Steroidogenesis enzyme inhibitors in Cushing's syndrome

被引:64
作者
Daniel, Eleni [1 ]
Newell-Price, John D. C. [2 ]
机构
[1] Univ Sheffield, Dept Human Metab, Sheffield S10 2RX, S Yorkshire, England
[2] Univ Sheffield, Dept Endocrinol, Acad Unit Endocrinol, Sheffield S10 2RX, S Yorkshire, England
关键词
ALDOSTERONE SYNTHASE INHIBITION; MULTIPLE TRAUMA PATIENTS; CRITICALLY-ILL PATIENTS; IDEAL INDUCTION AGENT; LONG-TERM MANAGEMENT; LOW-DOSE ETOMIDATE; OF-THE-LITERATURE; ADRENOCORTICAL CARCINOMA; ADRENAL STEROIDOGENESIS; DOUBLE-BLIND;
D O I
10.1530/EJE-14-1014
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Steroidogenesis enzyme inhibitors are the mainstay of medical therapy in Cushing's syndrome (CS). Ketoconazole (KTZ) and metyrapone are the most commonly used agents. Although there is considerable experience of their use in individual specialist centres, these drugs have not been rigorously tested in prospective clinical trials. Clinicians face uncertainties and concerns with respect to the safety profile of these agents, and best means to monitor effect. We review steroidogenesis inhibitors in the management of CS, including older agents (KTZ, metyrapone, etomidate and mitotane) and those currently under development (LCI699, non-racemic KTZ), and offer a practical approach for their use in clinical practice.
引用
收藏
页码:R263 / R280
页数:18
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