Evidence map›Paper›PMID 30555696›Full record

ArticleJournal of therapeutic ultrasound2018

Transcranial and pulsed focused ultrasound that activates brain can accelerate remyelination in a mouse model of multiple sclerosis.

T A Olmstead, P A Chiarelli, D J Griggs, A M McClintic, A N Myroniv, P D Mourad

Abstract read
In one paragraph

Article in Journal of therapeutic ultrasound, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 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

6 authors.

T A Olmstead1Department of Neurological Surgery, University of Washington, Seattle, WA 98195 USA.
P A Chiarelli1Department of Neurological Surgery, University of Washington, Seattle, WA 98195 USA.
D J Griggs2Division of Engineering and Mathematics, University of Washington, Bothell, WA 98011 USA.
A M McClintic1Department of Neurological Surgery, University of Washington, Seattle, WA 98195 USA.
A N Myroniv1Department of Neurological Surgery, University of Washington, Seattle, WA 98195 USA.
P D Mourad1Department of Neurological Surgery, University of Washington, Seattle, WA 98195 USA.

Funding

Towards deep brain monitoring with superficial EEG sensors plus neuromodulatory focused ultrasoundR21EY027557 · NEI · UNIVERSITY OF WASHINGTON · PI MOURAD, PIERRE D · 2016 to 2017
$464k
NEI NIH HHS R21 EY027557
6 · The paper itself

Abstract

backgroundMultiple sclerosis (MS) impacts approximately 400,000 in the United States and is the leading cause of disability among young to middle aged people in the developed world. Characteristic of this disease, myelin within generally focal volumes of brain tissue wastes away under an autoimmune assault, either inexorably or through a cycle of demyelination and remyelination. This centrally located damage produces central and peripheral symptoms tied to the portion of brain within the MS lesion site. Interestingly, Gibson and colleagues noted that optical activation of transgenically tagged central neurons increased the thickness of the myelin sheath around those neurons. Since ultrasound, delivered transcranially, can also activate brain focally, we hypothesized that ultrasound stimulation that followed the temporal pattern of Gibson et al. applied to MS lesions in a mouse model might either decelerate the demyelination phase or accelerate its remyelination phase.

methodsWe created a temporal pattern of ultrasound delivery that conformed to that of Gibson et al. and capable of activating mouse brain. We then applied ultrasound, transcranially, following that temporal pattern to separate cohorts of a mouse model of multiple sclerosis, using three different ultrasound carrier frequencies (0.625 MHz, 1.09 MHz, 2.0 MHz), during each of the demyelinating and remyelinating phases. After identifying the most promising protocol and MS brain state through qualitative analysis of myelin content, we performed additional studies for that condition then assayed for change in myelin content via quantitative analysis.

resultsWe identified one ultrasound protocol that significantly accelerated remyelination, without damage, as demonstrated with histological analysis.

conclusionMRI-guided focused ultrasound systems exist that can, in principle, deliver the ultrasound protocol we successfully tested here. In addition, MRI, as the clinical gold standard, can readily identify MS lesions. Given the relatively low intensity values of our ultrasound protocol - close to FDA limits - we anticipate that future success with this approach to MS therapy as tested using more realistic MS mouse models may one day translate to clinical trials that help address this devastating disease.

Indexed as

Brain activationFocused ultrasoundMultiple sclerosisNeuromodulationTherapy

Identifiers

PMID30555696
PMCPMC6287362

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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.