Evidence map›Paper›PMID 34222868›Full record

ArticleBrain communications2021

Increased facial asymmetry in focal epilepsies associated with unilateral lesions.

Simona Balestrini, Seymour M Lopez, Krishna Chinthapalli, Narek Sargsyan, Rita Demurtas, Sjoerd Vos, Andre Altmann, Michael Suttie, Peter Hammond, Sanjay M Sisodiya

Open access · goldAbstract readComment
In one paragraph

Article in Brain communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 31% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Observational
  4. Steps to Improve Precision Medicine in Epilepsy.Molecular diagnosis & therapy · 2023
    Article
  5. Article
  6. Article
  7. Article
  8. Editorial April 2021.Brain communications · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Simona BalestriniDepartment of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London.ORCID https://orcid.org/0000-0001-5639-1969
Seymour M LopezDepartment of Medical Physics, Centre for Medical Image Computing, UCL, London, UK.ORCID https://orcid.org/0000-0003-0736-4811
Krishna ChinthapalliDepartment of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London.
Narek SargsyanDepartment of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London.
Rita DemurtasDepartment of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London.
Sjoerd VosDepartment of Medical Physics, Centre for Medical Image Computing, UCL, London, UK.
Andre AltmannDepartment of Medical Physics, Centre for Medical Image Computing, UCL, London, UK.ORCID https://orcid.org/0000-0002-9265-2393
Michael SuttieNuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, UK.
Peter HammondNuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, UK.
Sanjay M SisodiyaDepartment of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London.
Chalfonts and Gerrards Cross Hospital · GBOpen Data Institute · GBUniversity College London · GBNational Hospital for Neurology and Neurosurgery · GB

Funding

Medical Research Council MR/L016311/1
6 · The paper itself

Abstract

The epilepsies are now conceptualized as network disruptions: focal epilepsies are considered to have network alterations in the hemisphere of seizure onset, whilst generalized epilepsies are considered to have bi-hemispheric network changes. Increasingly, many epilepsies are also considered to be neurodevelopmental disorders, with early changes in the brain underpinning seizure biology. The development of the structure of the face is influenced by complex molecular interactions between surface ectoderm and underlying developing forebrain and neural crest cells. This influence is likely to continue postnatally, given the evidence of facial growth changes over time in humans until at least 18 years of age. In this case-control study, we hypothesized that people with lateralized focal epilepsies (i.e. unilateral network changes) have an increased degree of facial asymmetry, compared with people with generalized epilepsies or controls without epilepsy. We applied three-dimensional stereophotogrammetry and dense surface models to evaluate facial asymmetry in people with epilepsy, aiming to generate new tools to explore pathophysiological mechanisms in epilepsy. We analysed neuroimaging data to explore the correlation between face and brain asymmetry. We consecutively recruited 859 people with epilepsy attending the epilepsy clinics at a tertiary referral centre. We used dense surface modelling of the full face and signature analyses of three-dimensional facial photographs to analyse facial differences between 378 cases and 205 healthy controls. Neuroimaging around the time of the facial photograph was available for 234 cases. We computed the brain asymmetry index between contralateral regions. Cases with focal symptomatic epilepsy associated with unilateral lesions showed greater facial asymmetry compared to controls (

Indexed as

brain asymmetrydense surface modellingfacial asymmetryfocal epilepsynetworks

Identifiers

PMID34222868
PMCPMC8244637
OpenAlexW3156073307

What OpenQuestion holds

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LicenceCC BY
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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.