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Early or deferred initiation of efavirenz during rifampicin-based TB therapy has no significant effect on CYP3A induction in TB-HIV infected patients.
Aklillu, Eleni; Zumla, Alimuddin; Habtewold, Abiy; Amogne, Wondwossen; Makonnen, Eyasu; Yimer, Getnet; Burhenne, Jürgen; Diczfalusy, Ulf.
Afiliação
  • Aklillu E; Division of Clinical Pharmacology, Department of Laboratory Medicine, Karolinska University Hospital Huddinge C1:68, Karolinska Institutet, Stockholm, Sweden.
  • Zumla A; Division of Infection and Immunity, University College London, NIHR Biomedical Research Centre at UCL Hospitals NHS Foundation Trust, London, UK.
  • Habtewold A; UNZA-UCLMS Research and Training Program, Department of Medicine, University Teaching Hospital, Lusaka, Zambia.
  • Amogne W; Department of Pharmaceutical Sciences, School of Pharmacy, William Carey University, Biloxi, MS, USA.
  • Makonnen E; Department of Internal Medicine, College of Health Science, Addis Ababa University, Addis Ababa, Ethiopia.
  • Yimer G; Department of Pharmacology, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.
  • Burhenne J; Department of Pharmacology, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.
  • Diczfalusy U; Department of Clinical Pharmacology and Pharmacoepidemiology, University of Heidelberg, Heidelberg, Germany.
Br J Pharmacol ; 178(16): 3294-3308, 2021 08.
Article em En | MEDLINE | ID: mdl-33155675
ABSTRACT
BACKGROUND AND

PURPOSE:

In TB-HIV co-infection, prompt initiation of TB therapy is recommended but anti-retroviral treatment (ART) is often delayed due to potential drug-drug interactions between rifampicin and efavirenz. In a longitudinal cohort study, we evaluated the effects of efavirenz/rifampicin co-treatment and time of ART initiation on CYP3A induction. EXPERIMENTAL

APPROACH:

Treatment-naïve TB-HIV co-infected patients (n = 102) were randomized to efavirenz-based-ART after 4 (n = 69) or 8 weeks (n = 33) of commencing rifampicin-based anti-TB therapy. HIV patients without TB (n = 94) receiving efavirenz-based-ART only were enrolled as control. Plasma 4ß-hydroxycholesterol/cholesterol (4ß-OHC/Chol) ratio, an endogenous biomarker for CYP3A activity, was determined at baseline, at 4 and 16 weeks of ART. KEY

RESULTS:

In patients treated with efavirenz only, median 4ß-OHC/Chol ratios increased from baseline by 269% and 275% after 4 and 16 weeks of ART, respectively. In TB-HIV patients, rifampicin only therapy for 4 and 8 weeks increased median 4ß-OHC/Chol ratios from baseline by 378% and 576% respectively. After efavirenz/rifampicin co-treatment, 4ß-OHC/Chol ratios increased by 560% of baseline (4 weeks) and 456% of baseline (16 weeks). Neither time of ART initiation, sex, genotype nor efavirenz plasma concentration were significant predictors of 4ß-OHC/Chol ratios after 4 weeks of efavirenz/rifampicin co-treatment. CONCLUSION AND IMPLICATIONS Rifampicin induced CYP3A more potently than efavirenz, with maximum induction occurring within the first 4 weeks of rifampicin therapy. We provide pharmacological evidence that early (4 weeks) or deferred (8 weeks) ART initiation during anti-TB therapy has no significant effect on CYP3A induction. LINKED ARTICLES This article is part of a themed issue on Oxysterols, Lifelong Health and Therapeutics. To view the other articles in this section visit http//onlinelibrary.wiley.com/doi/10.1111/bph.v178.16/issuetoc.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article