Skip to main content

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 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.

Peer Review reports

Background

Viral load testing is the gold standard for HIV treatment monitoring and is recommended as the preferred approach to diagnose and confirm treatment failure [1, 2]. The WHO recommends that routine VL testing should be done at 6 and 12 months after initiation of ART for adult HIV patients and every 12 months thereafter if the patient is stable on ART [1].

Given that VL assessment is not done routinely at ART initiation, ART-naïve HIV-infected individuals with suppressed or undetectable VL (uVL) are not identified. Detecting suppressed/undetectable VL in HIV-infected individuals newly initiating ART may be useful in identifying “elite controllers” or unreported ART use. In this paper, we analysed the prevalence of virological 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

Study design and population

The FLC for Option B+ study was an open-label RCT with two parallel intervention and control arms. This RCT was undertaken in South Central Uganda, at Mulago National Referral Hospital and Kampala Capital City Authority (KCCA) health units in Kampala (urban) district as well as at Mityana District hospital and six surrounding health centers in Mityana (rural) district. The RCT goal was to test an enhanced peer group support system called “Friends for Life Circles” (FLCs) to help HIV-infected pregnant women initiating PMTCT Option B+ during the antenatal period adhere to lifelong ART and postpartum care visits [3]. Eligible participants were HIV-positive pregnant women ≥ 18 years of age, newly initiating ART Option B+, who agreed to come to the study clinic for scheduled appointments and to be home visited as needed to ensure follow up [3]. In this RCT, ART-naïve women were defined as those who started on ART on or shortly (≤ 14 days) before their enrolment into the FLC Option B+ trial. Additional inclusion criteria included residing within a 20 km radius around the study clinic and not planning to move out of the catchment area within the next 2 years [3]. Exclusion criteria included any medical, social or other circumstancse that might prevent a mother from adhering to the study protocol [3]. At trial commencement, the study relied on documented pregnancy and positive HIV test from the health units which resulted in enrolment of some participants that were neither pregnant nor HIV positive. The protocol was subsequently amended so that confirmatory testing for pregnancy and HIV positivity could be done by the study prior to enrolment.

Data collection procedures

Pregnant women testing HIV-positive and started on ART on the same day as part of the National PMTCT Program were screened for the RCT. Eligible women were enrolled and randomized into the RCT within 14 days of ART initiation. At enrolment into the RCT, each participant had whole blood samples collected for assessment of baseline plasma HIV-RNA as well as standardized questionnaires administered to capture data on socio-demographic characteristics, adherence to ARVs and HIV status disclosure.

Blood sample collection and HIV testing

Whole blood collected in sterile EDTA tubes was stored at room temperature. Plasma was then separated from whole blood by centrifugation within 24 h of sample collection after which plasma was transferred to sterile cryovials. In Kampala, processing and storage was done at the VL testing Laboratory while in Mityana, plasma was stored frozen at – 20 °C in the Mityana Hospital Laboratory and transported to Kampala for storage and VL testing every 1–2 weeks on frozen icepacks in temperature-controlled cool boxes. Plasma VL testing was conducted in batches at the Infectious Disease Institute (IDI) Core Lab in Mulago Hospital using COBAS Ampliprep /COBAS Taqman HIV-1 test whose lower limit of detection was 20 copies/ml. Participants in whom no viral copies were detected had repeat rapid HIV antibody testing done to confirm HIV diagnosis and if found negative, had HIV DNA PCR testing done. Undetectable viral load in this study was defined as VL count < 20 copies/ml while virological suppression was defined as VL count < 400 copies/ml.

Statistical analysis

STATA software (StataCorp LP, 4905 Lakeway Drive, College Station, TX, USA) was used for all statistical analyses. All collected data on socio-demographic variables were considered for inclusion in the univariate logistic regression analysis and variables with a significance level of p < 0.1 were considered for inclusion in the full multivariate model. Using a backward elimination method, only variables with a significance level of p < 0.05 were kept in the final model. Odds ratios were used to measure the magnitude of the effect and a Wald test was used to evaluate the statistical significance of each coefficient in the model assessing the relationship between socio-demographic characteristics and the different binary viral load outcome groups [(0 = detectable VL, 1 = undetectable VL) or (0 = unsuppressed VL, 1 = suppressed VL)]. The likelihood ratio test (LHRT) was used to compare the goodness of fit for two nested models.

