MORNING OR EVENING ADMINISTRATION OF NASAL CALCITONIN - EFFECTS ON BIOCHEMICAL MARKERS OF BONE TURNOVER

Citation
A. Schlemmer et al., MORNING OR EVENING ADMINISTRATION OF NASAL CALCITONIN - EFFECTS ON BIOCHEMICAL MARKERS OF BONE TURNOVER, Bone, 20(1), 1997, pp. 63-67
Citations number
34
Categorie Soggetti
Endocrynology & Metabolism
Journal title
BoneACNP
ISSN journal
87563282
Volume
20
Issue
1
Year of publication
1997
Pages
63 - 67
Database
ISI
SICI code
8756-3282(1997)20:1<63:MOEAON>2.0.ZU;2-I
Abstract
The purpose of this study was to examine the effect of intranasal salm on calcitonin (sCT) administration (200 IE), given either in the morni ng (8:00) or evening (21:00), on the known circadian variation in bioc hemical markers of bone turnover. An open, placebo-controlled, randomi zed, crossover study, with three 24 h studies of blood samples drawn e very third hour and urine collected in 3 h aliquots was undertaken. Su bjects consisted of nine healthy postmenopausal women, aged 58 +/- 7 y ears. Urinary CrossLaps (a measure of bone resorption) was measured by ELISA and corrected for creatinine (Cr), Serum osteocalcin (sOC) was measured by radioimmunoassay (RIA). The first 24 h study was performed without intervention. Prior to this control study the participants we re randomized to either morning (8:00) or evening (21:00) sCT (200 LE) , sCT administrations were given 4-5 days prior to and during the seco nd study, After a washing-out period of 2 weeks the participants were given 200 IE of sCT at the reverse time of the day 5 days prior to and during the third study. At all timepoints, urinary CrossLaps/Cr exhib ited a significant (p < 0.001) circadian rhythm with its zenith in ear ly morning and nadir in late afternoon. Both morning and evening admin istration of sCT significantly decreased the urinary excretion of Cros sLaps/Cr approximately 3-6 h after administration with a subsequent re bound effect, sOC did not exhibit a significant circadian variation an d was not affected by the calcitonin. The 24 h mean urinary CrossLaps/ Cr and sOC remained unchanged. Both morning and evening sCT significan tly decreased the urinary excretion of CrossLaps/Cr 3-6 h after admini stration, with a rebound effect approximately 12 h later. However, the present study does not indicate that neither evening nor twice-daily administration is superior to morning administration. (C) 1997 by Else vier Science Inc.