3 results match your criteria: "Ayers Children's Medical Center[Affiliation]"

Histological chorioamnionitis shapes the neonatal transcriptomic immune response.

Early Hum Dev

July 2016

Department of Pediatrics, University of Florida College of Medicine, Gainesville, FL, United States; Department of Pathology, Immunology, and Laboratory Medicine, University of Florida College of Medicine, Gainesville, FL, United States. Electronic address:

Background: Histologic chorioamnionitis (HCA) is commonly associated with preterm birth and deleterious post-natal outcomes including sepsis and necrotizing enterocolitis. Transcriptomic analysis has been used to uncover gene signatures that permit diagnosis and prognostication, show new therapeutic targets, and reveal mechanisms that underlie differential outcomes with other complex disease states in neonates such as sepsis.

Aims: To define the transcriptomic and inflammatory protein response in peripheral blood among infants with exposure to histologic chorioamnionitis.

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Neonatal ventricular fibrillation and an elusive ALCAPA: things are not always as they seem.

BMJ Case Rep

March 2016

Mildred Stahlman Division of Neonatology, Vanderbilt University, Nashville, Tennessee, USA Department of Neonatology, Ayers Children's Medical Center, Jackson, Tennessee, USA.

An anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital cardiac condition that typically presents with poor feeding and failure to thrive from progressive myocardial ischaemia. Previous reports of ALCAPA presenting with ventricular fibrillation (VF) have suggested a causative relationship. In this case, we present a neonate with VF without apparent cause after an extensive evaluation.

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Neonates manifest a unique host response to sepsis even among other children. Preterm neonates may experience sepsis soon after birth or during often-protracted birth hospitalizations as they attain physiologic maturity. We examined the transcriptome using genome-wide expression profiling on prospectively collected peripheral blood samples from infants evaluated for sepsis within 24 h after clinical presentation.

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