Systematic Literature Review and Meta-Analysis of Renal Function in Human Immunodeficiency Virus (HIV)-Infected Patients Treated with Atazanavir (ATV)-Based Regimens

PLoS One. 2015 May 4;10(5):e0124666. doi: 10.1371/journal.pone.0124666. eCollection 2015.

Abstract

Some HIV antiretroviral therapies (ART) have been associated with renal toxicities, which become of increasing concern as HIV-infected patients age and develop comorbidities. The objective of this study was to evaluate the relative impact of atazanavir (ATV)-based regimens on the renal function of adult patients with HIV. We conducted a systematic literature review by searching PubMed, EMBASE, Cochrane library, and the CRD from 2000 until March 2013. Major HIV-related conferences occurring in the past two years were also searched. All randomized clinical trials and large cohort studies assessing renal function in treatment-naïve and/or treatment-experienced HIV patients on ATV-based regimens were included. Fixed-effect mixed-treatment network analyses were carried out on the most frequently reported renal outcomes. 23 studies met the inclusion criteria, and change in estimated glomerular filtration rate (eGFR) from baseline to 48 weeks was identified as the main outcome. Two networks including, respectively, six studies (using the Cockcroft-Gault method) and four studies (using MDRD and CKD-EPI) were analysed. With CG network, ATV/r + TDF/FTC was associated with lower impact on the decline of eGFR than ATV/cobicistat + TDF/FTC but with higher decrease in eGFR than ATV/r + ABC/3TC (difference in mean change from baseline in eGFR respectively +3.67 and -3.89). The use of ATV/cobicistat + TDF/FTC led to a similar decline in eGFR as EVG/cobicistat/TDF/FTC. With respect to third agents combined with TDF/FTC, ATV/r had a lower increase in eGFR in comparison to EFV, and no difference was shown when compared to SQV/r and DRV/r. The effect of ATV-based regimens on renal function at 48 weeks appears similar to other ART regimens and appears to be modest regardless of boosting agent or backbone, although TDF containing backbones consistently leads to greater decline in eGFR.

Publication types

  • Meta-Analysis
  • Review
  • Systematic Review

MeSH terms

  • Adult
  • Anti-HIV Agents / therapeutic use*
  • Atazanavir Sulfate / therapeutic use*
  • Demography
  • Female
  • Glomerular Filtration Rate
  • HIV Infections / drug therapy*
  • HIV Infections / physiopathology*
  • Humans
  • Kidney Function Tests*
  • Male
  • Renal Insufficiency, Chronic / epidemiology
  • Renal Insufficiency, Chronic / physiopathology
  • Risk Factors

Substances

  • Anti-HIV Agents
  • Atazanavir Sulfate

Grants and funding

Helene Hardy (HH), Lisa Rosenblatt (LR), and Timothy Juday (TJ) are affiliated with BMS as the funding organization and have had a role in the study design, preparation of the manuscript, and decision to publish. The authors Sandrine Cure (SC), Florence Bianic (FB), and Caroline Espinas (CE) are affiliated with the commercial company OptumInsight and have had a role in the design, data collection, analysis, preparation of the manuscript, and decision to publish. Furthermore, SC, FB, and CE are employees of OPTUM who have received consultancy fees from BMS; and HH, LR, and TJ have an affiliation to the commercial funders of this research study, Bristol-Myers Squibb.