Prediction of clinically relevant drug-induced liver injury from structure using machine learning

被引:32
作者
Hammann, Felix [1 ]
Schoning, Verena [1 ]
Drewe, Jurgen [1 ]
机构
[1] Univ Hosp Basel, Div Clin Pharmacol & Toxicol, Schanzenstr 55, CH-4031 Basel, Switzerland
关键词
drug-induced liver injury; hepatotoxicity; machine learning; network analysis; structure-activity relationships; CAUSALITY ASSESSMENT; CYTOCHROME-P450; 3A; ADVERSE REACTIONS; ORAL MEDICATIONS; POTENTIAL ROLE; HEPATOTOXICITY; PHARMACOGENOMICS; LIPOPHILICITY; TRANSPORTERS; CHOLESTASIS;
D O I
10.1002/jat.3741
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Drug-induced liver injury (DILI) is the most common cause of acute liver failure and often responsible for drug withdrawals from the market. Clinical manifestations vary, and toxicity may or may not appear dose-dependent. We present several machine-learning models (decision tree induction, k-nearest neighbor, support vector machines, artificial neural networks) for the prediction of clinically relevant DILI based solely on drug structure, with data taken from published DILI cases. Our models achieved corrected classification rates of up to 89%. We also studied the association of a drug's interaction with carriers, enzymes and transporters, and the relationship of defined daily doses with hepatotoxicity. The results presented here are useful as a screening tool both in a clinical setting in the assessment of DILI as well as in the early stages of drug development to rule out potentially hepatotoxic candidates.
引用
收藏
页码:412 / 419
页数:8
相关论文
共 50 条
[1]   Antiepileptic drugs and liver disease [J].
Ahmed, SN ;
Siddiqi, ZA .
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2006, 15 (03) :156-164
[2]   Human Drug-Induced Liver Injury Severity Is Highly Associated With Dual Inhibition of Liver Mitochondrial Function and Bile Salt Export Pump [J].
Aleo, Michael D. ;
Luo, Yi ;
Swiss, Rachel ;
Bonin, Paul D. ;
Potter, David M. ;
Will, Yvonne .
HEPATOLOGY, 2014, 60 (03) :1015-1022
[3]  
Barysz M., 1983, Chemical Application of Topology Graph theory, P222
[4]   COMPARATIVE-STUDY OF LIPOPHILICITY VERSUS TOPOLOGICAL MOLECULAR DESCRIPTORS IN BIOLOGICAL CORRELATIONS [J].
BASAK, SC ;
HARRISS, DK ;
MAGNUSON, VR .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1984, 73 (04) :429-437
[5]   CAUSALITY ASSESSMENT OF ADVERSE REACTIONS TO DRUGS .2. AN ORIGINAL MODEL FOR VALIDATION OF DRUG CAUSALITY ASSESSMENT METHODS - CASE-REPORTS WITH POSITIVE RECHALLENGE [J].
BENICHOU, C ;
DANAN, G ;
FLAHAULT, A .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 1993, 46 (11) :1331-1336
[6]   Lipid-Metabolizing CYPs in the Regulation and Dysregulation of Metabolism [J].
Bishop-Bailey, David ;
Thomson, Scott ;
Askari, Ara ;
Faulkner, Ashton ;
Wheeler-Jones, Caroline .
ANNUAL REVIEW OF NUTRITION, VOL 34, 2014, 34 :261-279
[7]   Mechanisms of isoniazid-induced idiosyncratic liver injury: Emerging role of mitochondrial stress [J].
Boelsterli, Urs A. ;
Lee, Kang Kwang .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2014, 29 (04) :678-687
[8]   MOLECULAR-IDENTIFICATION NUMBER FOR SUBSTRUCTURE SEARCHES [J].
BURDEN, FR .
JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES, 1989, 29 (03) :225-227
[9]   Elevated hepatic multidrug resistance-associated protein 3/ATP-binding cassette subfamily C 3 expression in human obstructive cholestasis is mediated through tumor necrosis factor alpha and c-Jun NH2-terminal kinase/stress-activated protein kinase-signaling pathway [J].
Chai, Jin ;
He, Yu ;
Cai, Shi-Ying ;
Jiang, Zhongyong ;
Wang, Huaizhi ;
Li, Qiong ;
Chen, Lei ;
Peng, Zhihong ;
He, Xiaochong ;
Wu, Xiaoping ;
Xiao, Tianli ;
Wang, Rongquan ;
Boyer, James L. ;
Chen, Wensheng .
HEPATOLOGY, 2012, 55 (05) :1485-1494
[10]   Drug-induced liver injury: what was new in 2013? [J].
Chalhoub, Walid M. ;
Sliman, Kayla D. ;
Arumuganathan, Meera ;
Lewis, James H. .
EXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY, 2014, 10 (07) :959-980