Evidence map›Paper›PMID 26754787›Full record

ArticleBrain : a journal of neurology2016

Memory network plasticity after temporal lobe resection: a longitudinal functional imaging study.

Meneka K Sidhu, Jason Stretton, Gavin P Winston, Andrew W McEvoy, Mark Symms, Pamela J Thompson, Matthias J Koepp, John S Duncan

Abstract read
In one paragraph

Article in Brain : a journal of neurology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing 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

48 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  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

8 authors.

Meneka K Sidhu1 Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK 2 Epilepsy Society MRI Unit, Chesham Lane, Chalfont St. Peter SL9 0RJ, Buckinghamshire, UK.
Jason Stretton1 Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK 2 Epilepsy Society MRI Unit, Chesham Lane, Chalfont St. Peter SL9 0RJ, Buckinghamshire, UK 3 MRC Cognition and Brain Science Unit, Chaucer Road, Cambridge, CB2 7EF, UK.
Gavin P Winston1 Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK 2 Epilepsy Society MRI Unit, Chesham Lane, Chalfont St. Peter SL9 0RJ, Buckinghamshire, UK.
Andrew W McEvoy1 Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK 2 Epilepsy Society MRI Unit, Chesham Lane, Chalfont St. Peter SL9 0RJ, Buckinghamshire, UK.
Mark Symms1 Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK 2 Epilepsy Society MRI Unit, Chesham Lane, Chalfont St. Peter SL9 0RJ, Buckinghamshire, UK.
Pamela J Thompson1 Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK 2 Epilepsy Society MRI Unit, Chesham Lane, Chalfont St. Peter SL9 0RJ, Buckinghamshire, UK.
Matthias J Koepp1 Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK 2 Epilepsy Society MRI Unit, Chesham Lane, Chalfont St. Peter SL9 0RJ, Buckinghamshire, UK.
John S Duncan1 Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK 2 Epilepsy Society MRI Unit, Chesham Lane, Chalfont St. Peter SL9 0RJ, Buckinghamshire, UK j.duncan@ucl.ac.uk.

Funding

Medical Research Council G0802012Medical Research Council MC_U105579215Wellcome Trust 083148Wellcome Trust 093875
6 · The paper itself

Abstract

Anterior temporal lobe resection can control seizures in up to 80% of patients with temporal lobe epilepsy. Memory decrements are the main neurocognitive complication. Preoperative functional reorganization has been described in memory networks, but less is known of postoperative reorganization. We investigated reorganization of memory-encoding networks preoperatively and 3 and 12 months after surgery. We studied 36 patients with unilateral medial temporal lobe epilepsy (19 right) before and 3 and 12 months after anterior temporal lobe resection. Fifteen healthy control subjects were studied at three equivalent time points. All subjects had neuropsychological testing at each of the three time points. A functional magnetic resonance imaging memory-encoding paradigm of words and faces was performed with subsequent out-of-scanner recognition assessments. Changes in activations across the time points in each patient group were compared to changes in the control group in a single flexible factorial analysis. Postoperative change in memory across the time points was correlated with postoperative activations to investigate the efficiency of reorganized networks. Left temporal lobe epilepsy patients showed increased right anterior hippocampal and frontal activation at both 3 and 12 months after surgery relative to preoperatively, for word and face encoding, with a concomitant reduction in left frontal activation 12 months postoperatively. Right anterior hippocampal activation 12 months postoperatively correlated significantly with improved verbal learning in patients with left temporal lobe epilepsy from preoperatively to 12 months postoperatively. Preoperatively, there was significant left posterior hippocampal activation that was sustained 3 months postoperatively at word encoding, and increased at face encoding. For both word and face encoding this was significantly reduced from 3 to 12 months postoperatively. Patients with right temporal lobe epilepsy showed increased left anterior hippocampal activation on word encoding from 3 to 12 months postoperatively compared to preoperatively. On face encoding, left anterior hippocampal activations were present preoperatively and 12 months postoperatively. Left anterior hippocampal and orbitofrontal cortex activations correlated with improvements in both design and verbal learning 12 months postoperatively. On face encoding, there were significantly increased left posterior hippocampal activations that reduced significantly from 3 to 12 months postoperatively. Postoperative changes occur in the memory-encoding network in both left and right temporal lobe epilepsy patients across both verbal and visual domains. Three months after surgery, compensatory posterior hippocampal reorganization that occurs is transient and inefficient. Engagement of the contralateral hippocampus 12 months after surgery represented efficient reorganization in both patient groups, suggesting that the contralateral hippocampus contributes to memory outcome 12 months after surgery.

Indexed as

AdultEpilepsy, Temporal LobeFemaleHumansLongitudinal StudiesMagnetic Resonance ImagingMaleMemoryMiddle AgedNerve NetNeuronal PlasticityTemporal LobeYoung Adultanterior temporal lobe resectionfunctional MRImemory encodingtemporal lobe epilepsy

Identifiers

PMID26754787
PMCPMC4805088

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.