C
Coleman Gross
Publications - 5
Citations - 564
Coleman Gross is an academic researcher. The author has contributed to research in topics: Mifepristone & Cushing syndrome. The author has an hindex of 5, co-authored 5 publications receiving 487 citations.
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Journal ArticleDOI
Mifepristone, a Glucocorticoid Receptor Antagonist, Produces Clinical and Metabolic Benefits in Patients with Cushing's Syndrome
Maria Fleseriu,Beverly M. K. Biller,James W. Findling,Mark E. Molitch,David E. Schteingart,Coleman Gross +5 more
TL;DR: Mifepristone produced significant clinical and metabolic improvement in patients with CS with an acceptable risk-benefit profile during 6 months of treatment, and had significant improvement in clinical status.
Journal ArticleDOI
Changes in plasma ACTH levels and corticotroph tumor size in patients with Cushing's disease during long-term treatment with the glucocorticoid receptor antagonist mifepristone.
Maria Fleseriu,James W. Findling,Christian A. Koch,Sven Schlaffer,Michael Buchfelder,Coleman Gross +5 more
TL;DR: In the largest prospective study to date, long-term mifepristone treatment increased ACTH in approximately two-thirds of patients with Cushing's disease patients and generally remained stable over time.
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A new therapeutic approach in the medical treatment of Cushing's syndrome: glucocorticoid receptor blockade with mifepristone.
Maria Fleseriu,Mark E. Molitch,Coleman Gross,David E. Schteingart,T. Brooks Vaughan,Beverly M. K. Biller +5 more
TL;DR: Clinical trial data have shown that mifepristone improves glycemic control and blood pressure, causes weight loss and a decrease in waist circumference, lessens depression, and improves overall wellbeing, however, adverse effects include adrenal insufficiency, hypokalemia, and endometrial thickening with vaginal bleeding.
Journal ArticleDOI
Impact of Mifepristone, a Glucocorticoid/Progesterone Antagonist, on HDL Cholesterol, HDL Particle Concentration, and HDL Function
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,Tomas Vaisar +12 more
TL;DR: Treatment with mifepristone reduced HDL-C, HDL particle concentration, and serum HDL cholesterol efflux in postmenopausal women, however, on a per particle basis, the efflux capacity of serum HDL increased and support the concept that a decrease in HDL- C may not represent proportional impairment of HDL function.
Journal ArticleDOI
Improvement in insulin sensitivity during mifepristone treatment of Cushing syndrome: early and late effects.
TL;DR: Using oral glucose tolerance test data from SEISMIC, whole-body insulin sensitivity, β-cell function, insulinogenic index, homeostasis model assessment-β [HOMA-β], disposition index, weight, and waist circumference over time were assessed.