Population Pharmacokinetics of Perphenazine in Schizophrenia Patients From CATIE: Impact of Race and Smoking

被引:23
|
作者
Jin, Yuyan [2 ]
Pollock, Bruce G. [3 ,5 ]
Coley, Kim [4 ]
Miller, Del [6 ]
Marder, Stephen R. [7 ]
Florian, Jeff [2 ]
Schneider, Lon [8 ]
Lieberman, Jeffrey [9 ]
Kirshner, Margaret [5 ]
Bies, Robert R. [1 ,2 ,5 ]
机构
[1] Indiana Univ, Div Clin Pharmacol, Sch Med, Indianapolis, IN 46204 USA
[2] Univ Pittsburgh, Sch Pharm, Dept Pharmaceut Sci, Pittsburgh, PA 15261 USA
[3] Univ Toronto, Rotman Res Inst, Baycrest Hosp, Toronto, ON M5S 1A1, Canada
[4] Univ Pittsburgh, Sch Pharm, Dept Pharm & Therapeut, Pittsburgh, PA 15261 USA
[5] Univ Pittsburgh, Dept Psychiat, Pittsburgh, PA USA
[6] Univ Iowa, Coll Med, Dept Psychiat, Iowa City, IA 52242 USA
[7] Univ Calif Los Angeles, Sch Med, Dept Psychiat, Los Angeles, CA 90024 USA
[8] Univ So Calif, Sch Med, Dept Psychiat, Los Angeles, CA USA
[9] Columbia Univ, Dept Psychiat, Med Ctr, New York, NY USA
来源
JOURNAL OF CLINICAL PHARMACOLOGY | 2010年 / 50卷 / 01期
关键词
Perphenazine; population pharmacokinetics; Clinical Antipsychotic Trials for Intervention Effectiveness (CATIE); race and smoke; schizophrenia; CONCENTRATION-CONTROLLED TRIAL; AIRWAYS OBSTRUCTION; ANTIPSYCHOTICS; PARAMETERS; ADHERENCE; WHITE;
D O I
10.1177/0091270009343694
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The goal of the study was to characterize population pharmacokinetics (PPK) for perphenazine in patients with schizophrenia from the Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE). Patients (n = 156) received 8 to 32 mg of perphenazine daily for 14 to 600 days for a total of 421 plasma concentrations measurements. Nonlinear mixed-effects modeling was used to determine PPK characteristics of perphenazine. One- and 2-compartment models with various random effect implementations and mixture distributions were evaluated. Objective function values and goodness-of-fit plots were used as model selection criteria. Age, weight, sex, race, smoking, and concomitant medications were evaluated as covariates. A 1-compartment linear model with proportional error best described the data. The population mean clearance and volume of distribution for perphenazine were 483 L/h and 18 200 L, respectively. Race and smoking status had significant impacts on perphenazine clearance estimates. In addition, the estimated population mean clearance was 48% higher in nonsmoking African Americans than in nonsmoking other races (512 L/h vs 346 L/h). Active smokers eliminated perphenazine 159 L/h faster than nonsmokers in each race. Clearances for smoking African Americans versus smokers in other races were 671 L/h versus 505 L/h, respectively.
引用
收藏
页码:73 / 80
页数:8
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