Abstract

There were significant differences in response and pharmacokinetic characteristics to the peginterferon α2a treatment among Chronic Hepatitis B (CHB) patients. The aim of this study is to identify factors which could significantly impact the peginterferon α2a pharmacokinetic characteristics in CHB patients. There were 208 blood samples collected from 178 patients who were considered as CHB and had been treated with peginterferon α2a followed by blood concentration measurement and other laboratory tests. The covariates such as demographic and clinical characteristics of the patients were retrieved from medical records. Nonlinear mixed-effects modeling method was used to develop the population pharmacokinetic model with NONMEM software. A population pharmacokinetic model for peginterferon α2a has been successfully developed which shows that distribution volume (V) was associated with body mass index (BMI), and drug clearance (CL) had a positive correlation with creatinine clearance (CCR). The final population pharmacokinetic model supports the use of BMI and CCR-adjusted dosing in hepatitis B virus patients.

Details

Title
Population pharmacokinetics of peginterferon α2a in patients with chronic hepatitis B
Author
Bi, Jingfeng 1   VIAFID ORCID Logo  ; Li, Xingang 2 ; Liu, Jia 3 ; Chen, Dawei 4 ; Li, Shuo 5 ; Hou, Jun 1 ; Zhou, Yuxia 6 ; Zhu, Shanwei 7 ; Zhao, Zhigang 2 ; Qin, Enqiang 4 ; Zhenman Wei 1 

 Research Center for Clinical & Translational Medicine, 302 Military Hospital, Beijing, China 
 Department of Pharmacy, Beijing Tiantan Hospital, Capital Medical University, Beijing, China 
 Laboratory Center, 302 Military Hospital, Beijing, China 
 Infectious Disease Treatment Center, 302 Military Hospital, Beijing, China 
 Ministry of Health, 302 Military Hospital, Beijing, China 
 Medical Information Center, 302 Military Hospital, Beijing, China 
 Department of Pharmacy, 302 Military Hospital, Beijing, China 
Pages
1-9
Publication year
2017
Publication date
Aug 2017
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
1957201649
Copyright
© 2017. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.