He Rui, Li Yuhong, Ruan Jinguang
Department of Anesthesiology, Shaoxing People's Hospital, Shaoxing, Zhejiang, China (mainland).
Department of Anesthesiology, First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, Zhejiang, China (mainland).
Med Sci Monit. 2015 Feb 4;21:396-402. doi: 10.12659/MSM.892044.
Microsomal enzyme P450 (CYP450) plays an important role in metabolism of most xenobiotics. The activity of CYP3A decreases in patients with liver dysfunction. However, whether serum concentrations of liver enzymes reflect the activity of CYP3A is unclear. We aimed to search for a new clue to predict the activity of CYP3A and guide clinical medication.
Forty-five patients undergoing surgery under general anesthesia were enrolled in the study, including 15 cases with normal liver function (Group N), 15 cases with moderate fatty liver according to both the results of ultrasonic diagnosis of moderate fatty liver and the laboratory results of elevated alanine transaminase less than 3 times the normal (Group M), and 15 cases with end-stage liver disease (Group S). Each patient received a single dose of 5 mg midazolam intravenously. CYP3A activity was measured by plasma 1'hydroxymidsazolam/midazolam (1'-OH-MDZ/MDZ) ratio at 2 h after administration of midazolam.
They was no significant difference in CYP3A activity between the patients with normal liver function and moderate fatty liver (P=0.332). The activity of CYP3A in Group S was lower than in Group N and Group M (P=0.000). Multiple linear regression analysis showed a statistically significant linear relationship between the activity of CYP3A and alanine transaminase (ALT, R2=0.682, P=0.000), and total bilirubin (TB, R2=0.519, P=0.002). There were no other factors, including albumin (ALB, P=0.881) and alkaline phosphatase (ALP, P=0.497), correlated with the activity of CYP3A.
We conclude that the activity of CYP3A in patients with end-stage liver disease decreased. The decrease in the activity of CYP3A was determined by the increase in the serum concentration of ALT and TB and not by patient's age or body weight. ALT and TB therefore might have predictive value for the activity of CYP3A. An abnormal liver function test likely gives the clinician a hint about dosage adjustment.
微粒体酶P450(CYP450)在大多数外源性物质的代谢中起重要作用。肝功能不全患者的CYP3A活性降低。然而,血清肝酶浓度是否反映CYP3A的活性尚不清楚。我们旨在寻找预测CYP3A活性的新线索并指导临床用药。
纳入45例接受全身麻醉手术的患者,包括15例肝功能正常者(N组)、15例根据超声诊断为中度脂肪肝且实验室检查丙氨酸转氨酶升高小于正常3倍者(M组)和15例终末期肝病患者(S组)。每位患者静脉注射单剂量5mg咪达唑仑。在给予咪达唑仑后2小时,通过血浆1'-羟基咪达唑仑/咪达唑仑(1'-OH-MDZ/MDZ)比值测定CYP3A活性。
肝功能正常患者与中度脂肪肝患者的CYP3A活性无显著差异(P = 0.332)。S组的CYP3A活性低于N组和M组(P = 0.000)。多元线性回归分析显示,CYP3A活性与丙氨酸转氨酶(ALT,R2 = 0.682,P = 0.000)和总胆红素(TB,R2 = 0.519,P = 0.002)之间存在统计学显著的线性关系。没有其他因素,包括白蛋白(ALB,P = 0.881)和碱性磷酸酶(ALP,P = 0.497),与CYP3A活性相关。
我们得出结论,终末期肝病患者的CYP3A活性降低。CYP3A活性的降低由ALT和TB血清浓度的升高决定,而非患者年龄或体重。因此,ALT和TB可能对CYP3A活性具有预测价值。肝功能检查异常可能会给临床医生调整剂量提供提示。