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Calculation of QT shift in non clinical safety pharmacology studies.

机译:非临床安全药理研究中QT偏移的计算。

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INTRODUCTION: Drug-induced QT interval prolongation is a major concern in new drug candidate development. This study presents a method of assessment of drug-induced QT interval prolongation without need for QT correction in conscious Beagle dogs and Cynomolgus monkeys monitored by telemetry. Accuracy and reliability are analysed by comparison with a reference QT correction method (Holzgrefe) from experiments performed with reference substances terfenadine, thioridazine and sotalol. METHODS: The QT shift method principle is assessment of any drug-induced QT interval shift directly from the individual QT/RR relationship. The individual QT/RR relationship is built from a treatment-free 24-hour recording period. QT and RR intervals are determined from a beat-to-beat analysis. A probabilistic method is used to define the individual QT/RR relationships. Checks were performed to compare results obtained with the QT shift method and the QT correction methods. The robustness of the QT shift method was tested under various conditions of drug-induced heart rate change (i.e. normal, bradycardia and tachycardia). RESULTS: The extent of agreement with the used reference QT correction method, Holzgrefe formula, was excellent (3-4 ms) in both animal species under the various drug induced effects on heart rate. The statistical sensitivity threshold for detection of QT prolongation according to a standard safety pharmacology study design was 7-8 ms. DISCUSSION: When combined with the probabilistic determination of individual QT/RR relationships, this simple method provides a direct assessment of a drug-induced effect on QT interval, without any curve fitting or application of correction formula. Despite noticeably different shapes in QT/RR relationships, the QT shift method is applicable to both Beagle dogs and Cynomolgus monkeys. It is likely that the QT shift method will be particularly helpful in problematic cases, enabling detection of drug-induced prolongation of less than 10 ms.
机译:简介:药物诱导的QT间隔延长是新药候选药物开发中的主要关注点。这项研究提出了一种评估遥测监测的有意识的比格犬和食蟹猴不需要QT校正的药物诱导的QT间隔延长的方法。通过与参考QT校正方法(Holzgrefe)进行比较,分析了准确性和可靠性,该方法来自参考物质​​特非那定,硫代哒嗪和索他洛尔的实验。方法:QT移位方法原理是直接根据个体QT / RR关系评估任何药物引起的QT间隔移位。单独的QT / RR关系是从24小时无治疗记录期开始的。 QT和RR间隔是根据心跳分析确定的。概率方法用于定义各个QT / RR关系。进行检查以比较使用QT偏移方法和QT校正方法获得的结果。在药物引起的心率变化的各种条件下(即正常,心动过缓和心动过速)测试了QT移位方法的鲁棒性。结果:在各种药物诱发的心率影响下,两种动物中与参考的QT校正方法Holzgrefe公式的吻合程度极佳(3-4毫秒)。根据标准安全药理研究设计,检测QT延长的统计学敏感性阈值为7-8 ms。讨论:当与单个QT / RR关系的概率确定相结合时,这种简单的方法可以直接评估药物对QT间隔的影响,而无需任何曲线拟合或应用校正公式。尽管QT / RR关系的形状明显不同,但QT漂移方法适用于比格犬和食蟹猴。 QT移位方法在有问题的情况下可能特别有用,可以检测到小于10毫秒的药物诱导的延长。

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