Journal article
Per- and polyfluoroalkyl substances (PFAS) in early life is associated with childhood intestinal inflammation: analyses of three birth cohorts
Clinical gastroenterology and hepatology
07/10/2026
DOI: 10.1016/j.cgh.2026.07.001
PMID: 42431496
Abstract
Early life exposures shape intestinal and immune development and later risk of inflammatory bowel disease (IBD). Per- and polyfluoroalkyl substances (PFAS), or forever chemicals, are associated with intestinal inflammation and IBD. However, the impact of early life PFAS exposure on later intestinal inflammation is not known.
We conducted untargeted PFAS analyses in early life samples from mother-offspring dyads across three cohorts. These included dried blood spots from offspring (n=84) and cord blood (n=93) from two prospective birth cohorts of mothers with and without IBD in New York, United States, and maternal serum during pregnancy (n=14) from a birth cohort in Mexico City, Mexico. Fecal calprotectin (FC), a biomarker of intestinal inflammation, was measured longitudinally in offspring stool. Covariate-adjusted weighted quantile sum regression models were used to estimate associations between PFAS and FC.
PFAS metabolites were detected across all sample types. Higher levels of PFAS mixtures were associated with higher FC between 1 and 6 years of age in both dried blood spot and cord blood analyses (covariate-adjusted β estimates for change in log-transformed fecal calprotectin at age 6 years per decile increase in the PFAS mixture was 0.44, 95% CI 0.18, 0.70 and 0.69, 95% CI 0.53, 0.85, respectively) Similarly, higher levels of PFAS mixtures in maternal serum were associated with higher FC in late childhood (β 0.19, 95% CI 0.05, 0.33). Compared to mothers-offspring dyads without maternal IBD, those with maternal IBD were more likely to have higher perfluoro-1-octane sulfonamide acetic acid and 3-perfluorohexyl-2-hydroxypropyl acrylate levels in dried blood spots and cord blood, respectively; these PFAS metabolites were also the top contributors to offspring FC.
PFAS chemicals are detectable in early life samples, indicating exposure during this period of vulnerability, and are associated with higher FC in childhood across three birth cohorts.
Details
- Title: Subtitle
- Per- and polyfluoroalkyl substances (PFAS) in early life is associated with childhood intestinal inflammation: analyses of three birth cohorts
- Creators
- Vishal Midya - Icahn School of Medicine at Mount SinaiAmith S Maroli - Icahn School of Medicine at Mount SinaiMellissa Picker - Icahn School of Medicine at Mount SinaiGeorgia Dolios - Icahn School of Medicine at Mount SinaiDamaskini Valvi - Icahn School of Medicine at Mount SinaiIsabella Nguyen - Icahn School of Medicine at Mount SinaiTaegyu Kim - Icahn School of Medicine at Mount SinaiAlexa Rendon - Icahn School of Medicine at Mount SinaiRosemary Chen - Icahn School of Medicine at Mount SinaiKaitlyn Weinstein - Icahn School of Medicine at Mount SinaiHaibin Guan - Icahn School of Medicine at Mount SinaiGary Joseph - Icahn School of Medicine at Mount SinaiJoseph Eggers - University of IowaLibni A Torres-Olascoaga - Instituto Nacional de Salud PúblicaRohitha Ravisekar - Icahn School of Medicine at Mount SinaiBhargavi Srinath - Icahn School of Medicine at Mount SinaiRomana Ranchadiya - Icahn School of Medicine at Mount SinaiSyam S Andra - Icahn School of Medicine at Mount SinaiDavid Achaintre - Icahn School of Medicine at Mount SinaiChris Gennings - Icahn School of Medicine at Mount SinaiMartha M Téllez-Rojo - Instituto Nacional de Salud PúblicaRobert O Wright - Icahn School of Medicine at Mount SinaiManish Arora - Icahn School of Medicine at Mount SinaiMaria José Rosa - Icahn School of Medicine at Mount SinaiMegan Niedzwiecki - Icahn School of Medicine at Mount SinaiJoana Torres - Hospital da LuzCecilia S Alcala - Icahn School of Medicine at Mount SinaiJamil M Lane - Icahn School of Medicine at Mount SinaiShoshannah Eggers - University of IowaJean-Frederic Colombel - Icahn School of Medicine at Mount SinaiInga Peter - Icahn School of Medicine at Mount SinaiLauren Petrick - Sheba Medical CenterManasi Agrawal - Icahn School of Medicine at Mount Sinai
- Resource Type
- Journal article
- Publication Details
- Clinical gastroenterology and hepatology
- DOI
- 10.1016/j.cgh.2026.07.001
- PMID
- 42431496
- NLM abbreviation
- Clin Gastroenterol Hepatol
- ISSN
- 1542-7714
- eISSN
- 1542-7714
- Publisher
- Elsevier
- Language
- English
- Electronic publication date
- 07/10/2026
- Academic Unit
- Epidemiology; Injury Prevention Research Center
- Record Identifier
- 9985180970402771
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