THE ANTIESTROGEN TAMOXIFEN PRODUCES HEMODILUTION IN NORMAL POSTMENOPAUSAL WOMEN

Citation
Ab. Grey et al., THE ANTIESTROGEN TAMOXIFEN PRODUCES HEMODILUTION IN NORMAL POSTMENOPAUSAL WOMEN, Journal of internal medicine, 242(5), 1997, pp. 383-388
Citations number
19
Categorie Soggetti
Medicine, General & Internal
ISSN journal
09546820
Volume
242
Issue
5
Year of publication
1997
Pages
383 - 388
Database
ISI
SICI code
0954-6820(1997)242:5<383:TATPHI>2.0.ZU;2-9
Abstract
Objectives. To report the effects of the anti-oestrogen tamoxifen on b iochemical and haematological parameters. Design. Randomized, double-b lind comparison of tamoxifen 20 mg per day and placebo, over two years . Setting. A university hospital. Subjects. Forty-six healthy late-pos tmenopausal women (mean, SD time since menopause; 11, seven years). Ma in outcome measures. Blood specimens were drawn in the fasting state a t baseline, six months and two years for measurement of haemoglobin, h aematocrit, erythrocyte mean cell volume, mean erythrocyte haemoglobin , leucocyte count, platelet count, urea, electrolytes, creatinine and albumin. Results. There was a significant decline in the haemoglobin c oncentration in the tamoxifen group (-4.4, 1.2 g/L; mean, SE) and its levels were lower in this group than in those receiving placebo (P = 0 .004). Similarly, haematocrit, erythrocyte count and total leucocyte c ount were lower in those on placebo (P = 0.002, P = 0.01 and P = 0.01, respectively) and platelet count showed a similar trend (P = 0.08). I n the tamoxifen group, the level of serum albumin fell significantly ( -2.2, 0.4 g/L) and was lower throughout the study than that in the pla cebo group (P = 0.006). That of serum urea tended to fall (-0.4, 0.2 m mol L) but the between-groups comparison was not significant (P = 0.18 ). Conclusions. These data suggest that tamoxifen exerts a haemodiluto ry effect in normal postmenopausal women. Since a similar effect has b een reported in response to postmenopausal oestrogen therapy, it is li kely that the observed changes represent another oestrogenic effect of tamoxifen in postmenopausal women. Haemodilution may contribute to th e reduced incidence of cardiovascular disease reported in tamoxifen-tr eated women, and, therefore, its assessment in the new oestrogen agoni sts/antagonists being developed for cardiovascular disease prevention may be important.