Evidence map›Paper›PMID 32683693›Full record

ArticleEpilepsia2020

Peri-ictal hypoxia is related to extent of regional brain volume loss accompanying generalized tonic-clonic seizures.

Luke A Allen, Ronald M Harper, Sjoerd B Vos, Catherine A Scott, Nuria Lacuey, Laura Vilella, Joel S Winston, Benjamin P Whatley, Rajesh Kumar, Jennifer Ogren and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Epilepsia, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 2 pooled it
4.1field-weighted citation impact, top 5% 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

23 citing papers in PubMed, 2 syntheses or guidelines pooled it, 42 citations in OpenAlex.

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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

16 authors at 5 institutions in 3 countries.

Luke A AllenDepartment of Clinical and Experimental Epilepsy, UCL Institute of Neurology, University College London, London, UK.ORCID 0000-0002-4988-1457
Ronald M HarperThe Center for SUDEP Research, National Institute of Neurological Disorders and Stroke, Bethesda, MD, USA.
Sjoerd B VosThe Center for SUDEP Research, National Institute of Neurological Disorders and Stroke, Bethesda, MD, USA.ORCID 0000-0002-8502-4487
Catherine A ScottDepartment of Clinical and Experimental Epilepsy, UCL Institute of Neurology, University College London, London, UK.
Nuria LacueyThe Center for SUDEP Research, National Institute of Neurological Disorders and Stroke, Bethesda, MD, USA.
Laura VilellaThe Center for SUDEP Research, National Institute of Neurological Disorders and Stroke, Bethesda, MD, USA.
Joel S WinstonDepartment of Clinical and Experimental Epilepsy, UCL Institute of Neurology, University College London, London, UK.
Benjamin P WhatleyDepartment of Clinical and Experimental Epilepsy, UCL Institute of Neurology, University College London, London, UK.ORCID 0000-0001-8824-367X
Rajesh KumarThe Center for SUDEP Research, National Institute of Neurological Disorders and Stroke, Bethesda, MD, USA.
Jennifer OgrenThe Center for SUDEP Research, National Institute of Neurological Disorders and Stroke, Bethesda, MD, USA.
Jaison S HampsonDepartment of Neurology, University of Texas Health Sciences Center at Houston, Houston, TX, USA.
Sandhya RaniDepartment of Neurology, University of Texas Health Sciences Center at Houston, Houston, TX, USA.
Gavin P WinstonDepartment of Clinical and Experimental Epilepsy, UCL Institute of Neurology, University College London, London, UK.ORCID 0000-0001-9395-1478
Louis LemieuxDepartment of Clinical and Experimental Epilepsy, UCL Institute of Neurology, University College London, London, UK.
Samden D LhatooThe Center for SUDEP Research, National Institute of Neurological Disorders and Stroke, Bethesda, MD, USA.ORCID 0000-0002-0260-3855
Beate DiehlDepartment of Clinical and Experimental Epilepsy, UCL Institute of Neurology, University College London, London, UK.ORCID 0000-0002-6896-854X
National Institute of Neurological Disorders and Stroke · USUniversity College London · GBUniversity of California, Los Angeles · USThe University of Texas Health Science Center at Houston · USQueen's University · CA

Funding

SUDEP Translational Research Alliance (SUTRA): Autonomic and Imaging Biomarkers of SUDEP; SUTRA 3 of 7U01NS090407 · NINDS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI DIEHL, BEATE, HARPER, RONALD MARVEN · 2014 to 2018
$7.3M
Medical Research Council G0301067Medical Research Council G0802012Medical Research Council MR/M00841X/1NINDS NIH HHS U01 NS090407
6 · The paper itself

Abstract

objectivesHypoxia, or abnormally low blood-oxygen levels, often accompanies seizures and may elicit brain structural changes in people with epilepsy which contribute to central processes underlying sudden unexpected death in epilepsy (SUDEP). The extent to which hypoxia may be related to brain structural alterations in this patient group remains unexplored.

methodsWe analyzed high-resolution T1-weighted magnetic resonance imaging (MRI) to determine brain morphometric and volumetric alterations in people with generalized tonic-clonic seizures (GTCS) recorded during long-term video-electroencephalography (VEEG), recruited from two sites (n = 22), together with data from age- and sex-matched healthy controls (n = 43). Subjects were sub-divided into those with mild/moderate (GTCS-hypox-mild/moderate, n = 12) and severe (GTCS-hypox-severe, n = 10) hypoxia, measured by peripheral oxygen saturation (SpO

resultsMorphometric and volumetric alterations appeared in association with peri-GTCS hypoxia, including volume loss in the periaqueductal gray (PAG), thalamus, hypothalamus, vermis, cerebellum, parabrachial pons, and medulla. Thalamic and PAG volume was significantly reduced in GTCS patients with severe hypoxia compared with GTCS patients with mild/moderate hypoxia. Brainstem volume loss appeared in both hypoxia groups, although it was more extensive in those with severe hypoxia. Significant negative partial correlations emerged between thalamic and hippocampal volume and extent of hypoxia, whereas vermis and accumbens volumes declined with increasing hypoxia duration. SIGNIFICANCE: Brain structural alterations in patients with GTCS are related to the extent of hypoxia in brain sites that serve vital functions. Although the changes are associative only, they provide evidence of injury to regulatory brain sites related to respiratory manifestations of seizures.

Indexed as

Sudden Unexpected Death in EpilepsyAdultBrainCase-Control StudiesElectroencephalographyEpilepsy, Tonic-ClonicFemaleGray MatterHumansHypoxiaImaging, Three-DimensionalMagnetic Resonance ImagingMaleMiddle AgedOrgan SizeProspective StudiesepilepsyhypoxiaMRISUDEP

Identifiers

PMID32683693
PMCPMC7496610
OpenAlexW3043084974

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.