Evidence map›Paper›PMID 36674629›Full record

ArticleInternational journal of molecular sciences2023

Genetic Risk Factors for Neurological Disorders in Children with Adverse Events Following Immunization: A Descriptive Study of a Polish Case Series.

Agnieszka Charzewska, Iwona Terczyńska, Agata Lipiec, Tomasz Mazurczak, Paulina Górka-Skoczylas, Róża Szlendak, Karolina Kanabus, Renata Tataj, Mateusz Dawidziuk, Bartosz Wojtaś and 4 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 37% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Current issues in molecular biology · 2024
    Article
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 at 2 institutions in 1 country.

Agnieszka CharzewskaDepartment of Medical Genetics, Institute of Mother and Child, Kasprzaka 17A, 01-211 Warsaw, Poland.ORCID 0000-0003-0279-8370
Iwona TerczyńskaInstitute of Mother and Child, Clinic of Paediatric Neurology, Kasprzaka 17A, 01-211 Warsaw, Poland.
Agata LipiecInstitute of Mother and Child, Clinic of Paediatric Neurology, Kasprzaka 17A, 01-211 Warsaw, Poland.
Tomasz MazurczakInstitute of Mother and Child, Clinic of Paediatric Neurology, Kasprzaka 17A, 01-211 Warsaw, Poland.
Paulina Górka-SkoczylasDepartment of Medical Genetics, Institute of Mother and Child, Kasprzaka 17A, 01-211 Warsaw, Poland.
Róża SzlendakDepartment of Medical Genetics, Institute of Mother and Child, Kasprzaka 17A, 01-211 Warsaw, Poland.
Karolina KanabusDepartment of Medical Genetics, Institute of Mother and Child, Kasprzaka 17A, 01-211 Warsaw, Poland.
Renata TatajDepartment of Medical Genetics, Institute of Mother and Child, Kasprzaka 17A, 01-211 Warsaw, Poland.
Mateusz DawidziukDepartment of Medical Genetics, Institute of Mother and Child, Kasprzaka 17A, 01-211 Warsaw, Poland.ORCID 0000-0001-5102-8722
Bartosz WojtaśLaboratory of Molecular Neurobiology, Nencki Institute of Experimental Biology PAS, Pasteura 3, 02-093 Warsaw, Poland.ORCID 0000-0002-9967-910X
Bartłomiej GielniewskiLaboratory of Molecular Neurobiology, Nencki Institute of Experimental Biology PAS, Pasteura 3, 02-093 Warsaw, Poland.
Jerzy BalDepartment of Medical Genetics, Institute of Mother and Child, Kasprzaka 17A, 01-211 Warsaw, Poland.
Elżbieta StawickaInstitute of Mother and Child, Clinic of Paediatric Neurology, Kasprzaka 17A, 01-211 Warsaw, Poland.ORCID 0000-0003-1329-846X
Dorota Hoffman-ZacharskaDepartment of Medical Genetics, Institute of Mother and Child, Kasprzaka 17A, 01-211 Warsaw, Poland.ORCID 0000-0001-7367-512X
Instytut Biologii Doświadczalnej im. Marcelego Nenckiego · PLUniversity of Warsaw · PL

Funding

Polish National Science Centre 2015/17/B/NZ4/02669
6 · The paper itself

Abstract

Studies conducted on large populations show a lack of connection between vaccination and serious neurological symptoms. However, there are isolated cases that indicate such a relationship. These reports on adverse effects following immunization (AEFI) reduce social confidence in vaccination; however, their background may be rare genetic defects. The aim of the presented study was to examine if neurological AEFI in children may be associated with variants in genes related to neurodevelopment. To identify such possible associations, a descriptive study of the Polish case series was conducted. We performed next-generation sequencing in patients who, up to 4 weeks of injection of any vaccine, manifested neurological AEFI. We included 23 previously normally developing children with first seizures that occurred after vaccination. We identified pathogenic/likely pathogenic variants in genes engaged in neurodevelopment in nine patients and variants of uncertain significance in another nine patients. The mutated genes belonged to the group of genes related to epilepsy syndromes/epileptic encephalopathy. We showed that AEFI might have a genetic background. We hypothesized that in some AEFI patients, the vaccine might only trigger neurological symptoms that would have been manifested anyway as a result of a pathogenic variant in a gene engaged in neurodevelopment.

Indexed as

Drug-Related Side Effects and Adverse ReactionsVaccinesAdverse Drug Reaction Reporting SystemsChildHumansImmunizationPolandRisk FactorsSeizuresVaccinationVaccinesdrug-related side effects and adverse reactionsepilepsyexome sequencingvaccination

Identifiers

PMID36674629
PMCPMC9864286
OpenAlexW4313647005

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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.