Literature DB >> 33464624

Drug exposure of first-line anti-tuberculosis drugs in China: A prospective pharmacological cohort study.

Yazhou Gao1, Lina Davies Forsman2,3, Weihua Ren4, Xubin Zheng1, Ziwei Bao5, Yi Hu1, Judith Bruchfeld2,3, Jan-Willem Alffenaar6.   

Abstract

AIM: Exploring the need for optimization of drug exposure to improve tuberculosis (TB) treatment outcome is of great importance. We aimed to describe drug exposure at steady state as well as the population pharmacokinetics (PK) of rifampicin (RIF), isoniazid (INH) and pyrazinamide (PZA) in Chinese TB patients.
METHODS: A prospective multicentre PK study of RIF, INH and PZA was conducted in China between January 2015 and December 2017. Six blood samples were collected from each subject for drug concentration measurement. Nonlinear mixed effect analyses were used to develop population PK models.
RESULTS: In total, 217 patients were included. Positive correlations between body weight, clearance and volume of distribution were identified for RIF and PZA, whereas body weight only influenced clearance for INH. In addition, males had higher RIF clearance and thus lower RIF exposure than women. Acetylator status was significantly associated with INH clearance as INH exposure in intermediate and fast acetylators was significantly lower than in slow acetylators, especially in low-weight bands. Simulations also showed significantly lower drug exposures in low-weight bands for all three drugs. Patients weighing <38 kg were respectively exposed to 30.4%, 45.9% and 18.0% lower area under the concentration-time curve of RIF, INH and PZA than those weighing ≥70 kg. Higher doses by addition of one fixed-dose combination tablet or 150 mg INH were simulated and found to be effective in improving INH drug exposures, especially in low-weight bands.
CONCLUSION: PK variability of first-line anti-TB drugs is common in Chinese TB patients. The developed population PK models can be used to optimize drug exposures in Chinese patients. Moreover, standard dosing needs to be adjusted to increase target attainment.
© 2020 The British Pharmacological Society.

Entities:  

Keywords:  antituberculosis drugs; dosing strategy; drug exposure; population pharmacokinetics

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Year:  2020        PMID: 33464624     DOI: 10.1111/bcp.14522

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


  3 in total

1.  Population Pharmacokinetic Modelling and Limited Sampling Strategies for Therapeutic Drug Monitoring of Pyrazinamide in Patients with Tuberculosis.

Authors:  Reihaneh Abolhassani-Chimeh; Onno W Akkerman; Antonia M I Saktiawati; Nieko C Punt; Mathieu S Bolhuis; Yanri W Subronto; Tjip S van der Werf; Jos G W Kosterink; Jan-Willem C Alffenaar; Marieke G G Sturkenboom
Journal:  Antimicrob Agents Chemother       Date:  2022-06-21       Impact factor: 5.938

2.  Paradoxical development of pleural-based masses in patients with pleural tuberculosis during treatment: a clinical observational study in China.

Authors:  Zhengwei Dong; Wei Zhang; Wenwen Sun; Shaojun Zhang; Chenlu Yang; Chunyan Wu; Lin Fan
Journal:  BMC Pulm Med       Date:  2022-04-04       Impact factor: 3.317

Review 3.  Influence of N-acetyltransferase 2 (NAT2) genotype/single nucleotide polymorphisms on clearance of isoniazid in tuberculosis patients: a systematic review of population pharmacokinetic models.

Authors:  Levin Thomas; Arun Prasath Raju; Sonal Sekhar M; Muralidhar Varma; Kavitha Saravu; Mithu Banerjee; Chidananda Sanju Sv; Surulivelrajan Mallayasamy; Mahadev Rao
Journal:  Eur J Clin Pharmacol       Date:  2022-07-19       Impact factor: 3.064

  3 in total

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