High prevalence of pre-treatment HIV drug resistance in Papua New Guinea: findings from the first nationally representative pre-treatment HIV drug resistance study.


Journal

BMC infectious diseases
ISSN: 1471-2334
Titre abrégé: BMC Infect Dis
Pays: England
ID NLM: 100968551

Informations de publication

Date de publication:
19 Mar 2022
Historique:
received: 15 04 2021
accepted: 08 03 2022
entrez: 20 3 2022
pubmed: 21 3 2022
medline: 23 3 2022
Statut: epublish

Résumé

Determining the prevalence of pre-treatment HIV drug resistance (PDR) is important to assess the effectiveness of first-line therapies. To determine PDR prevalence in Papua New Guinea (PNG), we conducted a nationally representative survey. We used a two-stage cluster sampling method to recruit HIV treatment initiators with and without prior exposure to antiretroviral therapies (ART) in selected clinics. Dried blood spots were collected and tested for PDR. A total of 315 sequences were available for analysis. The overall PDR prevalence rate was 18.4% (95% CI 13.8-24.3%). The prevalence of PDR to non-nucleoside analog reverse-transcriptase inhibitors (NNRTIs) was 17.8% (95% CI 13.6-23.0%) and of PDR to nucleoside reverse transcriptase inhibitors (NRTIs) was 6.3% (95% CI 1.6-17.1%). The PDR prevalence rate among people reinitiating ART was 42.4% (95% CI 29.1-56.4%). PNG has a high PDR prevalence rate, especially to NNRTI-based first-line therapies. Our findings suggest that removing NNRTIs as part of first-line treatment is warranted and will lead to improving viral suppression rates in PNG.

Sections du résumé

BACKGROUND BACKGROUND
Determining the prevalence of pre-treatment HIV drug resistance (PDR) is important to assess the effectiveness of first-line therapies. To determine PDR prevalence in Papua New Guinea (PNG), we conducted a nationally representative survey.
METHODS METHODS
We used a two-stage cluster sampling method to recruit HIV treatment initiators with and without prior exposure to antiretroviral therapies (ART) in selected clinics. Dried blood spots were collected and tested for PDR.
RESULTS RESULTS
A total of 315 sequences were available for analysis. The overall PDR prevalence rate was 18.4% (95% CI 13.8-24.3%). The prevalence of PDR to non-nucleoside analog reverse-transcriptase inhibitors (NNRTIs) was 17.8% (95% CI 13.6-23.0%) and of PDR to nucleoside reverse transcriptase inhibitors (NRTIs) was 6.3% (95% CI 1.6-17.1%). The PDR prevalence rate among people reinitiating ART was 42.4% (95% CI 29.1-56.4%).
CONCLUSIONS CONCLUSIONS
PNG has a high PDR prevalence rate, especially to NNRTI-based first-line therapies. Our findings suggest that removing NNRTIs as part of first-line treatment is warranted and will lead to improving viral suppression rates in PNG.

Identifiants

pubmed: 35305571
doi: 10.1186/s12879-022-07264-y
pii: 10.1186/s12879-022-07264-y
pmc: PMC8934451
doi:

Substances chimiques

Anti-HIV Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

266

Subventions

Organisme : World Health Organization
ID : 001
Pays : International
Organisme : World Health Organization
ID : WHO-CO PTAEO: WPPNG1611068/64156/7.2
Pays : International

Informations de copyright

© 2022. The Author(s).

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Auteurs

Janet Gare (J)

Sexual and Reproductive Health Unit, PNG Institute of Medical Research, Corner of Leigh Vial & Homate St, Goroka, Eastern Highlands Province, 441, Papua New Guinea. janet.gare@pngimr.org.pg.

Ben Toto (B)

Sexual and Reproductive Health Unit, PNG Institute of Medical Research, Corner of Leigh Vial & Homate St, Goroka, Eastern Highlands Province, 441, Papua New Guinea.

Percy Pokeya (P)

United States Centres for Disease Control and Prevention Country Office of Papua New Guinea, Port Moresby, National Capital District, Papua New Guinea.

Linh-Vi Le (LV)

HIV, Hepatitis and STI Unit, Division of Communicable Disease, World Health Organization Regional Office of the Western Pacific, Manila, Philippines.

Nick Dala (N)

Director's Office, National AIDS Council Secretariat, Port Moresby, National Capital District, Papua New Guinea.

Namarola Lote (N)

World Health Organization Country Office of Papua New Guinea, Port Moresby, National Capital District, Papua New Guinea.

Bangan John (B)

World Health Organization Country Office of Papua New Guinea, Port Moresby, National Capital District, Papua New Guinea.

Abel Yamba (A)

United States Centres for Disease Control and Prevention Country Office of Papua New Guinea, Port Moresby, National Capital District, Papua New Guinea.

Kevin Soli (K)

United States Centres for Disease Control and Prevention Country Office of Papua New Guinea, Port Moresby, National Capital District, Papua New Guinea.

Joshua DeVos (J)

Division of Global HIV and TB, International Lab Branch, United States Centers for Disease Control and Prevention, Atlanta, GA, USA.

Heather Paulin (H)

Division of Global HIV and TB, HIV Care and Treatment Branch, United States Centers for Disease Control and Prevention, Atlanta, GA, USA.

Nick Wagar (N)

Division of Global HIV and TB, International Lab Branch, United States Centers for Disease Control and Prevention, Atlanta, GA, USA.

Du-Ping Zheng (DP)

Division of Global HIV and TB, International Lab Branch, United States Centers for Disease Control and Prevention, Atlanta, GA, USA.

Takeshi Nishijima (T)

National Center for Global Health and Medicine, Tokyo, Japan.

Peniel Boas (P)

National HIV Program Division, National Department of Health, Port Moresby, National Capital District, Papua New Guinea.

Angela Kelly-Hanku (A)

Sexual and Reproductive Health Unit, PNG Institute of Medical Research, Corner of Leigh Vial & Homate St, Goroka, Eastern Highlands Province, 441, Papua New Guinea.
Kirby Institute for Infection and Immunity in Society, University of New South Wales, Sydney, NSW, Australia.

Anup Gurung (A)

World Health Organization Country Office of Papua New Guinea, Port Moresby, National Capital District, Papua New Guinea.

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