Evidence map›Paper›PMID 23294289›Full record

ArticleEpilepsia2013

Evidence for a shared genetic susceptibility to migraine and epilepsy.

Melodie R Winawer, Robert Connors, EPGP Investigators

Open access · bronzeAbstract read
In one paragraph

Article in Epilepsia, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 6% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 80 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Epilepsy and the gut: Perpetrator or victim?World journal of gastrointestinal pathophysiology · 2022
    Review
  6. Action Potentials Are Critical for the Propagation of Focally Elicited Spreading Depolarizations.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  7. Headache in people with epilepsy.Nature reviews. Neurology · 2021
    Review
  8. Article
  9. Article
  10. Article
  11. Painful Seizures: a Review of Epileptic Ictal Pain.Current pain and headache reports · 2019
    Review
  12. Review
  13. Studies on the Mechanism of Glutamate Metabolism in NTG-Induced Migraine Rats Treated with DCXF.Evidence-based complementary and alternative medicine : eCAM · 2019
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. A systematic approach for identifying shared mechanisms in epilepsy and its comorbidities.Database : the journal of biological databases and curation · 2018
    Article
  19. Headache and Epilepsy.Journal of epilepsy research · 2017
    Review
  20. Shared mechanisms of epilepsy, migraine and affective disorders.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 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

3 authors at 1 institution in 1 country.

Melodie R WinawerGH Sergievsky Center, Columbia University, New York, New York 10032, USA. mw211@columbia.edu
Robert Connors
EPGP Investigators
Columbia University · US

Funding

The Epilepsy Phenome/ Genome Project (EPGP)U01NS053998 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LOWENSTEIN, DANIEL H · 2007 to 2013
$26.4M
NINDS NIH HHS NINDS U01 NS 053998NINDS NIH HHS U01 NS053998
6 · The paper itself

Abstract

purposeAlthough epilepsy and migraine are known to co-occur within individuals, the contribution of a shared genetic susceptibility to this comorbidity remains unclear. We investigated the hypothesis of shared genetic effects on migraine and epilepsy in the Epilepsy Phenome/Genome Project (EPGP) cohort.

methodsWe studied prevalence of a history of migraine in 730 EPGP participants aged ≥ 12 years with nonacquired focal epilepsy (NAFE) or generalized epilepsy (GE) from 501 families containing two or more individuals with epilepsy of unknown cause. Information on migraine without aura (MO) and migraine with aura (MA) was collected using an instrument validated for individuals ≥ 12 years. Because many individuals have both MO and MA, we considered two nonoverlapping groups of individuals with migraine: those who met criteria for MA in any of their headaches (MA), and those who did not ("MO-only"). EPGP participants were interviewed about the history of seizure disorders in additional nonenrolled family members. We evaluated associations of migraine prevalence in enrolled subjects with a family history of seizure disorders in additional nonenrolled relatives, using generalized estimating equations to control for the nonindependence of observations within families. KEY

findingsPrevalence of a history of MA (but not MO-only) was significantly increased in enrolled participants with two or more additional affected first-degree relatives. SIGNIFICANCE: These findings support the hypothesis of a shared genetic susceptibility to epilepsy and MA.

Indexed as

AdolescentAdultChildData CollectionDNAElectroencephalographyEpilepsies, PartialEpilepsyEpilepsy, GeneralizedFemaleGenetic Predisposition to DiseaseGenomeHumansMaleMiddle AgedMigraine DisordersDNA

Identifiers

PMID23294289
PMCPMC3566298
OpenAlexW2150473239

What OpenQuestion holds

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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.