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Record W3192601169 · doi:10.1002/epi4.12528

Response: Sotos Syndrome and the added value of genetic workup in epilepsy surgery

2021· letter· en· W3192601169 on OpenAlexafffundabout
Kenneth A. Myers

Bibliographic record

VenueEpilepsia Open · 2021
Typeletter
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicGenetic Syndromes and Imprinting
Canadian institutionsMcGill UniversityMcGill University Health CentreMontreal Children's Hospital
FundersSavoy FoundationLivaNovaBiogen
KeywordsSotos syndromeEpilepsyLevetiracetamMedicinePediatricsMalignancyEpilepsy surgeryEpileptogenesisEpilepsy syndromesSurgeryPathologyPsychiatry

Abstract

fetched live from OpenAlex

I thank Bättig et al for their very interesting letter in response to our paper, “Seizures in Sotos syndrome: Phenotyping in 49 patients.”1 They recently described a patient with drug-resistant focal epilepsy and a diffuse astrocytoma, who continued to have seizures following resection of the lesion.2 The patient was subsequently diagnosed with Sotos syndrome and found to carry a pathogenic variant in NSD1. Sotos syndrome is associated with an increased risk for malignancy, though cerebral tumors are extremely rare. Our cohort did not include any patients in whom seizures occurred due to an intracranial neoplastic process. Interestingly, of the other two patients with Sotos syndrome and brain tumors described in the literature, one was a boy with intractable epilepsy that also continued after resection of a ganglioglioma.3 The other was an adult male with a low-grade glioma identified when he presented with left face and arm paresthesia; the authors noted that he had a past history of generalized tonic-clonic seizures, but it was not clear that these were thought related to the neoplastic process.4 Based on this admittedly very small sample, it appears that for Sotos syndrome patients with brain tumors and epilepsy, resection of the lesion often has little to no impact on seizure control. The experience of Bättig et al highlights the importance of genetic testing as part of an epilepsy presurgical workup. Although in many cases a genetic diagnosis will not change the recommendation to proceed with surgery, the finding of an underlying genetic condition that predisposes to epilepsy will change the counseling of the individual and his/her family regarding the long-term prognosis. At present, genetic testing is performed in a relatively small fraction of patients undergoing epilepsy presurgical evaluation.5 However, given that the cost of an epilepsy gene panel is relatively small in the context of the financial investment made in patients considered for epilepsy surgery, it is probably reasonable that genetic testing becomes a standard element of such evaluations. Dr Myers receives/has received research funding from the Fonds de Recherches du Québec – Santé, Research Institute of the McGill University Health Center, Citizens United for Research in Epilepsy, Liam Foundation, Savoy Foundation, Koolen-de Vries Foundation and dravet Canada; he is a site principal investigator on a study by LivaNova and a sub-investigator on studies by Ionis/Biogen. I confirm that I have read the Journal's position on issues involved in ethical publication and affirm that this report is consistent with those guidelines.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.002
metaresearch head score (Gemma)0.001
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Not applicable · Consensus signal: Not applicable
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.341
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0020.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0010.001
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.017
GPT teacher head0.251
Teacher spread0.234 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

Study designNot applicable
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2021
Admission routes3
Has abstractyes

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