Human Immunodeficiency Virus Infection in Adolescents and Mode of Transmission in Southern Africa: A Multinational Analysis of Population-Based Survey Data.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
16 08 2021
Historique:
received: 18 09 2020
pubmed: 30 4 2021
medline: 23 9 2021
entrez: 29 4 2021
Statut: ppublish

Résumé

Adolescents aged 10-19 years living with human immunodeficiency virus (HIV) (ALHIV), both perinatally infected adolescents (APHIV) and behaviorally infected adolescents (ABHIV), are a growing population with distinct care needs. We characterized the epidemiology of HIV in adolescents included in Population-based HIV Impact Assessments (2015-2017) in Zimbabwe, Malawi, Zambia, Eswatini, and Lesotho. Adolescents were tested for HIV using national rapid testing algorithms. Viral load (VL) suppression (VLS) was defined as VL <1000 copies/mL, and undetectable VL (UVL) as VL <50 copies/mL. Recent infection (within 6 months) was measured using a limiting antigen avidity assay, excluding adolescents with VLS or with detectable antiretrovirals (ARVs) in blood. To determine the most likely mode of infection, we used a risk algorithm incorporating recency, maternal HIV and vital status, history of sexual activity, and age at diagnosis. HIV prevalence ranged from 1.6% in Zambia to 4.8% in Eswatini. Of 707 ALHIV, 60.9% (95% confidence interval, 55.3%-66.6%) had HIV previously diagnosed, and 47.1% (41.9%-52.3%) had VLS. Our algorithm estimated that 72.6% of ALHIV (485 of 707) were APHIV, with HIV diagnosed previously in 69.5% of APHIV and 39.4% of ABHIV, and with 65.3% of APHIV and 33.5% of ABHIV receiving ARV treatment. Only 67.2% of APHIV and 60.5% of ABHIV receiving ARVs had UVL. These findings suggest that two-thirds of ALHIV were perinatally infected, with many unaware of their status. The low prevalence of VLS and UVL in those receiving treatment raises concerns around treatment effectiveness. Expansion of opportunities for HIV diagnoses and the optimization of treatment are imperative.

Sections du résumé

BACKGROUND
Adolescents aged 10-19 years living with human immunodeficiency virus (HIV) (ALHIV), both perinatally infected adolescents (APHIV) and behaviorally infected adolescents (ABHIV), are a growing population with distinct care needs. We characterized the epidemiology of HIV in adolescents included in Population-based HIV Impact Assessments (2015-2017) in Zimbabwe, Malawi, Zambia, Eswatini, and Lesotho.
METHODS
Adolescents were tested for HIV using national rapid testing algorithms. Viral load (VL) suppression (VLS) was defined as VL <1000 copies/mL, and undetectable VL (UVL) as VL <50 copies/mL. Recent infection (within 6 months) was measured using a limiting antigen avidity assay, excluding adolescents with VLS or with detectable antiretrovirals (ARVs) in blood. To determine the most likely mode of infection, we used a risk algorithm incorporating recency, maternal HIV and vital status, history of sexual activity, and age at diagnosis.
RESULTS
HIV prevalence ranged from 1.6% in Zambia to 4.8% in Eswatini. Of 707 ALHIV, 60.9% (95% confidence interval, 55.3%-66.6%) had HIV previously diagnosed, and 47.1% (41.9%-52.3%) had VLS. Our algorithm estimated that 72.6% of ALHIV (485 of 707) were APHIV, with HIV diagnosed previously in 69.5% of APHIV and 39.4% of ABHIV, and with 65.3% of APHIV and 33.5% of ABHIV receiving ARV treatment. Only 67.2% of APHIV and 60.5% of ABHIV receiving ARVs had UVL.
CONCLUSIONS
These findings suggest that two-thirds of ALHIV were perinatally infected, with many unaware of their status. The low prevalence of VLS and UVL in those receiving treatment raises concerns around treatment effectiveness. Expansion of opportunities for HIV diagnoses and the optimization of treatment are imperative.

Identifiants

pubmed: 33912973
pii: 6257705
doi: 10.1093/cid/ciab031
pmc: PMC8366830
doi:

Substances chimiques

Anti-Retroviral Agents 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

594-604

Subventions

Organisme : CGH CDC HHS
ID : U2G GH001226
Pays : United States
Organisme : PEPFAR
Pays : United States

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America.

Auteurs

Andrea Low (A)

ICAP at Columbia, Mailman School of Public Health, New York, New York,USA.
Department of Epidemiology, Mailman School of Public Health, New York,USA.

Chloe Teasdale (C)

ICAP at Columbia, Mailman School of Public Health, New York, New York,USA.
Department of Epidemiology, Mailman School of Public Health, New York,USA.
Department of Epidemiology and Biostatistics, CUNY Graduate School of Public Health and Health Policy, New York, New York,USA.

Kristin Brown (K)

US Centers for Disease Control and Prevention, Atlanta, Georgia,USA.

Danielle T Barradas (DT)

US Centers for Disease Control and Prevention, Lusaka, Zambia.

Owen Mugurungi (O)

Ministry of Health and Child Welfare, AIDS and TB Programme, Harare, Zimbabwe.

Karam Sachathep (K)

ICAP at Columbia, Mailman School of Public Health, New York, New York,USA.

Harriet Nuwagaba-Biribonwoha (H)

ICAP at Columbia, Mailman School of Public Health, New York, New York,USA.
Department of Epidemiology, Mailman School of Public Health, New York,USA.

Sehin Birhanu (S)

US Centers for Disease Control and Prevention, Atlanta, Georgia,USA.

Andrew Banda (A)

Ministry of Health, Lusaka, Zambia.

Koen Frederix (K)

ICAP at Columbia, Mailman School of Public Health, New York, New York,USA.

Danielle Payne (D)

US Centers for Disease Control and Prevention, Lilongwe, Malawi.

Elizabeth Radin (E)

ICAP at Columbia, Mailman School of Public Health, New York, New York,USA.
Department of Epidemiology, Mailman School of Public Health, New York,USA.

Lubbe Wiesner (L)

Division of Clinical Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa.

Choice Ginindza (C)

Eswatini Central Statistical Office, Mbabane, Eswatini.

Neena Philip (N)

ICAP at Columbia, Mailman School of Public Health, New York, New York,USA.
Department of Epidemiology, Mailman School of Public Health, New York,USA.

Godfrey Musuka (G)

ICAP at Columbia, Mailman School of Public Health, New York, New York,USA.

Sakhile Sithole (S)

ICAP at Columbia, Mailman School of Public Health, New York, New York,USA.

Hetal Patel (H)

US Centers for Disease Control and Prevention, Atlanta, Georgia,USA.

Limpho Maile (L)

Ministry of Health, Maseru, Lesotho.

Elaine J Abrams (EJ)

ICAP at Columbia, Mailman School of Public Health, New York, New York,USA.
Department of Epidemiology, Mailman School of Public Health, New York,USA.
Department of Pediatrics, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York,USA.

Stephen Arpadi (S)

ICAP at Columbia, Mailman School of Public Health, New York, New York,USA.
Department of Epidemiology, Mailman School of Public Health, New York,USA.
Department of Pediatrics, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York,USA.

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