Evidence mapPaperPMID 41275763Full record

ArticleEnvironment international2025

Association of in utero exposure to phthalate and DINCH metabolites with placental DNA methylation.

Hana Vespalcova, Bethany Knox, Amrit Kaur Sakhi, Cathrine Thomsen, Sofía Aguilar-Lacasaña, Marta Cosin-Tomas, Laura Gómez-Herrera, Olga Sánchez García, Elisa Llurba, María Dolores Gómez-Roig and 4 more

Abstract read
In one paragraph

Article in Environment international, 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. 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

14 authors.

Hana VespalcovaISGlobal, Barcelona, Spain; Universitat Pompeu Fabra (UPF), Barcelona, Spain. Electronic address: hana.vespalcova@isglobal.org.
Bethany KnoxISGlobal, Barcelona, Spain; Universitat Pompeu Fabra (UPF), Barcelona, Spain; CIBER Epidemiología y Salud Pública (CIBERESP), Madrid, Spain.
Amrit Kaur SakhiDepartment of Food Safety, Norwegian Institute of Public Health, Oslo, Norway.
Cathrine ThomsenDepartment of Food Safety, Norwegian Institute of Public Health, Oslo, Norway.
Sofía Aguilar-LacasañaISGlobal, Barcelona, Spain; Universitat Pompeu Fabra (UPF), Barcelona, Spain; CIBER Epidemiología y Salud Pública (CIBERESP), Madrid, Spain.
Marta Cosin-TomasISGlobal, Barcelona, Spain; Universitat Pompeu Fabra (UPF), Barcelona, Spain; CIBER Epidemiología y Salud Pública (CIBERESP), Madrid, Spain.
Laura Gómez-HerreraISGlobal, Barcelona, Spain; CIBER Epidemiología y Salud Pública (CIBERESP), Madrid, Spain; Facultat de Medicina, Universitat de Barcelona (UB), Barcelona, Spain.
Olga Sánchez GarcíaDepartment of Obstetrics and Gynaecology, Institut de Recerca (IR SANT PAU). Hospital de la Santa Creu i Sant Pau, Barcelona, Spain; Primary Care Interventions to Prevent Maternal and Child Chronic Diseases of Perinatal and Developmental Origin Network (RICORS-SAMID), RD21/0012/0001, Instituto de Salud Carlos III, Madrid, Spain.
Elisa LlurbaDepartment of Obstetrics and Gynaecology, Institut de Recerca (IR SANT PAU). Hospital de la Santa Creu i Sant Pau, Barcelona, Spain; Primary Care Interventions to Prevent Maternal and Child Chronic Diseases of Perinatal and Developmental Origin Network (RICORS-SAMID), RD21/0012/0001, Instituto de Salud Carlos III, Madrid, Spain.
María Dolores Gómez-RoigBCNatal, Fetal Medicine Research Center, Hospital Sant Joan de Déu and Hospital Clínic, University of Barcelona, Barcelona, Spain; Primary Care Interventions to Prevent Maternal and Child Chronic Diseases of Perinatal and Developmental Origin Network (RICORS-SAMID), RD21/0012/0003, Instituto de Salud Carlos III, Madrid, Spain; Institut de Recerca Sant Joan de Déu, Barcelona, Spain.
Jordi SunyerISGlobal, Barcelona, Spain; Universitat Pompeu Fabra (UPF), Barcelona, Spain; CIBER Epidemiología y Salud Pública (CIBERESP), Madrid, Spain; IMIM (Hospital del Mar Medical Research Institute), Barcelona, Catalonia, Spain.
Payam DadvandISGlobal, Barcelona, Spain; Universitat Pompeu Fabra (UPF), Barcelona, Spain; CIBER Epidemiología y Salud Pública (CIBERESP), Madrid, Spain.
Mariona BustamanteISGlobal, Barcelona, Spain; Universitat Pompeu Fabra (UPF), Barcelona, Spain; CIBER Epidemiología y Salud Pública (CIBERESP), Madrid, Spain. Electronic address: mariona.bustamante@isglobal.org.
Martine VrijheidISGlobal, Barcelona, Spain; Universitat Pompeu Fabra (UPF), Barcelona, Spain; CIBER Epidemiología y Salud Pública (CIBERESP), Madrid, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Phthalates and DINCH are non-persistent chemicals widely used in consumer products. In utero exposure to these compounds has been linked to adverse reproductive and long-term health outcomes, potentially through epigenetic changes in the placenta. This study investigated associations between maternal phthalate and DINCH metabolite levels and placental DNA methylation in 469 mother-child pairs from the Barcelona Life Study Cohort (BiSC). Fifteen phthalate and two DINCH metabolites were measured in pooled maternal urine samples collected at 19 and 35 weeks of gestation using liquid chromatography-tandem mass spectrometry (LC-MS/MS. Placental DNA methylation was assessed using the Illumina EPIC array. We applied robust linear regression models to test associations between single exposures at 19 weeks, 35 weeks, and whole pregnancy (average of the two time points), with each CpG site. In secondary analyses, quantile g-computation was used to test associations between exposure mixtures and suggestive CpGs (p-value < 1E-05). We identified 38 Bonferroni significant associations in the single exposure models (p-value < 1E-07)- 24 at 19 weeks, 8 at 35 weeks and 6 for the whole pregnancy period. Suggestive CpGs (p-value < 1E-05) were annotated to genes involved in metabolic, immune and vascular pathways, steroid biosynthesis, and sex hormone signaling. Sex-stratified analyses revealed 49 female-specific and 42 male-specific associations, most of which were identified at a single time point. Mixture analyses revealed 20 significant associations, all consistent in direction with the single-metabolite models. These results suggest that prenatal exposure to phthalates and DINCH may contribute to placental epigenetic alterations supporting a role for endocrine disruption, metabolism, and vascular and immune modulation in mediating their effects.

Indexed as

DNA MethylationEnvironmental PollutantsMaternal ExposurePhthalic AcidsPlacentaAdultFemaleHumansMalePregnancyEnvironmental Pollutantsphthalic acidPhthalic AcidsDINCHEndocrine disruptorEpigenome-wide association study (EWAS)Phthalate metabolitesPlacental DNA methylationPregnancySex-specific

Identifiers

PMID41275763
PMCPMC12696147

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.