Evidence map›Paper›PMID 25523813›Full record

ArticleExperimental neurology2015

Optimized methods for epilepsy therapy development using an etiologically realistic model of focal epilepsy in the rat.

Clifford L Eastman, Jason S Fender, Nancy R Temkin, Raimondo D'Ambrosio

Open access · greenAbstract read
In one paragraph

Article in Experimental neurology, 2015. 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
1.7field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 20 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

4 authors at 2 institutions in 1 country.

Clifford L EastmanDepartment of Neurological Surgery, University of Washington, School of Medicine, Seattle, WA 98104, USA.
Jason S FenderDepartment of Neurological Surgery, University of Washington, School of Medicine, Seattle, WA 98104, USA.
Nancy R TemkinDepartment of Neurological Surgery, University of Washington, School of Medicine, Seattle, WA 98104, USA; Department of Biostatistics, University of Washington, School of Medicine, Seattle, WA 98104, USA.
Raimondo D'AmbrosioDepartment of Neurological Surgery, University of Washington, School of Medicine, Seattle, WA 98104, USA; Regional Epilepsy Center, University of Washington, School of Medicine, Seattle, WA 98104, USA. Electronic address: raid@u.washington.edu.
Neurological Surgery · USUniversity of Washington · US

Funding

Optimization of the FPI model for epilepsy therapy developmentR21NS076570 · NINDS · UNIVERSITY OF WASHINGTON · PI D'AMBROSIO, RAIMONDO · 2012 to 2013
$416k
NINDS NIH HHS NS076570NINDS NIH HHS R21 NS076570
6 · The paper itself

Abstract

Conventionally developed antiseizure drugs fail to control epileptic seizures in about 30% of patients, and no treatment prevents epilepsy. New etiologically realistic, syndrome-specific epilepsy models are expected to identify better treatments by capturing currently unknown ictogenic and epileptogenic mechanisms that operate in the corresponding patient populations. Additionally, the use of electrocorticography permits better monitoring of epileptogenesis and the full spectrum of acquired seizures, including focal nonconvulsive seizures that are typically difficult to treat in humans. Thus, the combined use of etiologically realistic models and electrocorticography may improve our understanding of the genesis and progression of epilepsy, and facilitate discovery and translation of novel treatments. However, this approach is labor intensive and must be optimized. To this end, we used an etiologically realistic rat model of posttraumatic epilepsy, in which the initiating fluid percussion injury closely replicates contusive closed-head injury in humans, and has been adapted to maximize epileptogenesis and focal non-convulsive seizures. We obtained week-long 5-electrode electrocorticography 1 month post-injury, and used a Monte-Carlo-based non-parametric bootstrap strategy to test the impact of electrode montage design, duration-based seizure definitions, group size and duration of recordings on the assessment of posttraumatic epilepsy, and on statistical power to detect antiseizure and antiepileptogenic treatment effects. We found that use of seizure definition based on clinical criteria rather than event duration, and of recording montages closely sampling the activity of epileptic foci, maximize the power to detect treatment effects. Detection of treatment effects was marginally improved by prolonged recording, and 24h recording epochs were sufficient to provide 80% power to detect clinically interesting seizure control or prevention of seizures with small groups of animals. We conclude that appropriate electrode montage and clinically relevant seizure definition permit convenient deployment of fluid percussion injury and electrocorticography for epilepsy therapy development.

Indexed as

Disease Models, AnimalAnimalsElectroencephalographyEpilepsies, PartialHead Injuries, ClosedMaleProbabilityRatsRats, Sprague-DawleySpectrum AnalysisTime FactorsDrug developmentFocal epilepsyNon-convulsive seizurePharmacoresistancePreclinical drug screeningStatistical power analysis

Identifiers

PMID25523813
PMCPMC4327986
OpenAlexW2081974100

What OpenQuestion holds

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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.