Results

A total of 540 HIV-positive pregnant women participants were enrolled into the FLC for Option B+ RCT between May 2016 and September 2017. Of these, eight participants were subsequently terminated due to inappropriate enrolment and are excluded from the data analyses. Three of these did not disclose information on ineligibility status during screening while five of these were found to be neither pregnant nor HIV-positive upon confirmatory testing.

The mean duration from date of ART initiation to time of sample collection for baseline VL assessment was 4.4 days (SD 3.6) and the median was 4 days (range 0–30 days, IQR 2–6 days). Table 1 shows the univariate analysis of the proportions of the 532 eligible study participants with baseline suppressed (< 400 copies/ml) and undetectable (< 20 copies/ml) HIV VL by socio-demographics characteristics.

Table 1 Proportions of pregnant women with baseline suppressed and undetectable HIV viral load by socio-demographic characteristics

Participants’ median age was 25 years; 137 (25.8%) were from rural Mityana and 395 (74.2%) from urban Kampala. Twenty-nine (5.5%) of 532 enrolled women had baseline uVL (< 20 copies/ml) and 84 (15.8%) had baseline viral suppression (20–399 copies/ml), all with no self-reported prior ART use. Therefore, the prevalence of undetectable VL was 5.5% and the proportion of patients with suppressed VL (< 400 copies/ml) was 21.2%. The median VL counts and frequencies of the different VL categories by RCT site are summarized in Table 2.

Table 2 Baseline VL and distribution of pregnant women across VL ranges in Kampala and Mityana districts

The median age in years for participants with and without uVL at baseline was 25 (IQR: 21, 30) and 25 (IQR: 22, 30) respectively. The multivariate analysis (Table 3) shows that disclosure of HIV status to any person other than a partner was the only factor associated with baseline VL suppression (VL < 400 copies/ml); there was no association between gravidity, marital status, religion, tribe, mean monthly income, educational level attained, disclosure of HIV status to partner and uVL (VL < 20 copies/ml) or VL suppression (VL < 400 copies/ml) at baseline as illustrated in Table 3. The adjusted odds ratio for VL suppression (< 400 copies/ml) in those who did not disclose compared to those who disclosed to any person other than their partner was 0.640 (95% CI 0.416–0.982, p = 0.041), after adjusting for marital status. (Table 3).

Table 3 Multivariate analysis of factors associated with baseline VL suppression in FLC for Option B+ RCT participants

Discussion

Our results show that 5.5% of HIV-infected pregnant women who initiated ART in the study had uVL at baseline and were potential elite controllers (EC). This is higher than previous findings in Uganda where a prevalence of 1% and 0.26% of HIV controllers (ECs and aviraemic controllers) were reported by Laeyendecker et al. [4] and Kayongo et al. [5] in 2009 and 2018 respectively. However, our findings are consistent with the findings of a 2014 systematic review where the proportion of ECs was 0.15–7.7% and did not necessarily reflect the length of follow-up [6].

ECs are HIV-positive individuals who are able to suppress viral replication to undetectable levels for extended periods of time without ART. This definition of elite controllers thus requires factoring in longitudinal characteristics of VL suppression over a certain period of time [6, 7], which was not documented in our study since it was a baseline analysis. ECs are believed to control viral replication through mechanisms involving host immune responses [6]. Consistent with our findings, previous reports have not documented any association between elite controllers and specific socio-demographic characteristics [7].

We also identified a high proportion of women who were virally suppressed (< 400 copies/ml) at baseline (N = 113, 21.2%). This is in contrast to the HPTN068 study [8] which, in spite of using a higher threshold for viral suppression (< 2000 copies/ml), had only 15.7% of patients virally suppressed in the absence of ART. In our study, women who had not disclosed to an other person than their partner were less likely to be virally suppressed (OR 0.64; 95% CI 0.416–0.982, p = 0.041) than those who had disclosed. It is difficult to interpret this finding without more information but disclosure of HIV remains a challenge in Uganda because of stigma, particularly for women bearing children for fear of the consequences such women might face from their partner or others [9]. It might indicate that some of these women have been infected for some time and did not disclose nor get appropriate care and treatment for fear of discrimination from their social network [10].

