Gestational diabetes in women living with HIV in Botswana: lower rates with dolutegravir- than with efavirenz-based antiretroviral therapy

K. N. Mmasa*, K. Powis, S. Sun, J. Makhema, M. Mmalane, S. Kgole, G. Masasa, S. Moyo, M. Gerschenson, T. Mohammed, J. Legbedze, E. J. Abrams, I. J. Kurland, M. E. Geffner, J. Jao

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

Background: There are few data on the prevalence of gestational diabetes (GDM) in pregnant women living with HIV (WLHIV) in sub-Saharan Africa, particularly those using integrase strand transfer inhibitors such as dolutegravir (DTG). Methods: We prospectively enrolled pregnant WLHIV and pregnant women without HIV ≥18 years old in Gaborone, Botswana, excluding those with pre-existing diabetes. We screened for GDM using a 75 g oral glucose tolerance test (OGTT) performed at 24–28 weeks’ gestation or at the earliest prenatal visit for those presenting after 28 weeks. Logistic regression models were fitted to assess the association between maternal HIV infection and GDM. Subgroup analyses were performed among WLHIV to assess the association between maternal antiretroviral therapy (ART) in pregnancy [DTG vs. efavirenz (EFV) with tenofovir/emtricitabine] and GDM. Results: Of 486 pregnant women, 66.5% were WLHIV, and they were older than women without HIV (median age 30 vs. 25 years, P < 0.01). Among WLHIV, 97.8% had an HIV-1 RNA level < 400 copies/mL at enrolment. Overall, 8.4% had GDM with similar rates between WLHIV and those without HIV (9.0% vs. 7.4%). The WLHIV receiving DTG-based ART had a 60% lower risk for GDM compared with those on EFV-based ART (adjusted odds ratio = 0.40, 95% CI: 0.18–0.92) after adjusting for confounders. Conclusions: Pregnant WLHIV on ART in Botswana were not at increased risk of GDM compared with women without HIV. Among WLHIV, the risk of GDM was lower with DTG- than with EFV-based ART. Further studies with larger cohorts are warranted to confirm these findings.

Original languageEnglish (US)
Pages (from-to)715-722
Number of pages8
JournalHIV Medicine
Volume22
Issue number8
DOIs
StatePublished - Sep 2021

Funding

We would like to thank the women who participated in this study as well as the study staff for their support of this research. Conflict of interest: The authors have no financial disclosures to report. Financial disclosure: This study was funded by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), National Institutes of Health (NIH) through R01DK109881. MG was also funded by the National Institute of General Medicine Sciences, NIH grant no. P20-GM113134. MEG receives consultant fees from Gilead Sciences, Inc. IJK was supported by the Stable Isotope and Metabolomics Core Facility of the Diabetes Research and Training Center (DRTC) of the Albert Einstein College of Medicine (NIH P60DK020541). : This study was funded by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), National Institutes of Health (NIH) through R01DK109881. MG was also funded by the National Institute of General Medicine Sciences, NIH grant no. P20‐GM113134. MEG receives consultant fees from Gilead Sciences, Inc. IJK was supported by the Stable Isotope and Metabolomics Core Facility of the Diabetes Research and Training Center (DRTC) of the Albert Einstein College of Medicine (NIH P60DK020541). Financial disclosure

Keywords

  • Africa
  • HIV
  • dolutegravir
  • efavirenz
  • gestational diabetes

ASJC Scopus subject areas

  • Infectious Diseases
  • Pharmacology (medical)
  • Health Policy

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