Isoniazid pharmacokinetics, pharmacodynamics, and dosing in South African infants
- PMID: 22695364
- PMCID: PMC3397663
- DOI: 10.1097/FTD.0b013e31825c4bc3
Isoniazid pharmacokinetics, pharmacodynamics, and dosing in South African infants
Abstract
Aims: There are limited data on isoniazid (INH) pharmacokinetics in infants and young children and, therefore, uncertainty on appropriate dosing.
Methods: Pharmacokinetic data were obtained from perinatally HIV-exposed South African infants aged 3-24 months receiving INH 10-20 mg·kg·d orally for Mycobacterium tuberculosis prophylaxis. INH pharmacokinetic parameters were characterized using a population pharmacokinetic approach. Dosing simulations were performed to evaluate weight-based INH doses in children based on N-acetyltransferase 2 enzyme (NAT2) genotype, age, maximum concentrations (Cmax) ≥3 mg/L, and area under the curve (AUC0-24) ≥10.52 mg·h/L.
Results: In 151 infants (53% female, 48% HIV positive) receiving a mean INH dose of 14.5 mg·kg·d, mean (±SD) Cmax at 3, 6, and 23 months of age were 10.0 (3.5), 8.6 (2.6), and 9.3 (3.8) mg/L, respectively, mean (±SD) AUC0-24 were 53.6 (26.8), 42 (19.9), and 44 (30.7) mg·h/L, respectively, and mean (±SD) half-lives were 2.1 (0.7), 1.9 (0.6), and 1.8 (0.9) hours, respectively. A trimodal apparent oral clearance of INH as a function of the NAT2 genotype was apparent as early as 3 months. INH was well tolerated. At an average INH dose of 14.5 mg·kg·d, 99% of infants aged 3-24 months have an INH Cmax ≥3 mg/L, and 98% have an INH AUC0-24 ≥10.52 mg·h/L.
Conclusions: INH at an average dose of 14.5 mg/kg once daily was well tolerated in infants and achieved INH Cmax values ≥3 mg/L and AUC0-24 values ≥10.52 mg·h/L.
Figures


Similar articles
-
The pharmacogenetics of NAT2 enzyme maturation in perinatally HIV exposed infants receiving isoniazid.J Clin Pharmacol. 2012 Apr;52(4):511-9. doi: 10.1177/0091270011402826. Epub 2011 May 10. J Clin Pharmacol. 2012. PMID: 21558457 Free PMC article. Clinical Trial.
-
Influence of NAT2 Genotype and Maturation on Isoniazid Exposure in Low-Birth-Weight and Preterm Infants With or Without Human Immunodeficiency Virus (HIV) Exposure.Clin Infect Dis. 2022 Sep 29;75(6):1037-1045. doi: 10.1093/cid/ciac001. Clin Infect Dis. 2022. PMID: 35134861 Free PMC article.
-
Pharmacokinetics of isoniazid in low-birth-weight and premature infants.Antimicrob Agents Chemother. 2014;58(4):2229-34. doi: 10.1128/AAC.01532-13. Epub 2014 Feb 3. Antimicrob Agents Chemother. 2014. PMID: 24492365 Free PMC article.
-
A Systematic Review and Meta-analysis of Isoniazid Pharmacokinetics in Healthy Volunteers and Patients with Tuberculosis.Clin Ther. 2020 Nov;42(11):e220-e241. doi: 10.1016/j.clinthera.2020.09.009. Epub 2020 Oct 5. Clin Ther. 2020. PMID: 33032843
-
Parametric population pharmacokinetics of isoniazid: a systematic review.Expert Rev Clin Pharmacol. 2023 May;16(5):467-489. doi: 10.1080/17512433.2023.2196401. Epub 2023 Apr 3. Expert Rev Clin Pharmacol. 2023. PMID: 36971782
Cited by
-
Optimization of dosing regimens of isoniazid and rifampicin in children with tuberculosis in India.Br J Clin Pharmacol. 2019 Mar;85(3):644-654. doi: 10.1111/bcp.13846. Epub 2019 Jan 17. Br J Clin Pharmacol. 2019. PMID: 30588647 Free PMC article. Clinical Trial.
-
Pharmacokinetics of First-Line Anti-Tubercular Drugs.Indian J Pediatr. 2019 May;86(5):468-478. doi: 10.1007/s12098-019-02911-w. Epub 2019 Mar 26. Indian J Pediatr. 2019. PMID: 30915644 Review.
-
The Non-Linear Child: Ontogeny, Isoniazid Concentration, and NAT2 Genotype Modulate Enzyme Reaction Kinetics and Metabolism.EBioMedicine. 2016 Sep;11:118-126. doi: 10.1016/j.ebiom.2016.07.031. Epub 2016 Jul 27. EBioMedicine. 2016. PMID: 27528266 Free PMC article.
-
Adequacy of the 10 mg/kg Daily Dose of Antituberculosis Drug Isoniazid in Infants under 6 Months of Age.Antibiotics (Basel). 2023 Jan 30;12(2):272. doi: 10.3390/antibiotics12020272. Antibiotics (Basel). 2023. PMID: 36830184 Free PMC article.
-
The Development of an Age-Appropriate Fixed Dose Combination for Tuberculosis Using Physiologically-Based Pharmacokinetic Modeling (PBBM) and Risk Assessment.Pharmaceutics. 2024 Dec 12;16(12):1587. doi: 10.3390/pharmaceutics16121587. Pharmaceutics. 2024. PMID: 39771565 Free PMC article.
References
-
- Swaminathan S, Rekha B. Pediatric tuberculosis: global overview and challenges. Clin Infect Dis. 2010;50(Suppl 3):S184–94. - PubMed
-
- Weber WW, Hein DW. Clinical pharmacokinetics of isoniazid. Clinical pharmacokinetics. 1979;4(6):401–22. - PubMed
-
- Walker K, Ginsberg G, Hattis D, et al. Genetic polymorphism in N-Acetyltransferase (NAT): Population distribution of NAT1 and NAT2 activity. Journal of toxicology and environmental health. 2009;12(5–6):440–72. - PubMed
-
- Preziosi P. Isoniazid: metabolic aspects and toxicological correlates. Current drug metabolism. 2007;8(8):839–51. - PubMed
-
- Donald PR, Sirgel FA, Venter A, et al. The influence of human N-acetyltransferase genotype on the early bactericidal activity of isoniazid. Clin Infect Dis. 2004;39(10):1425–30. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical