help button home button Endocrine Society JCEM
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Submit a related Letter to the Editor
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Copyright Permission
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lamberts, S. W.
Right arrow Articles by de Jong, F. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lamberts, S. W.
Right arrow Articles by de Jong, F. H.
Right arrowPubmed/NCBI databases
*Compound via MeSH
*Substance via MeSH
Medline Plus Health Information
*Brain Cancer
Hazardous Substances DB
*DEXAMETHASONE
*ESTRADIOL
*HYDROCORTISONE
*RU-486

Journal of Clinical Endocrinology & Metabolism, Vol 73, 187-191, Copyright © 1991 by Endocrine Society


ARTICLES

The endocrine effects of long-term treatment with mifepristone (RU 486)

SW Lamberts, JW Koper and FH de Jong
Department of Medicine, Erasmus University, Rotterdam, The Netherlands.

Mifepristone (RU 486) is a compound with progesterone as well as cortisol-blocking activities. We investigated the endocrine effects of long-term therapy of 10 patients with meningiomas with 200 mg mifepristone daily for 1 yr. Most patients initially complained of nausea, vomiting, and/or tiredness. In four patients prednisone (7.5 mg/day) had to be given simultaneously in order to overcome these side- effects. In retrospect those patients who presented with the most severe side-effects showed the most rapidly occurring activation of the hypothalamo-pituitary-adrenal-axis, as measured by an increase of circulating cortisol levels as well as of urinary cortisol excretion. Therapy with RU 486 activated the hypothalamo-pituitary-adrenal axis, resulting in a resetting of this system at a higher level at which the diurnal rhythm and the responsiveness to CRH stimulation were maintained, whereas the sensitivity to dexamethasone had diminished. Secondarily the production of androstenedione and estradiol increased considerably. These endocrine changes were caused by the induction of partial cortisol receptor resistance during therapy with RU 486. The compensatory overproduction of androgens and consequently of estrogens during long-term RU 486 therapy might limit its use as a single treatment in the treatment of estrogen-dependent cancer.


This article has been cited by other articles:


Home page
Eur J EndocrinolHome page
S. Johanssen and B. Allolio
Mifepristone (RU 486) in Cushing's syndrome
Eur. J. Endocrinol., November 1, 2007; 157(5): 561 - 569.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
P. B. Jacobson, T. W. von Geldern, L. Ohman, M. Osterland, J. Wang, B. Zinker, D. Wilcox, P. T. Nguyen, A. Mika, S. Fung, et al.
Hepatic Glucocorticoid Receptor Antagonism Is Sufficient to Reduce Elevated Hepatic Glucose Output and Improve Glucose Control in Animal Models of Type 2 Diabetes
J. Pharmacol. Exp. Ther., July 1, 2005; 314(1): 191 - 200.
[Abstract] [Full Text] [PDF]


Home page
Hum Reprod UpdateHome page
N. Chabbert-Buffet, G. Meduri, P. Bouchard, and I. M. Spitz
Selective progesterone receptor modulators and progesterone antagonists: mechanisms of action and clinical applications
Hum. Reprod. Update, May 1, 2005; 11(3): 293 - 307.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
T. C. Sandeep, J. L. W. Yau, A. M. J. MacLullich, J. Noble, I. J. Deary, B. R. Walker, and J. R. Seckl
From The Cover: 11{beta}-Hydroxysteroid dehydrogenase inhibition improves cognitive function in healthy elderly men and type 2 diabetics
PNAS, April 27, 2004; 101(17): 6734 - 6739.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
M. D. Passaro, J. Piquion, N. Mullen, D. Sutherland, S. Zhai, W. D. Figg, R. Blye, and L. K. Nieman
Luteal phase dose-response relationships of the antiprogestin CDB-2914 in normally cycling women
Hum. Reprod., September 1, 2003; 18(9): 1820 - 1827.
[Abstract] [Full Text] [PDF]


Home page
NEJMHome page
I. M. Spitz and C.W. Bardin
Mifepristone (RU 486) -- A Modulator of Progestin and Glucocorticoid Action
N. Engl. J. Med., August 5, 1993; 329(6): 404 - 412.
[Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Endocrinology Endocrine Reviews J. Clin. End. & Metab.
Molecular Endocrinology Recent Prog. Horm. Res. All Endocrine Journals
Copyright © 1991 by The Endocrine Society