A population pharmacokinetic model is beneficial in quantifying hair concentrations of ritonavir-boosted atazanavir: a study of HIV-infected Zimbabwean adolescents

被引:3
|
作者
Ngara, Bernard [1 ]
Zvada, Simbarashe [2 ]
Chawana, Tariro Dianah [3 ]
Stray-Pedersen, Babill [4 ]
Nhachi, Charles Fungai Brian [3 ]
Rusakaniko, Simbarashe [1 ]
机构
[1] Univ Zimbabwe, Dept Community Med, Coll Hlth Sci, Mazowe St,Parirenyatwa Complex,POB A178 Avondale, Harare, Zimbabwe
[2] Stellenbosch Univ, Dept Clin Pharmacol, Private Bag X1, ZA-7602 Stellenbosch, South Africa
[3] Univ Zimbabwe, Coll Hlth Sci, Dept Clin Pharmacol, Mazowe St,Parirenyatwa Complex,POB A178 Avondale, Harare, Zimbabwe
[4] Oslo Univ Hosp, Inst Clin Med, Womens Clin, N-0027 Oslo, Norway
来源
BMC PHARMACOLOGY & TOXICOLOGY | 2020年 / 21卷 / 01期
关键词
Pharmacokinetic modelling; HIV; AIDS; Adolescents; Adherence; Hair; NONMEM; ADHERENCE; EXPOSURE; COCAINE; CONTAMINATION; EFAVIRENZ; HIV/AIDS; CYP2B6;
D O I
10.1186/s40360-020-00437-y
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background Adolescents experience higher levels of non-adherence to HIV treatment. Drug concentration in hair promises to be reliable for assessing exposure to antiretroviral (ARV) drugs. Pharmacokinetic modelling can explore utility of drug in hair. We aimed at developing and validating a pharmacokinetic model based on atazanavir/ritonavir (ATV/r) in hair and identify factors associated with variabilities in hair accumulation. Methods We based the study on secondary data analysis whereby data from a previous study on Zimbabwean adolescents which collected hair samples at enrolment and 3 months follow-up was used in model development. We performed model development in NONMEM (version 7.3) ADVAN 13. Results There is 16% / 18% of the respective ATV/r in hair as a ratio of steady-state trough plasma concentrations. At follow-up, we estimated an increase of 30% /42% of respective ATV/r in hair. We associated a unit increase in adherence score with 2% increase in hair concentration both ATV/r. Thinner participants had 54% higher while overweight had 21% lower atazanavir in hair compared to normal weight participants. Adolescents receiving care from fellow siblings had atazanavir in hair at least 54% less compared to other forms of care. Conclusion The determinants of increased ATV/r concentrations in hair found in our analysis are monitoring at follow up event, body mass index, and caregiver status. Measuring drug concentration in hair is feasibly accomplished and could be more accurate for monitoring ARV drugs exposure.
引用
收藏
页数:9
相关论文
共 50 条
  • [21] Population pharmacokinetics (PK) of ritonavir (RTV)-boosted atazanavir (ATV) in HIV-infected and healthy individuals
    Dickinson, L.
    Aarons, L.
    Back, D.
    Waters, L.
    Else, L.
    Khoo, S.
    Pozniak, A.
    Boffito, M.
    HIV MEDICINE, 2009, 10 : 51 - 52
  • [22] Population pharmacokinetic models for ritonavir boosted atazanavir and tenofovir in highly pretreated HIV infected patients.
    Taburet, A
    Barrail-Tran, A
    Mentré, F
    Piketty, C
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2006, 79 (02) : P47 - P47
  • [23] Dual therapy with dolutegravir plus ritonavir-boosted or unboosted atazanavir as a maintenance treatment in highly experienced HIV-infected patients
    Faycal, A.
    Abdi, B.
    Peytavin, G.
    Tebano, G.
    Schneider, L.
    Seang, S.
    Simon, A.
    Tubiana, R.
    Valantin, M.
    Marcelin, A.
    Katlama, C.
    Palich, R.
    JOURNAL OF THE INTERNATIONAL AIDS SOCIETY, 2018, 21
  • [24] Substitution of raltegravir for ritonavir-boosted protease inhibitors in HIV-infected patients: the SPIRAL study
    Martinez, Esteban
    Larrousse, Maria
    Llibre, Josep M.
    Gutierrez, Felix
    Saumoy, Maria
    Antela, Antonio
    Knobel, Hernando
    Murillas, Javier
    Berenguer, Juan
    Pich, Judit
    Perez, Ignacio
    Gatell, Jose M.
    AIDS, 2010, 24 (11) : 1697 - 1707
  • [25] Safety and Efficacy of a 36-Week Induction Regimen of Abacavir/Lamivudine and Ritonavir-Boosted Atazanavir in HIV-Infected Patients
    Squires, Kathleen E.
    Young, Benjamin
    DeJesus, Edwin
    Bellos, Nicholas
    Murphy, Daniel
    Sutherland-Phillips, Denise H.
    Zhao, Henry H.
    Patel, Lisa G.
    Ross, Lisa L.
    Wannamaker, Paul G.
    Shaefer, Mark S.
    HIV CLINICAL TRIALS, 2010, 11 (02): : 69 - 79
  • [26] Development and validation of a population pharmacokinetic model for atazanavir in HIV-infected patients
    Lopez, Rosa M.
    Colom, Helena
    Pou, Leonor
    Azuaje, Carlos
    Curran, Adrian
    Ribera, Esteve
    Monterde, Josep
    THERAPEUTIC DRUG MONITORING, 2007, 29 (04) : 476 - 476
  • [27] Simplification from tenofovir disoproxil fumarate plus lamivudine or emtricitabine plus ritonavir-boosted protease inhibitor to ritonavir-boosted atazanavir plus lamivudine in virologically suppressed HIV-infected adults with osteopenia: a pilot study
    Blanco, Jose L.
    Rojas, Jhon
    de Lazzari, Elisa
    Inciarte, Alexy
    Subirana, Mar
    Callau, Pilar
    Martinez-Rebollar, Maria
    Laguno, Montserrat
    Mallolas, Josep
    de la Mora, Lorena
    Torres, Berta
    Gonzalez-Cordon, Ana
    Martinez, Esteban
    JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2022, 77 (07) : 1974 - 1979
  • [28] Safety of atazanavir/ritonavir with tenofovir disoproxil fumarate in HIV-infected adolescents
    Bunupuradah, T.
    Techasaensiri, C.
    Keadpudsa, S.
    Srimuan, A.
    Sahakijpicharn, T.
    Sriheara, C.
    Thammajaruk, N.
    Prasitsuebsai, W.
    Ananworanich, J.
    Puthanakit, T.
    INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES, 2014, 21 : 296 - +
  • [29] Simultaneous Population Pharmacokinetic Model for Lopinavir and Ritonavir in HIV-Infected Adults
    José Moltó
    Manuel José Barbanoj
    Cristina Miranda
    Asunción Blanco
    José Ramón Santos
    Eugenia Negredo
    Joan Costa
    Pere Domingo
    Bonaventura Clotet
    Marta Valle
    Clinical Pharmacokinetics, 2008, 47 : 681 - 692
  • [30] Simultaneous population pharmacokinetic model for lopinavir and ritonavir in HIV-infected adults
    Molto, Jose
    Barbanoj, Manuel Jose
    Miranda, Cristina
    Blanco, Asuncion
    Santos, Jose Ramon
    Negredo, Eugenia
    Costa, Joan
    Domingo, Pere
    Clotet, Bonaventura
    Valle, Marta
    CLINICAL PHARMACOKINETICS, 2008, 47 (10) : 681 - 692