Prevalence of undetectable and suppressed viral load in HIV-infected pregnant women initiating Option B+ in Uganda: an observational study nested within a randomized controlled trial.


Journal

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

Informations de publication

Date de publication:
04 Sep 2021
Historique:
received: 15 04 2021
accepted: 17 08 2021
entrez: 5 9 2021
pubmed: 6 9 2021
medline: 25 9 2021
Statut: epublish

Résumé

Viral load (VL) testing is key in monitoring adherence to antiretroviral therapy (ART) and documenting HIV treatment response. As per HIV treatment guidelines in Uganda, the first VL test is recommended 6 months after initiation of ART. Undetectable VL (uVL) at ART initiation may be helpful in detecting elite controllers in the absence of previous ART use. We investigated viral suppression at ART initiation among a cohort of HIV-positive pregnant women enrolled in the Friends for Life Circles (FLC) for Option B+ randomized controlled trial (RCT). Pregnant women ≥ 18 years of age testing positive for HIV at their first antenatal care visit and starting on ART Option B+ as per the National PMTCT Program guidelines were enrolled into the FLC for Option B+ RCT in urban Kampala and rural Mityana districts of Uganda. Each participant had whole blood samples collected at enrolment to assess baseline VL. Plasma HIV-1 RNA was quantified using COBAS Ampliprep /COBAS Taqman. Baseline VL below 400 RNA copies/ml was considered as viral suppression while baseline VL below 20 RNA copies/ml was considered uVL. The mean duration from the date of ART initiation to time of sample collection for baseline VL assessment was 4.4 days (SD 3.6). Of the 532 HIV-positive pregnant women enrolled in the FLC for Option B+ study and newly starting Option B+ without a self-reported history of prior ART use, 29 (5.5%) had uVL and 113 (21.4%) had suppressed VL at baseline. There was no association between participants' age, gravidity, marital status, mean monthly income, educational level, disclosure of HIV status to partner, and uVL or viral suppression at baseline. However, non-disclosure of HIV status to any other person was associated with decreased odds of viral suppression at baseline (OR 0.640; 0.416-0.982). Twenty-one percent of HIV-positive Ugandan pregnant women initiating ART (Option B+) showed virological suppression at baseline and were presumed to be "elite controllers" or to have misreported being ART-naive. Further studies are needed to better understand the biologic mechanisms of elite controllers among pregnant women as well as to differentiate elite controllers from concealed ART use. Trial Registration The trial was registered as NCT02515370 (04/08/2015) on Clinicaltrials.gov.

Sections du résumé

BACKGROUND BACKGROUND
Viral load (VL) testing is key in monitoring adherence to antiretroviral therapy (ART) and documenting HIV treatment response. As per HIV treatment guidelines in Uganda, the first VL test is recommended 6 months after initiation of ART. Undetectable VL (uVL) at ART initiation may be helpful in detecting elite controllers in the absence of previous ART use. We investigated viral suppression at ART initiation among a cohort of HIV-positive pregnant women enrolled in the Friends for Life Circles (FLC) for Option B+ randomized controlled trial (RCT).
METHODS METHODS
Pregnant women ≥ 18 years of age testing positive for HIV at their first antenatal care visit and starting on ART Option B+ as per the National PMTCT Program guidelines were enrolled into the FLC for Option B+ RCT in urban Kampala and rural Mityana districts of Uganda. Each participant had whole blood samples collected at enrolment to assess baseline VL. Plasma HIV-1 RNA was quantified using COBAS Ampliprep /COBAS Taqman. Baseline VL below 400 RNA copies/ml was considered as viral suppression while baseline VL below 20 RNA copies/ml was considered uVL.
RESULTS RESULTS
The mean duration from the date of ART initiation to time of sample collection for baseline VL assessment was 4.4 days (SD 3.6). Of the 532 HIV-positive pregnant women enrolled in the FLC for Option B+ study and newly starting Option B+ without a self-reported history of prior ART use, 29 (5.5%) had uVL and 113 (21.4%) had suppressed VL at baseline. There was no association between participants' age, gravidity, marital status, mean monthly income, educational level, disclosure of HIV status to partner, and uVL or viral suppression at baseline. However, non-disclosure of HIV status to any other person was associated with decreased odds of viral suppression at baseline (OR 0.640; 0.416-0.982).
CONCLUSION CONCLUSIONS
Twenty-one percent of HIV-positive Ugandan pregnant women initiating ART (Option B+) showed virological suppression at baseline and were presumed to be "elite controllers" or to have misreported being ART-naive. Further studies are needed to better understand the biologic mechanisms of elite controllers among pregnant women as well as to differentiate elite controllers from concealed ART use. Trial Registration The trial was registered as NCT02515370 (04/08/2015) on Clinicaltrials.gov.