It is also possible the women failed to report prior ART use since our findings are based on self-report. Much as we found no association between gravidity and VL suppression, there is a possibility that women with previous pregnancies after 2012 when Uganda rolled out Option B, could have received ART for PMTCT and developed viral suppression. Findings elsewhere have documented under-reporting of ART use by HIV patients [11,12,13]. In South Africa, blood donors reporting no history of ART use and identified as HIV-positive with undetectable viral load, were presumed ECs. However, when plasma samples of these presumed ECs were later tested for ARVs, undisclosed ART use was discovered in 66.4% of participants [11].

In addition to stigma mentioned above, other possible reasons why women may not report prior ART use are that they may have defaulted on their ART regimen and are thus concerned about being reprimanded. Additionally, participation in a study often implies better care which may prompt women to conceal prior ART use.

Our study had a number of strengths: first, the sample size was relatively large and included both rural and urban Ugandan populations, which increases the generalizability of our results in Uganda. Second, we used a highly sensitive validated assay for measurement of viral load and thus were able to measure VL copies at a very low level of detection. Finally, we were able to conduct HIV DNA PCR testing to confirm HIV status and to guard against including women incorrectly diagnosed as HIV positive based on a falsely positive rapid HIV screening test.

Our study however had some limitations. First, plasma drug levels were not yet available prior to ART initiation and baseline hair collection for measurement of ARV drug concentrations was not done. Baseline hair samples would have been helpful in assessing prolonged ARVs exposure and validation of ART naïve self-reports. Also, baseline VL assessment was done after ART initiation which could raise the question as to whether these women were truly ART-naïve at the time of VL measurement. However, the mean duration from date of ART initiation to time of blood sample collection was 4.4 days (median 4 days, range 0–30 days, IQR 2–6 days) which is very unlikely to have impacted VL measurements, as a period of 5 to 15 weeks has been reported as time to uVL after initiation of ART among HIV-infected pregnant women [14]. We also did not have data on CD4 levels because, since the adoption of Option B+ for PMTCT and the introduction of test and treat HIV policy in Uganda, ART is initiated immediately after confirming HIV infection without the need to measure CD4 levels. Additionally, our multivariate analysis only evaluated suppressed viral load (< 400 copies/ml) but not undetectable viral load because of small numbers in the undetectable category (< 20 copies/ml + TND). Lastly, much as partner and relatives’ HIV and ART status are important determinants of viral suppression, we did not have these data. This is incumbent on the premise that HIV disclosure and stigma are still challenges and many pregnant women do not share this information.

Conclusions

In the FLC for Options B+ RCT, over 5% of pregnant HIV-positive women initiating ART (Option B+) had undetectable viral load at baseline and were presumed to be either potential “elite controllers” or did not report previous use of ART. No specific maternal socio-demographic factors aside from disclosure of HIV status to person others than their partner was associated with baseline uVL. Further studies are needed to better understand the biological mechanisms of pregnant women who may be elite controllers; as well as the need and feasibility of screening for baseline antiretroviral drug detection among self-reporting ART-naïve pregnant women with uVL, in order to better inform their care and treatment.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author upon reasonable request. The study protocol has been provided under related files.

Abbreviations

VL:

Viral load

ART:

Antiretroviral therapy

uVL:

Undetectable VL

FLC:

Friends for Life Circles

EC:

Elite controllers

References

  1. WHO. WHO | Consolidated guidelines on the use of antiretroviral drugs for treating and preventing HIV infection. Recommendations for a public health approach- second edition [Internet]. WHO. World Health Organization; 2016. https://www.who.int/hiv/pub/arv/arv-2016/en/. accessed 22 May 2019.

  2. Unaids. The need for routine viral load testing [Internet]. 2016 [cited 2019 May 15]. https://www.unaids.org/sites/default/files/media_asset/JC2845_en.pdf

  3. Friends for Life Circles for Option B Plus - Full Text View - ClinicalTrials.gov [Internet]. [cited 2021 May 24]. https://clinicaltrials.gov/ct2/show/NCT02515370

  4. Laeyendecker O, Redd AD, Lutalo T, Gray RH, Wawer M, Ssempijja V, et al. Frequency of long-term nonprogressors in HIV-1 seroconverters From Rakai Uganda. J Acquir Immune Defic Syndr. 2009;52(3):316–9.

