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Distinct cord blood C-peptide, adipokine, and lipidomic signatures by in utero HIV exposure.
Jao, Jennifer; Balmert, Lauren C; Sun, Shan; Qiu, Yunping; Kraus, Thomas A; Kirmse, Brian; Sperling, Rhoda S; Abrams, Elaine J; Myer, Landon; Arpadi, Stephen; Geffner, Mitchell E; LeRoith, Derek; Kurland, Irwin J.
Afiliação
  • Jao J; Department of Pediatrics, Division of Pediatric Infectious Diseases, Department of Medicine, Division of Adult Infectious Diseases, Northwestern University Feinberg School of Medicine, Chicago, IL, USA. jennifer.jao@northwestern.edu.
  • Balmert LC; Department of Preventive Medicine, Division of Biostatistics, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Sun S; Department of Pediatrics, Division of Pediatric Infectious Diseases, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.
  • Qiu Y; Department of Medicine, Division of Endocrinology, Fleischer Institute for Diabetes and Metabolism, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Kraus TA; Center for Therapeutic Antibody Development, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Kirmse B; Department of Medical Genetics, University of Mississippi Medical Center, Jackson, MS, USA.
  • Sperling RS; Department of Obstetrics, Gynecology, and Reproductive Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Abrams EJ; ICAP at Columbia, Mailman School of Public Health and Vagelos College of Physicians and Surgeons, Columbia University, New York, NY, USA.
  • Myer L; G.H. Sergievsky Center, Department of Pediatrics, Department of Epidemiology, Vagelos College of Physicians & Surgeons and Mailman School of Public Health, Columbia University, New York, NY, USA.
  • Arpadi S; School of Public Health & Family Medicine, Faculty of Health Sciences, Division of Epidemiology & Biostatistics, University of Cape Town, Cape Town, South Africa.
  • Geffner ME; School of Public Health & Family Medicine, Faculty of Health Sciences, Division of Epidemiology & Biostatistics, University of Cape Town, Cape Town, South Africa.
  • LeRoith D; The Saban Research Institute of Children's Hospital Los Angeles, Keck School of Medicine of USC, Los Angeles, CA, USA.
  • Kurland IJ; Department of Medicine, Division of Endocrinology, Diabetes and Bone Diseases, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Pediatr Res ; 92(1): 233-241, 2022 07.
Article em En | MEDLINE | ID: mdl-34446848
BACKGROUND: Early-life metabolic derangements in HIV-exposed uninfected (HEU) infants have been reported. METHODS: Pregnant women with HIV and HIV-uninfected pregnant women were enrolled with their newborns in a US cohort from 2011 to 2015. We measured cord insulin, C-peptide, and metabolic cytokines of HEU and HIV-unexposed uninfected (HUU) newborns using ELISA and metabolites, lipid subspecies, and eicosanoids via liquid chromatography/mass spectrometry. Linear regression was employed to assess the association of intrauterine HIV/ART with insulin and C-peptide. Graphical lasso regression was used to identify differences between metabolite/lipid subspecies networks associated with C-peptide. RESULTS: Of 118 infants, 56 were HEU, ART exposed. In adjusted analyses, mean cord insulin (ß = 0.295, p = 0.03) and C-peptide (ß = 0.522, p < 0.01) were significantly higher in HEU vs. HUU newborns. HEU neonates exhibited primarily positive associations between complex lipids and C-peptide, indicative of fuel storage, and augmented associations between cord eicosanoids and cytokines. HUU neonates exhibited negative associations with lipids and C-peptide indicative of increased fuel utilization. CONCLUSION: Higher cord insulin and C-peptide in HEU vs. HUU newborns as well as differences in cord metabolites, metabolic-related cytokines, and eicosanoids may reflect a propensity for fuel storage and an inflammatory milieu suggestive of fetal metabolic changes associated with in utero HIV/ART exposure. IMPACT: There is a paucity of studies assessing cord blood and neonatal metabolic health in HIV-exposed uninfected (HEU) newborns, an increasing population worldwide. Compared to HIV-unexposed uninfected (HUU) newborns, HEU newborns exhibit alterations in fuel homeostasis and an inflammatory milieu associated with in utero HIV/antiretroviral therapy (ART) exposure. The long-term implications of these neonatal findings are as yet unknown, but merit continued evaluation as this important and growing population ages into adulthood.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Complicações Infecciosas na Gravidez / Infecções por HIV Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Infant / Newborn / Pregnancy Idioma: En Revista: Pediatr Res Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Complicações Infecciosas na Gravidez / Infecções por HIV Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Infant / Newborn / Pregnancy Idioma: En Revista: Pediatr Res Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos