Title
Association of age, baseline kidney function, and medication exposure with declines in creatinine clearance on pre-exposure prophylaxis: an observational cohort study
Date Issued
01 November 2016
Access level
open access
Resource Type
journal article
Author(s)
Gandhi M.
Glidden D.V.
Mayer K.
Schechter M.
Buchbinder S.
Grinsztejn B.
Hosek S.
Bekker L.G.
Louie A.
Horng H.
Benet L.Z.
Liu A.
Grant R.M.
Publisher(s)
Elsevier Ltd
Abstract
Background As pre-exposure prophylaxis (PrEP) with tenofovir disoproxil fumarate and emtricitabine for the prevention of HIV infection is rolled out internationally, strategies to maintain effectiveness and to minimise adverse effects merit consideration. In this study, we aimed to assess reductions in renal function and predictors of renal toxicity in a large open-label study of PrEP. Methods As part of the iPrEx open-label extension (OLE) study, men who have sex with men or transgender women aged 18–70 years who were HIV negative and had participated in three previous PrEP trials from Brazil, Ecuador, Peru, South Africa, Thailand, and the USA were enrolled into an open-label PrEP study. There were no restrictions on current renal function for enrolment into iPrEx OLE, in which participants were given combination tablets of tenofovir disoproxil fumarate (300 mg) and emtricitabine (200 mg) and advised to take one tablet per day. At follow-up sessions every 12 weeks, participants' creatinine clearance on PrEP was estimated and in a subset of participants, hair samples were collected to measure tenofovir and emtricitabine concentrations (a measure of adherence and exposure) via liquid-chromatography–tandem-mass-spectrometry. Reductions in creatinine clearance from baseline were calculated and predictors of decline were identified by use of multivariate models. iPrEx is registered with ClinicalTrials.com, number NCT00458393. Findings Baseline characteristics were similar between all participants in iPrEx-OLE (1224 participants with 7475 person-visits) and those participating in the hair substudy (220 participants with 1114 person-visits). During a median of 72 weeks, the mean decline in creatinine clearance was −2·9% (95% CI −2·4 to −3·4; p trend <0·0001), but declines were greater for those who started PrEP at older ages: participants aged 40–50 years at baseline had declines of −4·2% (95% CI −2·8 to −5·5) and participants older than 50 years at baseline had declines of −4·9% (−3·1 to −6·8). In multivariate models, age and baseline creatinine clearance less than 90 mL/min predicted declines in renal function. We identified a monotonic association between percentage decrease in creatinine clearance and the number of doses of tenofovir disoproxil fumarate and emtricitabine taken per week, as estimated by hair concentrations of tenofovir and emtricitabine (p trend =0·008). Interpretation Our data suggest that the frequency of safety monitoring for PrEP might need to be different between age groups and that pharmacological measures can monitor for toxic effects as well as adherence. Funding National Institutes of Health.
Start page
e521
End page
e528
Volume
3
Issue
11
Language
English
OCDE Knowledge area
Farmacología, Farmacia
Scopus EID
2-s2.0-84994182520
PubMed ID
Source
The Lancet HIV
Sponsor(s)
Gilead Sciences donated emtricitabine and tenofovir disoproxil fumarate for the study, but provided no other financial support and did not contribute to data interpretation or manuscript development. RG has received research funding from ViiV Healthcare for a competing PrEP product and has received grants from Gilead Sciences to attend annual investigator meetings and to support a study video project. DG is a member of a data safety and monitoring board for a ViiV-sponsored trial. KM reports unrestricted research grants from Gilead Sciences and ViiV Healthcare during the conduct of the study. The other authors declare no competing interests. This work was supported by the Division of Acquired Immunodeficiency Syndrome (DAIDS), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), as a cooperative agreement (UO1 AI84735, UO1 AI64002, 2R01 AI062333 to RG and UM1 AI068619). NIAID also supported the hair assays for this work (R01 AI098472, principal investigator MG) and data analysis (R03 AI120819, R03 AI122908, principal investigator DG). U01 AI034989 (Women's Interagency HIV Study) supported positive controls and reagents for the hair assays. We thank the participants in the iPrEx OLE study and the study staff. We also thank the Hair Analytical Laboratory at University of California, San Francisco (CA, USA) for work on the hair assays, as well as Stephen May for research coordination work. We acknowledge and are grateful to Hao Zhang (programme officer at NIAD for R01 AI098472) for his invaluable support and scientific input. This work was supported by the Division of Acquired Immunodeficiency Syndrome (DAIDS), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH) , as a cooperative agreement ( UO1 AI84735, UO1 AI64002, 2R01 AI062333 to RG and UM1 AI068619 ). NIAID also supported the hair assays for this work (R01 AI098472, principal investigator MG) and data analysis (R03 AI120819, R03 AI122908, principal investigator DG). U01 AI034989 (Women's Interagency HIV Study) supported positive controls and reagents for the hair assays. We thank the participants in the iPrEx OLE study and the study staff. We also thank the Hair Analytical Laboratory at University of California, San Francisco (CA, USA) for work on the hair assays, as well as Stephen May for research coordination work. We acknowledge and are grateful to Hao Zhang (programme officer at NIAD for R01 AI098472) for his invaluable support and scientific input.
Sources of information: Directorio de Producción Científica Scopus