ArticleJournal of clinical tuberculosis and other mycobacterial diseases2026
Acetylator status-guided rapid reintroduction of isoniazid in tuberculosis patients with drug-induced hepatotoxicity.
Article in Journal of clinical tuberculosis and other mycobacterial diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Background: People who slowly metabolize isoniazid are at increased risk of drug-induced liver injury (DILI) and interruption of tuberculosis treatment. We hypothesized that immediate identification of slow acetylators among patients with DILI will facilitate rapid and safe reintroduction of isoniazid. Methods: Between 2021 and 2023, at our tuberculosis referral centre in The Netherlands, we evaluated an isoniazid acetylator status-guided rapid reintroduction of anti-tuberculous drugs in a cohort of patients with DILI. Patients' acetylator status was determined by phenotyping after a single dose of isoniazid, regardless of liver function abnormalities. Results: In total, 49 tuberculosis patients underwent Therapeutic Drug Monitoring (TDM) from 2021 to 2023, with 67% being slow acetylators as assessed by phenotyping. Out of 10 patients with DILI, 8 were slow acetylators, and the total exposure to isoniazid (AUC Conclusion: In tuberculosis patients with DILI, assessment of isoniazid acetylator status can guide rapid reintroduction of isoniazid. Combined with AUC
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