Evidence map›Paper›PMID 42608976›Full record

ArticlePediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology2026

Plasma metabolomics in infancy reveals early signatures of a stringently-defined otitis-prone phenotype.

Nicole Prince, Jing Chen, Ravinder Kaur, Caitlin Syphurs, Annmarie Hoch, Asimenia Angelidou, Kerry McEnaney, Bo Chawes, Ole Bæk, Tingting Wang and 6 more

Abstract read
In one paragraph

Article in Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, 2026. 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. Plasma metabolomics in infancy reveals early signatures of a stringently-defined otitis-prone phenotype.Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2026
    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

16 authors.

Nicole PrinceChanning Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0002-8506-1122
Jing ChenPrecision Vaccines Program, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts, USA.ORCID https://orcid.org/0009-0006-5900-7460
Ravinder KaurCenter for Infectious Diseases and Immunology, Rochester General Hospital Research Institute, Rochester, New York, USA.ORCID https://orcid.org/0000-0001-6539-5339
Caitlin SyphursPrecision Vaccines Program, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts, USA.ORCID https://orcid.org/0009-0004-5066-3985
Annmarie HochPrecision Vaccines Program, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0003-0836-2164
Asimenia AngelidouHarvard Medical School, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0002-6716-6561
Kerry McEnaneyPrecision Vaccines Program, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0002-0378-3456
Bo ChawesCOPSAC, Copenhagen Prospective Studies on Asthma in Childhood, Copenhagen University Hospital - Herlev and Gentofte, Copenhagen, Denmark.ORCID https://orcid.org/0000-0001-6846-6243
Ole BækCOPSAC, Copenhagen Prospective Studies on Asthma in Childhood, Copenhagen University Hospital - Herlev and Gentofte, Copenhagen, Denmark.ORCID https://orcid.org/0000-0003-0598-0952
Tingting WangCOPSAC, Copenhagen Prospective Studies on Asthma in Childhood, Copenhagen University Hospital - Herlev and Gentofte, Copenhagen, Denmark.ORCID https://orcid.org/0000-0002-9100-3447
Nicklas BrustadCOPSAC, Copenhagen Prospective Studies on Asthma in Childhood, Copenhagen University Hospital - Herlev and Gentofte, Copenhagen, Denmark.ORCID https://orcid.org/0000-0001-6383-8845
Ofer LevyHarvard Medical School, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0002-5859-1945
Joann Diray-ArceHarvard Medical School, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0003-2183-4269
Michael PichicheroCenter for Infectious Diseases and Immunology, Rochester General Hospital Research Institute, Rochester, New York, USA.ORCID https://orcid.org/0000-0002-8276-3938
Jessica A Lasky-SuChanning Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0001-6236-4705
IDEaL Consortium

Funding

Proteomics and Metabolomics Core: IDEAL shapes vaccine response, susceptibility to respiratory infectious disease and asthmaU19AI168643 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI OFER LEVY · 2022 to 2026
$10.0M
NTHi Immunity in Young ChildrenR01DC008671 · NIDCD · UNIVERSITY OF ROCHESTER · PI PICHICHERO, MICHAEL E · 2007 to 2016
$5.8M
Immunometabolic signatures of BCG-induced neonatal trained immunityK08AI168487 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI Asimenia Angelidou · 2023 to 2026
$704k
Inflammatory subtypes and multi-omic determinants of early life infection riskK01HL175261 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI Nicole Prince · 2024 to 2026
$533k
National Institute of Allergy and Infectious Diseases K08AI168487National Institute of Allergy and Infectious Diseases U19AI168643NHLBI NIH HHS 1K01HL175261NHLBI NIH HHS K01 HL175261NIAID NIH HHS K08 AI168487NIAID NIH HHS U19 AI168643NIDCD NIH HHS R01 DC008671NIDCD NIH HHS R01 DC08671
6 · The paper itself

Abstract

backgroundOtitis media is highly prevalent during early life, yet the molecular factors that predispose children to recurrent episodes are poorly defined. Metabolomics captures dynamic biochemical changes and may help identify pathways influencing otitis susceptibility. We examined whether longitudinal infant plasma metabolomic profiles were associated with development of stringently-defined otitis proneness in the Rochester Combined Cohort (RCC; Rochester, NY).

methodsGlobal plasma metabolomic profiling was performed in RCC samples collected between ~6 and 18 months of age using liquid chromatography-tandem mass spectrometry (LC-MS/MS). Children were classified as stringently-defined otitis prone (sOP) if they experienced ≥3 acute otitis media (AOM) episodes within a 6-month period or ≥4 AOM episodes within a 12-month period during the first 3 years of life; all AOM episodes were tympanocentesis-confirmed. Generalized additive mixed models (GAMMs) assessed age-dependent differences in plasma metabolite levels between sOP and non-otitis-prone (nOP) children, adjusting for potential confounders.

resultsSeveral metabolites demonstrated age-related declines in lipid and amino acid pathways, with consistently lower metabolite trajectories in the sOP group. Compared with nOP children, sOP children exhibited significantly lower levels of 16 metabolites related to inflammatory lipid signaling, redox metabolism, and fatty acid metabolism (p < 4.4 × 10

conclusionChildren who subsequently met sOP criteria by age 3 years exhibited distinct plasma metabolomic signatures during infancy, suggesting altered immune-metabolic programming preceding recurrent otitis media. Longitudinal metabolomics provides a promising framework to identify biochemical mechanisms underlying otitis proneness.

Indexed as

Otitis MediaBiomarkersChromatography, LiquidCohort StudiesFemaleHumansInfantLongitudinal StudiesMaleMetabolomeMetabolomicsPhenotypeTandem Mass SpectrometryBiomarkersimmune developmentlongitudinal omicsmetabolomicsotitis proneness

Identifiers

PMID42608976
PMCPMC13482141

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.