Evidence map›Paper›PMID 30469023›Full record

ArticleMultiple sclerosis and related disorders2019

Sequential phases of RGC axonal and somatic injury in EAE mice examined using DTI and OCT.

Christopher Nishioka, Hsiao-Fang Liang, Barsam Barsamian, Shu-Wei Sun

Abstract read
In one paragraph

Article in Multiple sclerosis and related disorders, 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
2.3field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 35 citations in OpenAlex.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Christopher NishiokaBasic Sciences, School of Medicine, Loma Linda University, CA, United States; Neuroscience Graduate Program, University of California, Riverside, United States.
Hsiao-Fang LiangBasic Sciences, School of Medicine, Loma Linda University, CA, United States; Pharmaceutical Science, School of Pharmacy, Loma Linda University, CA, United States.
Barsam BarsamianBasic Sciences, School of Medicine, Loma Linda University, CA, United States; Neuroscience Graduate Program, University of California, Riverside, United States.
Shu-Wei SunBasic Sciences, School of Medicine, Loma Linda University, CA, United States; Neuroscience Graduate Program, University of California, Riverside, United States; Pharmaceutical Science, School of Pharmacy, Loma Linda University, CA, United States. Electronic address: rsun@llu.edu.
Loma Linda University · USUniversity of California, Riverside · US

Funding

Understanding neuronal and axonal degeneration in a murine model of human MSR01NS062830 · NINDS · LOMA LINDA UNIVERSITY · PI SUN, SHU-WEI · 2011 to 2014
$1.3M
NINDS NIH HHS R01 NS062830
6 · The paper itself

Abstract

backgroundClinical imaging modalities including optical coherence tomography (OCT) and diffusion tensor imaging (DTI) are vital in Multiple Sclerosis (MS), but their relationships during the different phases of Retinal ganglion cell (RGC) degeneration are not clear. We hypothesize that initial injury in optic nerve causes axonal degeneration leading to RGC loss in retina, which can be characterized by a combination of DTI and OCT. Our objective was to examine the correlation between noninvasive and histological data to chronicle the degeneration profile of RGCs in the retina and optic nerve in a mouse model of MS. MATERIALS AND

methodsExperimental Autoimmune Encephalomyelitis (EAE) was induced in 11 C57Bl/6 mice, with 8 mice reserved as controls. OCT and DTI was conducted 2-8 weeks after induction of EAE. The thickness of the retinal ganglion cell complex (GCC) was measured using OCT and compared to DTI indices measured in optic nerves. End-stage histology was used to quantify axon/myelin loss in the optic nerve and retinal thinning/RGC loss in the retina.

resultsSignificant changes in DTI-derived Axial Diffusivity (AD, -17.2%) and Trace Diffusivity (TR, -18.3%) began after 2 weeks of EAE. Later significant reductions in Fractional Anisotropy (FA) and AD, with increases in Radial Diffusion (RD) were apparent after 4 and 8 weeks. OCT-derived measures of GCC thickness were reduced after 4 weeks, and reached significant reduction after 8 weeks. Among EAE mice, DTI (FA, AD and RD measures) and OCT measures were all significantly correlated after 4 and 8 weeks. Among histology measures, RGC density (-23%), RGC size (-27%), and the number of SMI31+ axons (-54%) were reduced significantly. DTI measures of FA and AD along with GCC thinning were the best independent predictors of axon loss.

conclusionsDTI and OCT measures are tightly correlated during the chronic phase of axonal degeneration (4-8 weeks) in EAE mice. After 8 weeks of EAE, both OCT and DTI measures are strong predictors of axon loss in the Optic Nerve.

Indexed as

Diffusion Tensor ImagingTomography, Optical CoherenceAnimalsAxonsDisease Models, AnimalEncephalomyelitis, Autoimmune, ExperimentalFemaleMice, Inbred C57BLMultiple SclerosisOptic NerveRetinal DegenerationRetinal Ganglion CellsDiffusion tensor imaging (DTI)Experimental Autoimmune Encephalomyelitis (EAE)longitudinal studyOptical coherence tomography (OCT)Retinal ganglion cell (RGC)

Identifiers

PMID30469023
PMCPMC6392031
OpenAlexW2900889362

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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.