High efavirenz serum concentrations in TB/HIV-coinfected Ugandan adults with a CYP2B6 516 TT genotype on anti-TB treatment

被引:8
作者
von Braun, Amrei [1 ,2 ,5 ]
Castelnuovo, Barbara [1 ]
Ledergerber, Bruno [2 ]
Cusato, Jessica [3 ]
Buzibye, Allan [1 ]
Kambugu, Andrew [1 ]
Fehr, Jan [2 ,4 ]
Calcagno, Andrea [3 ]
Lamorde, Mohammed [1 ]
Sekaggya-Wiltshire, Christine [1 ]
机构
[1] Makerere Univ, Infect Dis Inst, Coll Hlth Sci, Kampala, Uganda
[2] Univ Zurich, Univ Zurich Hosp, Div Infect Dis & Hosp Epidemiol, Zurich, Switzerland
[3] Univ Torino, Dept Med Sci, Infect Dis Unit, Turin, Italy
[4] Univ Zurich, Epidemiol Biostat & Prevent Inst, Dept Publ Hlth, Zurich, Switzerland
[5] Leipzig Univ Hosp, Div Infect Dis & Trop Med, Liebigstr 20, D-04103 Leipzig, Germany
关键词
PHARMACOKINETICS; THERAPY;
D O I
10.1093/jac/dky379
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: To report the efavirenz serum concentrations in TB/HIV-coinfected Ugandan adults on concomitant anti-TB treatment and analyse factors associated with elevated concentrations in this specific population. Methods: Serum efavirenz concentrations in TB/HIV-coinfected Ugandan adults on efavirenz-based ART (600 mg daily) were measured onsite at 2, 8, 12 and 24 weeks of concomitant anti-TB treatment, including rifampicin. Genetic analysis was done retrospectively through real-time PCR by allelic discrimination (CYP2B6 516G>T, rs3745274). Univariable and multivariable logistic regression analyses were done to assess factors potentially associated with elevated efavirenz serum concentrations. Results: A total of 166 patients were included in the analysis. The median age was 34 (IQR = 30-40) years, 99 (59.6%) were male, the median CD4 cell count was 195 (IQR = 71-334) cells/mm(3) and the median BMI was 19 (IQR = 17.6-21.5) kg/m(2). Almost half of all patients (82, 49.4%) had at least one efavirenz serum concentration above the reference range of 4 mg/L. The serum efavirenz concentrations of patients with genotype CYP2B6 516 TT were consistently above 4 mg/L and significantly higher than those of patients with GG/GT genotypes: CYP2B6 516 TT 9.6 mg/L (IQR = 7.3-13.3) versus CYP2B6 516 GT 3.4 mg/L (IQR = 2.1-5.1) and CYP2B6 516 GG 2.6 mg/L (IQR = 1.3-4.0) (Wilcoxon rank-sum test: P < 0.0001). Conclusions: A large proportion of our study participants had at least one efavirenz serum concentration >4 mg/L. The CYP2B6 516 TT genotype was the strongest predictor of high concentration. Physicians should be vigilant that efavirenz serum concentrations may be elevated in patients on concomitant anti-TB treatment and that individualized care is warranted whenever possible.
引用
收藏
页码:135 / 138
页数:4
相关论文
共 13 条
[1]   Efficacy and safety of efavirenz 400 mg daily versus 600 mg daily: 96-week data from the randomised, double-blind, placebo-controlled, non-inferiority ENCORE1 study [J].
Amin, Janaki ;
Becker, Stephen ;
Belloso, Waldo ;
To, Marta Boffi ;
Cooper, David ;
Crabtree-Ramirez, Brenda ;
Duncombe, Chris ;
Emery, Sean ;
Foulkes, Sharne ;
Hill, Andrew ;
Jessen, Heiko ;
Kumar, Suresh ;
Lee, Man-Po ;
Losso, Marcelo ;
Nwizu, Chidi ;
Phanuphak, Praphan ;
Rooney, Tim Read Jim ;
Er, Kim Schaff ;
Shahar, Eduardo ;
Winston, Alan ;
Wolff, Marcelo ;
Young, Barnaby ;
Abela, Cecilia ;
Amin, Janaki ;
Avihingsanon, Anchalee ;
Belloso, Waldo ;
Boyd, Mark ;
Carey, Dianne ;
Clarke, Amanda ;
Cooper, David ;
Courtney-Vega, Kymme ;
No, Marina Delfi ;
Donaldson, Anna ;
Emery, Sean ;
Espinosa, Natalie ;
Johannesen, Tanya ;
Lin, Enmoore ;
Losso, Marcelo ;
Moricz, Alejandra ;
Pett, Sarah ;
Phanupak, Praphan ;
Puls, Rebekah ;
Pussadee, Kanitta ;
Sutheerasak, Parinya ;
Tomlins, Louise ;
Ubolyam, Sasiwimol ;
Belloso, Waldo ;
Azwa, Raja Iskandar Shah bin Raja ;
Bissio, Emiliano ;
Calanni, Liliana .
