Literature DB >> 34034303

Placental Vascular Abnormalities in Association With Prenatal and Long-Term Health Characteristics Among HIV-Exposed Uninfected Adolescents and Young Adults.

Lindsay T Fourman1, Sarah B Mueller2, Autumn Boutin1, Isabel Zheng1, Chelsea S Pan1, Marisa E Gerard1, Takara L Stanley1,3, Drucilla J Roberts2.   

Abstract

BACKGROUND: HIV-exposed uninfected (HEU) individuals are predisposed to adverse health outcomes, which in part may stem from the influence of an altered intrauterine milieu on fetal programming. The placenta serves as a readout for the effects of the maternal environment on the developing fetus and may itself contribute to the pathogenesis of disease.
SETTING: US academic health system.
METHODS: We leveraged a previously established registry-based cohort of HEU adolescents and young adults to identify 26 subjects for whom placental histopathology was available. We further obtained placental tissue from 29 HIV-unexposed pregnancies for comparison. We examined differences in placental histopathology between the groups and related villous vascularity in the HEU group to prenatal maternal characteristics and long-term health outcomes.
RESULTS: Placentas from HEU pregnancies demonstrated a higher blood vessel count per villus as compared with controls (5.9 ± 1.0 vs. 5.4 ± 0.8; P = 0.05), which was independent of maternal prenatal age, race, body mass index, smoking status, hemoglobin, and gestational age. Furthermore, within the HEU group, lower CD4+ T-cell count during pregnancy was associated with greater placental vascularity (r = -0.44; P = 0.03). No significant relationships were observed between placental blood vessel count per villus and body mass index z-score or reactive airway disease among HEU individuals later in life.
CONCLUSIONS: Placentas from HEU pregnancies demonstrated increased villous vascularity compared with HIV-unexposed controls in proportion to the severity of maternal immune dysfunction. Further studies are needed to examine intrauterine exposure to hypoxia as a potential mechanism of fetal programming in HIV.
Copyright © 2021 Wolters Kluwer Health, Inc. All rights reserved.

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Year:  2021        PMID: 34034303      PMCID: PMC8373807          DOI: 10.1097/QAI.0000000000002734

Source DB:  PubMed          Journal:  J Acquir Immune Defic Syndr        ISSN: 1525-4135            Impact factor:   3.771


  34 in total

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4.  Increased risk for and mortality from invasive pneumococcal disease in HIV-exposed but uninfected infants aged <1 year in South Africa, 2009-2013.

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6.  A framework for elimination of perinatal transmission of HIV in the United States.

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9.  Prenatal hypoxia independent of undernutrition promotes molecular markers of insulin resistance in adult offspring.

Authors:  E J Camm; M S Martin-Gronert; N L Wright; J A Hansell; S E Ozanne; D A Giussani
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10.  Placental Structure in Preterm Birth Among HIV-Positive Versus HIV-Negative Women in Kenya.

Authors:  Moses M Obimbo; Yan Zhou; Michael T McMaster; Craig R Cohen; Zahida Qureshi; John Ong'ech; Julius A Ogeng'o; Susan J Fisher
Journal:  J Acquir Immune Defic Syndr       Date:  2019-01-01       Impact factor: 3.731

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