Evidence map›Paper›PMID 33178126›Full record

ArticleFrontiers in neurology2020

Prediction of Neurodevelopment in Infants With Tuberous Sclerosis Complex Using Early EEG Characteristics.

Jessie De Ridder, Mario Lavanga, Birgit Verhelle, Jan Vervisch, Katrien Lemmens, Katarzyna Kotulska, Romina Moavero, Paolo Curatolo, Bernhard Weschke, Kate Riney and 17 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neurology, 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
2.4field-weighted citation impact, top 10% 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, 34 citations in OpenAlex.

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  9. aEEG in the first 3 days after extremely preterm delivery relates to neurodevelopmental outcomes.Journal of perinatology : official journal of the California Perinatal Association · 2024
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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

27 authors at 16 institutions in 11 countries.

Jessie De RidderPediatric Neurology, Department of Development and Regeneration, University of Leuven KU Leuven, Leuven, Belgium.
Mario LavangaDepartment of Electrical Engineering (ESAT), STADIUS Centre for Dynamical Systems, Signal Processing and Data Analytics, KU Leuven, Leuven, Belgium.
Birgit VerhellePediatric Neurology, Department of Development and Regeneration, University of Leuven KU Leuven, Leuven, Belgium.
Jan VervischPediatric Neurology, Department of Development and Regeneration, University of Leuven KU Leuven, Leuven, Belgium.
Katrien LemmensPediatric Neurology, Department of Development and Regeneration, University of Leuven KU Leuven, Leuven, Belgium.
Katarzyna KotulskaDepartment of Neurology and Epileptology, The Children's Memorial Health Institute, Warsaw, Poland.
Romina MoaveroChild Neurology and Psychiatry Unit, Systems Medicine Department, Tor Vergata University, Rome, Italy.
Paolo CuratoloChild Neurology and Psychiatry Unit, Systems Medicine Department, Tor Vergata University, Rome, Italy.
Bernhard WeschkeDepartment of Child Neurology, Charité University Medicine Berlin, Berlin, Germany.
Kate RineyNeuroscience Unit, Queensland Children's Hospital, Brisbane, QLD, Australia.
Martha FeuchtDepartment of Pediatrics, Medical University Vienna, Vienna, Austria.
Pavel KrsekDepartment of Paediatric Neurology, Charles University, Second Faculty of Medicine, Motol University Hospital, Prague, Czechia.
Rima NabboutDepartment of Pediatric Neurology, Reference Centre for Rare Epilepsies, Imagine Institute, Necker- Enfants Malades Hospital, University Paris Descartes, Paris, France.
Anna C JansenPediatric Neurology Unit, Universitair Ziekenhuis Brussel, Brussels, Belgium.
Konrad WojdanTransition Technologies, Warsaw, Poland.
Dorota Domanska-PakiełaDepartment of Neurology and Epileptology, The Children's Memorial Health Institute, Warsaw, Poland.
Magdalena Kaczorowska-FrontczakDepartment of Neurology and Epileptology, The Children's Memorial Health Institute, Warsaw, Poland.
Christoph HertzbergDiagnose und Behandlungszentrum für Kinder und Jugendliche, Vivantes Klinikum Neuköln, Berlin, Germany.
Cyrille H FerrierDepartment of Child Neurology, Brain Centre, University Medical Centre Utrecht, Utrecht, Netherlands.
Sharon SamueliDepartment of Pediatrics, Medical University Vienna, Vienna, Austria.
Barbora BenovaDepartment of Paediatric Neurology, Charles University, Second Faculty of Medicine, Motol University Hospital, Prague, Czechia.
Eleonora AronicaDepartment of (Neuro)Pathology, Amsterdam Universitair Medisch Centrum, University of Amsterdam, Amsterdam, Netherlands.
David J KwiatkowskiHarvard Medical School, Brigham and Women's Hospital, Boston, MA, United States.
Floor E JansenDepartment of Child Neurology, Brain Centre, University Medical Centre Utrecht, Utrecht, Netherlands.
Sergiusz JóźwiakDepartment of Neurology and Epileptology, The Children's Memorial Health Institute, Warsaw, Poland.
Sabine Van HuffelDepartment of Electrical Engineering (ESAT), STADIUS Centre for Dynamical Systems, Signal Processing and Data Analytics, KU Leuven, Leuven, Belgium.
Lieven LagaePediatric Neurology, Department of Development and Regeneration, University of Leuven KU Leuven, Leuven, Belgium.
KU Leuven · BEChildren's Memorial Health Institute · PLMedical University of Vienna · ATUniversity Medical Center Utrecht · NLUniversity of Rome Tor Vergata · ITCharité - Universitätsmedizin Berlin · DECharles University · CZHarvard University · USInstitut National de Recherche en Santé Publique · MLTransition Technologies (Poland) · PLUniversitair Ziekenhuis Brussel · BEUniversité Paris Cité · FRUniversity Hospital in Motol · CZUniversity of Amsterdam · NLUniversity of Queensland · AUVivantes Klinikum · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tuberous Sclerosis Complex (TSC) is a multisystem genetic disorder with a high risk of early-onset epilepsy and a high prevalence of neurodevelopmental comorbidities, including intellectual disability and autism spectrum disorder (ASD). Therefore, TSC is an interesting disease model to investigate early biomarkers of neurodevelopmental comorbidities when interventions are favourable. We investigated whether early EEG characteristics can be used to predict neurodevelopment in infants with TSC. The first recorded EEG of 64 infants with TSC, enrolled in the international prospective EPISTOP trial (recorded at a median gestational age 42 4/7 weeks) was first visually assessed. EEG characteristics were correlated with ASD risk based on the ADOS-2 score, and cognitive, language, and motor developmental quotients (Bayley Scales of Infant and Toddler Development III) at the age of 24 months. Quantitative EEG analysis was used to validate the relationship between EEG background abnormalities and ASD risk. An abnormal first EEG (OR = 4.1,

Indexed as

autism (ASD)biomarkerEEGneurodevelomentTAND profiletuberous sclerosis complex (TSC)

Identifiers

PMID33178126
PMCPMC7596378
OpenAlexW3093031525

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.