Use of Contemporary Protease Inhibitors and Risk of Incident Chronic Kidney Disease in Persons With Human Immunodeficiency Virus: the Data Collection on Adverse Events of Anti-HIV Drugs (D:A:D) Study

Author:

Ryom Lene1,Dilling Lundgren Jens1ORCID,Reiss Peter23,Kirk Ole1,Law Matthew4,Ross Mike5,Morlat Phillip6,Andreas Fux Christoph7,Fontas Eric8,De Wit Stephane9,D’Arminio Monforte Antonella10,El-Sadr Wafaa11,Phillips Andrew12,Ingrid Hatleberg Camilla1,Sabin Caroline12,Mocroft Amanda12ORCID,

Affiliation:

1. Rigshospitalet, University of Copenhagen, CHIP, Department of Infectious Diseases, Centre for Cardiac, Vascular, Pulmonary and Infectious Diseases, Copenhagen, Denmark

2. Amsterdam University Medical Centres (Location AMC), Department of Global Health and Division of Infectious Diseases, University of Amsterdam

3. HIV Monitoring Foundation, Amsterdam, The Netherlands

4. Kirby Institute, University of New South Wales Sydney, Australia

5. Albert Einstein College of Medicine/Montefiore Medical Center, Bronx, and

6. Université de Bordeaux, INSERM

7. Clinic for Infectious Diseases and Hospital Hygiene, Kantonsspital Aarau, Switzerland

8. Department of Public Health, Nice University Hospital, France

9. Division of Infectious Diseases, Saint Pierre University Hospital, Université Libre de Bruxelles, Brussels, Belgium

10. Dipartimento di Scienze della Salute, Clinica di Malattie Infettive e Tropicali, Azienda Ospedaliera-Polo Universitario San Paolo, Milan, Italy

11. ICAP at Columbia University and Harlem Hospital, New York

12. Centre for Clinical Research, Epidemiology, Modelling and Evaluation, Institute for Global Health, University College London, London, United Kingdom

Abstract

Abstract Background It is unclear whether use of contemporary protease inhibitors pose a similar risk of chronic kidney disease (CKD) as use of older protease inhibitors. Methods Participants in the Data Collection on Adverse Events of Anti-HIV Drugs (D:A:D) study were followed up until the earliest occurrence of CKD, the last visit plus 6 months, or 1 February 2016. Adjusted Poisson regression was used to assess associations between CKD and the use of ritonavir-boosted atazanavir (ATV/r) or ritonavir-boosted darunavir (DRV/r). Results The incidence of CKD (10.0/1000 person-years of follow-up; 95% confidence interval, 9.5–10.4/1000 person-years of follow-up) increased gradually with increasing exposure to ATV/r, but the relation was less clear for DRV/r. After adjustment, only exposure to ATV/r (adjusted incidence rate ratio, 1.4; 95% confidence interval, 1.2–1.6), but not exposure to DRV/r (1.0; .8–1.3), remained significantly associated with CKD. Conclusion While DRV/r use was not significantly associated with CKD an increasing incidence with longer ATV/r use was confirmed.

Funder

Highly Active Antiretroviral Therapy Oversight Committee

Danish National Research Foundation

Australian Government Department of Health and Ageing

National Institute of Allergy and Infectious Diseases

National Institutes of Health

Janssen Research & Development

Merck

Pfizer

GlaxoSmithKline

Swiss National Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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