Evidence map›Paper›PMID 37441820›Full record

ArticleNeuroImage. Clinical2023

Multi-spectral diffusion MRI mega-analysis in genetic generalized epilepsy: Relation to outcomes.

Barbara A K Kreilkamp, Christina Stier, Erik H Rauf, Pascal Martin, Silke Ethofer, Holger Lerche, Raviteja Kotikalapudi, Justus Marquetand, Peter Dechent, Niels K Focke

Open access · goldAbstract read
In one paragraph

Article in NeuroImage. Clinical, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. 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

10 authors at 4 institutions in 1 country.

Barbara A K KreilkampClinic for Neurology, University Medical Center Göttingen, Göttingen, Germany. Electronic address: barbara.kreilkamp@med.uni-goettingen.de.
Christina StierClinic for Neurology, University Medical Center Göttingen, Göttingen, Germany; Department of Neurology and Epileptology, Hertie Institute of Clinical Brain Research, University of Tübingen, Tübingen, Germany. Electronic address: christina.stier@med.uni-goettingen.de.
Erik H RaufClinic for Neurology, University Medical Center Göttingen, Göttingen, Germany. Electronic address: erik.rauf@med.uni-goettingen.de.
Pascal MartinDepartment of Neurology and Epileptology, Hertie Institute of Clinical Brain Research, University of Tübingen, Tübingen, Germany. Electronic address: pascal.martin@med.uni-tuebingen.de.
Silke EthoferDepartment of Neurosurgery, University of Tübingen, Tübingen, Germany. Electronic address: silke.ethofer@uni-tuebingen.de.
Holger LercheDepartment of Neurology and Epileptology, Hertie Institute of Clinical Brain Research, University of Tübingen, Tübingen, Germany. Electronic address: holger.lerche@unituebingen.de.
Raviteja KotikalapudiLaboratory for Predictive Neuroimaging, University of Duisburg-Essen, Essen, Germany.
Justus MarquetandDepartment of Neurology and Epileptology, Hertie Institute of Clinical Brain Research, University of Tübingen, Tübingen, Germany; Department of Neural Dynamics and Magnetoencephalography, Hertie-Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany; MEG-Center, University of Tübingen, Tübingen, Germany. Electronic address: Justus.Marquetand@med.uni-tuebingen.de.
Peter DechentDepartment of Cognitive Neurology, University Medical Center Göttingen, Göttingen, Germany. Electronic address: Peter.Dechent@medizin.uni-goettingen.de.
Niels K FockeClinic for Neurology, University Medical Center Göttingen, Göttingen, Germany. Electronic address: niels.focke@med.uni-goettingen.de.
Universitätsmedizin Göttingen · DEUniversity of Tübingen · DEHertie Institute for Clinical Brain Research · DEUniversity of Duisburg-Essen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesGenetic generalized epilepsy (GGE) is the most common form of generalized epilepsy. Although individual patients with GGE typically present without structural alterations, group differences have been demonstrated in GGE and some GGE subtypes like juvenile myoclonic epilepsy (GGE-JME). Previous studies usually involved only small cohorts from single centers and therefore could not assess imaging markers of multiple GGE subtypes.

methodsWe performed a diffusion MRI mega-analysis in 192 participants consisting of 126 controls and 66 patients with GGE from four different cohorts and two different epilepsy centers. We applied whole-brain multi-site harmonization and analyzed fractional anisotropy (FA), as well as mean, radial and axial diffusivity (MD/RD/AD) to assess differences between controls, patients with GGE and the common GGE subtypes, i.e. GGE with generalized tonic-clonic seizures only (GGE-GTCS), GGE-JME and absence epilepsy (GGE-AE). We also analyzed relationships with patients' response to anti-seizure-medication (ASM).

resultsRelative to controls, we identified decreased anisotropy and increased RD in patients with GGE. We found no significant effects of disease duration, age of onset or seizure frequency on diffusion metrics. Patients with JME had increased MD and RD when compared to controls, while patients with GGE-GTCS showed decreased MD/AD when compared to controls. Compared to patients with GGE-AE, patients with GGE-GTCS had lower AD/MD. Compared to patients with GGE-GTCS, patients with GGE-JME had higher MD/RD and AD. Moreover, we found lower FA in patients with refractory when compared to patients with non-refractory GGE in the right cortico-spinal tract, but no significant differences in patients with active versus controlled epilepsy. DISCUSSION: We provide evidence that clinically defined GGE as a whole and GGE-subtypes harbor marked microstructural differences detectable with diffusion MRI. Moreover, we found an association between microstructural changes and treatment resistance. Our findings have important implications for future full-resolution multi-site studies when assessing GGE, its subtypes and ASM refractoriness.

Indexed as

Epilepsy, AbsenceEpilepsy, GeneralizedMyoclonic Epilepsy, JuvenileBrainDiffusion Magnetic Resonance ImagingHumansComBatMulti-cohortMulti-siteTBSS

Identifiers

PMID37441820
PMCPMC10509527
OpenAlexW4383618859

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.