ArticlePrecision nutrition2025
Integrating Exposures and Multi-Omics in the Boston Birth Cohort to Elucidate Immune Development across the Life Course: Rationale and Study Design.
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.
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.
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.
Who cites it
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
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
Identifiers
41425477PMC12716885What Socratic holds
Registered trials
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.