Evidence map›Paper›PMID 25012388›Full record

ReviewAdvances in experimental medicine and biology2014

How might novel technologies such as optogenetics lead to better treatments in epilepsy?

Esther Krook-Magnuson, Marco Ledri, Ivan Soltesz, Merab Kokaia

Abstract readReview
In one paragraph

Review in Advances in experimental medicine and biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Review
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  4. Article
  5. Review
  6. Review
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  8. Article
  9. Review
  10. Future of seizure prediction and intervention: closing the loop.Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society · 2015
    Review
  11. Article
  12. Review
  13. Article
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  15. 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

4 authors.

Esther Krook-MagnusonDepartment of Anatomy and Neurobiology, University of California, 192 Irvine Hall, Irvine, CA, 92697, USA, ekrookma@uci.edu.
Marco Ledri
Ivan Soltesz
Merab Kokaia

Funding

GABAergic regulation of entorhino-hippocampal excitability in epilepsy.R01NS074432 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI SOLTESZ, IVAN · 2011 to 2015
$1.6M
On-demand optogenetic cerebellar intervention for temporal lobe epilepsyK99NS087110 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI KROOK-MAGNUSON, ESTHER · 2014 to 2014
$90k
NINDS NIH HHS K99 NS087110NINDS NIH HHS NS74432NINDS NIH HHS R01 NS074432
6 · The paper itself

Abstract

Recent technological advances open exciting avenues for improving the understanding of mechanisms in a broad range of epilepsies. This chapter focuses on the development of optogenetics and on-demand technologies for the study of epilepsy and the control of seizures. Optogenetics is a technique which, through cell-type selective expression of light-sensitive proteins called opsins, allows temporally precise control via light delivery of specific populations of neurons. Therefore, it is now possible not only to record interictal and ictal neuronal activity, but also to test causality and identify potential new therapeutic approaches. We first discuss the benefits and caveats to using optogenetic approaches and recent advances in optogenetics related tools. We then turn to the use of optogenetics, including on-demand optogenetics in the study of epilepsies, which highlights the powerful potential of optogenetics for epilepsy research.

Indexed as

OptogeneticsEpilepsyHumansNeurons

Identifiers

PMID25012388
PMCPMC4968566

What OpenQuestion holds

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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.