Evidence mapPaperPMID 40132045Full record

ArticleThe Journal of clinical endocrinology and metabolism2025

Prenatal Concentrations of Perfluoroalkyl Substances and Maternal Beta Cell Function at 7 to 9 Years of Follow-Up.

Jana Palaniyandi, Jennifer E Bruin, Mandy Fisher, Michael M Borghese, Myriam P Hoyeck, Constadina Panagiotopoulos, Jillian Ashley-Martin

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Article in The Journal of clinical endocrinology and metabolism, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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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

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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.

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4 · The record

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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

7 authors.

Jana PalaniyandiDepartment of Biology and Institute of Biochemistry, Carleton University, Ottawa, ON, Canada K1S 5B6.ORCID 0009-0005-3956-553X
Jennifer E BruinDepartment of Biology and Institute of Biochemistry, Carleton University, Ottawa, ON, Canada K1S 5B6.ORCID 0000-0003-2326-7819
Mandy FisherEnvironmental Health Science and Research Bureau, Health Canada, Ottawa, ON, Canada K1A 0K9.ORCID 0000-0003-4656-3813
Michael M BorgheseEnvironmental Health Science and Research Bureau, Health Canada, Ottawa, ON, Canada K1A 0K9.ORCID 0000-0003-0007-1565
Myriam P HoyeckDepartment of Biology and Institute of Biochemistry, Carleton University, Ottawa, ON, Canada K1S 5B6.ORCID 0000-0003-4021-5770
Constadina PanagiotopoulosDepartment of Pediatrics, University of British Columbia, and BC Children's Hospital, Vancouver, BC, Canada V6H 3V4.ORCID 0000-0002-1379-7472
Jillian Ashley-MartinEnvironmental Health Science and Research Bureau, Health Canada, Ottawa, ON, Canada K1A 0K9.ORCID 0000-0001-9958-7531

Funding

BC Children's Hospital FoundationBC Children's Hospital Research InstituteCanadian Institutes for Health Research (CIHR) MOP-81285CIHR Canadian Graduate Scholarship-DoctorateCIHR Project PJT-186282Guiding interdisciplinary ResearchHealth Canada Chemicals Management PlanOntario Early ResearcherOntario Graduate ScholarshipOntario Ministry of the Environment
6 · The paper itself

Abstract

contextEpidemiological evidence regarding prenatal per- and polyfluoroalkyl substance (PFAS) exposure and long-term maternal metabolic health outcomes is lacking.

objectiveQuantify associations between prenatal PFAS concentrations and maternal metabolic biomarkers of glucose homeostasis 7 to 9 years later.

methodsWe measured second trimester plasma concentrations of 9 PFAS in participants enrolled in the Maternal-Infant Research on Environmental Chemicals (MIREC) study. We measured individual biomarkers of glucose homeostasis (fasting intact proinsulin, C-peptide, insulin, glucose, and hemoglobin A1C levels) in samples collected 7 to 9 years after the MIREC pregnancy (n = 258) and derived indicators of pancreatic beta cell function (proinsulin to insulin [PI:INS], proinsulin to C-peptide [PI:CP] ratios) and insulin resistance (homeostatic model assessment for insulin resistance [HOMA-IR], triglyceride-glucose index). Using multivariable linear regression models, we quantified the percent change in each outcome per doubling of individual PFAS concentrations. We used quantile g-computation and weighted quantile sum regression to evaluate the mixture of PFAS.

resultsPrenatal perfluorononanoic acid and perfluorodecanoic acid concentrations were associated with 13.9% (95% CI: 0.8, 28.8) and 10.5% (95% CI: -1.0, 23.4) higher HOMA-IR values as well as 11.9% (95% CI: 0.1, 25.1) and 8.9% (95% CI: -1.5, 20.3) higher fasting insulin concentrations, respectively. A doubling of perfluorooctanoic acid concentrations was associated with increases in intact proinsulin concentrations (12.8% [95% CI: -3.5, 31.8]) and beta cell function ratios (PI:INS: 11.5% [95% CI: -4.4, 30.1]; PI:CP: 13.5% [95% CI: -2.4, 32.0]).

conclusionPrenatal exposure to PFAS may impact long-term maternal insulin resistance and beta cell function, key risk factors for type 2 diabetes. These associations differ by specific PFAS.

Indexed as

Environmental PollutantsFluorocarbonsInsulin-Secreting CellsMaternal ExposurePrenatal Exposure Delayed EffectsAdultBiomarkersBlood GlucoseCaprylatesChildFemaleFollow-Up StudiesHumansInsulinInsulin ResistancePregnancyBiomarkersBlood GlucoseCaprylatesEnvironmental PollutantsFluorocarbonsInsulinperfluorooctanoic acidbiomarkersfluorocarbonsinsulin resistancemetabolismpostpartumpregnancy

Identifiers

PMID40132045
PMCPMC12972668

What Socratic holds

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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.