Evidence map›Paper›PMID 42852388›Full record

ArticleEnvironmental health perspectives2026

Associations of Urinary Triclosan Concentrations Across Gestation and Childhood with the Adolescent Gut Microbiome.

Hannah E Laue, Abby F Fleisch, Antonia M Calafat, Bruce P Lanphear, Kim M Cecil, Kimberly Yolton, Jessie P Buckley, Margaret R Karagas, Juliette C Madan, Amy D Willis and 1 more

Abstract read
In one paragraph

Article in Environmental health perspectives, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

11 authors.

Hannah E LaueDepartment of Biostatistics & Epidemiology, University of Massachusetts Amherst School of Public Health and Health Sciences, Amherst, Massachusetts 01003, United States.ORCID https://orcid.org/0000-0002-2578-103X
Abby F FleischCenter for Interdisciplinary and Population Health Research, Maine Institute for Research, Westbrook, Maine 04092, United States.
Antonia M CalafatDivision of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, Georgia 30329, United States.
Bruce P LanphearFaculty of Health Sciences, Simon Fraser University, Vancouver V5A 1S6, Canada.
Kim M CecilDepartment of Radiology, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio 45267, United States.
Kimberly YoltonDepartment of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio 45267, United States.
Jessie P BuckleyDepartment of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States.ORCID https://orcid.org/0000-0001-7976-0157
Margaret R KaragasDepartment of Epidemiology, Dartmouth Geisel School of Medicine, Hanover, New Hampshire 03755, United States.
Juliette C MadanDepartment of Epidemiology, Dartmouth Geisel School of Medicine, Hanover, New Hampshire 03755, United States.
Amy D WillisDepartment of Biostatistics, University of Washington Hans Rosling Center for Population Health, Seattle, Washington 98195, United States.
Joseph M BraunDepartment of Epidemiology, Brown University, Providence, Rhode Island 02912, United States.ORCID https://orcid.org/0000-0002-5239-3235

Funding

LCenter for Clinical and Translational Science and TrainingUL1TR001425 · NCATS · UNIVERSITY OF CINCINNATI · PI HEUBI, JAMES E., KISSELA, BRETT M · 2015 to 2024
$37.5M
Study of Prevalent Neurotoxicants in ChildrenP01ES011261 · NIEHS · CINCINNATI CHILDRENS HOSP MED CTR · PI LANPHEAR, BRUCE P · 2001 to 2006
$6.4M
Early life perfluoroalkyl substance exposure & obesity: Mechanisms & phenotypingR01ES025214 · NIEHS · BROWN UNIVERSITY · PI BRAUN, JOSEPH M · 2016 to 2020
$3.1M
A Community-Based Trial to Prevent Lead Poisoning and InjuriesR01ES014575 · NIEHS · CINCINNATI CHILDRENS HOSP MED CTR · PI YOLTON, KIMBERLY · 2007 to 2011
$2.9M
Longitudinal study of exposure to PBDEs and PFCs and child neurobehaviorR01ES020349 · NIEHS · UNIVERSITY OF CINCINNATI · PI CHEN, AIMIN, LANPHEAR, BRUCE P · 2011 to 2015
$2.9M
Statistical methods to enhance reproducible microbiome discoveryR35GM133420 · NIGMS · UNIVERSITY OF WASHINGTON · PI Amy D Willis · 2019 to 2026
$2.8M
Endocrine Disrupting Chemicals, Thyroid Hormones, and Child NeurobehaviorR01ES024381 · NIEHS · BROWN UNIVERSITY · PI BRAUN, JOSEPH M · 2015 to 2018
$2.4M
Triclosan, pubertal hormones, and the gut microbiome: implications for neurobehaviorR00ES034086 · NIEHS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI LAUE, HANNAH ELIZABETH · 2024 to 2025
$743k
Triclosan, pubertal hormones, and the gut microbiome: implications for neurobehaviorK99ES034086 · NIEHS · DARTMOUTH COLLEGE · PI LAUE, HANNAH ELIZABETH · 2023 to 2024
$220k
NCATS NIH HHS UL1 TR001425NIEHS NIH HHS K99 ES034086NIEHS NIH HHS P01 ES011261NIEHS NIH HHS R00 ES034086NIEHS NIH HHS R01 ES014575NIEHS NIH HHS R01 ES020349NIEHS NIH HHS R01 ES024381NIEHS NIH HHS R01 ES025214NIGMS NIH HHS R35 GM133420
6 · The paper itself

Abstract

Research on the influence of repeated exposure to antimicrobial chemicals, such as triclosan, on the microbiome is lacking. The goal of this study was to elucidate the associations of time-varying urinary triclosan concentrations with the adolescent gut microbiome. We used data from a prospective cohort based in Cincinnati, OH (enrolled 2003-2006, n = 146), to assess the time-varying associations of urinary triclosan concentrations with adolescent (age ∼ 12 years) gut microbiome diversity and composition. Individuals ≥ 18-years-old were recruited during the second trimester of pregnancy, and urinary triclosan concentrations were measured in pregnant women up to 2 times in pregnancy and up to 7 times in the child from ages 1 through 12 years. At age ∼ 12 years, fecal microbiome diversity and composition was characterized with metagenomic sequencing. We estimated differences in the relative abundance of prevalent (≥50%) bacterial species and gene pathways using linear regression and generalized estimating equations to assess windows of heightened susceptibility adjusted for sociodemographic characteristics. Additionally, we examined sex-specific associations by including an interaction term. The adolescent median Shannon diversity was 3.5 (IQR: 3.3, 3.5). Higher gestational triclosan concentrations with lower gut microbiome diversity [β = -0.13 per 10-fold increase (95%CI: -0.24, -0.02)]. Triclosan concentrations were also positively associated with higher abundance of antibiotic resistance genes and differential abundance of some bacterial species, with the strongest associations observed in early life and at age 12 years. We also found differences depending on sex, with more significant associations observed among males. Our findings provide insight into windows of triclosan exposure that are relevant to gut microbiome composition and the impacts of antimicrobial agents.

Indexed as

Anti-Infective Agents, LocalGastrointestinal MicrobiomeTriclosanAdolescentChildChild, PreschoolFecesFemaleHumansInfantMaleOhioPregnancyProspective StudiesAnti-Infective Agents, LocalTriclosan

Identifiers

PMID42852388
PMCPMC13648101

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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.