Evidence map›Paper›PMID 40342157›Full record

ArticleEpilepsia2025

Prospective neuroimaging and neuropsychological evaluation in adults with newly diagnosed focal epilepsy.

Christophe E de Bezenac, Nicola Leek, Guleed Adan, Ahmad M S Ali, Rajiv Mohanraj, Shubhabrata Biswas, Ronan N Mcginty, Kieran Murphy, Helen Malone, Gus Baker and 3 more

Abstract read
In one paragraph

Article in Epilepsia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
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.

Christophe E de BezenacDepartment of Pharmacology and Therapeutics, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, UK.ORCID https://orcid.org/0000-0002-2433-9776
Nicola LeekDepartment of Pharmacology and Therapeutics, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, UK.
Guleed AdanDepartment of Pharmacology and Therapeutics, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, UK.
Ahmad M S AliThe Walton Centre NHS Foundation Trust, Liverpool, UK.
Rajiv MohanrajDepartment of Neurology, Manchester Centre for Clinical Neurosciences, Salford Royal NHS Foundation Trust, Salford, UK.
Shubhabrata BiswasThe Walton Centre NHS Foundation Trust, Liverpool, UK.
Ronan N McgintyThe Walton Centre NHS Foundation Trust, Liverpool, UK.ORCID https://orcid.org/0000-0002-4606-7783
Kieran MurphyLiverpool Magnetic Resonance Imaging Centre, University of Liverpool, Liverpool, UK.
Helen MaloneThe Walton Centre NHS Foundation Trust, Liverpool, UK.
Gus BakerThe Walton Centre NHS Foundation Trust, Liverpool, UK.
Perry MooreThe Walton Centre NHS Foundation Trust, Liverpool, UK.
Anthony G MarsonDepartment of Pharmacology and Therapeutics, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, UK.
Simon S KellerDepartment of Pharmacology and Therapeutics, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, UK.ORCID https://orcid.org/0000-0001-5247-9795

Funding

Medical Research Council (MRC) MR/S00355X/1
6 · The paper itself

Abstract

objectiveFew prospective studies exist on newly diagnosed focal epilepsy (NDFE), a critical period for understanding epilepsy's biology and identifying biomarkers and potential interventions. We report a prospective cohort study in patients with NDFE and age-, sex-, and education-matched healthy controls.

methodsWe recruited 104 patients with NDFE and 45 controls for research-grade 3 Tesla multi-modal magnetic resonance imaging (MRI), electroencephalography (EEG), comprehensive neuropsychological testing, and blood biomarker investigations. Baseline clinical, neuroradiological, MRI morphometric, and neuropsychological findings are reported in this article.

resultsFollowing neuroradiological reporting, MRI was unremarkable in 38% of patients, showed lesions associated with epilepsy in 12%, abnormalities of unknown significance in 49%, and incidental findings in 23%. For controls, these figures were 56%, 7%, 33%, and 16%, respectively. Patients had more white matter hyperintensities, classified as abnormalities of unknown significance, than controls. Reduced bihemispheric frontal lobe cortical thickness and thalamic volumes with moderate effect sizes were observed in patients. Compared to controls, patients scored lower on executive function, processing speed, and visual, delayed, and immediate memory tasks, and higher on depression and anxiety assessments. Cluster analysis identified four distinct patient cognitive profiles, two of which were associated with high levels of anxiety and depression and lower executive function and memory scores. SIGNIFICANCE: Adults with focal NDFE have more MRI-positive findings than previously reported. Subtle white matter lesions may have clinical significance and a pathophysiological basis in focal epilepsy. Morphometric and neuropsychological changes at epilepsy diagnosis suggest that brain and cognitive alterations are not solely due to chronic epilepsy.

Indexed as

BrainEpilepsies, PartialNeuroimagingNeuropsychological TestsAdultCohort StudiesElectroencephalographyFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedProspective StudiesYoung Adultneuroimagingneuropsychologynewly diagnosed focal epilepsy

Identifiers

PMID40342157
PMCPMC12371684

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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.