Department of Obstetrics and Gynecology, Oregon Health and Science University, Portland, USA.
Br J Clin Pharmacol. 2012 Sep;74(3):510-4. doi: 10.1111/j.1365-2125.2012.04209.x.
AIM(S): While it is known that CYP3A4/5 activity is decreased with combined oral contraceptive (COC) use and obesity suppresses CYP expression, the combined effects of obesity and COC use on CYP3A4/5 activity are unclear. Therefore, our aim was to examine the effect of COC usage on CYP3A4/5 activity in obese women.
Thirty-four, obese (body mass index, BMI > 30 kg m(-2)) women of reproductive age (18-35 years old) were placed on a COC pill containing 20 µg ethinylestradiol/100 µg levonorgestrel for 21 days starting at the onset of menses. A midazolam pharmacokinetic study was conducted prior to initiation and after 21 days of COC treatment. Serial blood samples were collected and plasma concentrations of midazolam were measured using liquid chromatography tandem mass spectrometry. Pharmacokinetic parameters were estimated using a non-compartmental method.
Midazolam clearance, a surrogate measure of CYP3A4/5 activity, was significantly decreased upon COC use (63.3 l h(-1) vs. 53.9 l h(-1), P < 0.05). A median decrease of 5.6 l h(-1) (95% CI -4.1, 13.3 l h(-1)) was observed. However, the magnitude of change was similar to that reported in women with normal BMI.
Although we hypothesized that obesity might amplify the impact on CYP3A4/5 activity in COC users, we found that this was not the case. This finding is reassuring regarding potential additional drug-drug interactions in obese COC users as CYP3A4/5 is a major enzyme in the metabolism of many marketed drugs.
已知 CYP3A4/5 活性随口服避孕药(COC)联合使用而降低,肥胖抑制 CYP 表达,但肥胖和 COC 联合使用对 CYP3A4/5 活性的综合影响尚不清楚。因此,我们的目的是研究 COC 使用对肥胖女性 CYP3A4/5 活性的影响。
34 名肥胖(体重指数,BMI > 30 kg m(-2)) 的育龄妇女(18-35 岁)在月经来潮时开始服用含有 20 µg 炔雌醇/100 µg 左炔诺孕酮的 COC 药丸,共 21 天。在开始和 COC 治疗 21 天后进行咪达唑仑药代动力学研究。采集连续血样,使用液相色谱串联质谱法测定咪达唑仑的血浆浓度。使用非房室模型法估算药代动力学参数。
咪达唑仑清除率(CYP3A4/5 活性的替代指标)在 COC 使用时显著降低(63.3 l h(-1) 比 53.9 l h(-1),P < 0.05)。观察到中位数下降 5.6 l h(-1)(95%CI -4.1,13.3 l h(-1))。然而,变化幅度与 BMI 正常的女性报告的相似。
尽管我们假设肥胖可能会放大 COC 用户对 CYP3A4/5 活性的影响,但我们发现并非如此。这一发现令人放心,因为 CYP3A4/5 是许多上市药物代谢的主要酶,肥胖的 COC 用户可能会出现潜在的额外药物相互作用。