Evidence map›Paper›PMID 40072664›Full record

Observational studyEuropean journal of pediatrics2025

Prognostic significance of asymmetric dimethyl arginine level in pediatric patients with COVID-19 infection and MIS-C.

Memduha Sari, Fatih Akin, Abdullah Yazar, Ahmet Osman Kilic, Ozge Metin Akcan, Abdullah Akkus, Mehmet Uyar, Cemile Topcu, Mustafa Genceli

Abstract readObservational Study
In one paragraph

Observational study in European journal of pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Memduha SariDepartment of Pediatrics, Mut State Hospital, 33600, Mersin, Turkey. menduhaakcay@gmail.com.ORCID http://orcid.org/0000-0002-3251-786X
Fatih AkinDepartment of Pediatrics, Faculty of Medicine Hospital, Necmettin Erbakan University, Konya, Turkey.ORCID http://orcid.org/0000-0001-5725-3867
Abdullah YazarDepartment of Pediatrics, Faculty of Medicine Hospital, Necmettin Erbakan University, Konya, Turkey.ORCID http://orcid.org/0000-0003-0733-3943
Ahmet Osman KilicDepartment of Pediatrics, Faculty of Medicine Hospital, Necmettin Erbakan University, Konya, Turkey.ORCID http://orcid.org/0000-0002-3451-6764
Ozge Metin AkcanDepartments of Pediatric Infectious Diseases, Faculty of Medicine Hospital, Necmettin Erbakan University, Konya, Turkey.ORCID http://orcid.org/0000-0002-3465-6994
Abdullah AkkusDepartment of Pediatrics, Faculty of Medicine Hospital, Necmettin Erbakan University, Konya, Turkey.ORCID http://orcid.org/0000-0002-0642-8759
Mehmet UyarDepartment of Public Health, Faculty of Medicine Hospital, Necmettin Erbakan University, Konya, Turkey.ORCID http://orcid.org/0000-0002-3954-7471
Cemile TopcuDepartment of Biochemistry, Faculty of Medicine Hospital, Necmettin Erbakan University, Konya, Turkey.ORCID http://orcid.org/0000-0003-2596-7894
Mustafa GenceliDepartments of Pediatric Infectious Diseases, Faculty of Medicine Hospital, Necmettin Erbakan University, Konya, Turkey.ORCID http://orcid.org/0000-0001-9455-2735

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coronavirus disease 2019 (COVID-19) and COVID-19-related multisystem inflammatory syndrome in children (MIS-C) is known to be a life-threatening health problem worldwide. The study investigates the potential relationship between asymmetric dimethylarginine (ADMA) levels and disease severity in such conditions. We conducted an observational, prospective study between July 2021 and January 2022. The study enrolled 98 patients diagnosed with COVID-19, 21 patients diagnosed with MIS-C, and 42 healthy individuals who served as a control group. The COVID-19 patients were further categorized into three subgroups based on their level of care: outpatients, those requiring hospitalization, and those requiring intensive care. The MIS-C patients formed a distinct fourth group. COVID-19 outpatients had a median ADMA level of 8097.0 ng/L (interquartile range: 6436.06-10840.0 ng/L), while those requiring hospitalization had a higher level of 13,195.60 ng/L (11,472.4-15,862.2 ng/L). Patients in intensive care exhibited the highest median ADMA level at 19,361.4 ng/L (15,596.65-23,367.9 ng/L). MIS-C patients also had elevated ADMA levels, with a median of 15,735.50 ng/L (13,486.6-20,532.5 ng/L). Receiver operating characteristic (ROC) curve analysis revealed that an ADMA level of 6135.15 ng/L could distinguish between patients and controls with 95% sensitivity, 100% specificity, 100% positive predictive value, and 87.5% negative predictive value.

conclusionsIn conclusion, our study is the first to investigate ADMA levels in children with COVID-19 and MIS-C. We found that ADMA levels were significantly elevated in children with COVID-19 requiring intensive care and those with MIS-C, suggesting a potential role for ADMA as a biomarker of endothelial dysfunction in these populations. WHAT IS KNOWN: • Endothelial dysfunction is a determinant of poor prognosis in various cardiovascular diseases and plays a critical role in the pathogenesis of COVID-19 and MIS-C. • Asymmetric dimethylarginine (ADMA) is a well-known biomarker of endothelial dysfunction. Elevated levels of ADMA adversely affect vascular endothelial function by reducing nitric oxide production. WHAT IS NEW: • It is the first to show that elevated ADMA levels in children with COVID-19 and MIS-C are associated with disease severity. • ADMA has been identified as a potential biomarker that can be used to assess the prognosis of COVID-19 and MIS-C in children and to predict the severity of the disease.

Indexed as

ArginineCOVID-19Systemic Inflammatory Response SyndromeAdolescentBiomarkersCase-Control StudiesChildChild, PreschoolFemaleHospitalizationHumansInfantMalePrognosisProspective StudiesROC CurveArginineBiomarkersN,N-dimethylarginineADMAChildrenCOVID-19Endothelial damageMIS-C

Identifiers

PMID40072664
PMCPMC11903618

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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.