Evidence map›Paper›PMID 38072180›Full record

ArticleToxicology in vitro : an international journal published in association with BIBRA2024

In vitro screening of per- and polyfluorinated substances (PFAS) for interference with seven thyroid hormone system targets across nine assays.

Sigmund J Degitz, Jennifer H Olker, Jeffery S Denny, Philip P Degoey, Phillip C Hartig, Mary C Cardon, Stephanie A Eytcheson, Jonathan T Haselman, Sally A Mayasich, Michael W Hornung

Open access · greenAbstract read
In one paragraph

Article in Toxicology in vitro : an international journal published in association with BIBRA, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.5field-weighted citation impact, top 5% of its field
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

15 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Article
  3. PFAS Alter Thyroid Histology and Cellular SignalingJournal of the Endocrine Society · 2026
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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

10 authors at 2 institutions in 1 country.

Sigmund J DegitzUS Environmental Protection Agency, Office of Research and Development, Center for Computational Toxicology and Exposure (CCTE), Great Lakes Toxicology and Ecology Division (GLTED), Duluth, MN 55804, USA. Electronic address: degitz.sigmund@epa.gov.
Jennifer H OlkerUS Environmental Protection Agency, Office of Research and Development, Center for Computational Toxicology and Exposure (CCTE), Great Lakes Toxicology and Ecology Division (GLTED), Duluth, MN 55804, USA.
Jeffery S DennyUS Environmental Protection Agency, Office of Research and Development, Center for Computational Toxicology and Exposure (CCTE), Great Lakes Toxicology and Ecology Division (GLTED), Duluth, MN 55804, USA.
Philip P DegoeyUS Environmental Protection Agency, Office of Research and Development, Center for Computational Toxicology and Exposure (CCTE), Great Lakes Toxicology and Ecology Division (GLTED), Duluth, MN 55804, USA.
Phillip C HartigUS Environmental Protection Agency, Office of Research and Development Center for Public Health and Environmental Assessment, Public Health and Integrated Toxicology Division, Research Triangle Park, NC 27709, USA.
Mary C CardonUS Environmental Protection Agency, Office of Research and Development Center for Public Health and Environmental Assessment, Public Health and Integrated Toxicology Division, Research Triangle Park, NC 27709, USA.
Stephanie A EytchesonUS Environmental Protection Agency, Office of Research and Development, Center for Computational Toxicology and Exposure (CCTE), Great Lakes Toxicology and Ecology Division (GLTED), Duluth, MN 55804, USA; Oak Ridge Institute for Science and Education, Oak Ridge, TN, USA.
Jonathan T HaselmanUS Environmental Protection Agency, Office of Research and Development, Center for Computational Toxicology and Exposure (CCTE), Great Lakes Toxicology and Ecology Division (GLTED), Duluth, MN 55804, USA.
Sally A MayasichUS Environmental Protection Agency, Office of Research and Development, Center for Computational Toxicology and Exposure (CCTE), Great Lakes Toxicology and Ecology Division (GLTED), Duluth, MN 55804, USA; Oak Ridge Institute for Science and Education, Oak Ridge, TN, USA.
Michael W HornungUS Environmental Protection Agency, Office of Research and Development, Center for Computational Toxicology and Exposure (CCTE), Great Lakes Toxicology and Ecology Division (GLTED), Duluth, MN 55804, USA.
Environmental Protection Agency · USOak Ridge Associated Universities · US

Funding

Intramural EPA EPA999999
6 · The paper itself

Abstract

The US Environmental Protection Agency is evaluating the ecological and toxicological effects of per- and polyfluorinated chemicals. A number of perfluorinated chemicals have been shown to impact the thyroid axis in vivo suggesting that the thyroid hormone system is a target of these chemicals. The objective of this study was to evaluate the activity of 136 perfluorinated chemicals at seven key molecular initiating events (MIE) within the thyroid axis using nine in vitro assays. The potential MIE targets investigated are Human Iodothyronine Deiodinase 1 (hDIO1), Human Iodothyronine Deiodinase 2 (hDIO2), Human Iodothyronine Deiodinase 3 (hDIO3), Xenopus Iodothyronine Deiodinase (xDIO3); Human Iodotyrosine Deiodinase (hIYD), Xenopus Iodotyrosine Deiodinase (xIYD), Human Thyroid Peroxidase (hTPO); and the serum binding proteins Human Transthyretin (hTTR) and Human Thyroxine Binding Globulin (hTBG). Of the 136 PFAS chemicals tested, 85 had sufficient activity to produce a half-maximal effect concentration (EC50) in at least one of the nine assays. In general, most of these PFAS chemicals did not have strong potency towards the seven MIEs examined, apart from transthyretin binding, for which several PFAS had potency similar to the respective model inhibitor. These data sets identify potentially active PFAS chemicals to prioritize for further testing in orthogonal in vitro assays and at higher levels of biological organization to evaluate their capacity for altering the thyroid hormone system and causing potential adverse health and ecological effects.

Indexed as

FluorocarbonsPrealbuminHumansIodide PeroxidaseThyroid GlandThyroid HormonesFluorocarbonsIodide PeroxidasePrealbuminThyroid HormonesAdverse outcome pathwaysMolecular initiating eventPerfluorinatedPrioritizationScreeningThyroid

Identifiers

PMID38072180
PMCPMC11081714
OpenAlexW4389515031

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.