Evidence map›Paper›PMID 26798959›Full record

ArticleBrain connectivity2016

Plasticity of Interhemispheric Temporal Lobe White Matter Pathways Due to Early Disruption of Corpus Callosum Development in Spina Bifida.

Kailyn A Bradley, Jenifer Juranek, Anna Romanowska-Pawliczek, H Julia Hannay, Paul T Cirino, Maureen Dennis, Larry A Kramer, Jack M Fletcher

Open access · greenAbstract read
In one paragraph

Article in Brain connectivity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Assessment of longitudinal brain development using super-resolution magnetic resonance imaging following fetal surgery for open spina bifida.Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology · 2023
    Article
  4. Review
  5. Review
  6. Observational
  7. Neuropsychological care guidelines for people with spina bifida.Journal of pediatric rehabilitation medicine
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 2 countries.

Kailyn A Bradley1 Department of Psychology, University of Houston , Houston, Texas.
Jenifer Juranek3 Department of Pediatrics, Children's Learning Institute, University of Texas Health Science Center at Houston , Houston, Texas.
Anna Romanowska-Pawliczek3 Department of Pediatrics, Children's Learning Institute, University of Texas Health Science Center at Houston , Houston, Texas.
H Julia Hannay1 Department of Psychology, University of Houston , Houston, Texas.
Paul T Cirino1 Department of Psychology, University of Houston , Houston, Texas.
Maureen Dennis4 Program in Neurosciences and Mental Health, The Hospital for Sick Children , Toronto, Canada .
Larry A Kramer5 Department of Diagnostic and Interventional Radiology, University of Texas Health Science Center at Houston , Houston, Texas.
Jack M Fletcher1 Department of Psychology, University of Houston , Houston, Texas.
University of Houston · USThe University of Texas Health Science Center at Houston · USHospital for Sick Children · CAIcahn School of Medicine at Mount Sinai · US

Funding

SUBJECT RECRUITMENT AND EVALUATION COREP01HD035946 · NICHD · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI FLETCHER, JACK M · 1998 to 2009
$10.8M
NICHD NIH HHS P01-HD35946-06
6 · The paper itself

Abstract

Spina bifida myelomeningocele (SBM) is commonly associated with anomalous development of the corpus callosum (CC) because of congenital partial hypogenesis and hydrocephalus-related hypoplasia. It represents a model disorder to examine the effects of early disruption of CC neurodevelopment and the plasticity of interhemispheric white matter connections. Diffusion tensor imaging was acquired on 76 individuals with SBM and 27 typically developing individuals, aged 8-36 years. Probabilistic tractography was used to isolate the interhemispheric connections between the posterior superior temporal lobes, which typically traverse the posterior third of the CC. Early disruption of CC development resulted in restructuring of interhemispheric connections through alternate commissures, particularly the anterior commissure (AC). These rerouted fibers were present in people with SBM and both CC hypoplasia and hypogenesis. In addition, microstructural integrity was reduced in the interhemispheric temporal tract in people with SBM, indexed by lower fractional anisotropy, axial diffusivity, and higher radial diffusivity. Interhemispheric temporal tract volume was positively correlated with total volume of the CC, such that more severe underdevelopment of the CC was associated with fewer connections between the posterior temporal lobes. Therefore, both the macrostructure and microstructure of this interhemispheric tract were reduced, presumably as a result of more extensive CC malformation. The current findings suggest that early disruption in CC development reroutes interhemispheric temporal fibers through both the AC and more anterior sections of the CC in support of persistent hypotheses that the AC may serve a compensatory function in atypical CC development.

Indexed as

AdolescentAdultAgenesis of Corpus CallosumCase-Control StudiesChildCorpus CallosumDiffusion Tensor ImagingFemaleHumansMaleMeningomyeloceleNerve Fibers, MyelinatedNeural PathwaysNeuronal PlasticitySpinal DysraphismTemporal Lobecorpus callosumdiffusion tensor imagingfiber trackingneural plasticitytemporal lobe

Identifiers

PMID26798959
PMCPMC4827308
OpenAlexW2273771579

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.