Effect of endogenous steroid hormones on 17-alpha-hydroxyprogesterone caproate metabolism

被引:9
|
作者
Cuppett, Courtney D. [1 ]
Zhao, Yang [2 ]
Caritis, Steve [1 ]
Zhang, Shimin [2 ]
Zhao, Wenchen [2 ]
Venkataramanan, Raman [2 ]
机构
[1] Magee Womens Hosp, Dept Obstet Gynecol & Reprod Sci, Div Maternal Fetal Med, Pittsburgh, PA USA
[2] Univ Pittsburgh, Sch Pharm, Pittsburgh, PA USA
关键词
17-alpha-hydroxyprogesterone caproate; drug-drug interaction; human liver microsome; metabolism; steroid hormone; PROGESTERONE LEVELS; PRETERM DELIVERY; ESTRADIOL; PRESCRIPTION; OXIDATION; 3A4; PREVENTION; PREGNANCY; ESTRIOL; ESTRONE;
D O I
10.1016/j.ajog.2012.09.021
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: Plasma concentrations of 17-alpha-hydroxyprogesterone caproate (17-OHPC) vary substantially in pregnant patients who receive an identical dose. Endogenous steroid hormones may alter 17-OHPC metabolism, which contributes to this large variability. STUDY DESIGN: Pooled human liver microsomes were incubated with 17-OHPC alone or in combination with progesterone, hydroxyprogesterone, estrone, estradiol, or estriol. High-performance liquid chromatography with ultraviolet detection was used to quantify 17-OHPC. RESULTS: Under the conditions that were studied, 17-OHPC metabolism was inhibited by 37% by a combination of endogenous steroid hormones. Progesterone alone significantly inhibited 17-OHPC metabolism by 28% (P<.001). CONCLUSION: 17-OHPC metabolism is inhibited significantly by endogenous steroids and, in particular, progesterone. This effect may account for some of the large variation in plasma 17-OHPC concentrations that is seen in pregnant patients who receive a fixed dose of medication.
引用
收藏
页码:86.e1 / 86.e6
页数:6
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