Evidence map›Paper›PMID 41120462›Full record

ArticleScientific reports2025

Clinical manifestations and severity of COVID-19 caused by Omicron among paediatric patients aged 0-17 years in Italy.

Rossana Scutari, Valeria Fox, Jennifer L Nguyen, Luna Colagrossi, Andrea Smarrazzo, Anna Chiara Vittucci, Laura Cursi, Martina Mastropaolo, Lorena Forquè Rodriguez, Carmen D'amore and 19 more

Abstract read
In one paragraph

Article in Scientific reports, 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

29 authors.

Rossana Scutari *Multimodal Laboratory Research Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Valeria Fox *Multimodal Laboratory Research Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Jennifer L NguyenPfizer Inc, New York, NY, USA.
Luna ColagrossiMicrobiology and Diagnostic Immunology Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Andrea SmarrazzoPediatrics Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Anna Chiara VittucciGeneral Pediatrics and Emergency Unit 2nd Level, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Laura CursiInfectious Disease Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Martina MastropaoloMultimodal Laboratory Research Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Lorena Forquè RodriguezMultimodal Laboratory Research Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Carmen D'amoreEpidemiology, Clinical Pathways and Clinical Risk Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Luciano PacelliPfizer Inc, New York, NY, USA.
Mustapha M MustaphaPfizer Inc, New York, NY, USA.
Claudia AlteriDepartment of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.
Jingyan YangPfizer Inc, New York, NY, USA.
Antonella De SantisPediatrics Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Romina QuerciaPfizer Inc, New York, NY, USA.
Alessandra PagliaroPfizer Inc, New York, NY, USA.
Annarita GranagliaMicrobiology and Diagnostic Immunology Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Vanessa FiniMicrobiology and Diagnostic Immunology Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Srinivas R ValluriPfizer Inc, New York, NY, USA.
Cristina RussoMicrobiology and Diagnostic Immunology Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Catia MarquesPfizer Inc, New York, NY, USA.
John M McLaughlinPfizer Inc, New York, NY, USA.
Laura LancellaInfectious Disease Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Marta Luisa Ciofi Degli AttiEpidemiology, Clinical Pathways and Clinical Risk Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Andrea CampanaPediatrics Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Massimiliano RaponiMedical Direction, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Alberto VillaniGeneral Pediatrics and Emergency Unit 2nd Level, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Carlo Federico PernoMultimodal Laboratory Research Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy. carlofederico.perno@opbg.net.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SARS-CoV-2 Omicron variant evolved into multiple sub-lineages, some showing increased transmissibility and immune evasion. Despite decreased risk of severe disease, paediatric hospitalization rose. However, factors influencing clinical outcomes remain unclear. A total of 458 whole-genome Omicron sequences from patients 0-17 years, diagnosed with SARS-CoV-2 at Bambino Gesù Children's Hospital (January-December 2023) were analysed. Clinical features, disease severity and circulating variants were assessed. Phylogenetic analysis was performed, and logistic regression identified factors associated with hospitalization. Among patients, 249 (54.4%) were male, with median age 0.6 years. Comorbidities were present in 105 (22.9%) patients, mainly immunocompromised (21.0%). Infections were predominantly from XBB (75.0%), JN.1 (12.4%), BA.5 (7.4%) and BA.2 (5.2%) clades. Upper respiratory infections predominated (73.8%), followed by asymptomatic (17.2%) and lower respiratory infections (4.6%), with nine patients having ≥ 1 co-infection. Comorbidities and lower respiratory infections were positively associated with hospitalization, while upper respiratory infections showed a negative association. Given the recent shift to RGN integrin-binding motif in Omicron sub-lineages, leading to altered pathogenesis, its presence was evaluated, revealing a predominance of RGN (N = 378, 84.6%). In conclusion, COVID-19 severity in paediatric patients was primarily driven by comorbidities and co-infections, while milder cases in healthy children may be associated with RGN integrin-binding motif.

Indexed as

COVID-19SARS-CoV-2AdolescentChildChild, PreschoolFemaleHospitalizationHumansInfantInfant, NewbornItalyMalePhylogenySeverity of Illness IndexClinical outcomesCOVID-19 in childrenOmicron cladeSARS-CoV-2 genomic characterization

Identifiers

PMID41120462
PMCPMC12540900

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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.