Lower Insulin Sensitivity in Newborns With In Utero HIV and Antiretroviral Exposure Who Are Uninfected in Botswana

Author:

Jao Jennifer123ORCID,Sun Shan2,Bonner Lauren B4,Legbedze Justine2,Mmasa Keolebogile N4,Makhema Joseph4,Mmalane Mompati4,Kgole Samuel4,Masasa Gosego4,Moyo Sikhulile4,Gerschenson Mariana5,Mohammed Terence4,Abrams Elaine J6,Kurland Irwin J7,Geffner Mitchell E8,Powis Kathleen M391011

Affiliation:

1. Department of Pediatrics, Division of Pediatric Infectious Diseases, Northwestern University Feinberg School of Medicine , Chicago, Illinois , USA

2. Department of Pediatrics, Ann and Robert H. Lurie Children's Hospital of Chicago , Chicago, Illinois , USA

3. Botswana-Harvard AIDS Institute Partnership , Gaborone , Botswana

4. Department of Preventive Medicine, Northwestern University Feinberg School of Medicine , Chicago, Illinois , USA

5. Department of Cell and Molecular Biology, John A. Burns School of Medicine, University of Hawaii at Manoa , Honolulu, Hawaii , USA

6. ICAP at Columbia University, Mailman School of Public Health and Vagelos College of Physicians and Surgeons, Columbia University , New York, New York , USA

7. Department of Medicine, Albert Einstein College of Medicine , Bronx, New York , USA

8. Saban Research Institute of Children's Hospital Los Angeles, Keck School of Medicine of University of Southern California , Los Angeles, California , USA

9. Department of Internal Medicine, Massachusetts General Hospital , Boston, Massachusetts , USA

10. Department of Pediatrics, Massachusetts General Hospital , Boston, Massachusetts , USA

11. Department of Immunology and Infectious Diseases, Harvard T. H. Chan School of Public Health , Boston, Massachusetts , USA

Abstract

AbstractBackgroundFew data exist on early-life metabolic perturbations in newborns with perinatal HIV and antiretroviral (ARV) exposure but uninfected (HEU) compared to those perinatally HIV unexposed and uninfected (HUU).MethodsWe enrolled pregnant persons with HIV (PWH) receiving tenofovir (TDF)/emtricitabine or lamivudine (XTC) plus dolutegravir (DTG) or efavirenz (EFV), and pregnant individuals without HIV, as well as their liveborn infants. Newborns were randomized to receive either zidovudine (AZT) or nevirapine (NVP) postnatal prophylaxis. Preprandial homeostasis model assessment for insulin resistance (HOMA-IR) was assessed at birth and 1 month. Linear mixed models were fit to assess the association between in utero HIV/ARV exposure and average HOMA-IR from birth to 1 month, adjusting for confounders.ResultsOf 450 newborns, 306 were HEU. HOMA-IR was higher in newborns HEU versus HUU after adjusting for confounders (mean difference of 0.068 in log HOMA-IR, P = .037). Among newborns HEU, HOMA-IR was not significantly different between TDF/XTC/DTG versus TDF/XTC/EFV in utero ARV exposure and between AZT versus NVP newborn postnatal prophylaxis arms.ConclusionsNewborns HEU versus HUU had lower insulin sensitivity at birth and at 1 month of life, raising potential concern for obesity and other metabolic perturbations later in life for newborns HEU.Clinical Trials RegistrationNCT03088410.

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

National Institutes of Health

National Institute of General Medical Sciences

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

Reference33 articles.

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