Evidence map›Paper›PMID 37316509›Full record

ArticleScientific reports2023

The role of superficial and deep layers in the generation of high frequency oscillations and interictal epileptiform discharges in the human cortex.

Daniel Fabo, Virag Bokodi, Johanna-Petra Szabó, Emilia Tóth, Pariya Salami, Corey J Keller, Boglárka Hajnal, Thomas Thesen, Orrin Devinsky, Werner Doyle and 7 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. 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
2.2field-weighted citation impact, top 13% 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, 10 citations in OpenAlex.

  1. Article
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  4. Intracranial Voltage Profiles from Untangled Human Deep Sources Reveal Multisource Composition and Source Allocation Bias.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
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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

17 authors at 11 institutions in 2 countries.

Daniel Fabo *Epilepsy Unit, Department of Neurology, National Institute of Mental Health, Neurology and Neurosurgery, Amerikai Út 57. 1145, Budapest, Hungary. fabo@oiti.hu.
Virag Bokodi *Epilepsy Unit, Department of Neurology, National Institute of Mental Health, Neurology and Neurosurgery, Amerikai Út 57. 1145, Budapest, Hungary.
Johanna-Petra SzabóEpilepsy Unit, Department of Neurology, National Institute of Mental Health, Neurology and Neurosurgery, Amerikai Út 57. 1145, Budapest, Hungary.
Emilia TóthEpilepsy Unit, Department of Neurology, National Institute of Mental Health, Neurology and Neurosurgery, Amerikai Út 57. 1145, Budapest, Hungary.
Pariya SalamiEpilepsy Division, Department of Neurology, Department of Neurosurgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Corey J KellerDepartment of Psychiatry and Behavioral Sciences, Stanford University Medical Center, Stanford, CA, USA.
Boglárka HajnalEpilepsy Unit, Department of Neurology, National Institute of Mental Health, Neurology and Neurosurgery, Amerikai Út 57. 1145, Budapest, Hungary.
Thomas ThesenComprehensive Epilepsy Center, New York University School of Medicine, New York, NY, USA.
Orrin DevinskyComprehensive Epilepsy Center, New York University School of Medicine, New York, NY, USA.
Werner DoyleComprehensive Epilepsy Center, New York University School of Medicine, New York, NY, USA.
Ashesh MehtaDepartment of Neurosurgery, Zucker School of Medicine at Hofstra/Northwell and Feinstein Institute for Medical Research, Manhasset, NY, USA.
Joseph MadsenThe Children's Hospital, Boston, MA, USA.
Emad EskandarMassachusetts General Hospital Neurosurgery Research, Boston, MA, USA.
Lorand ErőssDepartment of Functional Neurosurgery, National Institute of Mental Health, Neurology and Neurosurgery, Budapest, Hungary.
István UlbertEpilepsy Unit, Department of Neurology, National Institute of Mental Health, Neurology and Neurosurgery, Amerikai Út 57. 1145, Budapest, Hungary.
Eric HalgrenDepartment of Radiology, Neurosciences and Psychiatry, University of California, San Diego, San Diego, CA, USA.
Sydney S CashEpilepsy Division, Department of Neurology, Department of Neurosurgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA. scash@mgh.harvard.edu.
Massachusetts General Hospital · USNew York University · USSzent János Kórház · HUBoston Children's Hospital · USBudapest University of Economics and Business · HUEötvös Loránd University · HUFeinstein Institute for Medical Research · USOrszágos Idegsebészeti Tudományos Intézet · HUStanford University · USThe University of Texas Health Science Center at Houston · USUniversity of California San Diego · US

Funding

Neurophysiology of Human Cortical EpilepsyR01NS062092 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI CASH, SYDNEY S · 2010 to 2021
$4.7M
NIH HHS R01NS062092
6 · The paper itself

Abstract

Describing intracortical laminar organization of interictal epileptiform discharges (IED) and high frequency oscillations (HFOs), also known as ripples. Defining the frequency limits of slow and fast ripples. We recorded potential gradients with laminar multielectrode arrays (LME) for current source density (CSD) and multi-unit activity (MUA) analysis of interictal epileptiform discharges IEDs and HFOs in the neocortex and mesial temporal lobe of focal epilepsy patients. IEDs were observed in 20/29, while ripples only in 9/29 patients. Ripples were all detected within the seizure onset zone (SOZ). Compared to hippocampal HFOs, neocortical ripples proved to be longer, lower in frequency and amplitude, and presented non-uniform cycles. A subset of ripples (≈ 50%) co-occurred with IEDs, while IEDs were shown to contain variable high-frequency activity, even below HFO detection threshold. The limit between slow and fast ripples was defined at 150 Hz, while IEDs' high frequency components form clusters separated at 185 Hz. CSD analysis of IEDs and ripples revealed an alternating sink-source pair in the supragranular cortical layers, although fast ripple CSD appeared lower and engaged a wider cortical domain than slow ripples MUA analysis suggested a possible role of infragranularly located neural populations in ripple and IED generation. Laminar distribution of peak frequencies derived from HFOs and IEDs, respectively, showed that supragranular layers were dominated by slower (< 150 Hz) components. Our findings suggest that cortical slow ripples are generated primarily in upper layers while fast ripples and associated MUA in deeper layers. The dissociation of macro- and microdomains suggests that microelectrode recordings may be more selective for SOZ-linked ripples. We found a complex interplay between neural activity in the neocortical laminae during ripple and IED formation. We observed a potential leading role of cortical neurons in deeper layers, suggesting a refined utilization of LMEs in SOZ localization.

Indexed as

Body FluidsColeopteraEndocrine GlandsEpilepsies, PartialHigh-Frequency VentilationAnimalsHumans

Identifiers

PMID37316509
PMCPMC10267175
OpenAlexW4380681728

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.