Evidence map›Paper›PMID 40817859›Full record

ArticleJournal of medical virology2025

Genetic Variants Affect Distinct Metabolic Pathways in Pediatric Multisystem Inflammatory Syndrome and Severe COVID-19.

Alysson Henrique Urbanski, Flávia Cristina de Paula Freitas, Tiago Minuzzi Freire da Fontoura Gomes, Michelle Orane Schemberger, Bárbara Carvalho Santos Dos Reis, Flavia Amêndola Anísio de Carvalho, Roberta Soares Faccion, Lucas de Almeida Machado, Deborah Antunes Dos Santos, Daniela Prado Cunha and 34 more

Abstract read
In one paragraph

Article in Journal of medical virology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

44 authors.

Alysson Henrique UrbanskiInstituto Carlos Chagas, FIOCRUZ, Curitiba, Paraná, Brazil.
Flávia Cristina de Paula FreitasInstituto Carlos Chagas, FIOCRUZ, Curitiba, Paraná, Brazil.
Tiago Minuzzi Freire da Fontoura GomesInstituto Carlos Chagas, FIOCRUZ, Curitiba, Paraná, Brazil.
Michelle Orane SchembergerInstituto Carlos Chagas, FIOCRUZ, Curitiba, Paraná, Brazil.
Bárbara Carvalho Santos Dos ReisLaboratório de Alta Complexidade (LACIFF), Unidade de Pesquisa Clínica, Instituto Fernandes Figueira, FIOCRUZ, Rio de Janeiro, Brazil.
Flavia Amêndola Anísio de CarvalhoLaboratório de Alta Complexidade (LACIFF), Unidade de Pesquisa Clínica, Instituto Fernandes Figueira, FIOCRUZ, Rio de Janeiro, Brazil.
Roberta Soares FaccionLaboratório de Alta Complexidade (LACIFF), Unidade de Pesquisa Clínica, Instituto Fernandes Figueira, FIOCRUZ, Rio de Janeiro, Brazil.
Lucas de Almeida MachadoLaboratório de Alta Complexidade (LACIFF), Unidade de Pesquisa Clínica, Instituto Fernandes Figueira, FIOCRUZ, Rio de Janeiro, Brazil.
Deborah Antunes Dos SantosLaboratório de Genômica Aplicada e Bioinovações (IOC), Instituto Oswaldo Cruz, FIOCRUZ, Rio de Janeiro, Brazil.
Daniela Prado CunhaLaboratório de Alta Complexidade (LACIFF), Unidade de Pesquisa Clínica, Instituto Fernandes Figueira, FIOCRUZ, Rio de Janeiro, Brazil.
Margarida Dos Santos SalúLaboratório de Alta Complexidade (LACIFF), Unidade de Pesquisa Clínica, Instituto Fernandes Figueira, FIOCRUZ, Rio de Janeiro, Brazil.
Daniella Campelo Batalha Cox MooreDepartamento de Pediatria, IFF, Unidade de Pacientes Graves, FIOCRUZ, Rio de Janeiro, RJ, Brazil.
Mayra Marinho PresibellaLaboratório Central do Estado do Paraná (LACEN), São José dos Pinhais, Paraná, Brazil.
Juliana Fontes NoguchiFaculdade Evangélica Mackenzie Do Paraná, Curitiba, Paraná, Brazil.ORCID 0000-0002-9128-8796
Henrique Lira BorgesFaculdade Evangélica Mackenzie Do Paraná, Curitiba, Paraná, Brazil.
Lais Kimie TomiuraFaculdade Evangélica Mackenzie Do Paraná, Curitiba, Paraná, Brazil.
Luiza Silva de CastroFaculdade Evangélica Mackenzie Do Paraná, Curitiba, Paraná, Brazil.
Letícia Graziela Costa SantosInstituto Carlos Chagas, FIOCRUZ, Curitiba, Paraná, Brazil.
Esdras Matheus Gomes da SilvaInstituto Carlos Chagas, FIOCRUZ, Curitiba, Paraná, Brazil.
Vinícius Da Silva Coutinho ParreiraInstituto Carlos Chagas, FIOCRUZ, Curitiba, Paraná, Brazil.
Luis Gustavo MorelloInstituto Carlos Chagas, FIOCRUZ, Curitiba, Paraná, Brazil.
Fabricio Klerynton MarchiniInstituto Carlos Chagas, FIOCRUZ, Curitiba, Paraná, Brazil.
Maria Regina TizzotFaculdade Evangélica Mackenzie Do Paraná, Curitiba, Paraná, Brazil.
Mauricio Marcondes RibasHospital Universitário Evangélico Mackenzie, Curitiba, Paraná, Brazil.
Gilberto PascolatHospital Universitário Evangélico Mackenzie, Curitiba, Paraná, Brazil.
Carmen Australia Paredes Marcondes RibasFaculdade Evangélica Mackenzie Do Paraná, Curitiba, Paraná, Brazil.
Fábio Fernandes da Rocha VicenteFederal University of Technology - Paraná (UTFPR), Cornélio Procópio, Paraná, Brazil.
Alexandre Rossi PaschoalFederal University of Technology - Paraná (UTFPR), Cornélio Procópio, Paraná, Brazil.
Rubens CatDepartamento de Pediatria, Universidade Federal do Paraná, Curitiba, Paraná, Brazil.
Benilton de Sá CarvalhoDepartamento de Estatística, Universidade Estadual de Campinas, Campinas, São Paulo, Brazil.
Jaqueline Carvalho de OliveiraDepartamento de Genética, Universidade Federal do Paraná, Curitiba, Paraná, Brazil.
Marcus F OliveiraUniversidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Luiz Lehmann CoutinhoEscola Superior de Agricultura Luiz de Queiroz (ESALQ), Universidade de São Paulo, Piracicaba, São Paulo, Brazil.
Acácia Maria Lourenço Francisco NasrSecretaria da Saúde do Estado do Paraná (SESA), Curitiba, Paraná, Brazil.
Irina Nastassja RiedigerLaboratório Central do Estado do Paraná (LACEN), São José dos Pinhais, Paraná, Brazil.
Jeanine Marie NardinEscola de Medicina e Ciências da Vida (EMCV), Pontifícia Universidade Católica do Paraná - PUCPR, Curitiba, Paraná, Brazil.
Liya Regina MikamiFaculdade Evangélica Mackenzie Do Paraná, Curitiba, Paraná, Brazil.
Ana Carolina Ramos GuimarãesLaboratório de Genômica Aplicada e Bioinovações (IOC), Instituto Oswaldo Cruz, FIOCRUZ, Rio de Janeiro, Brazil.
Patricia Savio de Araujo-SouzaUniversidade Federal do Paraná, Curitiba, Paraná, Brazil.ORCID 0000-0002-4489-9148
Arnaldo Prata-BarbosaInstituto D'or de Pesquisa e Ensino, Rio de Janeiro, Brazil.
Zilton Farias Meira de VasconcelosLaboratório de Alta Complexidade (LACIFF), Unidade de Pesquisa Clínica, Instituto Fernandes Figueira, FIOCRUZ, Rio de Janeiro, Brazil.
Helisson FaoroInstituto Carlos Chagas, FIOCRUZ, Curitiba, Paraná, Brazil.
Hellen Geremias Dos SantosInstituto Carlos Chagas, FIOCRUZ, Curitiba, Paraná, Brazil.
Fabio PassettiInstituto Carlos Chagas, FIOCRUZ, Curitiba, Paraná, Brazil.ORCID 0000-0001-5672-7848