Identifiants

pubmed: 34481464
doi: 10.1186/s12879-021-06608-4
pii: 10.1186/s12879-021-06608-4
pmc: PMC8417996
doi:

Substances chimiques

Anti-HIV Agents 0

Banques de données

ClinicalTrials.gov
['NCT02515370']

Types de publication

Journal Article Observational Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

907

Informations de copyright

© 2021. The Author(s).

Références

BMC Public Health. 2019 Jul 15;19(1):950
pubmed: 31307455
AIDS. 2018 Jan 28;32(3):363-369
pubmed: 29194115
J Acquir Immune Defic Syndr. 2018 Nov 1;79(3):394-398
pubmed: 30063647
Reprod Health. 2017 Aug 30;14(1):107
pubmed: 28854944
J Infect Dis. 2013 Nov 15;208(10):1624-8
pubmed: 23908493
J Acquir Immune Defic Syndr. 2009 Nov 1;52(3):316-9
pubmed: 19726998
PLoS One. 2014 Jan 28;9(1):e86719
pubmed: 24489776
HIV Clin Trials. 2018 Oct;19(5):202-208
pubmed: 30522410
Clin Infect Dis. 2007 Jun 15;44(12):1647-56
pubmed: 17516411
J Infect Dis. 2019 Jul 19;220(4):643-647
pubmed: 30950501

Auteurs

Grace Gabagaya (G)

Makerere University - Johns Hopkins University Research Collaboration, P.O. Box 23491, Kampala, Uganda.

Gordon Rukundo (G)

Makerere University - Johns Hopkins University Research Collaboration, P.O. Box 23491, Kampala, Uganda.

Alexander Amone (A)

Makerere University - Johns Hopkins University Research Collaboration, P.O. Box 23491, Kampala, Uganda.

Priscilla Wavamunno (P)

Makerere University - Johns Hopkins University Research Collaboration, P.O. Box 23491, Kampala, Uganda.

Joyce Namale-Matovu (J)

Makerere University - Johns Hopkins University Research Collaboration, P.O. Box 23491, Kampala, Uganda.

Irene Lubega (I)

Makerere University - Johns Hopkins University Research Collaboration, P.O. Box 23491, Kampala, Uganda.

Clemensia Nakabiito (C)

Makerere University - Johns Hopkins University Research Collaboration, P.O. Box 23491, Kampala, Uganda.

Zikulah Namukwaya (Z)

Makerere University - Johns Hopkins University Research Collaboration, P.O. Box 23491, Kampala, Uganda.

Monica Nolan (M)

Makerere University - Johns Hopkins University Research Collaboration, P.O. Box 23491, Kampala, Uganda.

Samuel S Malamba (SS)

Uganda Virus Research Institute, Entebbe, Uganda.

Rachel King (R)

Institute for Global Health Sciences, University of California, San Francisco, USA.

Jaco Homsy (J)

Institute for Global Health Sciences, University of California, San Francisco, USA.

Mary Glenn Fowler (MG)

Department of Pathology, Johns Hopkins University, School of Medicine, Baltimore, USA.

Philippa Musoke (P)

Makerere University - Johns Hopkins University Research Collaboration, P.O. Box 23491, Kampala, Uganda. pmusoke@mujhu.org.
Department of Paediatrics & Child Health, School of Medicine, College of Health Sciences, Makerere University, Kampala, Uganda. pmusoke@mujhu.org.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH