Project II - Repair in High Risk Newborns with Congenital Heart Disease Congenital heart disease (CHD) is the most common birth defect, and neonatal surgery is often necessary for survival. Despite the complexity of these surgeries, most infants with CHD survive. Although severe neurologic disability is rare, school age children with CHD frequently exhibit behavioral, emotional, cognitive and motor impairments. The pervasive nature of these disabilities suggests fundamental problems with brain development. Using advanced magnetic resonance imaging techniques, we have discovered that newborns with CHD have delayed brain development compared with normal babies and are at high risk of acquiring new brain injuries before and after surgery. The overall goal of this proposal is to understand neurodevelopmental impairment following neonatal CHD surgery at a structural brain network level and to determine the capacity for repair following neonatal brain injury. To achieve this goal, this study will use new techniques for analyzing the complete set of brain connections - the so-called 'connectome'. Newborns with two types of CHD will be studied before and after surgery and again at six months of age. The groups differ in the number of surgeries needed to restore heart function and blood oxygen levels to near normal levels. By performing MRIs at three time points, we will learn how development of brain networks are affected in CHD and how repair and recovery from brain injury proceeds following neonatal surgery. This information will be useful for developing new treatments to optimize brain development and recovery from brain injury in any condition where newborn brain injury occurs because of low brain oxygen and/or blood flow.
Congenital heart disease (CHD) is the most common birth defect and survivors often exhibit neurologic disability at school age. This proposal aims to understand neurodevelopmental impairment in CHD using new magnetic resonance imaging techniques that visualize the complete network of brain connections. Results will inform how newborns brains develop and repair following injury.
|Peyvandi, Shabnam; De Santiago, Veronica; Chakkarapani, Elavazhagan et al. (2016) Association of Prenatal Diagnosis of Critical Congenital Heart Disease With Postnatal Brain Development and the Risk of Brain Injury. JAMA Pediatr 170:e154450|
|Kim, Hosung; Lepage, Claude; Maheshwary, Romir et al. (2016) NEOCIVET: Towards accurate morphometry of neonatal gyrification and clinical applications in preterm newborns. Neuroimage 138:28-42|
|Gano, Dawn; Ho, Mai-Lan; Partridge, John Colin et al. (2016) Antenatal Exposure to Magnesium Sulfate Is Associated with Reduced Cerebellar Hemorrhage in Preterm Newborns. J Pediatr 178:68-74|
|Kim, Hosung; Gano, Dawn; Ho, Mai-Lan et al. (2016) Hindbrain regional growth in preterm newborns and its impairment in relation to brain injury. Hum Brain Mapp 37:678-88|
|Kim, Hosung; Joo, EunYeon; Suh, Sooyeon et al. (2016) Effects of long-term treatment on brain volume in patients with obstructive sleep apnea syndrome. Hum Brain Mapp 37:395-409|
|Tam, Emily W Y; Chau, Vann; Barkovich, A James et al. (2016) Early postnatal docosahexaenoic acid levels and improved preterm brain development. Pediatr Res 79:723-30|
|Kansagra, Akash P; Mabray, Marc C; Ferriero, Donna M et al. (2016) Microstructural maturation of white matter tracts in encephalopathic neonates. Clin Imaging 40:1009-13|
|Gano, Dawn; Andersen, Sarah K; Partridge, J Colin et al. (2015) Diminished white matter injury over time in a cohort of premature newborns. J Pediatr 166:39-43|
|Peyvandi, S; Feldstein, V A; Hirose, S et al. (2015) Twin-reversed arterial perfusion sequence associated with decreased fetal cerebral vascular impedance. Ultrasound Obstet Gynecol 45:447-51|
|Chen, Yiran; Tymofiyeva, Olga; Hess, Christopher P et al. (2015) Effects of rejecting diffusion directions on tensor-derived parameters. Neuroimage 109:160-70|
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