Evidence map›Paper›PMID 40411393›Full record

Observational studyThe Journal of international medical research2025

Surgical decision-making in adult patients with epilepsy related to germline mutations: A single-center study.

Irina Podkorytova, Sasha Alick Lindstrom, Kan Ding, Ghazala Perven, Ryan Hays

Abstract readObservational Study
In one paragraph

Observational study in The Journal of international medical research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

5 authors.

Irina PodkorytovaDepartment of Neurology, University of Texas Southwestern Medical Center, USA.ORCID 0000-0003-2143-3123
Sasha Alick LindstromDepartment of Neurology, University of Texas Southwestern Medical Center, USA.
Kan DingDepartment of Neurology, University of Texas Southwestern Medical Center, USA.
Ghazala PervenDepartment of Neurology, University of Texas Southwestern Medical Center, USA.
Ryan HaysDepartment of Neurology, University of Texas Southwestern Medical Center, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ObjectivesGenetic testing is not routinely performed during presurgical evaluation of adult patients with epilepsy.MethodsIn this retrospective observational study, we analyzed the diagnostic yield of an epilepsy multigene panel and patient characteristics in adult epilepsy surgery candidates from 2014 to 2024. We compared data collected from patients with GTPase-activating protein activity toward Rags 1 (GATOR1) and non-GATOR1 pathway mutations.ResultsIn total, 31 of the 236 (13%) patients tested positive for monogenic epilepsy disorders. The epilepsy multigene panel diagnostic yield was 12% (28 of the 233 patients). Overall, 9 of the 31 patients had GATOR1 pathway mutations. Moreover, 15 of the 31 patients underwent invasive electroencephalography evaluations, with 6 exhibiting GATOR1 and 9 exhibiting non-GATOR1 pathway mutations. In the GATOR1 mutations group, three of the six (50%) patients had focal ictal onset. In the non-GATOR1 mutations group, two of the nine (22%) patients had focal ictal onset. Overall, 8 of the 31 patients underwent resection or laser ablation, with 4 exhibiting GATOR1 and 4 exhibiting non-GATOR1 pathway mutations. In the GATOR1 mutations group, four of the nine (44.4%) patients underwent resection or laser ablation, and all had favorable outcomes (Engel I-II). In the non-GATOR1 mutations group, 4 of the 22 (18.2%) patients underwent resection. One patient had a favorable outcome (Engel I).ConclusionsGenetic testing may be helpful for selection of epilepsy surgery candidates and for counseling regarding expected epilepsy surgery outcome. These findings may be valuable for large multicenter studies with the goal to streamline the surgical journey of epilepsy patients with germline mutations.

Indexed as

Clinical Decision-MakingEpilepsyGerm-Line MutationAdolescentAdultElectroencephalographyFemaleGenetic TestingGTPase-Activating ProteinsHumansMaleMiddle AgedRetrospective StudiesYoung AdultGTPase-Activating ProteinsEpilepsy surgeryGATOR1 mutationsgenetic testingneuromodulationstereoelectroencephalography

Identifiers

PMID40411393
PMCPMC12103672

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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.