Incomplete Reversibility of Estimated Glomerular Filtration Rate Decline Following Tenofovir Disoproxil Fumarate Exposure

被引:93
作者
Jose, Sophie [1 ]
Hamzah, Lisa [2 ,3 ]
Campbell, Lucy J. [2 ,3 ]
Hill, Teresa [1 ]
Fisher, Martin [10 ]
Leen, Clifford [11 ]
Gilson, Richard [4 ]
Walsh, John [5 ]
Nelson, Mark [6 ]
Hay, Phillip [7 ]
Johnson, Margaret [8 ]
Chadwick, David [12 ]
Nitsch, Dorothea [9 ]
Jones, Rachael [6 ]
Sabin, Caroline A. [1 ]
Post, Frank A. [2 ,3 ]
机构
[1] UCL, Res Dept Infect & Populat Hlth, London NW3 2PF, England
[2] Kings Coll Hosp Natl Hlth Serv NHS Fdn Trust, London, England
[3] Kings Coll London, Sch Med, London WC2R 2LS, England
[4] Univ Coll Med Sch, Mortimer Market Ctr, London, England
[5] Imperial Coll Healthcare NHS Trust, London, England
[6] Chelsea & Westminster NHS Fdn Trust, London, England
[7] St Georges Healthcare NHS Trust, London, England
[8] Royal Free Hampstead NHS Trust, London, England
[9] London Sch Hyg & Trop Med, London WC1, England
[10] Brighton & Sussex Univ Hosp NHS Trust, Brighton, E Sussex, England
[11] Lothian Univ Hosp NHS Trust, Edinburgh, Midlothian, Scotland
[12] South Tees Hosp NHS Fdn Trust, Middlesbrough, Cleveland, England
基金
英国医学研究理事会; 美国国家卫生研究院;
关键词
tenofovir; highly active antiretroviral therapy; eGFR; eGFR slopes; renal function; kidney; CHRONIC KIDNEY-DISEASE; RENAL-FUNCTION; ANTIRETROVIRAL THERAPY; TUBULAR DYSFUNCTION; NAIVE PATIENTS; RISK-FACTORS; HIV PATIENTS; NEPHROTOXICITY; TOXICITY; SAFETY;
D O I
10.1093/infdis/jiu107
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Tenofovir disoproxil fumarate (TDF) has been linked to renal impairment, but the extent to which this impairment is reversible is unclear. We aimed to investigate the reversibility of renal decline during TDF therapy. Methods. Cox proportional hazards models assessed factors associated with discontinuing TDF in those with an exposure duration of >6 months. In those who discontinued TDF therapy, linear piecewise regression models estimated glomerular filtration rate (eGFR) slopes before initiation of, during, and after discontinuation of TDF therapy. Factors associated with not achieving eGFR recovery 6 months after discontinuing TDF were assessed using multi-variable logistic regression. Results. We observed declines in the eGFR during TDF exposure (mean slopes, -15.7 mL/minute/1.73 m(2)/year [95% confidence interval {CI}, -20.5 to -10.9] during the first 3 months and -3.1 mL/minute/1.73 m(2)/year [95% CI, -4.6 to -1.7] thereafter) and evidence of eGFR increases following discontinuation of TDF therapy (mean slopes, 12.5 mL/minute/1.73 m(2)/year [95% CI, 8.9-16.1] during the first 3 months and 0.8 mL/minute/1.73 m(2)/year [95% CI,.1-1.5] thereafter). Following TDF discontinuation, 38.6% of patients with a decline in the eGFR did not experience recovery. A higher eGFR at baseline, a lower eGFR after discontinuation of TDF therapy, and more-prolonged exposure to TDF were associated with an increased risk of incomplete recovery 6 months after discontinuation of TDF therapy. Conclusions. This study shows that a decline in the eGFR during TDF therapy was not fully reversible in one third of patients and suggests that prolonged TDF exposure at a low eGFR should be avoided.
引用
收藏
页码:363 / 373
页数:11
相关论文
共 49 条
[1]  
[Anonymous], 2010, ANTIRETROVIRAL THEOR
[2]   The uncertainty of the eGFR [J].
Badrick T. ;
Turner P. .
Indian Journal of Clinical Biochemistry, 2013, 28 (3) :242-247
[3]   Intra-individual variation in creatinine and cystatin C [J].
Bandaranayake, Niluka ;
Ankrah-Tetteh, Thelma ;
Wijeratne, Sethsiri ;
Swaminathan, Ramasamyiyer .
CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2007, 45 (09) :1237-1239
[4]   Evaluation of mitochondrial DNA content and enzyme levels in tenofovir DF-treated rats, rhesus monkeys and woodchucks [J].
Biesecker, G ;
Karimi, S ;
Desjardins, J ;
Meyer, D ;
Abbott, B ;
Bendele, R ;
Richardson, F .
ANTIVIRAL RESEARCH, 2003, 58 (03) :217-225
[5]   Assessment of mitochondrial toxicity in human cells treated with tenofovir: Comparison with other nucleoside reverse transcriptase inhibitors [J].
Birkus, G ;
Hitchcock, MJM ;
Cihlar, T .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (03) :716-723
[6]   High rate of reversibility of renal damage in a cohort of HIV-infected patients receiving tenofovir-containing antiretroviral therapy [J].
Bonjoch, Anna ;
Echeverria, Patricia ;
Perez-Alvarez, Nuria ;
Puig, Jordi ;
Estany, Carla ;
Clotet, Bonaventura ;
Negredo, Eugenia .
ANTIVIRAL RESEARCH, 2012, 96 (01) :65-69
[7]   Relationship between renal dysfunction, nephrotoxicity and death among HIV adults on tenofovir [J].
Brennan, Alana ;
Evans, Denise ;
Maskew, Mhairi ;
Naicker, Saraladevi ;
Ive, Prudence ;
Sanne, Ian ;
Maotoe, Thapelo ;
Fox, Matthew .
AIDS, 2011, 25 (13) :1603-1609
[8]  
CAMPBELL L, 2009, US FOR SERV GEN TECH, V39, P11
[9]   Spectrum of chronic kidney disease in HIV-infected patients [J].
Campbell, L. J. ;
Ibrahim, F. ;
Fisher, M. ;
Holt, S. G. ;
Hendry, B. M. ;
Post, F. A. .
HIV MEDICINE, 2009, 10 (06) :329-336
[10]   Is Tenofovir-Related Renal Toxicity Incompletely Reversible? [J].
Campbell, Lucy J. ;
Hamzah, Lisa ;
Post, Frank A. .
JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2011, 56 (03) :E95-E95