Impact of Mifepristone, a Glucocorticoid/Progesterone Antagonist, on HDL Cholesterol, HDL Particle Concentration, and HDL Function
Author(s) -
Stephanie T. Page,
Ronald M. Krauss,
Coleman Gross,
Brian Y. Ishida,
Jay W. Heinecke,
Chongren Tang,
John K. Amory,
Peter M. Schaefer,
Cheryl J. Cox,
John P. Kane,
Jonathan Q. Purnell,
Richard L. Weinstein,
Tomáš Vaisar
Publication year - 2012
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.2011-2813
Subject(s) - mifepristone , medicine , endocrinology , cholesterol , placebo , antiglucocorticoid , high density lipoprotein , cholesterylester transfer protein , glucocorticoid , progestin , lipoprotein , biology , glucocorticoid receptor , estrogen , pregnancy , genetics , alternative medicine , pathology
Mifepristone is a glucocorticoid and progestin antagonist under investigation for the treatment of Cushing's syndrome. Mifepristone decreases high-density lipoprotein (HDL) cholesterol (HDL-C) levels in treated patients, but the clinical significance of this is unclear because recent studies suggest that functional properties of HDL predict cardiovascular disease status better than does HDL-C concentration.
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