Evidence map›Paper›PMID 42881263›Full record

ArticlePediatric research2026

PFAS exposure in 12-year-old children and its association with metabolic markers.

Naomi Lejeune, Elke Rouxel, Christine Monfort, Hélène Tillaut, Corentin Goxe, Florence Rouget, Frank Giton, Éric Gaudreau, Fabrice Lainé, Ronan Garlantézec and 3 more

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

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Naomi LejeuneInstitut de recherche en santé, environnement et travail (Irset), Inserm, EHESP, University of Rennes, Rennes, France. naomi.lejeune@inserm.fr.
Elke RouxelInstitut de recherche en santé, environnement et travail (Irset), Inserm, EHESP, University of Rennes, Rennes, France.
Christine MonfortInstitut de recherche en santé, environnement et travail (Irset), Inserm, EHESP, University of Rennes, Rennes, France.
Hélène TillautInstitut de recherche en santé, environnement et travail (Irset), Inserm, EHESP, University of Rennes, Rennes, France.
Corentin GoxeInstitut de recherche en santé, environnement et travail (Irset), Inserm, EHESP, University of Rennes, Rennes, France.
Florence RougetCHU Rennes, Inserm UMR S 1085, Irset, Université de Rennes, Rennes, France.
Frank GitonAP-HP, Pôle Biologie-Pathologie Henri Mondor, Inserm, IMRB, Créteil, France.
Éric GaudreauCentre de Toxicologie du Québec (CTQ), Institut national de santé publique du Québec (INSPQ), Québec City, QC, Canada.
Fabrice LainéCentre d'Investigation Clinique CHU-Rennes (CIC 1414), CHU Rennes, Institut National de la Santé et de la Recherche Médicale, Inserm, Rennes, France.
Ronan GarlantézecCHU Rennes, Inserm UMR S 1085, Irset, Université de Rennes, Rennes, France.
Sylvaine CordierInstitut de recherche en santé, environnement et travail (Irset), Inserm, EHESP, University of Rennes, Rennes, France.
Cécile ChevrierInstitut de recherche en santé, environnement et travail (Irset), Inserm, EHESP, University of Rennes, Rennes, France.
Charline WarembourgInstitut de recherche en santé, environnement et travail (Irset), Inserm, EHESP, University of Rennes, Rennes, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPer- and polyfluoroalkyl substances (PFAS) are long-lasting industrial chemicals with widespread exposure, but their effects on adolescent cardiometabolic health remain underexplored. This cross-sectional study evaluated associations between PFAS concentrations and metabolic biomarkers at age 12.

methodsThe study included 451 participants from the French PELAGIE mother-child cohort. At age 12, serum levels of six PFAS and metabolic biomarkers (leptin, adiponectin, fructosamine, total cholesterol, LDL, HDL, triglycerides) were measured. Cross-sectional associations were assessed using multivariable linear regression models and Quantile G-computation mixture models, adjusted for potential confounders and stratified by sex and pubertal stage.

resultsIn the overall population, perfluoroundecanoic acid (PFUdA) was associated with higher total cholesterol and LDL cholesterol levels. In pre-menarcheal girls, perfluorohexane sulfonate (PFHxS) was associated with higher total cholesterol and LDL cholesterol levels, and PFAS mixture analyses also showed positive associations with these lipid markers. In boys, perfluorononanoic acid (PFNA) and perfluorodecanoic acid (PFDA) were associated with higher triglyceride levels in peripubertal boys, whereas perfluorooctane sulfonate (PFOS) was associated with lower triglyceride levels in postpubertal boys.

conclusionFindings indicate potential associations between PFAS exposure and metabolic biomarkers at age 12, with variations by sex and pubertal status, emphasizing the need for longitudinal investigations. IMPACT: PFAS were detected in all serum samples, showing widespread exposure among the adolescents. Exposure to PFAS was associated with blood lipid markers at age 12, with differences in associations observed across sex- and pubertal stage-specific groups. This study is one of the few to consider the stage of pubertal development in the associations between PFAS and metabolic health markers. The findings suggest that pubertal development should be considered when evaluating the health effects of PFAS exposure during adolescence.

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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.