Evidence map›Paper›PMID 35726354›Full record

ArticleAnnals of neurology2022

Networks Underlie Temporal Onset of Dysplasia-Related Epilepsy: A MELD Study.

Nathan T Cohen, Xiaozhen You, Manu Krishnamurthy, Leigh N Sepeta, Anqing Zhang, Chima Oluigbo, Matthew T Whitehead, Taha Gholipour, Torsten Baldeweg, Konrad Wagstyl and 3 more

Open access · greenAbstract read
In one paragraph

Article in Annals of neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.8field-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

16 citing papers in PubMed, 20 citations in OpenAlex.

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  6. Review
  7. ILAE neuroimaging task force highlight: MRI detection of early life epilepsy caused by focal cortical dysplasia.Epileptic disorders : international epilepsy journal with videotape · 2025
    Article
  8. Article
  9. ILAE genetic literacy series: Focal cortical dysplasia.Epileptic disorders : international epilepsy journal with videotape · 2025
    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

13 authors at 3 institutions in 2 countries.

Nathan T CohenCenter for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, DC.ORCID 0000-0002-1410-3487
Xiaozhen YouCenter for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, DC.
Manu KrishnamurthyCenter for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, DC.
Leigh N SepetaCenter for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, DC.
Anqing ZhangCenter for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, DC.
Chima OluigboCenter for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, DC.
Matthew T WhiteheadCenter for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, DC.
Taha GholipourCenter for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, DC.ORCID 0000-0002-8751-0593
Torsten BaldewegGreat Ormond Street Institute for Child Health, University College of London, London, UK.
Konrad WagstylWellcome Centre for Human Neuroimaging, London, UK.ORCID 0000-0003-3439-5808
Sophie AdlerGreat Ormond Street Institute for Child Health, University College of London, London, UK.
William D GaillardCenter for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, DC.
Multi-Centre Epilepsy Lesion Detection (MELD) Project
George Washington University Hospital · USGreat Ormond Street Hospital · GBWellcome Centre for Human Neuroimaging · GB

Funding

Clinical and Translational Science Institute at Childrens NationalUL1TR001876 · NCATS · CHILDREN'S RESEARCH INSTITUTE · PI BELL, MICHAEL J · 2016 to 2021
$25.6M
Neurobehavioral Evaluation CoreP50HD105328 · NICHD · CHILDREN'S RESEARCH INSTITUTE · PI LAUREN KENWORTHY · 2021 to 2026
$9.3M
Research_ProjectU54HD090257 · NICHD · CHILDREN'S RESEARCH INSTITUTE · PI VITTORIO GALLO, VITTORIO GALLO VITTORIO GALLO · 2016 to 2020
$5.9M
Imaging the Impact of Childhood Epilepsy on Memory Development - SupplementK23NS093152 · NINDS · CHILDREN'S RESEARCH INSTITUTE · PI SEPETA, LEIGH · 2018 to 2023
$912k
NCATS NIH HHS UL1 TR001876NCATS NIH HHS UL1TR001876NICHD NIH HHS P50 HD105328NICHD NIH HHS U54 HD090257NINDS NIH HHS K23 NS093152
6 · The paper itself

Abstract

objectiveThe purpose of this study was to evaluate if focal cortical dysplasia (FCD) co-localization to cortical functional networks is associated with the temporal distribution of epilepsy onset in FCD.

methodsInternational (20 center), retrospective cohort from the Multi-Centre Epilepsy Lesion Detection (MELD) project. Patients included if >3 years old, had 3D pre-operative T1 magnetic resonance imaging (MRI; 1.5 or 3 T) with radiologic or histopathologic FCD after surgery. Images processed using the MELD protocol, masked with 3D regions-of-interest (ROI), and co-registered to fsaverage_sym (symmetric template). FCDs were then co-localized to 1 of 7 distributed functional cortical networks. Negative binomial regression evaluated effect of FCD size, network, histology, and sulcal depth on age of epilepsy onset. From this model, predictive age of epilepsy onset was calculated for each network.

resultsThree hundred eighty-eight patients had median age seizure onset 5 years (interquartile range [IQR] = 3-11 years), median age at pre-operative scan 18 years (IQR = 11-28 years). FCDs co-localized to the following networks: limbic (90), default mode (87), somatomotor (65), front parietal control (52), ventral attention (32), dorsal attention (31), and visual (31). Larger lesions were associated with younger age of onset (p = 0.01); age of epilepsy onset was associated with dominant network (p = 0.04) but not sulcal depth or histology. Sensorimotor networks had youngest onset; the limbic network had oldest age of onset (p values <0.05).

interpretationFCD co-localization to distributed functional cortical networks is associated with age of epilepsy onset: sensory neural networks (somatomotor and visual) with earlier onset, and limbic latest onset. These variations may reflect developmental differences in synaptic/white matter maturation or network activation and may provide a biological basis for age-dependent epilepsy onset expression. ANN NEUROL 2022;92:503-511.

Indexed as

EpilepsyMalformations of Cortical DevelopmentChildChild, PreschoolHumansMagnetic Resonance ImagingRetrospective StudiesTreatment Outcome

Identifiers

PMID35726354
PMCPMC10410674
OpenAlexW4283204381

What OpenQuestion holds

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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.