Evidence map›Paper›PMID 40214943›Full record

ArticleIndian pediatrics2025

FCGR2A Gene Polymorphism Association in Children with Multisystem Inflammatory Syndrome.

Esra Yeşiltepe, Derya Duman, Necdet Kuyucu, Sevcan Tuğ Bozdoğan, Lara Çıtırık, Edanur Yeşil, Derya Karpuz

Abstract read
In one paragraph

Article in Indian pediatrics, 2025. 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
–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

1 citing paper in PubMed.

  1. 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

7 authors.

Esra YeşiltepeDepartment of Pediatrics, Faculty of Medicine, Mersin University, 33343, Mersin, Turkey.
Derya DumanDepartment of Pediatric Cardiology, Faculty of Medicine, University of Mersin, 34. Cadde, Ciftlikkoy Kampusu, 33343, Mersin, Turkey. drderyaduman@gmail.com.ORCID 0000-0002-4176-1709
Necdet KuyucuDepartment of Pediatric Infectious Disease, Faculty of Medicine, University of Mersin, 34. Cadde, Ciftlikkoy Kampusu, 33343, Mersin, Turkey.ORCID 0000-0002-6721-4105
Sevcan Tuğ BozdoğanDepartment of Medical Genetics, Faculty of Medicine, Çukurova University, Balcalı Kampüsü, 01330, Adana, Turkey.ORCID 0000-0003-3853-8212
Lara ÇıtırıkDepartment of Pediatric Cardiology, Faculty of Medicine, Mersin University, 33343, Mersin, Turkey.
Edanur YeşilDepartment of Pediatric Infectious Disease, Faculty of Medicine, University of Mersin, 34. Cadde, Ciftlikkoy Kampusu, 33343, Mersin, Turkey.ORCID 0000-0002-8926-9959
Derya KarpuzDepartment of Pediatric Cardiology, Faculty of Medicine, University of Mersin, 34. Cadde, Ciftlikkoy Kampusu, 33343, Mersin, Turkey.ORCID 0000-0002-3007-1403

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveFc gamma receptor IIa (FCGR2A) gene polymorphism is associated with increased susceptibility to autoimmune and infectious diseases. The aim of the present study was to evaluate the association of FCGR2A rs1801274 polymorphism with the development and severity of multisystem inflammatory syndrome in children (MIS-C).

methodsThis case-control study was conducted in a single center with MIS-C patients and healthy children. Clinical and cardiac imaging data of the participants was collected. The association between the clinical severity of the disease and FCGR2A rs1801274 polymorphism were investigated.

resultsThere was no significant association between FCGR2A rs1801274 polymorphism and cardiovascular complications in MIS-C patients. However, those with homozygous FCGR2A rs1801274 gene polymorphism developed severe cardiac dysfunction and required immunomodulatory agents other than intravenous immunoglobulin. The mean age of the patients with severe MIS-C was significantly higher than those with mild MIS-C, and systolic dysfunction was significant.

conclusionsFurther multicenter studies in different ethnic groups are needed to evaluate the association between differences in the FCGR2A rs1801274 gene and severity of MIS-C and/or other inflammatory diseases. TRIAL REGISTRY: Mersin University Clinical Trial Registry, Decision number 2022/280 dated April 20, 2022.

Indexed as

COVID-19Receptors, IgGSystemic Inflammatory Response SyndromeAdolescentCase-Control StudiesChildChild, PreschoolFemaleGenetic Predisposition to DiseaseHumansInfantMalePolymorphism, GeneticPolymorphism, Single NucleotideFCGR2A protein, humanReceptors, IgGCardiovascular systemChildGeneticsMultisystem inflammation

Identifiers

PMID40214943
PMCPMC12041097

What Socratic holds

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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 Socratic graph.