Department of Clinical Pharmacy, St. Antonius Hospital, Koekoekslaan 1, 3435 CM, Nieuwegein, The Netherlands.
Division of Pharmacology, Leiden Academic Centre for Drug Research, Leiden University, Leiden, The Netherlands.
Clin Pharmacokinet. 2017 Dec;56(12):1577-1587. doi: 10.1007/s40262-017-0544-2.
Obesity is associated with many pathophysiological changes that may result in altered drug metabolism. The aim of this study is to investigate the influence of obesity on the pharmacokinetics of morphine, morphine-3-glucuronide (M3G), and morphine-6-glucuronide (M6G) through a combined analysis in morbidly obese patients and non-obese healthy volunteers.
In this analysis, data from 20 morbidly obese patients [mean body mass index 49.9 kg/m (range 37.6-78.6 kg/m) and weight 151.3 kg (range 112-251.9 kg)] and 20 healthy volunteers [mean weight 70.6 kg (range 58-85 kg)] were included. Morbidly obese patients received 10 mg of intravenous (I.V.) morphine after gastric bypass surgery, with additional morphine I.V. doses as needed. Healthy volunteers received an I.V. bolus of morphine of 0.1 mg/kg followed by an infusion of 0.030 mg kg h for 1 h. Population pharmacokinetic modeling was performed using NONMEM 7.2.
In morbidly obese patients, elimination clearance of M3G and M6G was decreased substantially compared with healthy volunteers (p < 0.001). Regarding glucuronidation, only a slight decrease in the formation of M6G and a delay in the formation of M3G was found (both p < 0.001). Obesity was also identified as a covariate for the peripheral volume of distribution of morphine (p < 0.001).
Metabolism of morphine is not altered in morbidly obese patients. However, decreased elimination of both M3G and M6G is evident, resulting in a substantial increase in exposure to these two metabolites. A rational explanation of this finding is that it results from alterations in membrane transporter function and/or expression in the liver. ClinicalTrials.gov identifier: NCT01097148.
肥胖与许多病理生理变化相关,这些变化可能导致药物代谢改变。本研究旨在通过对病态肥胖患者和非肥胖健康志愿者进行联合分析,探讨肥胖对吗啡、吗啡-3-葡萄糖醛酸苷(M3G)和吗啡-6-葡萄糖醛酸苷(M6G)药代动力学的影响。
本分析纳入 20 例病态肥胖患者(平均体重指数 49.9kg/m²,范围 37.6-78.6kg/m²,体重 151.3kg,范围 112-251.9kg)和 20 例健康志愿者(平均体重 70.6kg,范围 58-85kg)的数据。病态肥胖患者在胃旁路手术后接受 10mg 静脉(I.V.)吗啡,根据需要额外给予吗啡 I.V.剂量。健康志愿者接受 0.1mg/kg 的 I.V.吗啡推注,随后以 0.030mg·kg-1·h-1 的速度输注 1h。采用 NONMEM 7.2 进行群体药代动力学建模。
与健康志愿者相比,病态肥胖患者 M3G 和 M6G 的消除清除率显著降低(p<0.001)。关于葡萄糖醛酸化,仅发现 M6G 的形成略有减少,M3G 的形成延迟(均 p<0.001)。肥胖也被确定为吗啡外周分布容积的协变量(p<0.001)。
在病态肥胖患者中,吗啡代谢未发生改变。然而,M3G 和 M6G 的消除减少明显,导致这两种代谢物的暴露量显著增加。对这一发现的合理解释是,这是由于肝脏膜转运体功能和/或表达的改变所致。临床试验注册号:NCT01097148。