Evidence map›Paper›PMID 40781296›Full record

Trial reportBMC pregnancy and childbirth2025

Maternal phthalate exposure, gestational length, and preterm birth risk: a prospective cohort study nested within a randomised trial.

Karen P Best, Lisa N Yelland, Liu Ge, Zumin Shi, Shalem Leemaqz, Robert Gibson, Maria Makrides, Philippa Middleton

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in BMC pregnancy and childbirth, 2025. 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

8 authors.

Karen P BestSAHMRI Women and Kids, South Australian Health and Medical Research Institute, North Adelaide, South Australia. karen.best@sahmri.com.
Lisa N YellandSAHMRI Women and Kids, South Australian Health and Medical Research Institute, North Adelaide, South Australia.
Liu GeSAHMRI Women and Kids, South Australian Health and Medical Research Institute, North Adelaide, South Australia.
Zumin ShiDepartment of Nutrition Sciences, College of Health Sciences, Qatar University, Doha, Qatar.
Shalem LeemaqzSAHMRI Women and Kids, South Australian Health and Medical Research Institute, North Adelaide, South Australia.
Robert GibsonSAHMRI Women and Kids, South Australian Health and Medical Research Institute, North Adelaide, South Australia.
Maria MakridesSAHMRI Women and Kids, South Australian Health and Medical Research Institute, North Adelaide, South Australia.
Philippa MiddletonSAHMRI Women and Kids, South Australian Health and Medical Research Institute, North Adelaide, South Australia.

Funding

National Health and Medical Research Council APP1135155Women's and Children's Hospital Foundation MS McLeod Research Fund Postdoctoral FellowshipWomen's and Children's Hospital Foundation Research Project Grant
6 · The paper itself

Abstract

backgroundPreterm birth (< 37 weeks gestation) is a leading cause of infant morbidity and mortality, yet the underlying causes remain unknown in many cases. Environmental exposures, including endocrine-disrupting chemicals such as phthalates, have been implicated in preterm birth risk. Phthalates are commonly used as plasticisers in consumer products, resulting in widespread human exposure. While some studies suggest an association between maternal phthalate exposure and reduced gestational length, findings remain inconsistent. This study aimed to investigate the relationship between urinary phthalate metabolite concentrations and gestational length in an Australian pregnancy cohort.

methodsThis prospective cohort study was nested within the Omega-3 to Reduce the Incidence of Prematurity (ORIP) trial. A total of 605 women with singleton pregnancies from South Australia provided urine samples between 22- and 26-weeks' gestation for phthalate metabolite analysis. Thirteen phthalate metabolites were quantified using liquid chromatography-tandem mass spectrometry. Gestational age at birth was determined from medical records. Linear regression models assessed associations between phthalate concentrations and gestational length, adjusting for maternal characteristics including age, BMI, socioeconomic status, education, smoking, and alcohol consumption.

resultsPhthalate metabolites were detected in > 99% of urine samples, with the highest concentrations observed for mono-ethyl phthalate (MEP), mono-isobutyl phthalate (MiBP), and mono-butyl phthalate (MBP). There was no evidence of an association between phthalate exposure and gestational length in either unadjusted or adjusted analyses. No significant association was found between phthalate exposure and preterm birth risk.

conclusionsDespite widespread phthalate exposure, no clear link was identified between maternal phthalate levels and shortened gestation in this Australian cohort. However, continued surveillance is needed to monitor emerging plasticiser exposures and inform public health policies on maternal and infant health. TRIAL REGISTRATION NUMBER: Australian New Zealand Clinical Trials Registry number, ACTRN12613001142729. Date of registration: 27/09/2013.

Indexed as

Gestational AgeMaternal ExposurePhthalic AcidsPremature BirthAdultFemaleHumansInfant, NewbornPregnancyProspective StudiesRisk FactorsSouth AustraliaYoung Adultphthalic acidPhthalic AcidsEndocrine disrupting chemicalsEnvironmentExposurePhthalatesPregnancyPrematurityPrenatal

Identifiers

PMID40781296
PMCPMC12335031

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.