Evidence map›Paper›PMID 39341532›Full record

ArticleEnvironmental research2024

An evaluation of in utero polycyclic aromatic hydrocarbon exposure on the neonatal meconium microbiome.

Divya Keerthy, Miranda J Spratlen, Lingsheng Wen, Dwayne Seeram, Heekuk Park, Lehyla Calero, Anne-Catrin Uhlemann, Julie B Herbstman

Abstract read
In one paragraph

Article in Environmental research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
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.

Divya KeerthyNeonatal and Perinatal Medicine, Columbia University, New York, NY, United States; Neonatal and Perinatal Medicine, NewYork Presbyterian Queens, Flushing, NY, United States. Electronic address: divyarky@gmail.com.
Miranda J SpratlenDepartment of Environmental Health Sciences, Mailman School of Public Health, Columbia University, New York, NY, United States.
Lingsheng WenDivision of Infectious Diseases, Columbia University, New York, NY, United States.
Dwayne SeeramDivision of Infectious Diseases, Columbia University, New York, NY, United States.
Heekuk ParkDivision of Infectious Diseases, Columbia University, New York, NY, United States.
Lehyla CaleroDepartment of Environmental Health Sciences, Mailman School of Public Health, Columbia University, New York, NY, United States.
Anne-Catrin UhlemannDivision of Infectious Diseases, Columbia University, New York, NY, United States.
Julie B HerbstmanDepartment of Environmental Health Sciences, Mailman School of Public Health, Columbia University, New York, NY, United States.

Funding

True Metal fac coreP30ES009089 · NIEHS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Steven N. Chillrud · 1998 to 2026
$44.7M
Not whether but how: The ethics of reporting individual results in a pregnancy cohort.UH3OD023290 · OD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Julie Beth Herbstman, AMY MARGOLIS · 2018 to 2026
$18.8M
To Maintain and Enrich Resource Infrastructure for Existing Environmental Epidemiology CohortsR24ES029489 · NIEHS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Julie Beth Herbstman, Marcela Tamayo-Ortiz · 2020 to 2026
$2.3M
NIEHS NIH HHS P30 ES009089NIEHS NIH HHS R24 ES029489NIH HHS UH3 OD023290
6 · The paper itself

Abstract

introductionIn utero exposure to environmental polycyclic aromatic hydrocarbon (PAH) is associated with neurodevelopmental impairments[1-8], prematurity[9-12] and low birthweight[9,13-15]. The gut microbiome serves as an intermediary between self and external environment; therefore, exploring the impact of PAH on microbiota may elucidate their role in disease. Here, we evaluated the effect of in utero PAH exposure on meconium microbiome.

methodsWe evaluated 49 mother-child dyads within Fair Start Birth Cohort with full term delivery and adequate meconium sampling. Prenatal PAH was measured using personal active samplers worn for 48 h during third trimester. Post-processing, 35 samples with adequate biomass were evaluated for association between tertile of PAH exposure (high (H) vs low/medium (L/M)) and microbiome diversity.

resultsNo significant differences were observed in alpha diversity metrics, Chao1 and Shannon index, between exposure groups for total PAH. However, alpha diversity metrics were negatively associated with log benzo[a]anthracene (BaA) and log chrysene (Chry) with high exposure, but positively associated with log benzo[a]pyrene (BaP) with low/medium exposure. After adjustment for birthweight and sex, alpha diversity metrics were negatively associated with log BaA, BaP, Chry, Indeno (Zhang et al., 2021; Perera et al., 2018)pyrene (IcdP) and total PAH with high exposure. Conversely, with low/medium exposure, alpha diversity metrics positively correlated with log BaP and benzo[b]fluoranthane (BbF). No significant difference in beta diversity was observed across groups using UniFrac, weighted UniFrac, or Bray-Curtis methods. Differential expression analysis showed differentially abundant taxa between exposure groups.

conclusionBacterial taxa were detectable in 35/49 (71%) meconium samples. Altered alpha diversity metrics and differentially abundant taxa between groups suggest in utero PAH exposure may impede early colonization. Sample size is limited, but these findings provide supporting evidence for wider scale research. Research on long-term impact of prenatal PAH exposure on childhood health outcomes is ongoing. Differential effects of specific PAHs need further evaluation.

Indexed as

Maternal ExposureMeconiumPolycyclic Aromatic HydrocarbonsAdultEnvironmental PollutantsFemaleGastrointestinal MicrobiomeHumansInfant, NewbornMaleMicrobiotaPregnancyPrenatal Exposure Delayed EffectsYoung AdultEnvironmental PollutantsPolycyclic Aromatic HydrocarbonsAir pollutantsAir pollutionMeconium microbiomeNeonatalPolycyclic aromatic hydrocarbonPrenatal exposure

Identifiers

PMID39341532
PMCPMC11816390

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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 OpenQuestion graph.