Evidence map›Paper›PMID 41566972›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2026

Symptomatic and Asymptomatic Norovirus Infections in Early Life; the PREVAIL Cohort, 2017-2020.

Julia M Baker, Jennifer L Cannon, Claire P Mattison, Hannah Browne, Kenny Nguyen, Rachel M Burke, Eddie Bartlett, Shannon C Conrey, Allison R Burrell, Mary Allen Staat and 5 more

Abstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2026. 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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0cells of the map it votes in
0citing papers in PubMed
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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

15 authors.

Julia M BakerDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.ORCID 0000-0001-7872-316X
Jennifer L CannonCDC Foundation, Atlanta, Georgia, USA.
Claire P MattisonDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Hannah BrowneDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Kenny NguyenDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.ORCID 0000-0003-1727-5441
Rachel M BurkeDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.ORCID 0000-0002-5678-5826
Eddie BartlettDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Shannon C ConreyDepartment of Environmental and Public Health Sciences, Division of Epidemiology, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.ORCID 0000-0003-3715-5842
Allison R BurrellDivision of Infectious Diseases, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.ORCID 0000-0002-2271-8430
Mary Allen StaatDivision of Infectious Diseases, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Ardythe L MorrowDepartment of Environmental and Public Health Sciences, Division of Epidemiology, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.
Umesh D ParasharDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Jan VinjéDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Sara A MirzaDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.ORCID 0000-0003-3144-6569
Daniel C PayneDivision of Infectious Diseases, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.

Funding

Impact of the Initial Influenza Exposure on the Quality, Magnitude, Breadth, Potency and Durability of Influenza ImmunityU01AI144673 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI STAAT, MARY A · 2019 to 2025
$36.4M
Molecular Epidemiology in Children's Environmental Health Training Program (MECEH)T32ES010957 · NIEHS · UNIVERSITY OF CINCINNATI · PI Kelly J Brunst · 2001 to 2026
$11.1M
Center for Clinical and Translational Science and TrainingUM1TR005265 · NCATS · UNIVERSITY OF CINCINNATI · PI Jareen Meinzen-Derr, Jeffrey Robert Strawn · 2025 to 2026
$10.6M
MOM2CHild Study: Leveraging systems biology toward discoveries in Maternal Obesity, Milk, and Translation To Child HealthR01HD109915 · NICHD · UNIVERSITY OF CINCINNATI · PI ARDYTHE L MORROW · 2022 to 2026
$3.9M
Good Ventures FoundationNCATS NIH HHS UM1 TR005265NCIRD CDC HHS U01 IP001059NIAID NIH HHS R01HD109915NIAID NIH HHS U01A1144673NIAID NIH HHS U01 AI144673NIEHS NIH HHS T32 ES010957US Centers for Disease Control and Prevention IP16-004
6 · The paper itself

Abstract

introductionNorovirus is the leading cause of medically attended acute gastroenteritis in the United States. Efforts to reduce the disease burden are constrained by uncertainty around fundamental aspects of norovirus epidemiology. This study describes characteristics of norovirus infections and explores potential risk factors for symptomatic infections in early life.

methodsThe Pediatric Respiratory and Enteric Virus Acquisition and Immunogenesis Longitudinal (PREVAIL) birth cohort study followed 245 children from birth to 2 years of age with weekly stool sample collection and symptom surveys. Stool samples were tested by reverse transcriptase-realtime polymerase chain reaction to detect norovirus genogroup (G)I and GII; positive samples were genotyped. Infections accompanied by diarrhea and/or vomiting were considered symptomatic. Children were categorized as adherent if they participated for ≥18 months and submitted ≥70% of samples.

resultsA total of 72 GI and 330 GII norovirus infections (among 156 children) were identified. One-fifth (20.8%) of adherent children experienced ≥1 norovirus infection by 6 months of age, increasing to 84.2% of children by 2 years of age. About one-third of infections were symptomatic, including half of infections with cycle threshold values <25. Infection with norovirus genotype GII.4 Sydney was the strongest predictor of symptomatic infection in adjusted analyses, as was older age and higher viral load. Childcare attendance, breastfeeding, mother's secretor status, and prior infections were not predictive of symptom status.

conclusionsThis study highlights fundamental characteristics of norovirus epidemiology in early life with implications for understanding the full natural history of the disease, disease transmission, and prevention approaches.

Indexed as

Asymptomatic InfectionsCaliciviridae InfectionsGastroenteritisNorovirusBirth CohortChild, PreschoolCohort StudiesDiarrheaFecesFemaleGenotypeHumansInfantInfant, NewbornLongitudinal StudiesMalebirth cohortchildgastroenteritisnorovirusUnited States

Identifiers

PMID41566972
PMCPMC13284834

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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.