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A preliminary study of the effect of fluoxetine treatment on the 2:16-alpha-hydroxyestrone ratio in young women.

机译:氟西汀治疗对年轻女性2:16-α-羟基雌酮比例的影响的初步研究。

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摘要

Cytochrome P450 isoenzymes are known to contribute to estrone metabolism. The authors hypothesized that fluoxetine, a known inhibitor of multiple P450 isoenzymes including 3A4, 2C9, and 2D6, would affect estrone metabolism, altering the 2-hydroxyestrone:16-alpha-hydroxyestrone (2OHE1:16OHE1) ratio. In this preliminary study, four of eight recruited women with regular menstrual cycles, aged 21-37 years, completed a 24-hour urine collection prior to initiation of fluoxetine therapy and after at least 5 weeks of antidepressant treatment. In three of the four women who were nonsmokers, the 2OHE1:16OHE1 ratio was significantly higher after 5 weeks of fluoxetine therapy (pretreatment, 2.08 +/- 0.11; posttreatment, 3.50 +/- 0.46; paired Student's t-test P = 4.72, P = 0.021).
机译:已知细胞色素P450同工酶可促进雌酮的代谢。作者假设氟西汀是一种已知的多种P450同工酶(包括3A4、2C9和2D6)的抑制剂,会影响雌酮的代谢,从而改变2-羟基雌酮:16-α-羟基雌酮(2OHE1:16OHE1)的比例。在这项初步研究中,八名年龄在21-37岁之间的月经周期正常的新招募女性中,有四名在开始氟西汀治疗之前和抗抑郁治疗至少5周后完成了24小时尿液收集。在四名非吸烟女性中,有三名女性接受氟西汀治疗5周后2OHE1:16OHE1比率显着更高(治疗前为2.08 +/- 0.11;治疗后为3.50 +/- 0.46;配对的学生t检验P = 4.72, P = 0.021)。

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