Prevalence of Human Immunodeficiency Virus-1 Integrase Strand Transfer Inhibitor Resistance in British Columbia, Canada Between 2009 and 2016: A Longitudinal Analysis

Author:

Kamelian Kimia12ORCID,Lepik Katherine J13,Chau William1,Yip Benita1,Zhang Wendy W12,Lima Viviane Dias12,Robbins Marjorie A1,Woods Conan1,Olmstead Andrea12,Joy Jeffrey B12,Barrios Rolando14,Harrigan P Richard2

Affiliation:

1. BC Centre for Excellence in HIV/AIDS, Vancouver, British Columbia, Canada

2. University of British Columbia, Department of Medicine, Division of AIDS, Vancouver, Canada

3. Pharmacy Department, St. Paul’s Hospital, Vancouver, British Columbia, Canada

4. University of British Columbia, School of Population and Public Health, Vancouver, Canada

Abstract

AbstractBackgroundIntegrase strand transfer inhibitors (INSTIs) are highly efficacious and well tolerated antiretrovirals with fewer adverse side-effects relative to other classes of antiretrovirals. The use of INSTIs raltegravir, elvitegravir, and dolutegravir has increased dramatically over recent years. However, there is limited information about the evolution and prevalence of INSTI resistance mutations in clinical human immunodeficiency virus populations.MethodsHuman immunodeficiency virus-1-positive individuals ≥19 years were included if they received ≥1 dispensed prescription of antiretroviral therapy (ART) in British Columbia between 2009 and 2016 (N = 9358). Physician-ordered drug resistance tests were analyzed and protease inhibitor (PI), reverse-transcriptase inhibitor (RT), and INSTI resistance were defined as having ≥1 sample with a combined, cumulative score ≥30 by Stanford HIV Drug Resistance Algorithm version 7.0.1.ResultsAlthough most ART-treated individuals were tested for PI and RT resistance, INSTI resistance testing lagged behind the uptake of INSTIs among INSTI-treated individuals (11% in 2009; 34% in 2016). The prevalence of INSTI resistance was relatively low, but it increased from 1 to 7 per 1000 ART-treated individuals between 2009 and 2016 (P < .0001, R2 = 0.98). Integrase strand transfer inhibitor resistance mutations increased at integrase codons 66, 97, 140, 148, 155, and 263.ConclusionsThe prevalence of INSTI resistance remains low compared with PI and RT resistance in ART-treated populations but is expanding with increased INSTI use.

Funder

Large-Scale Applied Research Project in Genomics and Personalized Health

Genome Canada

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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