Evidence map›Paper›PMID 31663115›Full record

ArticleEpilepsia2019

Tau deposition in young adults with drug-resistant focal epilepsy.

Kelsey M Smith, Melissa M Blessing, Joseph E Parisi, Jeffrey W Britton, Jay Mandrekar, Gregory D Cascino

Open access · hybridAbstract read
In one paragraph

Article in Epilepsia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Exploring biomarkers of neurodegeneration in epilepsy: Critical insights.Epileptic disorders : international epilepsy journal with videotape · 2025
    Review
  4. Article
  5. Cellular and pathological functions of tau.Nature reviews. Molecular cell biology · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Chronic Traumatic Encephalopathy in a Routine Neuropathology Service in Australia.Journal of neuropathology and experimental neurology · 2022
    Article
  15. Article
  16. Review
  17. Nodding Syndrome: A Scoping Review.Tropical medicine and infectious disease · 2021
    Article
  18. Review
  19. Article
  20. 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

6 authors at 1 institution in 1 country.

Kelsey M SmithDepartment of Neurology, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0001-8659-3801
Melissa M BlessingDepartment of Pathology, Mayo Clinic, Rochester, Minnesota.
Joseph E ParisiDepartments of Laboratory Medicine and Pathology, and Neurology, Mayo Clinic, Rochester, Minnesota.
Jeffrey W BrittonDepartment of Neurology, Mayo Clinic, Rochester, Minnesota.
Jay MandrekarDivision of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, Minnesota.
Gregory D CascinoDepartment of Neurology, Mayo Clinic, Rochester, Minnesota.
Mayo Clinic · US

Funding

Mayo Foundation for Medical Education and Research
6 · The paper itself

Abstract

objectiveTo evaluate the presence of tau deposition and pathologic features of chronic traumatic encephalopathy (CTE) in young adult patients treated with focal cortical resections for drug-resistant epilepsy.

methodsSixty consecutive patients who had undergone surgical treatment for drug-resistant focal epilepsy between 18 and 45 years of age were identified (2010-2017). Medical records were reviewed to determine clinical factors, including history of head trauma, age at seizure onset, age at surgical resection, seizure type(s) and frequency, imaging findings, and surgical outcome. All formalin-fixed, paraffin-embedded blocks from the surgical specimens from each subject were sectioned and stained with hematoxylin and eosin and antibodies to tau (Thermo Fisher Scientific Clone AT8), and examined blindly for tau pathology, including lesions characteristic of CTE.

resultsThe median age at resection was 29.5 years (range = 19-45). A history of head trauma was reported in 19 patients. Although none of the patients had pathological findings characteristic of CTE, 23 patients (38%) demonstrated tau-immunoreactive lesions, including neurites, neurofibrillary pretangles, neurofibrillary tangles, subpial tau, and/or glial tau. In 4 of the 23 patients (7% of the cohort; 17% of those with tau pathology), substantial tau burden was identified. Three of these 4 patients had no significant history of head trauma; 1 patient had multiple sports-related concussions. No specific clinical factors correlated with the presence of tau pathology. SIGNIFICANCE: Tau-immunoreactive lesions were found in 38% of 60 patients who underwent a focal cortical resection for drug-resistant focal epilepsy. Diagnostic features of CTE were not detected in any patient; however, the pathological evaluation for CTE was limited to a surgical specimen. The prominent and excessive tau deposition in 23 patients (38%) is abnormal in this age group and warrants further investigation.

Indexed as

AdultBrainBrain ChemistryDrug Resistant EpilepsyEpilepsies, PartialHumansMiddle Agedtau ProteinsYoung AdultMAPT protein, humantau Proteinschronic traumatic encephalopathyepilepsy surgeryneuropathology

Identifiers

PMID31663115
PMCPMC6973032
OpenAlexW2982423301

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.