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In Silico Study Supports the Efficacy of a Reduced Dose Regimen for Stavudine

Overview
Journal Antiviral Res
Publisher Elsevier
Date 2011 Aug 31
PMID 21875620
Citations 5
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Abstract

Stavudine (d4T) is used extensively as part of HAART in resource poor settings, despite its toxicities. The revised WHO guidelines specify replacement of d4T with less toxic but more expensive drugs when feasible, and that d4T doses be standardized to 30 mg twice daily (bid) (irrespective of body-weight), from the approved 40 mg bid in adults (body-weight ≥60 kg). Therefore, an in silico population pharmacokinetic and biochemical model was utilized to compare relative efficacies of the two doses in humans. Assessment of predicted quartile ranges of simulated concentrations of the triphosphate of d4T suggested sufficient trough concentrations to inhibit wild type HIV-1 reverse transcriptase at the reduced dose, lending support to the revised WHO recommendations.

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References
1.
Hurwitz S, Asif G, Schinazi R . Development of a population simulation model for HIV monotherapy virological outcomes using lamivudine. Antivir Chem Chemother. 2008; 18(6):329-41. DOI: 10.1177/095632020701800605. View

2.
Becher F, Landman R, Mboup S, Kane C, Canestri A, Liegeois F . Monitoring of didanosine and stavudine intracellular trisphosphorylated anabolite concentrations in HIV-infected patients. AIDS. 2004; 18(2):181-7. DOI: 10.1097/00002030-200401230-00006. View

3.
Diamond T, Roshal M, Jamburuthugoda V, Reynolds H, Merriam A, Lee K . Macrophage tropism of HIV-1 depends on efficient cellular dNTP utilization by reverse transcriptase. J Biol Chem. 2004; 279(49):51545-53. PMC: 1351161. DOI: 10.1074/jbc.M408573200. View

4.
Dube M, Komarow L, Mulligan K, Grinspoon S, Parker R, Robbins G . Long-term body fat outcomes in antiretroviral-naive participants randomized to nelfinavir or efavirenz or both plus dual nucleosides. Dual X-ray absorptiometry results from A5005s, a substudy of Adult Clinical Trials Group 384. J Acquir Immune Defic Syndr. 2007; 45(5):508-14. DOI: 10.1097/QAI.0b013e3181142d26. View

5.
Pedrol E, Martin T, del Pozo M, Flores J, Sanz J, Carton J . [Efficacy and safety of a reduced-dose of stavudine in HIV-infected patients under immunological and virological stable conditions]. Med Clin (Barc). 2007; 129(10):361-5. DOI: 10.1157/13110209. View