Evidence mapPaperPMID 41425477Full record

ArticlePrecision nutrition2025

Integrating Exposures and Multi-Omics in the Boston Birth Cohort to Elucidate Immune Development across the Life Course: Rationale and Study Design.

Xiumei Hong, Pamela A Frischmeyer-Guerrerio, Guoying Wang, Colleen Pearson, William G Adam, H Benjamin Larman, Hongkai Ji, Xiaobin Wang

Abstract read
In one paragraph

Article in Precision nutrition, 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

8 authors.

Xiumei HongCenter on the Early Life Origins of Disease, Department of Population, Family and Reproductive Health, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD, 21205, USA.
Pamela A Frischmeyer-GuerrerioLaboratory of Allergic Diseases, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD; USA.
Guoying WangCenter on the Early Life Origins of Disease, Department of Population, Family and Reproductive Health, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD, 21205, USA.
Colleen PearsonDepartment of Pediatrics, Boston University School of Medicine and Boston Medical Center, Boston, MA, 02118, USA.
William G AdamDepartment of Pediatrics, Boston University School of Medicine and Boston Medical Center, Boston, MA, 02118, USA.
H Benjamin LarmanInstitute for Cell Engineering, Division of Immunology, Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Hongkai JiDepartment of Biostatistics, Johns Hopkins University Bloomberg School of Public Health, 615 N Wolfe St, Baltimore, MD 21205, USA.
Xiaobin WangCenter on the Early Life Origins of Disease, Department of Population, Family and Reproductive Health, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD, 21205, USA.

Funding

Preterm Birth, Maternal and Cord Blood Metabolome, and Child Metabolic RiskR01HD041702 · NICHD · LURIE CHILDREN'S HOSPITAL OF CHICAGO · PI Frank B Hu, XIAOBIN WANG · 2001 to 2026
$11.1M
Immune Development Across the Life Course: Integrating Exposures and Multi-Omics in the Boston Birth CohortU01ES034983 · NIEHS · JOHNS HOPKINS UNIVERSITY · PI Hongkai Ji, Harry Benjamin Larman · 2022 to 2026
$3.9M
Boston University Clinical and Translational Science Institute - U ProgramU54TR001012 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI CENTER, DAVID M. · 2014 to 2014
$3.9M
The Hopkins Population CenterP2CHD042854 · NICHD · JOHNS HOPKINS UNIVERSITY · PI FEINIAN CHEN · 2021 to 2026
$3.0M
Post Genome-Wide Association Study of Food AllergyU01AI090727 · NIAID · LURIE CHILDREN'S HOSPITAL OF CHICAGO · PI WANG, XIAOBIN · 2010 to 2014
$2.3M
Functional RNA Modifications, Micronutrient Exposure, Developmental DisabilitiesR01ES031521 · NIEHS · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI WANG, XIAOBIN, XIE, HEHUANG · 2020 to 2024
$1.9M
Maternal Exposure to Low Level Mercury, Metabolome, and Child Cardiometabolic Risk in Multi-Ethnic Prospective Birth CohortsR01ES031272 · NIEHS · JOHNS HOPKINS UNIVERSITY · PI WANG, GUOYING, WANG, XIAOBIN · 2020 to 2024
$1.2M
Maternal and Cord Blood Metabolome, Infant Feeding, and Development of Food Allergy in a Prospective Birth CohortR21AI154233 · NIAID · JOHNS HOPKINS UNIVERSITY · PI HONG, XIUMEI · 2020 to 2021
$450k
Interplay of the T Cell Repertoire Development and Early Life Exposure on Incident Risk of Peanut AllergyR21AI171059 · NIAID · JOHNS HOPKINS UNIVERSITY · PI HONG, XIUMEI, SMITH, KELLIE NICOLE · 2023 to 2024
$450k
Establishing Precursors of Food Allergy in NewbornsR21AI079872 · NIAID · LURIE CHILDREN'S HOSPITAL OF CHICAGO · PI WANG, XIAOBIN · 2008 to 2009
$447k
NCATS NIH HHS U54 TR001012NIAID NIH HHS R21 AI079872NIAID NIH HHS R21 AI154233NIAID NIH HHS R21 AI171059NIAID NIH HHS U01 AI090727NICHD NIH HHS P2C HD042854NICHD NIH HHS R01 HD041702NIEHS NIH HHS R01 ES031272NIEHS NIH HHS R01 ES031521NIEHS NIH HHS U01 ES034983
6 · The paper itself

Abstract

In-utero and the first few years of life represent critical windows for immune development, and early life exposures to microbes and environmental pollutants may have a profound impact on future risk of allergic diseases. However, few studies have examined the interplay among early life exposures, immune responses, and multi-omics on allergic outcomes across the critical developmental windows. Funded by the National Institute of Health, we launched a prospective study in the Boston Birth Cohort (BBC) to investigate the impact of early-life exposure to environmental pollutants and immune response to a broad array of microbes on the development and prognosis of allergic diseases from birth up to age 18 years and their underlying molecular pathways (referred as "The BBC IDeaL study"). The objective of this paper is to describe the study rationale, hypotheses, and study design of the BBC IDeaL study. This study included a total of 990 mother-child dyads, with almost equal number of boys and girls. About 58% mothers self-identified as Black, 6% as White, 22% as Hispanic and 14% as others. These children were followed from birth onwards, with an average of 12 ± 5 years of follow-up. The incident rate for food allergy and asthma was 8% and 21%, respectively. The key strengths of this study include its prospective birth cohort design, large sample size, diverse race/ethnicity, comprehensive and high-quality exposure assessment, standardized clinical outcome ascertainment, cutting-edge immune and multi-omics assays. We anticipate that successful completion of the BBC IDeaL study will help identify important early life risk and protective factors, along with novel biomarkers for prediction or therapeutic targets. Ultimately, the expected findings may contribute to identification of high-risk newborns and can inform effective interventions during the earliest developmental windows when they may have the greatest lifelong benefit.

Indexed as

Allergic diseasesAsthmaEnvironmental exposureImmune developmentPhIP-SeqProspective Birth Cohort Study

Identifiers

PMID41425477
PMCPMC12716885

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.