Evidence map›Paper›PMID 31163675›Full record

ArticleJournal of clinical medicine2019

Early Clinical Predictors of Autism Spectrum Disorder in Infants with Tuberous Sclerosis Complex: Results from the EPISTOP Study.

Romina Moavero, Arianna Benvenuto, Leonardo Emberti Gialloreti, Martina Siracusano, Katarzyna Kotulska, Bernhard Weschke, Kate Riney, Floor E Jansen, Martha Feucht, Pavel Krsek and 14 more

2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
6.1field-weighted citation impact, top 3% 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.

NCT02098759 naunknown statusnot on this map

Long-term, Prospective Study Evaluating Clinical and Molecular Biomarkers of Epileptogenesis in a Genetic Model of Epilepsy - Tuberous Sclerosis Complex

TypeinterventionalSponsorSergiusz JozwiakRan2013 to 2018Enrolled100ConditionsTSC, Tuberous Sclerosis Complex, EpilepsyArmsepilepsy early diagnosis protocol
NCT05161494 completednot on this mapstarted 2022, after this paper: background citation

Identification of Gait Disorders in Children, Adolescents and Young Adults With Rare Genetic Diseases

TypeobservationalSponsorUniversiteit AntwerpenRan2022 to 2026Enrolled41ConditionsTuberous Sclerosis, STXBP1 Encephalopathy With Epilepsy
3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 72 citations in OpenAlex.

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  4. Is autism driven by epilepsy in infants with Tuberous Sclerosis Complex?Annals of clinical and translational neurology · 2020
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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

24 authors at 15 institutions in 10 countries.

