Pharmacogenetics and Pharmacokinetics of Moxifloxacin in MDR-TB Patients in Indonesia: Analysis for ABCB1 and SLCO1B1

被引:0
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作者
Annisa, Nurul [1 ,2 ]
Afifah, Nadiya N. [1 ,3 ]
Santoso, Prayudi [4 ,5 ]
Yunivita, Vycke [5 ,6 ]
te Brake, Lindsey H. M. [7 ]
Aarnoutse, Rob E. [7 ]
Barliana, Melisa I. [1 ,8 ]
Ruslami, Rovina [5 ,6 ]
机构
[1] Univ Padjadjaran, Fac Pharm, Dept Biol Pharm, Jl Ir Soekarno Km 21, Jatinangor 45363, West Java, Indonesia
[2] Univ Mulawarman, Fac Pharm, Div Clin & Community Pharm, Jl Kuaro Gunung Kelua, Samarinda 75119, East Kalimantan, Indonesia
[3] Univ Esa Unggul, Fac Hlth Sci, Dept Pharm, Jl Arjuna Utara, Jakarta 11510, Indonesia
[4] Univ Padjadjaran, Hasan Sadikin Gen Hosp, Fac Med, Dept Internal Med,Div Pulm & Crit Care, Jl Prof Eyckman, Bandung 40162, West Java, Indonesia
[5] Univ Padjadjaran, Res Ctr Care & Control Infect Dis, Jl Prof Eyckman, Bandung 40162, West Java, Indonesia
[6] Univ Padjadjaran, Fac Med, Dept Biomed Sci, Div Pharmacol & Therapy, Jl Ir Soekarno Km 21, Jatinangor 45363, West Java, Indonesia
[7] Radboud Univ Nijmegen, Radboud Inst Med Innovat, Med Ctr, Dept Pharm, Geert Grooteplein Zuid 10, NL-6525 GA Nijmegen, Netherlands
[8] Univ Padjadjaran, Ctr Excellence Pharmaceut Care Innovat, Jl Ir Soekarno Km 21, Jatinangor 45363, West Java, Indonesia
来源
ANTIBIOTICS-BASEL | 2025年 / 14卷 / 02期
关键词
pharmacogenetics; pharmacokinetics; AUC(0-24); C-max; moxifloxacin; ABCB1; rs2032582; MDR-TB; GENDER; AGE; RIFAMPICIN; EXPRESSION; ABSENCE; DRUGS;
D O I
10.3390/antibiotics14020204
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background/Objectives: Studies show that SNPs in ABCB1 rs2032582 and SLCO1B1 rs4149015 affect the PK profile of moxifloxacin, a key drug for MDR-TB. This study aimed to assess the genotype frequencies of ABCB1 rs2032582 and SLCO1B1 rs4149015; describe moxifloxacin AUC(0-24) and C-max; and evaluate the association between genotype variations and moxifloxacin AUC(0-24) and C-max, corrected for the effect of other determinants in MDR-TB patients in Indonesia. Methods: The genotypes were identified using DNA sequencing. Plasma samples for PK analysis were collected at either two or four timepoints post-dose, at steady state. AUC(0-24) values were assessed with a limited sampling formula. A multivariate linear regression analysis identified the determinants for moxifloxacin AUC(0-24) and C-max. Results: We recruited 204 MDR-TB patients for PG analysis, with 80 providing PK samples. The majority of the ABCB1 and SLCO1B1 genotypes were wildtype (GG), 41.7% and 93.6%, respectively. The geometric mean AUC(0-24) for moxifloxacin was 78.6 mg center dot h/L and that for C-max was 6.1 mg/L. No statistically significant difference in exposure to moxifloxacin could be shown between the genotypes. Sex, age, and dose in mg/kg/body weight were significant determinants of the AUC(0-24) of moxifloxacin. Conclusions: The major genotype of ABCB1 rs2032582 and SLCO1B1 rs4149015 was wildtype, and the exposure to moxifloxacin was high but not related to the studied genotype in an Indonesian population.
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页数:12
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