Evidence map›Paper›PMID 41604608›Full record

ArticleNeurology2026

Progressive Changes in Brain Morphology in People With Idiopathic Generalized Epilepsy.

Fenglai Xiao, Yingying Zhang, Britta Wandschneider, Lawrence P Binding, Davide Giampiccolo, Marine Fleury, Luisa Delazer, Bernardo Crespo Pimentel, Isha Puntambekar, Kazuki Fukuma and 5 more

Abstract read
In one paragraph

Article in Neurology, 2026. 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
–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

2 citing papers in PubMed.

  1. Article
  2. Article
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

15 authors.

Fenglai XiaoDepartment of Clinical & Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, United Kingdom.ORCID 0000-0003-1308-6539
Yingying ZhangDepartment of Neurology, West China Hospital, Sichuan University, Chengdu, China.
Britta WandschneiderDepartment of Clinical & Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, United Kingdom.ORCID 0000-0001-7181-2637
Lawrence P BindingDepartment of Clinical & Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, United Kingdom.ORCID 0000-0002-5658-4960
Davide GiampiccoloDepartment of Clinical & Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, United Kingdom.ORCID 0000-0003-3849-4168
Marine FleuryDepartment of Clinical & Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, United Kingdom.
Luisa DelazerDepartment of Clinical & Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, United Kingdom.ORCID 0009-0002-1330-3628
Bernardo Crespo PimentelDepartment of Clinical & Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, United Kingdom.ORCID 0000-0002-8965-8081
Isha PuntambekarDepartment of Clinical & Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, United Kingdom.
Kazuki FukumaDepartment of Clinical & Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, United Kingdom.ORCID 0000-0001-8117-8916
Lorenzo CaciagliDepartment of Clinical & Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, United Kingdom.ORCID 0000-0001-7189-9699
Josemir W SanderDepartment of Clinical & Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, United Kingdom.ORCID 0000-0001-6041-9661
John S DuncanDepartment of Clinical & Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, United Kingdom.ORCID 0000-0002-1373-0681
Dong ZhouDepartment of Neurology, West China Hospital, Sichuan University, Chengdu, China.ORCID 0000-0001-7101-4125
Matthias J KoeppDepartment of Clinical & Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, United Kingdom.ORCID 0000-0002-4277-8000

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesIdiopathic generalized epilepsy (IGE) is typically responsive to treatment, yet some people remain poorly controlled despite multiple antiseizure medication trials. Whether this subgroup shows progressive structural brain changes remains uncertain. We aimed to investigate whether people with poorly controlled chronic IGE exhibit progressive morphological brain alterations and how these differ from those in early-stage IGE.

methodsThis longitudinal case-control neuroimaging study included 2 cohorts: an early-stage IGE group from West China Hospital (Chengdu, China) and a chronic IGE group from the National Hospital for Neurology and Neurosurgery (London, United Kingdom). Participants had a history of generalized seizures and no focal pathology. Matched healthy controls were drawn from 3 public imaging data sets. Participants underwent 2 high-resolution T1-weighted MRI scans at least 12 months apart. Cortical thickness and hippocampal and subcortical volumes were measured on paired scans. Longitudinal changes were assessed using linear mixed-effects models, correcting for age and interscan interval. Structural covariance analysis was conducted to examine inter-regional relationships over time, focusing on thalamo-cortical coupling.

resultsForty-two people with early-stage IGE and 67 with chronic IGE were recruited from 2 separate epilepsy centers, and 109 matched controls were included. The early-stage IGE group showed progressive atrophy limited to the left putamen. Chronic IGE was associated with widespread cortical thinning, primarily in frontal and temporal regions, and thickening in posterior and occipital areas. Subcortical atrophy involves the putamen, thalamus, and pallidum. People with ongoing generalized tonic-clonic seizures showed thickening in the precentral gyrus and additional thinning in the frontal cortex and precuneus. Photosensitive IGE was associated with thickening in the lingual gyrus and occipital cortex. Valproate use was associated with attenuated structural changes in motor, visual, and subcortical regions. Increased structural covariance was observed between the left thalamus and left lingual gyrus in chronic IGE. DISCUSSION: Chronic IGE, particularly with persistent generalized tonic-clonic seizures or photosensitivity, is associated with more extensive progressive brain changes compared with matched controls. Valproate may have a protective association with these structural changes, although further validation is needed. Longitudinal MRI may help monitor disease progression and treatment effects in poorly controlled IGE.

Indexed as

BrainEpilepsy, GeneralizedAdolescentAdultAtrophyCase-Control StudiesDisease ProgressionFemaleHumansLongitudinal StudiesMagnetic Resonance ImagingMaleMiddle AgedYoung Adult

Identifiers

PMID41604608
PMCPMC12857813

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.