CIRCADIAN VARIATION IN SERUM CORTISOL AND CIRCULATING NEUTROPHILS AREMARKERS FOR CIRCADIAN VARIATION OF BONE-MARROW PROLIFERATION IN CANCER-PATIENTS

Citation
Jf. Abrahamsen et al., CIRCADIAN VARIATION IN SERUM CORTISOL AND CIRCULATING NEUTROPHILS AREMARKERS FOR CIRCADIAN VARIATION OF BONE-MARROW PROLIFERATION IN CANCER-PATIENTS, European journal of haematology, 50(4), 1993, pp. 206-212
Citations number
28
Categorie Soggetti
Hematology
ISSN journal
09024441
Volume
50
Issue
4
Year of publication
1993
Pages
206 - 212
Database
ISI
SICI code
0902-4441(1993)50:4<206:CVISCA>2.0.ZU;2-E
Abstract
Serum cortisol, circulating white blood cells and DNA cell cycle distr ibution in bone marrow cells were measured during daytime (11.00) and at midnight (24.00) over single 24-hour periods in 15 cancer patients. The neutrophils and fraction of bone marrow cells in S-phase showed t he same circadian variation as cortisol with higher values in daytime as compared to midnight in 11 patients with a normal cortisol rhythm ( p < 0.05). The lymphocytes, eosinophils and basophils all had signific antly higher values at midnight as compared to daytime. There were sig nificant correlations between cortisol and neutrophils, lymphocytes, e osinophils and basophils. The correlation between neutrophils and frac tions of bone marrow cells in S-phase and S + G2/M-phase were highly s ignificant (r = 0.74, p = 0.0001 and r = 0.72, p = 0.0001, respectivel y). In 8 of 13 patients (61.5%) without bone marrow infiltration both cortisol and neutrophils showed identical circadian variation as bone marrow cells in S-phase and S + G2/M-phase. Furthermore, for the total series a significant correlation between S-phase, cortisol and neutro phils was found by multiple regression analysis (p < 0.0001). These fi ndings strengthen the possibility of using the circadian variation in cortisol and neutrophils as marker rhythms for circadian variation in bone marrow proliferation, thus allowing optimization of cytotoxic the rapy and individualization of chronotherapy.