Fetal growth assessed via ultrasound in relation to maternal HIV infection status and antiretroviral regimens

Author:

Williams Paige L.123,Karalius Brad3,Patel Kunjal13,Aschengrau Ann4,Chakhtoura Nahida5,Enriquez Naomi1,Moye Jack5,Garvie Patricia A.6,Monte Dina7,Seage George R.3,Zorrilla Carmen8,Mussi-Pinhata Marisa M.6

Affiliation:

1. Center for Biostatistics in AIDS Research, Harvard T. H. Chan School of Public Health, Boston, MA, USA

2. Department of Biostatistics, Harvard T. H. Chan School of Public Health, Boston, MA, USA

3. Department of Epidemiology, Harvard T. H. Chan School of Public Health, Boston, MA, USA

4. Department of Epidemiology, Boston University School of Public Health, Boston, MA, USA

5. Eunice Kennedy ShriverNational Institute of Child Health and Human Development, Bethesda, MD, USA

6. Research Department, Children's Diagnostic & Treatment Center, Fort Lauderdale, FL, USA

7. Westat, Inc, Rockville, MD, USA

8. University of Puerto Rico, San Juan, Puerto Rico, USA

Abstract

Objective: :To evaluate effects of maternal HIV and antiretroviral treatment (ART) on intrauterine fetal growth. Design: :Prospective cohort studies of HIV and ZIKA infection among women living with HIV (WLHIV) and women not living with HIV (WNLHIV) conducted in Brazil and the US from 2016-2020. Methods: :We evaluated fetal growth via repeated ultrasounds and calculated Z-scores for fetal growth measures using Intergrowth-21st standards among women with singleton pregnancies. Adjusted linear mixed models were fit for each fetal growth Z-score by HIV status. Among WLHIV, we compared fetal growth Z-scores by the most common maternal ART regimens, stratified by timing of ART initiation. Results: :We included 166 WLHIV and 705 WNLHIV; none had Zika infection. Z-scores were similar for WLHIV and WNLHIV for femur length (latest 3rd trimester median = 1.08) and estimated fetal weight (median≈0.60); adjusted mean differences in fetal weight Z-scores by HIV status were <0.1 throughout gestation. Other fetal growth measurements were lower for WLHIV than WNLHIV early in gestation but increased more rapidly over gestation. Among WLHIV not on ART at conception, adjusted mean Z-scores were generally similar across regimens initiated during pregnancy but somewhat lower for atazanavir-based regimens for biparietal diameter compared to efavirenz- or raltegravir-based regimens. Among WLHIV on ART at conception, mean Z-scores were similar across ART regimens. Conclusions: :Within our cohorts, fetal growth was lower in WLHIV than WNLHIV early in gestation but similar by the end of gestation, which is reassuring. Among WLHIV, fetal growth measures were generally similar across ART regimens evaluated.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Infectious Diseases,Immunology,Immunology and Allergy

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