Evidence map›Paper›PMID 39177951›Full record

ArticleEnvironmental health perspectives2024

Exposure of

Katherine Roth, Zhao Yang, Manisha Agarwal, Johnna Birbeck, Judy Westrick, Todd Lydic, Katherine Gurdziel, Michael C Petriello

Abstract read
In one paragraph

Article in Environmental health perspectives, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Synergistic toxicity in alcohol-associated liver disease and PFAS exposure.Toxicological sciences : an official journal of the Society of Toxicology · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Article
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.

Katherine RothInstitute of Environmental Health Sciences, Wayne State University, Detroit, Michigan, USA.
Zhao YangInstitute of Environmental Health Sciences, Wayne State University, Detroit, Michigan, USA.
Manisha AgarwalDepartment of Pharmacology, School of Medicine, Wayne State University, Detroit, Michigan, USA.
Johnna BirbeckDepartment of Chemistry, Lumigen Instrumentation Center, Wayne State University, Detroit, Michigan, USA.
Judy WestrickDepartment of Chemistry, Lumigen Instrumentation Center, Wayne State University, Detroit, Michigan, USA.
Todd LydicDepartment of Physiology, Michigan State University, East Lansing, Michigan, USA.
Katherine GurdzielInstitute of Environmental Health Sciences, Wayne State University, Detroit, Michigan, USA.
Michael C PetrielloInstitute of Environmental Health Sciences, Wayne State University, Detroit, Michigan, USA.

Funding

Research Experience & Training Coordination CoreP42ES030991 · NIEHS · WAYNE STATE UNIVERSITY · PI Glen Ray Hood · 2022 to 2026
$13.9M
Pilot Project ProgramP30ES020957 · NIEHS · WAYNE STATE UNIVERSITY · PI PARKER, GRAHAM C · 2014 to 2021
$10.1M
Translational Research Support CoreP30ES036084 · NIEHS · WAYNE STATE UNIVERSITY · PI Melissa A Runge-Morris · 2024 to 2026
$5.2M
PFAS accelerate atherosclerosis through modulation of bile acid metabolismR01ES034407 · NIEHS · WAYNE STATE UNIVERSITY · PI Michael Curtis Petriello · 2023 to 2026
$2.3M
Exposure to PFAS mixture induces atherosclerosis via modulation of bile acid transportF32ES034638 · NIEHS · WAYNE STATE UNIVERSITY · PI ROTH, KATHERINE · 2023 to 2024
$151k
NIEHS NIH HHS F32 ES034638NIEHS NIH HHS P30 ES020957NIEHS NIH HHS P30 ES036084NIEHS NIH HHS P42 ES030991NIEHS NIH HHS R01 ES034407
6 · The paper itself

Abstract

backgroundPrevious epidemiological studies have repeatedly found per- and polyfluoroalkyl substances (PFAS) exposure associated with higher circulating cholesterol, one of the greatest risk factors for development of coronary artery disease. The main route of cholesterol catabolism is through its conversion to bile acids, which circulate between the liver and ileum via enterohepatic circulation. Patients with coronary artery disease have decreased bile acid excretion, indicating that PFAS-induced impacts on enterohepatic circulation may play a critical role in cardiovascular risk.

objectivesUsing a mouse model with high levels of low-density and very low-density lipoprotein (LDL and VLDL, respectively) cholesterol and aortic lesion development similar to humans, the present study investigated mechanisms linking exposure to a PFAS mixture with increased cholesterol.

methodsMale and female

resultsAfter 7 wk of PFAS exposure, average circulating PFAS levels were measured at 21.6, 20.1, 31.2, 23.5, and DISCUSSION: Mice exposed to a PFAS mixture displayed higher circulating cholesterol and bile acids perhaps due to impacts on enterohepatic circulation. This study implicates PFAS-mediated effects at the site of the ileum as a possible critical mediator of increased cardiovascular risk following PFAS exposure. https://doi.org/10.1289/EHP14339.

Indexed as

Bile Acids and SaltsFluorocarbonsAlkanesulfonic AcidsAnimalsCholesterolEnvironmental PollutantsFemaleLipidsMaleMiceReceptors, LDLAlkanesulfonic AcidsBile Acids and SaltsCholesterolEnvironmental PollutantsFluorocarbonsLipidsReceptors, LDL

Identifiers

PMID39177951
PMCPMC11343043

What OpenQuestion holds

Textmetadata
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.