growth hormone

Elizabeth B. Klerman,1,* Gail K. Adler,2,* Moonsoo Jin,3 Anne M. Maliszewski,2 and Emery N. Brown3

1Division of Sleep Medicine and 2Division of Endocrinology, Diabetes, and Hypertension, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston 02115; and 3Neuroscience Statistics Research Laboratory, Department of Anesthesia and Critical Care, Massachusetts General Hospital, Division of Health Sciences and Technology, Harvard Medical School/Massachusetts Institute of Technology, Boston, Massachusetts 02114

Submitted 23 December 2002 ; accepted in final form 8 July 2003

The diurnal pattern of growth hormone (GH) serum levels depends on the frequency and amplitude of GH secretory events, the kinetics of GH infusion into and clearance from the circulation, and the feedback of GH on its secretion. We present a two-dimensional linear differential equation model based on these physiological principles to describe GH diurnal patterns. The model characterizes the onset times of the secretory events, the secretory event amplitudes, as well as the infusion, clearance, and feedback half-lives of GH. We illustrate the model by using maximum likelihood methods to fit it to GH measurements collected in 12 normal, healthy women during 8 h of scheduled sleep and a 16-h circadian constant-routine protocol. We assess the importance of the model components by using parameter standard error estimates and Akaike's Information Criterion. During sleep, both the median infusion and clearance half-life estimates were 13.8 min, and the median number of secretory events was 2. During the constant routine, the median infusion half-life estimate was 12.6 min, the median clearance half-life estimate was 11.7 min, and the median number of secretory events was 5. The infusion and clearance half-life estimates and the number of secretory events are consistent with current published reports. Our model gave an excellent fit to each GH data series. Our analysis paradigm suggests an approach to decomposing GH diurnal patterns that can be used to characterize the physiological properties of this hormone under normal and pathological conditions.

compartment model; constant routine



Address for reprint requests and other correspondence: E. B. Klerman, Division of Sleep Medicine, 221 Longwood Ave., Boston, MA 02115 (E-mail: ebklerman{at}hms.harvard.edu).




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