Evidence map›Paper›PMID 36011376›Full record

ArticleGenes2022

Genetics of Pediatric Epilepsy: Next-Generation Sequencing in Clinical Practice.

Antonela Blazekovic, Kristina Gotovac Jercic, Sarah Meglaj, Vlasta Duranovic, Igor Prpic, Bernarda Lozic, Masa Malenica, Silvana Markovic, Lucija Lujic, Zeljka Petelin Gadze and 4 more

Abstract read
In one paragraph

Article in Genes, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Article
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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

14 authors.

Antonela BlazekovicDepartment for Functional Genomics, Center for Translational and Clinical Research, University Hospital Center Zagreb, University of Zagreb School of Medicine, 10000 Zagreb, Croatia.ORCID 0000-0002-3669-7941
Kristina Gotovac JercicDepartment for Functional Genomics, Center for Translational and Clinical Research, University Hospital Center Zagreb, University of Zagreb School of Medicine, 10000 Zagreb, Croatia.
Sarah MeglajDepartment for Functional Genomics, Center for Translational and Clinical Research, University Hospital Center Zagreb, University of Zagreb School of Medicine, 10000 Zagreb, Croatia.ORCID 0000-0001-5143-7913
Vlasta DuranovicDepartment of Neuropediatrics, Children's Hospital Zagreb, 10000 Zagreb, Croatia.
Igor PrpicDepartment of Pediatrics, Clinical Hospital Center Rijeka, Faculty of Medicine, University of Rijeka, 51000 Rijeka, Croatia.ORCID 0000-0001-9000-7684
Bernarda LozicDepartment of Pediatrics, University Hospital of Split, University of Split School of Medicine, 21000 Split, Croatia.
Masa MalenicaDepartment of Pediatrics, University Hospital Center Sestre Milosrdnice, 10000 Zagreb, Croatia.
Silvana MarkovicDr. Tomislav Bardek General Hospital Koprivnica, 48000 Koprivnica, Croatia.
Lucija LujicDepartment of Neuropediatrics, Children's Hospital Zagreb, 10000 Zagreb, Croatia.
Zeljka Petelin GadzeDepartment of Neurology, University Hospital Center Zagreb, University of Zagreb School of Medicine, 10000 Zagreb, Croatia.
Romana Gjergja JuraskiNeuropediatric Clinic, Srebrnjak Children's Hospital, 10000 Zagreb, Croatia.
Nina BarišicDepartment of Pediatrics, University Hospital Center Zagreb, 10000 Zagreb, Croatia.
Ivo BaricDepartment of Pediatrics, University Hospital Center Zagreb, 10000 Zagreb, Croatia.
Fran BoroveckiDepartment for Functional Genomics, Center for Translational and Clinical Research, University Hospital Center Zagreb, University of Zagreb School of Medicine, 10000 Zagreb, Croatia.ORCID 0000-0002-5178-7929

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epilepsy is one of the most common neurological disorders with diverse phenotypic characteristics and high genetic heterogeneity. Epilepsy often occurs in childhood, so timely diagnosis and adequate therapy are crucial for preserving quality of life and unhindered development of a child. Next-generation-sequencing (NGS)-based tools have shown potential in increasing diagnostic yield. The primary objective of this study was to evaluate the impact of genetic testing and to investigate the diagnostic utility of targeted gene panel sequencing. This retrospective cohort study included 277 patients aged 6 months to 17 years undergoing NGS with an epilepsy panel covering 142 genes. Of 118 variants detected, 38 (32.2%) were not described in the literature. We identified 64 pathogenic or likely pathogenic variants with an overall diagnostic yield of 23.1%. We showed a significantly higher diagnostic yield in patients with developmental delay (28.9%). Furthermore, we showed that patients with variants reported as pathogenic presented with seizures at a younger age, which led to the conclusion that such children should be included in genomic diagnostic procedures as soon as possible to achieve a correct diagnosis in a timely manner, potentially leading to better treatment and avoidance of unnecessary procedures. Describing and discovering the genetic background of the disease not only leads to a better understanding of the mechanisms of the disorder but also opens the possibility of more precise and individualized treatment based on stratified medicine.

Indexed as

EpilepsyQuality of LifeChildGenetic TestingHigh-Throughput Nucleotide SequencingHumansRetrospective Studiesclinical decision makingepilepsygene panelnext-generation sequencingpediatric

Identifiers

PMID36011376
PMCPMC9407986

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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.