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评估用于过敏性接触性皮炎结构-活性关系建模的临床病例报告数据。

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

作者信息

Gealy R, Graham C, Sussman N B, Macina O T, Rosenkranz H S, Karol M H

机构信息

Department of Environmental and Occupational Health, University of Pittsburgh, Pennsylvania 15238, USA.

出版信息

Hum Exp Toxicol. 1996 Jun;15(6):489-93. doi: 10.1177/096032719601500605.

Abstract

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 represented 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 previously 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.

摘要

临床病例报告可能是向卫生专业人员警示潜在健康危害存在的重要信息来源。然而,孤立的病例报告对于暴露与疾病之间的因果关系而言是薄弱的证据,因为它们并未提供导致疾病事件的特定暴露频率的指示。为了识别结构 - 活性关系,编制了一个引起过敏性接触性皮炎(ACD)的化学物质数据库。临床报告占数据的相当一部分。使用多重计算机自动结构评估(MultiCASE)来创建一个结构 - 活性模型,用于预测未经测试的化学物质的ACD活性。我们研究了将病例报告数据纳入模型如何影响模型的预测能力。此外,该模型还用于预测从临床病例报告中识别出的化学物质的活性。获得了以下结果:当仅由一两个病例报告确定为皮肤致敏剂的化学物质被纳入模型时,模型的特异性降低。在这些化学物质中,不到一半被证据最充分的模型预测为有活性。这些化学物质具有任何模型以前都未遇到过的子结构。我们得出结论,基于孤立临床病例报告分类为致敏剂的化学物质应从我们的ACD模型中排除。当数据相应有限时,这里描述的基于稀疏证据评估化学物质活性的方法应考虑用于其他毒性终点。

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