Exploring Variability in Rifampicin Plasma Exposure and Development of Anti-Tuberculosis Drug-Induced Liver Injury among Patients with Pulmonary Tuberculosis from the Pharmacogenetic Perspective

• Published in: Pharmaceutics Vol. 16; no. 3; p. 388
• Main Authors: Kivrane, Agnija, Ulanova, Viktorija, Grinberga, Solveiga, Sevostjanovs, Eduards, Viksna, Anda, Ozere, Iveta, Bogdanova, Ineta, Zolovs, Maksims, Ranka, Renate
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.03.2024; MDPI
• Subjects: Analysis; Care and treatment; Drug dosages; Drug resistance; drug-induced liver injury; Efavirenz; Enzymes; Ethylenediaminetetraacetic acid; Genetic testing; Genomes; HIV; Hospitals; Human immunodeficiency virus; liquid chromatography–tandem mass spectrometry; Liver; Liver diseases; next-generation sequencing; Patients; pharmacogenetics; pharmacokinetics; Plasma; Plasma physics; Rifampin; Rifapentine; RNA polymerase; Telmisartan; Tuberculosis; Latvia; Timor-Leste; drug-induced liver injury; pharmacokinetics; liquid chromatography–tandem mass spectrometry; next-generation sequencing; pharmacogenetics; tuberculosis
• ISSN: 1999-4923; 1999-4923
• DOI: 10.3390/pharmaceutics16030388

Genetic polymorphisms can exert a considerable impact on drug pharmacokinetics (PK) and the development of adverse drug reactions (ADR). However, the effect of genetic polymorphisms on the anti-tuberculosis (anti-TB) drug, and particularly rifampicin (RIF), exposure or anti-TB drug-induced liver injury (DILI) remains uncertain. Here, we evaluated the relationship between single nucleotide polymorphisms (SNPs) detected in the RIF pharmacogenes ( , , , , and ) and RIF PK parameters, as well as anti-TB treatment-associated DILI. In total, the study enrolled 46 patients with drug-susceptible pulmonary TB. The RIF plasma concentration was measured using the LC-MS/MS method in the blood samples collected pre-dose and 2 and 6 h post-dose, whilst the DILI status was established using the results from blood biochemical analysis performed before and 10-12 days after treatment onset. The genotyping was conducted using a targeted NGS approach. After adjustment for confounders, the patients carrying the rs3732357 GA/AA genotype of the gene were found to have significantly lower RIF plasma AUC in comparison to those with GG genotype, while the difference in RIF plasma C was insignificant. None of the analyzed SNPs was related to DILI. Hence, we are the first to report intronic SNP rs3732357 as the genetic component of variability in RIF exposure. Regarding anti-TB treatment-associated DILI, the other preexisting factors promoting this ADR should be considered.