Evidence map›Paper›PMID 23761699›Full record

ArticleJournal of neurophysiology2013

Temporal changes of neocortical high-frequency oscillations in epilepsy.

Allison Pearce, Drausin Wulsin, Justin A Blanco, Abba Krieger, Brian Litt, William C Stacey

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 2 pooled it
2.9field-weighted citation impact, top 9% 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

42 citing papers in PubMed, 2 syntheses or guidelines pooled it, 66 citations in OpenAlex.

  1. The role of high-frequency oscillations in epilepsy surgery planning.The Cochrane database of systematic reviews · 2017
    Pooled it
  2. The role of high-frequency oscillations in epilepsy surgery planning.The Cochrane database of systematic reviews · 2014
    Pooled it
  3. Review
  4. Article
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  7. Review
  8. Optimizing automated detection of high frequency oscillations using visual markings does not improve SOZ localization.Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2024
    Article
  9. Article
  10. Networks through the lens of high-frequency oscillations.Frontiers in network physiology · 2024
    Review
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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 at 3 institutions in 1 country.

Allison PearceDepartment of Computer Science, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Drausin Wulsin
Justin A Blanco
Abba Krieger
Brian Litt
William C Stacey
University of Pennsylvania · USUnited States Naval Academy · USUniversity of Michigan–Ann Arbor · US

Funding

An Implantable Device to predict and Prevent SeizuresR01NS041811 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI DICHTER, MARC A · 2001 to 2011
$13.0M
The International epilepsy electrophysiology databaseU24NS063930 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI LITT, BRIAN · 2010 to 2014
$5.6M
Modeling seizure precursors and antiepileptic brain stimulationK08NS069783 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI STACEY, WILLIAM CHARLES · 2011 to 2015
$886k
Neuralynx for Translational ResearchS10RR031724 · NCRR · UNIVERSITY OF PENNSYLVANIA · PI LITT, BRIAN · 2011 to 2011
$225k
NCRR NIH HHS S10 RR031724NINDS NIH HHS 1K08-NS-069783-02NINDS NIH HHS 1-U24-NS-063930-02NINDS NIH HHS 2R01-NS0-41811-06NINDS NIH HHS K08 NS069783NINDS NIH HHS U24 NS063930
6 · The paper itself

Abstract

High-frequency (100-500 Hz) oscillations (HFOs) recorded from intracranial electrodes are a potential biomarker for epileptogenic brain. HFOs are commonly categorized as ripples (100-250 Hz) or fast ripples (250-500 Hz), and a third class of mixed frequency events has also been identified. We hypothesize that temporal changes in HFOs may identify periods of increased the likelihood of seizure onset. HFOs (86,151) from five patients with neocortical epilepsy implanted with hybrid (micro + macro) intracranial electrodes were detected using a previously validated automated algorithm run over all channels of each patient's entire recording. HFOs were characterized by extracting quantitative morphologic features and divided into four time epochs (interictal, preictal, ictal, and postictal) and three HFO clusters (ripples, fast ripples, and mixed events). We used supervised classification and nonparametric statistical tests to explore quantitative changes in HFO features before, during, and after seizures. We also analyzed temporal changes in the rates and proportions of events from each HFO cluster during these periods. We observed patient-specific changes in HFO morphology linked to fluctuation in the relative rates of ripples, fast ripples, and mixed frequency events. These changes in relative rate occurred in pre- and postictal periods up to thirty min before and after seizures. We also found evidence that the distribution of HFOs during these different time periods varied greatly between individual patients. These results suggest that temporal analysis of HFO features has potential for designing custom seizure prediction algorithms and for exploring the relationship between HFOs and seizure generation.

Indexed as

AdultBiomarkersBrain WavesData Interpretation, StatisticalElectroencephalographyEpilepsyFemaleHumansMaleNeocortexTime FactorsYoung AdultBiomarkersclassifierepilepsyHFOmachine learningoscillation

Identifiers

PMID23761699
PMCPMC3763087
OpenAlexW2109909859

What OpenQuestion holds

Textmetadata
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.