Literature DB >> 15881750

Spinal lesion level in spina bifida: a source of neural and cognitive heterogeneity.

Jack M Fletcher1, Kim Copeland, Jon A Frederick, Susan E Blaser, Larry A Kramer, Hope Northrup, H Julia Hannay, Michael E Brandt, David J Francis, Grace Villarreal, James M Drake, John P Laurent, Irene Townsend, Susan Inwood, Amy Boudousquie, Maureen Dennis.   

Abstract

OBJECT: The aim of this study was to evaluate whether the level of a spinal lesion is associated with variations in anomalous brain development and neurobehavioral outcomes in children suffering from the meningomyelocele form of spina bifida and hydrocephalus (SBM-H).
METHODS: Two hundred sixty-eight children with SBM-H were divided into upper (T-12 and above; 82 patients) and lower (L-1 and below; 186 patients) lesion-level groups. Magnetic resonance images were qualitatively coded by radiologists and quantitatively segmented for cerebrum and cerebellum volumes. Psychometric assessments of handedness, intelligence, academic skills, and adaptive behavior were compared between lesion-level groups and also used to determine the number of children who met research-based criteria for mental retardation, attention deficit hyperactivity disorder, and learning disabilities. The magnetic resonance images obtained in children with upper-level spinal lesions demonstrated more qualitative abnormalities in the midbrain and tectum, pons, and splenium, although not in the cerebellum, compared with images obtained in children with lower-level spinal lesions. Upper-level lesions were also associated with reductions in cerebrum and cerebellum volumes, lower scores on measures of intelligence, academic skills, and adaptive behavior, and with a higher frequency of individuals meeting the criteria for mental retardation. Hispanic children (who were also more economically disadvantaged) were more likely to have upper-level lesions and poorer neurobehavioral outcomes, but lesion-level effects were generally independent of ethnicity.
CONCLUSIONS: A higher level of spinal lesion in SBM-H is a marker for more severe anomalous brain development, which is in turn associated with poorer neurobehavioral outcomes in a wide variety of domains that determine levels of independent functioning for these children at home and school.

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Mesh:

Year:  2005        PMID: 15881750     DOI: 10.3171/ped.2005.102.3.0268

Source DB:  PubMed          Journal:  J Neurosurg        ISSN: 0022-3085            Impact factor:   5.115


  76 in total

1.  Multiple spinal anomalies associated with dysgenesis of the corpus callosum.

Authors:  F S Erol
Journal:  Ir J Med Sci       Date:  2010-04-22       Impact factor: 1.568

2.  Mother-adolescent agreement regarding decision-making autonomy: a longitudinal comparison of families of adolescents with and without spina bifida.

Authors:  Katie A Devine; Rachel M Wasserman; Lily S Gershenson; Grayson N Holmbeck; Bonnie S Essner
Journal:  J Pediatr Psychol       Date:  2010-10-13

3.  Age and factors associated with self-clean intermittent catheterization in patients with spina bifida.

Authors:  T J Atchley; P P Dangle; B D Hopson; A Graham; A A Arynchyna; B G Rocque; D B Joseph; T S Wilson
Journal:  J Pediatr Rehabil Med       Date:  2018

4.  Cerebellar vermis morphology in children with spina bifida and Chiari type II malformation.

Authors:  Michael S Salman; Susan E Blaser; James A Sharpe; Maureen Dennis
Journal:  Childs Nerv Syst       Date:  2005-12-22       Impact factor: 1.475

5.  Age-related differences in executive function among children with spina bifida/hydrocephalus based on parent behavior ratings.

Authors:  Reem A Tarazi; T Andrew Zabel; E Mark Mahone
Journal:  Clin Neuropsychol       Date:  2007-08-18       Impact factor: 3.535

6.  Examination of frontal and parietal tectocortical attention pathways in spina bifida meningomyelocele using probabilistic diffusion tractography.

Authors:  Victoria J Williams; Jenifer Juranek; Karla Stuebing; Paul T Cirino; Maureen Dennis; Jack M Fletcher
Journal:  Brain Connect       Date:  2013-09-21

7.  Genetic variations in the GLUT3 gene associated with myelomeningocele.

Authors:  Brendan D Connealy; Hope Northrup; Kit Sing Au
Journal:  Am J Obstet Gynecol       Date:  2014-05-09       Impact factor: 8.661

Review 8.  Age, plasticity, and homeostasis in childhood brain disorders.

Authors:  Maureen Dennis; Brenda J Spiegler; Jenifer J Juranek; Erin D Bigler; O Carter Snead; Jack M Fletcher
Journal:  Neurosci Biobehav Rev       Date:  2013-10-03       Impact factor: 8.989

9.  Profiles of Neuropsychological Functioning in Children and Adolescents with Spina Bifida: Associations with Biopsychosocial Predictors and Functional Outcomes.

Authors:  Rachel M Wasserman; Grayson N Holmbeck
Journal:  J Int Neuropsychol Soc       Date:  2016-08-30       Impact factor: 2.892

10.  Sustained attention in children with two etiologies of early hydrocephalus.

Authors:  Maegan D Swartwout; Paul T Cirino; Amy W Hampson; Jack M Fletcher; Michael E Brandt; Maureen Dennis
Journal:  Neuropsychology       Date:  2008-11       Impact factor: 3.295

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