Evidence map›Paper›PMID 23167847›Full record

ArticleEpilepsia2013

mRNA blood expression patterns in new-onset idiopathic pediatric epilepsy.

Hansel M Greiner, Paul S Horn, Katherine Holland, James Collins, Andrew D Hershey, Tracy A Glauser

Abstract read
In one paragraph

Article in Epilepsia, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 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.

Hansel M GreinerDivision of Neurology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio 45229-3039, USA. hansel.greiner@cchmc.org
Paul S Horn
Katherine Holland
James Collins
Andrew D Hershey
Tracy A Glauser

Funding

Cincinnati Center for Clinical and Translational Sciences and TrainingUL1TR000077 · NCATS · UNIVERSITY OF CINCINNATI · PI HEUBI, JAMES E. · 2012 to 2014
$9.9M
Cincinnati Neuroscience Clinical Trials Research Center (CinciNEXT)U10NS077311 · NINDS · UNIVERSITY OF CINCINNATI · PI GLAUSER, TRACY A, WOO, DANIEL · 2011 to 2017
$2.1M
Sodium Channel Gene Variation in the Treatment of EpilepsyR01NS062756 · NINDS · CINCINNATI CHILDRENS HOSP MED CTR · PI HOLLAND, KATHERINE D · 2009 to 2013
$1.6M
Blood Genomics of Anticonvulsant Efficacy in ChildrenR21NS044956 · NINDS · CHILDREN'S HOSPITAL MED CTR (CINCINNATI) · PI GLAUSER, TRACY A · 2003 to 2004
$325k
NCATS NIH HHS UL1 TR000077NINDS NIH HHS NS044956NINDS NIH HHS R01 NS062756NINDS NIH HHS R21 NS044956NINDS NIH HHS U10 NS077311
6 · The paper itself

Abstract

purposeDetermine if blood messenger RNA (mRNA) expression patterns in children with newly diagnosed untreated idiopathic epilepsy are different from those in healthy controls. Determine the differential expression patterns between epilepsy patients with generalized onset or partial onset seizures compared to healthy controls.

methodsWhole blood was obtained from otherwise healthy pediatric patients with newly diagnosed untreated idiopathic epilepsy along with healthy pediatric controls. mRNA was isolated and hybridized to Affymetrix HGU 133 2.0+ microarrays. Analysis was performed using Genespring. Differentially expressed gene lists resulted from comparison of (1) epilepsy and control groups and (2) seizure type subgroups with controls. Tissue expression and gene ontology analysis was performed using DAVID. KEY

findingsThirty-seven epilepsy patients and 28 controls were included. Overall, 575 genes were differentially expressed in subjects with epilepsy compared to controls. The generalized seizure subgroup versus control (GvC) gene list and the partial seizure subgroup versus control (PvC) gene list were different (p < 0.05). Tissue expression analysis identified almost half of the genes in GvC and PvC as brain based. Functional group analysis identified several biologically relevant pathways. In GvC, these included mitochondria and lymphocyte activation. In PvC, we identified apoptosis, inflammatory defense, and cell motion pathways. SIGNIFICANCE: A unique, biologically meaningful mRNA expression pattern is detectable in whole blood of pediatric subjects with new-onset and untreated epilepsy. This analysis finds many similar pathways to those identified in brain studies examining lesional intractable epilepsy. Blood mRNA expression patterns show promise as a target for biomarker development in pediatric epilepsy.

Indexed as

AdolescentAge of OnsetChildChild, PreschoolCluster AnalysisCohort StudiesEpilepsies, PartialEpilepsyEpilepsy, GeneralizedFemaleGene Expression RegulationGenetic MarkersHumansLymphocyte ActivationMaleMicroarray AnalysisGenetic MarkersRNARNA, Messenger

Identifiers

PMID23167847
PMCPMC3566372

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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.