陈卓佳, 王雪丁, 周列民, 方子妍, 王红胜, 李嘉丽, 周珏倩, 黄红兵, 黄民. 卡马西平对癫痫患者丙戊酸及其毒性代谢物血药浓度的影响J. 药学学报, 2014,49(4): 530-534.
引用本文: 陈卓佳, 王雪丁, 周列民, 方子妍, 王红胜, 李嘉丽, 周珏倩, 黄红兵, 黄民. 卡马西平对癫痫患者丙戊酸及其毒性代谢物血药浓度的影响J. 药学学报, 2014,49(4): 530-534.
CHEN Zhuo-jia, WANG Xue-ding, ZHOU Lie-min, FANG Zi-yan, WANG Hong-sheng, LI Jia-li, ZHOU Jue-qian, HUANG Hong-bing, HUANG Min. Effects of carbamazepine on plasma concentrations of valproic acid and its toxic metabolite in epileptic patientsJ. Acta Pharmaceutica Sinica, 2014,49(4): 530-534.
Citation: CHEN Zhuo-jia, WANG Xue-ding, ZHOU Lie-min, FANG Zi-yan, WANG Hong-sheng, LI Jia-li, ZHOU Jue-qian, HUANG Hong-bing, HUANG Min. Effects of carbamazepine on plasma concentrations of valproic acid and its toxic metabolite in epileptic patientsJ. Acta Pharmaceutica Sinica, 2014,49(4): 530-534.

卡马西平对癫痫患者丙戊酸及其毒性代谢物血药浓度的影响

Effects of carbamazepine on plasma concentrations of valproic acid and its toxic metabolite in epileptic patients

  • 摘要: 本文探讨了卡马西平(carbamazepine,CBZ)对癫痫患者丙戊酸(valproic acid,VPA)及其毒性代谢物2-丙基-4-戊烯酸(4-ene VPA)血药浓度的影响。测定癫痫患者血浆中VPA及4-ene VPA的浓度,明确卡马西平对丙戊酸的影响。共纳入VPA单药组87例,VPA+CBZ组19例,年龄和性别组间无显著性差异。与VPA单药组比较,合用CBZ可以显著(P <0.01)降低VPA谷浓度 VPA单药组:(69.5 ± 28.8)µg·mL-1;VPA+CBZ组:(46.3 ± 25.6)µg·mL-1 及体重剂量调整谷浓度 VPA单药组:(4.89 ± 2.21)µg·mL-1·mg-1·kg-1;VPA+CBZ组:(3.14 ± 1.74)µg·mL-1·mg-1·kg-1,而合用CBZ对4-ene VPA浓度没有影响。合用CBZ会导致VPA血药浓度降低,进而可能影响VPA的临床疗效,建议临床上VPA与CBZ合用时需监测VPA血药浓度以调整VPA用药剂量。

     

    Abstract: To investigate the effects of carbamazepine (CBZ) on the plasma concentrations of valproic acid (VPA) and its toxic metabolite 2-propyl-4-pentenoic acid (4-ene VPA) in epileptic patients, the plasma concentrations of VPA and 4-ene VPA were determined, and the effect of CBZ on pharmacokinetics of VPA was evaluated. All patients had been divided into two groups (VPA group, n = 87; and VPA+CBZ group, n = 19). As compared to VPA group, the combination of CBZ significantly (P < 0.01) decreased the trough concentration of VPA VPA group, (69.5 ± 28.8) �g·mL-1; VPA+CBZ group, (46.3 ± 25.6) �g·mL-1 and does-adjusted VPA trough concentration VPA group, (4.89 ± 2.21) �g·mL-1·mg-1·kg-1; VPA+CBZ group, (3.14 ± 1.74) �g·mL-1·mg-1·kg-1. However, the addition of CBZ did not influence the concentration of 4-ene VPA. The present study revealed that coadministration of CBZ can reduce VPA plasma concentration and may impact VPA clinical effect, therefore therapeutic drug mornitoring of VPA should be used when combined use of CBZ and VPA.

     

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