Evidence map›Paper›PMID 25087843›Full record

ArticleAnnals of neurology2014

Neurodevelopment in new-onset juvenile myoclonic epilepsy over the first 2 years.

Jack J Lin, Kevin Dabbs, Jeffrey D Riley, Jana E Jones, Daren C Jackson, David A Hsu, Carl E Stafstrom, Michael Seidenberg, Bruce P Hermann

Abstract read
In one paragraph

Article in Annals of neurology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

  1. Article
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  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Neuroimaging in the Epileptic Baboon.Frontiers in veterinary science · 2022
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Observational
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Jack J LinDepartment of Neurology, University of California, Irvine, Irvine, CA.
Kevin Dabbs
Jeffrey D Riley
Jana E Jones
Daren C Jackson
David A Hsu
Carl E Stafstrom
Michael Seidenberg
Bruce P Hermann

Funding

Institutional Clinical and Translational Science AwardUL1TR000427 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2012 to 2016
$32.2M
Neuropsychological Progression of New Onset EpilepsyR01NS044351 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI HERMANN, BRUCE PHILLIP · 2003 to 2015
$6.3M
Institutional Clinical and Translational Science AwardKL2TR000428 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2012 to 2016
$6.2M
Early-onset epilepsy and genetics influence white matter tracts and cognitionK23NS060993 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI LIN, JACK J · 2009 to 2013
$818k
NCATS NIH HHS KL2 TR000428NCATS NIH HHS UL1 TR000427NCATS NIH HHS UL1TR000427NINDS NIH HHS K23 NS060993NINDS NIH HHS R01 NS044351PHS HHS 3R01-44351
6 · The paper itself

Abstract

objectiveAdults with juvenile myoclonic epilepsy (JME) have subtle brain structural abnormalities in the frontothalamocortical network, poorer cognitive function, and worse long-term social outcomes, even when their seizures are controlled and/or remitted. The natural history of JME and development of abnormalities in brain structure and cognition from epilepsy onset has not been studied.

methodsThe maturational trajectories of cognitive and brain development were prospectively compared between 19 children with new-onset JME in the first 2 years after diagnosis and 57 healthy controls.

resultsCognitive abilities of children with JME were similar to or worse than healthy controls at baseline but failed to reach the competence level of healthy controls at follow-up across most of the tested cognitive abilities. Abnormal patterns of brain development, as assessed by magnetic resonance imaging studies, were evident in children with JME and included attenuation of age-related decline in cortical volume, thickness, and surface area compared to typically developing children. The altered brain developmental trajectory in the JME group was evident in higher-association frontoparietotemporal brain regions (p < 0.05, corrected for multiple comparisons).

interpretationChildren with JME have abnormal structural brain development and impaired cognitive development early in the course of their epilepsy.

Indexed as

AdolescentAge of OnsetAnticonvulsantsBrainCerebral CortexChildCognition DisordersDisease ProgressionExecutive FunctionFemaleHumansLongitudinal StudiesMaleMyoclonic Epilepsy, JuvenileNeuropsychological TestsAnticonvulsants

Identifiers

PMID25087843
PMCPMC4362677

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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.