LANCET INFECTIOUS DISEASES, 2015, 15 (07) :793-802
[2]  
[Anonymous], 2010, TREATM TUB GUID
[3]   Efavirenz and the CNS: what we already know and questions that need to be answered [J].
Apostolova, Nadezda ;
Funes, Haryes A. ;
Blas-Garcia, Ana ;
Galindo, Maria J. ;
Alvarez, Angeles ;
Esplugues, Juan V. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2015, 70 (10) :2693-2708
[4]   Interpatient variability in the pharmacokinetics of the HIV non-nucleoside reverse transcriptase inhibitor efavirenz:: the effect of gender, race, and CYP2B6 polymorphism [J].
Burger, D ;
van der Heiden, I ;
la Porte, C ;
van der Ende, M ;
Groeneveld, P ;
Richter, C ;
Koopmans, P ;
Kroon, F ;
Sprenger, H ;
Lindemans, J ;
Schenk, P ;
van Schaik, R .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2006, 61 (02) :148-154
[5]  
Cohen K, 2009, ANTIVIR THER, V14, P687
[6]   Pharmacokinetics of Efavirenz and Treatment of HIV-1 Among Pregnant Women With and Without Tuberculosis Coinfection [J].
Dooley, Kelly E. ;
Denti, Paolo ;
Martinson, Neil ;
Cohn, Silvia ;
Mashabela, Fildah ;
Hoffmann, Jennifer ;
Haas, David W. ;
Hull, Jennifer ;
Msandiwa, Regina ;
Castel, Sandra ;
Wiesner, Lubbe ;
Chaisson, Richard E. ;
McIlleron, Helen .
JOURNAL OF INFECTIOUS DISEASES, 2015, 211 (02) :197-205
[7]   Prediction of neuropsychiatric adverse events associated with long-term efavirenz therapy, using plasma drug level monitoring [J].
Gutiérrez, F ;
Navarro, A ;
Padilla, S ;
Antón, R ;
Masiá, M ;
Borrás, J ;
Martín-Hidalgo, A .
CLINICAL INFECTIOUS DISEASES, 2005, 41 (11) :1648-1653
[8]   Efavirenz plasma levels can predict treatment failure and central nervous system side effects in HIV-1-infected patients [J].
Marzolini, C ;
Telenti, A ;
Decosterd, LA ;
Greub, G ;
Biollaz, J ;
Buclin, T .
AIDS, 2001, 15 (01) :71-75
[9]   CYP2B6 genotype-based efavirenz dose recommendations during rifampicin-based antituberculosis cotreatment for a sub-Saharan Africa population [J].
Mukonzo, Jackson K. ;
Bisaso, Ronald K. ;
Ogwal-Okeng, Jasper ;
Gustafsson, Lars L. ;
Owen, Joel S. ;
Aklillu, Eleni .
PHARMACOGENOMICS, 2016, 17 (06) :603-613
[10]   Pharmacokinetic and pharmacogenomic modelling of the CYP3A activity marker 4β-hydroxycholesterol during efavirenz treatment and efavirenz/rifampicin co-treatment [J].
Ngaimisi, E. ;
Minzi, O. ;
Mugusi, S. ;
Sasi, P. ;
Riedel, K. -D. ;
Suda, A. ;
Ueda, N. ;
Bakari, M. ;
Janabi, M. ;
Mugusi, F. ;
Bertilsson, L. ;
Burhenne, J. ;
Aklillu, E. ;
Diczfalusy, U. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2014, 69 (12) :3311-3319