Evidence map›Paper›PMID 40114338›Full record

ArticleExperimental dermatology2025

Effects of Emissions From Oriented Strand Board on the Development of Atopic Dermatitis Using Two Different Experimental Mouse Models.

Evelyn Schneider, Katja Butter, Benjamin Schnautz, Stephanie Musiol, Johanna Grosch, Sonja Schindela, Manuel Garcia-Käufer, Richard Gminski, Stefan Haak, Martin Ohlmeyer and 4 more

Abstract read
In one paragraph

Article in Experimental dermatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

14 authors.

Evelyn SchneiderCenter of Allergy and Environment (ZAUM), Technical University of Munich (TUM) and Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
Katja ButterThünen Institute of Wood Research, Hamburg, Germany.
Benjamin SchnautzCenter of Allergy and Environment (ZAUM), Technical University of Munich (TUM) and Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
Stephanie MusiolCenter of Allergy and Environment (ZAUM), Technical University of Munich (TUM) and Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
Johanna GroschCenter of Allergy and Environment (ZAUM), Technical University of Munich (TUM) and Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
Sonja SchindelaCenter of Allergy and Environment (ZAUM), Technical University of Munich (TUM) and Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
Manuel Garcia-KäuferInstitute for Infection Prevention and Control, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Richard GminskiInstitute for Infection Prevention and Control, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Stefan HaakCenter of Allergy and Environment (ZAUM), Technical University of Munich (TUM) and Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
Martin OhlmeyerThünen Institute of Wood Research, Hamburg, Germany.
Carsten B Schmidt-WeberCenter of Allergy and Environment (ZAUM), Technical University of Munich (TUM) and Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
Stefanie EyerichCenter of Allergy and Environment (ZAUM), Technical University of Munich (TUM) and Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
Julia Esser-von BierenCenter of Allergy and Environment (ZAUM), Technical University of Munich (TUM) and Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
Francesca AlessandriniCenter of Allergy and Environment (ZAUM), Technical University of Munich (TUM) and Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.ORCID https://orcid.org/0000-0002-9854-8968

Funding

Bundesministerium für Ernährung und Landwirtschaft
6 · The paper itself

Abstract

Atopic dermatitis (AD) is an allergic skin disease widespread in children, which later in life can predispose them to asthma. Oriented strand board (OSB), increasingly used in the construction industry, emits volatile organic compounds in the indoor air, some of which may exacerbate AD development in humans. The aim of this study was to evaluate the effects of OSB emissions on the development of AD and lung inflammation. Two different murine AD models, induced by calcipotriol or oxazolone, were exposed to higher- or lower-emitting OSB throughout the experiments. Physiological, biochemical, and immunological parameters of skin disease development, as well as lung inflammatory parameters, were evaluated. Exposure to higher-emitting OSB, characterised especially by high 3-carene emissions, exacerbated some parameters of AD, such as skin barrier function and thickness, with accumulation of eosinophils and 15-lipoxygenase (15-LOX)-driven mediators in both models, whereas IL-4 or 5-LOX-positive cells were increased in only the calcipotriol or oxazolone model, respectively. In the lungs of calcipotriol-treated mice, higher-emitting OSB increased lung eosinophil recruitment. Exposure to lower-emitting OSB had no or even beneficial effects on the skin or lungs of murine AD models. 3-carene in OSB emissions, alone or in combination with other substances, may promote the development of AD and prime the lungs towards an allergic phenotype. Identification and quantification of potentially harmful emitting sources in indoor air may be important for AD prevention or control.

Indexed as

AsthmaConstruction MaterialsDermatitis, AtopicVolatile Organic CompoundsAnimalsBicyclic MonoterpenesCalcitriolDisease Models, AnimalEosinophilsHumansLipid MetabolismMiceOxazolone3-careneBicyclic MonoterpenescalcipotrieneCalcitriolOxazoloneVolatile Organic Compoundsatopic dermatitisatopic marchinflammationlipid mediatorsmouse modelsoriented strand boardvolatile organic compounds

Identifiers

PMID40114338
PMCPMC11926298

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Registered trials

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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.