Evidence map›Paper›PMID 26696839›Full record

ArticleFrontiers in neuroanatomy2015

Synchronous Changes of Cortical Thickness and Corresponding White Matter Microstructure During Brain Development Accessed by Diffusion MRI Tractography from Parcellated Cortex.

Tina Jeon, Virendra Mishra, Minhui Ouyang, Min Chen, Hao Huang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neuroanatomy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

30 citing papers in PubMed, 46 citations in OpenAlex.

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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

5 authors at 5 institutions in 1 country.

Tina JeonRadiology Research, Children's Hospital of Philadelphia, Philadelphia PA, USA ; Advanced Imaging Research Center, University of Texas Southwestern Medical Center at Dallas, Dallas TX, USA.
Virendra MishraAdvanced Imaging Research Center, University of Texas Southwestern Medical Center at Dallas, Dallas TX, USA ; Lou Ruvo Center for Brain Health, Cleveland Clinic, Las Vegas NV, USA.
Minhui OuyangRadiology Research, Children's Hospital of Philadelphia, Philadelphia PA, USA ; Advanced Imaging Research Center, University of Texas Southwestern Medical Center at Dallas, Dallas TX, USA.
Min ChenDepartment of Mathematical Sciences, University of Texas at Dallas, Richardson TX, USA.
Hao HuangRadiology Research, Children's Hospital of Philadelphia, Philadelphia PA, USA ; Department of Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia PA, USA.
Advanced Imaging Research (United States) · USChildren's Hospital of Philadelphia · USLou Ruvo Brain Institute · USThe University of Texas at Dallas · USThe University of Texas Southwestern Medical Center · US

Funding

The Intellectual and Developmental Disabilities Research Center at CHOP/PennU54HD086984 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI YUDKOFF, MARC · 2016 to 2020
$6.3M
Structural Development of Human Fetal BrainR01MH092535 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · PI HUANG, HAO · 2011 to 2020
$4.6M
Digital probabilistic MRI atlas of primate brain with toolkits for surgery guidanR21EB009545 · NIBIB · UT SOUTHWESTERN MEDICAL CENTER · PI HUANG, HAO · 2009 to 2010
$451k
NIBIB NIH HHS R21 EB009545NICHD NIH HHS U54 HD086984NIMH NIH HHS R01 MH092535
6 · The paper itself

Abstract

Cortical thickness (CT) changes during normal brain development is associated with complicated cellular and molecular processes including synaptic pruning and apoptosis. In parallel, the microstructural enhancement of developmental white matter (WM) axons with their neuronal bodies in the cerebral cortex has been widely reported with measurements of metrics derived from diffusion tensor imaging (DTI), especially fractional anisotropy (FA). We hypothesized that the changes of CT and microstructural enhancement of corresponding axons are highly interacted during development. DTI and T1-weighted images of 50 healthy children and adolescents between the ages of 7 and 25 years were acquired. With the parcellated cortical gyri transformed from T1-weighted images to DTI space as the tractography seeds, probabilistic tracking was performed to delineate the WM fibers traced from specific parcellated cortical regions. CT was measured at certain cortical regions and FA was measured from the WM fibers traced from same cortical regions. The CT of all frontal cortical gyri, including Brodmann areas 4, 6, 8, 9, 10, 11, 44, 45, 46, and 47, decreased significantly and heterogeneously; concurrently, significant, and heterogeneous increases of FA of WM traced from corresponding regions were found. We further revealed significant correlation between the slopes of the CT decrease and the slopes of corresponding WM FA increase in all frontal cortical gyri, suggesting coherent cortical pruning and corresponding WM microstructural enhancement. Such correlation was not found in cortical regions other than frontal cortex. The molecular and cellular mechanisms of these synchronous changes may be associated with overlapping signaling pathways of axonal guidance, synaptic pruning, neuronal apoptosis, and more prevalent interstitial neurons in the prefrontal cortex. Revealing the coherence of cortical and WM structural changes during development may open a new window for understanding the underlying mechanisms of developing brain circuits and structural abnormality associated with mental disorders.

Indexed as

brain developmentcircuitscortical thicknesssynchronoustractographywhite matter microstructure

Identifiers

PMID26696839
PMCPMC4667005
OpenAlexW2185375039

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.