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Original Studies |
Departamento de Pediatría (A.M.-H., R.J., A.M.-C., J.M.F.-G.) and Departamento de Fisiología, Instituto de Biotecnología (D.A.-C., G.E., M.M.), E-18012 Granada, Spain; and Department of Cellular and Structural Biology, University of Texas Health Science Center (R.J.R.), San Antonio, Texas
Address all correspondence and requests for reprints to: Dr. D. Acuña-Castroviejo, Departamento de Fisiología, Facultad de Medicina, Avenida de Madrid 11, E-18012 Granada, Spain. E-mail: dacuna{at}goliat.ugr.es
To assess the existence of a possible nocturnal ultradian rhythm of melatonin in children, we analyzed 28 pediatric patients (mean age, 9.08 ± 2.2 yr) with GH-dependent and GH-independent growth delay. Plasma melatonin was measured by RIA in children sampled every 30 min between 21000900 h. Statistical analysis consisted of cluster analysis to examine the presence of peaks and troughs. The pattern of melatonin levels was related to the cause of growth delay, although the means of the nocturnal concentrations of melatonin were similar in all children. Interestingly, children with a GH deficit showed a nearly normal melatonin profile, whereas children with normal GH values but abnormal growth displayed atypical profiles of melatonin. The results also prove the existence of an ultradian rhythm of melatonin in most of the patients studied. The ultradian rhythm of melatonin in children was characterized by irregular interburst intervals, thus differing from the rhythm previously described in adults that had an almost constant pulse frequency. Moreover, the existence of low and high melatonin producers was revealed in the study, a feature unrelated to the cause of growth delay. The group of children with a GH deficit showed the lowest values of integrated melatonin production and of the area of peaks and troughs. These results prove that children exhibit an ultradian rhythm of melatonin like that in adults. Whereas it is not clear whether the episodic production of melatonin is required for its biological actions, the existence of irregular pulses may reflect endocrine influences at this age and/or the immaturity of the intrinsic pulse generator.
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