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Model-Based Assessment of Variability in Isoniazid Pharmacokinetics and Metabolism in Patients Co-Infected With Tuberculosis and HIV: Implications for a Novel Dosing Strategy

Artikel i vetenskaplig tidskrift
Författare Jesper Sundell
E. Bienvenu
D. Janzen
Sofia Birgersson
Angela Äbelö
Michael Ashton
Publicerad i Clinical Pharmacology & Therapeutics
Volym 108
Nummer/häfte 1
Sidor 73-80
ISSN 0009-9236
Publiceringsår 2020
Publicerad vid Institutionen för neurovetenskap och fysiologi, sektionen för farmakologi
Sidor 73-80
Språk en
Länkar dx.doi.org/10.1002/cpt.1806
Ämnesord antituberculosis drug concentrations, nat2 genotype, rifampin, efavirenz, therapy, hepatotoxicity, plasma, polymorphisms, hydrazine, phenotype, Pharmacology & Pharmacy
Ämneskategorier Farmaceutisk vetenskap

Sammanfattning

Tuberculosis is the most common cause of death in HIV-infected patients. Isoniazid is used as a first-line drug to treat tuberculosis infection. However, variability in isoniazid pharmacokinetics can result in hepatotoxicity or treatment failure. Determination of clinical factors affecting isoniazid pharmacokinetics and metabolic pathways in HIV co-infected patients is therefore critical. Plasma levels of isoniazid, acetyl-isoniazid, and isonicotinic acid from 63 patients co-infected with tuberculosis and HIV were analyzed by liquid chromatography with tandem mass spectrometry followed by nonlinear mixed-effects modeling. Patients were genotyped to determine acetylator status. Patients were either on concomitant efavirenz-based antiretroviral therapy or HIV treatment naive. Clearances of isoniazid were 1.3-fold and 2.3-fold higher in intermediate and rapid acetylators, respectively, compared with slow acetylators. Patients on concomitant efavirenz-based antiretroviral therapy had 64% and 80% higher population predicted clearances of acetyl-isoniazid and isonicotinic acid, respectively, compared with patients who were HIV treatment naive. Both sex and CD4 cell count affected the bioavailability of isoniazid. Variability in isoniazid exposure could be reduced by dose adaptions based on acetylator type and sex in addition to the currently used weight bands. A novel dosing strategy that has the potential to reduce isoniazid-related toxicity and treatment failure is presented.

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