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Determination of the Potential of Drug Candidates to Cause Severe Skin Disorders Using Computational Modeling

机译:使用计算模型确定可能导致严重皮肤疾病的候选药物

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摘要

Efficient and accurate prediction for drugs' potential to cause rare and severe adverse drug reactions (ADRs) is needed to facilitate the evaluation of risk-benefit ratio of drug candidates during drug development. Severe skin disorders like the Stevens Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN), which are life-threatening dermatological conditions, are such ADRs that have not received sufficient attention so far. In this study, a total of 1127 marketed drugs were screened for their potential to cause SJS/TEN, of which 255 were found to cause SJS/TEN and 239 were unlikely to cause SJS/TEN. One-class classification method was used to develop multiple prediction models. An applicability domain was determined to define the applicability of the model. Ensemble method was used to develop ensemble models to improve prediction ability. The final ensemble model achieved a sensitivity and specificity of 81 % and 67.4%, respectively, when estimated using the external 5-fold cross validation method, and a sensitivity of 66.7% when assessed using an external positive set. The results suggest the methods used in this study are potentially useful for facilitating the prediction of rare and severe ADRs.
机译:需要有效,准确地预测药物引起罕见和严重不良药物反应(ADR)的潜力,以帮助评估药物开发过程中候选药物的风险收益比。严重的皮肤疾病,如史蒂文森·约翰逊综合症(SJS)和有毒的表皮坏死溶解症(TEN),是威胁生命的皮肤病,是迄今为止尚未引起足够重视的这类ADR。在这项研究中,总共筛选了1127种市售药物引起SJS / TEN的潜力,其中发现255种引起SJS / TEN,而239种不太可能引起SJS / TEN。一类分类方法用于开发多个预测模型。确定适用性域以定义模型的适用性。使用集成方法开发集成模型以提高预测能力。最终的集成模型在使用外部5倍交叉验证方法进行评估时,分别达到81%和67.4%的灵敏度和特异性,而在使用外部阳性结果进行评估时,达到66.7%的灵敏度。结果表明,本研究中使用的方法可能有助于简化罕见和严重ADR的预测。

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