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HIV-1 drug resistance mutations among individuals with low-level viraemia while taking combination ART in Botswana.
Bareng, Ontlametse T; Moyo, Sikhulile; Zahralban-Steele, Melissa; Maruapula, Dorcas; Ditlhako, Tsotlhe; Mokaleng, Baitshepi; Mokgethi, Patrick; Choga, Wonderful T; Moraka, Natasha O; Pretorius-Holme, Molly; Mine, Madisa O; Raizes, Elliot; Molebatsi, Kesaobaka; Motswaledi, Modisa S; Gobe, Irene; Mohammed, Terence; Gaolathe, Tendani; Shapiro, Roger; Mmalane, Mompati; Makhema, Joseph M; Lockman, Shahin; Essex, Max; Novitsky, Vlad; Gaseitsiwe, Simani.
Afiliación
  • Bareng OT; Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
  • Moyo S; School of Allied Health Professions, Faculty of Health Sciences, University of Botswana, Gaborone, Botswana.
  • Zahralban-Steele M; Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
  • Maruapula D; Department of Immunology and Infectious Diseases, Harvard T. H. Chan School of Public Health, Boston, MA, USA.
  • Ditlhako T; Department of Immunology and Infectious Diseases, Harvard T. H. Chan School of Public Health, Boston, MA, USA.
  • Mokaleng B; Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
  • Mokgethi P; Department of Biological Sciences, Faculty of Science, University of Botswana, Gaborone, Botswana.
  • Choga WT; Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
  • Moraka NO; Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
  • Pretorius-Holme M; School of Allied Health Professions, Faculty of Health Sciences, University of Botswana, Gaborone, Botswana.
  • Mine MO; Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
  • Raizes E; Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
  • Molebatsi K; Division of Human Genetics, Department of Pathology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
  • Motswaledi MS; Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
  • Gobe I; Division of Medical Virology, Stellenbosch University, Cape Town, South Africa.
  • Mohammed T; Department of Immunology and Infectious Diseases, Harvard T. H. Chan School of Public Health, Boston, MA, USA.
  • Gaolathe T; Botswana Ministry of Health and Wellness, Gaborone, Botswana.
  • Shapiro R; U.S. Centers for Disease Control and Prevention, Atlanta, USA.
  • Mmalane M; Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
  • Makhema JM; Department of Statistics, University of Botswana, Gaborone, Botswana.
  • Lockman S; School of Allied Health Professions, Faculty of Health Sciences, University of Botswana, Gaborone, Botswana.
  • Essex M; School of Allied Health Professions, Faculty of Health Sciences, University of Botswana, Gaborone, Botswana.
  • Novitsky V; Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
  • Gaseitsiwe S; Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
J Antimicrob Chemother ; 77(5): 1385-1395, 2022 04 27.
Article en En | MEDLINE | ID: mdl-35229102
ABSTRACT

OBJECTIVES:

To assess whether a single instance of low-level viraemia (LLV) is associated with the presence of drug resistance mutations (DRMs) and predicts subsequent virological failure (VF) in adults receiving ART in 30 communities participating in the Botswana Combination Prevention Project.

METHODS:

A total of 6078 HIV-1 C pol sequences were generated and analysed using the Stanford HIV drug resistance database. LLV was defined as plasma VL = 51-999 copies/mL and VF was defined as plasma VL ≥ 1000 copies/mL.

RESULTS:

Among 6078 people with HIV (PWH), 4443 (73%) were on ART for at least 6 months. Of the 332 persons on ART with VL > 50 copies/mL, 175 (4%) had VL ≥ 1000 copies/mL and 157 (4%) had LLV at baseline. The prevalence of any DRM was 57 (36%) and 78 (45%) in persons with LLV and VL ≥ 1000 copies/mL, respectively. Major DRMs were found in 31 (20%) with LLV and 53 (30%) with VL ≥ 1000 copies/mL (P = 0.04). Among the 135 PWH with at least one DRM, 17% had NRTI-, 35% NNRTI-, 6% PI- and 3% INSTI-associated mutations. Among the 3596 participants who were followed up, 1709 (48%) were on ART for ≥6 months at entry and had at least one subsequent VL measurement (median 29 months), 43 (3%) of whom had LLV. The OR of experiencing VF in persons with LLV at entry was 36-fold higher than in the virally suppressed group.

CONCLUSIONS:

A single LLV measurement while on ART strongly predicted the risk of future VF, suggesting the use of VL > 50 copies/mL as an indication for more intensive adherence support with more frequent VL monitoring.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Infecciones por VIH / VIH-1 / Seropositividad para VIH / Fármacos Anti-VIH Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Adult / Humans País/Región como asunto: Africa Idioma: En Revista: J Antimicrob Chemother Año: 2022 Tipo del documento: Article País de afiliación: Botswana

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Infecciones por VIH / VIH-1 / Seropositividad para VIH / Fármacos Anti-VIH Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Adult / Humans País/Región como asunto: Africa Idioma: En Revista: J Antimicrob Chemother Año: 2022 Tipo del documento: Article País de afiliación: Botswana