    Article  Google Scholar 

  5. Kayongo A, Gonzalo-Gil E, Gümüşgöz E, Niwaha AJ, Semitala F, Kalyesubula R, et al. Brief report: identification of elite and viremic controllers from a large urban HIV Ambulatory Center in Kampala. Uganda J Acquir Immune Defic Syndr. 2018;79(3):394–8.

    Article  Google Scholar 

  6. Olson AD, Meyer L, Prins M, Thiebaut R, Gurdasani D, Guiguet M, et al. An evaluation of HIV elite controller definitions within a large seroconverter cohort collaboration Okulicz JF. PLoS ONE. 2014;9(1):e86719.

    Article  Google Scholar 

  7. Okulicz F, Elite J. Controllers and long-term nonprogressors: models for HIV vaccine development? J AIDS Clin Res. 2012;03(01):1.

    Article  Google Scholar 

  8. Sivay MV, Fogel JM, Wang J, Zhang Y, Piwowar-Manning E, Clarke W, et al. Natural control of HIV infection in young women in South Africa: HPTN 068. HIV Clin Trials. 2018;19(5):202–8.

    Article  CAS  Google Scholar 

  9. Naigino R, Makumbi F, Mukose A, et al. HIV status disclosure and associated outcomes among pregnant women enrolled in antiretroviral therapy in Uganda: a mixed methods study. Reprod Health. 2017;14:107. https://doi.org/10.1186/s12978-017-0367-5.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Masereka EM, Ngabirano TD, Osingada CP, et al. Increasing retention of HIV positive pregnant and breastfeeding mothers on option-b plus by upgrading and providing full time HIV services at a lower health facility in rural Uganda. BMC Public Health. 2019;19:950. https://doi.org/10.1186/s12889-019-7280-5.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Sykes W, Van den Berg K, Jacobs G, Jauregui A, Roubinian N, Wiesner L, et al. Discovery of false elite controllers: HIV antibody-positive RNA-negative blood donors found to be on antiretroviral therapy. J Infect Dis. 2019;220(4):643–7.

    Article  CAS  Google Scholar 

  12. Grabowski MK, Reynolds S, Kagaayi J, Gray R, Clarke W, Chang L, et al. The validity of self-reported antiretroviral use in persons living with HIV. AIDS. 2017;32(3):1.

    Google Scholar 

  13. Fogel JM, Wang L, Parsons TL, Ou S-S, Piwowar-Manning E, Chen Y, et al. Undisclosed antiretroviral drug use in a multinational clinical trial (HIV Prevention Trials Network 052). J Infect Dis. 2013;208(10):1624–8.

    Article  CAS  Google Scholar 

  14. European Collaborative Study. Time to undetectable viral load after highly active antiretroviral therapy initiation among hiv-infected pregnant women. Clin Infect Dis. 2007;44(12):1647–56.

    Article  Google Scholar 

Download references

Acknowledgements

We would like to thank the FLC for Option B+ study team who were vital in the collection of the data and the study participants without whom this study would not have been possible.

Funding

These data are from the Friends for Life Circles for Option B+ study which was funded by NIH/Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) grant # IR01HD080476-01.

Author information

Authors and Affiliations

Authors

Contributions

GG wrote original draft. GR contributed to data curation. GG, AA, PW, SM, RK, CN, JH, MGF and PM edited the manuscript. SM carried out the statistical analyses. JNM, IL, RK, JH, CN, ZN, MN, MGF and PM made contributions to the conception and design of the study and provided input on the manuscript. All authors reviewed and approved final manuscript.

Corresponding author

Correspondence to Philippa Musoke.

Ethics declarations

Ethics approval and consent to participate

All study procedures were conducted in compliance with the relevant national laws and international regulatory requirements. Written informed consent was obtained from all study participants prior to any protocol-specified procedures being conducted. The study protocol, informed consent forms, and other study instruments administered to participants were reviewed and approved by the Joint Clinical Research Centre (JCRC) Institutional Review Board in Uganda; the Uganda National Council for Science and Technology (UNCST), Johns Hopkins University (JHU) and University of California San Francisco (UCSF) Ethics committees prior to participant enrolment or study procedures.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Gabagaya, G., Rukundo, G., Amone, A. et al. 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 Infect Dis 21, 907 (2021). https://doi.org/10.1186/s12879-021-06608-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12879-021-06608-4

Keywords