Spina bifida meningomyelocele is the major severely disabling birth defect in North America, but our knowledge of the factors responsible for neurobehavioral outcome is fragmentary. The program project aims to make these fragments coherent. The overall objective of this program project is to identify sources of variability-genetic, environmental, and CNS-that explain variations in the neurobehavioral outcomes of children with spina bifida meningomyelocele and hydrocephalus (SBH). To accomplish this objective, we propose to evaluate 583 children with spina bifida and 159 controls in five projects and three cores at two primary data collection sites: the University of Texas-Houston Medical School and the Hospital for Sick Children, Toronto. Project 1 (Genetics; Northrup, P.I.) evaluates genetic factors associated with spina bifida and related neural tube defects in Hispanic and Caucasian cohorts. Approximately 100 candidate genes will be tested and a genome-wide search will be initiated that permits testing of 150 of 330 possible markers. Projects 2 (Early Learning; Landry, P.I.) is a longitudinal study of infants with SBH from 7-36 months of age. This study addresses the relationship of core neurobiological deficits and the environment in producing early learning deficits in children with SBH. Project 3 (Cerebellum; Dennis, P.I.) evaluates the role of cerebellum/midbrain dysmorphology in producing the motor, spatial, and attentional deficits associated with SBH. Project 4 (Corpus Callosum; Hannay, P.I.) examines the corpus callosum anomalies characteristic of SBH in relationship to interhemispheric transmission and hemispheric specialization. Project 5 (Discourse and Academic Skills; Barnes, P.I. evaluates factors producing deficits in discourse, reading comprehension, and math in children with SBH. These 5 projects are supported by an Administrative Services Core (A; Fletcher, P.I.), Subject Recruitment and Evaluation Core (B; Fletcher, P.I.), and Database, Computer, and Statistics Core (C; Francis, P.I.) Core B provides for comprehensive medical, neuroimaging and psychometric evaluations of each child. Core C provides databases, project-specific data analyses, and overall data analyses. Altogether, this comprehensive program project should facilitate an integrated, multi-disciplinary understanding of spina bifida, a common and significantly handicapping disability.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Program Projects (P01)
Project #
3P01HD035946-03S1
Application #
6096322
Study Section
Special Emphasis Panel (ZHD1-MRG-C (JF))
Program Officer
Hanson, James W
Project Start
1998-03-20
Project End
2002-02-28
Budget Start
2000-05-31
Budget End
2001-02-28
Support Year
3
Fiscal Year
2000
Total Cost
$101,419
Indirect Cost
Name
University of Texas Health Science Center Houston
Department
Pediatrics
Type
Schools of Medicine
DUNS #
City
Houston
State
TX
Country
United States
Zip Code
77225
Ware, Ashley L; Kulesz, Paulina A; Juranek, Jenifer et al. (2017) Cognitive control and associated neural correlates in adults with spina bifida myelomeningocele. Neuropsychology 31:411-423
Raghubar, Kimberly P; Barnes, Marcia A (2017) Early numeracy skills in preschool-aged children: a review of neurocognitive findings and implications for assessment and intervention. Clin Neuropsychol 31:329-351
Ware, Ashley L; Kulesz, Paulina A; Williams, Victoria J et al. (2016) Gray matter integrity within regions of the dorsolateral prefrontal cortical-subcortical network predicts executive function and fine motor dexterity in spina bifida. Neuropsychology 30:492-501
Dennis, Maureen; Cirino, Paul T; Simic, Nevena et al. (2016) White and grey matter relations to simple, choice, and cognitive reaction time in spina bifida. Brain Imaging Behav 10:238-51
Bradley, Kailyn A; Juranek, Jenifer; Romanowska-Pawliczek, Anna et al. (2016) Plasticity of Interhemispheric Temporal Lobe White Matter Pathways Due to Early Disruption of Corpus Callosum Development in Spina Bifida. Brain Connect 6:238-48
Arrington, C Nikki; Ware, Ashley L; Ahmed, Yusra et al. (2016) Are Shunt Revisions Associated with IQ in Congenital Hydrocephalus? A Meta -Analysis. Neuropsychol Rev 26:329-339
Ruggiero, Jaclyn E; Northrup, Hope; Au, Kit Sing (2015) Association of facilitated glucose transporter 2 gene variants with the myelomeningocele phenotype. Birth Defects Res A Clin Mol Teratol 103:479-87
Treble-Barna, Amery; Juranek, Jenifer; Stuebing, Karla K et al. (2015) Prospective and episodic memory in relation to hippocampal volume in adults with spina bifida myelomeningocele. Neuropsychology 29:92-101
Kulesz, Paulina A; Tian, Siva; Juranek, Jenifer et al. (2015) Relations between volumetric measures of brain structure and attentional function in spina bifida: utilization of robust statistical approaches. Neuropsychology 29:212-25
Kulesz, Paulina A; Treble-Barna, Amery; Williams, Victoria J et al. (2015) Attention in spina bifida myelomeningocele: Relations with brain volume and integrity. Neuroimage Clin 8:72-8

Showing the most recent 10 out of 128 publications