Evidence map›Paper›PMID 26909329›Full record

ArticleNeuroImage. Clinical2016

Spatially selective 2D RF inner field of view (iFOV) diffusion kurtosis imaging (DKI) of the pediatric spinal cord.

Chris J Conklin, Devon M Middleton, Mahdi Alizadeh, Jürgen Finsterbusch, David L Raunig, Scott H Faro, Pallav Shah, Laura Krisa, Rebecca Sinko, Joan Z Delalic and 2 more

Abstract read
In one paragraph

Article in NeuroImage. Clinical, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

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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

12 authors.

Chris J ConklinElectrical Engineering, Temple University, Philadelphia, PA, United States; Radiology, Thomas Jefferson University, Philadelphia, PA, United States. Electronic address: Christopher.conklin@jefferson.edu.
Devon M MiddletonRadiology, Temple University, Philadelphia, PA, United States; Bioengineering, Temple University, Philadelphia, PA, United States.
Mahdi AlizadehRadiology, Temple University, Philadelphia, PA, United States; Bioengineering, Temple University, Philadelphia, PA, United States.
Jürgen FinsterbuschSystems Neuroscience, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
David L RaunigICON Medical Imaging, Warrington, PA, United States.
Scott H FaroRadiology, Temple University, Philadelphia, PA, United States; Bioengineering, Temple University, Philadelphia, PA, United States.
Pallav ShahRadiology, Temple University, Philadelphia, PA, United States.
Laura KrisaPhysical Therapy, Thomas Jefferson University, Philadelphia, PA, United States; Occupational Therapy, Thomas Jefferson University, Philadelphia, PA, United States.
Rebecca SinkoOccupational Therapy, Thomas Jefferson University, Philadelphia, PA, United States.
Joan Z DelalicElectrical Engineering, Temple University, Philadelphia, PA, United States.
M J MulcaheyOccupational Therapy, Thomas Jefferson University, Philadelphia, PA, United States.
Feroze B MohamedBioengineering, Temple University, Philadelphia, PA, United States; Radiology, Thomas Jefferson University, Philadelphia, PA, United States.

Funding

Neuroimaging based on DTI as a biomarker for spinal cord injury in children.R01NS079635 · NINDS · THOMAS JEFFERSON UNIVERSITY · PI MOHAMED, FEROZE B, MULCAHEY-HERSHEY, MARYJANE · 2013 to 2017
$1.7M
NINDS NIH HHS R01 NS079635NINDS NIH HHS R01 NS079635-01A1
6 · The paper itself

Abstract

Magnetic resonance based diffusion imaging has been gaining more utility and clinical relevance over the past decade. Using conventional echo planar techniques, it is possible to acquire and characterize water diffusion within the central nervous system (CNS); namely in the form of Diffusion Weighted Imaging (DWI) and Diffusion Tensor Imaging (DTI). While each modality provides valuable clinical information in terms of the presence of diffusion and its directionality, both techniques are limited to assuming an ideal Gaussian distribution for water displacement with no intermolecular interactions. This assumption neglects pathological processes that are not Gaussian therefore reducing the amount of potentially clinically relevant information. Additions to the Gaussian distribution measured by the excess kurtosis, or peakedness, of the probabilistic model provide a better understanding of the underlying cellular structure. The objective of this work is to provide mathematical and experimental evidence that Diffusion Kurtosis Imaging (DKI) can offer additional information about the micromolecular environment of the pediatric spinal cord. This is accomplished by a more thorough characterization of the nature of random water displacement within the cord. A novel DKI imaging sequence based on a tilted 2D spatially selective radio frequency pulse providing reduced field of view (FOV) imaging was developed, implemented, and optimized on a 3 Tesla MRI scanner, and tested on pediatric subjects (healthy subjects: 15; patients with spinal cord injury (SCI):5). Software was developed and validated for post processing of the DKI images and estimation of the tensor parameters. The results show statistically significant differences in mean kurtosis (p < 0.01) and radial kurtosis (p < 0.01) between healthy subjects and subjects with SCI. DKI provides incremental and novel information over conventional diffusion acquisitions when coupled with higher order estimation algorithms.

Indexed as

Diffusion Magnetic Resonance ImagingDiffusion Tensor ImagingImage Processing, Computer-AssistedAdolescentAlgorithmsBrainChildFemaleHumansMaleSpinal Cord DiseasesDiffusionDiffusion kurtosis imaging (DKI)PediatricsSpinal cord injury

Identifiers

PMID26909329
PMCPMC4735660

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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.