Evidence map›Paper›PMID 32388570›Full record

ArticleALTEX2021

Evaluation of the global performance of eight in silico skin sensitization models using human data.

Emily Golden, Donna S Macmillan, Greg Dameron, Petra Kern, Thomas Hartung, Alexandra Maertens

Abstract read
In one paragraph

Article in ALTEX, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Development ofNAM journal · 2025
    Article
  8. AI: the Apollo guidance computer of the Exposome moonshot.Frontiers in artificial intelligence · 2025
    Article
  9. Article
  10. Article
  11. Use ofFrontiers in toxicology · 2024
    Article
  12. Article
  13. SkinSensPred as a Promising in Silico Tool for Integrated Testing Strategy on Skin Sensitization.International journal of environmental research and public health · 2022
    Article
  14. PreS/MD: Predictor of Sensitization Hazard for Chemical Substances Released From Medical Devices.Toxicological sciences : an official journal of the Society of Toxicology · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. Frontiers in pharmacology · 2021
    Review
  19. 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

6 authors.

Emily GoldenCenter for Alternatives to Animal Testing (CAAT), Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Donna S MacmillanLhasa Limited, Leeds, UK.
Greg DameronProcter & Gamble NV, Bever, Belgium.
Petra KernProcter & Gamble NV, Bever, Belgium.
Thomas HartungCenter for Alternatives to Animal Testing (CAAT), Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Alexandra MaertensCenter for Alternatives to Animal Testing (CAAT), Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.

Funding

Traning Program in Environmental Health SciencesT32ES007141 · NIEHS · JOHNS HOPKINS UNIVERSITY · PI Marsha Wills-Karp · 1985 to 2026
$22.2M
NIEHS NIH HHS T32 ES007141
6 · The paper itself

Abstract

Allergic contact dermatitis, or the clinical manifestation of skin sensitization, is a leading occupational hazard. Several testing approaches exist to assess skin sensitization, but in silico models are perhaps the most advantageous due to their high speed and low-cost results. Many in silico skin sensitization models exist, though many have only been tested against results from animal studies (e.g., LLNA); this creates uncertainty in human skin sensitization assessments in both a screening and regulatory context. This project’s aim was to evaluate the accuracy of eight in silico skin sensitization models against two human data sets: one highly curated (Basketter et al., 2014) and one screening level (HSDB). The binary skin sen­sitization status of each chemical in each of the two data sets was compared to the prediction from eight in silico skin sensitization tools (Toxtree, PredSkin, OECD’s QSAR Toolbox, UL’s REACHAcross™, Danish QSAR Database, TIMES-SS, and Lhasa Limited’s Derek Nexus). Models were assessed for coverage, accuracy, sensitivity, and specificity, as well as optimization features (e.g., probability of accuracy, applicability domain, etc.), if available. While there was a wide range of sensitivity and specificity, the models generally performed comparably to the LLNA in predicting human skin sensitization status (i.e., approximately 70-80% accuracy). Additionally, the models did not mispredict the same com­pounds, suggesting there might be an advantage in combining models. In silico skin sensitization models offer accurate and useful insights in a screening context; however, further improvements are necessary so these models may be con­sidered fully reliable for regulatory applications.

Indexed as

Computer SimulationModels, BiologicalAnimalsAnimal Testing AlternativesDermatitis, ContactHumansQSARread-acrossskin sensitizationstructural alerts

Identifiers

PMID32388570
PMCPMC11316520

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.