Evaluating clinical case report data for SAR modeling of allergic contact dermatitis

1996 ◽  
Vol 15 (6) ◽  
pp. 489-493 ◽  
Author(s):  
Robert Gealy ◽  
Cynthia Graham ◽  
Nancy B Sussman ◽  
Orest T Macina ◽  
Herbert S Rosenkranz ◽  
...  

Clinical case reports can be important sources of information for alerting health professionals to the existence of possible health hazards. Isolated case reports, however, are weak evidence of causal relationships between exposure and disease because they do not provide an indication of the frequency of a particular exposure leading to a disease event. A database of chemicals causing allergic contact dermatitis (ACD) was compiled to discern structure-activity relationships. Clinical reports repre sented a considerable fraction of the data. Multiple Computer Automated Structure Evaluation (MultiCASE) was used to create a structure-activity model to be used in predicting the ACD activity of untested chemicals. We examined how the predictive ability of the model was influenced by including the case report data in the model. In addition, the model was used to predict the activity of chemicals identified from clinical case reports. The following results were obtained: • When chemicals which were identified as dermal sensitizers by only one or two case reports were included in the model, the specificity of the model was reduced. • Less than one half of these chemicals were predicted to be active by the most highly evidenced model. • These chemicals possessed substructures not pre viously encountered by any of the models. We conclude that chemicals classified as sensitizers based on isolated clinical case reports be excluded from our model of ACD. The approach described here for evaluating activity of chemicals based on sparse evidence should be considered for use with other endpoints of toxicity when data are correspondingly limited.

2021 ◽  
Vol 7 (2) ◽  
pp. 16100-16106
Author(s):  
Cynthia Vitória Lopes da Fonsêca ◽  
Elba Soraya Magalhães da Luz ◽  
Walfrido José B. da Costa Neto ◽  
Gabriela Pinho de Alcântara ◽  
Letícia Maria Silva Soares ◽  
...  

2018 ◽  
Vol 78 (3) ◽  
pp. 228-229 ◽  
Author(s):  
Austin Jiang ◽  
Joel C. Harrison ◽  
Paul D. Siegel ◽  
Howard Maibach

2003 ◽  
Vol 31 (4) ◽  
pp. 393-399
Author(s):  
Herbert S. Rosenkranz

The increased acceptance of the use of structure–activity relationship (SAR) approaches to toxicity modelling has necessitated an evaluation of the limitations of the methodology. In this study, the limit of the capacity of the MULTICASE SAR program to model complex biological and toxicological phenomena was assessed. It was estimated that, provided the data set consists of at least 300 chemicals, divided equally between active and inactive compounds, the program is capable of handling phenomena that are even more “complex” than those modelled up to now (for example, allergic contact dermatitis, Salmonella mutagenicity, biodegradability, inhibition of tubulin polymerisation). However, within the data sets currently used to generate SAR models, there are limits to the complexity that can be handled. This may be the situation with regard to the modelling of systemic toxicity (for example, the LD50).


Sign in / Sign up

Export Citation Format

Share Document