High residual inflammation despite HIV viral suppression: Lessons learned from real-time adherence monitoring among people with HIV in Africa.


Journal

HIV medicine
ISSN: 1468-1293
Titre abrégé: HIV Med
Pays: England
ID NLM: 100897392

Informations de publication

Date de publication:
05 2022
Historique:
revised: 22 09 2021
received: 16 08 2021
accepted: 10 10 2021
pubmed: 28 10 2021
medline: 15 4 2022
entrez: 27 10 2021
Statut: ppublish

Résumé

Lower antiretroviral therapy (ART) adherence is associated with higher systemic inflammation in virally suppressed people with HIV (PWH); however, previous studies have mostly relied on subjective adherence measures and have not assessed this association by disease stage upon ART initiation. In the Monitoring Early Treatment Adherence study, adherence was monitored electronically in real time among adult, treatment-naïve PWH in Uganda and South Africa who initiated tenofovir disoproxil fumarate/emtricitabine/efavirenz during early-stage (CD4 > 350 cells/µL) or late-stage (CD4 < 200 cells/µL) disease. Participants who achieved viral suppression (< 400 copies/mL) at 6 months and remained suppressed after 12 months were analysed. The association between average ART adherence and plasma concentrations of interleukin 6 (IL-6), soluble CD14 (sCD14) and D-dimer was evaluated using adjusted multivariable linear regression, stratified by disease stage. In all, 488 PWH (61% women, mean age 35 years) were included in the analysis. Median ART adherence overall was 87%. In adjusted models, every 10% increase in average adherence was associated with a 3.0% decrease in IL-6 [95% confidence interval (CI): -5.9 to -0.01, p = 0.05] at 12 months. This relationship was observed in PWH with both early-stage (5.9%, 95% CI: -10.1 to -1.6, p = 0.009) and late-stage disease (3.7%, 95% CI: -7.2 to -0.2, p = 0.039). No significant associations were found with sCD14 or D-dimer. Objective ART adherence measurement was inversely associated with systemic inflammation in PWH who achieved viral suppression after ART initiation in sub-Saharan Africa, with a greater association in those with early-stage HIV. This finding underscores the importance of ART adherence beyond establishing viral suppression.

Sections du résumé

BACKGROUND
Lower antiretroviral therapy (ART) adherence is associated with higher systemic inflammation in virally suppressed people with HIV (PWH); however, previous studies have mostly relied on subjective adherence measures and have not assessed this association by disease stage upon ART initiation.
METHODS
In the Monitoring Early Treatment Adherence study, adherence was monitored electronically in real time among adult, treatment-naïve PWH in Uganda and South Africa who initiated tenofovir disoproxil fumarate/emtricitabine/efavirenz during early-stage (CD4 > 350 cells/µL) or late-stage (CD4 < 200 cells/µL) disease. Participants who achieved viral suppression (< 400 copies/mL) at 6 months and remained suppressed after 12 months were analysed. The association between average ART adherence and plasma concentrations of interleukin 6 (IL-6), soluble CD14 (sCD14) and D-dimer was evaluated using adjusted multivariable linear regression, stratified by disease stage.
RESULTS
In all, 488 PWH (61% women, mean age 35 years) were included in the analysis. Median ART adherence overall was 87%. In adjusted models, every 10% increase in average adherence was associated with a 3.0% decrease in IL-6 [95% confidence interval (CI): -5.9 to -0.01, p = 0.05] at 12 months. This relationship was observed in PWH with both early-stage (5.9%, 95% CI: -10.1 to -1.6, p = 0.009) and late-stage disease (3.7%, 95% CI: -7.2 to -0.2, p = 0.039). No significant associations were found with sCD14 or D-dimer.
CONCLUSIONS
Objective ART adherence measurement was inversely associated with systemic inflammation in PWH who achieved viral suppression after ART initiation in sub-Saharan Africa, with a greater association in those with early-stage HIV. This finding underscores the importance of ART adherence beyond establishing viral suppression.

Identifiants

pubmed: 34704355
doi: 10.1111/hiv.13200
doi:

Substances chimiques

Anti-HIV Agents 0
Interleukin-6 0
Lipopolysaccharide Receptors 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

465-473

Informations de copyright

© 2021 British HIV Association.

Références

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Auteurs

Jose R Castillo-Mancilla (JR)

University of Colorado-AMC, Aurora, Colorado, USA.

Nicholas Musinguzi (N)

Mbarara University of Science and Technology-Massachusetts General Hospital Global Health Collaborative, Mbarara, Uganda.

Stephen Asiimwe (S)

Mbarara University of Science and Technology-Massachusetts General Hospital Global Health Collaborative, Mbarara, Uganda.

Mark J Siedner (MJ)

Massachusetts General Hospital Center for Global Health, Boston, Massachusetts, USA.
Harvard Medical School, Boston, Massachusetts, USA.
Africa Health Research Institute, Durban, South Africa.

Catherine Orrell (C)

Desmond Tutu HIV Centre, Institute of Infectious Diseases and Molecular Medicine & Department of Medicine, University of Cape Town, Cape Town, South Africa.

David R Bangsberg (DR)

Oregon Health & Science University-Portland State University School of Public Health, Portland, Oregon, USA.

Jessica E Haberer (JE)

Massachusetts General Hospital Center for Global Health, Boston, Massachusetts, USA.
Harvard Medical School, Boston, Massachusetts, USA.

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