Safety and tolerability of isoniazid preventive therapy for tuberculosis for persons with HIV with and without alcohol use

Author:

Hahn Judith A.12,Ngabirano Christine3,Fatch Robin1,Emenyonu Nneka I.1,Cheng Debbie M.4,Adong Julian3,Tumwegamire Adah3,Terrault Norah A.5,Linas Benjamin P.6,Jacobson Karen R.6,Muyindike Winnie R.37

Affiliation:

1. Department of Medicine

2. Department of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, California, USA

3. Faculty of Medicine, Mbarara University of Science and Technology, Mbarara, Uganda

4. School of Public Health, Boston University School of Public Health, Boston, Massachusetts

5. Keck School of Medicine, University of Southern California, Los Angeles, California

6. Boston University Chobanian & Avedisian School of Medicine, Boston University, Boston, Massachusetts, USA

7. Mbarara Regional Referral Hospital, Mbarara, Uganda.

Abstract

Objective: Isoniazid (INH) preventive therapy is recommended to prevent tuberculosis (TB) disease for persons with HIV (PWH), except for those with regular and heavy alcohol consumption, due to hepatotoxicity concerns. We aimed to quantify the incidence of severe INH-related toxicity among PWH with and without recent alcohol consumption. Design: A prospective study of PWH receiving INH. Methods: We included PWH in southwest Uganda with recent (prior 3 months) (n = 200) or no (prior year) self-reported alcohol consumption (n = 101), on antiretroviral therapy, TB infected (≥5 mm on tuberculin skin test), and alanine aminotransferase (ALT) and aspartate aminotransferase (AST) 2× or less the upper limit of normal (ULN). Grade 3+ INH-related toxicity was ALT or AST at least 5× the ULN or severe symptoms; we stopped IPT upon detection. Grade 2 INH-related toxicity was ALT or AST 2–5× the ULN or moderate symptoms. Results: The cumulative incidence of Grade 3+ INH-related toxicity was 8.3% [95% confidence interval (95% CI) 5.4–12.0]; all resolved after INH cessation. Incidence was 6.0% (95% CI 3.1–10.2) among those reporting recent alcohol use and 12.9% (95% CI 7.0–21.0) among those reporting no prior year alcohol use. We found no differences by baseline phosphatidylethanol-confirmed alcohol severity. The cumulative incidence of Grade 2 toxicities (without Grade 3+) was 21.7% (95% CI 17.0–27.1); 25.0% (95% CI 19.0–31.8) among those with recent alcohol use and 14.8% (95% CI 8.1–23.9) among those with no prior year alcohol use. Conclusion: Alcohol use does not appear to increase risk for serious INH-related toxicity among PWH without significant liver enzyme elevations at baseline (≤2x ULN).

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Infectious Diseases,Immunology,Immunology and Allergy

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