Evidence map›Paper›PMID 30771034›Full record

ArticleMagma (New York, N.Y.)2019

Detection of axonal degeneration in a mouse model of Huntington's disease: comparison between diffusion tensor imaging and anomalous diffusion metrics.

Rodolfo G Gatto, Allen Q Ye, Luis Colon-Perez, Thomas H Mareci, Anna Lysakowski, Steven D Price, Scott T Brady, Muge Karaman, Gerardo Morfini, Richard L Magin

Open access · greenAbstract readComparative Study
In one paragraph

Article in Magma (New York, N.Y.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Animal models of Huntington's disease. Pros and cons.Brain, behavior, & immunity - health · 2025
    Review
  3. Article
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  5. Review
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  8. Review
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  12. Article
  13. Genes · 2021
    Article
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  18. Article
  19. MR Imaging of SCA3/MJD.Frontiers in neuroscience · 2020
    Review
  20. Article
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

10 authors at 3 institutions in 1 country.

Rodolfo G GattoDepartment of Anatomy and Cell Biology, University of Illinois at Chicago, Chicago, IL, USA.ORCID http://orcid.org/0000-0002-5103-1611
Allen Q YeDepartment of Bioengineering, University of Illinois at Chicago, 851 S Morgan St, 218 SEO (MC 063), Chicago, IL, 60607, USA.
Luis Colon-PerezDepartment of Neurology and Behavior, University of California at Irvine, Irvine, CA, USA.
Thomas H MareciDepartment of Biochemistry and Molecular Biology, University of Florida, Gainesville, FL, USA.
Anna LysakowskiDepartment of Anatomy and Cell Biology, University of Illinois at Chicago, Chicago, IL, USA.
Steven D PriceDepartment of Anatomy and Cell Biology, University of Illinois at Chicago, Chicago, IL, USA.
Scott T BradyDepartment of Anatomy and Cell Biology, University of Illinois at Chicago, Chicago, IL, USA.
Muge KaramanDepartment of Bioengineering, University of Illinois at Chicago, 851 S Morgan St, 218 SEO (MC 063), Chicago, IL, 60607, USA.
Gerardo MorfiniDepartment of Anatomy and Cell Biology, University of Illinois at Chicago, Chicago, IL, USA.
Richard L MaginDepartment of Bioengineering, University of Illinois at Chicago, 851 S Morgan St, 218 SEO (MC 063), Chicago, IL, 60607, USA. rmagin@uic.edu.
University of Illinois Chicago · USUniversity of California, Irvine · USUniversity of Florida · US

Funding

CELLULAR MECHANISMS OF THE VESTIBULAR SYSTEMR01DC002058 · NIDCD · UNIVERSITY OF ILLINOIS AT CHICAGO · PI GOLDBERG, JAY M, LYSAKOWSKI, ANNA · 1993 to 2014
$5.3M
Cellular Mechanisms of the Vestibular SystemR56DC002058 · NIDCD · UNIVERSITY OF CHICAGO · PI GOLDBERG, JAY M, LYSAKOWSKI, ANNA · 2009 to 2009
$471k
Addressing the contribution of JNK3 to axonal pathology in Huntington's diseaseR21NS096642 · NINDS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MORFINI, GERARDO ANDRES · 2016 to 2017
$430k
Chicago Biomedical Consortium Award #085740National Center for Advancing Translational Science NCATS TLTR000049National Science Foundation DMR-1157490NIDCD NIH HHS R01 DC002058NIDCD NIH HHS R56 DC002058NIH HHS CHDI #A-11872NIH HHS NIH DC02058NIH HHS NIH R21NS096642NINDS NIH HHS R21 NS096642
6 · The paper itself

Abstract

objectiveThe goal of this work is to study the changes in white matter integrity in R6/2, a well-established animal model of Huntington's disease (HD) that are captured by ex vivo diffusion imaging (DTI) using a high field MRI (17.6 T). MATERIALS AND

methodsDTI and continuous time random walk (CTRW) models were used to fit changes in the diffusion-weighted signal intensity in the corpus callosum of controls and in R6/2 mice.

resultsA significant 13% decrease in fractional anisotropy, a 7% increase in axial diffusion, and a 33% increase in radial diffusion were observed between R6/2 and control mice. No change was observed in the CTRW beta parameter, but a significant decrease in the alpha parameter (- 21%) was measured. Histological analysis of the corpus callosum showed a decrease in axonal organization, myelin alterations, and astrogliosis. Electron microscopy studies demonstrated ultrastructural changes in degenerating axons, such as an increase in tortuosity in the R6/2 mice.

conclusionsDTI and CTRW diffusion models display quantitative changes associated with the microstructural alterations observed in the corpus callosum of the R6/2 mice. The observed increase in the diffusivity and decrease in the alpha CTRW parameter providing support for the use of these diffusion models for non-invasive detection of white matter alterations in HD.

Indexed as

AxonsDiffusion Tensor ImagingMagnetic Resonance ImagingAnimalsAnisotropyCorpus CallosumFemaleHuntington DiseaseMaleMiceMicroscopy, FluorescenceMyelin SheathWhite MatterAnomalous diffusionDiffusion tensor imagingHuntington diseaseMagnetic resonance imagingMice

Identifiers

PMID30771034
PMCPMC7837609
OpenAlexW2912762199

What OpenQuestion holds

Textmetadata
LicenceTDM
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.