Do Chinese HIV-infected adult patients with altered renal function need to adjust tenofovir disoproxil fumarate dosage? A population pharmacokinetics analysis

被引:0
|
作者
Chen, Rui [1 ,2 ]
Zhang, Ren-fang [1 ]
Xing, Ya-ru [1 ,3 ]
Liu, Li [1 ]
Yin, Lin [1 ]
Li, Ying-ying [3 ]
Jiao, Zheng [2 ]
Zhang, Li-jun [1 ]
机构
[1] Fudan Univ, Dept Clin Res Ctr, Shanghai Publ Hlth Clin Ctr, Shanghai 201508, Peoples R China
[2] Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Sch Med, Dept Pharm, 241 Huaihai West Rd, Shanghai 200030, Peoples R China
[3] Guilin Med Univ, Sch Pharm, 1 Zhiyuan Rd, Guilin 541199, Peoples R China
关键词
Tenofovir; HIV; Population pharmacokinetics; Renal impairment; Monte Carlo simulation; GLOMERULAR-FILTRATION-RATE; ANTIRETROVIRAL ACTIVITY; THERAPY; SAFETY; DF; EXPOSURE; MODEL;
D O I
10.1016/j.ejps.2024.106851
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Tenofovir disoproxil fumarate (TDF), a prodrug of tenofovir (TFV), is an effective drug in treating patients infected with human immunodeficiency virus (HIV). Previous population pharmacokinetics (PPK) studies have showed the large variabilities in PK of TFV. Furthermore, limited information was known in Chinese populations. Therefore, the aim of this study was to characterize PPK of TDF in Chinese and identify factors that may affect its PK. TFV concentrations (n = 552) from 30 healthy subjects and 162 HIV-infected Chinese adult patients were pooled for PPK analysis by a nonlinear mixed-effects method. The PK of TFV was adequately described as a twocompartment model with first order absorption and elimination. The typical apparent clearance (CL/F) of TFV in 70-kg adults was 137 L/h, higher than that reported in Caucasians and Blacks (45.8-93 L/h). Estimated glomerular filtration rate was identified to be a significant factor influencing CL/F. Monte Carlo simulation showed that the exposure of standard dosing regimen of TDF 300 mg every 24 h in Chinese people with mild renal impairment (60 to 90 ml/min/1.73 m2) was close to that in individuals with normal renal function (90 mL/ min). Dose adjustment is not required for patients with mild renal impairment. Our study might offer new clues for optimal dosing strategies in Chinese patients with HIV-infected.
引用
收藏
页数:8
相关论文
共 45 条
  • [31] Urinary β2 microglobulin can predict tenofovir disoproxil fumarate-related renal dysfunction in HIV-1-infected patients who initiate tenofovir disoproxil fumarate-containing antiretroviral therapy
    Nishijima, Takeshi
    Kurosawa, Takuma
    Tanaka, Noriko
    Kawasaki, Yohei
    Kikuchi, Yoshimi
    Oka, Shinichi
    Gatanaga, Hiroyuki
    AIDS, 2016, 30 (10) : 1563 - 1571
  • [32] Renal function change after switching tenofovir disoproxil fumarate for tenofovir alafenamide in the HIV-positive patients of a metropolitan sexual health service
    Turner, Dane
    Drak, Douglas
    O'Connor, Catherine C.
    Templeton, David J.
    Gracey, David M.
    AIDS RESEARCH AND THERAPY, 2019, 16 (01)
  • [33] Renal function in Japanese HIV-1-positive patients who switch to tenofovir alafenamide fumarate after long-term tenofovir disoproxil fumarate: a single-center observational study
    Abe, Kensuke
    Obara, Taku
    Kamio, Satomi
    Kondo, Asahi
    Imamura, Junji
    Goto, Tatsuya
    Ito, Toshihiro
    Sato, Hiroshi
    Takahashi, Nobuyuki
    AIDS RESEARCH AND THERAPY, 2021, 18 (01)
  • [34] Evaluation of hypophosphataemia in tenofovir disoproxil fumarate (TDF)-exposed and TDF-unexposed HIV-infected out-patients receiving highly active antiretroviral therapy
    Buchacz, K.
    Brooks, J. T.
    Tong, T.
    Moorman, A. C.
    Baker, R. K.
    Holmberg, S. D.
    Greenberg, A.
    HIV MEDICINE, 2006, 7 (07) : 451 - 456
  • [35] Renal function in Japanese HIV-1-positive patients who switch to tenofovir alafenamide fumarate after long-term tenofovir disoproxil fumarate: a single-center observational study
    Kensuke Abe
    Taku Obara
    Satomi Kamio
    Asahi Kondo
    Junji Imamura
    Tatsuya Goto
    Toshihiro Ito
    Hiroshi Sato
    Nobuyuki Takahashi
    AIDS Research and Therapy, 18
  • [36] Prospective study of renal function in HIV-infected pediatric patients receiving tenofovir-containing HAART regimens
    Soler-Palacin, Pere
    Melendo, Susana
    Noguera-Julian, Antoni
    Fortuny, Claudia
    Navarro, Maria L.
    Mellado, Maria J.
    Garcia, Lourdes
    Uriona, Sonia
    Martin-Nalda, Andrea
    Figueras, Concepcio
    AIDS, 2011, 25 (02) : 171 - 176
  • [37] Long-Term Renal Safety of Tenofovir Disoproxil Fumarate in Vertically HIV-Infected Children, Adolescents and Young AdultsA 60-Month Follow-Up Study
    Alessandra Viganò
    Giorgio Bedogni
    Valeria Manfredini
    Vania Giacomet
    Chiara Cerini
    Francesca di Nello
    Francesca Penagini
    Cristiana Caprio
    Gian Vincenzo Zuccotti
    Clinical Drug Investigation, 2011, 31 : 407 - 415
  • [38] Long-term Renal Effects of Tenofovir-Disoproxil-Fumarate in Vertically HIV-Infected Children, Adolescents, and Young Adults: A 132-Month Follow-Up Study
    Giacomet, Vania
    Nannini, Pilar
    Vigano, Alessandra
    Erba, Paola
    Benincaso, Annarita
    Bedogni, Giorgio
    Cattaneo, Dario
    Falvella, Felicia Stefania
    Zuccotti, Gian Vincenzo
    CLINICAL DRUG INVESTIGATION, 2015, 35 (07) : 419 - 426
  • [39] Association between tenofovir plasma trough concentrations in the early stage of administration and discontinuation of up to five years tenofovir disoproxil fumarate due to renal function-related adverse events in Japanese HIV-1 infected patients
    Yagura, Hiroki
    Watanabe, Dai
    Nakauchi, Takao
    Kushida, Hiroyuki
    Hirota, Kazuyuki
    Nishida, Yasuharu
    Yoshino, Munehiro
    Uehira, Tomoko
    Shirasaka, Takuma
    JOURNAL OF PHARMACEUTICAL HEALTH CARE AND SCIENCES, 2024, 10 (01):
  • [40] Vitamin D and Calcium Supplement Attenuate Bone Loss among HIV-Infected Patients Receiving Tenofovir Disoproxil Fumarate/Emtricitabine/Efavirenz: An Open-Label, Randomized Controlled Trial
    Boontanondha, Patawee
    Nimitphong, Hataikarn
    Musikarat, Suchawadee
    Ragkho, Aschara
    Kiertiburanakul, Sasisopin
    CURRENT HIV RESEARCH, 2020, 18 (01) : 52 - 62