Evidence map›Paper›PMID 25616449›Full record

ArticleEpilepsy research2015

Factors affecting reorganisation of memory encoding networks in temporal lobe epilepsy.

M K Sidhu, J Stretton, G P Winston, M Symms, P J Thompson, M J Koepp, J S Duncan

Open access · hybridAbstract read
In one paragraph

Article in Epilepsy research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.7field-weighted citation impact, top 11% 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, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Recent Advances in Neuroimaging of Epilepsy.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2021
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Naming fMRI predicts the effect of temporal lobe resection on language decline.Annals of clinical and translational neurology · 2019
    Article
  15. Article
  16. Article
  17. Neurostimulation for Memory Enhancement in Epilepsy.Current neurology and neuroscience reports · 2018
    Review
  18. Article
  19. Article
  20. Neuronal network models of epileptogenesis.Neurosciences (Riyadh, Saudi Arabia) · 2017
    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

7 authors at 2 institutions in 1 country.

M K SidhuDepartment of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London WC1 N 3BG, UK; Epilepsy Society MRI Unit, Chesham Lane, Chalfont St. Peter SL9 0RJ, UK. Electronic address: m.sidhu@ucl.ac.uk.
J StrettonDepartment of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London WC1 N 3BG, UK; Epilepsy Society MRI Unit, Chesham Lane, Chalfont St. Peter SL9 0RJ, UK. Electronic address: j.stretton@ucl.ac.uk.
G P WinstonDepartment of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London WC1 N 3BG, UK; Epilepsy Society MRI Unit, Chesham Lane, Chalfont St. Peter SL9 0RJ, UK. Electronic address: g.winston@ucl.ac.uk.
M SymmsDepartment of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London WC1 N 3BG, UK; Epilepsy Society MRI Unit, Chesham Lane, Chalfont St. Peter SL9 0RJ, UK. Electronic address: m.symms@ucl.ac.uk.
P J ThompsonDepartment of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London WC1 N 3BG, UK; Epilepsy Society MRI Unit, Chesham Lane, Chalfont St. Peter SL9 0RJ, UK. Electronic address: p.thompson@ucl.ac.uk.
M J KoeppDepartment of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London WC1 N 3BG, UK; Epilepsy Society MRI Unit, Chesham Lane, Chalfont St. Peter SL9 0RJ, UK. Electronic address: m.koepp@ucl.ac.uk.
J S DuncanDepartment of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London WC1 N 3BG, UK; Epilepsy Society MRI Unit, Chesham Lane, Chalfont St. Peter SL9 0RJ, UK. Electronic address: j.duncan@ucl.ac.uk.
University College London · GBNational Hospital for Neurology and Neurosurgery · GB

Funding

Medical Research Council MC_U105579215Wellcome Trust 083148
6 · The paper itself

Abstract

aimsIn temporal lobe epilepsy (TLE) due to hippocampal sclerosis reorganisation in the memory encoding network has been consistently described. Distinct areas of reorganisation have been shown to be efficient when associated with successful subsequent memory formation or inefficient when not associated with successful subsequent memory. We investigated the effect of clinical parameters that modulate memory functions: age at onset of epilepsy, epilepsy duration and seizure frequency in a large cohort of patients.

methodsWe studied 53 patients with unilateral TLE and hippocampal sclerosis (29 left). All participants performed a functional magnetic resonance imaging memory encoding paradigm of faces and words. A continuous regression analysis was used to investigate the effects of age at onset of epilepsy, epilepsy duration and seizure frequency on the activation patterns in the memory encoding network.

resultsEarlier age at onset of epilepsy was associated with left posterior hippocampus activations that were involved in successful subsequent memory formation in left hippocampal sclerosis patients. No association of age at onset of epilepsy was seen with face encoding in right hippocampal sclerosis patients. In both left hippocampal sclerosis patients during word encoding and right hippocampal sclerosis patients during face encoding, shorter duration of epilepsy and lower seizure frequency were associated with medial temporal lobe activations that were involved in successful memory formation. Longer epilepsy duration and higher seizure frequency were associated with contralateral extra-temporal activations that were not associated with successful memory formation.

conclusionAge at onset of epilepsy influenced verbal memory encoding in patients with TLE due to hippocampal sclerosis in the speech-dominant hemisphere. Shorter duration of epilepsy and lower seizure frequency were associated with less disruption of the efficient memory encoding network whilst longer duration and higher seizure frequency were associated with greater, inefficient, extra-temporal reorganisation.

Indexed as

AdultAge of OnsetEpilepsy, Temporal LobeFaceFemaleFunctional LateralityHippocampusHumansMagnetic Resonance ImagingMaleMemoryMiddle AgedNeural PathwaysNeuropsychological TestsPattern Recognition, VisualPhotic StimulationDurationEpisodic memoryFunctional MRISeizure frequencyTemporal lobe epilepsy

Identifiers

PMID25616449
PMCPMC4315807
OpenAlexW2058037067

What OpenQuestion holds

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LicenceCC BY
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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.