Funding

This study was supported by Fundação Araucária, Conselho Nacional de Desenvolvimento Científico e Tecnológico, Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior and Fundação Oswaldo Cruz.
6 · The paper itself

Abstract

The coronavirus disease 2019 (COVID-19) pandemic has triggered a global health crisis, with over 700 million confirmed cases and at least 7 million deaths reported by early 2024. Children are less vulnerable to severe SARS-CoV-2 infection than adults and typically experience milder respiratory symptoms. However, a rare but significant complication, known as multisystem inflammatory syndrome in children (MIS-C), can develop weeks after infection, characterized by a spectrum of inflammatory symptoms. This study employed whole-exome sequencing and over-representation analysis to identify genetic variants of potential clinical significance related to MIS-C or severe COVID-19 in a group of children with acute respiratory distress syndrome (ARDS), all of whom were unvaccinated for COVID-19. We observed the enrichment of potentially pathogenic genetic variants in genes related to carbohydrate metabolism, particularly glycogen breakdown, in severe COVID-19 pediatric patients, and in genes related to cholesterol and lipoprotein metabolism in MIS-C patients. These findings offer insights into the genetic underpinnings of MIS-C and severe COVID-19, suggesting potential genes and biological pathways for further research.

Indexed as

COVID-19Genetic VariationMetabolic Networks and PathwaysSystemic Inflammatory Response SyndromeAdolescentCarbohydrate MetabolismChildChild, PreschoolExome SequencingFemaleHumansInfantMaleSARS-CoV-2carbohydrate metabolismcholesterol metabolismCOVID‐19genetic variantsMIS‐C (multisystem inflammatory syndrome in children)whole‐exome sequencing

Identifiers

PMID40817859
PMCPMC12357531

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