Romina MoaveroChild Neurology and Psychiatry Unit, Systems Medicine Department, Tor Vergata University, Via Montpellier 1, 00133 Rome, Italy. rominamoavero@hotmail.com.ORCID 0000-0002-6200-060X
Arianna BenvenutoChild Neurology and Psychiatry Unit, Systems Medicine Department, Tor Vergata University, Via Montpellier 1, 00133 Rome, Italy. ariannabenvenuto@yahoo.it.
Leonardo Emberti GialloretiDepartment of Biomedicine and Prevention, Tor Vergata University of Rome, Via Montpellier 1, 00133 Rome, Italy. leonardo.emberti.gialloreti@uniroma2.it.
Martina SiracusanoDepartment of Biomedicine and Prevention, Tor Vergata University of Rome, Via Montpellier 1, 00133 Rome, Italy. siracusanomartina@hotmail.it.
Katarzyna KotulskaDepartment of Neurology and Epileptology, The Children's Memorial Health Institute, Al. Dzieci Polskich 20, 04-730 Warsaw, Poland. kotulska.jozwiak@gmail.com.
Bernhard WeschkeDepartment of Child Neurology, Charité University Medicine Berlin, Augustenburger Platz 1, 13353 Berlin, Germany. bernhard.weschke@charite.de.
Kate RineyNeuroscience Unit, Queensland Children's Hospital, 501 Stanley Street, South Brisbane, QLD 4101, Australia. drkateriney@gccn.com.au.
Floor E JansenDepartment of Child Neurology, Brain Center, University Medical Center Utrecht, 3584 Utrecht, The Netherlands. F.E.Jansen@umcutrecht.nl.
Martha FeuchtDepartment of Pediatrics, University Hospital Vienna, 1090 Vienna, Austria. martha.feucht@meduniwien.ac.at.
Pavel KrsekMotol University Hospital, Charles University, 150 06 Prague, Czech Republic. pavel.krsek@post.cz.
Rima NabboutDepartment of Pediatric Neurology, Reference Centre for Rare Epilepsies, Necker- Enfants Malades Hospital, University Paris Descartes, Imagine Institute, 75015 Paris, France. rimanabbout@yahoo.com.
Anna C JansenPediatric Neurology Unit-UZ Brussel, 1050 Brussels, Belgium. Anna.Jansen@uzbrussel.be.ORCID 0000-0002-3835-2824
Konrad WojdanWarsaw University of Technology, Institute of Heat Engineering, 00-661 Warsaw, Poland. K.Wojdan@tt.com.pl.
Julita BorkowskaDepartment of Neurology and Epileptology, The Children's Memorial Health Institute, Al. Dzieci Polskich 20, 04-730 Warsaw, Poland. J.Borkowska@IPCZD.PL.
Krzystof SadowskiDepartment of Neurology and Epileptology, The Children's Memorial Health Institute, Al. Dzieci Polskich 20, 04-730 Warsaw, Poland. K.Sadowski@IPCZD.PL.
Christoph HertzbergDiagnose und Behandlungszentrum für Kinder und Jugendliche, Vivantes Klinikum Neuköln, 12351 Berlin, Germany. Christoph.Hertzberg@vivantes.de.
Hanna HulshofDepartment of Child Neurology, Brain Center, University Medical Center Utrecht, 3584 Utrecht, The Netherlands. H.M.Hulshof-3@umcutrecht.nl.
Sharon SamueliDepartment of Pediatrics, University Hospital Vienna, 1090 Vienna, Austria. sharon.samueli@meduniwien.ac.at.
Barbora BenovaMotol University Hospital, Charles University, 150 06 Prague, Czech Republic. barbora.benova@gmail.com.
Eleonora AronicaAmsterdam UMC, University of Amsterdam, Department of (Neuro)Pathology, Amsterdam Neuroscience, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands. e.aronica@amc.uva.nl.
David J KwiatkowskiBrigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA. dk@rics.bwh.harvard.edu.
Lieven LagaeDepartment of Development and Regeneration-Section Pediatric Neurology, University Hospitals KU Leuven, 3000 Leuven, Belgium. lieven.lagae@uzleuven.be.
Sergiusz JozwiakDepartment of Neurology and Epileptology, The Children's Memorial Health Institute, Al. Dzieci Polskich 20, 04-730 Warsaw, Poland. sergiusz.jozwiak@gmail.com.ORCID 0000-0003-3350-6326
Paolo CuratoloChild Neurology and Psychiatry Unit, Systems Medicine Department, Tor Vergata University, Via Montpellier 1, 00133 Rome, Italy. curatolo@uniroma2.it.
University of Rome Tor Vergata · ITChildren's Memorial Health Institute · PLCharles University · CZUniversity Medical Center Utrecht · NLVienna General Hospital · ATAmsterdam Neuroscience · NLBrigham and Women's Hospital · USCharité - Universitätsmedizin Berlin · DEKU Leuven · BEMedical University of Warsaw · PLThe University of Queensland · AUUniversitair Ziekenhuis Brussel · BEUniversité Paris Cité · FRVivantes Klinikum · DEWarsaw University of Technology · PL

Funding

European Community's Seventh Framework Programme 602391
6 · The paper itself

Abstract

Autism spectrum disorder (ASD) is highly prevalent in subjects with Tuberous Sclerosis Complex (TSC), but we are not still able to reliably predict which infants will develop ASD. This study aimed to identify the early clinical markers of ASD and/or developmental delay (DD) in infants with an early diagnosis of TSC. We prospectively evaluated 82 infants with TSC (6-24 months of age), using a detailed neuropsychological assessment (Bayley Scales of Infant Development-BSID, and Autism Diagnostic Observation Schedule-ADOS), in the context of the EPISTOP (Long-term, prospective study evaluating clinical and molecular biomarkers of EPIleptogenesiS in a genetic model of epilepsy-Tuberous SclerOsis ComPlex) project (NCT02098759). Normal cognitive developmental quotient at 12 months excluded subsequent ASD (negative predictive value 100%). The total score of ADOS at 12 months clearly differentiated children with a future diagnosis of ASD from children without (

Indexed as

autismdevelopmental delaydiagnosisepilepsyEPISTOPintellectual disabilitymarkersrisk factorstreatmenttuberous sclerosis complex

Identifiers

PMID31163675
PMCPMC6617179
OpenAlexW2948816809

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.