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DICTrank: The largest reference list of 1318 human drugs ranked by risk of drug-induced cardiotoxicity using FDA labeling.
Qu, Yanyan; Li, Ting; Liu, Zhichao; Li, Dongying; Tong, Weida.
Afiliação
  • Qu Y; National Center for Toxicological Research, US Food and Drug Administration, Jefferson, AR, USA; University of Arkansas at Little Rock and University of Arkansas for Medical Sciences Joint Bioinformatics Program, Little Rock, AR, USA.
  • Li T; National Center for Toxicological Research, US Food and Drug Administration, Jefferson, AR, USA.
  • Liu Z; National Center for Toxicological Research, US Food and Drug Administration, Jefferson, AR, USA.
  • Li D; National Center for Toxicological Research, US Food and Drug Administration, Jefferson, AR, USA. Electronic address: Dongying.Li@fda.hhs.gov.
  • Tong W; National Center for Toxicological Research, US Food and Drug Administration, Jefferson, AR, USA. Electronic address: Weida.Tong@fda.hhs.gov.
Drug Discov Today ; 28(11): 103770, 2023 Nov.
Article em En | MEDLINE | ID: mdl-37714406
Drug-induced cardiotoxicity (DICT) is a leading cause of drug trial failure and discontinuation. Current drug annotations for cardiotoxicity largely focus on individual outcomes or mechanisms. Considering the broad spectrum of adverse cardiac events, we developed Drug-Induced Cardiotoxicity Rank (DICTrank) using FDA labeling and comprehensively classified 1318 human drugs into four categories: Most-DICT-Concern (n = 341), Less-DICT-Concern (n = 528), No-DICT-Concern (n = 343), and Ambiguous-DICT-Concern (n = 106). Notably, DICTrank covers diverse therapeutic categories, of which several were enriched with Most-DICT-Concern drugs, such as antineoplastic agents, sex hormones, anti-inflammatory drugs, beta-blockers, and cardiac therapy. DICTrank currently presents the largest drug list of DICT annotation, and it could contribute to the development of new approach methods, including AI models for early identification of DICT risk during drug development and beyond.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cardiotoxicidade / Antineoplásicos Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cardiotoxicidade / Antineoplásicos Idioma: En Ano de publicação: 2023 Tipo de documento: Article