Coupling Data Mining and Laboratory Experiments to Discover Drug Interactions Causing QT Prolongation

被引:64
作者
Lorberbaum, Tal [1 ,2 ]
Sampson, Kevin J. [3 ]
Chang, Jeremy B. [2 ]
Iyer, Vivek [4 ]
Woosley, Raymond L. [5 ]
Kass, Robert S. [3 ]
Tatonetti, Nicholas P. [2 ]
机构
[1] Columbia Univ, Dept Physiol & Cellular Biophys, New York, NY USA
[2] Columbia Univ, Dept Biomed Informat, 622 West 168th St,PH20, New York, NY 10032 USA
[3] Columbia Univ, Dept Pharmacol, New York, NY USA
[4] Columbia Univ, Dept Cardiol, New York, NY USA
[5] Azcert Inc, Oro Valley, AZ USA
基金
美国国家卫生研究院;
关键词
data mining; data science; drug-drug interaction; long QT syndrome; INTERVAL; LANSOPRAZOLE; SCIENCE;
D O I
10.1016/j.jacc.2016.07.761
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND QT interval-prolonging drug-drug interactions (QT-DDIs) may increase the risk of life-threatening arrhythmia. Despite guidelines for testing from regulatory agencies, these interactions are usually discovered after drugs are marketed and may go undiscovered for years. OBJECTIVES Using a combination of adverse event reports, electronic health records (EHR), and laboratory experiments, the goal of this study was to develop a data-driven pipeline for discovering QT-DDIs. METHODS 1.8 million adverse event reports were mined for signals indicating a QT-DDI. Using 1.6 million electrocardiogram results from 380,000 patients in our institutional EHR, these putative interactions were either refuted or corroborated. In the laboratory, we used patch-clamp electrophysiology to measure the human ether-a-go-go-related gene (hERG) channel block (the primary mechanism by which drugs prolong the QT interval) to evaluate our top candidate. RESULTS Both direct and indirect signals in the adverse event reports provided evidence that the combination of ceftriaxone (a cephalosporin antibiotic) and lansoprazole (a proton-pump inhibitor) will prolong the QT interval. In the EHR, we found that patients taking both ceftriaxone and lansoprazole had significantly longer QTc intervals (up to 12ms in white men) and were 1.4 times more likely to have a QTc interval above 500 ms. In the laboratory, we found that, in combination and at clinically relevant concentrations, these drugs blocked the hERG channel. As a negative control, we evaluated the combination of lansoprazole and cefuroxime (another cephalosporin), which lacked evidence of an interaction in the adverse event reports. We found no significant effect of this pair in either the EHR or in the electrophysiology experiments. Class effect analyses suggested this interaction was specific to lansoprazole combined with ceftriaxone but not with other cephalosporins. CONCLUSIONS Coupling data mining and laboratory experiments is an efficient method for identifying QT-DDIs. Combination therapy of ceftriaxone and lansoprazole is associated with increased risk of acquired long QT syndrome. (C) 2016 by the American College of Cardiology Foundation.
引用
收藏
页码:1756 / 1764
页数:9
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