Clinical Relevance of Human Immunodeficiency Virus Low-level Viremia in the Dolutegravir era: Data From the Viral Load Cohort North-East Lesotho (VICONEL)

Author:

Kohler Maurus1,Brown Jennifer A1,Tschumi Nadine1,Lerotholi Malebanye12,Motaboli Lipontso3,Mokete Moliehi3,Chammartin Frédérique1,Labhardt Niklaus D14

Affiliation:

1. Division of Clinical Epidemiology, Department of Clinical Research, University Hospital Basel , Basel , Switzerland

2. Ministry of Health Lesotho , Maseru , Lesotho

3. SolidarMed, Partnerships for Health , Maseru , Lesotho

4. Division of Infectious Diseases and Hospital Epidemiology, University Hospital Basel , Basel , Switzerland

Abstract

Abstract Background Human immunodeficiency virus low-level viremia (LLV) is associated with subsequent treatment failure at least with non nucleoside reverse transcriptase inhibitor (NNRTI)-containing antiretroviral therapy. Data on implications of LLV occurring under dolutegravir, which has largely replaced NNRTIs in Africa, are scarce, however. Methods We included adults with human immunodeficiency virus in Lesotho who had ≥2 viral loads (VLs) taken after ≥6 months of NNRTI- or dolutegravir-based antiretroviral therapy. Within VL pairs, we assessed the association of viral suppression (<50 copies/mL) and low- and high-range LLV (50–199 and 200–999 copies/mL, respectively) with virological failure (≥1000 copies/mL) using a mixed-effects regression model. Participants could contribute VLs to the NNRTI and the dolutegravir group. Results Among 18 550 participants, 12 216 (65.9%) were female and median age at first VL included was 41.2 years (interquartile range, 33.4–51.5). In both groups, compared with a suppressed VL, odds of subsequent virological failure were higher for low-range LLV (NNRTI: adjusted odds ratio; 95% confidence interval: 1.9; 1.4–2.4 and dolutegravir: 2.1; 1.3–3.6) and high-range LLV (adjusted odds ratio; 95% confidence interval, 4.2; 3.1–5.7 and 4.4; 2.4–7.9). Conclusions In the dolutegravir era, LLV remains associated with virological failure, endorsing the need for close clinical and laboratory monitoring of those with a VL ≥50 copies/mL.

Funder

Swiss National Science Foundation

Janggen-Pöhn Foundation

Publisher

Oxford University Press (OUP)

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