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

Abstract 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...

Full description

Bibliographic Details
Main Authors: Grace Gabagaya, Gordon Rukundo, Alexander Amone, Priscilla Wavamunno, Joyce Namale-Matovu, Irene Lubega, Clemensia Nakabiito, Zikulah Namukwaya, Monica Nolan, Samuel S. Malamba, Rachel King, Jaco Homsy, Mary Glenn Fowler, Philippa Musoke
Format: Article
Language:English
Published: BMC 2021-09-01
Series:BMC Infectious Diseases
Subjects:
Online Access:https://doi.org/10.1186/s12879-021-06608-4
_version_ 1819115381169586176
author Grace Gabagaya
Gordon Rukundo
Alexander Amone
Priscilla Wavamunno
Joyce Namale-Matovu
Irene Lubega
Clemensia Nakabiito
Zikulah Namukwaya
Monica Nolan
Samuel S. Malamba
Rachel King
Jaco Homsy
Mary Glenn Fowler
Philippa Musoke
author_facet Grace Gabagaya
Gordon Rukundo
Alexander Amone
Priscilla Wavamunno
Joyce Namale-Matovu
Irene Lubega
Clemensia Nakabiito
Zikulah Namukwaya
Monica Nolan
Samuel S. Malamba
Rachel King
Jaco Homsy
Mary Glenn Fowler
Philippa Musoke
author_sort Grace Gabagaya
collection DOAJ
description Abstract 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 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 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 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.
first_indexed 2024-12-22T05:00:17Z
format Article
id doaj.art-a6e60a87db6b4a80a90a07879223d0fd
institution Directory Open Access Journal
issn 1471-2334
language English
last_indexed 2024-12-22T05:00:17Z
publishDate 2021-09-01
publisher BMC
record_format Article
series BMC Infectious Diseases
spelling doaj.art-a6e60a87db6b4a80a90a07879223d0fd2022-12-21T18:38:17ZengBMCBMC Infectious Diseases1471-23342021-09-012111710.1186/s12879-021-06608-4Prevalence of undetectable and suppressed viral load in HIV-infected pregnant women initiating Option B+ in Uganda: an observational study nested within a randomized controlled trialGrace Gabagaya0Gordon Rukundo1Alexander Amone2Priscilla Wavamunno3Joyce Namale-Matovu4Irene Lubega5Clemensia Nakabiito6Zikulah Namukwaya7Monica Nolan8Samuel S. Malamba9Rachel King10Jaco Homsy11Mary Glenn Fowler12Philippa Musoke13Makerere University - Johns Hopkins University Research CollaborationMakerere University - Johns Hopkins University Research CollaborationMakerere University - Johns Hopkins University Research CollaborationMakerere University - Johns Hopkins University Research CollaborationMakerere University - Johns Hopkins University Research CollaborationMakerere University - Johns Hopkins University Research CollaborationMakerere University - Johns Hopkins University Research CollaborationMakerere University - Johns Hopkins University Research CollaborationMakerere University - Johns Hopkins University Research CollaborationUganda Virus Research InstituteInstitute for Global Health Sciences, University of CaliforniaInstitute for Global Health Sciences, University of CaliforniaDepartment of Pathology, Johns Hopkins University, School of MedicineMakerere University - Johns Hopkins University Research CollaborationAbstract 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 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 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 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.https://doi.org/10.1186/s12879-021-06608-4HIVPregnancyViral loadViral or virological suppressionUgandaHIV transmission
spellingShingle Grace Gabagaya
Gordon Rukundo
Alexander Amone
Priscilla Wavamunno
Joyce Namale-Matovu
Irene Lubega
Clemensia Nakabiito
Zikulah Namukwaya
Monica Nolan
Samuel S. Malamba
Rachel King
Jaco Homsy
Mary Glenn Fowler
Philippa Musoke
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
BMC Infectious Diseases
HIV
Pregnancy
Viral load
Viral or virological suppression
Uganda
HIV transmission
title 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
title_full 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
title_fullStr 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
title_full_unstemmed 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
title_short 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
title_sort 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
topic HIV
Pregnancy
Viral load
Viral or virological suppression
Uganda
HIV transmission
url https://doi.org/10.1186/s12879-021-06608-4
work_keys_str_mv AT gracegabagaya prevalenceofundetectableandsuppressedviralloadinhivinfectedpregnantwomeninitiatingoptionbinugandaanobservationalstudynestedwithinarandomizedcontrolledtrial
AT gordonrukundo prevalenceofundetectableandsuppressedviralloadinhivinfectedpregnantwomeninitiatingoptionbinugandaanobservationalstudynestedwithinarandomizedcontrolledtrial
AT alexanderamone prevalenceofundetectableandsuppressedviralloadinhivinfectedpregnantwomeninitiatingoptionbinugandaanobservationalstudynestedwithinarandomizedcontrolledtrial
AT priscillawavamunno prevalenceofundetectableandsuppressedviralloadinhivinfectedpregnantwomeninitiatingoptionbinugandaanobservationalstudynestedwithinarandomizedcontrolledtrial
AT joycenamalematovu prevalenceofundetectableandsuppressedviralloadinhivinfectedpregnantwomeninitiatingoptionbinugandaanobservationalstudynestedwithinarandomizedcontrolledtrial
AT irenelubega prevalenceofundetectableandsuppressedviralloadinhivinfectedpregnantwomeninitiatingoptionbinugandaanobservationalstudynestedwithinarandomizedcontrolledtrial
AT clemensianakabiito prevalenceofundetectableandsuppressedviralloadinhivinfectedpregnantwomeninitiatingoptionbinugandaanobservationalstudynestedwithinarandomizedcontrolledtrial
AT zikulahnamukwaya prevalenceofundetectableandsuppressedviralloadinhivinfectedpregnantwomeninitiatingoptionbinugandaanobservationalstudynestedwithinarandomizedcontrolledtrial
AT monicanolan prevalenceofundetectableandsuppressedviralloadinhivinfectedpregnantwomeninitiatingoptionbinugandaanobservationalstudynestedwithinarandomizedcontrolledtrial
AT samuelsmalamba prevalenceofundetectableandsuppressedviralloadinhivinfectedpregnantwomeninitiatingoptionbinugandaanobservationalstudynestedwithinarandomizedcontrolledtrial
AT rachelking prevalenceofundetectableandsuppressedviralloadinhivinfectedpregnantwomeninitiatingoptionbinugandaanobservationalstudynestedwithinarandomizedcontrolledtrial
AT jacohomsy prevalenceofundetectableandsuppressedviralloadinhivinfectedpregnantwomeninitiatingoptionbinugandaanobservationalstudynestedwithinarandomizedcontrolledtrial
AT maryglennfowler prevalenceofundetectableandsuppressedviralloadinhivinfectedpregnantwomeninitiatingoptionbinugandaanobservationalstudynestedwithinarandomizedcontrolledtrial
AT philippamusoke prevalenceofundetectableandsuppressedviralloadinhivinfectedpregnantwomeninitiatingoptionbinugandaanobservationalstudynestedwithinarandomizedcontrolledtrial